以胸苷激酶基因相对保守区域为靶点的聚合酶链反应标准化快速检测传染性喉气管炎病毒

S. Chakma, S. Sarker, S. Talukder, Md. Hakimul Haque, E. Chowdhury, A. Bari
{"title":"以胸苷激酶基因相对保守区域为靶点的聚合酶链反应标准化快速检测传染性喉气管炎病毒","authors":"S. Chakma, S. Sarker, S. Talukder, Md. Hakimul Haque, E. Chowdhury, A. Bari","doi":"10.3329/UJZRU.V29I1.9468","DOIUrl":null,"url":null,"abstract":"Infectious laryngotracheitis is an acute upper respiratory tract infection of chickens caused by infectious laryngotracheitis virus. The study was conducted to standardize the polymerase chain reaction targeting a relatively conserved region of the thymidine kinase gene for the rapid detection of infectious laryngotracheitis virus. The vaccine samples were collected from two renowned company of Bangladesh. DNA was extracted from diluted vaccine samples by using Wizard® Genomic DNA purification kit and thymidine kinase gene was amplified by using PCR system 9600 Thermocycler. Two vaccine samples were positively amplified by polymerase chain reaction. A procedure was developed for rapid detection of infectious laryngotracheitis virus by polymerase chain reaction of the conserved region of viral thymidine kinase gene containing DNA fragments. The results obtained in this study suggested that the polymerase chain reaction procedure could serve as a fast and sensitive method for the detection of vaccine strains of infectious laryngotracheitis viruses. Key words: Infectious laryngotracheitis virus; viral thymidine kinase (TK) gene; polymerase chain reaction DOI: http://dx.doi.org/10.3329/ujzru.v29i1.9468 UJZRU 2010; 29(1): 61-64","PeriodicalId":23467,"journal":{"name":"University Journal of Zoology, Rajshahi University","volume":"45 1","pages":"61-64"},"PeriodicalIF":0.0000,"publicationDate":"2012-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Rapid detection of infectious laryngotracheitis virus by standardization of polymerase chain reaction targeting a relatively conserved region of the thymidine kinase gene\",\"authors\":\"S. Chakma, S. Sarker, S. Talukder, Md. Hakimul Haque, E. Chowdhury, A. Bari\",\"doi\":\"10.3329/UJZRU.V29I1.9468\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Infectious laryngotracheitis is an acute upper respiratory tract infection of chickens caused by infectious laryngotracheitis virus. The study was conducted to standardize the polymerase chain reaction targeting a relatively conserved region of the thymidine kinase gene for the rapid detection of infectious laryngotracheitis virus. The vaccine samples were collected from two renowned company of Bangladesh. DNA was extracted from diluted vaccine samples by using Wizard® Genomic DNA purification kit and thymidine kinase gene was amplified by using PCR system 9600 Thermocycler. Two vaccine samples were positively amplified by polymerase chain reaction. A procedure was developed for rapid detection of infectious laryngotracheitis virus by polymerase chain reaction of the conserved region of viral thymidine kinase gene containing DNA fragments. The results obtained in this study suggested that the polymerase chain reaction procedure could serve as a fast and sensitive method for the detection of vaccine strains of infectious laryngotracheitis viruses. Key words: Infectious laryngotracheitis virus; viral thymidine kinase (TK) gene; polymerase chain reaction DOI: http://dx.doi.org/10.3329/ujzru.v29i1.9468 UJZRU 2010; 29(1): 61-64\",\"PeriodicalId\":23467,\"journal\":{\"name\":\"University Journal of Zoology, Rajshahi University\",\"volume\":\"45 1\",\"pages\":\"61-64\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2012-01-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"University Journal of Zoology, Rajshahi University\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3329/UJZRU.V29I1.9468\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"University Journal of Zoology, Rajshahi University","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3329/UJZRU.V29I1.9468","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3

摘要

传染性喉气管炎是由传染性喉气管炎病毒引起的鸡的急性上呼吸道感染。本研究旨在规范针对胸苷激酶基因相对保守区域的聚合酶链反应,用于传染性喉气管炎病毒的快速检测。疫苗样本来自孟加拉国两家知名公司。用Wizard®基因组DNA纯化试剂盒从稀释后的疫苗样品中提取DNA,用PCR系统9600 Thermocycler扩增胸苷激酶基因。两种疫苗经聚合酶链反应扩增阳性。建立了一种利用病毒胸苷激酶基因保守区DNA片段聚合酶链反应快速检测传染性喉气管炎病毒的方法。本研究结果表明,聚合酶链反应法可作为一种快速、灵敏的检测传染性喉气管炎疫苗株的方法。关键词:传染性喉气管炎病毒;病毒性胸苷激酶(TK)基因;聚合酶链反应DOI: http://dx.doi.org/10.3329/ujzru.v29i1.9468 UJZRU 2010;29 (1): 61 - 64
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rapid detection of infectious laryngotracheitis virus by standardization of polymerase chain reaction targeting a relatively conserved region of the thymidine kinase gene
Infectious laryngotracheitis is an acute upper respiratory tract infection of chickens caused by infectious laryngotracheitis virus. The study was conducted to standardize the polymerase chain reaction targeting a relatively conserved region of the thymidine kinase gene for the rapid detection of infectious laryngotracheitis virus. The vaccine samples were collected from two renowned company of Bangladesh. DNA was extracted from diluted vaccine samples by using Wizard® Genomic DNA purification kit and thymidine kinase gene was amplified by using PCR system 9600 Thermocycler. Two vaccine samples were positively amplified by polymerase chain reaction. A procedure was developed for rapid detection of infectious laryngotracheitis virus by polymerase chain reaction of the conserved region of viral thymidine kinase gene containing DNA fragments. The results obtained in this study suggested that the polymerase chain reaction procedure could serve as a fast and sensitive method for the detection of vaccine strains of infectious laryngotracheitis viruses. Key words: Infectious laryngotracheitis virus; viral thymidine kinase (TK) gene; polymerase chain reaction DOI: http://dx.doi.org/10.3329/ujzru.v29i1.9468 UJZRU 2010; 29(1): 61-64
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信