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Molecular epidemiology and whole genome sequencing analysis of clinical Mycobacterium bovis from Ghana

BACKGROUND: Bovine tuberculosis (bTB) caused by Mycobacterium bovis is a re-emerging problem in both livestock and humans. The association of some M. bovis strains with hyper-virulence, MDR-TB and disseminated disease makes it imperative to understand the biology of the pathogen. METHODS: Mycobacter...

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Autores principales: Otchere, Isaac Darko, van Tonder, Andries J., Asante-Poku, Adwoa, Sánchez-Busó, Leonor, Coscollá, Mireia, Osei-Wusu, Stephen, Asare, Prince, Aboagye, Samuel Yaw, Ekuban, Samuel Acquah, Yahayah, Abdallah Iddrisu, Forson, Audrey, Baddoo, Akosua, Laryea, Clement, Parkhill, Julian, Harris, Simon R., Gagneux, Sebastien, Yeboah-Manu, Dorothy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6398925/
https://www.ncbi.nlm.nih.gov/pubmed/30830912
http://dx.doi.org/10.1371/journal.pone.0209395
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author Otchere, Isaac Darko
van Tonder, Andries J.
Asante-Poku, Adwoa
Sánchez-Busó, Leonor
Coscollá, Mireia
Osei-Wusu, Stephen
Asare, Prince
Aboagye, Samuel Yaw
Ekuban, Samuel Acquah
Yahayah, Abdallah Iddrisu
Forson, Audrey
Baddoo, Akosua
Laryea, Clement
Parkhill, Julian
Harris, Simon R.
Gagneux, Sebastien
Yeboah-Manu, Dorothy
author_facet Otchere, Isaac Darko
van Tonder, Andries J.
Asante-Poku, Adwoa
Sánchez-Busó, Leonor
Coscollá, Mireia
Osei-Wusu, Stephen
Asare, Prince
Aboagye, Samuel Yaw
Ekuban, Samuel Acquah
Yahayah, Abdallah Iddrisu
Forson, Audrey
Baddoo, Akosua
Laryea, Clement
Parkhill, Julian
Harris, Simon R.
Gagneux, Sebastien
Yeboah-Manu, Dorothy
author_sort Otchere, Isaac Darko
collection PubMed
description BACKGROUND: Bovine tuberculosis (bTB) caused by Mycobacterium bovis is a re-emerging problem in both livestock and humans. The association of some M. bovis strains with hyper-virulence, MDR-TB and disseminated disease makes it imperative to understand the biology of the pathogen. METHODS: Mycobacterium bovis (15) among 1755 M. tuberculosis complex (MTBC) isolated between 2012 and 2014 were characterized and analyzed for associated patient demography and other risk factors. Five of the M. bovis isolates were whole-genome sequenced and comparatively analyzed against a global collection of published M. bovis genomes. RESULTS: Mycobacterium bovis was isolated from 3/560(0.5%) females and 12/1195(1.0%) males with pulmonary TB. The average age of M. bovis infected cases was 46.8 years (7-72years). TB patients from the Northern region of Ghana (1.9%;4/212) had a higher rate of infection with M. bovis (OR = 2.7,p = 0.0968) compared to those from the Greater Accra region (0.7%;11/1543). Among TB patients with available HIV status, the odds of isolating M. bovis from HIV patients (2/119) was 3.3 higher relative to non-HIV patients (4/774). Direct contact with livestock or their unpasteurized products was significantly associated with bTB (p<0.0001, OR = 124.4,95% CI = 30.1–508.3). Two (13.3%) of the M. bovis isolates were INH resistant due to the S315T mutation in katG whereas one (6.7%) was RIF resistant with Q432P and I1491S mutations in rpoB. M. bovis from Ghana resolved as mono-phyletic branch among mostly M. bovis from Africa irrespective of the host and were closest to the root of the global M. bovis phylogeny. M. bovis-specific amino acid mutations were detected among MTBC core genes such as mce1A, mmpL1, pks6, phoT, pstB, glgP and Rv2955c. Additional mutations P6T in chaA, G187E in mgtC, T35A in Rv1979c, S387A in narK1, L400F in fas and A563T in eccA1 were restricted to the 5 clinical M. bovis from Ghana. CONCLUSION: Our data indicate potential zoonotic transmission of bTB in Ghana and hence calls for intensified public education on bTB, especially among risk groups.
