TY - JOUR
T1 - Wave succession in the pandemic clone of Vibrio parahaemolyticus driven by gene loss
AU - Yang, Chao
AU - Qiu, Hongling
AU - Svensson, Sarah L.
AU - Ni, Chengpei
AU - Gao, Song
AU - Jia, Zhizhou
AU - Wen, Huiqi
AU - Xie, Li
AU - Xu, Wenxuan
AU - Qin, Yujiao
AU - Lin, Shuzhu
AU - Wang, Jiancheng
AU - Zhang, Yiquan
AU - Li, Yinghui
AU - Jiang, Min
AU - Shi, Xiaolu
AU - Hu, Qinghua
AU - Zhou, Zhemin
AU - Chao, Yanjie
AU - Yang, Ruifu
AU - Cui, Yujun
AU - Martinez-Urtaza, Jaime
AU - Wang, Hui
AU - Falush, Daniel
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature Limited 2025.
PY - 2025/8/27
Y1 - 2025/8/27
N2 - While spontaneous mutation and gene acquisition are well-established drivers of pathogen adaptation, the role of gene loss remains underexplored. Here we investigated the emergence and diversification of the pandemic clone of Vibrio parahaemolyticus through large-scale phylogenomic analysis of 8,684 global isolates. The pandemic clone rapidly acquired multiple marker genes and genomic islands, subsequently diverging into successive sublineages mediating independent waves of cross-country transmission, as also observed in Vibrio cholerae. Wave succession in the last two decades was driven by loss of putrescine utilization (Puu) genes, conferring phenotypic advantages for environmental adaptation (enhanced biofilm formation) and human transmission (increased cell adhesion and intestinal colonization and reduced virulence), consistent with the virulence trade-off hypothesis. We identified Puu-gene loss in several bacterial genera, with effects on biofilm and adhesion replicated in V. cholerae and Escherichia coli, suggesting convergent evolution and universal phenotypic effects. Our results highlight the indispensable role of gene loss in bacterial pathogen adaptation.
AB - While spontaneous mutation and gene acquisition are well-established drivers of pathogen adaptation, the role of gene loss remains underexplored. Here we investigated the emergence and diversification of the pandemic clone of Vibrio parahaemolyticus through large-scale phylogenomic analysis of 8,684 global isolates. The pandemic clone rapidly acquired multiple marker genes and genomic islands, subsequently diverging into successive sublineages mediating independent waves of cross-country transmission, as also observed in Vibrio cholerae. Wave succession in the last two decades was driven by loss of putrescine utilization (Puu) genes, conferring phenotypic advantages for environmental adaptation (enhanced biofilm formation) and human transmission (increased cell adhesion and intestinal colonization and reduced virulence), consistent with the virulence trade-off hypothesis. We identified Puu-gene loss in several bacterial genera, with effects on biofilm and adhesion replicated in V. cholerae and Escherichia coli, suggesting convergent evolution and universal phenotypic effects. Our results highlight the indispensable role of gene loss in bacterial pathogen adaptation.
KW - Escherichia-coli
KW - Antivirulence genes
KW - Black-holes
KW - Bacterial
KW - Pathogen
KW - Evolution
KW - Virulence
KW - Cholera
KW - O3-k6
KW - Inactivation
UR - https://www.scopus.com/pages/publications/105014284472
UR - https://portalrecerca.uab.cat/en/publications/c958830d-57b1-4b61-9c71-1633737a1063
U2 - 10.1038/s41559-025-02827-z
DO - 10.1038/s41559-025-02827-z
M3 - Article
C2 - 40866534
AN - SCOPUS:105014284472
SN - 2397-334X
JO - Nature Ecology and Evolution
JF - Nature Ecology and Evolution
ER -