Epidemiology of Clinical Sporotrichosis in the Americas in the Last Ten Years

Hernández-Castro, Rigoberto; Pinto-Almazán, Rodolfo; Arenas, Roberto; Sánchez-Cárdenas, Carlos Daniel; Espinosa-Hernández, Víctor Manuel; Sierra-Maeda, Karla Yaeko; Conde-Cuevas, Esther; Juárez-Durán, Eder R.; Xicohtencatl-Cortes, Juan; Carrillo-Casas, Erika Margarita; Steven-Velásquez, Jimmy; Martínez-Herrera, Erick; Rodríguez-Cerdeira, Carmen

doi:10.3390/jof8060588

Open AccessReview

Epidemiology of Clinical Sporotrichosis in the Americas in the Last Ten Years

by

Rigoberto Hernández-Castro

^1,†

,

Rodolfo Pinto-Almazán

^2,3,†

,

Roberto Arenas

^4,5,†

,

Carlos Daniel Sánchez-Cárdenas

⁶,

Víctor Manuel Espinosa-Hernández

⁷,

Karla Yaeko Sierra-Maeda

¹,

Esther Conde-Cuevas

⁷,

Eder R. Juárez-Durán

⁴

,

Juan Xicohtencatl-Cortes

⁸

,

Erika Margarita Carrillo-Casas

⁹,

Jimmy Steven-Velásquez

¹⁰

,

Erick Martínez-Herrera

^2,5,*

and

Carmen Rodríguez-Cerdeira

^5,11,12,*

¹

Departamento de Ecología de Agentes Patógenos, Hospital General “Dr. Manuel Gea González”, Ciudad de México 14080, Mexico

²

Sección de Estudios de Posgrado e Investigación, Escuela Superior de Medicina, Instituto Politécnico Nacional, Plan de San Luis y Díaz Mirón, Ciudad de México 11340, Mexico

³

Noncommunicable Diseases Research Group, Universidad La Salle-México, Benjamín Franklin 45, Mexico City 06140, Mexico

⁴

Sección de Micología, Hospital General “Dr. Manuel Gea González”, Tlalpan, Ciudad de México 14080, Mexico

⁵

Efficiency, Quality, and Costs in Health Services Research Group (EFISALUD), Galicia Sur Health Research Institute (IIS Galicia Sur), SERGAS-UVIGO, 36213 Vigo, Spain

⁶

Servicio de Dermatología, Centro Médico Nacional La Raza, Paseo de las Jacarandas S/N, La Raza, Azcapotzalco, Ciudad de México 02990, Mexico

⁷

Maestría en Ciencias de la Salud, Escuela Superior de Medicina, Instituto Politécnico Nacional, Plan de San Luis y Díaz Mirón, Ciudad de México 11340, Mexico

⁸

Laboratorio de Bacteriología Intestinal, Hospital Infantil de México “Dr. Federico Gómez”, Ciudad de México 06720, Mexico

⁹

Departamento de Biología Molecular e Histocompatibilidad, Hospital General “Dr. Manuel Gea González”, Tlalpan, Ciudad de México 14080, Mexico

¹⁰

Hospital General San Juan de Dios, 1ra Avenida “A” 10-50, zona 1, Ciudad de Guatemala 01001, Guatemala

¹¹

Dermatology Department, Hospital Vithas Vigo and University of Vigo, 36206 Vigo, Spain

¹²

Campus Universitario, University of Vigo, 36310 Vigo, Spain

Show full affiliation list

Hide full affiliation list

^*

Authors to whom correspondence should be addressed.

^†

These authors contributed equally to this work.

J. Fungi 2022, 8(6), 588; https://doi.org/10.3390/jof8060588

Submission received: 14 April 2022 / Revised: 24 May 2022 / Accepted: 24 May 2022 / Published: 30 May 2022

(This article belongs to the Special Issue Sporothrix and Sporotrichosis 2.0)

Download

Browse Figures

Review Reports Versions Notes

Abstract

:

Background: Sporotrichosis is a fungal infection caused by species of the Sporothrix genus. Presently, the prevalence of sporotrichosis in the Americas is unknown, so this study aims to analyze the cases reported in the past 10 years. Methods: An advanced search was conducted from 2012 to 2022 in English and Spanish in PUBMED, SciELO, and Cochrane, with the terms: “sporotrichosis”, “lymphocutaneous sporotrichosis”, “fixed sporotrichosis”, “mycosis”, “Sporothrix spp.”, “Sporothrix complex”, “S. schenckii sensu stricto”, “S. schenckii sensu lato”, “S. globose”, “S. brasiliensis”, “S. luriei”. Sporotrichosis is a fungal infection caused by species of the Sporothrix genus associated with “pathogenicity” or “epidemiology”. Results: A total of 124 articles were found in the Americas, corresponding to 12,568 patients. Of these, 87.38% of cases were reported in South America, 11.62% in North America, and 1.00% in Central America and the Caribbean. Brazil, Peru, and Mexico had the highest number of cases. The most prevalent etiological agents were S. schenckii complex/Sporothrix spp. (52.91%), S. schenckii (42.38%), others (4.68%), and Not Determined (ND) (0.03%). The most frequent form of the disease was lymphocutaneous infection; however, the infection type was not determined in 5639 cases. Among the diagnostic methods, culture was the most used. Conclusions: There is a high occurrence of cases reported in the literature. South America is the region with the highest number of reports because of its environment (climate, inhalation of spores, etc.), zoonotic transmission (scratches and sneezes from contaminated animals), and possible traumatic inoculation due to outdoor activities (agriculture, gardening, and related occupations). Molecular diagnosis has not been sufficiently developed due to its high cost.

Keywords:

sporotrichosis; Sporothrix schenckii sensu stricto; Sporothrixschenckii complex; lymphocutaneous sporotrichosis; fixed cutaneous sporotrichosis; disseminated sporotrichosis; the Americas

1. Introduction

Sporotrichosis is a fungal infection caused by thermo-dimorphic fungi species of the Sporothrix genus. Previously, the classification of the species of sporotrichosis was conducted through the classification of the Sporothrix schenckii complex, which included Sporothrix schenckii sensu stricto, Sporothrix brasiliensis (S. brasiliensis), Sporothrix globosa (S. globosa), Sporothrix luriei (S. lurieri), Sporothrix pallida (S. pallida), Sporothrix mexicana (S. mexicana), and Sporothrix chilensis (S. chilensis) [1,2]. However, since 2016, the taxonomical classification of Sporothrix has been changed into a clinical clade that includes Sporothrix schenckii, S. globosa, S. brasiliensis, and S. luriei. On some occasions, the species of the environmental clade, such as S. pallida, S. mexicana, and S. chilensis may cause infection upon contact with an individual [1,2,3,4]. The infections occur mainly cutaneously or subcutaneously with lymphatic involvement [1,2,3,4]. This infection has been considered the most frequent subcutaneous mycosis in Latin America [2]. Such infections can be difficult to diagnose with the naked eye since they can be similar to infiltrative or ulcerative lesions from vascular and inflammatory disorders [1,3].

For this subcutaneous infection to develop, a direct trauma must occur first. For example, inoculation occurs when the skin is punctured by plants with thorns, gardeners are a classic case of this. Also, inoculation can occur through fomites that contact contaminated soil. For instance, people who wear sandals can suffer trauma from stones, firewood, or thorns with fungal spores on their surface [2,3]. With all the above, it can be inferred that this type of fungal infection is associated with regions where the main livelihood is agriculture, that is, in environments where the climate is tropical and subtropical. Another form of transmission, which has been increasing in recent times in some regions of the continent such as Brazil, Argentina, Paraguay, and Panama, has been reported to result from scratches, bites, pecks, and stings from different animals [1,2,3,4].

There are several techniques for detecting sporotrichosis, including Sabouraud dextrose agar cultures, lactophenol blue or erythromycin staining, histopathological studies, and PCR sequencing, among others [5,6,7] (Figure 1).

As for the clinical forms of sporotrichosis, various types have been described, such as the lymphocutaneous, fixed cutaneous, and, as mentioned earlier, the disseminated or hematogenous forms where both organs and tissues can be affected [5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28]. The latter is the rarest because the recommended antifungal regimens are usually effective; however, in patients with alterations in cellular immunity, these infections can spread [2,3,4].

2. Materials and Methods

An advanced search was conducted in English and Spanish languages in the engines Medical Literature Analysis and Retrieval System Online (MEDLINE/PUBMED), Scientific Electronic Library Online (SciELO), and Cochrane Database. Because the systematic review was performed for the 10 last years (2012–2022), both taxonomical classifications were used. The applied terms were “sporotrichosis”, “lymphocutaneous sporotrichosis”, “fixed sporotrichosis”, “Sporothrix spp.” and “Sporothrix schenckii complex”, “S. schenckii sensu stricto”, and “S. schenckii sensu lato”, Sporothrix schenckii, (Sporothrix schenckii), Sporothrix brasiliensis (S. brasiliensis), Sporothrix globosa (S. globosa), Sporothrix luriei (S. lurieri), Sporothrix pallida (S. pallida), Sporothrix mexicana (S. mexicana), and Sporothrix chilensis (S. chilensis) associated with “pathogenicity” or “epidemiology”. The total number of articles found was 243. The review was performed based on the preferred reporting items for systematic reviews and meta-analyses (PRISMA) (Figure 2). After reading the titles and reviewing the complete text, the most relevant papers to develop this article were identified. At the end of the selection process, 127 articles were chosen. The review was performed based on the preferred reporting items for systematic reviews and meta-analyses (PRISMA).

3. Epidemiology of Sporotrichosis in North America

A total of 48 publications related to sporotrichosis were found in North America [5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52]. There were 1460 patients in total associated with infection caused by species of the genus Sporothrix. According to the previous classification, it was found that in Canada, only two case reports were found, one from Ontario and the other from Toronto [5,6]. In the US, 27 reports containing 1 clinical case were found (81.5% S. schenckii, 18.5% Sporothrix spp., S. schenckii complex, and S. schenckii sensu lato) [7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33]. Of these, seven cases came from California, three from Oklahoma, two cases from Kansas, Texas, Arizona, Minnesota, and Florida, one case from Michigan, Nebraska, Oregon, Pennsylvania, and finally, one case without a specific city or region. In Mexico, there were 19 reports registered with 1431 reported cases (84.7% Sporothrix spp., 14.47% S. schenckii, 0.55% S. globosa, 0.21% S. schenckii sensu stricto, 0.07% S. mexicana) [34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52]. Jalisco reported 1060 cases, Guerrero 150, Nayarit 23, Zacatecas 21, Michoacan 20, Guanajuato 14, Oaxaca 9, Puebla, and San Luis Potosí 8 each, Mexico City 6, Chihuahua, Nuevo León, Querétaro, and Veracruz 2 each, Baja California, Durango, State of Mexico, and Morelos 1 each, and 99 cases were reported with an unspecified city (Table 1). When classifying according to the current taxonomy [1,2,3,4], we can mention that in Canada, 50% of the sporotrichosis was due to S. schenckii and 50% to Sporothrix spp. [5,6]. In the US, it was reported that Sporothrix spp. (85.19%) and S. schenckii (14.81%) were responsible for this pathology [7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33]. Finally, in Mexico, 85.05% were due to Sporothrix spp., 14.33% S. schenckii, 0.55% S. globosa, and 0.07% S. mexicana [34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52].

The most frequent variety reported was lymphocutaneous with 956 cases, followed by fixed cutaneous with 388 cases, and the disseminated form with 83 [5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52]. A lymphocutaneous presentation evolved into a disseminated after 10 months. The least frequent varieties were the disseminated cutaneous with 16 cases, disseminated cutaneous with affected mucous membranes and arthritis with 3 cases each, and the pulmonary form with 2 cases. Finally, lymphadenitis, meningitis, laryngotracheal joint, visceral fungemia, visceral infection associated with fungemia, an atypical presentation, and a visceral presentation with fungemia and mucosal involvement were only reported in one case each. The most common reported etiological agent with the new taxonomical classification was Sporothrix spp. with 85.00% (1241/1460), followed by S. schenckii with 14.38% (210/1460), S. globosa with 0.54% (8/1460), and S. mexicana with 0.068% (1/1460) [5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52].

In terms of the diagnosis, fungal culture was the most frequently used diagnostic methodology with 33/48, followed by histopathological examination with 20/48. It is worth noting that the histopathological examination was always accompanied by fungal cultures. PCR sequencing was the third method used in 11/48 studies. For this diagnostic tool, the Calmodulin gene was used in 7 cases, the ITS1-2 region in 3 cases, and an unspecified gene in 1 case. Also, the MALDI-TOF and the agglutination latex test were used for diagnosis in two reports. Finally, the use of the Sporotrichin Skin Test and physical examination was mentioned in one report, and one case was reported without describing the employed diagnostic method [5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52].

