High quality reference genomes for toxigenic and non-toxigenic Vibrio cholerae serogroup O139.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
10 04 2019
Historique:
received: 05 09 2018
accepted: 13 03 2019
entrez: 12 4 2019
pubmed: 12 4 2019
medline: 7 10 2020
Statut: epublish

Résumé

Toxigenic Vibrio cholerae of the O139 serogroup have been responsible for several large cholera epidemics in South Asia, and continue to be of clinical and historical significance today. This serogroup was initially feared to represent a new, emerging V. cholerae clone that would lead to an eighth cholera pandemic. However, these concerns were ultimately unfounded. The majority of clinically relevant V. cholerae O139 isolates are closely related to serogroup O1, biotype El Tor V. cholerae, and comprise a single sublineage of the seventh pandemic El Tor lineage. Although related, these V. cholerae serogroups differ in several fundamental ways, in terms of their O-antigen, capsulation phenotype, and the genomic islands found on their chromosomes. Here, we present four complete, high-quality genomes for V. cholerae O139, obtained using long-read sequencing. Three of these sequences are from toxigenic V. cholerae, and one is from a bacterium which, although classified serologically as V. cholerae O139, lacks the CTXφ bacteriophage and the ability to produce cholera toxin. We highlight fundamental genomic differences between these isolates, the V. cholerae O1 reference strain N16961, and the prototypical O139 strain MO10. These sequences are an important resource for the scientific community, and will improve greatly our ability to perform genomic analyses of non-O1 V. cholerae in the future. These genomes also offer new insights into the biology of a V. cholerae serogroup that, from a genomic perspective, is poorly understood.

Identifiants

pubmed: 30971707
doi: 10.1038/s41598-019-41883-x
pii: 10.1038/s41598-019-41883-x
pmc: PMC6458141
doi:

Substances chimiques

O Antigens 0
Cholera Toxin 9012-63-9

Banques de données

figshare
['10.6084/m9.figshare.6480266']

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5865

Subventions

Organisme : Wellcome Trust
ID : 098051
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 206194
Pays : United Kingdom

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Auteurs

Matthew J Dorman (MJ)

Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, United Kingdom.

Daryl Domman (D)

Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, United Kingdom.

Muhammad Ikhtear Uddin (MI)

Infectious Diseases Division, International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh.

Salma Sharmin (S)

Infectious Diseases Division, International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh.

Mokibul Hassan Afrad (MH)

Infectious Diseases Division, International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh.

Yasmin Ara Begum (YA)

Infectious Diseases Division, International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh.

Firdausi Qadri (F)

Infectious Diseases Division, International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh. fqadri@icddrb.org.

Nicholas R Thomson (NR)

Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, United Kingdom. nrt@sanger.ac.uk.
London School of Hygiene and Tropical Medicine, Keppel Street, London, WC1E 7HT, United Kingdom. nrt@sanger.ac.uk.

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Classifications MeSH