Unveiling the Global Threat: Genomic Insights into Carbapenem-Resistant Salmonella enterica subsp . enterica in Human

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Authors: Shixing Liu, X D Zhang, Jintao Xia, Chao Fang, Yining Zhao, Mingming Zhou
Cited by: 1
References: 37

Abstract

The misuse of broad-spectrum antibiotics has facilitated the emergence of carbapenem-resistant Salmonella enterica subsp. enterica (CRSE). This study aims to investigate the genomic characteristics and epidemiological patterns of two strains isolated from pediatric patients, along with 21 CRSE strains collected from humans worldwide. The antimicrobial susceptibility tests were detected by the agar microdilution method. Whole-genome sequence of the two CRSE strains was sequenced using the Illumina platform. Acquisition and analysis of WGS data were performed by the NCBI Pathogen Detection Portal, BacWGSTdb 2.0, Salmonella In Silico Typing Resource, and the Center for Genomic Epidemiology. Two S. Typhimurium isolates from children carried the carbapenemase gene bla NDM-5 and belonged to ST34. The CRSE isolates predominantly contained the carbapenem resistance gene bla OXA-48 in the United Kingdom and bla NDM in China. The virulence gene profiles of these isolates were consistent across different regions. Carbapenem-resistant S. Typhimurium and S. Kentucky were predominantly found in China and the United Kingdom, respectively. ST198 strains were prevalent in the United Kingdom, whereas all ST34 strains were identified in China. This investigation underscores the global dissemination of carbapenem-resistant Salmonella in humans, revealing variations in drug resistance, serotypes, and sequence types across different regions. Therefore, the global detection of carbapenem resistance has important guiding significance for controlling its transmission, preventing infection, and clinical treatment.

Fields of Study & Subjects

Salmonella and Campylobacter epidemiology Antibiotic Resistance in Bacteria Cancer Research and Treatments

Publication details

Journal / source
Microbial Drug Resistance
Publisher
SAGE Publications
Volume
32
Issue
6
Pages
209–214
Publication date
5 March 2026
Language
EN