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Review

Leptospirosis and Coinfection: Should We Be Concerned?

by
Asmalia Md-Lasim
1,2,
Farah Shafawati Mohd-Taib
1,*,
Mardani Abdul-Halim
3,
Ahmad Mohiddin Mohd-Ngesom
4,
Sheila Nathan
1 and
Shukor Md-Nor
1
1
Department of Biological Sciences and Biotechnology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, UKM, Bangi 43600, Selangor, Malaysia
2
Herbal Medicine Research Centre (HMRC), Institute for Medical Research (IMR), National Institue of Health (NIH), Ministry of Health, Shah Alam 40170, Selangor, Malaysia
3
Biotechnology Research Institute, Universiti Malaysia Sabah, Jalan UMS, Kota Kinabalu 88400, Sabah, Malaysia
4
Center for Toxicology and Health Risk, Faculty of Health Sciences, Universiti Kebangsaan Malaysia, Kuala Lumpur 50300, Federal Territory of Kuala Lumpur, Malaysia
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2021, 18(17), 9411; https://doi.org/10.3390/ijerph18179411
Submission received: 18 May 2021 / Revised: 5 August 2021 / Accepted: 23 August 2021 / Published: 6 September 2021
(This article belongs to the Section Infectious Disease Epidemiology)
Browse Figure
Review Reports Versions Notes

Abstract

:
Pathogenic Leptospira is the causative agent of leptospirosis, an emerging zoonotic disease affecting animals and humans worldwide. The risk of host infection following interaction with environmental sources depends on the ability of Leptospira to persist, survive, and infect the new host to continue the transmission chain. Leptospira may coexist with other pathogens, thus providing a suitable condition for the development of other pathogens, resulting in multi-pathogen infection in humans. Therefore, it is important to better understand the dynamics of transmission by these pathogens. We conducted Boolean searches of several databases, including Google Scholar, PubMed, SciELO, and ScienceDirect, to identify relevant published data on Leptospira and coinfection with other pathogenic bacteria. We review the role of the host-microbiota in determining the synanthropic interaction of Leptospira sp. with other bacteria, thus creating a suitable condition for the leptospira to survive and persist successfully. We also discuss the biotic and abiotic factors that amplify the viability of Leptospira in the environment. The coinfection of leptospira with pathogenic bacteria has rarely been reported, potentially contributing to a lack of awareness. Therefore, the occurrence of leptospirosis coinfection may complicate diagnosis, long-lasting examination, and mistreatment that could lead to mortality. Identifying the presence of leptospirosis with other bacteria through metagenomic analysis could reveal possible coinfection. In conclusion, the occurrence of leptospirosis with other diseases should be of concern and may depend on the success of the transmission and severity of individual infections. Medical practitioners may misdiagnose the presence of multiple infections and should be made aware of and receive adequate training on appropriate treatment for leptospirosis patients. Physicians could undertake a more targeted approach for leptospirosis diagnosis by considering other symptoms caused by the coinfected bacteria; thus, more specific treatment could be given.

1. Introduction

Leptospirosis is a zoonotic disease caused by the spirochete bacteria Leptospira spp. that belongs to the genus Leptospira [1]. There are 20 species of Leptospira categorised into 24 serogroups with more than 300 serovars [2]. It is estimated that there are one million apparent Leptospira infections annually, with nearly 60,000 deaths [3,4], rendering leptospirosis a significant threat to the global public [5].
The number of leptospirosis outbreaks is widespread throughout tropical and subtropical countries and frequently associated with natural disasters such as extreme flooding and heavy rainfall [6,7]. Direct contact with water, soil and vegetation contaminated with pathogenic leptospires during water-related incidence has been widely documented as the risk factor for leptospirosis [8,9,10]. Occupational activities that place individuals at high risk of infection include farming, agriculture, mining, sewage maintenance, and military action [11,12,13,14,15].
The transmission of Leptospira between humans, animals, and the environment is complex and not well documented [16]. Although the presence and survival capability of multiple strains of Leptospira in environmental samples may vary (soil, water, streams, and sewers) [17,18], the dynamics and mechanism of Leptospira in the environment are still unclear [19]. Although pathogenic leptospira can produce biofilm in nature [20,21,22], the interaction with other microorganisms in the environment might support the survival and persistence of leptospiral pathogens outside the host [23,24].
Coinfection can influence epidemiology and disease severity [25]. A coinfection involving simultaneous infection of several pathogens in the same host may result in different types of diseases [26]. A coinfection is synonymous with simultaneous infection, mixed infection, multiple infections, concomitant infection, concurrent infection, polyinfection, polyparasitism, and multiple parasitism of an individual host [27,28]. Coinfection involves infectious pathogens from various taxa levels (bacteria, fungi, parasites, and viruses) and genetic variations of the same infectious agents [29]. Coinfections are more likely to have detrimental impacts on host health compared to mono-infections. High pathogen abundance and simultaneous interaction could significantly affect infection dynamics by changing host vulnerability and the risk of multiple infections simultaneously.
For instance, leptospirosis co-infection with other diseases such as melioidosis [30], dengue fever [31], malaria [32], and typhus [33] has been well documented. Such co-infection typically leads to misdiagnosis, increases the severity of the disease, and can even benefit the causative agents [34]. The treatment of leptospirosis coinfection with other diseases may bring additional challenges if the symptom of the coinfection is similar to other common diseases [35,36,37]. Environmental exposure and the similar nature between pathogenic environmental bacteria may increase the possibility of coinfection and lead to miss or underdiagnosis. However, it is important to develop a better knowledge of the dynamics of transmission of these pathogenic Leptospira and ecological drivers of coinfections to improve a targeted public health response. This review aims to provide an overview of the present knowledge of leptospirosis and the probability of leptospirosis coinfection with environmental pathogenic bacteria. Given the lack of data on leptospirosis coinfection with environmental bacteria, we also include other potential coinfection.

2. Leptospira—An Overview of Epidemiology, Transmission and Persistence in the Environment

Leptospira, derived from the Greek, term leptos (small) and the Latin word speira (a coil), is a single, motile, spiral-shaped, Gram-negative spirochete with internal flagella and finely coiled [38]. The bacteria are usually 0.1–0.2 µm in diameter and between 6 to 20 µm in length. Their helical amplitude is approximately 0.1 µm to 0.15 µm, with a wavelength of 0.5 µm. Leptospira demonstrates two forms of movement, translational and rotational [39]. Its morphology can differ when sub-cultured in vitro but restored when passaged in hamsters [40]. Leptospires are aerobic microbes with optimal growth between 28 °C and 30 °C. They also grow in simple media enriched with ammonium salts [41], vitamin B1, B12 [42], and long-chain fatty acids [43].
Leptospires are spirochaetes that belong to the order Spirochaetales, a family of Leptospiraceae. The Leptospiraceae family consists of two genera, Leptospira and Leptonema, and the genus Leptospira is divided into pathogenic, intermediate pathogenic, and non-pathogenic Leptospira [40]. Several species are classified within each category based on phenotypic properties and genotypic classification. The genus Leptopsira has been divided into three lineages based on pathogenicity and genetic analysis with pathogenic, saprophytic and intermediate pathogenic species (Table 1) [44,45,46,47,48]. Within each species, Leptospira is further subdivided into serovars, which is the smallest taxonomic unit of the bacteria. Approximately 300 pathogenic serovars have been identified, 88 of which belong to the well-characterised pathogenic species, Leptospira interrogans [36]. However, classification based on whole-genome sequencing may increase the number of the species in the future [48,49].

2.1. Epidemiology of Leptospira

Leptospirosis is distributed globally in rural and urban areas. The disease occurs in the temperate and tropical regions, with higher incidence rates in the tropics [50]. It remains one of the most important public health issues due to the wide range of serovars circulating within large reservoirs. Large populations of rodents, farm animals and dogs are capable of being colonised within the kidneys and shedding of Lepospira in urine which increases the spread to the environment [51,52,53]. If Leptospira that persist in the renal and urinary systems are shed from animals, the bacteria can survive under optimum environmental conditions for months and up to a year [54,55]. Animals that have recovered from leptospirosis may continue to be carriers of Leptospira within the renal tubules for several months [56].
Additionally, climate factors may influence Leptospira infectivity by providing ideal conditions for Leptospira to survive for prolonged periods of time, with transmissions becoming worse during heavy rainfall and flooding. Leptospira can easily contaminate the environment and pose a greater risk of infection through skin wounds during heavy rain. The water hits land surfaces and its either stored in the subsurface as soil moisture, or lost to evapotranspiration into freshwater bodies which leads to humans to be exposed [57,58,59]. This situation increases the possibility of Leptospira infections among rodents and increased interaction with humans will lead to increased occurrence of leptospirosis [60]. Reports on flooding is a significant factor for the increase in leptospirosis cases, and are common in Thailand, the Philippines, Sri Lanka, and Malaysia [61,62,63,64].
Other factors such as poverty, urbanisation, and rapid population growth may have an impact on the high prevalence of Leptospira infections in wildlife, domestic animals, and humans [65]. These situations increase reservoir populations and compromise basic health care services, sanitation, waste management, whilst exposing humans to Leptospira. The particular areas that overflow by heavy rainfalls that cannot be drained due to the faulty sanitation network, causing rodents to abandon their burrows and contaminate the water with their urine [66,67]. In addition to contaminated floodwater, rodents increase the possibility of transmitting bacteria to humans through cuts and abrasions of the skin [68], following prolonged immersion in contaminated water [51]. Transmission is most likely to occur during the cleaning of the flooded muddy houses and surroundings.
Occupational groups such as banana plantation farmers, sugarcane workers, paddy farmers, veterinarians, animal shelter employees, hunters, wet market workers and abattoir workers are at high risk of infection due to their job description involves contact with water and soils [69,70]. They are typically prone to skin cuts, abrasions during the activities in the particular areas which are providing a suitable environment and are rich with a source of food favouring the presence of rodents [71]. The rodent might share similar places with people, easily moving around and excreting bacteria into the environment via urine [72]. Farm labourers are especially vulnerable to injury, increasing their susceptibility to bacterial infections, partially due to a lack of adherence to the need for personal protective equipment.

