Leptospira spp. detection in bats from the Peninsula of Yucatán, México
Abstract
The records of Leptospira spp. in bats from México are scarce. It is known that several species of bats are hosts of pathogenic Leptospira spp.; therefore, they participate in the epidemiological cycle and can generate transmission scenarios to people and animals. The aim was to detect the DNA of Leptospira spp. in bats captured in four sites from the Yucatán Peninsula, México. A kidney fragment was collected from the bats and used to extract genomic DNA. Using a PCR, the DNA of Leptospira spp. was detected. Fifty–four bats of the species Desmodus rotundus, Mimon cozumelae, Pteronotus mesoamericanus, Pteronotus fulvus, Nyctinomops laticaudatus, Peropteryx macrotis, Molossus nigricans, Molossus aztecus, Noctilio leporinus, Saccopteryx bilineata and Mormoops megalophylla were studied. The PCR yielded a total frequency of Leptospira spp. of 44.4% (24/54, 95% CI 36.2–71.7%). Species with at least one positive individual were D. rotundus, M. cozumelae, P. mesoamericanus, N. laticaudatus, P. macrotis, M. nigricans, N. leporinus, M. aztecus, and S. bilineata. A high frequency of Leptospira spp. was found in different species of bats belonging to several trophic guilds. The presence of Leptospira spp. in bats is relevant for Public and Animal Health because the evidence indicates that they can generate zoonotic transmission cycles.
Downloads
References
Coburn J, Picardeau M, Woods CW, Veldman T, Haake, DA. Pathogenesis insights from an ancient and ubiquitous spirochete. PLoS Pathog. [Internet]. 2021; 17(10):e1009836. doi: https://doi.org/kq29
Torres–Castro M, Hernández–Betancourt S, Agudelo–Flórez P, Arroyave–Sierra E, Zavala–Castro J, Puerto FI. Revisión actual de la epidemiología de la leptospirosis. Rev. Med. Inst. Mex. Seguro Soc. 2016; 54(5):620–5. PMID: 27428344.
Costa F, Hagan JE, Calcagno J, Kane M, Torgerson P, Martinez–Silveira MS, Stein C, Abela–Ridder B, Ko AI. Global morbidity and mortality of leptospirosis: A systematic review. PLoS Negl. Trop. Dis. [Internet]. 2015; 9(9):e0003898. doi: https://doi.org/b7sd
Yescas–Benítez JE, Rivero–Perez N, Montiel–Díaz HE, Valladares–Carranza B, Peláez–Acero A, Morales–Ubaldo AL, Zaragoza–Bastida A. Comportamiento epidemiológico de la leptospirosis en México durante el periodo 2013–2019. Rev. Salud Publ. [Internet]. 2020; 22(4):421–7. doi: https://doi.org/kq3c
Lata KS, Kumar S, Vindal V, Patel S, Das J. A core and pan gene map of Leptospira genus and its interactions with human host. Microb. Pathog. [Internet]. 2022; 162:105347. doi: https://doi.org/kq3d
Santos AAN, Ribeiro PDS, da França GV, Souza FN, Ramos EAG, Figueira CP, Reis MG, Costa F, Ristow P. Leptospira interrogans biofilm formation in Rattus norvegicus (Norway rats) natural reservoirs. PLoS Negl. Trop. Dis. [Internet]. 2021; 15(9):e0009736. doi: https://doi.org/kq3f
Azócar–Aedo L. Basic aspects and epidemiological studies on leptospirosis carried out in animals in Chile: A bibliographic review. Trop. Med. Infect. Dis. [Internet]. 2023; 8(2):97. doi: https://doi.org/kq3h