4. Epidemiology of Sporotrichosis in Central America and the Caribbean

Only 8 publications with 126 cases of sporotrichosis were found in Central America and the Caribbean [53,54,55,56,57,58,59,60]. In the only article found from Costa Rica during the search period, 57 isolates were analyzed in San José, finding the presence of 2 species: S. schenckii sensu stricto (93%), S. brasiliensis (3.5%), and Sporothix spp. (3.5%) [53]. On the other hand, there were 3 reports in Guatemala with 65 cases (98.5% Sporothrix spp. and 1.5% S. schenckii sensu stricto), with all cases being from Guatemala City [54,55,56]. Finally, reports of a single case were found in Honduras (Tegucigalpa); the agent responsible for the infection was S. schenckii, and in Panama (Correa District), the agent was not determined [57,58]. In the Caribbean, only two reports of S. schenckii sensu lato from Cuba were found [59,60]. Regarding the new taxonomic classification, it was determined that in Costa Rica, 93% of the cases were caused by S. schenckii, 3.5% by S. brasiliensis, and 3.5% by Sporothix spp. [53]. Meanwhile, in Guatemala, the main pathogenic agent was Sporothrix spp. with 98.5% and S. schenckii with 1.5% [54,55,56]. In Honduras and Panama, it was observed that the agent Sporothrix spp. was responsible for sporotrichosis, with one case per country (100%) [57,58]. In Cuba, there were two reports of a case due to Sporothrix spp., which represents 100% [59,60].

The most frequently reported form was lymphocutaneous with 39 cases (30.95%), followed by fixed cutaneous with 26 (20.63%), the disseminated form with 2 (1.59%), 1 case of chancre (0.79%), and 58 ND cases (46.03%) [53,54,55,56,57,58,59,60]. The most common etiological agents noted were Sporothrix spp. with 55.56% (70/126), S. schenckii with 42.85% (54/126), and S. brasiliensis with 1.59% (2/126) [53,54,55,56,57,58,59,60].

Regarding diagnosis, fungal culture was used as a diagnostic method in all articles (8/8), followed by histopathological examination (5/8). In this case, also, the histopathological examination was always accompanied by fungal cultures. PCR sequencing (2/8) employing the calmodulin gene in one article and the ITS1-2 region in the other was also used as a diagnostic tool. Lastly, diagnosis with microscopy using lactophenol blue was mentioned in two reports (Table 2) [53,54,55,56,57,58,59,60].

5. Epidemiology of Sporotrichosis in South America

A total of 68 publications with 11,050 cases of sporotrichosis were found in South America [61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103,104,105,106,107,108,109,110,111,112,113,114,115,116,117,118,119,120,121,122,123,124,125,126,127,128,129,130,131]. Of these, 4 reports were found in Argentina during the analyzed period with 38 cases, of which 9 were caused by S. schenckii sensu stricto (23.68%), 26 by S. brasiliensis (68.52%), 1 by S. globosa (2.6%), 1 by S. schenckii (2.6%), and 1 by S. schenckii complex (2.6%) [61,62,63,64]. Brazil reported 42 articles with 5546 analyzed cases [65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103,104,105,106], identifying Sporothrix spp. and S. schenckii complex as the causative agent in 4906 cases (88.46%), S. schenckii in 302 (5.45%), S. brasiliensis in 125 (2.25%), Sporothrix sensu lato in 110 (1.98%), S. globosa plus S. schenckii in 91 cases (1.64%) Sporothrix sensu stricto in 5 (0.09%), S. globosa in 4 (0.07%), and S. mexicana in 3 (0.05%) during the studied period. In Colombia, 4 reports were found, adding up to 50 cases [56,107,108,109].S. Schenckii sensu stricto was identified in 22 cases (44.00%), Sporothrix spp. in 15 (30.00%), S. globosa in 12 (24.00%) and S. schenckii sensu lato in 1 (2.00%). Likewise, in Chile, 3 reported cases detected Sporothrix spp. in 1 (33.33%), S. globosa in 1 (33,33%), and Sporothrix pallida in 1 (33.33%) [110,111,112]. A total of 13 cases of Sporothrix spp. and S. schenckii complex (100%) were reported in Paraguay [113,114]. In Peru, from 4792 cases, S. schenckii was found in 4656 (97.16%), Sporothrix spp. and the Sporothrix complex in 116 (2.42%), S. schenkii sensu stricto in 19 (0.40%), and Sporothrix sensu lato in 1 (0.02%) [115,116,117,118,119,120,121,122,123]. There was 1 report of 157 cases of Sporothrix spp. (100%) found in Uruguay [124]. Finally, there were 4 reports from Venezuela with 452 cases of Sporothrix spp., and the Sporothrix complex was found in 220 of those cases (48.67%), S. schenckii sensu lato in 130 (28.76%), S. schenckii in 42 (9.29%), S. schenckii sensu stricto in 17 (3.76%), S. globosa in 39 (8.63%), 1 case of Ophiostoma stenoceras (0.22%) and 3 cases were ND (0.66%) [125,126,127,128].

Regarding the new taxonomic classification, in Argentina, 26.31% were S. schenckii, 68.42% S. brasiliensis, 2.63% S. globosa, and 2.63% Sporothrix spp. [61,62,63,64]. In Brazil, the main pathogenic agent was Sporothrix spp. with 95.56%, S. brasiliensis 2.25%, S. globosa plus S. schenckii 1.64%, S. schenckii 0.41%, S. globosa 0.07%, and S. mexicana 0.05% [65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103,104,105,106]. In Colombia, S. schenckii 44.00%, Sporothrix spp. 32.00%, and S. globosa 24.00% were the principal mycotic agents [56,107,108,109]. Regarding Chile, the pathogenic agents were Sporothrix spp., S. globose, and S. pallida (33.33% each) [110,111,112]. In Paraguay, the unique agent found was Sporothrix spp. (100%) [113,114]. For Peru, the most important pathogenic agents were Sporothrix spp. (99.54%), and S. schenckii (0.46%) [115,116,117,118,119,120,121,122,123]. In Uruguay, 100% of the cases were due to Sporothrix spp. (100%) [124]. In Venezuela, Sporothrix spp. (80.04%), S. schenckii (13.38%), and S. globose (6.57%) were the types of Sporothrix agents [125,126,127,128].

The most frequent types of disease were lymphocutaneous with 3293 cases (29.47%), fixed cutaneous with 1947 (17.43%), disseminated cutaneous with 34 (0.30%), systemic form with 18 (0.16%), and others with 177 cases (1.60%). However, there were 5702 cases (51.04%) with undetermined types from all the cases diagnosed as sporotrichosis [56,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103,104,105,106,107,108,109,110,111,112,113,114,115,116,117,118,119,120,121,122,123,124,125,126,127,128].

The most common reported etiological agent with the new taxonomical classification was Sporothrix spp. with 95.12% (10,511/11,050), followed by S. schenckii with 1.23% (136/11,050), S. brasiliensis with 2.27% (251/11,050), S. globosa plus S. schenckii with 0.82% (91/11,050), S. globosa with 0.52% (57/11,050), S. mexicana 0.027% (3/11,050), and S. pallida with 0.009% (1/11,050) [56,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103,104,105,106,107,108,109,110,111,112,113,114,115,116,117,118,119,120].

With reference to diagnosis, fungal culture was used as a diagnostic methodology in almost all articles (67/71), followed by PCR sequencing (26/71), where the calmodulin gene (15/23), the ITS 1-2 region (6/23), and other genes (15/23) were used. Other types of diagnoses (12/71) were applied, such as direct microscopy (19/71), histopathological examination, always accompanied by fungal culture (18/71), and microscopy with lactophenol blue (9/71) (Table 3).

6. Discussion

A total of 124 publications were found with reports related to sporotrichosis in the Americas in the last 10 years, with 12,636 patients associated with infection caused by species of the genus Sporothrix. Interestingly, it was observed that 87.45% (11,050) of these cases were reported in South America, 11.55% (1460) in North America, and 1.00% (126) in Central America and the Caribbean [5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103,104,105,106,107,108,109,110,111,112,113,114,115,116,117,118,119,120,121,122,123,124,125,126,127,128]. The countries that presented the highest number of cases during the analyzed period were Brazil (5546—43.89%), Peru (4792—37.92%), and Mexico (1431—11.32%). It should be noted that in the case of Brazil and Peru, there were various reports with several cases from a time period ranging from 25 to 50 years [66,67,75,86]. As previously mentioned, sporotrichosis is a disease caused by a thermodymorphic fungus of the genus Sporothrix. It is known that this subcutaneous disease, although cosmopolitan, generally occurs in both tropical and subtropical regions. The latter could explain, in some part, the high prevalence in Latin America, being endemic in this region [1,2,3,4,129]. However, three countries (Brazil, Peru, and Mexico) have specific characteristics that increase the number of cases. In Brazil and adjacent countries (for example, Argentina and Paraguay), an increasing number of cases have been associated with zoonotic infection, mainly from infected cats through scratches or sneezes [3,4]. Since the zoonotic transmission of S. brasiliensis is the most important form of communication, it is recommended that hygienic measures be taken regarding domestic animals such as cats, rodents, etc., due to possible infections. If it is diagnosed in animals, it must be treated immediately, and gloves must be used when handling animals with injuries [2,3,4].

In Mexico, sporotrichosis is considered endemic and an occupational disease due to the different sources of infection. The climate of some regions in Mexico is perfect for the characteristics of this type of mycosis to increase its incidence. Although tropical and subtropical climates are preferred by this fungus, in this country, the cold and dry seasons are the contagion peaks of these pathological agents. The states that are more affected are Mexico City, Puebla, Jalisco, Michoacan, the State of Mexico, and Guanajuato. In these states, agriculture is one of the most important economic activities, which explains the high incidence of the Sporothrix contagion [130]. Thus, the principal recommendation in this region is the use of gloves or long-sleeved clothing when carrying out work activities where these species are endemic.

Regarding the etiological agents responsible for the types of sporotrichosis, it is important to specify that they were referred to both in the table and in the text in the way they were named in the articles that were analyzed. Since most of them were written and published before the changes in taxonomical classification, they do not consider the clinical and environmental clades classification instead of the Sporothrix schenckii complex.

As for the etiological agent of sporotrichosis, the most prevalent, according to the reports with the old taxonomical classification, were S. schenckii complex and Sporothrix spp. with 6624 cases (52.41%), S. schenckii with 5302 (41.95%), S. schenckii sensu lato with 245 (1.94%), S. schenckii sensu stricto with 147 (1.16%), S. brasiliensis with 153 (1.21%), S. globosa plus S. Schenckii sensu stricto with 91 (0.72%), S. globosa with 65 (0.51%), S. mexicana with 4 (0.03%), S. pallida 1 (0.008%), Ophiostoma stenoceras 1 (0.008%), and 4 ND cases (0.032%). It is worth mentioning that, although there are other species, such as Sporothrix luriei, there were no reports found in the studied period in the Americas [1,131].

Likewise, within the systematic review, Ophiostoma stenoceras appears, which in the taxonomic classification of Sporothrix is represented in its sexual state, in the year the report was made. Nevertheless, in 2016, Beer et al. concluded through phylogenetic analyzes that the genus Sporothrix was different from the genus Ophiostoma, but that was before considering its sexual state. Officially, the sexual status of Sporothrix is not known, and in this case, Ophiostoma stenoceras was included according to the regulations that governed the taxonomy before the divorce between the two genders occurred [132].

After analyzing the articles to carry out the classification according to the new taxonomy, we found that the most common reported etiological agent was Sporothrix spp. with 94.34% (11,922/12,636), followed by S. schenckii with 3.16% (400/12,636), S. brasiliensis with 1.21% (153/12,636), S. globosa plus S. schenckii with 0.72% (91/12,636), S. globosa with 0.51% (65/12,636), S. mexicana 0.03% (4/12,636), and S. pallida with 0.007% (1/12,636) [61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103,104,105,106,107,108,109,110,111,112,113,114,115,116,117,118,119,120,121,122,123,124,125,126,127,128].

On the other hand, the most frequent type of sporotrichosis was the lymphocutaneous with 4288 cases, followed by the fixed cutaneous with 2340 cases, the disseminated or systemic with 103, the disseminated cutaneous with 52 cases, other with 215 cases, and 5760 cases were ND. By being a subcutaneous mycosis, the lymphocutaneous form is the most frequent one because sporotrichosis mainly affects the lymph nodes of the skin and the subcutaneous tissue, producing ulcers and thereby affecting the lymphocutaneous system [133]. The infection begins in the form of an inoculation chancre. Subsequently, erythematous nodular lesions arise, which follow the trajectory of the lymphatic vessels, mainly affecting the face and upper and lower limbs. Another common form is the fixed cutaneous, which occupies the second place in the Americas to the present date. This type is of a fixed form at the inoculation site of the fungus, affecting mainly children, and it is observed as a verrucous plaque. Its presence demonstrates a high immunity response from the patient. Being a disease of this body region, it has a low prevalence in other organs or tissues. However, the disseminated or hematogenous form may be cutaneous or systemic [5,6,7,8]. Systemic sporotrichosis can cause respiratory and lung disorders, osteomyelitis, arthritis, and meningitis. It is important to note that the type of condition affecting the patients (5760 cases) was not mentioned in several of the reported cases analyzed in this publication.

