Novel Borrelia genotypes in bats from the Macaregua Cave, Colombia.


Journal

Zoonoses and public health
ISSN: 1863-2378
Titre abrégé: Zoonoses Public Health
Pays: Germany
ID NLM: 101300786

Informations de publication

Date de publication:
02 2021
Historique:
received: 06 09 2020
revised: 04 11 2020
accepted: 05 11 2020
pubmed: 24 11 2020
medline: 14 4 2021
entrez: 23 11 2020
Statut: ppublish

Résumé

Bats have been implicated as reservoirs of relapsing fever group spirochaetes since the beginning of the last century. Recently, bat-associated spirochaetes have been reported as human pathogens. In 1968, a spirochaete was detected in blood of the bat Natalus tumidirostris captured inside the Macaregua cave, Colombia. Data on this microorganism were never published again. The aim of this study was to evaluate the presence of Borrelia DNA in blood from bats of Macaregua cave. We performed molecular analyses using a genus-specific real-time PCR targeting the 16S rRNA to detect DNA of Borrelia in blood samples from 46 bats captured in the Macaregua cave. Positive samples were submitted to a battery of PCRs aiming to amply Borrelia 16S rRNA, flaB, glpQ, p66, ospC, clpA, clpX, nifS, pepX, pyrG, recG, rplB and uvrA genes. Seventeen samples were positive for Borrelia after real-time PCR. With the exception of flaB gene, attempts to amplify further loci were unsuccessful. Nucleotide and amino acid divergences of four flaB haplotypes characterized from blood of Carollia perspicillata showed Borrelia burgdorferi sensu lato (Bbsl) as the most closely related group. A phylogenetic tree including 74 sequences of the genus confirmed this trend, since Borrelia genotypes detected in bats from Macaregua formed a monophyletic group basally positioned to Bbsl. Our results suggest that Borrelia genotypes characterized from bats roosting in the Macaregua cave might constitute a new taxon within the genus. This is the first molecular characterization of a Borrelia sp. in Colombia.

Identifiants

pubmed: 33226201
doi: 10.1111/zph.12789
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

12-18

Informations de copyright

© 2020 Wiley-VCH GmbH.

