Xiao Liu , Zhen Liu , Xuemei Bai , He Gao , Zhiwen Sun , Duochun Wang
{"title":"First report of a carbapenem-resistant Serratia sarumanii clinical strain co-harboring blaKPC-2 and blaNDM-1 genes in China","authors":"Xiao Liu , Zhen Liu , Xuemei Bai , He Gao , Zhiwen Sun , Duochun Wang","doi":"10.1016/j.crmicr.2025.100411","DOIUrl":null,"url":null,"abstract":"<div><div>Carbapenem-resistant <em>Enterobacteriaceae</em> (CRE), particularly those co-harboring multiple carbapenemase genes, pose a significant global health threat. However, the coexistence of <em>bla</em><sub>KPC-2</sub> and <em>bla</em><sub>NDM-1</sub> in <em>Serratia sarumanii</em> has not been previously reported. This study aims to report and characterize the first carbapenem-resistant <em>S. sarumanii</em> (CRSS) clinical strain MAS3954 in China co-harboring <em>bla</em><sub>KPC-2</sub> and <em>bla</em><sub>NDM-1</sub>, focusing on its genetic characteristics, plasmid stability, and transfer potential. Whole-genome analysis revealed that the <em>bla</em><sub>KPC-2</sub> and <em>bla</em><sub>NDM-1</sub> were located on two distinct plasmids. Plasmid pMAS3954-KPC (113,856 bp, IncFII/IncFIB) exhibited low similarity (<66%) to known plasmids, indicating a novel fusion event between pKPC-h2 and <em>S. marcescens</em> chromosome, while pMAS3954-NDM (55,235 bp, IncX3) was highly conserved (100% identity/coverage). Conjugation experiments showed that the <em>bla</em><sub>NDM-1</sub> was transferable, while <em>bla</em><sub>KPC-2</sub> was not. During 10 days of continuous passage, the genetic context of <em>bla</em><sub>NDM-1</sub> was gradually excised from the plasmids after the 8th day, whereas they maintained 100% retention for <em>bla</em><sub>KPC-2</sub>. <em>S. sarumanii</em> MAS3954 was multidrug-resistant (MDR), including carbapenems, β-lactams, β-lactam/β-lactamase inhibitors, trimethoprim-sulfamethoxazole, tetracycline, nitrofurantoin, colistin, and fluoroquinolones, but remained susceptible to certain aminoglycosides and tigecycline. Phylogenomic analysis identified a distinct clade for <em>S. sarumanii</em> MAS3954, diverging notably from other strains. Comparison of resistance genes further highlighted the unique co-harboring of <em>bla</em><sub>KPC-2</sub> and <em>bla</em><sub>NDM-1</sub> in MAS3954, absent in other strains. To our knowledge, this study represents the first characterization of clinical <em>S. sarumanii</em> strain co-harboring <em>bla</em><sub>KPC-2</sub> and <em>bla</em><sub>NDM-1</sub>. The findings highlight the need for enhanced surveillance and infection control to prevent the spread of these MDR strains in healthcare settings.</div></div>","PeriodicalId":34305,"journal":{"name":"Current Research in Microbial Sciences","volume":"9 ","pages":"Article 100411"},"PeriodicalIF":5.8000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Research in Microbial Sciences","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666517425000732","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Carbapenem-resistant Enterobacteriaceae (CRE), particularly those co-harboring multiple carbapenemase genes, pose a significant global health threat. However, the coexistence of blaKPC-2 and blaNDM-1 in Serratia sarumanii has not been previously reported. This study aims to report and characterize the first carbapenem-resistant S. sarumanii (CRSS) clinical strain MAS3954 in China co-harboring blaKPC-2 and blaNDM-1, focusing on its genetic characteristics, plasmid stability, and transfer potential. Whole-genome analysis revealed that the blaKPC-2 and blaNDM-1 were located on two distinct plasmids. Plasmid pMAS3954-KPC (113,856 bp, IncFII/IncFIB) exhibited low similarity (<66%) to known plasmids, indicating a novel fusion event between pKPC-h2 and S. marcescens chromosome, while pMAS3954-NDM (55,235 bp, IncX3) was highly conserved (100% identity/coverage). Conjugation experiments showed that the blaNDM-1 was transferable, while blaKPC-2 was not. During 10 days of continuous passage, the genetic context of blaNDM-1 was gradually excised from the plasmids after the 8th day, whereas they maintained 100% retention for blaKPC-2. S. sarumanii MAS3954 was multidrug-resistant (MDR), including carbapenems, β-lactams, β-lactam/β-lactamase inhibitors, trimethoprim-sulfamethoxazole, tetracycline, nitrofurantoin, colistin, and fluoroquinolones, but remained susceptible to certain aminoglycosides and tigecycline. Phylogenomic analysis identified a distinct clade for S. sarumanii MAS3954, diverging notably from other strains. Comparison of resistance genes further highlighted the unique co-harboring of blaKPC-2 and blaNDM-1 in MAS3954, absent in other strains. To our knowledge, this study represents the first characterization of clinical S. sarumanii strain co-harboring blaKPC-2 and blaNDM-1. The findings highlight the need for enhanced surveillance and infection control to prevent the spread of these MDR strains in healthcare settings.