高灵敏、快速检测肺炎克雷伯菌中 khe、blaKPC-2 和 blaNDM-1 基因的多重重组酶辅助 qPCR 分析法

IF 2.6 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY Journal of Clinical Laboratory Analysis Pub Date : 2024-04-08 DOI:10.1002/jcla.25038
Shao-wei Hua, Jie Wang, Zi-jin Zhao, Feng-yu Tian, Meng Zhao, Yu-xin Wang, Rui-qing Zhang, Zhi-qiang Han, Shi-jue Gao, Xiao-na Lv, Hong-yi Li, Xin-xin Shen, Xue-jun Ma, Zhi-shan Feng
{"title":"高灵敏、快速检测肺炎克雷伯菌中 khe、blaKPC-2 和 blaNDM-1 基因的多重重组酶辅助 qPCR 分析法","authors":"Shao-wei Hua,&nbsp;Jie Wang,&nbsp;Zi-jin Zhao,&nbsp;Feng-yu Tian,&nbsp;Meng Zhao,&nbsp;Yu-xin Wang,&nbsp;Rui-qing Zhang,&nbsp;Zhi-qiang Han,&nbsp;Shi-jue Gao,&nbsp;Xiao-na Lv,&nbsp;Hong-yi Li,&nbsp;Xin-xin Shen,&nbsp;Xue-jun Ma,&nbsp;Zhi-shan Feng","doi":"10.1002/jcla.25038","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Objective</h3>\n \n <p>This study aimed to establish a highly sensitive and rapid single-tube, two-stage, multiplex recombinase-aided qPCR (mRAP) assay to specifically detect the khe, bla<sub>KPC-2</sub>, and bla<sub>NDM-1</sub> genes in <i>Klebsiella pneumoniae</i>.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>mRAP was carried out in a qPCR instrument within 1 h. The analytical sensitivities of mRAP for khe, bla<sub>KPC-2</sub>, and bla<sub>NDM-1</sub> genes were tested using recombinant plasmids and dilutions of reference strains. A total of 137 clinical isolates and 86 sputum samples were used to validate the clinical performance of mRAP.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>mRAP achieved the sensitivities of 10, 8, and 14 copies/reaction for khe, bla<sub>KPC-2</sub>, and bla<sub>NDM-1</sub> genes, respectively, superior to qPCR. The Kappa value of qPCR and mRAP for detecting khe, bla<sub>KPC-2</sub>, and bla<sub>NDM-1</sub> genes was 1, 0.855, and 1, respectively (<i>p</i> &lt; 0.05).</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>mRAP is a rapid and highly sensitive assay for potential clinical identification of khe, bla<sub>KPC-2</sub>, and bla<sub>NDM-1</sub> genes in <i>K. pneumoniae</i>.</p>\n </section>\n </div>","PeriodicalId":15509,"journal":{"name":"Journal of Clinical Laboratory Analysis","volume":"38 9","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2024-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jcla.25038","citationCount":"0","resultStr":"{\"title\":\"A Multiplex Recombinase-Aided qPCR Assay for Highly Sensitive and Rapid Detection of khe, blaKPC-2, and blaNDM-1 Genes in Klebsiella pneumoniae\",\"authors\":\"Shao-wei Hua,&nbsp;Jie Wang,&nbsp;Zi-jin Zhao,&nbsp;Feng-yu Tian,&nbsp;Meng Zhao,&nbsp;Yu-xin Wang,&nbsp;Rui-qing Zhang,&nbsp;Zhi-qiang Han,&nbsp;Shi-jue Gao,&nbsp;Xiao-na Lv,&nbsp;Hong-yi Li,&nbsp;Xin-xin Shen,&nbsp;Xue-jun Ma,&nbsp;Zhi-shan Feng\",\"doi\":\"10.1002/jcla.25038\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Objective</h3>\\n \\n <p>This study aimed to establish a highly sensitive and rapid single-tube, two-stage, multiplex recombinase-aided qPCR (mRAP) assay to specifically detect the khe, bla<sub>KPC-2</sub>, and bla<sub>NDM-1</sub> genes in <i>Klebsiella pneumoniae</i>.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>mRAP was carried out in a qPCR instrument within 1 h. The analytical sensitivities of mRAP for khe, bla<sub>KPC-2</sub>, and bla<sub>NDM-1</sub> genes were tested using recombinant plasmids and dilutions of reference strains. A total of 137 clinical isolates and 86 sputum samples were used to validate the clinical performance of mRAP.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>mRAP achieved the sensitivities of 10, 8, and 14 copies/reaction for khe, bla<sub>KPC-2</sub>, and bla<sub>NDM-1</sub> genes, respectively, superior to qPCR. The Kappa value of qPCR and mRAP for detecting khe, bla<sub>KPC-2</sub>, and bla<sub>NDM-1</sub> genes was 1, 0.855, and 1, respectively (<i>p</i> &lt; 0.05).</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusion</h3>\\n \\n <p>mRAP is a rapid and highly sensitive assay for potential clinical identification of khe, bla<sub>KPC-2</sub>, and bla<sub>NDM-1</sub> genes in <i>K. pneumoniae</i>.</p>\\n </section>\\n </div>\",\"PeriodicalId\":15509,\"journal\":{\"name\":\"Journal of Clinical Laboratory Analysis\",\"volume\":\"38 9\",\"pages\":\"\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2024-04-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jcla.25038\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Clinical Laboratory Analysis\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/jcla.25038\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MEDICAL LABORATORY TECHNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical Laboratory Analysis","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jcla.25038","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICAL LABORATORY TECHNOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

