{"title":"Genomic portrayal of emerging carbapenem-resistant El Tor variant <i>Vibrio cholerae</i> O1.","authors":"Sreeja Shaw, Agila Kumari Pragasam, Goutam Chowdhury, Prosenjit Samanta, Deboleena Roy, Debjani Ghosh, Thandavarayan Ramamurthy, Jigna Karia, Govind Ninama, Shin-Ichi Miyoshi, Yukihiro Akeda, Hemanta Koley, Asish Kumar Mukhopadhyay","doi":"10.1128/aac.00740-25","DOIUrl":null,"url":null,"abstract":"<p><p>The escalating prevalence of carbapenem-resistant (CR) enteric pathogens elicits significant challenges to public health management and effective antimicrobial therapy. While carbapenem resistance is rare in <i>Vibrio cholerae</i> O1 (VC), the recent emergence of CR strains reveals a concerning shift in their antimicrobial resistance (AMR) landscape. This study aims to characterize the resistance mechanisms in newly identified El Tor CRVC isolated from cholera patients in Gujarat, India during 2019. Fifty VC isolates were screened for major virulence-associated genes along with the determination of their antibiotic resistance profiles using Kirby-Bauer disk diffusion and MIC assays. Whole-genome sequencing (WGS) was employed to investigate the underlying mechanisms of CR. All the isolates exhibited hypervirulent Haitian alleles of major virulence genes and AMR profiles of typical multidrug resistance (MDR). Strikingly, 12% (6/50) of them were resistant to carbapenems and other antibiotics. Molecular analysis revealed that these CR isolates were clonally related and harbored a 142 kbp IncA/C type conjugative mega-plasmid with several AMR encoding genes, including <i>bla</i><sub>NDM-1</sub>, that can be easily transferred to other bacterial species and confer donor AMR patterns. The plasmid's competence for horizontal gene transfer presents a significant risk of dissemination to other enteric pathogens and thereby may complicate the treatment. This finding emphasizes the urgent need for enhanced genomic surveillance and robust antimicrobial stewardship programs aimed at curbing the spread of CRVC strains and mitigating their impact on cholera treatment and containment strategies.</p>","PeriodicalId":8152,"journal":{"name":"Antimicrobial Agents and Chemotherapy","volume":" ","pages":"e0074025"},"PeriodicalIF":4.5000,"publicationDate":"2025-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Antimicrobial Agents and Chemotherapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1128/aac.00740-25","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The escalating prevalence of carbapenem-resistant (CR) enteric pathogens elicits significant challenges to public health management and effective antimicrobial therapy. While carbapenem resistance is rare in Vibrio cholerae O1 (VC), the recent emergence of CR strains reveals a concerning shift in their antimicrobial resistance (AMR) landscape. This study aims to characterize the resistance mechanisms in newly identified El Tor CRVC isolated from cholera patients in Gujarat, India during 2019. Fifty VC isolates were screened for major virulence-associated genes along with the determination of their antibiotic resistance profiles using Kirby-Bauer disk diffusion and MIC assays. Whole-genome sequencing (WGS) was employed to investigate the underlying mechanisms of CR. All the isolates exhibited hypervirulent Haitian alleles of major virulence genes and AMR profiles of typical multidrug resistance (MDR). Strikingly, 12% (6/50) of them were resistant to carbapenems and other antibiotics. Molecular analysis revealed that these CR isolates were clonally related and harbored a 142 kbp IncA/C type conjugative mega-plasmid with several AMR encoding genes, including blaNDM-1, that can be easily transferred to other bacterial species and confer donor AMR patterns. The plasmid's competence for horizontal gene transfer presents a significant risk of dissemination to other enteric pathogens and thereby may complicate the treatment. This finding emphasizes the urgent need for enhanced genomic surveillance and robust antimicrobial stewardship programs aimed at curbing the spread of CRVC strains and mitigating their impact on cholera treatment and containment strategies.
碳青霉烯耐药(CR)肠道病原体的流行率不断上升,给公共卫生管理和有效的抗菌治疗带来了重大挑战。虽然碳青霉烯耐药性在霍乱弧菌O1 (VC)中很少见,但最近出现的CR菌株揭示了其抗菌素耐药性(AMR)格局的一个令人担忧的转变。本研究旨在描述2019年从印度古吉拉特邦霍乱患者中分离到的新发现的El Tor CRVC的耐药机制。对50株VC分离株进行了主要毒力相关基因筛选,并采用Kirby-Bauer圆盘扩散法和MIC法测定了它们的抗生素耐药谱。采用全基因组测序(WGS)研究其发病机制,发现所有分离株均具有主要毒力基因的高毒力海地等位基因和典型多药耐药(MDR)的AMR谱。引人注目的是,其中12%(6/50)的人对碳青霉烯类和其他抗生素耐药。分子分析表明,这些CR分离株具有克隆相关性,具有142 kbp的IncA/C型偶联质粒,其中包含几个AMR编码基因,包括blaNDM-1,可以很容易地转移到其他细菌物种并赋予供体AMR模式。质粒的水平基因转移能力有可能传播给其他肠道病原体,从而使治疗复杂化。这一发现强调,迫切需要加强基因组监测和强有力的抗微生物管理规划,以遏制CRVC菌株的传播,减轻其对霍乱治疗和控制战略的影响。
期刊介绍:
Antimicrobial Agents and Chemotherapy (AAC) features interdisciplinary studies that build our understanding of the underlying mechanisms and therapeutic applications of antimicrobial and antiparasitic agents and chemotherapy.