Concerning diagnosis, various methods, both phenotypic and genotypic, have been used to detect the infection caused by this etiological agent [129]. Within the phenotypic methods, we can name (1) mycological cultures. This technique seeks the growth of the colony in a radial form (approximately 3 to 4 days) with a creamy consistency, and subsequently, the development of mycelium is observed for its identification (Gold Standard). Finally, it is suggested to perform a lactophenol blue staining to observe the microconidia in a sympodial arrangement along the mycelium. (2) serological diagnosis using sporotricine and immunodiffusion tests, immunoelectrophoresis, latex agglutination, etc. (3) histopathological diagnosis, an excisional biopsy of the nodular lesion is performed that may show granulomatous and necrotizing dermatitis, which can be stained with Hematoxylin and Eosin (HE) Schiff’s Periodic Acid (PAS), or Grocott-Gomori Methenamine Silver (MSG) to confirm the presence of asteroid bodies [5,6,7,8].

Nonetheless, genotypic identification tests are preferred since phenotypic techniques have disadvantages, such as being laborious, presenting variable results from the clinical field, and requiring many samples to reach a diagnosis. Therefore, different PCR techniques have been used for genotypic identification tests utilizing diverse genetic or molecular markers that have been developed [5].

In this systematic review, the culture turned out to be the most used diagnostic method throughout the continent, being performed in 107 of the 127 articles reviewed. Histopathological examination was the second most used diagnostic technique, found in 43 publications. In addition, PCR sequencing was used 38 times, direct microscopy 21 times, and microscopy with lactophenol blue was reported in 9 articles. Lastly, other techniques were used to detect sporotrichosis; however, these were not utilized routinely.

Author Contributions

R.H.-C., R.P.-A., R.A. and E.M.-H. designed the study and wrote the manuscript, contributing equally to the accomplishment of the work; R.P.-A., C.R.-C., C.D.S.-C., V.M.E.-H. and E.R.J.-D. contributed to the writing of the manuscript; K.Y.S.-M., E.M.-H., C.R.-C., E.C.-C., J.X.-C. and E.M.C.-C. planned, extracted data, wrote, and critically reviewed the manuscript; R.H-C., J.S.-V., C.R.-C. and E.M.-H. wrote and critically reviewed the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

