Revisiting the Global Epidemiology of Cholera in Conjunction With the Genomics of Vibrio cholerae

Переосмысление глобальной эпидемиологии холеры в сочетании с геномикой Vibrio cholerae
G. Balakrish Nair, Thandavarayan Ramamurthy, François‐Xavier Weill, Bhabatosh Das, Ankur Mutreja, Amit Ghosh
2019-07-23

CTX phage and ctxAB/ToxRS cholera toxin regulationVibrio cholerae O1 and O139integrative conjugative elements (ICE) and antibiotic resistanceseventh cholera pandemic (7CP)whole-genome sequencing (WGS) and SNP phylogenetics
Toxigenic Vibrio cholerae is responsible for 1.4 to 4.3 million cases with about 21,000-143,000 deaths per year. Dominance of O1 and O139 serogroups, classical and El tor biotypes, alterations in CTX phages and the pathogenicity Islands are some of the major features of V. cholerae isolates that are responsible for cholera epidemics. Whole-genome sequencing (WGS) based analyses of single-nucleotide polymorphisms (SNPs) and other infrequent genetic variants provides a robust phylogenetic framework. Recent studies on the global transmission of pandemic V. cholerae O1 strains have shown the existence of eight different phyletic lineages. In these, the classical and El Tor biotype strains were separated as two distinctly evolved lineages. The frequency of SNP accumulation and the temporal and geographical distribution supports the perception that the seventh cholera pandemic (7CP) has spread from the Bay of Bengal region in three independent but overlapping waves. The 2010 Haitian outbreak shared a common ancestor with South-Asian wave-3 strains. In West Africa and East/Southern Africa, cholera epidemics are caused by single expanded lineage, which has been introduced several times since 1970. The Latin American epidemics that occurred in 1991 and 2010 were the result of introductions of two 7CP sublineages. Sublineages representing wave-3 have caused huge outbreaks in Haiti and Yemen. The Ogawa-Inaba serotype switchover in several cholera epidemics are believed to be due to the involvement of certain selection mechanism(s) rather than due to random events. V. cholerae O139 serogroup is phylogenetically related to the 7CP El Tor, and almost all these isolates belonged to the multilocus sequence type-69. Additional phenotypic and genotypic information have been generated to understand the pathogenicity of classical and El Tor vibrios. Presence of integrative conjugative elements (ICE) with antibiotic resistance gene cassettes, clustered regularly interspaced short palindromic repeats-associated protein system and ctxAB promoter based ToxRS expression of cholera toxin separates classical and El Tor biotypes. With the availability of WGS information, several important applications including, molecular typing, antimicrobial resistance, new diagnostics and vaccination strategies could be generated.
1
Cholera epidemics in West Africa and East/Southern Africa arise from a single expanded lineage repeatedly introduced since 1970, while Latin American epidemics (1991, 2010) resulted from two separate 7CP sublineage introductions.
2
Genomic and phenotypic differences—ICE-borne antibiotic resistance cassettes, CRISPR-associated systems, and ctxAB promoter–linked ToxRS expression—distinguish classical and El Tor biotypes and inform diagnostics, AMR monitoring, and vaccine strategies.
3
Seventh cholera pandemic (7CP) spread from the Bay of Bengal in three independent overlapping waves; wave-3 strains seeded major outbreaks including Haiti (2010) and Yemen.
4
Toxigenic Vibrio cholerae causes an estimated 1.4–4.3 million cases and 21,000–143,000 deaths annually.
5
Whole-genome sequencing (WGS) SNP analyses reveal eight distinct phyletic lineages of pandemic V. cholerae O1, with classical and El Tor as separately evolved lineages.

Toxigenic Vibrio cholerae (global pandemic O1/O139 strains and their lineages)

Global epidemiology and genomic phylogeny including SNP-based lineage structure, serogroup/biotype distinctions, transmission waves, geographic-temporal spread, and genetic determinants of pathogenicity and antimicrobial resistance

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2019-07-23
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G. Balakrish Nair
Thandavarayan Ramamurthy
François‐Xavier Weill
Bhabatosh Das
Ankur Mutreja
Amit Ghosh
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