Abstract

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.

Highlights

  • Vibrio cholerae is the aetiological agent of cholera, an acute, life-threatening diarrhoea which has spread worldwide in seven pandemics since the nineteenth century

  • Genetic and biochemical studies demonstrated that O139 strains were closely related to O1 seventh pandemic El Tor strains, and it was suggested that V. cholerae O139 had arisen from an O1 El Tor ancestor[9,22,23,24]

  • The capsule is encoded by genes not found in other 7PET V. cholerae O1 genomes, which are located adjacent to the locus encoding lipopolysaccharide (LPS) biosynthesis genes in V. cholerae O13915,28–32

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Summary

Introduction

Vibrio cholerae is the aetiological agent of cholera, an acute, life-threatening diarrhoea which has spread worldwide in seven pandemics since the nineteenth century. Genetic and biochemical studies demonstrated that O139 strains were closely related to O1 seventh pandemic El Tor strains, and it was suggested that V. cholerae O139 had arisen from an O1 El Tor ancestor[9,22,23,24]. This was subsequently confirmed using whole-genome sequencing, which showed that toxigenic V. cholerae O139 formed a discrete sub-lineage within the seventh pandemic El Tor (7PET) lineage[25,26]. The MO10 genome sequence is currently used to represent V. cholerae O139 in comparative genomic analyses, but its genome sequence is incomplete and comprises 84 contigs (assembly accession number GCA_000152425.1)

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