Lopes-Bezerra, L.M.; Mora-Montes, H.M.; Zhang, Y.; Nino-Vega, G.; Rodrigues, A.M.; de Camargo, Z.P.; de Hoog, S. Sporotrichosis between 1898 and 2017: The evolution of knowledge on a changeable disease and on emerging etiological agents. Med. Mycol. 2018, 56, S126–S143. [Google Scholar] [CrossRef] [PubMed]
Rabello, V.B.S.; Almeida, M.A.; Bernardes-Engemann, A.R.; Almeida-Paes, R.; de Macedo, P.M.; Zancopé-Oliveira, R.M. The Historical Burden of Sporotrichosis in Brazil: A Systematic Review of Cases Reported from 1907 to 2020. Braz. J. Microbiol. 2022, 53, 231–244. [Google Scholar] [CrossRef] [PubMed]
Rodrigues, A.M.; Della Terra, P.P.; Gremião, I.D.; Pereira, S.A.; Orofino-Costa, R.; de Camargo, Z.P. The threat of emerging and re-emerging pathogenic Sporothrix species. Mycopathologia 2020, 185, 813–842. [Google Scholar] [CrossRef] [PubMed]
Gremião, I.D.F.; Evangelista Oliveira, M.M.; Monteiro de Miranda, L.H.; Saraiva Freitas, D.F.; Peraira, S.A. Geographic Expansion of Sporotrichosis, Brazil. Emergy Infect. Dis. 2020, 26, 621–662. [Google Scholar] [CrossRef] [Green Version]
Bunce, P.E.; Yang, L.; Chun, S.; Zhang, S.X.; Trinkaus, M.A.; Matukas, L.M. Disseminated sporotrichosis in a patient with hairy cell leukemia treated with amphotericin B and posaconazole. Med. Mycol. 2012, 50, 197–201. [Google Scholar] [CrossRef] [Green Version]
Tai, F.; Jakubovic, H.; Alabdulrazzaq, S.; Alavi, A. A case of sporotrichosis infection mimicking pyoderma gangrenosum and the role of tissue culture in diagnosis: A case report. SAGE Open Med. Case Rep. 2020, 8, 2050313X20919600. [Google Scholar] [CrossRef]
Hayfron, K.; Wiedeman, J.A. A 7-year-old girl with ulcerative lesion after a rodent bite. Pediatr. Infect. Dis. J. 2010, 29, 185–193. [Google Scholar] [CrossRef]
Kamal, A.; Orenstein, R. Disseminated sporotrichosis. J. Hosp. Med. 2010, 5, E29–E30. [Google Scholar] [CrossRef]
Lyengar, S.S.; Khan, J.A.; Brusco, M.; FitzSimmons, C.J. Cutaneous Sporothrix schenckii of the human eyelid. Ophthalmic Plast. Reconstr. Surg. 2010, 26, 305–306. [Google Scholar] [CrossRef]
Milby, A.H.; Pappas, N.D.; O’Donnell, J.; Bozentka, D.J. Sporotrichosis of the upper extremity. Orthopedics 2010, 33, 1–3. [Google Scholar]
Assi, M.; Lakkis, I.E.; Wheat, L.J. Cross-reactivity in the Histoplasma antigen enzyme immunoassay caused by sporotrichosis. Clin. Vaccine Immunol. 2011, 18, 1781–1782. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Parekh, P.K.; Butler, D.F. What is your diagnosis? Periorbital granulomatous plaque. Pediatr. Dermatol. 2011, 28, 457–458. [Google Scholar] [CrossRef] [PubMed]
Rees, R.K.; Swartzberg, J.E. Feline-transmitted sporotrichosis: A case study from California. Dermatol. Online. J. 2011, 17, 2. [Google Scholar] [CrossRef] [PubMed]
Sharon, V.R.; Kim, J.; Sudhakar, S.; Fung, M.A.; Maniar, A. Disseminated cutaneous sporotrichosis. Lancet Infect. Dis. 2013, 13, 95. [Google Scholar] [CrossRef]
Adnan, M.M.; Fierro-Fine, A.; Zhao, L.; Khalil, M.O. Metastic melanoma masquerading as disseminated sporotrichosis. J. Community Support. Oncol. 2014, 12, 339–340. [Google Scholar] [CrossRef]
Trotter, J.R.; Sriaroon, P.; Berman, D.; Petrovic, A.; Leiding, J.W. Sporothrix schenckii lymphadentitis in a male with X-linked chronic granulomatous disease. J. Clin. Immunol. 2014, 34, 49–52. [Google Scholar] [CrossRef]
Bahr, N.C.; Janssen, K.; Billings, J.; Loor, G.; Green, J.S. Respiratory failure due to possible donor-derived Sporothrix schenckii infection in a lung transplant recipient. Case Rep. Infect. Dis. 2015, 2015, 925718. [Google Scholar]
Hassan, K.; Turker, T.; Zangeneh, T. Disseminated sporotrichosis in an immunocompetent patient. Case Rep. Plast. Surg. Hand Surg. 2016, 3, 44–47. [Google Scholar] [CrossRef] [Green Version]
Lederer, H.T.; Sullivan, E.; Crum-Cianflone, N.F. Sporotrichosis as an unusual case of osteomyelitis: A case report and review of the literature. Med. Mycol. Case Rep. 2016, 11, 31–35. [Google Scholar] [CrossRef]
Aronowitz, P.B.; Gilroy, M.; Christiansen, K.N. Disseminated Sporotrichosis with Osteolytic Bone Involvement. J. Gen. Intern. Med. 2017, 32, 1063. [Google Scholar] [CrossRef] [Green Version]
Charles, K.; Lowe, L.; Shuman, E.; Cha, K.B. Painful linear ulcers: A case of cutaneous sporotrichosis mimicking pyoderma gangrenosum. JAAD Case Rep. 2017, 3, 519–552. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Hessler, C.; Kauffman, C.A.; Chow, F.C. The upside of bias: A case of chronic meningitis due to Sporothrix schenckii in an immunocompetent host. Neurohospitalist 2017, 7, 30–34. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Barbaryan, A.; El Atrouni, W.; Bailuc, S.; Jones, M.W.; Bhakta, M.; Mahmoud, K.H.; Mirrakhimov, A.E. Isolated Sporothrix schenckii monoarthritis. Case Rep. Infect. Dis. 2018, 2018, 9037657. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Farooqui, S.M.; Youness, H. The Infection Returns: A case of pulmonary sporotrichosis relapse after chemotherapy. Case Rep. Med. 2018, 2018, 1384029. [Google Scholar] [CrossRef] [Green Version]
Patel, R.; Busby, L.P.; Motamedi, D. Delayed diagnosis in a case of smoldering sporotrichal monoarthropathy. J. Radiol. Case Rep. 2019, 13, 17–23. [Google Scholar] [CrossRef]
Saeed, L.; Weber, R.J.; Puryear, S.B.; Bahrani, E.; Peluso, M.J.; Babik, J.M.; Haemel, A.; Coates, S.J. Disseminated cutaneous and osteoarticular sporotrichosis mimicking pyoderma gangrenosum. Open Forum Infect. Dis. 2019, 6, ofz395. [Google Scholar] [CrossRef]
White, M.; Adams, L.; Phan, C.; Erdag, G.; Totten, M.; Lee, R.; Lu, X.; Mehta, S.; Miller, L.S.; Zhang, S.X. Disseminated sporotrichosis following iatrogenic immunosuppression for suspected pyoderma gangrenosum. Lancet Infect. Dis. 2019, 19, e385–e391. [Google Scholar] [CrossRef]
Kaadan, M.I.; Dennis, M.; Desai, N.; Yadavalli, G.; Lederer, P. One health education for future physicians: A case report of cat-transmitted sporotrichosis. Open Forum Infect. Dis. 2020, 7, ofaa049. [Google Scholar] [CrossRef]
Parker, N.; Strong, N.; Pichetsurnthorn, P.; Lalich, D.; Moore, T. Disseminated sporotrichosis with brain abscesses in an HIV-Infected patient. Cureus 2020, 12, e8016. [Google Scholar] [CrossRef]
Shah, D.; Kim, A.E.; Elbadri, S.; Desai, B.; Ganti, L. An uncommon rash in the emergency department: Sporothrix Schenckii. Cureus 2021, 13, e16125. [Google Scholar] [CrossRef]
Wellington, T.; Hauschild, J.; Krauland, K.J.; Verwiebe, E.G.; Markelz, A.E. Sporotrichosis in a U.S. Army basic trainee. Mil. Med. 2021, usab463. [Google Scholar] [CrossRef] [PubMed]
Zambrano, A.I.; Church, E.C.; McKay, K.M.; Carnes, S.K.; Morse, R.J.; Leveque, T.K.; Roxby, A.C. A disfiguring rash. Open Forum Infect. Dis. 2021, 8, ofab332. [Google Scholar] [CrossRef] [PubMed]
Kenny, H.; Dougherty, M.; Churnin, I.; Early, S.; Gupta, A.; McGarey, P.O., Jr. Chronic laryngotracheal granulomatous disease secondary to Sporothrix schenckii in an immunocompromised patient. Ann. Otol. Rhinol. Laryngol. 2022, 34894211073002. [Google Scholar] [CrossRef] [PubMed]
Gutierrez-Morales, J.L.; Domínguez Romero, R.; Morales Esponda, M.; Rossiere Echazaleta, N.L.; Reyes Bonifant, G.; Santos Ramírez, A. Esporotricosis micematoide con invasión a médula espinal. Rev. Mex. Neuroci. 2011, 12, 50–54. [Google Scholar]
Romero-Cabello, R.; Bonifaz, A.; Romero-Feregrino, R.; Sánchez, C.J.; Linares, Y.; Zavala, J.T.; Romero, L.C.; Romero-Feregrino, R.; Vega, J.T. Disseminated sporotrichosis. BMJ Case Rep. 2011, 2011, bcr1020103404. [Google Scholar] [CrossRef] [Green Version]
Rojas-Padilla, R.; Pastrana, R.; Toledo, M.; Valencia, A.; Mena, C.; Bonifaz, A. Esporotricosis cutánea linfangítica por mordedura de araña. Dermatol. Rev. Mex. 2013, 57, 479–484. [Google Scholar]
Espinoza-Hernández, C.J.; Jesús-Silva, A.; Toussaint-Caire, S.; Arenas, R. Disseminated sporotrichosis with cutaneous and testicular involvement. Actas Dermosifiliogr. 2014, 105, 204–206. [Google Scholar] [CrossRef]
Chávez-López, G.; Estrada-Castañón, R.; Estrada-Chávez, G.; Vega-Memije, M.E.; Moreno-Coutiño, G. Esporotricosis cutánea diseminada: Un caso de la región de la montaña del estado de Guerrero, México. Dermatol. Rev. Mex. 2015, 59, 228–232. [Google Scholar]
Cotino Sánchez, A.; Torres-Alvarez, B.; Gurrola Morales, T.; Méndez Martínez, S.; Saucedo Gárate, M.; Castanedo-Cazares, J.P. Mycosis fungoides-like lesions in a patient with diffuse cutaneous sporotrichosis. Rev. Iberoam. Micol. 2015, 32, 200–203. [Google Scholar] [CrossRef]
Bonifaz, A.; Tirado-Sánchez, A.; Paredes-Solís, V.; Cepeda-Valdés, R.; González, G.M.; Treviño-Rangel, R.J.; Fierro-Arias, L. Cutaneous disseminated sporotrichosis: Clinical experience of 24 cases. J. Eur. Acad. Dermatol. Venereol. 2018, 32, e77–e79. [Google Scholar] [CrossRef]
Bonifaz, A.; Toriello, C.; Araiza, J.; Ramírez-Soto, M.C.; Tirado-Sánchez, A. Sporotrichin skin test for the diagnosis of sporotrichosis. J. Fungi 2018, 4, 55. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Estrada-Castañón, R.; Chávez-López, G.; Estrada-Chávez, G.; Bonifaz, A. Report of 73 cases of cutaneous sporotrichosis in Mexico. An. Bras. Dermatol. 2018, 93, 907–909. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Ochoa-Reyes, J.; Ramos-Martínez, E.; Treviño-Rangel, R.; González, G.M.; Bonifaz, A. Auricular sporotrichosis. Atypical case report simulating bacterial cellulitis. Rev. Chil. Infectol. 2018, 35, 83–87. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Puebla-Miranda, M.; Vásquez-Ramírez, M.; González-Ibarra, M.; Torres-López, I.H. Esporotricosis. Reporte de un caso ocupacional. Rev. Hosp. Jua. Mex. 2018, 85, 246–250. [Google Scholar]
Rangel-Gamboa, L.; Martinez-Hernandez, F.; Maravilla, P.; Flisser, A. A population genetics analysis in clinical isolates of Sporothrix schenckii based on calmodulin and calcium/calmodulin-dependent kinase partial gene sequences. Mycoses 2018, 61, 383–392. [Google Scholar] [CrossRef]
Rojas, O.C.; Bonifaz, A.; Campos, C.; Treviño-Rangel, R.J.; González-Álvarez, R.; González, G.M. Molecular identification, antifungal susceptibility, and geographic origin of clinical Strains of Sporothrix schenckii complex in Mexico. J. Fungi 2018, 4, 86. [Google Scholar] [CrossRef] [Green Version]
Estrada-Castañón, R.; Estrada-Chávez, G.; Chávez-López, M.G. Diagnosis and management of fungal neglected tropical diseases in community settings-mycetoma and sporotrichosis. Trop. Med. Infect. Dis. 2019, 4, 81. [Google Scholar] [CrossRef] [Green Version]
Mayorga-Rodríguez, J.; Mayorga-Garibaldi, J.L.; Muñoz-Estrada, V.F.; De León Ramírez, R.M. Esporotricosis: Serie de 1134 casos en una zona endémica de México. Med. Cut. Ibero Lat. Am. 2019, 47, 24–28. [Google Scholar]
Alvarez-Rivero, V.; Hernandez-Castro, R.; Moreno-Coutiño, G.; Lozano-Platonoff, A. Disseminated sporotrichosis: An important differential diagnosis for venous ulcers. Adv. Skin. Wound Care 2020, 33, 1–3. [Google Scholar] [CrossRef]
Bonifaz, A.; Morales-Peña, N.; Tirado-Sánchez, A.; Jiménez-Mendoza, D.R.; Treviño-Rangel, R.J.; González, G.M. Atypical sporotrichosis related to Sporothrix mexicana. Mycopathologia 2020, 185, 733–735. [Google Scholar] [CrossRef]
Bonifaz, A.; Tirado-Sánchez, A.; Araiza, J.; Treviño-Rangel, R.; González, G.M. Deep mycoses and pseudomycoses of the foot: A single-center retrospective study of 160 cases, in a tertiary-care center in Mexico. Foot 2021, 46, 101770. [Google Scholar] [CrossRef] [PubMed]
Martínez-Herrera, E.; Arenas, R.; Hernández-Castro, R.; Frías-De-León, M.G.; Rodríguez-Cerdeira, C. Uncommon clinical presentations of sporotrichosis: A two-case report. Pathogens 2021, 10, 1249. [Google Scholar] [CrossRef] [PubMed]
Lozada-Alvarado, S.; Salas-Campos, I.; Uribe-Lorío, L.; Gross, N.T. Molecular and Biochemical Identification and In Vitro Susceptibility to Itraconazole of Costa Rican Clinical Isolates of the Sporothrix schenckii Complex. Acta Sci. Microbiol. 2020, 3, 116–123. [Google Scholar] [CrossRef]
Román-Carrillo, M.; Porres-Paredes, S.; Orozco, R.; Argueta, V. Cutaneous Sporotrichosis. Case report. Rev. Médica Gt Colmedegua 2018, 157, 90–92. [Google Scholar]
Sánchez-Cárdenas, C.D.; Porras-López, C.; Morales-Ezquivel, O.; Frías-De-León, M.G.; Juárez-Durán, E.R.; Arenas, R.; Martínez-Herrera, E. Sporotrichosis: Epidemiological, clinical and mycological study of 53 cases in Guatemala. Life Sci. Press 2018, 2, 66–69. [Google Scholar] [CrossRef]
Flórez-Muñoz, S.V.; Alzate, J.F.; Mesa-Arango, A.C. Molecular Identification and Antifungal Susceptibility of Clinical Isolates of Sporothrix schenckii Complex in Medellin, Colombia. Mycopathologia 2019, 184, 53–63. [Google Scholar] [CrossRef]
Medina, R.; Flores, J.; Luque, M.T. Sporotrichosis in an Adolescent Patient. Honduras Pediátrica 2021, 34, 32–33. [Google Scholar] [CrossRef]
Rios, M.E.; Suarez, M.D.; Moreno, J.; Vallee, J.; Moreno, J.P. Zoonotic Sporotrichosis Related to Cat Contact: First Case Report from Panama in Central America. Cureus 2018, 10, e2906. [Google Scholar] [CrossRef] [Green Version]
Fernandez, M.C.; Reyes, N.; Gonzalez, J.C.; Montesino, M.; Apaulasa, K. Sporotrichosis. A propos of a case. Rev. Cubana Med. Trop. 2016, 68, 171–178. [Google Scholar]
Pérez-Morales, L.; Iglesias-López, M.; Quiñones-Cherta, O.; Reyes-Rodríguez, I. Microbiological Isolation of Sporothrix Schenckii in an Immunocompromised Patient. A Case Report. Rev. Cienc. Médicas Cienfuegos 2014, 12, 662–669. [Google Scholar]
Rojas, F.D.; Fernández, M.S.; Lucchelli, J.M.; Lombardi, D.; Malet, J.; Vetrisano, M.E.; Cattana, M.E.; de los Ángeles Sosa, M.; Giusiano, G. Cavitary Pulmonary Sporotrichosis: Case Report and Literature Review. Mycopathologia 2017, 182, 1119–1123. [Google Scholar] [CrossRef] [PubMed]
Etchecopaz, A.; Toscanini, M.A.; Gisbert, A.; Mas, J.; Scarpa, M.; Iovannitti, C.A.; Bendezú, K.; Nusblat, A.D.; Iachini, R.; Cuestas, M.L. Sporothrix brasiliensis: A review of an emerging south american fungal pathogen, its related disease, presentation and spread in Argentina. J. Fungi 2021, 7, 170. [Google Scholar] [CrossRef] [PubMed]
Córdoba, S.; Isla, G.; Szusz, W.; Vivot, W.; Hevia, A.; Davel, G.; Canteros, C.E. Molecular identification and susceptibility profile of Sporothrix schenckii sensu lato isolated in Argentina. Mycoses 2018, 61, 441–448. [Google Scholar] [CrossRef] [PubMed]
Picollo, M.; Epelbaum, C.; Bustos, A.C.; Carnovale, S.; Rosanova, M.T. Lymphocutaneous sporotrichosis in a pediatric patient, a case report. Rev. Chil. Infectol. 2021, 38, 811–815. [Google Scholar] [CrossRef] [PubMed]
Alzuguir, C.L.C.; Pereira, S.A.; Magalhães, M.A.F.M.; Almeida-Paes, R.; Freitas, D.F.S.; Oliveira, L.F.A.; Pimentel, M.I.F. Geo-epidemiology and socioeconomic aspects of human sporotrichosis in the municipality of Duque de Caxias, Rio de Janeiro, Brazil, between 2007 and 2016. Trans. R. Soc. Trop. Med. Hyg. 2020, 114, 99–106. [Google Scholar] [CrossRef]
Almeida-Paes, R.; de Oliveira, M.M.E.; Freitas, D.F.S.; do Valle, A.C.F.; Zancopé-Oliveira, R.M.; Gutierrez-Galhardo, M.C. Sporotrichosis in Rio de Janeiro, Brazil: Sporothrix brasiliensis Is Associated with Atypical Clinical Presentations. PLoS Negl. Trop. Dis. 2014, 8, e309. [Google Scholar] [CrossRef] [Green Version]
Freitas, D.F.S.; do Valle, A.C.F.; da Silva, M.B.T.; Campos, D.P.; Lyra, M.R.; De Souza, R.V.; Veloso, V.G.; Zancopé-Oliveira, R.M.; Bastos, F.I.; Galhardo, M.C.G. Sporotrichosis: An Emerging Neglected Opportunistic Infection in HIV-Infected Patients in Rio de Janeiro, Brazil. PLoS Negl. Trop. Dis. 2014, 8, e3110. [Google Scholar] [CrossRef]
Freitas, D.F.S.; de Siqueira Hoagland, B.; do Valle, A.C.F.; Fraga, B.B.; de Barros, M.B.; de Oliveira Schubach, A.; de Almeida-Paes, R.; Cuzzi, T.; Rosalino, C.M.V.; Zancopé-Oliveira, R.M.; et al. Sporotrichosis in HIV-infected patients: Report of 21 cases of endemic sporotrichosis in Rio de Janeiro, Brazil. Med. Mycol. 2012, 50, 170–178. [Google Scholar] [CrossRef] [Green Version]
