{"title":"多重pcr同时检测零售鸡肉中耐氟喹诺酮类和大环内酯类空肠弯曲菌/大肠弯曲菌","authors":"Akira Fukuda, Ayu Matsui, Yuma Furuya, Yasuhiko Suzuki, Yutaka Tamura, Chie Nakajima, Masaru Usui","doi":"10.1177/10766294251389592","DOIUrl":null,"url":null,"abstract":"<p><p><i>Campylobacter</i> contamination in chicken meat, particularly with fluoroquinolone- and macrolide-resistant strains, is a significant public health concern. Therefore, developing an easy and rapid detection method for fluoroquinolone- and macrolide-resistant <i>Campylobacter</i> will improve food safety. In this study, we designed and evaluated a multiplex-Polymerase Chain Reaction (PCR) method for the simultaneous detection of fluoroquinolone- and macrolide-resistant <i>Campylobacter jejuni</i> and <i>Campylobacter coli</i> in chicken meat. Our multiplex-PCR-targeted mutations in the <i>gyrA</i> and <i>rrl</i> genes of <i>Campylobacter</i> species confer resistance to fluoroquinolones and macrolides, respectively. Overall, this method could detect <i>Campylobacter</i> contamination and identify <i>C. jejuni</i> and <i>C. coli</i> as well as their susceptibility to fluoroquinolone and macrolide. Spiking of chicken meat samples revealed that multiplex-PCR can detect at least 0.72 Colony-Forming Unit (CFU)/g <i>C. jejuni</i>/<i>coli</i>. Among 277 retail chicken meat samples, <i>C. jejuni</i>/<i>coli</i> were detected in 54 samples using multiplex-PCR, with isolation from 52 samples using microbial culture. The susceptibility of the isolates to fluoroquinolones and macrolides was determined using both the PCR and culture methods, and a comparison of these methods showed that the accuracy, specificity, and sensitivity were all above 95%. The culture method required approximately 8 days for <i>Campylobacter</i> isolation and antimicrobial susceptibility testing. Multiplex-PCR could determine the contamination with <i>C. jejuni</i>/<i>coli</i> and susceptibility to fluoroquinolones and macrolides within 2-3 days from the enrichment culture to final determination. These results indicate that the proposed multiplex-PCR enables rapid and simultaneous detection of fluoroquinolone- and macrolide-resistant <i>C. jejuni</i>/<i>coli</i> in chicken meat and its utility for monitoring their contamination in food.</p>","PeriodicalId":18701,"journal":{"name":"Microbial drug resistance","volume":" ","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2025-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Simultaneous Detection of Fluoroquinolone- and Macrolide-Resistant <i>Campylobacter jejuni/Campylobacter coli</i> in Retail Chicken Meat Using Multiplex-PCR.\",\"authors\":\"Akira Fukuda, Ayu Matsui, Yuma Furuya, Yasuhiko Suzuki, Yutaka Tamura, Chie Nakajima, Masaru Usui\",\"doi\":\"10.1177/10766294251389592\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Campylobacter</i> contamination in chicken meat, particularly with fluoroquinolone- and macrolide-resistant strains, is a significant public health concern. Therefore, developing an easy and rapid detection method for fluoroquinolone- and macrolide-resistant <i>Campylobacter</i> will improve food safety. In this study, we designed and evaluated a multiplex-Polymerase Chain Reaction (PCR) method for the simultaneous detection of fluoroquinolone- and macrolide-resistant <i>Campylobacter jejuni</i> and <i>Campylobacter coli</i> in chicken meat. Our multiplex-PCR-targeted mutations in the <i>gyrA</i> and <i>rrl</i> genes of <i>Campylobacter</i> species confer resistance to fluoroquinolones and macrolides, respectively. Overall, this method could detect <i>Campylobacter</i> contamination and identify <i>C. jejuni</i> and <i>C. coli</i> as well as their susceptibility to fluoroquinolone and macrolide. Spiking of chicken meat samples revealed that multiplex-PCR can detect at least 0.72 Colony-Forming Unit (CFU)/g <i>C. jejuni</i>/<i>coli</i>. Among 277 retail chicken meat samples, <i>C. jejuni</i>/<i>coli</i> were detected in 54 samples using multiplex-PCR, with isolation from 52 samples using microbial culture. The susceptibility of the isolates to fluoroquinolones and macrolides was determined using both the PCR and culture methods, and a comparison of these methods showed that the accuracy, specificity, and sensitivity were all above 95%. The culture method required approximately 8 days for <i>Campylobacter</i> isolation and antimicrobial susceptibility testing. Multiplex-PCR could determine the contamination with <i>C. jejuni</i>/<i>coli</i> and susceptibility to fluoroquinolones and macrolides within 2-3 days from the enrichment culture to final determination. These results indicate that the proposed multiplex-PCR enables rapid and simultaneous detection of fluoroquinolone- and macrolide-resistant <i>C. jejuni</i>/<i>coli</i> in chicken meat and its utility for monitoring their contamination in food.