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本文引用的文献

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Ciprofloxacin resistance in Campylobacter jejuni isolates: detection of gyrA resistance mutations by mismatch amplification mutation assay PCR and DNA sequence analysis.空肠弯曲菌分离株对环丙沙星的耐药性:通过错配扩增突变分析PCR和DNA序列分析检测gyrA耐药突变
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PCR detection of bacteria in seven minutes.七分钟内通过聚合酶链式反应检测细菌。
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Campylobacter jejuni--an emerging foodborne pathogen.空肠弯曲菌——一种新出现的食源性病原体。
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Rapid emergence of high-level resistance to quinolones in Campylobacter jejuni associated with mutational changes in gyrA and parC.空肠弯曲菌中喹诺酮类高水平耐药性的快速出现与gyrA和parC的突变变化有关。
Antimicrob Agents Chemother. 1998 Dec;42(12):3276-8. doi: 10.1128/AAC.42.12.3276.
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Fluoroquinolone resistance mutations in the parC, parE, and gyrA genes of clinical isolates of viridans group streptococci.草绿色链球菌临床分离株的parC、parE和gyrA基因中的氟喹诺酮耐药突变
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PCR-based DNA amplification and presumptive detection of Escherichia coli O157:H7 with an internal fluorogenic probe and the 5' nuclease (TaqMan) assay.基于聚合酶链反应(PCR)的DNA扩增以及使用内部荧光探针和5'核酸酶(TaqMan)分析法对大肠杆菌O157:H7进行推定检测。
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Antimicrobial resistance of clinical strains of Campylobacter jejuni subsp. jejuni isolated from 1985 to 1997 in Quebec, Canada.1985年至1997年在加拿大魁北克分离出的空肠弯曲菌空肠亚种临床菌株的抗菌耐药性。
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Identification of novel mutation patterns in the parC gene of ciprofloxacin-resistant isolates of Neisseria gonorrhoeae.淋病奈瑟菌环丙沙星耐药菌株parC基因新突变模式的鉴定
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5' nuclease PCR assay to detect Yersinia pestis.用于检测鼠疫耶尔森菌的5'核酸酶聚合酶链反应检测法。
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Increased resistance to quinolones in Campylobacter jejuni: a genetic analysis of gyrA gene mutations in quinolone-resistant clinical isolates.空肠弯曲菌对喹诺酮类药物耐药性增加:喹诺酮耐药临床分离株中gyrA基因突变的遗传分析
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使用荧光定量聚合酶链反应检测法鉴定耐环丙沙星空肠弯曲菌

Identification of ciprofloxacin-resistant Campylobacter jejuni by use of a fluorogenic PCR assay.

作者信息

Wilson D L, Abner S R, Newman T C, Mansfield L S, Linz J E

机构信息

National Food Safety and Toxicology Center, Michigan State University, East Lansing, Michigan 48824, USA.

出版信息

J Clin Microbiol. 2000 Nov;38(11):3971-8. doi: 10.1128/JCM.38.11.3971-3978.2000.

DOI:10.1128/JCM.38.11.3971-3978.2000
PMID:11060054
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC87527/
Abstract

Fluoroquinolones are one class of antimicrobial agents commonly used to treat severe Campylobacter jejuni infection. C. jejuni strains resistant to high levels of the fluoroquinolone ciprofloxacin (MIC >/=16 microg/ml) have been predominantly characterized with a C-->T transition in codon 86 of gyrA. The gyrA gene encodes one subunit of DNA gyrase, which is a primary target for fluoroquinolone antibiotics. This study establishes a rapid PCR-based TaqMan method for identifying ciprofloxacin-resistant C. jejuni strains that carry the C-->T transition in codon 86 of gyrA. The assay uses real-time detection, eliminating the need for gel electrophoresis. Optimization of the assay parameters using purified Campylobacter DNA resulted in the ability to detect femtogram levels of DNA. The method should be useful for monitoring the development of ciprofloxacin resistance in C. jejuni. Compiled nucleotide sequence data on the quinolone resistance-determining region of gyrA in Campylobacter indicate that sequence comparison of this region is a useful method for tentative identification of Campylobacter isolates at the species level.

摘要

氟喹诺酮类是一类常用于治疗空肠弯曲菌严重感染的抗菌药物。对高水平氟喹诺酮环丙沙星耐药(最低抑菌浓度≥16微克/毫升)的空肠弯曲菌菌株,其主要特征是gyrA基因第86位密码子发生C→T转换。gyrA基因编码DNA回旋酶的一个亚基,而DNA回旋酶是氟喹诺酮类抗生素的主要作用靶点。本研究建立了一种基于PCR的快速TaqMan方法,用于鉴定gyrA基因第86位密码子发生C→T转换的耐环丙沙星空肠弯曲菌菌株。该检测方法采用实时检测,无需进行凝胶电泳。使用纯化的弯曲菌DNA对检测参数进行优化后,能够检测到飞克水平的DNA。该方法对于监测空肠弯曲菌中环丙沙星耐药性的发展应是有用的。弯曲菌中gyrA喹诺酮耐药决定区的汇编核苷酸序列数据表明,该区域的序列比较是在种水平上初步鉴定弯曲菌分离株的一种有用方法。