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Meta-analyses of the global multilocus genotypes of the human pathogen Campylobacter jejuni .

Authors :
Poorrashidi M
Hitchcock M
Xu J
Source :
Genome [Genome] 2024 Jun 01; Vol. 67 (6), pp. 189-203. Date of Electronic Publication: 2024 Mar 01.
Publication Year :
2024

Abstract

Campylobacter infections are a leading cause of bacterial diarrheal illness worldwide, with increasing reports of outbreaks in both developing and developed countries. Most studies investigating strain genotypes and epidemiology of Campylobacter jejuni examined on a local scale. Using the archived multilocus sequence typing data at seven loci, and associated strain metadata from the PubMLST database, here we investigated the spatial and temporal genetic structure of the global population of C. jejuni . Our analyses revealed evidence for clonal dispersals of multiple sequence types (STs) among countries and continents. However, despite the observed clonal dispersal and that most genetic variations were found within individual geographic subpopulations, both the non-clone-corrected and clone-corrected samples showed evidence of significant genetic differentiation among national and continental subpopulations, with non-clone-corrected samples showing greater differentiation than clone-corrected samples. Phylogenetic incompatibility analyses provided evidence for recombination within each continental subpopulation. However, linkage disequilibrium analyses rejected the hypothesis of random recombination across the samples. Temporally, multiple STs were found to persist across four decades and the five globally most common STs showed relatively stable frequencies over the last two decades. We discussed the implications of our results to food security, disease transmission, and public health management.<br />Competing Interests: The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

Details

Language :
English
ISSN :
1480-3321
Volume :
67
Issue :
6
Database :
MEDLINE
Journal :
Genome
Publication Type :
Academic Journal
Accession number :
38427983
Full Text :
https://doi.org/10.1139/gen-2023-0041