</p>\",\"PeriodicalId\":18701,\"journal\":{\"name\":\"Microbial drug resistance\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2025-10-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Microbial drug resistance\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1177/10766294251389592\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"INFECTIOUS DISEASES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbial drug resistance","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/10766294251389592","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0
摘要
鸡肉中的弯曲杆菌污染,特别是氟喹诺酮和大环内酯耐药菌株,是一个重大的公共卫生问题。因此,建立一种简便、快速的检测方法对氟喹诺酮类和大环内酯类耐药弯曲杆菌具有重要意义。本研究设计了一种多重聚合酶链反应(PCR)方法,用于同时检测鸡肉中对氟喹诺酮类和大环内酯类耐药的空肠弯曲菌和大肠弯曲菌。弯曲杆菌gyrA和rrl基因的多重pcr靶向突变分别赋予了对氟喹诺酮类药物和大环内酯类药物的耐药性。总体而言,该方法能检测出弯曲杆菌污染,并能鉴定空肠C.和大肠C.及其对氟喹诺酮类和大环内酯类药物的敏感性。对鸡肉样品进行pcr检测,结果表明多重pcr至少能检测出0.72个CFU /g C. jejuni/coli。在277份零售鸡肉样品中,多重pcr法检出54份空肠杆菌/大肠杆菌,微生物培养法分离出52份。采用PCR法和培养法测定分离菌株对氟喹诺酮类药物和大环内酯类药物的敏感性,两种方法的准确性、特异性和敏感性均在95%以上。培养方法需要8天左右进行弯曲杆菌的分离和药敏试验。从富集培养到最终检测,在2-3天内,多重聚合酶链反应(Multiplex-PCR)可以检测空肠杆菌/大肠杆菌的污染以及对氟喹诺酮类药物和大环内酯类药物的敏感性。上述结果表明,该多重pcr方法能够快速、同时检测鸡肉中对氟喹诺酮和大环内酯耐药的空肠杆菌/大肠杆菌,并可用于监测其在食品中的污染。
Simultaneous Detection of Fluoroquinolone- and Macrolide-Resistant Campylobacter jejuni/Campylobacter coli in Retail Chicken Meat Using Multiplex-PCR.
Campylobacter contamination in chicken meat, particularly with fluoroquinolone- and macrolide-resistant strains, is a significant public health concern. Therefore, developing an easy and rapid detection method for fluoroquinolone- and macrolide-resistant Campylobacter will improve food safety. In this study, we designed and evaluated a multiplex-Polymerase Chain Reaction (PCR) method for the simultaneous detection of fluoroquinolone- and macrolide-resistant Campylobacter jejuni and Campylobacter coli in chicken meat. Our multiplex-PCR-targeted mutations in the gyrA and rrl genes of Campylobacter species confer resistance to fluoroquinolones and macrolides, respectively. Overall, this method could detect Campylobacter contamination and identify C. jejuni and C. coli as well as their susceptibility to fluoroquinolone and macrolide. Spiking of chicken meat samples revealed that multiplex-PCR can detect at least 0.72 Colony-Forming Unit (CFU)/g C. jejuni/coli. Among 277 retail chicken meat samples, C. jejuni/coli were detected in 54 samples using multiplex-PCR, with isolation from 52 samples using microbial culture. The susceptibility of the isolates to fluoroquinolones and macrolides was determined using both the PCR and culture methods, and a comparison of these methods showed that the accuracy, specificity, and sensitivity were all above 95%. The culture method required approximately 8 days for Campylobacter isolation and antimicrobial susceptibility testing. Multiplex-PCR could determine the contamination with C. jejuni/coli and susceptibility to fluoroquinolones and macrolides within 2-3 days from the enrichment culture to final determination. These results indicate that the proposed multiplex-PCR enables rapid and simultaneous detection of fluoroquinolone- and macrolide-resistant C. jejuni/coli in chicken meat and its utility for monitoring their contamination in food.
期刊介绍:
Microbial Drug Resistance (MDR) is an international, peer-reviewed journal that covers the global spread and threat of multi-drug resistant clones of major pathogens that are widely documented in hospitals and the scientific community. The Journal addresses the serious challenges of trying to decipher the molecular mechanisms of drug resistance. MDR provides a multidisciplinary forum for peer-reviewed original publications as well as topical reviews and special reports.
MDR coverage includes:
Molecular biology of resistance mechanisms
Virulence genes and disease
Molecular epidemiology
Drug design
Infection control.