Références

Bunikis, J., Garpmo, U. F., Tsao, J., Berglund, J., Fish, D., & Barbour, A. (2004). Sequence typing reveals extensive strain diversity of the Lyme borreliosis agents Borrelia burgdorferi in North America and Borrelia afzelii in Europe. Microbiology, 150(6), 1741-1755. https://doi.org/10.1099/mic.0.26944-0
Dunn, L. H. (1927). Studies on the South American tick, Ornithodoros venezuelensis Brumpt, in Colombia. Its prevalence, distribution, and importance as an intermediate host of relapsing fever. Journal of Parasitology, 13, 249-255. https://doi.org/10.2307/3271661
Evans, N. J., Bown, K., Timofte, D., Simpson, V. R., & Birtles, R. J. (2009). Fatal borreliosis in bat caused by relapsing fever spirochete, United Kingdom. Emerging Infectious Diseases, 15, 1331-1333. https://doi.org/10.3201/eid1508.090475
Fukunaga, M., Okada, K., Nakao, M., Konishi, T., & Sato, Y. (1996). Phylogenetic analysis of Borrelia species based on Flagellin gene sequences and its application for molecular typing of Lyme Disease Borreliae. International Journal of Systematic Bacteriology, 46, 898-905. https://doi.org/10.1099/00207713-46-4-898
Guindon, S., & Gascuel, O. (2003). A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Systematic Biology, 52, 696-704. https://doi.org/10.1080/10635150390235520
Katoh, K., Misawa, K., Kima, K., & Miyata, T. (2002). MAFFT: A novel method for rapid multiple sequence alignment based on fast Fourier transform. Nucleic Acids Research, 30, 3059-3066. https://doi.org/10.1093/nar/gkf436
Kearse, M., Moir, R., Wilson, A., Stones-Havas, S., Cheung, M., Sturrock, S., Buxton, S., Cooper, A., Markowitz, S., Duran, C., Thierer, T., Ashton, B., Meintjes, P., & Drummond, A. (2012). Geneious Basic: An integrated and extendable desktop software platform for the organization and analysis of sequence data. Bioinformatics, 28, 1647-1649. https://doi.org/10.1093/bioinformatics/bts199
Kingry, L. C., Anacker, M., Pritt, B., Bjork, J., Respicio-Kingry, L., Liu, G., Sheldon, S., Boxrud, D., Strain, A., Oatman, S., Berry, J., Sloan, L., Mead, P., Neitzel, D., Kugeler, K. J., & Petersen, J. M. (2018). Surveillance for and discovery of Borrelia species in US patients suspected of Tickborne Illness. Clinical Infectious Diseases, 66, 1864-1871. https://doi.org/10.1093/cid/cix1107
Margos, G., Fingerle, V., Cutler, S., Gofton, A., Stevenson, B., & Estrada-Peña, A. (2020). Controversies in bacterial taxonomy: The example of the genus Borrelia. Ticks and Tick Borne Diseases, 11, e101335. https://doi.org/10.1016/j.ttbdis.2019.101335
Margos, G., Gatewood, A. G., Aanensen, D. M., Hanincova, K., Terekhova, D., Vollmer, S. A., Cornet, M., Piesman, J., Donaghy, M., Bormane, A., Hurn, M. A., Feil, E. J., Fish, D., Casjens, S., Wormser, G. P., Schwartz, I., & Kurtenbach, K. (2008). MLST of housekeeping genes captures geographic population structure and suggests a European origin of Borrelia burgdorferi. Proceedings of the National Academy of Sciences, 105, 8730-8735. https://doi.org/10.1073/pnas.0800323105
Margos, G., Gofton, A., Wibberg, D., Dangel, A., Marosevic, D., Loh, S.-M., Oskam, C., & Fingerle, V. (2018). The genus Borrelia reloaded. PLoS One, 13, e0208432. https://doi.org/10.1371/journal.pone.0208432
Marinkelle, C. J., & Grose, E. S. (1968). Species of Borrelia from a Colombian Bat (Natalus tumidirostris). Nature, 218, 487. https://doi.org/10.1038/218487a0
Marinkelle, C. J., & Grose, E. S. (1981). A list of ectoparasites of Colombian bats. Revista De Biología Tropical, 29, 11-20.
Mühldorfer, K. (2013). Bats and bacterial pathogens: a review. Zoonoses and Public Health, 60, 93-103. https://doi.org/10.1111/j.1863-2378.2012.01536.x
Muñoz-Leal, S., Faccini-Martínez, Á. A., Costa, F. B., Marcili, A., Mesquita, E. T. K. C., Marques, E. P., & Labruna, M. B. (2018). Isolation and molecular characterization of a relapsing fever Borrelia recovered from Ornithodoros rudis in Brazil. Ticks and Tick Borne Diseases, 9, 864-871. https://doi.org/10.1016/j.ttbdis.2018.03.008
Muñoz-Leal, S., Ramirez, D. G., Luz, H. R., Faccini, J. L. H., & Labruna, M. B. (2020). "Candidatus Borrelia ibitipoquensis," a Borrelia valaisiana-Related Genospecies Characterized from Ixodes paranaensis in Brazil. Microbial Ecology, 80(3), 682-689. https://doi.org/10.1007/s00248-020-01512-x
Nájera Angulo, L. (1945). Receptividad de los murciélagos cavernícolas españoles (Miniopterus schreibersii, Myotis myotis, Rhinolophus euryale y Rh. hipposideros minimus) al virus de la fiebre recurrente mediterránea. Boletin De La Real Sociedad Española De Historia Natural, 43, 217-228.
Nicolle, C., & Comte, C. (1906). Sur une spirollose d'un chéiroptère (Vespertilio kuhli). Annales De L'institut Pasteur, 20, 311-320.
Novy, F. G., & Knapp, R. E. (1906). Studies on Spirillum obermeieri and related organisms. Journal of Infectious Diseases, 3, 291-393.
Parola, P., Diatta, G., Socolovschi, C., Mediannikov, O., Tall, A., Bassene, H., Trape, J. F., & Raoult, D. (2011). Tick-borne relapsing fever borreliosis, rural senegal. Emerging Infectious Diseases, 17, 883-885. https://doi.org/10.3201/eid1705.100573
Peñuela-Salgado, M., & Pérez-Torres, J. (2015). Environmental and spatial characteristics that affect roost use by Seba's short-tailed bat (Carollia Perspicillata) in a Colombian cave. Journal of Cave and Karst Studies, 77, 160-164. https://doi.org/10.4311/2015LSC0105
Pérez-Torres, J., Martínez-Medina, D., Peñuela-Salgado, M., Ríos-Blanco, M. C., Estrada-Villegas, S., & Martínez-Luque, L. (2015). Macaregua: The cave with the highest bat richness in Colombia. Check List, 11, 1616. https://doi.org/10.15560/11.2.1616
Qiu, Y., Nakao, R., Hang'ombe, B. M., Sato, K., Kajihara, M., Kanchela, S., Changula, K., Eto, Y., Ndebe, J., Sasaki, M., Thu, M. J., Takada, A., Sawa, H., Sugimoto, C., & Kawabata, H. (2019). Human Borreliosis caused by a new world relapsing fever Borrelia-like organism in the old world. Clinical Infectious Diseases, 69, 107-112. https://doi.org/10.1093/cid/ciy850
Ramírez, J. D., Tapia-Calle, G., Muñoz-Cruz, G., Poveda, C., Rendón, L. M., Hincapié, E., & Guhl, F. (2014). Trypanosome species in neo-tropical bats: biological, evolutionary and epidemiological implications. Infection, Genetics and Evolution, 22, 250-256. https://doi.org/10.1016/j.meegid.2013.06.022
Ras, N. M., Lascola, B., Postic, D., Cutler, S. J., Rodhain, F., Baranton, G., & Raoult, D. (1996). Phylogenesis of Relapsing Fever Borrelia spp. International Journal of Systematic Bacteriology, 46, 859-865. https://doi.org/10.1099/00207713-46-4-859
Reeves, W. K., Streicker, D. G., Loftis, A. D., & Dasch, G. A. (2006). Serologic survey of Eptesicus fuscus from Georgia, U.S.A. for Rickettsia and Borrelia and laboratory transmission of a Rickettsia by bat ticks. Journal of Vector Ecology, 31, 386-389.
Ronquist, F., Teslenko, M., van der Mark, P., Ayres, D. L., Darling, A., Höhna, S. , Larget, B., Liu, L., Suchard, M. A., & Huelsenbeck, J. P. (2012). MrBayes 3.2: Efficient Bayesian phylogenetic inference and model choice across a large model space. Systematic Biology, 61(3), 539-542. https://doi.org/10.1093/sysbio/sys029
Schlegel, M., Ali, H. S., Stieger, N., Groschup, M. H., Wolf, R., & Ulrich, R. G. (2012). Molecular identification of small mammal species using novel cytochrome B gene-derived degenerated primers. Biochemical Genetics, 50, 440-447. https://doi.org/10.1007/s10528-011-9487-8
Schwan, T. G., Raffel, S. J., Schrumpf, M. E., Gill, J. S., & Piesman, J. (2009). Characterization of a novel relapsing fever spirochete in the midgut, coxal fluid, and salivary glands of the bat tick Carios kelleyi. Vector Borne and Zoonotic Diseases, 9, 643-647. https://doi.org/10.1089/vbz.2008.0177
Schwan, T. G., Raffel, S. J., Schrumpf, M. E., Policastro, P. F., Rawlings, J. A., Lane, R. S., Breitschwerdt, E. B., & Porcella, S. F. (2005). Phylogenetic analysis of the Spirochetes Borrelia parkeri and Borrelia turicatae and the potential for Tick-Borne relapsing fever in Florida. Journal of Clinical Microbiology, 43, 3851-3859. https://doi.org/10.1128/JCM.43.8.3851-3859.2005
Stromdahl, E. Y., Williamson, P. C., Kollars, T. M. J., Evans, S. R., Barry, R. K., Vince, M. A., & Dobbs, N. A. (2003). Evidence of Borrelia lonestari DNA in Amblyomma americanum (Acari: Ixodidae) removed from humans. Journal of Clinical Microbiology, 41, 5557-5562. https://doi.org/10.1128/jcm.41.12.5557-5562.2003

