检测核聚变的分子基因(F)和比较抑制酶作为纽卡斯尔病毒病因病因病因病因病因的定义因素进行比较

Medania Purwaningrum, Verawati Verawati, Ari Haryanto
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引用次数: 0

摘要

新城疫是一种由禽副粘病毒(APMV-1)引起的传染性病毒性疾病。这种病毒感染通过攻击神经、呼吸和消化系统而导致毁灭性的爆发。这种疾病通常会导致鸡蛋产量下降,并造成全球家禽业的经济损失。主要目的是利用BamH1、hin11和Apa 1进行逆转录聚合酶链反应(RT-PCR)和重条带酶分析,从ND病毒毒力标记物F基因中分离出ND病毒毒株和毒株。10份新城疫病毒样本来自动物疾病调查中心(ADIC) 2012-2013年从现场病例收集的沃茨病毒标本。从样本中提取新城疫病毒。提取的RNA产物作为模板进行RT-PCR扩增。RT-PCR扩增的目标为F基因。结果表明,由于存在长度为767 bp的DNA片段带,反应呈阳性。RT-PCR和重条带酶分析可以作为确定ND病毒病原型的工具,凝胶琼脂糖电泳显示出不同的酶切。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Deteksi Molekuler Gen Fusion (F) dan Analisis Perbandingan Beberapa Enzim Restriksi sebagai Penentu Patotipe Virus Newcastle Disease
Newcastle disease (ND) is a contagious viral disease caused by Avian Paramyxovirus Serotype-1 (APMV-1). This viral infection is responsible for devastating outbreak by attacking nerve, respiration, and also digestive system. This disease often followed with decreasing of eggs production and also responsible for economic losses in the poultry industries around the globe. The main goal was to differentiate virulent or avirulent strain of ND virus from F gene, which is the virulent marker of ND virus, by Reverse Transcription Polymerase Chain Reaction (RT-PCR) and Restrion Enzyme Analysis using BamH1, Hin 1l, and Apa 1. Ten ND virus samples came from Animal Disease Investigation Center (ADIC) Wates virus collection, collected from field case in 2012-2013. Newcastle disease virus was collected by extraction from the samples. The RNA product of extraction were used as a template for amplification in RT-PCR. The target of RT-PCR amplification was F gene. The results indicated positive reaction due to existing of DNA fragment band in size of 767 bp. RT-PCR and Restrion Enzyme Analysis can be used as tool to determine the pathotype of ND virus showed different restriction visualized by gel agarose electrophoresis.
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