2.2. Leptospira Persistence in the Environment

The ecological and environmental metabarcoding of DNA now routinely includes studies on the persistence and survival of Leptospira in the environment [73,74,75,76]. Using this approach, Sato et al. [75] discovered three pathogenic strains and non-pathogenic Leptospira strains from aquatic samples, which correlated with the level of precipitation. Further studies have also associated short to long term persistence in soil and water and the ability of the pathogen to survive and remain infectious outside the host [77]. Environmental parameters such as salinity, pH, temperature, humidity and high oxygen levels play a crucial role in the survival of Leptospira in the environment [38,78,79].
Many studies worldwide have shown a significant correlation between soil chemical properties and the survival of Leptospira bacteria. For example, in India, soil samples from rice fields and nearby stables were highly prevalent for Leptospira compared to urban sites [80]. Similarly, in Australian cane fields, the bacteria can survive up to seven weeks in acidic soil at pH 6.2 and three weeks in the rainwater-flooded soil [81]. Thibeaux et al. [48] reported that soil biochemical properties might determine the persistence of Leptospira strains and the risk of transmission to humans.
The presence of Leptospira is also prevalent in water bodies such as groundwater, rivers, sewage, and surface water in tropical and non-tropical regions [82]. The aqueous environment associated with salt concentration, high oxygen, pH, and alkalinity was also considered a key factor in the transmission of Leptospira to its host [83]. Optimal conditions for Leptospira growth have been reported at pH 6.7 to 7.3 in river water and dissolved solid salts surroundings [84]. However, a high concentration of salt is unsuitable for the long-term survival of pathogenic Leptospira [84], while other studies demonstrated the presence of Leptospira under neutral pH and slightly alkaline conditions (up to pH 8.0) [85]. Saito et al. [86] reported a steady decrease in pathogenic Leptospira motilities after 10 h of exposure. Hence, there is a critical need to address the survival of Leptospira in the environment with other factors such as biotic and abiotic interactions with other environmental pathogens leading to coinfections.
A study in Kelantan, Malaysia, identified pathogenic Leptospira from soil and water samples. Out of 42 samples of water and soil, 42.8% were positive for pathogenic Leptospira such as Leptospira kmetyi (17%), followed by intermediate strains of Leptospira wolffi (7%), Leptospira licerasiea (5%), Leptospira fainei (2%), and Leptospira inadai (2%). Culture-positive Leptospira obtained from the water samples was lower at 19.1%, likely due to toxic components within the sampled cloudy and foul-smelling water that limits Leptospira survivability [30].

3. Leptospira Coinfection, Is It Possible?

Currently, bacterial-viral coinfection is one of the biggest medical concerns, resulting in increased mortality rates is one of the biggest medical concerns. Approximately 30% of human diseases are caused by coinfection and could reach up to 80% in human communities [87]. Leptospirosis coinfection with other pathogenic bacteria in humans is a special case and also known as “the great mimicker” [35,88,89]. Unfortunately, no pathogenic effects and symptoms are observed in the patients at the early stage. The clinical presentations of leptospirosis coinfection are considerably overlapping, leading to misdiagnosis and mistreatment. Patients may develop fever, abdominal pain, myalgia, headache, vomitting, as well as long-term infections or death [35,36,90,91].
The majority of leptospirosis cases are mild and resolve spontaneously. Minor cases of leptospirosis resolve with time and oral antibiotics such as doxycycline, azithromycin, ampicillin and amoxicillin, which are administered based on the severity of the illness. Treatment with antibiotics must be initiated as soon as a provisional diagnosis of leptospirosis is suspected, regardless of the length of the symptom [92]. Furthermore, most of the coinfected patients respond effectively to fluid therapy, doxycycline and closely monitoring of their platelet count and hematocrit [93,94]. However, in some leptospirosis coinfections, treatment could not be assessed due to the lack of data, and it is critical to determine these different of infections that can provide relevant treatment decisions for patients with coinfections [95].

4. Leptospira Coinfection in Humans

It is often difficult to distinguish between the coinfection of Leptospira and other pathogens purely based on clinical presentation. Diagnosis is particularly challenging when broad spectrum of clinical phenotypes are presented [37]. Leptospira coinfection is more common with pathogenic agents causing dengue, malaria and scrub typhus although coinfection with arboviruses may also occur but is less frequently reported. During an outbreak of arboviruses-associated diseases, if conflicting microbiology or pathology results are obtained, clinicians should suspect a leptospiral coinfection, particularly among individuals from rural areas or travellers returning from epidemic areas [96]. The co-occurrence of leptospirosis with other diseases is summarised in Table 2.

4.1. Dengue

There have been increased reports of leptospirosis and dengue coinfection from several parts of the world especially Peru, Malaysia, and India [36,37,97,98]. The occurrence of leptospirosis and dengue coinfection has always been related to climate, with cases spiking during rainfall or monsoon seasons. During heavy rainfall, stagnant water is an ideal breeding ground for mosquitoes, while an increased rat population feeding on garbage brought to localities by flood waters transmits leptospira in their urine. Vella-Mendoza et al. [97] revealed that the prevalence of leptospirosis-dengue coinfection was higher in the age groups 20–44 and 45–59 at 37.5% and 25% respectively. Males are more vulnerable to coinfection, which could be due to a variety of factors such as work exposure, heavy rainfall and flooding.
Clinical features of coinfection may present as headache, myalgia and fatigue accompanying fever, making diagnosis more difficult, especially with an acute co-infection [37]. Diagnosis of leptospirosis includes detection of IgM antibodies by ELISA which is highly sensitive and IgM positive for dengue indicates a recent dengue infection. The polymerase chain reaction is also performed depending on the availability of the test. The majority of dengue treatments are driven by symptoms, whereas leptospirosis requires immediate administration of either penicillin, ceftriaxone or doxycycline to prevent complications.
Table
Table 2. Cases of leptopsira co-infections.
Table 2. Cases of leptopsira co-infections.
LocationYearStudy TypeNo. EnrolledNo.
Co-Infections		Co-Infection Prevalence (%)AgeDiagnostic TestReferences
Dengue
Malaysia2008Case report1110041ELISA IgM[99]
Malaysia2012Cross sectional study843238.1Mean: 39.4ELISA IgM, MAT[35]
Puerto Rico2012Case report1110042ELISA IgM, PCR[100]
Peru2015Case report1110010ELISA IgM, MAT[101]
Sri Lanka2015Case report1110052ELISA IgM, IgG[102]
Malaysia2017Retrospective study268114.130–32ELISA IgM, MAT, PCR[37]
Colombia2018Case study1110087ELISA IGM, PCR[103]
South India2018Retrospective study974333.4Mean: 37.4ELISA IgM[36]
Kelambakan2018Cross sectional study1004421–30ELISA IgM, PCR[104]
Sri Lanka2018Retrospective study6116.717–73ELISA IGM, PCR[105]
IndiaNMCase report1110039ELISA IgM, MAT, DFM[106]
Malaria
Thailand1999–2002Cross sectional study1873920–38ELISA IgM, MAT[107]
India2010Case report2210038 & 34ELISA IgM, MAT[108]
India2011Case report181810028–40ELISA IgM, SAT[109]
Tamil Nadu2012Case report2204822Mean: 29MSAT, MAT[110]
India2014Case report1110024RMAT, MAT[111]
Malaysia2011–2014Retrospective study1112623.4Mean: 33MAT, BFMP[112]
Melioidosis
Malaysia2010Case report2042029–60PCR, Blood C & S[113]
Malaysia2010Retrospective study15342.620–59ELISA IgM, PCR[114]
Malaysia2016Case report1110040PCR, ELISA IgM, MAT[86]
Typhus
Taiwan1997Retropective study86910.5Mean: 38ELISA IgM, MAT, IFA[115]
China2011Case report1110053ELISA IgM, MAT[116]
IndiaNMCase report1110040ELISA IgM, MAT[117]
IndiaNMCase report111009ELISA IgM, ICT[118]
India2015Cross sectional study258103.88NMELISA IgM, PCR[119]
Tamil Nadu2014–2015Retrospective study354236.5Mean: 31.48ELISA IgM, MAT[120]
Typhus
India2018Retrospective study22941Mean: 38ELISA IgM, PCR[121]
India2017Retrospective study72182–90ELISA IgM[122]
India2018–2019Retropective study6081142.31NAELISA IGM[123]
Note: N, Sample size, ELISA—Enzyme linked immunosorbent assay, PCR—Polymerase Chain reaction, IgM—Immunoglobulin M, MAT—Microscopic Agglutination Test, DFM—Dark Field Microscopy, RMAT—Rapid malaria antigen test, qPCR—Quantitative Polymerase Chain reaction, RT-PCR—Reverse Transcription Polymerase Chain reaction, BFMP—Blood Film for Microscopy Parasite, NA—not available.

4.2. Malaria

Malaria is a vector borne disease, transmitted by female Anopheles mosquitoes, with approximately 229 million cases and 435,000 deaths. Malaria epidemics can occur when climate and other conditions favour malaria transmission in areas where people have little or no immunity. They can also occur when people with low immunity travel to areas with high malaria transmission, for instance to find work, or as refugees. Symptoms of malaria range from asymptomatic or uncomplicated such as fever, headache, myalgia, and general malaise to severe complications.
Malaria and leptospirosis are significant global infections with overlapping geographic distribution, especially in tropical and subtropical countries. As malaria and leptospirosis are common in the tropics, co-infection is to be expected and is more likely to occur by chance. However, there is a common practice in a malaria endemic that if an acutely febrile patient is found to be malaria-positive, malaria is assumed to be the sole cause of fever. Fever, chills, body aches, yellow urine, jaundice, vomiting, and headache were all significant symptoms for coinfection patients [107,108,109,110,111,112]. Thus, the clinical symptom of malaria and leptospirosis were similar, making accurate diagnosis difficult without any laboratory confirmation [95]. Failure to recognize acute leptospirosis co-infection may cause a delay in initiating proper therapy and leading to severe complications of leptospirosis such as hepatic and renal failure [110].
The effect of age group, sex, socioeconomic background and living status was associated with poor housing areas, lives in or travels to an area with risk of malaria and leptospirosis. The high proportion of coinfection among male patients was also associated with their job description. However, there is no significant difference between the age of male and female patients. Furthermore, the clinician may also underdiagnose or fail to recognize the infection due to the similarity in clinical presentation resulting in late treatment.
Even though coinfection of leptospirosis and malaria has rarely been reported, there should have a high index of clinical suspicion and, for those who present with fever, thrombocytopenia, multiorgan failure, empirical treatment (3rd generation cephalosporin and doxycycline along with antimalarial) should cover most of the causative agents in case of coinfection. If diagnostic facilities for leptospirosis are not available, it is beneficial to treat the co-infection with a combination of Doxycycline and antimalarial treatment.
Artesunate is used to treat severe malaria cases, whereas Ceftriaxone is effective against bacterial infections and doxycycline is an appropriate therapy against atypical organisms such as Leptopsira and rickettsia. Critically ill patients with severe malaria should be given third generation cephalosporins, Chloroquine or Quinine with doxycycline for effective treatment of both infections simultaneously.

