دورية أكاديمية

Molecular epidemiology of Leptospira noguchii reveals important insights into a One Health context.

التفاصيل البيبلوغرافية
العنوان: Molecular epidemiology of Leptospira noguchii reveals important insights into a One Health context.
المؤلفون: Loureiro AP; Laboratório de Bacteriologia Veterinária, Departamento de Microbiologia e Parasitologia, Universidade Federal Fluminense, Niterói, Brazil., Jaeger LH; Laboratório de Bacteriologia Veterinária, Departamento de Microbiologia e Parasitologia, Universidade Federal Fluminense, Niterói, Brazil.; Laboratório de Epidemiologia e Sistemática Molecular, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil., Di Azevedo MIN; Laboratório de Bacteriologia Veterinária, Departamento de Microbiologia e Parasitologia, Universidade Federal Fluminense, Niterói, Brazil., Miraglia F; Laboratório de Bacteriologia Veterinária, Departamento de Microbiologia e Parasitologia, Universidade Federal Fluminense, Niterói, Brazil.; Departamento de Medicina Veterinária Preventiva e Saúde Animal, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, São Paulo, Brazil., Moreno LZ; Departamento de Medicina Veterinária Preventiva e Saúde Animal, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, São Paulo, Brazil., Moreno AM; Departamento de Medicina Veterinária Preventiva e Saúde Animal, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, São Paulo, Brazil., Pestana CP; Laboratório de Tecnologia Recombinante, Bio-Manguinhos, FIOCRUZ, Rio de Janeiro, Brazil., Carvalho-Costa FA; Laboratório de Epidemiologia e Sistemática Molecular, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil., Medeiros MA; Laboratório de Tecnologia Recombinante, Bio-Manguinhos, FIOCRUZ, Rio de Janeiro, Brazil., Lilenbaum W; Laboratório de Bacteriologia Veterinária, Departamento de Microbiologia e Parasitologia, Universidade Federal Fluminense, Niterói, Brazil.
المصدر: Transboundary and emerging diseases [Transbound Emerg Dis] 2020 Jan; Vol. 67 (1), pp. 276-283. Date of Electronic Publication: 2019 Sep 17.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Blackwell Verlag Country of Publication: Germany NLM ID: 101319538 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1865-1682 (Electronic) Linking ISSN: 18651674 NLM ISO Abbreviation: Transbound Emerg Dis Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Berlin : Blackwell Verlag
مواضيع طبية MeSH: One Health*, Cattle Diseases/*epidemiology , Leptospira/*genetics , Leptospirosis/*veterinary, Animals ; Bacterial Typing Techniques/veterinary ; Cattle ; Cattle Diseases/microbiology ; Electrophoresis, Gel, Pulsed-Field/veterinary ; Female ; Genotype ; Humans ; Leptospira/classification ; Leptospira/immunology ; Leptospira/pathogenicity ; Leptospirosis/epidemiology ; Leptospirosis/microbiology ; Molecular Epidemiology ; Multilocus Sequence Typing/veterinary ; Panama/epidemiology ; Phylogeny ; Serogroup ; Virulence ; Zoonoses
مستخلص: Leptospirosis presents a complex and dynamic epidemiology. Bovine leptospirosis has been described as a major infectious disease impairing reproductive efficiency. Although infections by Leptospira interrogans, L. santarosai and L. borgpetersenii are frequently reported in cattle, the presence of L. noguchii in these animals should not be neglected. In this study, we describe serological (MAT) and molecular characterization (rrs and secY gene sequencing, multilocus sequence typing [MLST] and pulsed-field gel electrophoresis [PFGE]) of eight L. noguchii strains obtained from slaughtered cows. Intraspecific genetic diversity was evaluated, and haplotype networks were constructed based on hosts and geographical localizations. Strains were characterized as belonging to serogroups Australis, Autumnalis and Panama, and molecular characterization showed a high heterogeneity of these strains. Ten different STs were found (including nine new STs and 39 novel alleles) as well as nine different pulsotypes. Two clonal complexes were found. Phylogenetic trees based on secY locus and concatenated MLST loci showed two main clusters, with sequences from the present study included in the first. In general, there was no relationship between the geographical origin and the secY phylogenetic clusters, as well as between secY phylogenetic clusters and serogroups. Molecular diversity indexes confirmed a high variability (H > 0.8). This high intraspecific variation observed may be related to differences in virulence, pathogenicity and antigenicity or even adaptability of the strains. In addition, haplotype networks clearly demonstrated the circulation of genotypes between humans and animals, confirming the zoonotic potential. The present study provides relevant data for the study of leptospirosis in the One Health context, where human, animal and environmental health is closely connected.
(© 2019 Blackwell Verlag GmbH.)
