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霍乱弧菌致病性基因检测引物的计算机分析。

In silico analyses of primers used to detect the pathogenicity genes of Vibrio cholerae.

机构信息

Centre de Biochimie, Université de Nice Sophia-Antipolis, Parc Valrose, F 06108 Nice, France.

出版信息

Microbes Environ. 2012;27(3):250-6. doi: 10.1264/jsme2.me11317. Epub 2012 May 17.

Abstract

In Vibrio cholerae, the etiological agent of cholera, most of the virulence genes are located in two pathogenicity islands, named TCP (Toxin-Co-regulated Pilus) and CTX (Cholera ToXins). For each V. cholerae pathogenicity gene, we retrieved every primer published since 1990 and every known allele in order to perform a complete in silico survey and assess the quality of the PCR primers used for amplification of these genes. Primers with a melting temperature in the range 55-60°C against any target sequence were considered valid. Our survey clearly revealed that two thirds of the published primers are not able to properly detect every genetic variant of the target genes. Moreover, the quality of primers did not improve with time. Their lifetime, i.e. the number of times they were cited in the literature, is also not a factor allowing the selection of valid primers. We were able to improve some primers or design new primers for the few cases where no valid primer was found. In conclusion, many published primers should be avoided or improved for use in molecular detection tests, in order to improve and perfect specificity and coverage. This study suggests that bioinformatic analyses are important to validate the choice of primers.

摘要

在霍乱弧菌(引起霍乱的病原体)中,大多数毒力基因位于两个致病性岛屿上,分别命名为 TCP(毒素调节菌毛)和 CTX(霍乱毒素)。对于每个霍乱弧菌的致病性基因,我们检索了自 1990 年以来发表的每一个引物,以及每一个已知的等位基因,以便对这些基因进行全面的计算机模拟调查,并评估用于扩增这些基因的 PCR 引物的质量。与任何靶序列的熔解温度在 55-60°C 范围内的引物被认为是有效的。我们的调查清楚地表明,三分之二的已发表引物不能正确检测目标基因的每个遗传变体。此外,引物的质量并没有随着时间的推移而提高。它们的“寿命”,即它们在文献中被引用的次数,也不是选择有效引物的因素。对于那些没有找到有效引物的少数情况,我们能够改进一些引物或设计新的引物。总之,为了提高和完善特异性和覆盖度,在分子检测试验中应避免或改进许多已发表的引物。这项研究表明,生物信息学分析对于验证引物的选择很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c322/4036039/7f3699ba443b/27_250f1.jpg

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