4.3. Melioidosis

Bukholderia pseudomallei is a soil and water surface bacterium found in tropical areas that causes melioidosis after exposure to contaminated water or soils [114]. Melioidosis has been reported in Malaysia and other endemic countries such as Brazil [124], Australia [125], India [126] and Thailand [127]. Infection with B. pseudomallei is most commonly associated with an inoculating injury, ingestion, or inhalation of aerosolized bacteria and occurs more frequently in the wet season or following extreme weather events such as tropical storms.
Co-occurrence of leptospirosis and melioidosis has rarely been reported. Based on our extensive literature review, there are only three publications on melioidosis and leptospirosis coinfection which may be attributed to a lack of awareness and underreporting. Clinical presentations are known to overlap fever, jaundice, headache, myalgia, diarrhoea, cough and vomiting. Furthermore, the relative risk of melioidosis in diabetic patients is strong leading to death. 83% (5/6) of the patients reported from the three publications died due to the misdiagnosis or delayed diagnosis [86,113,114], When the leptospira and melioidosis coinfection was recognized, the surviving patient was closely monitored and administered with appropriate antibiotics until his condition improved. His fever was completely recovered in 10 days and was discharged with oral doxycycline and co-trimoxazole for five months.
B. pseudomallei is commonly susceptible to ceftazidime, amoxycillin-clavulanic acid, penicillin, imipenem, azlocillin, doxycycline, aztreonam and ceftriaxone but resistant to gentamicin and colistin [128]. Intravenous ceftazidime or meropenem is the preferred choice for initial therapy for most patients with melioidosis. Moreover, most of the patients were treated with IV ceftriaxone and doxycycline during the initial phase and increased the dose to ceftazidime and cystaline Penicillin after the confirmation of the diseases.

4.4. Typhus

Scrub typhus is a rickettsial zoonosis caused by Orientia tsutsugamushi and transmitted through bites by infected chiggers. Fleas, ticks, louse or mites become carriers of the bacteria when they feed on the blood of infected humans (epidemic typhus) or infected rodents (a reservoir of Leptospira). Typhus and leptospirosis are likely to share similar routes of transmission when rats are abundant. Humans usually become infected when infected flea feces contaminates excoriated skin or are inhaled [129]. Other studies have found that R. rattus and R. norveigus are the primary host of R. typhi infected X. cheopsis fleas in Indonesia, as well as maintenance hosts for Leptospira spp. [129,130,131]. Incidence of leptospirosis increases after the rainy season due to water logging resulting in contact with animal urine, similar to scrub typhus that increases due to the large trombiculid mite population [115].
Generally, patients may present with clinical features such as headache, myalgia, cough, abdominal pain, rash, thrombocytopenia, leukocytosis and nausea. It is difficult to differentiate between leptospirosis and scrub typhus infection. Most of the coinfected patients have higher median platelet counts with lower blood bilirubin and creatine concentration compared to leptospirosis patients alone. It is important that the clinician kept in their mind to performed other appropriate diagnosis if the patient is travelling to or returning from any endemic areas. In serious situations, the coinfection cases can be fatal if not treated appropriately. In one example, a patient presented with leptospirosis and was treated appropriately with high doses of penicillin. However, the patient’s condition become worse and died from respiratory distress syndrome which is one of the common causes of death from O. tsutsugamuchi infections [115,132]. Intravenous penicillin is one of the choice treatment on severe leptospirosis, however O. tsutsugamushi was resistant to these antibiotics [133].
Hence, timely detection and appropriate management of leptospira co-infection with O. tsutsugamushi is important to significantly reduce the severity of the cases. An early detection of leptospirosis and rickettsioses was presumed when the 53 old healthy fruit salemans presented severe sepsis with impending respiratory failure. Empiric antibiotics with intravenous penicillin (treatment of leptospirosis) and levofloxacin (treatment of rickettsioses and other negative bacterial infection) were given and the patient’s condition improved and urine output increased gradually. The patient was discharged after 10 days in hospitals and was asymptomatic at 1 month follow up [116]. Tetracycline also been used to treat patients with leptospirosis and scrub typhus. Even though the doxycycline has usually been used for mild leptospirosis, but in the serious situation, high dose penicillin remains the choice. Other like ceftriaxone, ampicillin and cefotaxime can be considered as alternatives for penicillin [117].

5. High Potential for Coinfection with Environmental Bacteria

There is a unique interaction between the host and the resident microbiome by providing innate immunity, metabolism, diseases, and nutrition [134]. Microbial cells can quickly adapt to environmental differences through a wide range of genotypic and phenotypic properties. This adaptation is crucial for bacterial survival under extreme conditions. Therefore, bacteria play a crucial role in ecosystem cycles such as soil structure improvement, water recycling, soil aggregation, and soil nutrient sequence [135]. Various pathogenic bacteria may be shed between the pores of soil aggregates and embedded in the complex structure of clay. The interaction of coinfection between environment, vector and human was shown in Figure 1. However, the survival of the bacterial community is also influenced by pH, type of soil, nutrients, climate change and crop type. To date, environment bacterial pathogens such as Clostridium [136], Escherichia coli [137], and Bacillus [114] have contributed significantly to human health. Although rarely reported, the possibility of coinfection of these bacterial pathogens and Leptospira might occur because they are easily found in water, soil, and contaminated foods. To date, there is a novel case reported in a 32-year-old Malaysian coinfected with Leptospira and E. coli during her post-partum period. The patient suffered from acute neurological deterioration, pulmonary haemorrhage, disseminated intravascular coagulopathy, and multi-organ failure [138]. The observed symptoms mirrored clinical presentations typical of headaches, acute fever, rash, jaundice, malaise, myalgia, and lethargy [32]. Further investigations should address the probability that humans may be directly or indirectly exposed to multiple local infections [139].
The persistence of E. coli in the environment is becoming a major issue for farmers and public health. Most outbreaks were triggered by the consumption of undercooked beef and tainted raw vegetables [140], decomposed manure, human sewage, slaughterhouse wastes, and animal slurry. The bacteria can live under favourable conditions for up to a year. For example, Zhang et al. [141] found that E. coli O157: H7 could live for 33 days in neutral soils and 7 days in acid soils. They also reported that the relationship between soil pH and organic carbon could increase the period of E. coli survival time but negatively correlated with exchangeable K. Shiga-like toxin E. coli (STEC) produces two different toxins (Stx 1 and Stx 2) and causes haemorrhagic colitis [142], haemolytic-uremic syndrome [143], and intestinal pathogenic E. coli. Once infected, E. coli may persist for up to one year; however, the resident strain shift in the human intestine is not well understood [144].
Clostridium encompasses more than 200 species of Gram-positive bacteria, with 50 species contributing to intestinal diseases in humans and animals [145]. It prefers growth under low oxygen levels and ideal conditions that can multiply rapidly. Clostridium perfringens can produce more than 20 virulent toxins and be clinically associated with systemic and enteric diseases, including food poisoning, enterocolitis, gas gangrene, fever, muscle tissue destruction, and massive local oedema. The first profiling of co-regulated bacterial transcriptomes showed that TLR2 and NLRP3 inflammasome genes were induced by 33% during clostridial myonecrosis infections, with the C. perfringens gene successfully regulated [146].
Bacteria belonging to the genus Bacillus are Gram-positive, rod-shaped, spore-forming, motile and easily found in the soil. Although used to protect plants and animals from microbial infection by secretion of antibiotics, volatile compounds, and enzymes [147], it was not considered pathogenic to humans, except for a few strains such as Bacillus anthracis that can cause anthrax in humans and animals. Humans usually get infected during contact with infected animals or spore ingestion due to the inhalation of spores from soil management activities [148]. Amazingly, the bacteria are highly resistant to desiccation and remained inactive for a few years until the condition is ideal. Anthrax is also a potential biological weapon in a biological attack or bioterrorism [149].

6. Future Direction

Based on the frequency of coinfections, it is vital to enhance the clinical examination, protocols, and interpretation of laboratory results to enable accurate clinical diagnosis. During arbovirus-related outbreaks, a systematic diagnostic protocol should include Leptospira as a possible co-infecting agent [150], and clinical practitioners should be made aware of the possibilities of coinfection and seek further consultation with infectious disease physicians before the patient faces severe complications [151].
Several questions remain to be answered, such as it is unclear whether the presence of multiple infections in patients may present as short- or long-term clinical presentations. There is a gap describing the possibilities of leptospirosis coinfection transmission. As coinfection of leptospirosis with other diseases is now more frequently reported, early diagnosis of leptospirosis coinfection requires clinical awareness, and appropriate treatment to prevent any disease severity and complications.
On the other hand, it is difficult to control the emergence of new bacterial coinfections with leptospira, particularly bacteria which reside in various parts of soil and water. Unravelling the unique interaction between leptospira and other pathogenic bacteria may increase the knowledge of new potential transmission. Shotgun Metagenomic DNA sequencing allows the analysis of the taxonomic structure and functional genetic capacity of the microbiome community [152]. Microbiome research has gained tremendous attention over the last decade, and it has become evident that microbiota associated with other organisms is important to support the health, development, and well-being of their hosts [153]. However, the advancement of genomics practices to clinical microbiology has taken a long and complicated way [154].

