嗜冷黄杆菌a、B基因型实时PCR检测方法的建立

IF 0.6 4区 农林科学 Q4 FISHERIES
Fish Pathology Pub Date : 2019-09-15 DOI:10.3147/jsfp.54.58
Ryo Inoue, T. Takase
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引用次数: 0

摘要

-根据肽基脯氨酸顺式反式异构酶C (PPIC)基因多态性,嗜冷黄杆菌是细菌性冷水病的病原体,可分为A型和B型两种基因型。这些是常规检测使用限制性片段长度多态性的PCR扩增子(PCR- rflp)。由于这种方法既困难又费时,所以需要一种简单的方法。本研究建立了一种实时荧光定量PCR (TaqMan探针法)检测PPIC区域单核苷酸多态性(SNP)的新方法。我们在SNP位点上设计探针,并进行TaqMan探针基因分型。该方法与RFLP的结果基本一致。该方法可以简便、快速地确定嗜冷性冷梭菌的基因型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a Real-time PCR to Detect Genotypes A and B in Flavobacterium psychrophilum
― Flavobacterium psychrophilum , the causative agent of bacterial cold-water disease, is classified into two genotypes (A and B) based on peptidyl-prolyl cis-trans isomerase C (PPIC) gene polymorphism. These are routinely detected using restriction fragment length polymorphism of the PCR amplicon (PCR-RFLP). Since this method is difficult and time-consuming, a simple method is required. Here we developed a new method using real-time PCR assay (TaqMan probe assay) to detect single nucleotide polymorphism (SNP) in PPIC region. We designed the probes on a SNP site and performed TaqMan probe genotyping. The results obtained using this method was in line with those of RFLP. This new method could easily and rapidly determine F. psychrophilum genotypes.
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来源期刊
Fish Pathology
Fish Pathology 农林科学-兽医学
CiteScore
1.40
自引率
16.70%
发文量
13
审稿时长
6 months
期刊介绍: Information not localized
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