Arinelli, A.; Aleixo, A.L.Q.D.C.; Freitas, D.F.S.; Valle, A.C.F.D.; Almeida-Paes, R.; Gutierrez-Galhardo, M.C.; Curi, A.L.L. Ocular Sporotrichosis: 26 Cases with Bulbar Involvement in a Hyperendemic Area of Zoonotic Transmission. Ocul. Immunol. Inflamm. 2020, 28, 764–771. [Google Scholar] [CrossRef]
Pereira, M.A.; Freitas, R.J.; Nascimento, S.B.; Pantaleão, L.; Vilar, E.G. Sporotrichosis: A Clinicopathologic Study of 89 Consecutive Cases, Literature Review, and New Insights About Their Differential Diagnosis. Am. J. Dermatopathol. 2020, 42, 751–755. [Google Scholar] [CrossRef]
Rocha, I.D.C.B.; Della Terra, P.P.; de Oliveira, R.C.; Zanotti, R.L.; Falqueto, A.; de Camargo, Z.P.; Rodrigues, A.M.; Goncalves, S.S. Molecular-based assessment of diversity and population structure of Sporothrix spp. clinical isolates from Espírito Santo-Brazil. Mycoses 2021, 64, 420–427. [Google Scholar] [CrossRef] [PubMed]
Caus, A.L.O.; Zanotti, R.L.; Faccini-Martínez, Á.A.; Paterlini, G.V.; Falqueto, A. Epidemiological and clinical aspects of sporotrichosis in Espírito Santo State, southeast Brazil: A study of three decades (1982–2012). Am. J. Trop. Med. Hyg. 2019, 100, 706–713. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Poester, V.R.; Mattei, A.S.; Madrid, I.M.; Pereira, J.T.B.; Klafke, G.B.; Sanchotene, K.O.; Brandolt, T.M.; Xavier, M.O. Sporotrichosis in Southern Brazil, towards an epidemic? Zoonoses Public Health 2018, 65, 815–821. [Google Scholar] [CrossRef] [PubMed]
Benvegnú, A.M.; Dallazzem, L.N.D.; Chemello, R.M.L.; Beber, A.A.C.; Chemello, D. Case series of sporotrichosis at a teaching hospital in Brazil. Rev. Soc. Bras. Med. Trop. 2020, 53, e20190509. [Google Scholar] [CrossRef] [PubMed]
Grisolia, J.C.; Santos, L.A.; Coelho, L.M.L.; Silva, R.R.; de Camargo, Z.P.; Velloso, T.R.G.; Coelho, L.F.; Chavasco, J.K.; Malaquias, L.C.C. Seroepidemiological survey on sporotrichosis-infection in rural areas of the south of Minas Gerais State, Brazil. Braz. J. Microbiol. 2021, 52, 41–47. [Google Scholar] [CrossRef]
Filho, J.E.; dos Santos, I.B.; Reis, C.M.S.; Patané, J.S.L.; Paredes, V.; Bernardes, J.P.R.A.; Poggiani, S.D.S.C.; Castro, T.D.C.B.; Gomez, O.M.; Pereira, S.A.; et al. A novel Sporothrix brasiliensis genomic variant in Midwestern Brazil: Evidence for an older and wider sporotrichosis epidemic. Emerg. Microbes Infect. 2020, 9, 2515–2525. [Google Scholar] [CrossRef]
Marques, G.F.; Martins, A.L.G.P.; Sousa, J.M.P.; Brandão, L.S.G.; Wachholz, P.A.; Masuda, P.Y. Characterization of sporotrichosis cases treated in a dermatologic teaching unit in the State of São Paulo-Brazil, 2003–2013. Bras. Dermatol. 2015, 90, 273–275. [Google Scholar] [CrossRef] [Green Version]
Veasey, J.; Neto, M.; Ruiz, L.; Zaitz, C. Clinical and laboratory profile of urban sporotrichosis in a tertiary hospital in the city of São Paulo. Bras. Dermatol. 2021, 96, 243–245. [Google Scholar] [CrossRef]
Ferreira, L.C.; Barroso, P.F.; Tonomura, E.; Akiti, T.; Rodrigues, K.M. Osteomyelitis caused by Sporothrix schenckii in an immunocompetent patient. Rev. Soc. Bras. Med. Trop. 2016, 49, 527–529. [Google Scholar] [CrossRef] [Green Version]
Matos, A.M.F.; Moreira, L.M.; Barczewski, B.F.; De Matos, L.X.; De Oliveira, J.B.V.; Pimentel, M.I.F.; Almeida-Paes, R.; Oliveira, M.G.; Pinto, T.C.A.; Lima, N.; et al. Identification by MALDI-TOF MS of Sporothrix brasiliensis Isolated from a Subconjunctival Infiltrative Lesion in an Immunocompetent Patient. Microorganisms 2020, 8, 22. [Google Scholar] [CrossRef] [Green Version]
do Monte Alves, M.; Pipolo Milan, E.; da Silva-Rocha, W.P.; Soares de Sena da Costa, A.; Araújo Maciel, B.; Cavalcante Vale, P.H.; de Albuquerque, P.R.; Lopes Lima, S.; Salles de Azevedo Melo, A.; Messias Rodrigues, A.; et al. Fatal pulmonary sporotrichosis caused by Sporothrix brasiliensis in Northeast Brazil. PLoS Negl. Trop. Dis. 2020, 14, e0008141. [Google Scholar] [CrossRef] [PubMed]
Xavier, J.R.B.; Waller, S.B.; Osório, L.D.G.; Vives, P.S.; Albano, A.P.N.; de Aguiar, E.S.V.; Ferreira, M.R.A.; da Conceição, F.R.; de Faria, R.O.; Meireles, M.C.A.; et al. Human sporotrichosis outbreak caused by Sporothrix brasiliensis in a veterinary hospital in Southern Brazil. J. Mycol. Med. 2021, 31, 101163. [Google Scholar] [CrossRef] [PubMed]
de Sá Menezes Carvalho, G.; Verrinder Veasey, J. Immunoreactive cutaneous sporotrichosis. Bras. Dermatol. 2020, 95, 737–739. [Google Scholar] [CrossRef] [PubMed]
Lacerda Filho, A.M.; Cavalcante, C.M.; Da Silva, A.B.; Inácio, C.P.; de Lima-Neto, R.G.; De Andrade, M.C.L.; Magalhães, O.M.C.; Dos Santos, F.D.A.G.; Neves, R.P. High-Virulence Cat-Transmitted Ocular Sporotrichosis. Mycopathologia 2019, 184, 547–549. [Google Scholar] [CrossRef] [PubMed]
de Moura Barros, N.; de Souza Pessoa, A.; Martins Brotas, A. Systemic sporotrichosis in an alcoholic patient. Bras. Dermatol. 2020, 95, 376–378. [Google Scholar] [CrossRef]
Lemes, L.R.; Veasey, J.V.; Soutto-Mayor, S.; Contin-Proenca, C. Ocular involvement in sporotrichosis: Report of two cases in children. Bras. Derm. 2021, 96, 349–351. [Google Scholar] [CrossRef]
Henckens, N.F.T.; Rovers, J.F.J.; van Dommelen, L.; Bovenschen, H.J. Can cats cause colossal contagious cutaneous carbuncles? Derm. Online J. 2021, 27. [Google Scholar] [CrossRef]
Lora Barraza, L.; Bissoli Tolomelli, J.; Graça Cunha, C.; Bernardes Filho, F.; Towersey, L.; Hay, R.; Casz Schechtman, R.; da Costa Nery, J.A. Facial Cutaneous Sporotrichosis in a Boy. J. Emerg. Med. 2019, 56, 222–223. [Google Scholar] [CrossRef]
de Freitas Valente, M.; Bertazzoli Diogo, A.; Culau Merlo, V.F.; Pereira Pegas, J.R. Disseminated cutaneous sporotrichosis: Unusual presentation in an alcoholic patient. Rev. Inst. Med. Trop. São Paulo 2020, 62, e60. [Google Scholar] [CrossRef]
Crestani, L.; de Castro e Souza, B.; Kakizaki, P.; Sakai-Valente, N.Y. Therapeutic failure with itraconazole in sporotrichosis due to bariatric surgery. Bras. Derm. 2020, 95, 241–243. [Google Scholar] [CrossRef]
Arantes-Ferreira, G.S.; Watanabe, A.L.C.; Trevizoli, N.C.; Jorge, F.M.F.; Cajá, G.O.N.; Diaz, L.G.G.; Meireles, L.P.; Araújo, M.C.C.L. Disseminated Sporotrichosis in a Liver Transplant Patient: A Case Report. Transpl. Proc. 2019, 51, 1621–1624. [Google Scholar] [CrossRef] [PubMed]
Fichman, V.; Valle, A.C.F.D.; de Macedo, P.M.; Freitas, D.F.S.; Oliveira, M.M.E.; Almeida-Paes, R.; Gutierrez-Galhardo, M.C. Cryosurgery for the treatment of cutaneous sporotrichosis in four pregnant women. PLoS Negl. Trop. Dis. 2018, 12, e0006434. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Biancardi, A.L.; Freitas, D.F.; Vitor, R.D.; Andrade, H.B.; de Oliveira, M.M.; do Valle, A.C.; Zancope-Oliveira, R.M.; Galhardo, M.C.; Curi, A.L. Multifocal choroiditis in disseminated sporotrichosis in patients with HIV/AIDS. Retin. Cases Brief Rep. 2017, 11, 67–70. [Google Scholar] [CrossRef] [PubMed]
Fischman-Gompertz, O.; Rodrigues, A.M.; Fernandes, G.F.; Bentubo, H.D.L.; Pires de Camargo, Z.; Petri, V. Atypical Clinical Presentation of Sporotrichosis Caused by Sporothrix globosa Resistant to Itraconazole. Am. J. Trop. Med. Hyg. 2016, 94, 1218–1222. [Google Scholar] [CrossRef]
Aparecida-Grazziotin, N.; Gonçalves, I.L.; Todeschini, D.; Grazziotin-Vedana, L.; Canello-Todeschini, C.M.; Grazziotin, C. Squamous cell carcinoma subsequent to scarring caused by sporotrichosis: A case report. Rev. Iberoam. Micol. 2019, 36, 83–85. [Google Scholar] [CrossRef]
Ribeiro, B.N.; Ribeiro, R.N.; Penna, C.R.; Frota, A.C. Bone involvement by Sporothrix schenckii in an immunocompetent child. Pediatr. Radiol. 2015, 45, 1427–3140. [Google Scholar] [CrossRef]
Freitas, D.F.; Santos, S.S.; Almeida-Paes, R.; de Oliveira, M.M.; do Valle, A.C.; Gutierrez-Galhardo, M.C.; Zancopé-Oliveira, R.M.; Nosanchuk, J.D. Increase in virulence of Sporothrix brasiliensis over five years in a patient with chronic disseminated sporotrichosis. Virulence 2015, 6, 112–120. [Google Scholar] [CrossRef] [Green Version]
Nassif, P.W.; Granado, I.R.; Ferraz, J.S.; Souza, R.; Nassif, A.E. Atypical presentation of cutaneous sporotrichosis in an alcoholic patient. Dermatol. Online J. 2012, 18, 12. [Google Scholar]
Falqueto, A.; Bravim-Maifrede, S.; Araujo-Ribeiro, M. Unusual clinical presentation of sporotrichosis in three members of one family. Intern. J. Dermatol. 2012, 51, 434–438. [Google Scholar] [CrossRef]
Marques-de-Macedo, P.; Sztajnbok, D.C.N.; Camargo, Z.P.; Rodrigues, A.M.; Lopes-Bezerra, L.M.; Bernardes-Engemann, A.R.; Orofino-Costa, R. Dacryocystitis due to Sporothrix brasiliensis: A case report of a successful clinical and serological outcome with low-dose potassium iodide treatment and oculoplastic surgery. Br. J. Dermatol. 2015, 172, 1116–1119. [Google Scholar] [CrossRef]
Fichman, V.; Saraiva-Freitas, D.F.; Marques-de-Macedo, P.; Francesconi-do-Valle, A.C.; Almeida-Silva, F.; Zancopé-Oliveira, R.M.; Almeida-Paes, R.; Gutierrez-Galhardo, M.C. Sporotrichosis After Tattooing Caused by Sporothrix. Bras. Mycopathol. 2022, 187, 137–139. [Google Scholar] [CrossRef] [PubMed]
Nepomuceno Araújo, M.J.C.L.; Nihei, C.H.; Rodrigues, A.M.; Higashino, H.; Ponzio, V.; Campos Pignatari, A.C.; Barcellos, M.A.; Braga, O.; Duayer, I.F. Case Report: Invasive Sinusitis due to Sporothrix Brasiliensis in a Renal Transplant Recipient. Am. J. Trop. Med. Hyg. 2021, 105, 1218–1221. [Google Scholar] [CrossRef]
Lima, M.A.; Vallier, R.; Silva, M.M. Sporothrix brasiliensis meningitis in an immunocompetent patient. Pract. Neurol. 2021, 21, 241–242. [Google Scholar] [CrossRef]
Veasey, J.V.; Carvalho, G.S.M.; Ruiz, L.R.B.; Neves-Neto, M.F.; Zaitz, C. Epidemiological and geographical distribution profile of urban sporotrichosis in the city of São Paulo. Bras. Derm. 2022, 97, 228–230. [Google Scholar] [CrossRef]
Antonio, L.D.F.; Pimentel, M.I.F.; Lyra, M.R.; Madeira, M.D.F.; Miranda, L.D.F.C.; Paes, R.A.; Brito-Santos, F.; Carvalho, M.H.G.F.; Schubach, A.D.O. Sporothrix schenckii Sensu Lato identification in fragments of skin lesion cultured in NNN medium for differential diagnosis of cutaneous leishmaniasis. Diagn. Microbiol. Infect. Dis. 2017, 87, 118–120. [Google Scholar] [CrossRef] [PubMed]
Rodrigues, A.M.; de Hoog, S.; de Camargo, Z.P. Emergence of pathogenicity in the Sporothrix schenckii complex. Med Mycol. 2013, 51, 405–412. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Alvarado, Z.; Pereira, C. Fungal diseases in children and adolescents in a referral centre in Bogota, Colombia. Mycoses 2018, 61, 543–548. [Google Scholar] [CrossRef]
Macías, P.; Ordóñez, J.; Arenas, C.M.; Rodríguez, G. An eighteen-year-old man with tropical verrucous syndrome: Leishmaniasis vs, sporotrichosis. Biomedica 2021, 41, 240–246. [Google Scholar] [CrossRef]
Arenas-Soto, C.M.; Téllez-Kling, A.M.; Alvarado-Álvarez, Z.L. A Lesion on the Ear Resulting From Infection Acquired in the Tropics. Actas Dermosifiliogr. 2016, 107, 599–600. [Google Scholar] [CrossRef]
Niklitschek, S.; Porras, N.; González, S.; Romero, W. Sporotrichosis. Med. Clin. 2015, 145, 418. [Google Scholar] [CrossRef]
Cruz, R.; Vieille, P.; Oschilewski, D. Sporothrix globosa isolation related to a case of lymphocutaneous sporotrichosis. Rev. Chil. Infectol. 2012, 4, 401–405. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Cruz-Choappa, R.M.; Vieille-Oyarzo, P.I.; Carvajal-Silva, L.C. Aislamiento de Sporothrix pallida complex en muestras clínicas y ambientales de Chile. Rev. Argent Microbiol. 2014, 46, 311–314. [Google Scholar] [CrossRef] [Green Version]
García Duarte, J.M.; Wattiez Acosta, V.R.; Fornerón Viera, P.M.L.; Aldama Caballero, A.; Gorostiaga Matiauda1, G.A.; Rivelli de Oddone, V.B.; Pereira Brunelli, J.G. Sporotrichosis transmitted by domestic cat. A family case report. Rev. Del. Nacional. 2017, 9, 67–76. [Google Scholar] [CrossRef]
Aguilar Fernández, G.; Araújo López, V. Mycosis and nocardiosis implantation: Sporotrichosis, Chromoblastomycosis, Mycetomas and Nocardiosis. Casuistics in the Central Laboratory of Public Health, Paraguay, period 1997–2019. Rev. Nac. 2020, 12, 1–13. [Google Scholar] [CrossRef]
Ramirez-Soto, M.; Lizarraga-Trujillo, J. Granulomatous sporotrichosis: Report of two unusual cases. Rev. Chil. Infectol. 2013, 5, 548–553. [Google Scholar]
Ramírez-Soto, M.C. Sporotrichosis in the Ocular Adnexa: 21 Cases in an Endemic Area in Peru and Review of the Literature. Am. J. Ophthalmol. 2016, 162, 173–179.e3. [Google Scholar] [CrossRef]
Ramírez-Soto, M.C.; Malaga, G. Subcutaneous mycoses in Peru: A systematic review and meta-analysis for the burden of disease. Int. J. Dermatol. 2017, 56, 1037–1045. [Google Scholar] [CrossRef]
Ramírez-Soto, M.C.; Andagua-Castro, J.; Lizárraga-Trujillo, J. Palpebral sporotrichosis in a 6-year-old child. Int. J. Dermatol. 2016, 55, e625–e626. [Google Scholar] [CrossRef]
Wolff, D.; Feldt, T.; Reifenberger, J.; Sebald, H.; Bogdana, C. The brief case: Cutaneous sporotrichosis in an immunocompetent patient after travel to Peru. J. Clin. Microbiol. 2018, 56, e01958-17. [Google Scholar] [CrossRef] [Green Version]
Rueda, M.; Torres, N.; Bravo, F. Disseminated cutaneous sporotrichosis: An unusual case. Derm. Online J. 2018, 24. [Google Scholar] [CrossRef]
Oyarce, J.A.; García, C.; Alave, J.; Bustamante, B. Epidemiological clinical and laboratory characterization of sporotrichosis in patients of a tertiary care hospital in Lima, Peru, from 1991 to 2014. Rev. Chil. Infectol. 2016, 3, 315–321. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Schwalb, A.; Carcamo, P.M.; Seas, C. Lymphocutaneous Sporotrichosis. Am. J. Trop. Med. Hyg. 2022, 106, 758–759. [Google Scholar] [CrossRef] [PubMed]
Solorzano, S.; Ramirez, R.; Cabada, M.M.; Montoya, M.; Cazorla, E. Disseminated cutaneous sporotrichosis with joint involvement in a woman with type 2 diabetes. Rev. Peru Med. Exp. Salud Publica 2015, 32, 187–190. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Cabeza, E.; Arrillaga, A.; Dalcín, L.; Carbia, M.; Arteta, Z.; Perera, P. Clinical and Epidemiological Characteristics of Sporotrichosis in Reference Center of Uruguay. J. Fungi 2022, 8, 322. [Google Scholar] [CrossRef] [PubMed]
Barreto, L.; Velásquez, G.; Mendoza, M.; Camacho, E.; Goncalves, E.; Rodríguez, S.; Niño-Vega, G.A. Geographical distribution and ecological niche modeling of the etiological agents of human sporotrichosis in Venezuela. Braz. J. Microbiol. 2021, 52, 63–71. [Google Scholar] [CrossRef]
Mata-Essayag, S.; Delgado, A.; Colella, M.T.; Landaeta-Nezer, M.E.; Rosello, A.; de Salazar, C.P.; Olaizola, C.; Hartung, C.; Magaldi, S.; Velasquez, E. Epidemiology of sporotrichosis in Venezuela. Int. J. Dermatol. 2013, 52, 974–980. [Google Scholar] [CrossRef]
Martínez-Méndez, D.; Hernández-Valles, R.; Alvarado, P.; Mendoza, M. Mycoses In Venezuela: Working Groups in Mycology Reported Cases (1984–2010). Rev. Iberoam. Micol. 2013, 30, 39–46. [Google Scholar]
Camacho, E.; León-Navarro, I.; Rodríguez-Brito, S.; Mendoza, M.; Niño-Vega, G.A. Molecular epidemiology of human sporotrichosis in Venezuela reveals high frequency of Sporothrix globose. BMC Infect Dis. 2015, 15, 94. [Google Scholar] [CrossRef]
Orofino-Costa, R.; Marques-de-Macedo, P.; Messias-Rodrigues, A.; Bernardes-Engemann, A.R. Sporotrichosis: An update on epidemiology, etiopathogenesis, laboratory and clinical therapeutics. Bras. Dermatol. 2017, 92, 606–620. [Google Scholar] [CrossRef]
Rimma, Z.; Hernández Hernández, F. Sporotrichosis: The most frequent subcutaneous mycosis in Mexico. Rev. Fac. Med. 2019, 62, 48–55. [Google Scholar]
Chakrabarti, A.; Bonifaz, A.; Gutierrez-Galhardo, M.C.; Mochizuki, T.; Li, S. Global epidemiology of sporotrichosis. Med. Mycol. 2015, 53, 3–14. [Google Scholar] [CrossRef] [PubMed] [Green Version]
de Beer, Z.W.; Duong, T.A.; Wingfield, M.J. The divorce of Sporothrix and Ophiostoma: Solution to a problematic relationship. Stud. Mycol. 2016, 83, 165–191. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Toriello, C.; Brunner-Mendoza, C.; Ruiz-Baca, E.; Duarte-Escalante, E.; Pérez-Mejía, A.; Reyes-Montes, M.R. Sporotrichosis in Mexico. Braz. J. Microbiol. 2021, 52, 49–62. [Google Scholar] [CrossRef] [PubMed]

