Molecular identification of pathogenic free-living amoebae in various natural and artificial water bodies in the state of Chihuahua, Mexico. First part.

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Manuel Alejandro Borquez-Román
Rebeca Estefanya Payán-Sánchez
Claudia Carolina Hernández-Peña
Patricio Eduardo Byerly-Sosa
Luis-Fernando Lares-Jiménez
Libia Zulema Rodríguez-Anaya
José Reyes Gonzalez-Galaviz
Martín Renato Hernandez Castaños
Jaime Raúl Adame-Gallegos
Fernando Lares-Villa

Abstract

Free-living amoebae (AVL) are protozoa widely distributed in nature, and some of them are capable of causing serious infections in humans and animals. The genera Naegleria, Acanthamoeba, Balamuthia, Sappinia, Vermamoeba, Vahlkampfia y Paravahlkampfia, have gained relevance as they have species that behave as pathogenic and opportunistic parasites. To generate information on the geographic distribution and genetic diversity of pathogenic free-living amoebae in the northern region of Mexico, the findings of the sampling of various natural and artificial aquatic environments carried out in the state of Chihuahua are presented, particularly in the near the city of Chihuahua and Ciudad Juarez. Fourteen water samples were taken in one-liter containers, seven samples from the city of Chihuahua and its surroundings, and another seven samples from Ciudad Juarez and its suburbs, including the Rio Grande. Aliquots of 50 mL were duplicated after shaking the sampling bottle and centrifuged to concentrate the sample. Pellets were seeded on non-nutritive agar plates spiked with Escherichia coli and seeded at 37 and 42°C as isolation temperatures. 98 strains were isolated, 50 at 37°C and 48 at 42°C, keeping a total of 84 strains in culture. Once the morphological identification and PCR tests were carried out, N. fowleri, Naegleria spp., Acanthamoeba spp., and other genera of uncertain identity were confirmed, which amplified with the universal primers and are awaiting the result of the sequencing. The presence of free-living pathogenic amoebas in the North and South of Chihuahua and unrelated aquatic environments that may be a source of contamination for diseases caused by free-living pathogenic amoebas is confirmed. contamination for diseases caused by free-living pathogenic amoebas is confirmed

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Borquez-Román, M. A., Payán-Sánchez, R. E., Hernández-Peña, C. C., Byerly-Sosa, P. E., Lares-Jiménez, L.-F., Rodríguez-Anaya, L. Z., Gonzalez-Galaviz, J. R., Hernandez Castaños, M. R., Adame-Gallegos, J. R., & Lares-Villa, F. (2022). Molecular identification of pathogenic free-living amoebae in various natural and artificial water bodies in the state of Chihuahua, Mexico. First part . Revista Latinoamericana De Recursos Naturales, 18(3), 79-85. https://doi.org/10.33154/rlrn.2022.03.03
Section
Original Article

