Background <p>Carbapenem-resistant <i>Salmonella</i> Typhimurium (<i>S.</i> Typhimurium) is occasionally reported, primarily driven by the dissemination of the <i>bla</i><sub>NDM</sub> gene. Although this poses an emerging threat, its phylogenetic structure and epidemiological patterns remain insufficiently studied.</p> Methods <p>We characterized a clinical carbapenem-resistant <i>S.</i> Typhimurium isolate harboring <i>bla</i><sub>NDM−5</sub> from a tertiary hospital in China using antimicrobial susceptibility testing, plasmid conjugation, and stability assays. Whole-genome sequencing was integrated with data from GenBank to perform a series of bioinformatic analyses.</p> Results <p>The <i>bla</i><sub>NDM−5</sub> gene was located on a conjugative IncFII-type plasmid that demonstrated long-term stability in the recipient strain. Screening of GenBank identified four structurally related <i>bla</i><sub>NDM−5</sub>-carrying plasmids, all from bacterial hosts isolated in eastern Chinese cities. Comparative analysis revealed that <i>bla</i><sub>NDM−5</sub> was embedded within an identical truncated Tn<i>125</i> (ΔTn<i>125</i>) unit across all plasmids, suggesting a common genetic vehicle for its dissemination. Further structural analysis indicated the presence of IS<i>CR1</i> adjacent to ΔTn<i>125</i>, with the entire resistance region bounded by IS<i>26</i> elements, implying that IS<i>CR1</i> may facilitate the capture and mobilization of <i>bla</i><sub>NDM−5</sub>, while IS<i>26</i> could mediate co-transfer of multiple resistance modules. In addition, we systematically analyzed all available <i>bla</i><sub>NDM</sub>-positive <i>S.</i> Typhimurium genomes from GenBank (<i>n</i> = 28). Notably, all strains originated from China, and ST34 was the dominant clone (24/28, 85.7%) among <i>bla</i><sub>NDM</sub>-positive <i>S.</i> Typhimurium. Phylogenetic analysis classified the strains into three major clusters (I–III), showing strong concordance with Multi-Locus Sequence Types (MLST). Plasmid replicon screening identified IncHI2 and IncFII as the most prevalent plasmid types. Resistance gene profiling further confirmed <i>bla</i><sub>NDM−5</sub> as the predominant carbapenemase subtype, followed by <i>bla</i><sub>NDM−1</sub>.</p> Conclusion <p>This study identifies a conjugative and stable IncFII-type plasmid as an important vector for <i>bla</i><sub>NDM−5</sub> transmission in <i>S.</i> Typhimurium. The plasmid carries the carbapenemase gene within a conserved ΔTn<i>125</i> unit, and this plasmid type may have formed a regional epidemic in eastern China. IS<i>CR1</i> likely plays a key role in capturing ΔTn<i>125</i> and initiating <i>bla</i><sub>NDM−5</sub> transfer, while IS<i>26</i> facilitates co-mobilization of multidrug resistance modules. Epidemiological analysis further indicates that China is the primary region affected by <i>bla</i><sub>NDM</sub>-positive <i>S.</i> Typhimurium, with the ST34 clone and IncHI2/IncFII plasmids acting as potential major drivers of its dissemination. These findings provide a critical foundation for clinical and public health efforts to control the spread of carbapenem-resistant <i>S.</i> Typhimurium.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Tracing the evolutionary genomics of blaNDM-harboring Salmonella typhimurium in China

  • Jianbo Ye,
  • Yali Zheng,
  • Dakang Hu,
  • Huimin Chen,
  • Yuting Jin,
  • Qiran Ma,
  • Jiayu He,
  • Xinhua Luo

摘要

Background

Carbapenem-resistant Salmonella Typhimurium (S. Typhimurium) is occasionally reported, primarily driven by the dissemination of the blaNDM gene. Although this poses an emerging threat, its phylogenetic structure and epidemiological patterns remain insufficiently studied.

Methods

We characterized a clinical carbapenem-resistant S. Typhimurium isolate harboring blaNDM−5 from a tertiary hospital in China using antimicrobial susceptibility testing, plasmid conjugation, and stability assays. Whole-genome sequencing was integrated with data from GenBank to perform a series of bioinformatic analyses.

Results

The blaNDM−5 gene was located on a conjugative IncFII-type plasmid that demonstrated long-term stability in the recipient strain. Screening of GenBank identified four structurally related blaNDM−5-carrying plasmids, all from bacterial hosts isolated in eastern Chinese cities. Comparative analysis revealed that blaNDM−5 was embedded within an identical truncated Tn125 (ΔTn125) unit across all plasmids, suggesting a common genetic vehicle for its dissemination. Further structural analysis indicated the presence of ISCR1 adjacent to ΔTn125, with the entire resistance region bounded by IS26 elements, implying that ISCR1 may facilitate the capture and mobilization of blaNDM−5, while IS26 could mediate co-transfer of multiple resistance modules. In addition, we systematically analyzed all available blaNDM-positive S. Typhimurium genomes from GenBank (n = 28). Notably, all strains originated from China, and ST34 was the dominant clone (24/28, 85.7%) among blaNDM-positive S. Typhimurium. Phylogenetic analysis classified the strains into three major clusters (I–III), showing strong concordance with Multi-Locus Sequence Types (MLST). Plasmid replicon screening identified IncHI2 and IncFII as the most prevalent plasmid types. Resistance gene profiling further confirmed blaNDM−5 as the predominant carbapenemase subtype, followed by blaNDM−1.

Conclusion

This study identifies a conjugative and stable IncFII-type plasmid as an important vector for blaNDM−5 transmission in S. Typhimurium. The plasmid carries the carbapenemase gene within a conserved ΔTn125 unit, and this plasmid type may have formed a regional epidemic in eastern China. ISCR1 likely plays a key role in capturing ΔTn125 and initiating blaNDM−5 transfer, while IS26 facilitates co-mobilization of multidrug resistance modules. Epidemiological analysis further indicates that China is the primary region affected by blaNDM-positive S. Typhimurium, with the ST34 clone and IncHI2/IncFII plasmids acting as potential major drivers of its dissemination. These findings provide a critical foundation for clinical and public health efforts to control the spread of carbapenem-resistant S. Typhimurium.