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A molecular and epidemiological study of Vibrio cholerae isolates from cholera outbreaks in southern Ghana
Cholera remains a major global public health threat and continuous emergence of new Vibrio cholerae strains is of major concern. We conducted a molecular epidemiological study to detect virulence markers and antimicrobial resistance patterns of V. cholerae isolates obtained from the 2012–2015 choler...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351161/ https://www.ncbi.nlm.nih.gov/pubmed/32649692 http://dx.doi.org/10.1371/journal.pone.0236016 |
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author | Danso, Emelia Konadu Asare, Prince Otchere, Isaac Darko Akyeh, Lorenzo Moses Asante-Poku, Adwoa Aboagye, Samuel Yaw Osei-Wusu, Stephen Opare, David Ntoumi, Francine Zumla, Alimuddin Duodu, Samuel Yeboah-Manu, Dorothy |
author_facet | Danso, Emelia Konadu Asare, Prince Otchere, Isaac Darko Akyeh, Lorenzo Moses Asante-Poku, Adwoa Aboagye, Samuel Yaw Osei-Wusu, Stephen Opare, David Ntoumi, Francine Zumla, Alimuddin Duodu, Samuel Yeboah-Manu, Dorothy |
author_sort | Danso, Emelia Konadu |
collection | PubMed |
description | Cholera remains a major global public health threat and continuous emergence of new Vibrio cholerae strains is of major concern. We conducted a molecular epidemiological study to detect virulence markers and antimicrobial resistance patterns of V. cholerae isolates obtained from the 2012–2015 cholera outbreaks in Ghana. Archived clinical isolates obtained from the 2012, 2014 and 2015 cholera outbreaks in Ghana were revived by culture and subjected to microscopy, biochemical identification, serotyping, antibiotic susceptibility testing, molecular detection of distinct virulence factors and Multi-Locus Variable-Number of Tandem-Repeat Analysis (MLVA). Of 277 isolates analysed, 168 (60.6%) were confirmed to be V. cholerae and 109 (39.4%) isolates constituted other bacteria (Escherichia coli, Aeromonas sobria, Pseudomonas aeruginosa, Enterobacter cloacae and Enterococci faecalis). Serotyping the V. cholerae isolates identified 151 (89.9%) as Ogawa, 3 (1.8%) as Inaba and 14 (8.3%) as non-O1/O139 serogroup. The O1 serogroup isolates (154/168, 91.7%) carried the cholera toxin ctxB gene as detected by PCR. Additional virulence genes detected include zot, tcpA, ace, rtxC, toxR, rtxA, tcpP, hlyA and tagA. The most common and rare virulence factors detected among the isolates were rtxC (165 isolates) and tcpP (50 isolates) respectively. All isolates from 2014 and 2015 were multidrug resistant against the selected antibiotics. MLVA differentiated the isolates into 2 large unique clones A and B, with each predominating in a particular year. Spatial analysis showed clustering of most isolates at Ablekuma sub-district. Identification of several virulence genes among the two different genotypes of V. cholerae isolates and resistance to first- and second-line antibiotics, calls for scaleup of preventive strategies to reduce transmission, and strengthening of public health laboratories for rapid antimicrobial susceptibility testing to guide accurate treatment. Our findings support the current WHO licensed cholera vaccines which include both O1 Inaba and Ogawa serotypes. |
format | Online Article Text |
id | pubmed-7351161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-73511612020-07-20 A molecular and epidemiological study of Vibrio cholerae isolates from cholera outbreaks in southern Ghana Danso, Emelia Konadu Asare, Prince Otchere, Isaac Darko Akyeh, Lorenzo Moses Asante-Poku, Adwoa Aboagye, Samuel Yaw Osei-Wusu, Stephen Opare, David Ntoumi, Francine Zumla, Alimuddin Duodu, Samuel Yeboah-Manu, Dorothy PLoS One Research Article Cholera remains a major global public health threat and continuous emergence of new Vibrio cholerae strains is of major concern. We conducted a molecular epidemiological study to detect virulence markers and antimicrobial resistance patterns of V. cholerae isolates obtained from the 2012–2015 cholera outbreaks in Ghana. Archived clinical isolates obtained from the 2012, 2014 and 2015 cholera outbreaks in Ghana were revived by culture and subjected to microscopy, biochemical identification, serotyping, antibiotic susceptibility testing, molecular detection of distinct virulence factors and Multi-Locus Variable-Number of Tandem-Repeat Analysis (MLVA). Of 277 isolates analysed, 168 (60.6%) were confirmed to be V. cholerae and 109 (39.4%) isolates constituted other bacteria (Escherichia coli, Aeromonas sobria, Pseudomonas aeruginosa, Enterobacter cloacae and Enterococci faecalis). Serotyping the V. cholerae isolates identified 151 (89.9%) as Ogawa, 3 (1.8%) as Inaba and 14 (8.3%) as non-O1/O139 serogroup. The O1 serogroup isolates (154/168, 91.7%) carried the cholera toxin ctxB gene as detected by PCR. Additional virulence genes detected include zot, tcpA, ace, rtxC, toxR, rtxA, tcpP, hlyA and tagA. The most common and rare virulence factors detected among the isolates were rtxC (165 isolates) and tcpP (50 isolates) respectively. All isolates from 2014 and 2015 were multidrug resistant against the selected antibiotics. MLVA differentiated the isolates into 2 large unique clones A and B, with each predominating in a particular year. Spatial analysis showed clustering of most isolates at Ablekuma sub-district. Identification of several virulence genes among the two different genotypes of V. cholerae isolates and resistance to first- and second-line antibiotics, calls for scaleup of preventive strategies to reduce transmission, and strengthening of public health laboratories for rapid antimicrobial susceptibility testing to guide accurate treatment. Our findings support the current WHO licensed cholera vaccines which include both O1 Inaba and Ogawa serotypes. Public Library of Science 2020-07-10 /pmc/articles/PMC7351161/ /pubmed/32649692 http://dx.doi.org/10.1371/journal.pone.0236016 Text en © 2020 Danso 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 Danso, Emelia Konadu Asare, Prince Otchere, Isaac Darko Akyeh, Lorenzo Moses Asante-Poku, Adwoa Aboagye, Samuel Yaw Osei-Wusu, Stephen Opare, David Ntoumi, Francine Zumla, Alimuddin Duodu, Samuel Yeboah-Manu, Dorothy A molecular and epidemiological study of Vibrio cholerae isolates from cholera outbreaks in southern Ghana |
title | A molecular and epidemiological study of Vibrio cholerae isolates from cholera outbreaks in southern Ghana |
title_full | A molecular and epidemiological study of Vibrio cholerae isolates from cholera outbreaks in southern Ghana |
title_fullStr | A molecular and epidemiological study of Vibrio cholerae isolates from cholera outbreaks in southern Ghana |
title_full_unstemmed | A molecular and epidemiological study of Vibrio cholerae isolates from cholera outbreaks in southern Ghana |
title_short | A molecular and epidemiological study of Vibrio cholerae isolates from cholera outbreaks in southern Ghana |
title_sort | molecular and epidemiological study of vibrio cholerae isolates from cholera outbreaks in southern ghana |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351161/ https://www.ncbi.nlm.nih.gov/pubmed/32649692 http://dx.doi.org/10.1371/journal.pone.0236016 |
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