韩国多药耐药肠炎沙门氏菌和Virchow沙门氏菌携带质粒blaCTX-M-15的血清间转移和进化的基因组证据

IF 2.6 4区 医学 Q3 INFECTIOUS DISEASES
Tae-Min La, Sang-Won Lee, Ji-Yeon Hyeon
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引用次数: 0

摘要

携带blaCTX-M-15的多重耐药肠炎沙门氏菌(MDR)血清型肠炎(SE)在韩国出现;然而,质粒的遗传特性和进化动力学仍未得到充分研究。本研究旨在研究韩国人源和动物源SE菌株携带blactx - m -15质粒的结构、多样性和进化。采用不相容群分型和基因组比对工具对韩国产SE blactx - m -15阳性菌株的质粒结构进行分析。利用全基因组SNP分析和BEAST系统动力学分析确定了菌株的遗传关系和与最近共同祖先(tMRCA)的时间。根据耐药基因谱和不相容类群将质粒分为3种类型(I-III型)。比较基因组分析显示,这些质粒是协整的,是由SE毒力质粒(pSENV)和pIntAMR融合而成的。pIntAMR区域被鉴定为通过is26介导的转位获得的沙门氏菌(SV)的染色体整合形式。该区域含有多个耐药基因和共轭转移元件。携带blactx - m -15的SE菌株的tMRCA估计为2007年6月,III型质粒在2015年左右出现,表明在选择压力的驱动下发生了进化转变。本研究表明,SV和SE之间通过IS26转位介导的血清间质粒转移,促进了SV的质粒进化和MDR。了解这些机制对于制定减轻耐多药沙门氏菌传播的战略至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genomic evidence for interserovar transfer and evolution of blaCTX-M-15 carrying plasmid in multidrug-resistant Salmonella Enteritidis and Salmonella Virchow isolated in South Korea
Multidrug-resistant (MDR) Salmonella enterica serotype Enteritidis (SE) carrying blaCTX-M-15 has emerged in South Korea; however, the genetic characteristics and evolutionary dynamics of the plasmids remain understudied. This study aimed to characterize the structure, diversity, and evolution of blaCTX-M-15-carrying plasmids in SE strains from human and animal sources in South Korea. Plasmid structures of blaCTX-M-15-positive SE strains from South Korea were analyzed using incompatibility groups typing and genome alignment tools. Genetic relationships and the time to most recent common ancestor (tMRCA) for the strains were determined using whole-genome SNP analysis and BEAST phylodynamic analysis. The plasmids were classified into three types (Type I–III) based on antimicrobial resistance gene profiles and incompatibility groups. Comparative genomic analysis revealed that these plasmids were cointegrates, resulting from the fusion of the SE virulence plasmid (pSENV) and pIntAMR. The pIntAMR region was identified as a chromosomally integrated form in Salmonella Virchow (SV) acquired through IS26-mediated transposition. This region contained multiple antimicrobial resistance genes and conjugative transfer elements. The tMRCA for blaCTX-M-15-carrying SE strains was estimated as June 2007, with Type III plasmids emerging around 2015, suggesting an evolutionary shift driven by selective pressure. This study demonstrates interserovar plasmid transfer between SV and SE, mediated by IS26 transposition, contributing to plasmid evolution and MDR in SE. Understanding these mechanisms is crucial for developing strategies for mitigating the spread of MDR Salmonella.
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来源期刊
Infection Genetics and Evolution
Infection Genetics and Evolution 医学-传染病学
CiteScore
8.40
自引率
0.00%
发文量
215
审稿时长
82 days
期刊介绍: (aka Journal of Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases -- MEEGID) Infectious diseases constitute one of the main challenges to medical science in the coming century. The impressive development of molecular megatechnologies and of bioinformatics have greatly increased our knowledge of the evolution, transmission and pathogenicity of infectious diseases. Research has shown that host susceptibility to many infectious diseases has a genetic basis. Furthermore, much is now known on the molecular epidemiology, evolution and virulence of pathogenic agents, as well as their resistance to drugs, vaccines, and antibiotics. Equally, research on the genetics of disease vectors has greatly improved our understanding of their systematics, has increased our capacity to identify target populations for control or intervention, and has provided detailed information on the mechanisms of insecticide resistance. However, the genetics and evolutionary biology of hosts, pathogens and vectors have tended to develop as three separate fields of research. This artificial compartmentalisation is of concern due to our growing appreciation of the strong co-evolutionary interactions among hosts, pathogens and vectors. Infection, Genetics and Evolution and its companion congress [MEEGID](http://www.meegidconference.com/) (for Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases) are the main forum acting for the cross-fertilization between evolutionary science and biomedical research on infectious diseases. Infection, Genetics and Evolution is the only journal that welcomes articles dealing with the genetics and evolutionary biology of hosts, pathogens and vectors, and coevolution processes among them in relation to infection and disease manifestation. All infectious models enter the scope of the journal, including pathogens of humans, animals and plants, either parasites, fungi, bacteria, viruses or prions. The journal welcomes articles dealing with genetics, population genetics, genomics, postgenomics, gene expression, evolutionary biology, population dynamics, mathematical modeling and bioinformatics. We also provide many author benefits, such as free PDFs, a liberal copyright policy, special discounts on Elsevier publications and much more. Please click here for more information on our author services .
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