Figure 1. Sporothrix spp. culture and erythromycin staining 40×.

Figure 2. Flowchart of the different phases of the systematic review.

Table 1. Epidemiology of Sporotrichosis in North America.

Region	Country	City	Number of Reported Cases	Vulnerable Population		Diagnostic Method	Type of Sporotrichosis	Etiological Agents (%)		References
				Sex	Age (Years)			Taxonomy
				Sex	Age (Years)			Before 2017	After 2017
North America	Canada	Ontario	1	Male	44	PCR sequencing (ITS region)	Disseminated	S. schenckii	S. schenckii	[5]
	Canada	Toronto	1	Male	78	Fungal culture, Biopsy (Histopathology)	Lymphocutaneous	S. schenckii complex	Sporothrix spp.	[6]
	USA	California	1	Female	7	Fungal culture Biopsy (Histopathology)	Lymphocutaneous	S. schenckii	Sporothrix spp.	[7]
		Minnesota	1	Male	61	Fungal culture	Disseminated	S. schenckii	Sporothrix spp.	[8]
		ND	1	Female	87	Fungal culture	Lymphocutaneous on the eyelid	S. schenckii	Sporothrix spp.	[9]
		Pennsylvania	1	Male	67	Fungal culture Biopsy (Histopathology)	Lymphocutaneous	S. schenckii	Sporothrix spp.	[10]
		Texas	1	Male	34	Fungal culture Biopsy (Histopathology)	Disseminated	Sporothrix spp.	Sporothrix spp.	[11]
		Texas	1	Male	9	Fungal culture Biopsy (Histopathology)	Lymphocutaneous on the eyelid	S. schenckii	Sporothrix spp.	[12]
		California	1	Female	41	Fungal culture	Lymphocutaneous	S. schenckii	Sporothrix spp.	[13]
		Oregon	1	Male	53	Fungal culture	Disseminated	Sporothrix spp.	Sporothrix spp.	[14]
		Oklahoma	1	Male	66	Latex agglutination test	Disseminated	S. schenckii	Sporothrix spp.	[15]
		Florida	1	Male	33 month-Old	Fungal culture Biopsy (Histopathology)	Atypical lymphadenitis	S. schenckii	Sporothrix spp.	[16]
		Minnesota	1	Male	49	Fungal culture	Pulmonary sporotrichosis	Sporothrix spp.	Sporothrix spp.	[17]
		Arizona	1	Male	56	Fungal culture	Lymphocutaneous and disseminated (10 months later)	S. schenckii	Sporothrix spp.	[18]
		California	1	Male	39	Fungal culture	Sporothrical arthritis	S. schenckii	Sporothrix spp.	[19]
		California	1	Male	89	Fungal culture Biopsy (Histopathology)	Disseminated	S. schenckii	Sporothrix spp.	[20]
		Michigan	1	Female	57	Fungal culture Biopsy (Histopathology)	Lymphocutaneous	S. schenckii	Sporothrix spp.	[21]
		California	1	Male	34	Latex agglutination test	Chronic meningitis	S. schenckii	Sporothrix spp.	[22]
		Kansas	1	Male	33	Fungal culture MALDI-TOF	Sporothrical arthritis	S. schenckii	Sporothrix schenckii	[23]
		Oklahoma	1	Male	44	Fungal culture Biopsy (Histopathology)	Pulmonary sporotrichosis	S. schenckii sensu lato	Sporothrix spp.	[24]
		California	1	Male	41	Fungal culture	Sporothrical arthritis	S. schenckii	Sporothrix spp.	[25]
		California	1	Female	35	Fungal culture	Disseminated	S. schenckii	Sporothrix spp.	[26]
		Nebraska	1	Male	62	Fungal culture Biopsy (Histopathology)	Disseminated	S. schenckii	Sporothrix spp.	[27]
		Boston	1	Female	35	MALDI-TOF	Fixed cutaneous	S. schenckii	S. schenckii	[28]
		Kansas	1	Male	30	Fungal culture Biopsy (Histopathology)	Disseminated	S. schenckii	Sporothrix spp.	[29]
		Florida	1	Male	76	History and physical examination	Lymphocutaneous	Sporothrix spp.	Sporothrix spp.	[30]
		Oklahoma	1	Male	23	Fungal culture	Lymphocutaneous	S. schenckii complex	Sporothrix spp.	[31]
		Washington	1	Female	44	Fungal culture PCR sequencing (ITS 1–2)	Disseminated	S. schenckii	S. schenckii	[32]
		Arizona	1	Female	72	PCR DNA sequencing	Laryngotracheal granulomatous disease	S. schenckii	S. schenckii	[33]
	Mexico	Veracruz	1	Male	39	Fungal culture Biopsy (Histopathology)	Atypical	S. schenckii	Sporothrix spp.	[34]
		Puebla	1	Male	36	Fungal culture Biopsy (Histopathology)	Disseminated	S. schenckii	Sporothrix spp.	[35]
		Oaxaca	1	Male	13	Fungal culture	Lymphocutaneous on the left hand, forearm, and upper arm	Sporothrix spp.	Sporothrix spp.	[36]
		Mexico City	1	Male	54	Fungal culture Biopsy (Histopathology)	Disseminated (Testicular involvement)	S. schenckii	Sporothrix spp.	[37]
		Guerrero	1	Female	36	Fungal culture Biopsy (Histopathology)	Disseminated	Sporothrix spp.	Sporothrix spp.	[38]
		Durango	1	Male	68	Fungal culture Biopsy (Histopathology)	Disseminated	Sporothrix spp.	Sporothrix spp.	[39]
		ND	24	Male (16) Female (8)	Average: 35.5	PCR sequencing (calmodulin gene)	Cutaneous disseminated 16 (66.7%) Cutaneous disseminated + Mucosal 3 (12.5%) Joint 1 (4.1%) Visceral 1 (4.1%) Fungaemia 1 (4.1%) Mucosal + Visceral + Fungemia: 1 (4.1%) Visceral + Fungaemia 1 (4.1%)	S. schenckii 23 (95.5%). S. globosa 1 (4.5%)	S. schenckii 23 (95.5%). S. globosa 1 (4.5%)	[40]
		ND	55	Male (34) ND Female (18)		Sporotrichin Skin Test Fungal culture	Lymphocutaneous 32 (58.2%) Fixed cutaneous 19 (34.5%) Disseminated 4 (7.3%)	S. schenckii 54 (98%) S. globosa 1 (2%)	S. schenckii 54 (98%) S. globosa 1 (2%)	[41]
		Guerrero	73	Male (33) Female (40)	Average: 25.8	Fungal culture Biopsy (Histopathology)	Lymphocutaneous: 41 (56.16%) Fixed cutaneous 24 (32.87%) Disseminated 8 (10.95%)	S. schenckii	S. schenckii	[42]
		Chihuahua	1	Female	84	Multiplex PCR (Calmodulin gene)	Fixed cutaneous (Auricular sporotrichosis)	S. schenckii (sensu stricto)	S. schenckii	[43]
		Baja California	1	Male	23	Fungal culture Biopsy (Histopathology)	Lymphocutaneous	S. schenckii	Sporothrix spp.	[44]
		San Luis Potosi 8 Puebla 3 Mexico City 2 Queretaro 2 Guanajuato 2 Jalisco 1 Zacatecas 1 Michoacan 1 Morelos 1 State of Mexico 1	22	ND		PCR sequencing (Calmodulin and calcium-calmodulin-dependent kinase genes)	Lymphocutaneous: 17 (77.3%) Fixed cutaneous 4 (18.2%) Disseminated 1 (4.5%)	S. schenckii: 18 (81.8%) S. globosa 4 (18.2%)	S. schenckii: 18 (81.8%) S. globosa 4 (18.2%)	[45]
		Puebla 4 Nuevo Leon 2 Oaxaca 6 Mexico City 3 Jalisco 2	17	ND		PCR sequencing (Calmodulin gene)	Lymphocutaneous: 16 (94.11%) Disseminated: 1 (5.88%)	S. schenckii: 16 (94.11%) S. globosa 1 (5.88%)	S. schenckii: 16 (94.11%) S. globosa 1 (5.88%)	[46]
		Guerrero	76	Male (35) Female (41)	<18: 37 >18: 39	Fungal culture Biopsy (Histopathology)	Lymphocutaneous 43 (56.8%) Fixed cutaneous 24 (32.3%) Disseminated 8 (11%)	Sporothrix spp.	Sporothrix spp.	[47]
		Jalisco 1057 Nayarit 23 Zacatecas 20 Michoacan 19 Guanajuato 12 Veracruz 1 Chihuahua 1	1134	Male (669) Female (465)		ND	Lymphocutaneous: 782 (69%) Fixed cutaneous: 308 (27.2%) Disseminated 44 (38.8%)	S. schenckii complex	Sporothrix spp.	[48]
		ND	1	Male	45	PCR sequencing (Calmodulin gene)	Disseminated	S. schenckii complex	S. schenckii	[49]
		ND	1	Male	56	Fungal Culture Biopsy (Histopathology) PCR sequencing (ITS and calmodulin gene)	Fixed cutaneous sporotrichosis	S. mexicana	S. mexicana	[50]
		ND	18	Male (10) Female (8)	ND	PCR sequencing (ITS regions)	Lymphocutaneous 13 (72.2%) Fixed cutaneous 5 (27.8%)	S. schenckii 17 (94.4%) S. globosa: 1 (5.6%)	S. schenckii 17 (94.4%) S. globosa: 1 (5.6%)	[51]
		Oaxaca	2	Male	61	Multiplex PCR (Calmodulin gene)	Fixed cutaneous 1 (50%) Disseminated 1 (50%)	S. schenckii sensu stricto	S. schenckii	[52]
		Oaxaca	2	Male	21	Multiplex PCR (Calmodulin gene)	Fixed cutaneous 1 (50%) Disseminated 1 (50%)	S. schenckii sensu stricto	S. schenckii	[52]

ND: Not Determined.

