Dorman, MJ, Domman, D, Uddin, MI, Sharmin, S, Hassan Afrad, M, Begum, YA, Qadri, F and Thomson, NR. 2019. Supporting data for 'High quality reference genomes for toxigenic and non-toxigenic Vibrio cholerae serogroup O139'. [Online]. Figshare. Available from: https://doi.org/10.6084/m9.figshare.6480266.v1
Dorman, MJ, Domman, D, Uddin, MI, Sharmin, S, Hassan Afrad, M, Begum, YA, Qadri, F and Thomson, NR. Supporting data for 'High quality reference genomes for toxigenic and non-toxigenic Vibrio cholerae serogroup O139' [Internet]. Figshare; 2019. Available from: https://doi.org/10.6084/m9.figshare.6480266.v1
Dorman, MJ, Domman, D, Uddin, MI, Sharmin, S, Hassan Afrad, M, Begum, YA, Qadri, F and Thomson, NR (2019). Supporting data for 'High quality reference genomes for toxigenic and non-toxigenic Vibrio cholerae serogroup O139'. [Data Collection]. Figshare. https://doi.org/10.6084/m9.figshare.6480266.v1
Description
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.
Keywords
Data capture method | Experiment |
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Date (Date published in a 3rd party system) | 10 April 2019 |
Language(s) of written materials | English |
Data Creators | Dorman, MJ, Domman, D, Uddin, MI, Sharmin, S, Hassan Afrad, M, Begum, YA, Qadri, F and Thomson, NR |
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LSHTM Faculty/Department | Faculty of Infectious and Tropical Diseases > Dept of Pathogen Molecular Biology |
Participating Institutions | London School of Hygiene & Tropical Medicine, London, United Kingdom |
Funders |
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Date Deposited | 24 Jul 2019 11:20 |
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Last Modified | 08 Jul 2021 12:52 |
Publisher | Figshare |