Cilia G, Bertelloni F, Albini S, Fratini F. Insight into the epidemiology of leptospirosis: A review of Leptospira Isolations from "unconventional" hosts. Animals. [Internet]. 2021; 11(1):191. doi: https://doi.org/kq3j
Monroy FP, Solari S, Lopez JÁ, Agudelo–Flórez P, Peláez–Sánchez RG. High diversity of Leptospira species infecting bats captured in the Urabá Region (Antioquia–Colombia). Microorganisms. [Internet]. 2021; 9(9):1897. doi: https://doi.org/kq3k
Mühldorfer K. Bats and bacterial pathogens: a review. Zoonoses Public Health. [Internet]. 2013; 60(1):93–103. doi: https://doi.org/f4hsbm
Dietrich M, Mühldorfer K, Tortosa P, Markotter W. Leptospira and bats: Story of an emerging friendship. PLoS Pathog. [Internet]. 2015; 11(11):e1005176. doi: https://doi.org/kq3n
Torres–Castro M, Cruz–Camargo B, Medina–Pinto R, Reyes–Hernández B, Moguel–Lehmer C, Medina R, Ortiz–Esquivel J, Arcila–Fuentes W, López–Ávila A, Noh–Pech H, Panti–May A, Rodríguez–Vivas I, Puerto FI. Detección molecular de leptospiras patógenas en roedores sinantrópicos y silvestres capturados en Yucatán, México. Biomed. [Internet]. 2018; 38(Suppl 2):51–8. doi: https://doi.org/kq3q
Suárez–Galaz AR, Hernández–Betancourt S, Panti–May JA, Manrique–Saide P, Torres–Castro M. Evidencia de Leptospira spp. en musarañas Cryptotis mayensis. Nuevo hospedero en Yucatán, México. Rev. Biomed. [Internet]. 2021; 32(3):161–5. doi: https://doi.org/kq3r
Torres–Castro M, Febles–Solís V, Hernández–Betancourt S, Noh–Pech H, Estrella E, Peláez–Sánchez R, Panti–May A, Herrera–Flores B, Reyes–Hernández B, Sosa–Escalante J. Leptospira patógenas en murciélagos de Campeche y Yucatán, México. Rev. MVZ. Cordoba. [Internet]. 2020; 25(2):e1815. doi: https://doi.org/kq3t
Moguel–Chin WI, Hernández–Mena DI, Torres–Castro M, Barrientos–Medina RC, Hernández–Betancourt SF, MacSwiney G. MC, García–Prieto L, Vidal–Martínez VM, Selem–Salas CI, Panti–May JA. Survey on helminths of bats in the Yucatan Peninsula: infection levels, molecular information and host–parasite networks. Parasitology. [Internet]. 2023; 150(2):172–83. doi: https://doi.org/kq3x
Medellín R, Harita H, Sánchez O. Identificación de los Murciélagos de México. Clave de Campo, 2nd ed. Ciudad de México: Instituto de Ecología. 2008; p 26–63.
Dzib–Paredes G, Rodríguez–Vivas RI, Panti–May A, Noh–Pech H, Rosado–Aguilar JA, Torres–Castro M. Frecuencia de Borrelia burgdorferi sensu lato y Leptospira spp. en pequeños roedores de Yucatán, México. Rev. Cientif. Fac. Cien. Vet. [Internet]. 2022; 32:1–8. doi: https://doi.org/krvq
Haake DA, Suchard MA, Kelly MM, Dundoo M, Alt DP, Zuerner RL. Molecular evolution and mosaicism of leptospiral outer membrane proteins involves horizontal DNA transfer. J. Bacteriol. [Internet]. 2004; 186(9):2818–28. doi: https://doi.org/c9bctm
Shukla J. 16S rRNA PCR for differentiation of pathogenic and non–pathogenic leptospira isolates. Indian J. Med. Microbiol. 2003; 21(1):25–30. PMID: 17642970.
Torres–Castro M, Muñoz–Dueñas D, Hernández–Betancourt S, Bolio–González M, Noh–Pech H, Peláez–Sánchez R, Sosa–Escalante J. Infección con Toxoplasma gondii (Eucoccidiorida: Sarcocystidae) en murciélagos de Campeche y Yucatán, México. Rev. Biol. Trop. 2019; 67(3):633–42.