7. Conclusions

In conclusion, leptospirosis co-occurrence with other diseases is not often reported but is highly suspected, thus warrants further actions. As such, potential coinfection of Leptospira with other pathogens should be treated accordingly in high-risk patients. Medical practitioners may misdiagnose possible coinfections and should be aware of the appropriate diagnosis protocols prior to treatment. Although Leptospira infection occurs when humans are exposed directly to the infected animal and contaminated environment, there is a significant gap regarding the transmission of other pathogens and coinfection in leptospirosis patients. Further studies should focus on understanding the ecological aspect of the host and the persistence of Leptospira spp. with other pathogenic bacteria in the environment to provide optimal health control and prevention outcomes. Moreover, the development of a leptospirosis coinfection database from metagenom analysis could assist in the development of improved diagnostic and treatment of patients.

Author Contributions

A.M.-L., M.A.-H., S.N., A.M.M.-N., S.M.-N. and F.S.M.-T. participating in the; writing, reviewing and editing of all draft manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Fundamental Research Grant Scheme (FRGS), Ministry of Higher Education FRGS/1/2018/STG03/UKM/02/1.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Acknowledgments

We thank the Director General of Health Malaysia for his permission to published this article. We wish to thank Wildlife Ecology and Disease team (Wardah, Rosha, Zahin, Farisha).

Conflicts of Interest

The authors declare no conflict of interest and the funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