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spelling pubmed-63989252019-03-08 Molecular epidemiology and whole genome sequencing analysis of clinical Mycobacterium bovis from Ghana Otchere, Isaac Darko van Tonder, Andries J. Asante-Poku, Adwoa Sánchez-Busó, Leonor Coscollá, Mireia Osei-Wusu, Stephen Asare, Prince Aboagye, Samuel Yaw Ekuban, Samuel Acquah Yahayah, Abdallah Iddrisu Forson, Audrey Baddoo, Akosua Laryea, Clement Parkhill, Julian Harris, Simon R. Gagneux, Sebastien Yeboah-Manu, Dorothy PLoS One Research Article BACKGROUND: Bovine tuberculosis (bTB) caused by Mycobacterium bovis is a re-emerging problem in both livestock and humans. The association of some M. bovis strains with hyper-virulence, MDR-TB and disseminated disease makes it imperative to understand the biology of the pathogen. METHODS: Mycobacterium bovis (15) among 1755 M. tuberculosis complex (MTBC) isolated between 2012 and 2014 were characterized and analyzed for associated patient demography and other risk factors. Five of the M. bovis isolates were whole-genome sequenced and comparatively analyzed against a global collection of published M. bovis genomes. RESULTS: Mycobacterium bovis was isolated from 3/560(0.5%) females and 12/1195(1.0%) males with pulmonary TB. The average age of M. bovis infected cases was 46.8 years (7-72years). TB patients from the Northern region of Ghana (1.9%;4/212) had a higher rate of infection with M. bovis (OR = 2.7,p = 0.0968) compared to those from the Greater Accra region (0.7%;11/1543). Among TB patients with available HIV status, the odds of isolating M. bovis from HIV patients (2/119) was 3.3 higher relative to non-HIV patients (4/774). Direct contact with livestock or their unpasteurized products was significantly associated with bTB (p<0.0001, OR = 124.4,95% CI = 30.1–508.3). Two (13.3%) of the M. bovis isolates were INH resistant due to the S315T mutation in katG whereas one (6.7%) was RIF resistant with Q432P and I1491S mutations in rpoB. M. bovis from Ghana resolved as mono-phyletic branch among mostly M. bovis from Africa irrespective of the host and were closest to the root of the global M. bovis phylogeny. M. bovis-specific amino acid mutations were detected among MTBC core genes such as mce1A, mmpL1, pks6, phoT, pstB, glgP and Rv2955c. Additional mutations P6T in chaA, G187E in mgtC, T35A in Rv1979c, S387A in narK1, L400F in fas and A563T in eccA1 were restricted to the 5 clinical M. bovis from Ghana. CONCLUSION: Our data indicate potential zoonotic transmission of bTB in Ghana and hence calls for intensified public education on bTB, especially among risk groups. Public Library of Science 2019-03-04 /pmc/articles/PMC6398925/ /pubmed/30830912 http://dx.doi.org/10.1371/journal.pone.0209395 Text en © 2019 Otchere et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Otchere, Isaac Darko
van Tonder, Andries J.
Asante-Poku, Adwoa
Sánchez-Busó, Leonor
Coscollá, Mireia
Osei-Wusu, Stephen
Asare, Prince
Aboagye, Samuel Yaw
Ekuban, Samuel Acquah
Yahayah, Abdallah Iddrisu
Forson, Audrey
Baddoo, Akosua
Laryea, Clement
Parkhill, Julian
Harris, Simon R.
Gagneux, Sebastien
Yeboah-Manu, Dorothy
Molecular epidemiology and whole genome sequencing analysis of clinical Mycobacterium bovis from Ghana
title Molecular epidemiology and whole genome sequencing analysis of clinical Mycobacterium bovis from Ghana
title_full Molecular epidemiology and whole genome sequencing analysis of clinical Mycobacterium bovis from Ghana
title_fullStr Molecular epidemiology and whole genome sequencing analysis of clinical Mycobacterium bovis from Ghana
title_full_unstemmed Molecular epidemiology and whole genome sequencing analysis of clinical Mycobacterium bovis from Ghana
title_short Molecular epidemiology and whole genome sequencing analysis of clinical Mycobacterium bovis from Ghana
title_sort molecular epidemiology and whole genome sequencing analysis of clinical mycobacterium bovis from ghana
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6398925/
https://www.ncbi.nlm.nih.gov/pubmed/30830912
http://dx.doi.org/10.1371/journal.pone.0209395
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