Table 2. Epidemiology of Sporotrichosis in Central America and the Caribbean.

Region	Country	City	Number of Reported Cases	Vulnerable Population		Diagnostic Method	Type of Sporotrichosis	Etiological Agents (%)		References
				Sex	Age (Years)			Taxonomy
				Sex	Age (Years)			Before 2017	After 2017
Central America	Costa Rica	San José	57 (1994–2015)	No data		Direct microscopy, culture, PCR (enzymatic restriction and sequencing of the calmodulin gen)	ND	S. schenckii sensu stricto 53 (93%) S. brasiliensis 2 (3.5%) Sporothrix spp. 2 (3.5%)	S. schenckii 53 (93%) S. brasiliensis 2 (3.5%) Sporothrix spp. 2 (3.5%)	[53]
	Guatemala	Guatemala City	11	Male 7 Female 4	Average 49 years	Fungal culture, Histopathology	Fixed cutaneous 9 (81.8%) Lymphocutaneous 2 (18.2%)	Sporothrix spp. (100%)	Sporothrix spp. (100%)	[54]
		Guatemala City	53 (2007–2016)	Male 33 Female 20	Average 44.1 years	Fungal culture, microscope with Lactophenol cotton blue	Lymphocutaneous 33 (62.2%) Fixed cutaneous 17 (32.1%) Disseminated 2 (3.8%) Chancre 1 (1.9%)	Sporothrix schenckii complex. (100%)	Sporothrix spp. (100%)	[55]
		Guatemala City	1	ND		Fungal culture, PCR sequencing (ITS 1- 2 and β -tubulin)	ND	Sporothrix schenckii sensu stricto	Sporothrix schenckii	[56]
	Honduras	Tegucigalpa	1	Male 1	14 years	Fungal culture	Lymphocutaneous 1 (100%)	S. schenckii	Sporothrix spp.	[57]
	Panamá	Chorrera District	1	Male 1	34 years	Clinical, Direct Microscopy, Fungal culture.	Lymphocutaneous 1 (100%)	ND	Sporothrix spp.	[58]
Caribbean	Cuba	Pinar del Río	1	Female 1	57 years	Histopathology Fungal culture	Lymphocutaneous	Sporothrix schenckii sensu lato (100%)	Sporothrix spp. (100%)	[59]
Caribbean	Cuba	Cumanayagüa	1	Male	67	Histopathology, Fungal culture, Microscopy with lactophenol cotton blue	Lymphocutaneous	Sporothrix schenckii sensu lato (100%)	Sporothrix spp. (100%)	[60]

ND: Not Determined.

Table 3. Epidemiology of Sporotrichosis in South America.

