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Global Landscape of Clostridioides Difficile Phylogeography, Antibiotic Susceptibility, and Toxin Polymorphisms by Post-Hoc Whole-Genome Sequencing from the MODIFY I/II Studies

Authors :
Rebecca L. Blanchard
Ziqing Deng
Zhen Zeng
Shida Zhu
Judong Shen
Lan Chen
Ye Peng
Peter M. Shaw
Junhua Li
Jie Meng
Pierra Y T Law
Mary Beth Dorr
Xun Xu
Huanzi Zhong
David C. Nickle
Mark H. Wilcox
Hailong Zhao
Andrew Albright
Source :
Zhao, H, Nickle, D C, Zeng, Z, Law, P Y T, Wilcox, M H, Chen, L, Peng, Y, Meng, J, Deng, Z, Albright, A, Zhong, H, Xu, X, Zhu, S, Shen, J, Blanchard, R L, Dorr, M B, Shaw, P M & Li, J 2021, ' Global Landscape of Clostridioides Difficile Phylogeography, Antibiotic Susceptibility, and Toxin Polymorphisms by Post-Hoc Whole-Genome Sequencing from the MODIFY I/II Studies ', Infectious Diseases and Therapy, vol. 10, no. 2, pp. 853-870 . https://doi.org/10.1007/s40121-021-00426-6
Publication Year :
2021
Publisher :
Springer Science and Business Media LLC, 2021.

Abstract

Introduction Clostridioides (Clostridium) difficile infection, the leading cause of healthcare-associated diarrhea, represents a significant burden on global healthcare systems. Despite being a global issue, information on C. difficile from a global perspective is lacking. The aim of this study is to model the global phylogeography of clinical C. difficile. Methods Using samples collected from the MODIFY I and II studies (NCT01241552, NCT01513239), we performed whole-genome sequencing of 1501 clinical isolates including 37 novel sequence types (STs), representing the largest worldwide collection to date. Results Our data showed ribotypes, multi-locus sequence typing clades, and whole-genome phylogeny were in good accordance. The clinical C. difficile genome was found to be more conserved than previously reported (61% core genes), and modest recombination rates of 1.4-5.0 were observed across clades. We observed a significant continent distribution preference among five C. difficile clades (Benjamini-Hochberg corrected Fisher's exact test P

Details

ISSN :
21936382 and 21938229
Volume :
10
Database :
OpenAIRE
Journal :
Infectious Diseases and Therapy
Accession number :
edsair.doi.dedup.....9448e85a97714e7c1d1a65f93810ee27
Full Text :
https://doi.org/10.1007/s40121-021-00426-6