References

  1. Stimson, A.M. Note of an organism found in yellow-fever tissue. Public Health Rep. 1907, 22, 541. [Google Scholar] [CrossRef]
  2. Picardeau, M. Diagnosis and epidemiology of leptospirosis. Med. Mal. Infect. 2013, 43, 1–9. [Google Scholar] [CrossRef]
  3. Costa, F.; Wunder, E.A., Jr.; De Oliveira, D.; Bisht, V.; Rodrigues, G.; Reis, M.G.; Ko, A.I.; Begon, M.; Childs, J.E. Patterns in Leptopsira shedding in Norway rats (rattus norveigicus) from Brazilian slum communities at high risk of disease transmission. PLoS Negl. Trop. Dis. 2015, 9, e0003819. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Hotez, P.J.; Alvarado, M.; Basáñez, M.-G.; Bolliger, I.; Bourne, R.; Boussinesq, M.; Brooker, S.J.; Brown, A.S.; Buckle, G.; Budke, C.M.; et al. The global burden of disease study 2010: Interpretation and implications for the neglected tropical diseases. PLoS Negl. Trop. Dis. 2014, 8, e2865. [Google Scholar] [CrossRef] [Green Version]
  5. Jittimanee, J.; Wongbutdee, J. Prevention and control of leptospirosis in people and surveillance of the pathogenic Leptospira in rats and in surface water found at villages. J. Infect. Public Health 2019, 12, 705–711. [Google Scholar] [CrossRef] [PubMed]
  6. James, S.; Sathian, B.; Van Teijlingen, E.; Asim, M. Outbreak of leptospirosis in Kerala. Nepal J. Epidemiol. 2018, 8, 745–747. [Google Scholar] [CrossRef] [PubMed]
  7. Togami, E.; Kama, M.; Goarant, C.; Craig, S.B.; Lau, C.; Ritter, J.M.; Imrie, A.; Ko, A.I.; Nilles, E.J. A large leptospirosis outbreak following successive severe floods in Fiji, 2012. Am. J. Trop Med. Hyg. 2018, 99, 849–851. [Google Scholar] [CrossRef] [PubMed]
  8. Soo, Z.M.P.; Khan, N.A.; Siddiqul, R. Leptospirosis: Increasing importance in developing countries. Acta Trop. 2019, 201, 105183. [Google Scholar] [CrossRef] [PubMed]
  9. Teh, S.W.; Mok, P.L.; Subbiah, S.K. Misunderstanding in leptospirosis. Acta Trop. 2019, 197, 105046. [Google Scholar] [CrossRef]
  10. Mohamad-Hassan, S.N.; Bahaman, A.R.; Mutalib, A.R.; Khairani-Bejo, S. Serological prevalence of leptospiral infection in wild rats at the National Service Training Centres in Kelantan and Terengganu. Trop. Biomed. 2010, 27, 30–32. [Google Scholar]
  11. Neela, V.K.; Azhari, N.N.; Joseph, N.; Mimie, N.P.; Ramli, S.N.A.; Mustapha, N.F.; Ishak, S.N.; Mohd-Taib, F.S.; Yusof, M.A.; Desa, M.N.M.; et al. An outbreak of leptospirosis among reserve military recruits, Hulu Perdik, Malaysia. Eur. J. Clin. Microbiol. Infect. Dis. 2019, 38, 523–528. [Google Scholar] [CrossRef] [PubMed]
  12. Yupiana, Y.; Wilson, P.R.; Weston, J.F.; Vallee, E.; Collins-Emerson, J.M.; Benschop, J.; Scotland, T.; Heuer, C. Epidemiology investigation of Leptospira spp. in a dairy farming enterprise after the occurrence of three human leptospirosis cases. Zoonoses Public Health 2019, 66, 470–479. [Google Scholar] [CrossRef]
  13. Brinker, A.J.; Blazed, D.L. An outbreak of leptospirosis among united states military personnel in Guam. Trop. Dis. 2017, 3, 16. [Google Scholar] [CrossRef] [Green Version]
  14. Parveen, S.M.A.; Suganyaa, B.; Sathya, M.S.; Margreat, A.A.P.; Sivasankari, K.S.; Shanmughapriya, S.; Hoffman, N.E. Leptospirosis seroprevalence among blue metal mine workers of Tamil Nadu, India. Am. J. Trop. Med. Health 2016, 95, 38–42. [Google Scholar] [CrossRef]
  15. Ambekar, A.N.; Bharadwaj, R.S.; Joshi, S.A.; Kagal, A.S.; Bal, A.M. Sero surveillance of leptospirosis among sewer workers in Pune. Indian J. Public Health 2004, 48, 27–29. [Google Scholar]
  16. Barragan, V.; Olivas, S.; Keim, P.; Pearson, T. Critical knowledge gaps in our understanding of environmental cycling and transmission of leptospira spp. Appl. Environ. Microbiol. 2017, 83, e01190-17. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  17. Blasdell, K.R.; Morand, S.; Perera, D.; Firth, C. Association of rodent-borne leptospira spp. with urban environments in Malaysia Borneo. PLoS Negl. Trop. Dis. 2019, 13, e0007141. [Google Scholar] [CrossRef]
  18. Saito, M.; Villanueva, S.Y.A.M.; Chakraborty, A.; Miyahara, S.; Segawa, T.; Asoh, T.; Ozuru, R.; Gloriani, N.G.; Yanagihara, Y.; Yoshida, S.-I. Comparative analysis of Leptospira strains isolated from environmental soil and water in the Philippines and Japan. Appl. Environ. Microbiol. 2013, 79, 601–609. [Google Scholar] [CrossRef] [Green Version]
  19. Schneider, A.G.; Casanovas-Massana, A.; Hacker, K.; Wunder, E.A., Jr.; Begon, M.; Reis, M.G.; Childs, J.E.; Costa, F.; Lindow, J.; Ko, A.I. Quantification of pathogenic Leptospira in the soils of Brazilian urban slum. PLoS Negl. Trop. Dis. 2018, 12, e0006415. [Google Scholar] [CrossRef] [Green Version]
  20. Thibeaux, R.; Soupé-Gilbert, M.-E.; Kainiu, M.; Girault, D.; Bierque, E.; Fernandes, J.; Bähre, H.; Douyère, A.; Eskenazi, N.; Vinh, J.; et al. The zoonotic pathogen Leptospira interrogans mitigates environmental stress through cyclic-di-GMP-controlled biofilm production. NPJ Biofilms Microbiomes 2020, 6, 24. [Google Scholar] [CrossRef] [PubMed]
  21. Yamaguchi, T.; Higa, N.; Okura, N.; Matusmoto, A.; Hermawan, I.; Yamashiro, T.; Suzuki, T.; Toma, C. Characterizing interaction of Leptospira interrogans with proximal renal tubule epithelial cell. BMC Microbiol. 2018, 18, 64. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Vinod Kumar, K.; Lall, C.; Raj, R.V.; Vedhagiri, K.; Vijayachari, P. Molecular detection of pathogenic leptospiral protein encoding gene (lipL32) in environmental aquatic biofilms. Lett. Appl. Microbiol. 2016, 62, 311–315. [Google Scholar] [CrossRef]
  23. Barragan, V.A.; Mejia, M.E.; Travez, A.; Zapata, S.; Hartskeerl, R.A. Interaction of Leptospira with environmental bacteria from surface water. Curr. Microbiol. 2011, 62, 1802–1806. [Google Scholar] [CrossRef] [PubMed]
  24. Kumar, S.; Lata, K.S.; Sharma, P.; Bhairappanavar, S.B.; Soni, S.; Das, J. inferring pathogen-host interactions between Leptospira interrogans and homo sapiens using network theory. Sci. Rep. 2019, 9, 1434. [Google Scholar] [CrossRef] [Green Version]
  25. Thomas, V.; Anguita, J.; Barthold, S.W.; Fikrig, E. Coinfection with Borrelia burgdorferi and the agent of human granulocytic ehrlichiosis alters murine immune responses, pathogen burden, and severity of Lime arthiritis. Infect. Immun. 2001, 69, 3359–3371. [Google Scholar] [CrossRef] [Green Version]
  26. Martcheva, M.; Pilyugin, S.S.; Holt, R.D. Subthreshold and superthreshold coexistence of pathogen variants: The impact of host age-structure. Math. Biosci. 2007, 207, 58–77. [Google Scholar] [CrossRef] [PubMed]
  27. Rigaud, T.; Perrot-Minnot, M.J.; Brown, M.J.F. Parasite and host assemblages: Embracing the reality will improve our knowledge of parasite transmission and virulence. Proc. R. Soc. B 2010, 277, 3693–3702. [Google Scholar] [CrossRef] [Green Version]
  28. May, R.M.; Nowak, M.A. Coinfection and the evolution of parasite virulence. Proc. R. Soc. Lon. B 1995, 261, 209–215. [Google Scholar]
  29. Hoarau, A.O.G.; Mavingui, P.; Labarbenchon, C. Coinfections in wildlife: Focus on a neglected aspect of infectious diseases epidemiology. PLoS Pathog. 2020, 16, e1008790. [Google Scholar] [CrossRef] [PubMed]
  30. Ali, M.R.M.; Safiee, A.W.M.; Thangarajah, P.; Fauzi, M.H.; Besari, A.M. Molecular detection of leptospirosis and meliodosis co-infection: A case report. J. Infect. Public Health 2017, 10, 894–896. [Google Scholar]
  31. Turnier, P.L.; Bonifay, T.; Mosnier, E.; Schaub, R.; Jolivet, A. Usefulness of C-reactive protein in differentiating acute leptospirosis and dengue fever Guiana. Open Forum Infect. Dis. 2019, 6, ofz323. [Google Scholar] [CrossRef] [PubMed]
  32. Yong, L.S.; Koh, K.C. A case of mixed infections in patient presenting with acute febrile illness in the tropics. Case Rep. Infect. Dis. 2013, 2013, 562175. [Google Scholar] [CrossRef] [Green Version]
  33. Dev, N.; Kumar, R.; Kumar, D. Guillain-Barre syndrome: A rare complication of leptospirosis and scrub typhus co-infection. Trop. Dr. 2019, 49, 248–249. [Google Scholar] [CrossRef] [PubMed]
  34. McArdle, A.J.; Turkova, A.; Cunnington, A.J. When do co-infection matter? Curr. Opin. Infect. Dis. 2018, 31, 209–215. [Google Scholar] [CrossRef]
  35. Rafizah, A.A.N.; Aziah, B.D.; Azwany, Y.N.; Imran, M.K.; Rusli, A.M.; Nazri, S.M.; Nabilah, I.; Asma, H.S.; Zahiruddin, W.M.; Zaliha, I. Leptospirosis in Northeastern Malaysia: Misdiagnosed or coinfection? Int. J. Collab. Res. Intern. Med. Public Health 2012, 4, 1419–1427. [Google Scholar]
  36. Sachu, A.; Madhavan, A.; Vasudevan, A.; Vasudevapanicker, J. Prevalence of dengue and leptospirosis co-infection in a tertiary care hospital in South India. Iran. J. Microbiol. 2018, 10, 227–232. [Google Scholar] [PubMed]
  37. Suppiah, J.; Chan, S.-Y.; Ng, M.-W.; Khaw, Y.-S.; Ching, S.-M.; Mat-Nor, L.A.; Ahmad-Najimudin, N.A.; Chee, H.-Y. Clinical predictors of dengue fever co-infected with leptospirosis among patients admitted for dengue fever—A pilot study. J. Biomed. Sci. 2017, 24, 40. [Google Scholar] [CrossRef]
  38. Mohamed, H.; Nozha, C.; Hakim, K.; Abdelaziz, F.; Belahsen, R. Leptospira: Morphology, classification and pathogenesis. J. Bacteriol. Parasitol. 2011, 2, 6. [Google Scholar] [CrossRef]
  39. Berg, H.C.; Bromley, D.B.; Charon, N.W. Leptospiral motility. In Relations between Structure and Function in the Prokaryotic Cell: 28th Symposium of the Society for General Microbiology; Stanier, R.Y., Rogers, H.J., Ward, J.B., Eds.; Cambridge University Press: Cambridge, UK, 1978; pp. 285–294. [Google Scholar]
  40. Ellis, W.A.; Hovind-Hougen, K.; Moller, S.; Birch-Andresen, A. Morphological changes upon subculturing of freshly isolated strains of leptospira interrogans serovar hardjo. Zent. Bacteriol. Mikrobiol. Hyg. 1983, 255, 323–335. [Google Scholar] [CrossRef]