Region	Country	City	Number of Reported Cases	Vulnerable Population		Diagnostic Method	Type of Sporotrichosis	Etiological Agents (%)		References
				Sex (Number of Cases)	Age (Years)			Taxonomy
				Sex (Number of Cases)	Age (Years)			Before 2017	After 2017
South America	Argentina	Provincia de Chaco	1	Female	65	Bronchoalveolar lavage (BAL), Giemsa stain Fungal culture PCR sequencing (ITS 1–2)	Pulmonary	S. schenckii	S. schenckii	[61]
		Buenos Aires	16	Male (4) Female (10) ND (7)	Average 32.5	Fungal culture and PCR sequencing (Calmodulin gene)	Lymphocutaneous 33 (42.9%) Fixed cutaneous 17 (19.0%) ND (38.1%)	S. brasiliensis	S. brasiliensis	[62]
		Misiones	1			Fungal culture and PCR sequencing (Calmodulin gene)
		El Calafate	4			Fungal culture, PCR sequencing (Calmodulin gene) and histopathology
		Buenos Aires	15	ND		Fungal culture (agar potato dextrose and brain heart infusion agar) PCR sequencing (Calmodulin gene)	ND	S. schenckii sensu stricto 9 (56.5%) S. brasiliensis 5 (34.7%) S. globosa 1 (8.7%)	S. schenckii 9 (56.5%) S. brasiliensis 5 (34.7%) S. globosa 1 (8.7%)	[63]
		Buenos Aires	1	Female	5	Direct microscopy, Fungal culture (Sabouraud agar), Histopalology	Lymphocutaneous	S. schenckii complex	Sporothrix spp.	[64]
	Brazil	Rio de Janeiro (Duque de Caxias)	827 from 2007–2016	Female (541) Male (286)	42	Fungal culture	ND	Sporothrix spp.	Sporothrix spp.	[65]
		Rio de Janeiro ND Teresópolis ND	1563 (1999–2008 = 50 (3.20%))	Male (16) Female (34)	Average 47	Direct microscopy, Fungal culture, PCR sequencing (calmodulin gene)	Lymphocutaneous 24 (48%) Fixed cutaneous 15 (30%) Disseminated cutaneous 6 (12%) disseminated (involving internal tissues) 5 (10%)	S. brasiliensis 45 45 (90%) S. schenckii sensu stricto 5 (10%)	S. brasiliensis 45 (90%) S. schenckii 5 (10%)	[66]
		Rio de Janeiro	Group 1 48 (1.33%) Group 2 3570 (98.67%) 1987–2013	Group 1 HIV patients Male 33 Female 15 Group 2 Immunocompetent patients Male (1102) Female (2468)	Average: 38.4 Averag: 46.3	Direct microscopy, Fungal culture.	ND	Sporothrix spp.	Sporothrix spp.	[67]
		Rio de Janeiro	21/1750 cases in HIV patients (1.2%) from 1999–2009	Male (16) Female (5)	Average: 41.2	Direct microscopy, Fungal culture, Histopathology	Lymphocutaneous 7 (33.3%) Disseminated 7 (33.3%) widespread cutaneous 5 (23.8%) fixed cutaneous 2 (9.5%)	S. schenckii sensu lato	Sporothrix spp.	[68]
		Rio de Janeiro 16 Duque de Caxias 6 São João de Meriti 2 São Gonçalo 1 Maricá 1	26 from 2007–2017	Female (19) Male (7)	Average: 25	Direct microscopic, Fungal culture	Primary ocular 21 (80.8%) Associated cutaneous disease (3 lymphocutaneous, 1 the fixed cutaneous and 1 the disseminated 5 (19.2%)	Sporothrix spp.	Sporothrix spp.	[69]
		Rio de Janeiro	86 from 2009–2017	Male (26) Female (60)	Average: 36.3 Average: 46	Fungal culture Histopathology	ND	Sporothrix spp.	Sporothrix spp.	[70]
		Espíritu Santo	73 from 2016–2019	Male Female	ND	Fungal culture, Microscopy with lactophenol cotton blue, PCR sequencing (Calmodulin gene and Mating type (MAT) gene)	ND	S. brasiliensis 55 (76%) S. schenckii sensu stricto 18 (24%)	S. brasiliensis 55 (76%) S. schenckii 18 (24%)	[71]
		Espíritu Santo	171 cases from 1982–2012	Male (138) Female (33)	Average: 33.42	Fungal culture	ND	Sporothrix spp.	Sporothrix spp.	[72]
		Rio Grande do Sul	83 from 2010–2016	ND		Fungal culture	ND	Sporothrix spp.	Sporothrix spp.	[73]
		Rio Grande do Sul	43 from 2006–2015	Male (31) Female (7)	Average: 43	Fungal culture	Lymphocutaneous 22 (51%) Fixed cutaneous 14 (32.5%) Disseminated cutaneous 1 (2.5%) ND 6 (14%)	Sporothrix spp.	Sporothrix spp.	[74]
		Minas Gerais	282	Male (153) Female (129)	Average: 42.52	Fungal culture, Sporotrichin test, Histophatology, Production of S. schenckii antigens, Enzyme-linked immunosorbent assay	ND	S. schenckii	Sporothrix spp.	[75]
		Brasilia	91 from 1993–2018	Male (64) Female (27)	ND	Direct microscopy, Fungal culture, PCR sequencing (Calmodulin gene)	Lymphocutaneous 34 (37.36%) Cutaneous fixed 6 (6.59%) Disseminated 5 (5.49%) ND 46 (50.55%)	S. globosa (ND) S. schenckii (ND)	S. globosa (ND) S. schenckii (ND)	[76]
		São Paulo	25 from 2003–2013.	Male (18) Female (7)	Average: 42.48	Fungal culture Histopathology	Lymphocutaneous 20 (80%) Fixed cutaneous 5 (20%)	S. schencki sensu lato	Sporothrix spp.	[77]
		São Paulo	20 from 2012–2020	Male (9) Female (11)	Average: 2.2	Direct microscopy, Fungal culture, Histopathology	Lymphocutaneous 10 (50%) Multiple-inoculation 5 (25%) Fixed-cutaneous 3 (15%) Ocular-mucosal 2 (10%)	Sporothrix spp.	Sporothrix spp.	[78]
		Rio de Janeiro	1	Male	35	Direct microscopy, fungal culture	Osteomyelitis	S. schenckii complex	Sporothrix spp.	[79]
		Rio de Janeiro	1	Female	68	Direct microscopy (KOH), fungal culture (Sabouraud Dextrose Agar 2%, and Mycosel Agar, Brain Heart Infusion Agar, Potato Dextrose Agar), Lactophenol Cotton Blue and MALDI-TOF MS	Ocular	S. brasiliensis	S. brasiliensis	[80]
		Rio Grande do Norte	1	Male	50	Direct microscopy (KOH), fungal culture (Mycosel Agar), PCR sequencing >(Calmodulin gene)	Pulmonary	S. brasiliensis	S. brasiliensis	[81]
		Pelotas	7	ND		Gram-stain microscopy, fungal culture (Sabouraud-dextrose agar added with chloramphenicol and Mycosel), PCR sequencing (ITS1 and ITS4 and Calmodulin gene)	Lymphocutaneous 4 (57.1%) Ocular 3 (42.9%)	S. brasiliensis	S. brasiliensis	[82]
		São Paulo	1	Female	12	Histopatology (Grocott stainin), fungal culture.	Immunoreactive cutaneous	Sporothrix spp.	Sporothrix spp.	[83]
		Recife	1	Male	25	Histopatology (hematoxylin–eosin straining), fungal culture (Sabouraud dextrose agar with chloramphenicol), PCR sequencing (using the species-specific primers Sbra-F and Sbra-R and Calmodulin gene)	Ocular	S. brasilienis	S. brasilienis	[84]
		Rio de Janeiro	1	Male	44	Fungal culture	Disseminated	Sporothrix spp.	Sporothrix spp.	[85]
		São Paulo	2	Male	3 and 12	Fungal culture	Ocular	Sporothrix spp.	Sporothrix spp.	[86]
		ND	1	Female	45	Histopathology, Fungal culture (Sabouraud dextrose agar), PCR sequencing (Whole genome sequencing)	Cutaneos carbuncle	S. brasiliensis	S. brasiliensis	[87]
		Rio de Janeiro	1	Male	11	Fungal culture (Sabouraud’s dextrose agar), Culture microscopy with Lactofenol blue	Facial Cutaneous	Sporothrix spp.	Sporothrix spp.	[88]
		Guarulhos, Sao Paulo	1	Male	56	Fungal culture, Histopathology (Peryodic Acid Schiff staining),	Disseminated	Sporothrix spp.	Sporothrix spp.	[89]
		São Paulo	1	Female	39	Fungal culture (Sabouraud agar)	Lymphocutaneous	Sporothrix spp.	Sporothrix spp.	[90]
		Brasilia	1	Male	26	Fungal culture	Disseminated	Sporothrix spp.	Sporothrix spp.	[91]
		Rio de Janeiro	4 from 2006–2016	Female Age ranged from 18–34	Average 25	Fungal culture, PCR sequencing (Primer T3B fingerprintig assay)	Fixed cutaneous 2 (50%) Lymphocutaneous 2 (50%)	Sporothrix spp. 2 (50%) S. brasiliensis 2 (50%)	Sporothrix spp. 2 (50%) S. brasiliensis 2 (50%)	[92]
		Rio de Janeiro	3 from 2006 to 2013	Male Age ranged from 25–43	Average 32	Fungal culture, PCR sequencing (primer T3B fingerprinting assay )	Disseminated 3	S. brasiliensis	S. brasiliensis	[93]
		Rio de Janeiro	1	Male	66	Direct microscopy, fungal culture (Sabouraud dextrose agar, potato dextrose agar, corn meal agar and and brain heart infusion agar), Histopatology, PCR sequencing (Calmodulin gene)	Lymphocutaneous	S. globosa	S. globosa	[94]
		Palmeira das Missões	1	Male	73	Fungal culture	ND	S. schenckii complex	Sporothrix spp.	[95]
		Rio de Janeiro	1	Male	5	Fungal culture and Histopatology	Osteoarticular	S. schenckii	Sporothrix spp.	[96]
		Rio de Janeiro	1	Male	61	Fungal culture, PCR sequencing (primer T3B fingerprinting assay)	Disseminated	S. brasiliensis	S. brasiliensis	[97]
		ND	1	Male	49	Fungal culture	Disseminated	S. schenckii	Sporothrix spp.	[98]
		Espírito Santo	3	Female	30 and 10	Direct microscopy (KOH), fungal culture (Sabouraud Dextrose agar and Mycosel agar^®), assimilation of sugar test	Chancre 3	S. brasiliensis	S. brasiliensis	[99]
		Espírito Santo	3	Male	14		Chancre 3	S. brasiliensis	S. brasiliensis	[99]
		Rio de Janeiro	1	Female	9	PCR sequencing (calmodulina gene)	Dacryocystitis	S. brasiliensis	S. brasiliensis	[100]
		Rio de Janeiro	2	Female	22 and 27	Fungal culture, PCR sequencing (Calmodulina gene)	Fixed Cutaneous	S. brasiliensis	S. brasiliensis	[101]
		Rio de Janeiro	1	Male	6	Fungal culture, PCR sequencing	Invasive Sinusitis	S. brasiliensis	S. brasiliensis	[102]
		Rio de Janeiro	1	Male	56	Fungal culture, PCR sequencing	Meningitis, Lymphocutaneous	S. brasiliensis	S. brasiliensis	[103]
		São Paulo	20 from 2012–2020	Male 9 (45%)	Age ranged from 2–81 mean 32.2 ± 25.10	Fungal culture	ND	Sporothrix spp.	Sporothrix spp.	[104]
		São Paulo	20 from 2012–2020	Females 11 (55%)	Age ranged from 2–81 mean 32.2 ± 25.10	Fungal culture	ND	Sporothrix spp.	Sporothrix spp.	[104]
		Rio de Janeiro	64 from 2013–2015	ND		Fungal culture (Sabouraud Dextrosa Agar, Mycosel )	Lymphocutaneous 43 (67%) Fixed cutaneous 21 (33%)	S. schenckii sensu lato	Sporothrix spp.	[105]
		Minas Gerais 1 Ceará 1 Goiás 1 Pernambuco2 São Paulo 1	6	ND		Fungal culture (Potato Dextrose agar, Corn Meal agar), Carbohydrate assimilation tests, PCR sequiencing (calmodulin gene)	Lymphocutaneous 2 (33.3%) Disseminated 1 (16.7%) ND 3 (50%)	Sporothrix mexicana 3 (50%) Sporothrix globosa 3 (50%)	Sporothrix mexicana 3 (50%) Sporothrix globosa 3 (50%)	[106]
	Colombia	Antioquia	34	ND		Fungal culture, PCR sequencing (ITS 1–2 and β-tubulin)	ND	S. schenckii sensu stricto 22 (65.7%) S. globosa 12 (34.2%)	S. schenckii 22 (65.7%) S. globosa 12 (34.3%)	[56]
		Bogotá	2.28% (14 cases/612 patients)	Male ND Female ND	Between: 0–18	Fungal culture	ND	Sporothrix spp.	Sporothrix spp.	[107]
		Casanare	1	Male	18	Fungal culture, Histopathology	Verrucose	Sporothrix spp.	Sporothrix spp.	[108]
		Marandúa	1	Female	48	Fungal culture, Histopathology	Fixed cutaneous	S. schenckii sensu lato	Sporothrix spp.	[109]
	Chile	Santiago	1	Male	54	Histopathology	Lymphocutaneous	Sporothrix spp.	Sporothrix spp.	[110]
		Valparaíso	1	Female	75	Fungal culture Direct microscopy, Sugar assimilation (sucrose)	Lymphocutaneous	Sporothrix globosa	Sporothrix globosa	[111]
		Viña del Mar	1	Female	64	Direct microscopy, Fungal culture (Sabouraud with cycloheximide and potato dextrose agar) nitrogen-based agar, sequencing (D1/D2 region of the fungal 26S rRNA gene, it region; a partial fragment of the β-tubulin gene; ITS 1 and 2; and the 5.8S gene (SU)).	Onychomycosis	Sporothrix pallida	Sporothrix pallida	[112]
	Paraguay	Itá	2	Male Male	52	Histopathology (Peryodic Acid Schiff), Fungal culture, direct microscopy with Giensa strein	Lymphocutaneous 1 (50%) Fixed cutaneous 1 (50%)	Sporothrix spp.	Sporothrix spp.	[113]
	Paraguay	Cordillera 2 Guairá, Central 2 Misiones 2 San Pedro 2 Caaguazú 1	11 from 1997–2019.	Male 10 Female 1	Mean Age: 37,6 ± 20 Range: 24–69	Direct microscopy (KOH 10%), fungal culture (Sabouraud agar with glucose 2%, potato dextrose agar with chloramphenicol),	Lymphocutaneous 11 (100%)	Sporothrix schenckii complex	Sporothrix spp.	[114]
	Perú	Apurímac	2	Female	65	Direct microscopy, Giemsa stain Culture Microscopy with lactophenol cotton blue, Carbohydrate assimilation test (sucrose and raffinose) in nitrogen base	Fixed cutaneous	S. schenckii	S. schenckii	[115]
		Apurímac	2	Female	67		Fixed cutaneous	S. schenckii	S. schenckii	[115]
		Apurímac	21	Male (12) Female (9)	Average: 9	Fungal culture	Lymphocutaneous 13 (62%) Fixed cutaneous 8 (38%)	Sporothrix spp.	Sporothrix spp.	[116]
		Apurímac 2850	57 (15/100,000)	Male 1734 Female 1255	ND	Fungal culture, Microscopy with lactophenol cotton blue and PCR sequencing	Lymphocutaneous 2942 (63%) Fixed cutaneous 1728 (37%)	S. schenckii 4651 (99.6%) S. schenckii sensu stricto 19 (0.4%)	Sporothrix spp. 4651 (99.6%) S. schenckii 19 (0.4%)	[117]
		Cajamarca 1500	30 (3/100,000)
La Libertad 100		4 (0.5/100,000)
Cusco 200		2 (0.2/100,000)
Otras regiones 20		≤1 (0.1/100,000)
Abancay		1	Male	6	Fungal culture	Lymphocutaneous	Sporothrix spp.	Sporothrix spp.	[118]
Lima		1	Male	23	Fungal Culture Microscopy with lactophenol blue, MALDI-TOF MS, PCR sequencing (D1/D2 region of the fungal 26S rRNA gene)	Fixed cutaneous	S. schenckii	S. schenckii	[119]
Lima		1	Male	42	Histopathology, Microscopy, Fungal Culture	Disseminated cutaneous	S. schenkii sensu lato	Sporothrix spp.	[120]
Cajamarca		94 from 1991 to 2014	Males (67) Female (27)	Average: 36	Direct microscopy, Gram and Giemsa stain, Fungal culture, Histopathology	Lymphocutaneous 44 (47%) Fixed cutaneous 37 (39%) Disseminated cutaneous 11 (12%) Extra-cutaneous 1 (1%) ND 1 (1%)	S. schenckii	Sporothrix spp.	[121]
Apurímac
Amazonas
Ancash		1	Male	58	Fungal culture	Lymphocutaneous	S. schenckii	Sporothrix spp.	[122]
Cusco		1	Female	53	Fungal culture (Sabouraud)	Disseminated	S. schenckii	Sporothrix spp.	[123]
Uruguay	Tacuarembó 10 Cerro Largo 9 Canelones 9 Montevideo 5 Rocha 4 Paysandú 3 Flores 3 Río Negro 2 Colonia 2 Artigas 1 Rivera 1 Maldonado 1 Soriano 1 Non-registered 20	157 from 1983 to 2020	Male (152)	13–79 age range	Gram staining and culture in Sabouraud	Nodular Lymphatic 120 (76.4%) Fixed cutaneous 30 (19.1%) ND 7 (4.5%)	Sporothrix spp.	Sporothrix spp.	[124]
Uruguay		157 from 1983 to 2020	Female (5)	13–79 age range	Gram staining and culture in Sabouraud		Sporothrix spp.	Sporothrix spp.	[124]
Venezuela	Caracas	68	ND		Fungal culture, PCR sequencing (Calmodulin locus and ITS regions)	ND	S. schenckii 42 (62%) S. globosa 26 (38%)	S. schenckii 42 (62%) S. globosa 26 (38%)	[125]
	Aragua 55 Miranda 32 Other states 46	133 from 1963–2019	Male (95) Female (38)	0–15 15–30 >30	Direct microscopy Fungal culture	Lymphocutaneous 84 (63.15%) Fixed cutaneous 48 (36.09%) Cornea 1 (0.7%)	S. schenckii sensu lato 130 (97.7%) ND 3 (2.3%)	Sporothrix spp.	[126]
	Bolívar 14	0.55% (220 cases/39,806 patients)	ND	25–45 years	Microscopy and fungal culture	ND	Sporothrix spp.	Sporothrix spp.	[127]
	Caracas 160
	Carabobo 6
	Falcón 3
	Lara 5
	Mérida 1
	Monagas 24
	Sucre 1
	Táchira 2
	Zulia 4
	Costal Range 22	31 from 1973–2013	Male 64% Female 36%		Microscopy, fungal culture, pruebas bioquímicas, PCR sequencing (Calmodulin gene and ITS 4–5)	Fixed cutaneous 18 (60%) Lymphocutaneous 11 (36.33%) Disseminated 1 (3.33)%	S. schenckii sensu stricto 17 S. globosa 13 and Ophiostoma stenoceras 1	S. schenckii 17 (56.67%) S. globosa 13 (43.33%)	[128]
	Andes 7
	Plains 2

ND: Not Determined.

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

Share and Cite

MDPI and ACS Style

Hernández-Castro, R.; Pinto-Almazán, R.; Arenas, R.; Sánchez-Cárdenas, C.D.; Espinosa-Hernández, V.M.; Sierra-Maeda, K.Y.; Conde-Cuevas, E.; Juárez-Durán, E.R.; Xicohtencatl-Cortes, J.; Carrillo-Casas, E.M.; et al. Epidemiology of Clinical Sporotrichosis in the Americas in the Last Ten Years. J. Fungi 2022, 8, 588. https://doi.org/10.3390/jof8060588

AMA Style

Hernández-Castro R, Pinto-Almazán R, Arenas R, Sánchez-Cárdenas CD, Espinosa-Hernández VM, Sierra-Maeda KY, Conde-Cuevas E, Juárez-Durán ER, Xicohtencatl-Cortes J, Carrillo-Casas EM, et al. Epidemiology of Clinical Sporotrichosis in the Americas in the Last Ten Years. Journal of Fungi. 2022; 8(6):588. https://doi.org/10.3390/jof8060588

Chicago/Turabian Style

Hernández-Castro, Rigoberto, Rodolfo Pinto-Almazán, Roberto Arenas, Carlos Daniel Sánchez-Cárdenas, Víctor Manuel Espinosa-Hernández, Karla Yaeko Sierra-Maeda, Esther Conde-Cuevas, Eder R. Juárez-Durán, Juan Xicohtencatl-Cortes, Erika Margarita Carrillo-Casas, and et al. 2022. "Epidemiology of Clinical Sporotrichosis in the Americas in the Last Ten Years" Journal of Fungi 8, no. 6: 588. https://doi.org/10.3390/jof8060588

APA Style

Hernández-Castro, R., Pinto-Almazán, R., Arenas, R., Sánchez-Cárdenas, C. D., Espinosa-Hernández, V. M., Sierra-Maeda, K. Y., Conde-Cuevas, E., Juárez-Durán, E. R., Xicohtencatl-Cortes, J., Carrillo-Casas, E. M., Steven-Velásquez, J., Martínez-Herrera, E., & Rodríguez-Cerdeira, C. (2022). Epidemiology of Clinical Sporotrichosis in the Americas in the Last Ten Years. Journal of Fungi, 8(6), 588. https://doi.org/10.3390/jof8060588

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Menu

Epidemiology of Clinical Sporotrichosis in the Americas in the Last Ten Years

Abstract

1. Introduction

2. Materials and Methods

3. Epidemiology of Sporotrichosis in North America

4. Epidemiology of Sporotrichosis in Central America and the Caribbean

5. Epidemiology of Sporotrichosis in South America

6. Discussion

Author Contributions

Funding

Institutional Review Board Statement

Informed Consent Statement

Data Availability Statement

Conflicts of Interest

References

Share and Cite

Article Metrics

Article Access Statistics

Further Information

Guidelines

MDPI Initiatives

Follow MDPI