{"title":"geneLEAD VIII平台对万古霉素耐药基因vanA和vanB的自动分子检测。","authors":"Keiichiro Mori, Yasufumi Matsumura, Yusuke Tsuda, Koh Shinohara, Yasuhiro Tsuchido, Masaki Yamamoto, Miki Nagao","doi":"10.1099/acmi.0.001044.v4","DOIUrl":null,"url":null,"abstract":"<p><p>Rapid and accurate detection of vancomycin-resistant enterococci (VREs) can aid in the early application of appropriate antimicrobial treatment and the implementation of infection prevention measures. The VIASURE real-time PCR assay (Certest Biotec) is a multiplex nucleic acid-based <i>in vitro</i> diagnostic test intended for the detection of <i>vanA</i> and <i>vanB</i>, and geneLEAD VIII (Precision System Science) is a customizable, fully automated molecular detection platform. We evaluated the performance of the VIASURE assay on the geneLEAD VIII platform against 200 clinical enterococcal isolates consisting of 151 VREs and 49 vancomycin-susceptible enterococci collected in Japan, primarily in the Kinki region, and compared it to that of the in-house reference multiplex PCR assay. The performance of the VIASURE assay for the detection of <i>vanA</i> and <i>vanB</i> was comparable to that of the reference multiplex PCR assay, with both a sensitivity and specificity of 100%. Compared with the reference PCR assay, the VIASURE assay reduced the turn-around time by ~3 h 40 min (5 h 34 min vs. 1 h 54 min) and the hands-on time by 46 min per four samples. Fully automated molecular detection of <i>vanA</i> and <i>vanB</i> using the VIASURE assay and geneLEAD VIII for bacterial isolates can enable fast and reliable testing while reducing labour and is a promising tool for clinical laboratories and nosocomial infection control.</p>","PeriodicalId":94366,"journal":{"name":"Access microbiology","volume":"7 8","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12451298/pdf/","citationCount":"0","resultStr":"{\"title\":\"Automated molecular detection of the vancomycin resistance genes vanA and vanB using the geneLEAD VIII platform.\",\"authors\":\"Keiichiro Mori, Yasufumi Matsumura, Yusuke Tsuda, Koh Shinohara, Yasuhiro Tsuchido, Masaki Yamamoto, Miki Nagao\",\"doi\":\"10.1099/acmi.0.001044.v4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Rapid and accurate detection of vancomycin-resistant enterococci (VREs) can aid in the early application of appropriate antimicrobial treatment and the implementation of infection prevention measures. The VIASURE real-time PCR assay (Certest Biotec) is a multiplex nucleic acid-based <i>in vitro</i> diagnostic test intended for the detection of <i>vanA</i> and <i>vanB</i>, and geneLEAD VIII (Precision System Science) is a customizable, fully automated molecular detection platform. We evaluated the performance of the VIASURE assay on the geneLEAD VIII platform against 200 clinical enterococcal isolates consisting of 151 VREs and 49 vancomycin-susceptible enterococci collected in Japan, primarily in the Kinki region, and compared it to that of the in-house reference multiplex PCR assay. The performance of the VIASURE assay for the detection of <i>vanA</i> and <i>vanB</i> was comparable to that of the reference multiplex PCR assay, with both a sensitivity and specificity of 100%. Compared with the reference PCR assay, the VIASURE assay reduced the turn-around time by ~3 h 40 min (5 h 34 min vs. 1 h 54 min) and the hands-on time by 46 min per four samples. Fully automated molecular detection of <i>vanA</i> and <i>vanB</i> using the VIASURE assay and geneLEAD VIII for bacterial isolates can enable fast and reliable testing while reducing labour and is a promising tool for clinical laboratories and nosocomial infection control.</p>\",\"PeriodicalId\":94366,\"journal\":{\"name\":\"Access microbiology\",\"volume\":\"7 8\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-08-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12451298/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Access microbiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1099/acmi.0.001044.v4\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Access microbiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1099/acmi.0.001044.v4","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
快速准确地检测万古霉素耐药肠球菌(VREs)有助于早期应用适当的抗菌药物治疗和实施感染预防措施。VIASURE实时PCR检测(Certest Biotec)是一种基于多重核酸的体外诊断测试,用于检测vanA和vanB,而geneLEAD VIII (Precision System Science)是一种可定制的全自动分子检测平台。我们在geneLEAD VIII平台上评估了在日本(主要是在Kinki地区)收集的200株临床肠球菌分离物(包括151株VREs和49株万古霉素敏感肠球菌)的VIASURE检测性能,并将其与内部参考多重PCR检测进行了比较。VIASURE法检测vanA和vanB的性能与参考多重PCR法相当,灵敏度和特异性均为100%。与参考PCR法相比,VIASURE法每4个样品的周转时间缩短了约3 h 40 min (5 h 34 min vs 1 h 54 min),操作时间缩短了46 min。使用VIASURE测定法和geneLEAD VIII对细菌分离物进行vanA和vanB的全自动分子检测,可以实现快速可靠的检测,同时减少人工,是临床实验室和医院感染控制的有前途的工具。
Automated molecular detection of the vancomycin resistance genes vanA and vanB using the geneLEAD VIII platform.
Rapid and accurate detection of vancomycin-resistant enterococci (VREs) can aid in the early application of appropriate antimicrobial treatment and the implementation of infection prevention measures. The VIASURE real-time PCR assay (Certest Biotec) is a multiplex nucleic acid-based in vitro diagnostic test intended for the detection of vanA and vanB, and geneLEAD VIII (Precision System Science) is a customizable, fully automated molecular detection platform. We evaluated the performance of the VIASURE assay on the geneLEAD VIII platform against 200 clinical enterococcal isolates consisting of 151 VREs and 49 vancomycin-susceptible enterococci collected in Japan, primarily in the Kinki region, and compared it to that of the in-house reference multiplex PCR assay. The performance of the VIASURE assay for the detection of vanA and vanB was comparable to that of the reference multiplex PCR assay, with both a sensitivity and specificity of 100%. Compared with the reference PCR assay, the VIASURE assay reduced the turn-around time by ~3 h 40 min (5 h 34 min vs. 1 h 54 min) and the hands-on time by 46 min per four samples. Fully automated molecular detection of vanA and vanB using the VIASURE assay and geneLEAD VIII for bacterial isolates can enable fast and reliable testing while reducing labour and is a promising tool for clinical laboratories and nosocomial infection control.