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采用锁核酸探针的新型实时聚合酶链反应检测法评估法国氟喹诺酮敏感肺炎链球菌分离株中ParC突变的流行情况。

New real-time PCR assay using locked nucleic acid probes to assess prevalence of ParC mutations in fluoroquinolone-susceptible Streptococcus pneumoniae isolates from France.

作者信息

Decousser Jean-Winoc, Methlouthi Imen, Pina Patrick, Collignon Anne, Allouch Pierre

机构信息

Laboratoire de Biologie, Centre Hospitalier de Dourdan, 2 Rue du Potelet, 91415 Dourdan, France.

出版信息

Antimicrob Agents Chemother. 2006 Apr;50(4):1594-8. doi: 10.1128/AAC.50.4.1594-1598.2006.

Abstract

A real-time PCR assay with locked nucleic acid probes was developed to screen mutations at codons 79 and 83 of the Streptococcus pneumoniae parC gene. Only silent mutations were detected among 236 French invasive fluoroquinolone-susceptible strains. This test could be useful for some high-risk patients or in national surveys.

摘要

开发了一种使用锁核酸探针的实时聚合酶链反应检测方法,以筛查肺炎链球菌parC基因第79和83密码子处的突变。在236株法国侵袭性氟喹诺酮敏感菌株中仅检测到沉默突变。该检测方法可能对一些高危患者或全国性调查有用。

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引用本文的文献

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Real-time PCR detection of gyrA and parC mutations in Streptococcus pneumoniae.
Antimicrob Agents Chemother. 2008 Nov;52(11):4155-8. doi: 10.1128/AAC.00082-08. Epub 2008 Aug 25.

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