References: Ahmed, N., Devi, S. M., de Valverde, M. L., Vijayachari, P., Machang'u, R. S., Ellis, W. A., & Hartskeerl, R. A. (2006). Multilocus sequence typing method for identification and genotypic classification of pathogenic Leptospira species. Annals of Clinical Microbiology and Antimicrobials, 5(28), 1-10.
Ballados-González, G. G., Sánchez-Montes, S., Romero-Salas, D., Colunga Salas, P., Gutiérrez-Molina, R., León-Paniagua, L., … Cruz-Romero, A. (2018). Detection of pathogenic Leptospira species associated with phyllostomid bats (Mammalia: Chiroptera) from Veracruz, Mexico. Transboundary and Emerging Diseases, 65, 773-781.
Bandelt, H., Forster, P., & Röhl, A. (1999). Median-joining networks for inferring intraspecific phylogenies. Molecular Biology and Evolution, 16, 37-48. https://doi.org/10.1093/oxfordjournals.molbev.a026036.
Barragan, V., Chiriboga, J., Miller, E., Olivas, S., Birdsell, D., Hepp, C., … Pearson, T. (2016). High Leptospira diversity in animals and humans complicates the search for common reservoirs of human disease in rural ecuador. PLoS Neglected Tropical Diseases, 10, e0004990. https://doi.org/10.1371/journal.pntd.0004990.
Boonsilp, S., Thaipadungpanit, J., Amornchai, P., Wuthiekanun, V., Bailey, M. S., Holden, M. T., … Peacock, S. J. (2013). A single multilocus sequence typing (MLST) scheme for seven pathogenic Leptospira species. PLoS Neglected Tropical Diseases, 7, e1954. https://doi.org/10.1371/journal.pntd.0001954.
Cameron, C. E. (2015). Leptospiral structure, physiology, and metabolism. Current Topics in Microbiology and Immunology, 387, 21-41.
Ellis, W. A. (2015). Animal leptospirosis. Current Topics in Microbiology and Immunology, 387, 99-137.
Excoffier, L., & Lischer, H. E. L. (2010). Arlequin suite ver 3.5: A new series of programs to perform population genetics analyses under Linux and Windows. Molecular Ecology Resources, 10, 564-567. https://doi.org/10.1111/j.1755-0998.2010.02847.x.
Faine, S. B., Adler, B., Bolin, C., & Perolat, P. (1999). Leptospira and leptospirosis, (2nd ed.). Melbourne, Australia: MediSci.
Fenner, J. S., Anjum, M. F., Randall, L. P., Pritchard, G. C., Wu, G., Errington, J., … Woodward, M. J. (2010). Analysis of 16S rDNA sequences from pathogenic Leptospira serovars and use of single nucleotide polymorphisms for rapid speciation by D-HPLC. Research in Veterinary Science, 89, 48-57. https://doi.org/10.1016/j.rvsc.2009.12.014.
Flores, B. J., Pérez-Sánchez, T., Fuertes, H., Sheleby-Elías, J., Múzquiz, J. L., Jirón, W., … Halaihel, N. (2017). A cross-sectional epidemiological study of domestic animals related to human leptospirosis cases in Nicaragua. Acta Tropica, 170, 79-84. https://doi.org/10.1016/j.actatropica.2017.02.031.
Fouts, D. E., Matthias, M. A., Adhikarla, H., Adler, B., Amorim-Santos, L., Berg, D. E., … Vinetz, J. M. (2016). What makes a bsp bacterial species pathogenic? Comparative genomic analysis of the genus Leptospira. PLoS Neglected Tropical Diseases, 10, e0004403.
Francisco, A. P., Bugalho, M., Ramirez, M., & Carriço, J. A. (2009). Global optimal eBURST analysis of multilocus typing data using a graphic matroid approach. BMC Bioinformatics, 10, 152. https://doi.org/10.1186/1471-2105-10-152.
Galloway, R. L., & Levett, P. N. (2010). Application and validation of PFGE for serovar identification of Leptospira clinical isolates. PLoS Neglected Tropical Diseases, 4, e824. https://doi.org/10.1371/journal.pntd.0000824.
Hall, T. A. (1999). BioEdit: A user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symposium Series, 41, 95-98.
Hamond, C., Pestana, C. P., Medeiros, M. A., & Lilenbaum, W. (2016). Genotyping of Leptospira directly in urine samples of cattle demonstrates a diversity of species and strains in Brazil. Epidemiology and Infection, 144, 72-75.
Kumar, S., Stecher, G., & Tamura, K. (2016). MEGA7: Molecular evolutionary genetics analysis version 7.0 for bigger datasets. Molecular Biology and Evolution, 33, 1870-1874. https://doi.org/10.1093/molbev/msw054.
Leigh, J. W., & Bryant, D. (2015). Monte carlo strategies for selecting parameter values in simulation experiments. Systematic Biology, 64, 741-751. https://doi.org/10.1093/sysbio/syv030.