  41. Kadis, S.; Pugh, W.L. Urea utilisation by Leptospira. Infect. Immun. 1974, 10, 793–801. [Google Scholar] [CrossRef] [Green Version]
  42. Herman, H.S.; Mehta, S.; Cárdenas, W.; Stewart-Ibarra, A.; Finkelstein, J.L. Micronutrients and leptospirosis: A review of the current evidence. PLoS Negl. Trop. Dis. 2016, 10, e0004652. [Google Scholar] [CrossRef]
  43. Stern, N.; Shenberg, E.; Tietz, A. Studies on the metabolism of fatty acids in Leptospira: The biosynthesis of Δ9- and Δ11- monounsaturated acids. Eur. J. Biochem. 1969, 8, 101–108. [Google Scholar] [CrossRef]
  44. Carqueira, G.M.; Picardeau, M. A century of Leptospira strain typing. Infect. Gener. Evol. 2009, 9, 760–768. [Google Scholar] [CrossRef] [PubMed]
  45. Levett, P.N. Systematics of leptospiraceae. Curr. Top. Microbiol. Immunol. 2015, 387, 11–20. [Google Scholar]
  46. Sun, A.-H.; Liu, X.-X.; Yan, J. Leptospirosis is an invasive infectious and systemic inflammatory disease. Biomed. J. 2020, 43, 24–31. [Google Scholar] [CrossRef] [PubMed]
  47. Picardeau, M. Virulence of the zoonotic agent of leptospirosis: Still terra incognita? Nat. Rev. Micobiol. 2017, 15, 297–307. [Google Scholar] [CrossRef] [PubMed]
  48. Thibeaux, R.; Girault, D.; Bierque, E.; Soupé-Gilbert, M.-E.; Rettinger, A.; Douyère, A.; Meyer, M.; Iraola, G.; Picardeau, M.; Goarant, C. Biodiversity of environmental Leptospira: Improving identification and revisiting the diagnosis. Front. Microbiol. 2018, 9, 816. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  49. Casanovas-Massana, A.; Hamond, C.; Santos, L.A.; Oliveira, D.D.; Hacker, K.P.; Balassiano, I. Leptospira yasudae sp. nov. and Leptospira stimsonii sp. nov., two new species of the pathogenic group isolated from environmental sources. Int. J. Syst. Evol. Microbiol. 2020, 70, 1450–1456. [Google Scholar] [CrossRef] [PubMed]
  50. Hartskeerl, R.A.; Collares-Pereira, M.; Ellis, W.A. Emergence, control and re-emerging leptospirosis: Dynamics of infection in the changing world. Clin. Microbiol. Infect. 2011, 17, 494–501. [Google Scholar] [CrossRef] [Green Version]
  51. Garba, B.; Bahaman, A.R.; Bejo, S.K.; Zakaria, Z.; Mutalib, A.R.; Bande, F. Major epidemiological factors associated with leptospirosis in Malaysia. Acta Trop. 2018, 178, 242–247. [Google Scholar] [CrossRef] [PubMed]
  52. Levett, P.N. Leptospirosis. Clin. Microbiol. Rev. 2001, 14, 296–326. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  53. Cordonin, C.; Turpin, M.; Bringart, M.; Bascands, J.L.; Flores, O.; Dellagi, K. Pathogenetic Leptospira and their animal reserviors: Testing host specificity through experimental infection. Sci. Rep. 2020, 10, 7239. [Google Scholar] [CrossRef]
  54. Andre-Fontaine, G.; Aviat, F.; Thorin, C. Waterborne leptospirosis: Survival and preservation of the virulence of pathogenic Leptospira sp. in fresh water. Curr. Microbiol. 2015, 71, 136–142. [Google Scholar] [CrossRef]
  55. Bierque, M.; Thibeaux, R.; Girault, D.; Soupe-Gilbert, M.E. A systematic of Leptospira in water and soils. PLoS ONE 2020, 15, e0227055. [Google Scholar]
  56. Monahan, A.M.; Callanan, J.J.; Nally, J.E. Proteomic analysis of Leptospira interrogans shed in urine of chronically infected hosts. Infect. Immun. 2008, 76, 4952–4958. [Google Scholar] [CrossRef] [Green Version]
  57. Benacer, D.; Thong, K.L.; Verasahib, K.B.; Galloway, R.L.; Hartskeerl, R.A.; Lewis, J.W.; Mohd Zain, S.N. Human leptospirosis in Malaysia: Reviewing the challenges after 8 decades (1925–2012). Asia Pac. J. Public Health 2016, 28, 290–302. [Google Scholar] [CrossRef]
  58. Cucchi, K.; Liu, R.; Collender, P.A.; Cheng, Q.; Li, C.; Hoover, C.M.; Chang, H.H.; Liang, S.; Yang, C.; Remais, J.V. Hydroclimatic drivers of highly seasonal leptospirosis incidence suggest prominent soil reservoir of pathogenic Leptospira spp. in rural western China. PLoS Negl. Trop. Dis. 2019, 13, e0007968. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  59. Goarant, C. Leptospirosis: Risk factors and management challenges in developing countries. Res. Rep. Trop. Med. 2016, 7, 49–62. [Google Scholar] [CrossRef] [Green Version]
  60. Mohd-Taib, F.S.; Ishak, S.N.; Yusof, M.A.; Md-Lasim, A.; Md Nor, S.; Mohd-Sah, S.A.; Neela, V.K. Leptospirosis: An insight into community structure of small mammals host in urban environment. Trop. Biomed. 2020, 37, 142–154. [Google Scholar]
  61. Ehelepola, N.D.B.; Ariyaratne, K.; Dissanayake, W.P. The correlation between local weather and leptospirosis incidence in Kandy district, Sri Lanka from 2006 to 2015. Glob. Health Action 2019, 12, 1553283. [Google Scholar] [CrossRef] [PubMed]
  62. Rahmat, F.; Ishak, A.J.; Zulkafli, Z.; Yahaya, H.; Masrani, A. Prediction model of leptospirosis occurrence for Seremban (Malaysia) using meteorological data. Int. J. Integr. Eng. 2019, 11, 61–69. [Google Scholar] [CrossRef]
  63. Matsushita, N.; Ng, C.F.S.; Kim, Y.; Suzuki, M.; Saito, N.; Ariyoshi, K.; Salva, E.P.; Dimaano, E.M.; Villarama, J.B.; Go, W.S.; et al. The non-linear and lagged short-term relationship between rainfall and leptospirosis and the intermediate role of floods in the Philippines. PLoS Negl. Trop. Dis. 2018, 12, e0006331. [Google Scholar] [CrossRef] [PubMed]
  64. Chadsuthi, S.; Modchang, C.; Lenbury, Y.; Iamsirithaworn, S.; Triampo, W. Modelling seasonal leptospirosis transmission and its association with rainfall and temperature in Thailand using time-series and ARIMAX analysis. Asian Pac. J. Trop. Med. 2012, 5, 539–546. [Google Scholar] [CrossRef] [Green Version]
  65. Lau, C.L.; Townell, N.; Stephenson, E.; Berg, D.V. Leptospirosis: An important zoonosis acquired through work, play and travel. Aust. J. Gen. Pract. 2018, 47, 105–110. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  66. Okaka, F.O.; Odhiambo, B.D.O. Relationship between flooding and outbreak of infectious disease in Kenya: A review of the literature. J. Environ. Public Health 2018, 2018, 5452938. [Google Scholar] [CrossRef] [Green Version]
  67. Dobigny, G.; Gauthier, P.; Houemenou, G.; Choplin, A.; Dossou, H.J.; Badou, S.; Etougbétché, J.; Bourhy, P.; Koffi, S.; Durski, K.N.; et al. Leptospirosis and extensive urbanization in West Africa: A neglected and underestimated threat? Urban Sci. 2018, 2, 29. [Google Scholar] [CrossRef] [Green Version]
  68. Ferriman, A. UK considers logging adverse incidents. BMJ 1999, 319, 212. [Google Scholar] [CrossRef] [Green Version]
  69. Yatbandtoong, N.; Chaiyarat, R. Factors associated with leptospirosis in domestic cattle in Salakphra Wildlife Sanctuary, Thailand. Int. J. Environ. Res. Public Health 2019, 16, 1042. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  70. Atil, A.; Jeffree, M.S.; Rahim, S.S.S.A.; Hassan, M.R.; Lukman, K.A.; Ahmed, K. Occupational determinants of leptospirosis urban services workers. Int. J. Environ. Res. Public Health 2020, 17, 427. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  71. Yusof, M.A.; Mohd-Taib, F.S.; Ishak, S.N.; Md-Nor, S.; Md-Sah, S.A.; Mohamed, N.Z.; Azhari, N.N.; Neela, V.; Sekawi, Z. Microhabitat factors influenced the prevalence of pathogenic leptopsira spp. in small mammal host. Ecohealth 2019, 16, 260–274. [Google Scholar] [CrossRef] [PubMed]
  72. Rahman, M.S.A.A.; Hairon, S.M.; Hamat, R.A.; Jamaluddin, T.Z.M.T.; Shafei, M.N.; Idris, N. Seroprevalene and distribution of leptospirosis serovars among wet market workers in northeastern, Malaysia: A cross sectional study. BMC Infect. Dis. 2018, 18, 569. [Google Scholar] [CrossRef] [PubMed]
  73. Kumari, P.; Eo, K.Y.; Lee, W.S.; Kimura, J.; Yamamoto, N. DNA-based detection of Leptopsira wolffii, giardia intestinalis and Toxoplasma gondii in environmental feces of wild animals in Korea. J. Vet. Med. Sci. 2021, 83, 850–854. [Google Scholar] [CrossRef]
  74. Gamage, C.D.; Sato, Y.; Kimura, R.; Yamashiro, T.; Toma, C. Understanding leptospirosis eco-epidemiology by environmental DNA metabarcoding of irrigation water from two agro-ecological regions of Sri Lanka. PLoS Negl. Trop. Dis. 2020, 14, e0008437. [Google Scholar] [CrossRef] [PubMed]
  75. Sato, Y.; Mizuyama, M.; Sato, M.; Minamoto, T.; Kimura, R.; Toma, C. Environmental DNA metabarcoding to detect pathogenic Leptospira and associated organisms in leptospirosis-endemic areas of Japan. Sci. Rep. 2019, 9, 6575. [Google Scholar] [CrossRef]
  76. Casanovas-Massanan, A.; De Oliveira, D.; Schneider, A.G.; Begon, M.; Childs, J.E.; Costa, F.; Reis, M.G.; Ko, A.I.; Wunder, E.A. Genetic evidence for a potential environmental pathway to spillover infection of rat-borne leptospirosis. J. Infect. Dis. 2021, 17, jiab323. [Google Scholar] [CrossRef]
  77. Casanovas-Massana, A.; Pedra, G.G.; Wunder, E.A.; Diggle, P.J.; Begon, M.; Ko, A.I. Quantification of Leptospira interrogans survival in soil and water microcosms. Appl. Environ. Microbiol. 2018, 84, e00507–e00518. [Google Scholar] [CrossRef] [Green Version]
  78. Stoddard, R.A.; Buy, D.; Haberling, D.L.; Wuthiekanun, V.; Thaipadungpanit, J.; Hoffmaster, A.R. Viability of Leptospira isolates from a human outbreak in Thailand in various water types, pH and temperature conditions. Am. J. Trop. Med. Hyg. 2014, 91, 1020–1022. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  79. Li, S.; Li, P.; Zhang, L.; Hu, W.; Wang, M.; Liu, Y.; Tang, G.; Wang, D.; Zhou, B.; Yan, J. The role of reactive oxygen intermediates in the intracellular fate of Leptospira interrogans in the macrophages of different hosts. PLoS ONE 2017, 12, e0178618. [Google Scholar] [CrossRef] [PubMed]
  80. Zala, D.B.; Khan, V.; Sanghai, A.A.; Dalai, S.K.; Das, V.K. Leptospira in the different ecological niches of the tribal union territory of India. J. Infect. Dev. Ctries. 2018, 12, 849–854. [Google Scholar] [CrossRef] [PubMed]
  81. Smith, D.J.; Self, H.R. Observation on the survival of Leptospira australis A in soil and water. Epidemiol. Infect. 1995, 53, 436–444. [Google Scholar] [CrossRef] [Green Version]
