invA病毒基因的主要设计用于鸡的样本中识别和测序沙门氏菌

R. P. Melati, S. Nurjanah, W. P. Rahayu
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引用次数: 2

摘要

沙门氏菌的鉴定和测序需要一个特定的引物以及毒力标记。入侵基因(invA)是一种在所有沙门氏菌中都存在的基因,对沙门氏菌具有特异性,突变率低,因此可以作为沙门氏菌鉴定的靶基因。本研究旨在设计一种扩增子长、血清覆盖范围广的沙门氏菌invA基因引物,并获得最佳PCR条件。设计引物,用Primer-BLAST在硅片上检测其特异性,然后选择引物。对所选引物的退火温度和浓度进行了评价。通过序列选择得到一组invA基因引物,其正向序列为GCCGGTGAAATTATCGCCAC(起始碱基为297),反向序列为CTCGTAATTCGCCGCCATTG(起始碱基为1763)。基于引物- blast分析,该引物扩增子大小为1486 bp,退火温度为58℃,能够检测至少110种沙门氏菌血清型,能够检测鸡体内的沙门氏菌污染,而不能检测克雷伯氏菌、柠檬酸杆菌、沙雷氏菌、哈夫尼亚菌和大肠杆菌的存在。该引物在退火温度为58℃,引物浓度为1.2µM时,能很好地检测沙门氏菌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Desain Primer Gen Virulensi invA untuk Identifikasi dan Sekuensing Salmonella pada Sampel Karkas Ayam
Identification and sequencing of Salmonella require a specific primer as well as a virulence marker. Invasion gene (invA) is a gene found in all types of Salmonella, specific to Salmonella, and has a low mutation rate so that it can be used as a target gene for Salmonella identification. This study aimed to design a primer of invA gene of Salmonella spp. with long amplicons, has broad serovar coverage, and get an optimum PCR condition. Primers were designed and checked its specificity in silico using Primer-BLAST and then selected. Selected primer was evaluated for annealing temperature and primer concentration. Based on the sequential selection, it was obtained a set of invA gene primer with forwarding sequences GCCGGTGAAATTATCGCCAC (started at base 297) and reverses sequences CTCGTAATTCGCCGCCATTG (started at base 1763). Based on Primer-BLAST analysis, the primer gave an amplicon size of 1486 bp, has annealing temperature of 58 °C, capable of detecting at least 110 Salmonella serovars, capable to detect Salmonella contamination in chickens, and unable to detect the presence of Klebsiella sp., Citrobacter sp., Serratia sp., Hafnia sp., and E. coli. This primer can detect Salmonella very well with annealing temperature of 58 oC and primer concentration of 1.2 µM.
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