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Emergence and Evolutionary Response of Vibrio cholerae to Novel Bacteriophage, Democratic Republic of the Congo
Cholera causes substantial illness and death in Africa. We analyzed 24 toxigenic Vibrio cholerae O1 strains isolated in 2015–2017 from patients in the Great Lakes region of the Democratic Republic of the Congo. Strains originating in southern Asia appeared to be part of the T10 introduction event in...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Centers for Disease Control and Prevention
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9707599/ https://www.ncbi.nlm.nih.gov/pubmed/36417939 http://dx.doi.org/10.3201/eid2812.220572 |
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author | Alam, Meer T. Mavian, Carla Paisie, Taylor K. Tagliamonte, Massimiliano S. Cash, Melanie N. Angermeyer, Angus Seed, Kimberley D. Camilli, Andrew Maisha, Felicien Masanga Senga, R. Kabangwa Kakongo Salemi, Marco Morris, J. Glenn Ali, Afsar |
author_facet | Alam, Meer T. Mavian, Carla Paisie, Taylor K. Tagliamonte, Massimiliano S. Cash, Melanie N. Angermeyer, Angus Seed, Kimberley D. Camilli, Andrew Maisha, Felicien Masanga Senga, R. Kabangwa Kakongo Salemi, Marco Morris, J. Glenn Ali, Afsar |
author_sort | Alam, Meer T. |
collection | PubMed |
description | Cholera causes substantial illness and death in Africa. We analyzed 24 toxigenic Vibrio cholerae O1 strains isolated in 2015–2017 from patients in the Great Lakes region of the Democratic Republic of the Congo. Strains originating in southern Asia appeared to be part of the T10 introduction event in eastern Africa. We identified 2 main strain lineages, most recently a lineage corresponding to sequence type 515, a V. cholerae cluster previously reported in the Lake Kivu region. In 41% of fecal samples from cholera patients, we also identified a novel ICP1 (Bangladesh cholera phage 1) bacteriophage, genetically distinct from ICP1 isolates previously detected in Asia. Bacteriophage resistance occurred in distinct clades along both internal and external branches of the cholera phylogeny. This bacteriophage appears to have served as a major driver for cholera evolution and spread, and its appearance highlights the complex evolutionary dynamic that occurs between predatory phage and bacterial host. |
format | Online Article Text |
id | pubmed-9707599 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Centers for Disease Control and Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-97075992022-12-09 Emergence and Evolutionary Response of Vibrio cholerae to Novel Bacteriophage, Democratic Republic of the Congo Alam, Meer T. Mavian, Carla Paisie, Taylor K. Tagliamonte, Massimiliano S. Cash, Melanie N. Angermeyer, Angus Seed, Kimberley D. Camilli, Andrew Maisha, Felicien Masanga Senga, R. Kabangwa Kakongo Salemi, Marco Morris, J. Glenn Ali, Afsar Emerg Infect Dis Research Cholera causes substantial illness and death in Africa. We analyzed 24 toxigenic Vibrio cholerae O1 strains isolated in 2015–2017 from patients in the Great Lakes region of the Democratic Republic of the Congo. Strains originating in southern Asia appeared to be part of the T10 introduction event in eastern Africa. We identified 2 main strain lineages, most recently a lineage corresponding to sequence type 515, a V. cholerae cluster previously reported in the Lake Kivu region. In 41% of fecal samples from cholera patients, we also identified a novel ICP1 (Bangladesh cholera phage 1) bacteriophage, genetically distinct from ICP1 isolates previously detected in Asia. Bacteriophage resistance occurred in distinct clades along both internal and external branches of the cholera phylogeny. This bacteriophage appears to have served as a major driver for cholera evolution and spread, and its appearance highlights the complex evolutionary dynamic that occurs between predatory phage and bacterial host. Centers for Disease Control and Prevention 2022-12 /pmc/articles/PMC9707599/ /pubmed/36417939 http://dx.doi.org/10.3201/eid2812.220572 Text en https://creativecommons.org/licenses/by/4.0/Emerging Infectious Diseases is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited. |
spellingShingle | Research Alam, Meer T. Mavian, Carla Paisie, Taylor K. Tagliamonte, Massimiliano S. Cash, Melanie N. Angermeyer, Angus Seed, Kimberley D. Camilli, Andrew Maisha, Felicien Masanga Senga, R. Kabangwa Kakongo Salemi, Marco Morris, J. Glenn Ali, Afsar Emergence and Evolutionary Response of Vibrio cholerae to Novel Bacteriophage, Democratic Republic of the Congo |
title | Emergence and Evolutionary Response of Vibrio cholerae to Novel Bacteriophage, Democratic Republic of the Congo |
title_full | Emergence and Evolutionary Response of Vibrio cholerae to Novel Bacteriophage, Democratic Republic of the Congo |
title_fullStr | Emergence and Evolutionary Response of Vibrio cholerae to Novel Bacteriophage, Democratic Republic of the Congo |
title_full_unstemmed | Emergence and Evolutionary Response of Vibrio cholerae to Novel Bacteriophage, Democratic Republic of the Congo |
title_short | Emergence and Evolutionary Response of Vibrio cholerae to Novel Bacteriophage, Democratic Republic of the Congo |
title_sort | emergence and evolutionary response of vibrio cholerae to novel bacteriophage, democratic republic of the congo |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9707599/ https://www.ncbi.nlm.nih.gov/pubmed/36417939 http://dx.doi.org/10.3201/eid2812.220572 |
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