References

Benterki, M.S., Atachi, A., Bennoune, O., Regoudis, E., Pelandakis, M. (2016). Meningoencephalitis due to the amoeboflagellate Naegleria fowleri in ruminants in Algeria. Parasite; 23:11. DOI: 10.1051/parasite/2016011
De Jonckheere J.F. (2002). A century of research on the amoeboflagellate genus 522 Naegleria. Acta Protozool. 41: 309 – 342.
De Jonckheere, J.F. (2007). Recent interesting identifications of free-living amoebae from the Brussels laboratory (abstract). Japanese J Protozool. 40, 170.
De Jonckheere, J.F., (2011). Origin and evolution of the worldwide distributed pathogenic amoeboflagellate Naegleria fowleri. Infect. Genet. Evol. 11, 1520–1528 DOI: 10.1016/j.meegid.2011.07.023
Dykova, I., Nowak, B.F., Crosbie, P.B., Fiala, I., Peckova, H., Adams, M.B., Machackova, B., Dvorakova, H., 2005. Neoparamoeba branchiphila n. sp., and related species of the genus Neoparamoeba Page, 1987: morphological and molecular characterization of selected strains. J. Fish Dis. 28, 49–64. DOI: 10.1111/j.1365-2761.2004.00600.x
Gallegos-Neyra, E.M., Lugo-Vázquez, A., Calderón-Vega, A., Sánchez-Rodríguez, M.R. y Mayén-Estrada, R., 2014. Biodiversidad de protistas amébidos de vida libre en
México. Rev. Mex. Biodiv. 85:10-25. https://doi:10.7550/rmb.33691
Gallegos-Neyra, E. M., Becerra-Cigarroa, J. M., FigueroaMéndez, M. G., Fuentes-Zuno, S. A., Hernández-Zamarripa, A. R., Mendoza-Romero, M. J., Avier-Venegas, D.I., VillaDelavequia, G.S., 2018. Amibas de vida libre en playas de Tuxpan y Arrecife Ingeniero, Veracruz, México. Revista de Zoología, (29). Retrieved from:
https://www.redalyc.org/jatsRepo/498/49855322001/html/in dex.html
Hernández-Peña, CC., Saénz-Montoya, G., Alvarado-Soto, S., Carrillo-Méndez, JD., Soto-Padilla, MY., Otero-Ruiz, A., Lares-Jiménez, LF. 2019. Identificación de Naegleria spp. y Acanthamoeba spp. en agua de fuentes de Ciudad Juárez, Chihuahua. Rev Latinoamer Rec Nat 15(3):88-96.
Khan, N.A., 2006. Acanthamoeba: biology and increasing importance in human health. FEMS Microbiology Reviews, 30(4):564–595, https://doi.org/10.1111/j.15746976.2006.00023.xL.
Lares-Jiménez, L.F.; Borquez-Román, M.A.; Lares-García, C.; Otero-Ruiz, A.; Gonzalez-Galaviz, J.R.; Ibarra-Gámez, J.C.; Lares-Villa, F. (2018). Potentially pathogenic genera of freeliving amoebae coexisting in a thermal spring. Exp Parasitol, 195, 54-58. DOI: 10.1016/j.exppara.2018.10.006
Lares-Jimenez, L.F., Booton, G.C., Lares-Villa, F., VelazquezContreras, C.A., Fuerst, P.A., (2014). Genetic analysis among environmental strains of Balamuthia mandrillaris recovered from an artificial lagoon and from soil in Sonora, Mexico. Exp. Parasitol. 145, S57eS61. https://doi.org/10.1016/j.exppara.2014.07.007
Lares-Villa, F. y Hernández-Peña, C.C. (2010). Concentration of Naegleria fowleri in natural waters used for recreational purposes in Sonora, Mexico (November 2007-October 2008). Experimental Parasitology. 126(1):33-36 DOI: 10.1016/j.exppara.2010.04.011
Medeiros, M.L.Q., Araújo, M.F.F., Sodré-Neto, L., Amorim, A.S. (2013). Spatial and temporal distribution of free-living protozoa in aquatic environments of a Brazilian semiarid region. Ambi-Agua, Taubaté 8 (2), 46–56. 1129. https://doi.org/10.4136/ambi-agua.1129
Naqvi, A.A., Yazdani, N., Ahmad, R., Zehra, F., Ahmad, N., (2016). Epidemiology of primary amoebic meningoencephalitis-related deaths due to Naegleria fowleri infections from freshwater in Pakistan: an analysis of 8-year dataset. Arch. Pharm. Pract. 7 (4), 119e129. https://doi.org/10.4103/2045-080X.191924
Neelam, S., Niederkorn, J. (2017). Pathobiology and immunobiology of Acanthamoeba keratitis: insights from animal models. Yale J. Biol. Med. 90, 261-268. PMCID: PMC5482302
Page, F.C. 1988. A new key to freshwater and soil gymnamoebae. CCAP. Freshwater Biological Association. Pp 24-120
Pelandakis, M., Serre, S., Pernin, P., 2000. Analysis of the 5.8S rRNA gene and the internal transcribed spacers in Naegleria spp. and in N. fowleri. J. Eukaryot. Microbiol. 47, 116–121. https://doi.org/10.1111/j.1550-7408.2000.tb00020.x
Sousa-Ramos D, Reyes-Batlle M, Bellini NK, RodríguezExpósito RL, Martín-Real C. Piñero JE, Lorenzo-Morales J. (2022). Pathogenic free-living amoebae from water sources in Cape Verde. Parasitology Research 121:2399–2404 https://doi.org/10.1007/s00436-022-07563-y
Schroeder, J.M., Booton, G.C., Hay, J., Niszl, I.A., Seal, D.V., Markus, M.B., Fuerst, P.A., Byers, T.J., 2001. Use of subgenic 18S ribosomal DNA PCR and sequencing for genus and genotype identification of acanthamoebae from humans with keratitis and from sewage sludge. J. Clin. Microbiol. 39 (5), 1903–1911. https://doi.org/10.1128/JCM. 39.5.1903-1911.2001.
Visvesvara, G.S., Moura, H. y Schuster, F., 2007. Pathogenic and opportunistic free-living amoebae: Acanthamoeba spp., Balamuthia mandrillaris, Naegleria fowleri and Sappinia diploidea. FEMS Immunol Med Microbiol, 50(1), 1-26. https://doi:10.1111/j.1574-695X.2007.00232.x

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