Acanthamoeba is a free-living amoeba genus able to cause severe infections, such as Granulomatous amoebic encephalitis (GAE), epithelial disorders and a sight-threatening disease called
Acanthamoeba keratitis (AK) [
1,
2]. These opportunistic pathogenic protozoa have been isolated from different sources, with preference for soil and water niches [
3], and they can be classified into 23 genotypes based on their 18S rRNA sequences [
4]. Moreover, these organisms are capable of surviving in both external environments as well as inside an infected host as parasites. This double condition causes them to be called amphizoic organisms.
The genus
Acanthamoeba is considered an emerging parasite due to the difficulty of treating infections by these organisms [
5]. Furthermore, its clinical importance not only falls on its capability to produce infections, but also on its ability to harbor other pathogenic microorganisms as endosymbionts [
6]. The wide distribution of
Acanthamoeba in natural environments such as soil, airborne dust and water and the underdiagnosis of GAE and AK cases have made it difficult to investigate possible sources of infection. Moreover, the lack of a stable classification of this genus complicates the identification of individual isolates, including the matching of amoebae from infections with organisms from the environment.
Acanthamoeba is able to produce a life-threatening central nervous system (CNS) infection among the immunocompromised population, known as Granulomatous amoebic encephalitis (GAE). Although the prevalence of GAE worldwide is low, the mortality rate oscillates between 95 and 98% among infected patients [
7]. On the other hand, the most common pathology due to
Acanthamoeba is
Acanthamoeba keratitis (AK), produced in healthy individuals, especially contact lens wearers [
2]. Lately, the number of AK infections has been increasing from 17 to 70 per million among contact lens wearers [
8]. The contamination of contact lens cases with amoebae is the first step in AK infection [
8]. Generally, contact lens solutions include anti-fungal and anti-microbial components, which are not fully effective against
Acanthamoeba trophozoites and cysts [
9]. On the other hand, the current AK treatments are normally toxic, last a long time and are non-specific [
2]. Therefore, the development of new formulations against
Acanthamoeba strains are needed.
Acanthamoeba detection methods are mainly based on microscopic techniques, but these methods are laborious, long-lasting and require amoeba culture [
2]. In addition, amoeba culture is only positive in around 55% of the cases, and the quantity of the obtained sample could be not enough to see the protozoa. PCR (polymerase chain reaction) testing is a rapid detection technique of
Acanthamoeba parasites at the genotypic-level (T1-T23) [
10].
Acanthamoeba genotyping is gaining importance at the treatment level because different genotypes show variation in symptoms and response to the treatment [
11]. However, PCR presents different limitations, such as insufficient target DNA yield or non-specific DNA amplification [
12]. Thus, in order to reduce the AK infection damage, new rapid and reliable diagnostic tools need to be developed.
The current Pathogens Journal Special Issue, New Insights in Acanthamoeba, is focused on the most recent advances related to the pathogenesis, diagnosis and treatment of this opportunistic parasite. All these improvements mean significant and laborious research, which contributes to establishing further treatments and diagnosis tools, as well as to better understanding Acanthamoeba pathogenesis. From the Pathogens Journal and as Guest Editors, we would like to acknowledge the authors for their contributions and encourage them to continue with their interesting investigations.
Author Contributions
Conceptualization, M.R.-B., J.E.P. and J.L.-M.; methodology, M.R.-B., R.L.R.-E. and I.S.; resources, J.E.P. and J.L.-M.; data curation, M.R.-B.; writing—original draft preparation, M.R.-B.; writing—review and editing, M.R.-B., R.L.R.-E. and I.S.; visualization, J.E.P. and J.L.-M.; supervision, J.E.P. and J.L.-M.; project administration, J.E.P. and J.L.-M.; funding acquisition, J.E.P. and J.L.-M. All authors have read and agreed to the published version of the manuscript.
Funding
This study was supported by the RICET (project no. RD16/0027/0001 of the programme of Redes Temáticas de Investigación Cooperativa, FIS), CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III (CB21/13/00100), Spanish Ministry of Science, Innovation and Universities (MICINN), State Research Agency (AEI), the European Regional Development Funds (ERDF) (PGC2018–094503-B-C21), Ministerio de Sanidad, Gobierno de España and by the project N◦: 21/0587 funded by the Cabildo de Tenerife, Tenerife Innova, MEDI and FDCAN. RLRE was funded by a grant from Agencia Canaria de Investigación, Innovación y Sociedad de la Información (ACIISI) cofunded by Fondo Social Europeo (FSE) y FEDER, (TESIS2020010117).
Conflicts of Interest
The authors declare no conflict of interest.
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