家畜来源的空肠弯曲杆菌的比较基因组分析:抗菌素耐药性、毒力、可移动遗传元件和遗传亲缘性。

IF 2.5 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jae-Uk An, Junbum Lee, Seongbeom Cho, Hyokeun Song
{"title":"家畜来源的空肠弯曲杆菌的比较基因组分析:抗菌素耐药性、毒力、可移动遗传元件和遗传亲缘性。","authors":"Jae-Uk An, Junbum Lee, Seongbeom Cho, Hyokeun Song","doi":"10.4014/jmb.2411.11044","DOIUrl":null,"url":null,"abstract":"<p><p><i>Campylobacter jejuni</i> is a major cause of foodborne illnesses, and its increasing antimicrobial resistance (AMR) poses serious public health risks. Owing to their high genetic diversity and frequent intraspecific recombination, understanding the virulence traits of <i>Campylobacter</i> remains challenging. We elucidated the resistance and virulence mechanisms of <i>C. jejuni</i> in livestock using comparative genomic and phenotypic analyses. We analyzed <i>C. jejuni</i> strains isolated from chicken meat, chicken slaughterhouses, and dairy cattle farms. High resistance rates were observed for nalidixic acid, ciprofloxacin, and tetracycline. The chicken-derived strains showed significantly higher tetracycline resistance and marginally higher nalidixic acid resistance, whereas the cattle-derived strains showed marginally higher ciprofloxacin resistance. The key AMR determinants included <i>gyrA</i> and <i>tet(O)</i>, which were correlated with resistance phenotypes. Ten virulence factor families were identified with prevalences exceeding 90%. Biofilm formation was observed in 31.9% of strains and correlated with flagella-associated virulence factors. Eighteen plasmid types were detected, primarily in the pTet family, which carried various AMR genes and components of the Type IV secretion system, potentially facilitating the co-transfer of resistance and virulence traits. Conjugation experiments confirmed the horizontal transfer of two pTet plasmid types into the wild-type <i>C. jejuni</i> strain. Further, our analyses revealed over 95% genetic similarity with European <i>C. jejuni</i> strains in a public database-supporting the hypothesis of zoonotic transmission via global food chains-and the zoonotic risks of livestock-derived <i>Campylobacter jejuni</i>. These findings emphasize the need for extended global surveillance to mitigate the risk of zoonotic transmission.</p>","PeriodicalId":16481,"journal":{"name":"Journal of microbiology and biotechnology","volume":"35 ","pages":"e2411044"},"PeriodicalIF":2.5000,"publicationDate":"2025-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11876010/pdf/","citationCount":"0","resultStr":"{\"title\":\"Comparative Genomic Analysis of Livestock-Derived <i>Campylobacter jejuni</i>: Antimicrobial Resistance, Virulence, Mobile Genetic Elements, and Genetic Relatedness.\",\"authors\":\"Jae-Uk An, Junbum Lee, Seongbeom Cho, Hyokeun Song\",\"doi\":\"10.4014/jmb.2411.11044\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Campylobacter jejuni</i> is a major cause of foodborne illnesses, and its increasing antimicrobial resistance (AMR) poses serious public health risks. Owing to their high genetic diversity and frequent intraspecific recombination, understanding the virulence traits of <i>Campylobacter</i> remains challenging. We elucidated the resistance and virulence mechanisms of <i>C. jejuni</i> in livestock using comparative genomic and phenotypic analyses. We analyzed <i>C. jejuni</i> strains isolated from chicken meat, chicken slaughterhouses, and dairy cattle farms. High resistance rates were observed for nalidixic acid, ciprofloxacin, and tetracycline. The chicken-derived strains showed significantly higher tetracycline resistance and marginally higher nalidixic acid resistance, whereas the cattle-derived strains showed marginally higher ciprofloxacin resistance. The key AMR determinants included <i>gyrA</i> and <i>tet(O)</i>, which were correlated with resistance phenotypes. Ten virulence factor families were identified with prevalences exceeding 90%. Biofilm formation was observed in 31.9% of strains and correlated with flagella-associated virulence factors. Eighteen plasmid types were detected, primarily in the pTet family, which carried various AMR genes and components of the Type IV secretion system, potentially facilitating the co-transfer of resistance and virulence traits. Conjugation experiments confirmed the horizontal transfer of two pTet plasmid types into the wild-type <i>C. jejuni</i> strain. Further, our analyses revealed over 95% genetic similarity with European <i>C. jejuni</i> strains in a public database-supporting the hypothesis of zoonotic transmission via global food chains-and the zoonotic risks of livestock-derived <i>Campylobacter jejuni</i>. These findings emphasize the need for extended global surveillance to mitigate the risk of zoonotic transmission.</p>\",\"PeriodicalId\":16481,\"journal\":{\"name\":\"Journal of microbiology and biotechnology\",\"volume\":\"35 \",\"pages\":\"e2411044\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2025-02-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11876010/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of microbiology and biotechnology\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.4014/jmb.2411.11044\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of microbiology and biotechnology","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.4014/jmb.2411.11044","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

