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基于羟甲基胆色素原合酶(HMBS)基因的鸟类内源性内参

Hydroxymethylbilane synthase (HMBS) gene-based endogenous internal control for avian species.

作者信息

Wang Yaoyao, Zhang Jilei, Patrick Kelly, Li Min, Gong Jiansen, Xu Bu, Shen Qiuping, Yang Yi, Wei Lanjing, Zhang Yuanyuan, Peng Daxin, Ye Jianqiang, Poudel Anil, Wang Chengming

机构信息

Yangzhou University College of Veterinary Medicine, Yangzhou, Jiangsu, China.

Ross University School of Veterinary Medicine, Basseterre, West Indies, St. Kitts and Nevis.

出版信息

AMB Express. 2020 Oct 7;10(1):181. doi: 10.1186/s13568-020-01112-5.

Abstract

With PCR becoming one of the most important and widely-used diagnostic tools for infectious diseases of poultry, an urgent need has developed for an endogenous internal control (EIC) that monitors the quality and quantity of poultry DNA in test samples. In this study we developed a SYBR-qPCR to target the poultry homolog of the hydroxymethylbilane synthase (HMBS) gene as an EIC for avian species. The avian HMBS-based qPCR was very sensitive, detecting one HMBS gene copy in a 20 µL reaction, and is highly specific for avian species. It amplified DNA from 11 organs and tissues of chickens showing it can be used as an EIC on a large variety of samples. The application of the established EIC on clinically and experimentally infected samples demonstrated that false negativity and result variations could result from samples being collected using different operators, techniques, preservatives, and storage times. The high sensitivity and specificity of the avian HMBS-based qPCR, its ability to quantify DNAs extracted from a wide range of tissues and poultry species along with its usefulness in reducing false negativity in PCR results associated with inadequate sampling and storage degradation makes it an ideal EIC for poultry DNA and RNA PCR diagnostics. The study also highlights the importance of appropriate sampling and storage of samples in ensuring accuracy of molecular diagnostic testing.

摘要

随着聚合酶链反应(PCR)成为家禽传染病最重要且应用最广泛的诊断工具之一,迫切需要一种内源内参(EIC)来监测检测样本中家禽DNA的质量和数量。在本研究中,我们开发了一种基于荧光定量PCR(SYBR-qPCR),以家禽羟甲基胆色素原合酶(HMBS)基因的同源物作为禽类的内源内参。基于禽类HMBS的定量PCR非常灵敏,在20微升反应中能检测到一个HMBS基因拷贝,并且对禽类具有高度特异性。它能扩增鸡的11种器官和组织的DNA,表明其可用于多种样本作为内源内参。将建立的内源内参应用于临床和实验感染样本表明,使用不同操作人员、技术、防腐剂和储存时间采集的样本可能导致假阴性和结果差异。基于禽类HMBS的定量PCR具有高灵敏度和特异性,能够对从多种组织和家禽物种中提取的DNA进行定量,并且在减少与采样不足和储存降解相关的PCR结果假阴性方面很有用,使其成为家禽DNA和RNA PCR诊断的理想内源内参。该研究还强调了样本的适当采样和储存对确保分子诊断测试准确性的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcd2/7539256/c01ad19ea599/13568_2020_1112_Fig1_HTML.jpg

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