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First isolation, identification and genetic characterization of Brucella abortus biovar 3 from dairy cattle in Bangladesh

BACKGROUND: Brucellosis is a zoonotic disease caused by bacteria Brucella spp. belonging to the genus Brucella. It is endemic in domesticated animals in Bangladesh. Isolation, identification and genetic characterization of Brucella spp. in dairy cattle are essential to undertake appropriate control...

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Autores principales: Islam, Md. Sadequl, Garofolo, Giuliano, Sacchini, Lorena, Dainty, Amanda C., Khatun, Mst. Minara, Saha, Sukumar, Islam, Md. Ariful
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868452/
https://www.ncbi.nlm.nih.gov/pubmed/31452358
http://dx.doi.org/10.1002/vms3.193
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author Islam, Md. Sadequl
Garofolo, Giuliano
Sacchini, Lorena
Dainty, Amanda C.
Khatun, Mst. Minara
Saha, Sukumar
Islam, Md. Ariful
author_facet Islam, Md. Sadequl
Garofolo, Giuliano
Sacchini, Lorena
Dainty, Amanda C.
Khatun, Mst. Minara
Saha, Sukumar
Islam, Md. Ariful
author_sort Islam, Md. Sadequl
collection PubMed
description BACKGROUND: Brucellosis is a zoonotic disease caused by bacteria Brucella spp. belonging to the genus Brucella. It is endemic in domesticated animals in Bangladesh. Isolation, identification and genetic characterization of Brucella spp. in dairy cattle are essential to undertake appropriate control and preventive measures. The study was conducted to isolate and characterize the Brucella spp. circulating in dairy cattle. METHODS: Uterine discharge (n = 45), milk (n = 115), vaginal swab (n = 71), placenta (n = 7) and aborted fetus (n = 2) were collected. Brucella selective agar plates were inoculated with samples and incubated at 37 (◦)C for 14 days under 5% CO(2) for isolation of Brucella spp. Brucella suspected colonies were recovered from samples were confirmed by genus and species specific PCR assays. Genetic characterization was performed by Multi Locus Variable number tandem‐repeat Analysis‐16 (MLVA‐16). RESULTS: The isolates of Brucella recovered from samples were confirmed as B. abortus by AMOS‐ERY PCR assay. The classical biotyping method confirmed all 10 B. abortus isolates belonged to the biovar 3. The MLVA‐16 assay indicated all B. abortus isolates identical and the same genotype 40, based on panel 1 MLVA‐8. CONCLUSION: Dendrogram analysis revealed all B. abortus isolates of the study were identical to three isolates from Brazil, one isolate of France and closely related to Chinese isolates. This is the first report of isolation and genetic characterization of B. abortus from the dairy cattle in Bangladesh.
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spelling pubmed-68684522019-11-25 First isolation, identification and genetic characterization of Brucella abortus biovar 3 from dairy cattle in Bangladesh Islam, Md. Sadequl Garofolo, Giuliano Sacchini, Lorena Dainty, Amanda C. Khatun, Mst. Minara Saha, Sukumar Islam, Md. Ariful Vet Med Sci Original Articles BACKGROUND: Brucellosis is a zoonotic disease caused by bacteria Brucella spp. belonging to the genus Brucella. It is endemic in domesticated animals in Bangladesh. Isolation, identification and genetic characterization of Brucella spp. in dairy cattle are essential to undertake appropriate control and preventive measures. The study was conducted to isolate and characterize the Brucella spp. circulating in dairy cattle. METHODS: Uterine discharge (n = 45), milk (n = 115), vaginal swab (n = 71), placenta (n = 7) and aborted fetus (n = 2) were collected. Brucella selective agar plates were inoculated with samples and incubated at 37 (◦)C for 14 days under 5% CO(2) for isolation of Brucella spp. Brucella suspected colonies were recovered from samples were confirmed by genus and species specific PCR assays. Genetic characterization was performed by Multi Locus Variable number tandem‐repeat Analysis‐16 (MLVA‐16). RESULTS: The isolates of Brucella recovered from samples were confirmed as B. abortus by AMOS‐ERY PCR assay. The classical biotyping method confirmed all 10 B. abortus isolates belonged to the biovar 3. The MLVA‐16 assay indicated all B. abortus isolates identical and the same genotype 40, based on panel 1 MLVA‐8. CONCLUSION: Dendrogram analysis revealed all B. abortus isolates of the study were identical to three isolates from Brazil, one isolate of France and closely related to Chinese isolates. This is the first report of isolation and genetic characterization of B. abortus from the dairy cattle in Bangladesh. John Wiley and Sons Inc. 2019-08-26 /pmc/articles/PMC6868452/ /pubmed/31452358 http://dx.doi.org/10.1002/vms3.193 Text en © 2019 The Authors. Veterinary Medicine and Science Published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Islam, Md. Sadequl
Garofolo, Giuliano
Sacchini, Lorena
Dainty, Amanda C.
Khatun, Mst. Minara
Saha, Sukumar
Islam, Md. Ariful
First isolation, identification and genetic characterization of Brucella abortus biovar 3 from dairy cattle in Bangladesh
title First isolation, identification and genetic characterization of Brucella abortus biovar 3 from dairy cattle in Bangladesh
title_full First isolation, identification and genetic characterization of Brucella abortus biovar 3 from dairy cattle in Bangladesh
title_fullStr First isolation, identification and genetic characterization of Brucella abortus biovar 3 from dairy cattle in Bangladesh
title_full_unstemmed First isolation, identification and genetic characterization of Brucella abortus biovar 3 from dairy cattle in Bangladesh
title_short First isolation, identification and genetic characterization of Brucella abortus biovar 3 from dairy cattle in Bangladesh
title_sort first isolation, identification and genetic characterization of brucella abortus biovar 3 from dairy cattle in bangladesh
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868452/
https://www.ncbi.nlm.nih.gov/pubmed/31452358
http://dx.doi.org/10.1002/vms3.193
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