  82. Goarant, C.; Trueba, G.; Bierque, E.; Thibeaux, R.; Davis, B.; Moctezuma, D.P. Leptospira and Leptospirosis; Global Water Pathogen Project. Part 3 Bacteria; Rose, J.B., Jimenez-Cisneros, B., Pruden, A., Ashbolt, N., Miller, J., Eds.; Michigan State University: East Lansing, MI, USA, 2019; Available online: http://www.waterpathogens.org/book/leptospira-and-leptospriosis (accessed on 25 August 2021).
  83. Thibeaux, R.; Geroult, S.; Benezech, C.; Chabaud, S.; Soupé-Gilbert, M.-E.; Girault, D.; Bierque, E.; Goarant, C. Seeking the environmental source of leptospirosis reveals durable bacterial viability in river soils. PLoS Negl. Trop. Dis. 2017, 11, e0005414. [Google Scholar] [CrossRef] [Green Version]
  84. Bharti, A.R.; Nally, J.E.; Ricaldi, J.N.; Matthias, M.A.; Diaz, M.M.; Lovett, M.A.; Levett, P.N. Leptospirosis: A zoonotic disease of global importance. Lancet Infect. Dis. 2003, 3, 757–771. [Google Scholar] [CrossRef]
  85. Terpstra, W.J. Historical perspectives in leptospirosis. Indian J. Med. Microbiol. 2006, 23, 316–320. [Google Scholar] [CrossRef]
  86. Saito, M.; Miyahara, S.; Villanueva, S.Y.A.M.; Aramaki, N.; Ikejiri, M.; Kobayashi, Y. PCR and culture identification of pathogenic Leptospira spp. from coastal soil in Leyte, Philippines after a storm surge during super typhoon Haiyan (Yolanda). Appl. Environ. Microbiol. 2014, 80, 6926–6932. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  87. Vaumourin, R.; Vourc’h, G.P.; Vayssier-Taussat, M. The important of multiparasitism: Examining the consequences of co-infections for human and animal health. Parasit Vectors 2020, 8, 545. [Google Scholar] [CrossRef] [PubMed]
  88. Sembiring, E. Diagnostic approach in leptospirosis patients. IOP Conf. Ser. Earth Environ. Sci. 2018, 125, 012089. [Google Scholar] [CrossRef]
  89. Izurieta, R.; Galwanker, S.; Clem, A. Leptospirosis: The “mysterious” mimic. J. Emerg. Trauma Shock 2008, 1, 21–33. [Google Scholar]
  90. Smith, S.; Kennedy, B.J.; Dermedgoglou, A.; Poulgrain, S.S.; Paavola, M.P.; Minto, T.L. A simple score to predict severe leptospirosis. PLoS Negl. Trop. Dis. 2019, 13, e0007205. [Google Scholar] [CrossRef]
  91. Hishamshah, M.; Ahmad, N.; Ibrahim, H.M.; Halim, N.A.N.; Nawi, S.; Amran, F. Demographic, clinical and laboratory features of leptospirosis and dengue co-infection in Malaysia. J. Med. Microbiol. 2018, 67, 806–813. [Google Scholar] [CrossRef] [Green Version]
  92. Chacko, C.S.; Jayakumar, A.; Binu, S.L.; Pant, R.D.; Giri, A.; Chand, S.; Nandakumar, U.P. A short review on leptospirosis: Clinical manifestations, diagnosis and treatment. Clin. Epidemiol. Glob. Health 2021, 11, 100741. [Google Scholar] [CrossRef]
  93. Begam, N.N.; Kumar, A.; Sahu, M.; Soneja, M.; Bhatt, M.; Vishwakarma, V.K. Managemement of dengue wit coinfection: An updated narrative review. Drug Discov. Ther. 2021, 15, 130–138. [Google Scholar] [CrossRef]
  94. Parminder, K.; Jain, R.; Guglani, V.; Randev, S.; Kumar, P. Tropcal coinfection—A diagnostic dilemma: Case series from Northern India. J. Public Health Dis. Prev. 2021, 4, 102. [Google Scholar]
  95. Mala, W.; Wilairatana, P.; Kotepui, K.U.; Kotepui, M. Prevalence of malaria and chikungunya coinfection in febrile patients: A systematic review and meta-analysis. Trop. Med. Infect. Dis. 2021, 6, 119. [Google Scholar] [CrossRef]
  96. Kamath, V.; Ganguly, S.; Avinash, B.L. A comparative study of concurrent infections of rickettsial infection, malaria, typhoid, and chikungunya with dengue. APIK J. Int. Med. 2019, 7, 120–126. [Google Scholar] [CrossRef]
  97. Del Valle-Mendoza, J.; Palomares-Reyes, C.; Carrillo-Ng, H.; Tarazona-Castro, Y.; Kym, S.; Aguilar-Luis, M.A.; Del Valle, L.J.; Aquino-Ortega, R.; Martins-Luna, J.; Peña-Tuesta, I.; et al. Leptospirosis in febrile pateints with suspected diagnosis of dengue fever. BMC Res. Notes 2021, 14, 209. [Google Scholar] [CrossRef] [PubMed]
  98. Hartskeerl, R.A.; Smythe, L.D. The role of leptospirosis reference laboratory. Curr. Top. Microbiol. Immunol. 2015, 387, 273–288. [Google Scholar]
  99. Mohammad, E.; Mohsin, N.; Al-Abri, S.; Al-Abaidani, I.; Jha, A.; Camble, P.; Budruddin, M.; Khalil, M.; Pakyarra, A.; Al Busaidy, S. Acute renal failure in patient with both leptospirosis and dengue fever. Oman Med. J. 2008, 23, 100–102. [Google Scholar]
  100. Sharp, T.M.; Bracero, J.; Rivera, A.; Shieh, W.J.; Bhatnagar, J.; Rivera-Diez, I.; Hunsperger, E.; Munoz-Jordan, J.; Zaki, S.R.; Tomashek, K.M. Fatal human co-infection with Leptospira spp. and dengue virus Puerto Rico, 2010. Emerg. Infect. Dis. 2012, 18, 878–880. [Google Scholar] [CrossRef] [PubMed]
  101. Garbin, A.N.; Espinoza-Figueroa, J.; Sihuincha-Maldonado, M.; Suarez-Ognio, L. Coinfection of dengue and leptospirosis in a girl from the Peruvian Amazon. Rev. Peru. Med. Exp. Salud Publica 2015, 32, 179–182. [Google Scholar]
  102. Wijesinghe, A.; Gnanapraggash, N.; Ranasinghe, G.; Ragunathan, M.K. Fatal co-infection with leptospirosis and dengue in a Sri Langkan male. BMC Res. Notes 2015, 8, 348. [Google Scholar] [CrossRef] [Green Version]
  103. Cardona-Ospina, J.A.; Jiménez-Canizales, C.E.; Vásquez-Serna, H.; Garzón-Ramírez, J.A.; Alarcón-Robayo, J.F.; Cerón-Pineda, J.A.; Rodríguez-Morales, A.J. Fatal Dengue, Chikungunya and Leptospirosis: The Importance of Assessing Co-infections in Febrile Patients in Tropical Areas. Trop. Med. Infect. Dis. 2018, 3, 123. [Google Scholar] [CrossRef] [Green Version]
  104. Ravindar, A.; Shanmugam, P. Co-infection of dengue and leptospirosis in patients presenting to a tertiary care hospital with acute febrile illness: A cross-sectional study. J. Clin. Diagn. Res. 2018, 12, DC05–DC09. [Google Scholar] [CrossRef]
  105. Jayathilaka, P.G.N.S.; Mendis, A.S.V.; Perera, M.H.M.T.S.; Damsiri, H.M.T.; Gunaratne, A.V.C.; Agampodi, S.B. An outbreak of leptospirosis with predominant cardiac involvement: A case series. BMC Infect. Dis. 2019, 19, 265. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  106. Nithya, V.; Umadevi, R. Leptospirosis complicating dengue infection in a 39 year old female- a case report. Drug Invent. Today 2019, 12, 2407–2409. [Google Scholar]
  107. Wongsrichanalai, C.; Miller, R.S.; Gray, M.; Murray, C.K.; Magill, A.J.; Pickard, A.L.; Liao, W.J.; McDaniel, P. Co-infection with malaria and leptospirosis. Am. J. Trop. Med. Hyg. 2003, 68, 583–585. [Google Scholar] [CrossRef] [Green Version]
  108. Baliga, K.V.; Uday, Y.; Sood, V.; Nagpal, A. Acute febrile hepato-renal dysfunction in the tropics: Co-infection of malaria and leptospirosis. J. Infect. Chemother. 2011, 17, 694–697. [Google Scholar] [CrossRef]
  109. Gurjar, M.; Saigal, S.; Baronia, A.K.; Azim, A.; Poddar, B.; Singh, R.K. Clinical manifestations of co-infection with malaria and leptospirosis. Trop. Dr. 2011, 41, 175. [Google Scholar] [CrossRef]
  110. Loganathan, N.; Ramalingam, S.; Ravishankar, D.; Shivakumar, S. Co-infection of malaria and leptospirosis—A hospital based study from South India. Nat. J. Res. Com. Med. 2012, 1, 117–119. [Google Scholar]
  111. Samantha, S.; Samantha, S.; Haldar, R. Emergency caesarean delivery in a patient with cerebral malaria-Leptospira co infection: Anaesthetic and critical care considerations. Indian J. Anaesth. 2014, 58, 55–58. [Google Scholar] [CrossRef] [PubMed]
  112. Rao, M.; Atiqah, N.; Dasiman, M.; Amran, F. Demographic, clinical and laboratory features of leptospirosis-malaria co-infections in Peninsular Malaysia. J. Med. Microbiol. 2020, 69, 451–456. [Google Scholar] [CrossRef]
  113. Hin, H.S.; Ramalingam, R.; Chunn, K.Y.; Ahmad, N.; Rahman, J.A.; Mohamed, M.S. Case report: Fatal co-infection melioidosis and leptospirosis. Am. J. Trop. Med. Hyg. 2012, 87, 737–740. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  114. Sapian, M.; Khair, M.T.; How, S.H.; Rajalingam, R.; Sahhir, K.; Norazah, A.; Khebir, V.; Jamalludin, A.R. Outbreak of melioidosis and leptospirosis co-infection following a rescue operation. Med. J. Malays. 2012, 67, 293–297. [Google Scholar]
  115. Watt, G.; Jongsakul, K.; Suttinot, C. Possible scrub typhus coinfections in thai agricultural workers hospitalised with leptospirosis. Am. J. Trop. Med. Hyg. 2003, 68, 89–91. [Google Scholar] [CrossRef] [Green Version]
  116. Wei, Y.F.; Chiu, C.T.; Lai, Y.F.; Lai, C.H.; Lin, H.H. Successful treatment of septic shock and respiratory failure due to leptospirosis and scrub typhus coinfection with penicillin, levofloxacin and activated protein C. J. Microbiol. Immunol. Infect. 2012, 45, 251–254. [Google Scholar] [CrossRef] [Green Version]
  117. Mahajan, S.K.; Babu, S.N.M.; Singh, D.; Kanga, A.; Kaushal, S.S. Scrub typhus and leptospirosis co-infection in Himalayan region. Trop. Dr. 2012, 42, 176–177. [Google Scholar] [CrossRef] [PubMed]
  118. Chandramohan, A.; Venkatesh, S.; Dhandapany, G.; Stephen, S. Scrub typhus co-infection in an adolescent girl with varicella. Indian Pediatr. 2015, 52, 891–892. [Google Scholar] [CrossRef] [PubMed]
  119. Gupta, N.; Chaudhry, R.; Mirdha, B.; Das, B.; Dar, L.; Kabra, S.; Lodha, R.; Dey, A.; Sood, R.; Sreenivas, N.W.A.V. Scrub typhus and leptospirosis: The fallacy of diagnosing with IgM and enzyme linked immunosorbant assays. J. Microb. Biochem. Technol. 2016, 8, 071–075. [Google Scholar] [CrossRef]
  120. Kanagasabai, S.; Thatchinamoorthy, G.; Ganesan, A.; Pachiyappan, G.; Gouthami, P.; Valarmathi, S.; Jacob, S.M. Seroprevalence of scrub typhus and coinfection with leptospirosis in Chennai, Tamil Nadu. Int. J. Infect. Dis. 2016, 45, 178. [Google Scholar] [CrossRef] [Green Version]
  121. Malakar, S.; Negi, B.D.; Dutt, K.; Bharat, K.; Shah, B.; Raina, S.; Sharma, R. Concurrent coinfections in tropics: A hospital-based observational study from Himachal Pradesh, India. Recent Adv. Biol. Med. 2019, 5, 871388. [Google Scholar] [CrossRef]