Auteurs

Sebastián Muñoz-Leal (S)

Department of Pathology and Preventive Medicine, Faculty of Veterinary Sciences, University of Concepción, Chillán, Chile.
Department of Preventive Veterinary Medicine and Animal Health, Faculty of Veterinary Medicine and Zootechny, University of São Paulo, São Paulo, Brazil.

Álvaro A Faccini-Martínez (ÁA)

Instituto de Investigaciones Biológicas del Trópico, Universidad de Córdoba, Campus Berástegui, Córdoba, Colombia.
Committee of Tropical Medicine, Zoonoses and Travel Medicine, Asociación Colombiana de Infectología, Bogotá, Colombia.

Jairo Pérez-Torres (J)

Ecology and Systematics Unit (UNESIS), Laboratory of Functional Ecology, Faculty of Sciences, Pontificia Universidad Javeriana, Bogotá, Colombia.

Sandra M Chala-Quintero (SM)

Ecology and Systematics Unit (UNESIS), Laboratory of Functional Ecology, Faculty of Sciences, Pontificia Universidad Javeriana, Bogotá, Colombia.

Maria T Herrera-Sepúlveda (MT)

Ecology and Systematics Unit (UNESIS), Laboratory of Functional Ecology, Faculty of Sciences, Pontificia Universidad Javeriana, Bogotá, Colombia.
Infectious Diseases Group, Faculty of Sciences, Pontificia Universidad Javeriana, Bogotá, Colombia.

Claudia Cuervo (C)

Infectious Diseases Group, Faculty of Sciences, Pontificia Universidad Javeriana, Bogotá, Colombia.

Marcelo B Labruna (MB)

Department of Preventive Veterinary Medicine and Animal Health, Faculty of Veterinary Medicine and Zootechny, University of São Paulo, São Paulo, Brazil.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH