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首页> 外文期刊>Indian Journal of Experimental Biology >Evaluation of four methods of DNA recovery from Mycobacterium avium subspecies paratuberculosis present in intestine tissue of goats and comparative sensitivity of IS900 PCR with respect to culture for diagnosis of Johne's disease.
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Evaluation of four methods of DNA recovery from Mycobacterium avium subspecies paratuberculosis present in intestine tissue of goats and comparative sensitivity of IS900 PCR with respect to culture for diagnosis of Johne's disease.

机译:评价了四种从山羊肠道组织中存在的鸟分枝杆菌副结核分枝杆菌中回收DNA的方法,以及IS900 PCR对培养物进行约翰逊氏病诊断的比较敏感性。

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摘要

Low sensitivity of PCR reaction for detection of Mycoobacterium avium subspecies paratuberculosis (MAP) in tissues and fecal samples is mainly attributed to false negative results. Present study was undertaken to compare four methods of DNA isolation from tissues of infected animals and to determine most sensitive protocol for the recovery of DNA, suitable for IS900 PCR based detection of Johne's disease infection. Method I, the traditional van Soolingen2 method of DNA isolation was adopted for the isolation of DNA from tissues. Method II was modification (hexadecyl pyridinium chloride-HPC treatment) of van Soolingen2 method. Method III was traditional tissue DNA isolation method based on tissue lysis buffer. Method IV was modification of method III (HPC treatment). Using four methods of DNA isolation from 25 intestinal tissues of clinically infected goats, DNA was isolated from 15 (60.0%), 18 (72.0%), 13 (52.0%) and 13 (52.0%) tissues using method I, II, III and IV, respectively. All isolated DNA preparations were positive for MAP in IS900 PCR. HPC treatment enhanced the recovery of DNA from tissues of infected animals using method II. Therefore, method II can improve the diagnosis MAP infection using IS900 PCR.
机译:PCR反应检测组织和粪便样品中鸟分枝杆菌副结核分枝杆菌(MAP)的敏感性较低,这主要归因于假阴性结果。进行本研究以比较四种从感染动物组织中分离DNA的方法,并确定最敏感的DNA回收方案,适用于基于IS900 PCR的约翰尼氏病感染检测。方法一,采用传统的范索林根2 DNA分离方法从组织中分离DNA。方法II是van Soolingen2方法的改进方法(氯化十六烷基吡啶鎓-HPC处理)。方法III是基于组织裂解缓冲液的传统组织DNA分离方法。方法IV是方法III(HPC处理)的改进。使用四种从临床感染山羊的25个肠组织中分离DNA的方法,使用方法I,II,III从15个(60.0%),18个(72.0%),13个(52.0%)和13个(52.0%)组织中分离DNA。和IV。在IS900 PCR中,所有分离的DNA制剂MAP均为阳性。使用方法II,HPC处理可提高感染动物组织DNA的回收率。因此,方法II可以使用IS900 PCR改善MAP感染的诊断。

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