Loureiro, A. P., Martins, G., Pinto, P., Narduche, L., Teixeira, R. C., & Lilenbaum, W. (2015). Usage of a selective media (EMJH-STAFF) in primary culturing of pathogenic leptospires from bovine clinical samples. Letters in Applied Microbiology, 61, 603-606. https://doi.org/10.1111/lam.12501.
Martins, G., Loureiro, A. P., Hamond, C., Pinna, M. H., Bremont, S., Bourhy, P., & Lilenbaum, W. (2015). First isolation of Leptospira noguchii serogroups Panama and Autumnalis from cattle. Epidemiology and Infection, 143, 1538-1541.
Pellizzaro, M., Conrado, F. O., Martins, C. M., Joaquim, S. F., Ferreira, F., Langoni, H., & Biondo, A. W. (2017). Serosurvey of Leptospira spp. and Toxoplasma gondii in rats captured from two zoos in Southern Brazil. Revista Da Sociedade Brasileira De Medicina Tropical, 50, 857-860. https://doi.org/10.1590/0037-8682-0138-2017.
Pinto, P. S., Pestana, C., Medeiros, M. A., & Lilenbaum, W. (2017). Plurality of Leptospira strains on slaughtered animals suggest a broader concept of adaptability of leptospires to cattle. Acta Tropica, 172, 156-159. https://doi.org/10.1016/j.actatropica.2017.04.032.
Ribeiro-Gonçalves, B., Francisco, A. P., Vaz, C., Ramirez, M., & Carriço, J. A. (2016). PHYLOViZ Online: Web-based tool for visualization, phylogenetic inference, analysis and sharing of minimum spanning trees. Nucleic Acids Research, 44, W246-251. https://doi.org/10.1093/nar/gkw359.
Silva, E. F., Brod, C. S., Cerqueira, G. M., Bourscheidt, D., Seyffert, N., Queiroz, A., … Dellagostin, O. A. (2007). Isolation of Leptospira noguchii from sheep. Veterinary Microbiology, 121, 144-149. https://doi.org/10.1016/j.vetmic.2006.11.010.
Silva, E. F., Cerqueira, G. M., Seyffert, N., Seixas, F. K., Hartwig, D. D., Athanazio, D. A., … Dellagostin, O. A. (2009). Leptospira noguchii and human and animal leptospirosis, Southern Brazil. Epidemiology and Infection, 15, 621-623.
Van Belkum, A., Tassios, P. T., Dijkshoorn, L., Haeggman, S., Cookson, B., Fry, N. K., … Struelens, M. (2007). Guidelines for the validation and application of typing methods for use in bacterial epidemiology. Clinical Microbiology and Infection, 13, 1-46. https://doi.org/10.1111/j.1469-0691.2007.01786.x.
Vieira, A. S., D'Andrea, P. S., do Vilela, R., Loretto, D., Jaeger, L. H., Carvalho-Costa, F. A., & Lilenbaum, W. (2019). Pathogenic Leptospira species are widely disseminated among small mammals in Atlantic Forest biome. Transboundary and Emerging Diseases, 66, 1195-1201.
Xu, Y., Zhang, J., Cui, S., Li, M., Zhang, Y., Xue, H., … Wang, J. (2015). Genetic stability of vaccine strains by multilocus sequence typing and pulsed-field gel electrophoresis analysis: Implications for quality control of the leptospiral vaccine. Human Vaccines & Immunotherapeutics, 11, 1272-1276. https://doi.org/10.1080/21645515.2015.1020266.
Zarantonelli, L., Suanes, A., Meny, P., Buroni, F., Nieves, C., Salaberry, X., … Buschiazzo, A. (2018). Isolation of pathogenic Leptospira strains from naturally infected cattle in Uruguay reveals high serovar diversity, and uncovers a relevant risk for human leptospirosis. PLoS Neglected Tropical Diseases, 12, e0006694. https://doi.org/10.1371/journal.pntd.0006694.
معلومات مُعتمدة: 2011/18290-0 Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro; E-26/202.766/2016 Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro; E-26/202.370/2018 MINDA; 2013/17136-2 Fundação de Amparo à Pesquisa do Estado de São Paulo
فهرسة مساهمة: Keywords: Leptospira noguchii; MLST; PFGE; bovine leptospirosis; genotyping
سلسلة جزيئية: GENBANK KY113317; KY113324; MK579498; MK579566
تواريخ الأحداث: Date Created: 20190905 Date Completed: 20200526 Latest Revision: 20200526
رمز التحديث: 20221213
DOI: 10.1111/tbed.13349
PMID: 31484225
قاعدة البيانات: MEDLINE
الوصف
تدمد:1865-1682
DOI:10.1111/tbed.13349