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首页> 外文期刊>Journal of Microbiological Methods >HRM confirmation of Neisseria gonorrhoeae in clinical specimens by G -> A (position 857) mutation detection in the 16S rRNA gene before sequencing and after porA confirmation
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HRM confirmation of Neisseria gonorrhoeae in clinical specimens by G -> A (position 857) mutation detection in the 16S rRNA gene before sequencing and after porA confirmation

机译:在测序之前和porA确认之后,通过16S rRNA基因中的G-> A(位置857)突变检测对临床样本中的淋病奈瑟菌进行HRM确认

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摘要

A total of 2273 specimens submitted to the Austin Hospital Pathology Service for Neisseria gonorrhoeae screening between September 1, 2009 and May 11, 2011 were used in this study. Specimens were simultaneously screened and confirmed with a previously published real time PCR assay for the opa gene (extra primers were included to increase sensitivity) and the porA gene respectively. The opa gene screen and initial porA gene confirmation yielded an N. gonorrhoeae positivity rate of 0.88% (20/2273) and 0.49% (11/2191) for specimens and patients respectively. A 16S rDNA High Resolution Melt confirmatory PCR was developed subsequently; this reduced the N. gonorrhoeae positivity rate to 0.35% (8/2273) and 0.27% (6/2191) for specimens and patients respectively (not altered by 16S sequencing). The higher rate of secondary confirmation (16S HRM) in patients compared with samples was due to the detection of species other than N. gonorrhoeae detected by the initial screening and confirmation test. This underlines the importance of performing the secondary confirmatory test that has been developed in this study
机译:在此研究中,使用了2009年9月1日至2011年5月11日之间提交给奥斯汀医院病理学部门淋病奈瑟菌的2273个标本。同时筛选样品并用先前发布的实时PCR分析法分别检测opa基因(包括增加引物以提高灵敏度)和porA基因。 opa基因筛选和最初的porA基因确认分别使标本和患者的淋病奈瑟氏球菌阳性率为0.88%(20/2273)和0.49%(11/2191)。随后开发了16S rDNA高分辨率熔体确认PCR;这将标本和患者的淋病奈瑟氏球菌阳性率分别降低至0.35%(8/2273)和0.27%(6/2191)(未通过16S测序改变)。与样品相比,患者的二次确诊率更高(16S HRM)是由于通过初步筛选和确证测试检测到的淋病奈瑟氏球菌以外的物种。这强调了进行本研究中开发的二次确认测试的重要性

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