空肠弯曲杆菌是食源性疾病的主要原因,其日益增加的抗菌素耐药性(AMR)构成了严重的公共卫生风险。由于其高度的遗传多样性和频繁的种内重组,了解弯曲杆菌的毒力特性仍然具有挑战性。我们通过比较基因组和表型分析阐明了空肠梭菌在家畜体内的抗性和毒力机制。我们分析了从鸡肉、鸡屠宰场和奶牛养殖场分离的空肠杆菌菌株。对钠地酸、环丙沙星和四环素的耐药率较高。鸡源菌株对四环素的耐药性显著提高,对萘啶酸的耐药性略高,而牛源菌株对环丙沙星的耐药性略高。关键的AMR决定因子包括gyrA和tet(O),它们与抗性表型相关。十个毒力因子家族的流行率超过90%。在31.9%的菌株中观察到生物膜形成,并与鞭毛相关的毒力因子相关。共检测到18种类型的质粒,主要在ppet家族中,它们携带多种AMR基因和IV型分泌系统的成分,可能促进抗性和毒力性状的共同转移。偶联实验证实了两种ppet质粒水平转移到野生型空肠梭菌中。此外,我们的分析显示,在公共数据库中,与欧洲空肠弯曲杆菌菌株的遗传相似性超过95%,这支持了通过全球食物链进行人畜共患传播的假设,以及家畜源性空肠弯曲杆菌的人畜共患风险。这些发现强调需要扩大全球监测,以减轻人畜共患病传播的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative Genomic Analysis of Livestock-Derived Campylobacter jejuni: Antimicrobial Resistance, Virulence, Mobile Genetic Elements, and Genetic Relatedness.

Campylobacter jejuni is a major cause of foodborne illnesses, and its increasing antimicrobial resistance (AMR) poses serious public health risks. Owing to their high genetic diversity and frequent intraspecific recombination, understanding the virulence traits of Campylobacter remains challenging. We elucidated the resistance and virulence mechanisms of C. jejuni in livestock using comparative genomic and phenotypic analyses. We analyzed C. jejuni strains isolated from chicken meat, chicken slaughterhouses, and dairy cattle farms. High resistance rates were observed for nalidixic acid, ciprofloxacin, and tetracycline. The chicken-derived strains showed significantly higher tetracycline resistance and marginally higher nalidixic acid resistance, whereas the cattle-derived strains showed marginally higher ciprofloxacin resistance. The key AMR determinants included gyrA and tet(O), which were correlated with resistance phenotypes. Ten virulence factor families were identified with prevalences exceeding 90%. Biofilm formation was observed in 31.9% of strains and correlated with flagella-associated virulence factors. Eighteen plasmid types were detected, primarily in the pTet family, which carried various AMR genes and components of the Type IV secretion system, potentially facilitating the co-transfer of resistance and virulence traits. Conjugation experiments confirmed the horizontal transfer of two pTet plasmid types into the wild-type C. jejuni strain. Further, our analyses revealed over 95% genetic similarity with European C. jejuni strains in a public database-supporting the hypothesis of zoonotic transmission via global food chains-and the zoonotic risks of livestock-derived Campylobacter jejuni. These findings emphasize the need for extended global surveillance to mitigate the risk of zoonotic transmission.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of microbiology and biotechnology
Journal of microbiology and biotechnology BIOTECHNOLOGY & APPLIED MICROBIOLOGY-MICROBIOLOGY
CiteScore
5.50
自引率
3.60%
发文量
151
审稿时长
2 months
期刊介绍: The Journal of Microbiology and Biotechnology (JMB) is a monthly international journal devoted to the advancement and dissemination of scientific knowledge pertaining to microbiology, biotechnology, and related academic disciplines. It covers various scientific and technological aspects of Molecular and Cellular Microbiology, Environmental Microbiology and Biotechnology, Food Biotechnology, and Biotechnology and Bioengineering (subcategories are listed below). Launched in March 1991, the JMB is published by the Korean Society for Microbiology and Biotechnology (KMB) and distributed worldwide.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信