Torres–Castro M, Cuevas–Koh N, Hernández–Betancourt S, Noh–Pech H, Estrella E, Herrera–Flores B, Panti–May JA, Waleckx E, Sosa–Escalante J, Peláez–Sánchez R. Natural infection with Trypanosoma cruzi in bats captured in Campeche and Yucatán, México. Biomed. [Internet]. 2021; 41(Supl.1):131–40. doi: https://doi.org/gh3j
Torres–Castro M, Noh–Pech H, Hernández–Betancourt S, Peláez–Sánchez R, Lugo–Caballero C, Puerto FI. West Nile and Zika viruses in bats from a suburban area of Merida, Yucatan, Mexico. Zoonoses Public Health. [Internet]. 2021; 68(7):834–41. doi: https://doi.org/kq3z
Lugo–Caballero C, Torres–Castro M, López–Ávila K, Hernández–Betancourt S, Noh–Pech, H, Tello–Martín R, Puerto–Manzano F, Dzul–Rosado K. Molecular identification of zoonotic Rickettsia species closely related to R. typhi, R. felis, R. rickettsii in bats from Mexico. Indian J. Med. Res. [Internet]. 2021; 154(3):536–8. doi: https://doi.org/kq32
Panti–May JA, Hernández–Mena DI, Torres–Castro MA, Estrella–Martínez E, Lugo–Caballero C, Vidal–Martínez VM, Hernández–Betancourt SF. Morphological and molecular identification of helminths of the greater bulldog bat Noctilio leporinus (Quiroptera: Noctilionidae) from Campeche, Mexico. Parasitol. Int. [Internet]. 2021; 82:102302. doi: https://doi.org/kq33
Suárez–Galaz AR. Detección molecular de Leptospira spp. en quirópteros y roedores silvestres capturados en el estado de Yucatán, México. [Tesis de Licenciatura]. Mérida: Universidad Autónoma de Yucatán; 2020 [citado 05 jun 2023]. 55 p.
Ballados–González GG, Sánchez–Montes S, Romero–Salas D, Colunga–Salas P, Gutiérrez–Molina R, León–Paniagua L, Becker I, Méndez–Ojeda ML, Barrientos–Salcedo C, Serna–Lagunes R, Cruz–Romero, A. Detection of pathogenic Leptospira species associated with phyllostomid bats (Mammalia: Chiroptera) from Veracruz, Mexico. Transbound. Emerg. Dis. [Internet]. 2018; 65(3):773–81. doi: https://doi.org/gdjj3g
Szentivanyi T, McKee C, Jones G, Foster JT. Trends in bacterial pathogens of bats: Global distribution and knowledge gaps. Transbound. Emerg. Dis. [Internet]. 2023; 2023:1–17. doi: https://doi.org/kq35
Bevans AI, Fitzpatrick DM, Stone DM, Butler BP, Smith MP, Cheetham S. Phylogenetic relationships and diversity of bat–associated Leptospira and the histopathological evaluation of these infections in bats from Grenada, West Indies. PLoS Negl. Trop. Dis. [Internet]. 2020; 14(1):e0007940. doi: https://doi.org/kq36
Ulsenheimer BC, von Laer AE, Tonin AA, Campos AAS, Dos Santos HF, Sangioni LA, de Avila–Botton S. Leptospira interrogans in bats in Rio Grande do Sul State, Brazil: epidemiologic aspects and phylogeny. Braz. J. Microbiol. [Internet]. 2022; 53(4):2233–40. doi: https://doi.org/kq37
Vashi NA, Reddy P, Wayne DB, Sabin B. Bat–associated leptospirosis. J. Gen. Intern. Med. [Internet]. 2010; 25(2):162–4. doi: https://doi.org/cnc28n
