海产病原菌霍乱弧菌rtxA基因的PCR检测

Q3 Environmental Science
S. Ethica, Nurlaila Hidayati, H. Fuad, C. Arham, R. Ariyadi, E. Purwaningrum, K. Z. Rahman
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引用次数: 1

摘要

由霍乱弧菌引起的海产品传播疾病爆发,增加了对海产品食品安全风险评估的需要。本文对霍乱弧菌毒力基因rtxA作为产毒细菌DNA生物标志物的潜力进行了计算机研究。本研究的目的是利用细菌DNA生物标志物序列作为一种工具,促进霍乱感染的早期快速检测。利用Primer3Plus软件,从霍乱弧菌O1生物变体El Tor str. N16961基因组DNA的rtxA开放阅读框DNA中设计了5对特异性引物。然后,利用新设计的引物和从数据库中检索到的25个弧菌基因组DNA进行PCR检测。设计的5对引物RtxAOF-RtxAOR: ' 5- cgcaaaacagtttcagccga -3 '和5 ' - aggttggtcttgtggcca -3 '中,只有霍乱弧菌的单个DNA扩增子大小为518bp。使用类似的RtxAF-RtxAR引物研究的其他17个弧菌基因组未产生扩增带。进一步的检查表明,扩增子确实是霍乱弧菌rtxA基因的一部分。在此基础上,rtxA基因可作为霍乱弧菌的DNA生物标记物,为利用PCR技术快速诊断霍乱弧菌提供了可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection of rtxA Gene as a Biomarker of Seafood-Borne Pathogen Vibrio cholerae using In Silico PCR Assay
Seafood-borne outbreaks caused by Vibrio cholerae have led to the increased need for food safety risk assessment of marine products. An in silico investigation about the potential of virulence gene of V. cholerae, rtxA, as a DNA biomarker of the toxigenic bacterium has been carried out. The aim of this study was to use the bacterial DNA biomarker sequence as a tool to facilitate early rapid detection of cholera infection. Five specific pairs of primers were designed from the rtxA open reading frame DNA of V. cholerae O1 biovar El Tor str. N16961 genomic DNA using Primer3Plus. Next, in silico Polymerase Chain Reaction (PCR) assay was carried out using the newly designed primers and 25 genomic DNA of vibrio spp. retrieved from the in silico database. One of the five designed pairs of primers, RtxAOF-RtxAOR: ‘5-CGCAAAACAGTTTCAGCCGA-3’ and 5’-AGGTTGGTCTTTTGTGGCCA-3’, could result in single DNA amplicon sized 518 bp only from V. cholerae species. No amplicon bands were produced from 17 other vibrio genomes studied using similar RtxAF-RtxAR primers. A further check showed that the amplicon was indeed part of the rtxA gene of V. cholerae. Based on this in silico study, rtxA gene appeared to be a DNA biomarker of V. cholerae, which is potential to facilitate rapid diagnosis of the virulence bacterium using in silico PCR assay.
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来源期刊
CiteScore
1.40
自引率
0.00%
发文量
10
审稿时长
16 weeks
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