本研究旨在建立一种高灵敏度、快速的单管、两阶段、多重重组酶辅助qPCR(mRAP)检测方法,以特异性检测肺炎克雷伯菌中的khe、blaKPC-2和blaNDM-1基因。结果mRAP对khe、blaKPC-2和blaNDM-1基因的灵敏度分别为10、8和14拷贝/反应,优于qPCR。在检测 khe、blaKPC-2 和 blaNDM-1 基因方面,qPCR 和 mRAP 的 Kappa 值分别为 1、0.855 和 1(p < 0.05)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
A Multiplex Recombinase-Aided qPCR Assay for Highly Sensitive and Rapid Detection of khe, blaKPC-2, and blaNDM-1 Genes in Klebsiella pneumoniae

Objective

This study aimed to establish a highly sensitive and rapid single-tube, two-stage, multiplex recombinase-aided qPCR (mRAP) assay to specifically detect the khe, blaKPC-2, and blaNDM-1 genes in Klebsiella pneumoniae.

Methods

mRAP was carried out in a qPCR instrument within 1 h. The analytical sensitivities of mRAP for khe, blaKPC-2, and blaNDM-1 genes were tested using recombinant plasmids and dilutions of reference strains. A total of 137 clinical isolates and 86 sputum samples were used to validate the clinical performance of mRAP.

Results

mRAP achieved the sensitivities of 10, 8, and 14 copies/reaction for khe, blaKPC-2, and blaNDM-1 genes, respectively, superior to qPCR. The Kappa value of qPCR and mRAP for detecting khe, blaKPC-2, and blaNDM-1 genes was 1, 0.855, and 1, respectively (p < 0.05).

Conclusion

mRAP is a rapid and highly sensitive assay for potential clinical identification of khe, blaKPC-2, and blaNDM-1 genes in K. pneumoniae.

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 Clinical Laboratory Analysis
Journal of Clinical Laboratory Analysis 医学-医学实验技术
CiteScore
5.60
自引率
7.40%
发文量
584
审稿时长
6-12 weeks
期刊介绍: Journal of Clinical Laboratory Analysis publishes original articles on newly developing modes of technology and laboratory assays, with emphasis on their application in current and future clinical laboratory testing. This includes reports from the following fields: immunochemistry and toxicology, hematology and hematopathology, immunopathology, molecular diagnostics, microbiology, genetic testing, immunohematology, and clinical chemistry.
期刊最新文献
Development of Synthetic Antimicrobial Peptides Based on Genomic Analysis of Streptococcus salivarius. Evaluating Chromosomal Mosaicism in Prenatal Diagnosis: The Complementary Roles of Chromosomal Microarray Analysis and Karyotyping. Prevalence of Plasmid-Mediated Fluoroquinolone Resistance Genes in Pseudomonas aeruginosa Among Patients at Aleppo University Hospital, Syria. The Discovery of New Antibody in Autoimmune Disease Using a Novel Approach of Coombs Test Based on Flow Cytometry Method. B4GALNT1 Regulates Hepatocellular Carcinoma Cell Proliferation and Apoptosis via the PI3K-AKT-mTOR Pathway.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1