  122. Yaqoob, S.; Siddiqui, A.H.; Shukla, P. Scrub typhus: A neglected tropical disease and a potential threat in north india. J. Pure Appl. Microbiol. 2020, 14, 1589–1593. [Google Scholar] [CrossRef]
  123. Sengupta, M.; Tamasi, M.; Rajat, D.; Parthajit, B. Leptopsirosis and scrub typhus co-infection in febrile patients. World J. Adv. Res. Rev. 2020, 6, 233–236. [Google Scholar] [CrossRef]
  124. Lima, R.X.B.; Rolim, D.B. Melioidosis in children, Brazil 1989–2019. Emerg. Infect. Dis. 2021, 27, 1705–1708. [Google Scholar] [CrossRef] [PubMed]
  125. Hanson, J.; Smith, S.; Stewart, J.; Horne, P.; Ramsamy, N. Melioidosis—A disease of socioeconomic disadvantage. PLoS Negl. Trop. Dis. 2021, 15, e0009544. [Google Scholar] [CrossRef] [PubMed]
  126. Menon, R.; Baby, P.; Kumar, A.; Surendran, S.; Pradeep, M.; Rejendran, A.; Suju, G.; Ashok, A. Risk factor for mortality in melioidosis: A single-centre, 10 year retrospective cohort study. Sci. World J. 2021, 2021, 8154810. [Google Scholar] [CrossRef]
  127. Chaichana, P.; Kronsteiner, B.; Rongkard, P.; Teparrukkul, P.; Limmathurotsakul, D.; Chantratia, N.; Day, N.P.; Fletcher, H.A.; Dunachie, S.J. Serum from melioidosis survivors diminished intracellular Burkholderia pseudomallei growth in macrophages: A brief research report. Front. Cell Infect. Microbiol. 2020, 10, 442. [Google Scholar] [CrossRef] [PubMed]
  128. Wiersinga, W.J.; Virk, H.S.; Torres, A.G.; Currie, B.J.; Peacock, S.J.; Dance, D.A.B.; Limmathurotsakul, D. Melioidosis. Nat. Rev. Dis. Primers 2018, 4, 17107. [Google Scholar] [CrossRef]
  129. Gasem, M.H.; Wagenaar, J.F.; Goris, M.G.; Adi, M.S.; Isbandrio, B.B.; Hartskeerl, R.A.; Rolain, J.-M.; Raoult, D.; Van Gorp, E.C. Murine Typhus and Leptospirosis as Causes of Acute Undifferentiated Fever, Indonesia. Emerg. Infect. Dis. 2009, 15, 975–977. [Google Scholar] [CrossRef]
  130. Ibrahim, I.N.; Okabayashi, T.; Lestari, E.W.; Yanase, T.; Muramatsu, Y.; Ueno, H.; Morita, C. Serosurvey of wild rodents for ricketsioses Ispotted fever, murine typhus and Q fever) in Java Island, Indonesia. Eur. J. Epidemol. 1999, 15, 89–93. [Google Scholar] [CrossRef]
  131. Jiang, J.; Soetmadji, D.W.; Henry, K.M.; Ratiwayanto, S.; Bangs, M.J.; Richards, A.L. Rickettsia felis in Xenopsylla cheopis, Java Indonesia. Emerg. Infect. Dis. 2006, 12, 1281–1283. [Google Scholar] [CrossRef]
  132. Tsay, R.W.; Chang, F.Y. Serious complications in scrub typhus. J. Microbiol. Immunol. Infect. 1998, 31, 240–244. [Google Scholar]
  133. Silpapojakul, K. Scrub typhus in the western pacific region. Ann. Acad. Med. Singap. 1997, 26, 794–800. [Google Scholar]
  134. Gilbert, J.A.; Quinn, R.A.; Debelius, J.; Xu, Z.Z.; Morton, J. Microbiome-wide association studies link dynamic mmicrobiol consortia to disease. Nature 2016, 535, 94–103. [Google Scholar] [CrossRef]
  135. Ingham, E.R. Soil biology primer, Chapter 4: Soil fungus. In Soil and Water Conservation; Soil & Water Conservation Society: Ankeny, IA, USA, 2009; pp. 22–23. Available online: http://soils.usda.gov/sqi/concepts/soil_biology (accessed on 12 April 2021).
  136. Zhao, X.; Li, D.; Xu, S.; Guo, Z.; Zhang, Y.; Man, L.; Jiang, B.; Hu, X. Clostridium guangxiense spp. nov. Clostridium neunse sp. nov. two phylogenetically closely related hydrogen-producing species isolated from lake sediment. Int. J. Syst. Evol. Microbiol. 2017, 67, 710–715. [Google Scholar]
  137. Mathai, P.P.; Dunn, H.M.; Magnone, P.; Zhang, Q.; Ishii, S.; Chun, C.L.; Sadowsky, M.J. Association between submerged aquatic vegetation and elevated level of Escherichia coli and potential bacterial pathogens in freshwater lakes. Sci. Total. Environ. 2019, 657, 319–324. [Google Scholar] [CrossRef]
  138. Tan, T.L.; Lee, L.Y.; Lim, W.C. Fatal leptospirosis and Escherichia coli co-infection post-partum woman. Med. J. Malays. 2018, 73, 427–429. [Google Scholar]
  139. Dietrich, M.; Gomard, Y.; Lagadec, E.; Ramasindrazana, B.; Minter, G.L.; Guernier, V.; Benlali, A.; Rocamora, G.; Markotter, W.; Steven, M.; et al. Biogeography of Leptospira in wild animal communities inhabiting the insular ecosystem of the western Indian ocean island and neighboring Africa. Emerg. Microbes Infect. 2017, 7, 57. [Google Scholar] [CrossRef] [Green Version]
  140. Ibekwe, A.M.; Murinda, S.E.; Graves, A.K. Genetic diversity and antimicrobial resistance of Escherichia coli from human and animal sources uncovers multiple resistance from human sources. PLoS ONE 2011, 6, e20819. [Google Scholar] [CrossRef] [Green Version]
  141. Zhang, T.; Wang, H.; Wu, L.; Lou, J.; Wu, J.; Brookes, P.C.; Xu, J. Survival of Escherichia coli 0157:H7 in soils from Jiangsu province, China. PLoS ONE 2013, 8, e81178. [Google Scholar]
  142. Cohen, M.B.; Giannella, R.A. Hemorrhagic colitis associated with Escherichia coli 0157:H7. Adv. Intern. Med. 1992, 37, 173–195. [Google Scholar]
  143. Ko, H.; Maymani, H.; Rojas-Hernandez, C. Hemolytic uremic syndrome associated with Escherichia coli 0157:H7 infection in older adults: A case report and review of the literature. J. Med. Case Rep. 2016, 10, 175. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  144. Sousa, C.P. The versatile strategies of Escherichia coli pathotypes: A mini review. J. Venom. Anim. Toxins Incl. Trop. Dis. 2006, 12, 363–373. [Google Scholar] [CrossRef] [Green Version]
  145. Kiu, R.; Hall, L.J. An update on the human and animal enteric pathogen Clostridium perfringens. Emerg. Microbes Infect. 2018, 7, 141. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  146. Low, L.Y.; Harrison, P.F.; Gould, J.; Powell, D.R.; Choo, J.M.; Forster, S.C.; Chapman, R. Concurrent host-pathogen transcriptional responses in clostridium perfringens murine myonecrosis infections. mBio 2018, 9, e00473-18. [Google Scholar] [CrossRef] [Green Version]
  147. Foysal, M.J.; Lisa, A.K. Isolation and characterisation of Bacillus sp. strain BC01 from soil displaying potent antagonistic activity against plant and fish pathogenic fungi and bacteria. J. Genet. Eng. Biotechnol. 2018, 16, 387–392. [Google Scholar] [CrossRef] [PubMed]
  148. Dale, J.L.; Raynor, M.J.; Ty, M.C.; Hadjifrangiskou, M.; Koehler, T.M. A dual role for the Bacillus anthracis master virulence regulator AtxA: Control of sporulation and anthrax toxin production. Front. Microbiol. 2018, 9, 482. [Google Scholar] [CrossRef]
  149. Dizer, U.; Kenar, L.; Ortatath, M.; Karayilanoglu, T. How to weaponized anthrax? East. J. Med. 2004, 9, 13–16. [Google Scholar]
  150. Nhan, T.X.; Bonnieux, E.; Rovery, C.; De Pina, J.J.; Musso, D. Fatal leptospirosis and chikungunya co-infection: Do not forget leptospirosis during chikungunya outbreaks. IDCases 2016, 5, 12–14. [Google Scholar] [CrossRef] [Green Version]
  151. Sharma, S.; Mandal, A.; Vijayaachari, P. Investigation of malaria among patients of febrile illness and co-infection with leptospirosis in Andaman and Nicobar Islands. Res. J. Microbiol. 2014, 9, 104–110. [Google Scholar] [CrossRef] [Green Version]
  152. Hodkinson, B.P.; Grice, E.A. Next-generation sequencing: A review of technologies and tools for wound microbiome research. Adv. Wound Care 2015, 4, 50–58. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  153. Sessitsch, A.; Pfaffenbichler, N.; Mitter, B. Microbiome applications from lab to field: Facing complexity. Trends Plant Sci. 2019, 24, 194–198. [Google Scholar] [CrossRef]
  154. Brown, E.D.; Wright, G.D. Antibacterial drug discovery in the resistance era. Nature 2016, 529, 336–343. [Google Scholar] [CrossRef] [PubMed]
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Figure 1. Environment and vector infections occur as a result of coinfections in human.
Figure 1. Environment and vector infections occur as a result of coinfections in human.
Ijerph 18 09411 g001
Table
Table 1. Example of pathogenic, intermediate and saprophytic Leptospiral species.
Table 1. Example of pathogenic, intermediate and saprophytic Leptospiral species.
Genotypic ClassificationLeptospira Species
Pathogenic LeptospiraL. alexanderi, L. alstonii, L. borgpetersenii, L. interrogans, L. kirschneri, L. kmetyi, L. mayottensis, L. noguchii, L. santarosai, L. weilii.
Intermediate LeptospiraL. broomii, L. fainei, L. inadai, L. licerasiae, L. wolffii, L. venezelensis, L. broomii.
Sapropytic LeptospiraL. biflexa, L. meyeri, L. terpstrae, L. vanthielii, L. wolbachii, L. yanagawae, L. idonii.
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Md-Lasim, A.; Mohd-Taib, F.S.; Abdul-Halim, M.; Mohd-Ngesom, A.M.; Nathan, S.; Md-Nor, S. Leptospirosis and Coinfection: Should We Be Concerned? Int. J. Environ. Res. Public Health 2021, 18, 9411. https://doi.org/10.3390/ijerph18179411

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Md-Lasim A, Mohd-Taib FS, Abdul-Halim M, Mohd-Ngesom AM, Nathan S, Md-Nor S. Leptospirosis and Coinfection: Should We Be Concerned? International Journal of Environmental Research and Public Health. 2021; 18(17):9411. https://doi.org/10.3390/ijerph18179411

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Md-Lasim, Asmalia, Farah Shafawati Mohd-Taib, Mardani Abdul-Halim, Ahmad Mohiddin Mohd-Ngesom, Sheila Nathan, and Shukor Md-Nor. 2021. "Leptospirosis and Coinfection: Should We Be Concerned?" International Journal of Environmental Research and Public Health 18, no. 17: 9411. https://doi.org/10.3390/ijerph18179411

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Md-Lasim, A., Mohd-Taib, F. S., Abdul-Halim, M., Mohd-Ngesom, A. M., Nathan, S., & Md-Nor, S. (2021). Leptospirosis and Coinfection: Should We Be Concerned? International Journal of Environmental Research and Public Health, 18(17), 9411. https://doi.org/10.3390/ijerph18179411

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