Eby P, Peel AJ, Hoegh A, Madden W, Giles JR, Hudson PJ, Plowright RK. Pathogen spillover driven by rapid changes in bat ecology. Nature. [Internet]. 2023; 613(7943):340–4. doi: https://doi.org/jmr5
Nguyen L, Chimunda T. Neuro–leptospirosis – A batty diagnostic enigma. IDCases. [Internet]. 2023; 32:e01731. doi: https://doi.org/kq38
Bessa TA, Spichler A, Chapola EG, Husch AC, de Almeida MF, Sodré MM, Savani ES, Sacramento DR, Vinetz JM. The contribution of bats to leptospirosis transmission in Sao Paulo City, Brazil. Ame. J. Trop. Med. Hyg. [Internet]. 2010; 82(2):315–7. doi: https://doi.org/fpq3fs
Zhao M, Xiao X, Han HJ, Wang LJ, Lei SC, Liu JW, Qi R, Qin XR, Yu H, Yu XJ. Leptospira in Bats from Hubei Province, China, 2018. J. Wildl. Dis. [Internet]. 2019; 55(4):940–3. doi: 10.7589/2019–01–009.
Mateus J, Gómez N, Herrera–Sepúlveda MT, Hidalgo M, Pérez–Torres J, Cuervo C. Bats are a potential reservoir of pathogenic Leptospira species in Colombia. J. Infect. Dev. Ctries. [Internet]. 2019; 13(4):278–83. doi: https://doi.org/grssvg
McCutchan JL, Knox MA, Naikatini A, Hayman DTS, Gartrell BD. Molecular evidence of Leptospira spp. in isolated Fijian bats. J. Wildl. Dis. [Internet]. 2023; 59(1):202–6. doi: https://doi.org/kq39
Mayer FQ, Dos Reis EM, Bezerra AVA, Cerva C, Rosa J, Cibulski SP, Lima FES, Pacheco SM, Rodrigues RO. Pathogenic Leptospira spp. in bats: Molecular investigation in Southern Brazil. Comp. Immunol. Microbiol. Infect. Dis. [Internet]. 2017; 52:14–8. doi: https://doi.org/kq4b
Javati S, Guernier–Cambert V, Jonduo M, Robby S, Kimopa J, Maure T, McBryde ES, Pomat W, Aplin K, Helgen KM, Abdad MY, Horwood PF. Diversity of Leptospira spp. in bats and rodents from Papua New Guinea. Transboud. Emerg. Dis. [Internet]. 2022; 69(6):4048–54. doi: https://doi.org/kq4c
Harkin KR, Hays M, Davis R, Moore M. Use of PCR to identify Leptospira in kidneys of big brown bats (Eptesicus fuscus) in Kansas and Nebraska, USA. J. Wildl. Dis. [Internet]. 2014; 50(3):651–4. doi: https://doi.org/f6bcb7
Lagadec E, Gomard Y, Guernier V, Dietrich M, Pascalis H, Temmam S, Ramasindrazana, B, Goodman SM, Tortosa P, Dellagi K. Pathogenic Leptospira spp. in bats, Madagascar and Union of the Comoros. Emerg. Infect. Dis. [Internet]. 2012; 18(10):1696–8. doi: https://doi.org/kq4d
Esteves SB, Gaeta NC, Batista JMN, Dias RA, Heinemann MB. Leptospira spp. infection in bats: A systematic review and meta–analysis. Transbound. Emerg. Dis. [Internet]. 2022; 69(5):e2456–73. doi: https://doi.org/kq4f
Copyright (c) 2023 Marco Torres–Castro, Jesús Alonso Panti–May, María Cristina MacSwiney González, César Lugo–Caballero, Alejandro Suárez–Galaz, Melissa Suárez–Galaz, Aarón Yeh–Gorocica, Bayron Cruz–Camargo
This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.