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用于检测粪便样本中野生型A组轮状病毒株及疫苗株(Rotarix®和RotaTeq®)并进行基因分型的一步多重实时逆转录聚合酶链反应检测法。

One-step multiplex real-time RT-PCR assay for detecting and genotyping wild-type group A rotavirus strains and vaccine strains (Rotarix® and RotaTeq®) in stool samples.

作者信息

Gautam Rashi, Mijatovic-Rustempasic Slavica, Esona Mathew D, Tam Ka Ian, Quaye Osbourne, Bowen Michael D

机构信息

Division of Viral Diseases, Gastroenteritis and Respiratory Viruses Laboratory Branch, Centers for Disease Control and Prevention , Atlanta, Georgia , United States of America.

出版信息

PeerJ. 2016 Jan 11;4:e1560. doi: 10.7717/peerj.1560. eCollection 2016.

Abstract

Background. Group A rotavirus (RVA) infection is the major cause of acute gastroenteritis (AGE) in young children worldwide. Introduction of two live-attenuated rotavirus vaccines, RotaTeq® and Rotarix®, has dramatically reduced RVA associated AGE and mortality in developed as well as in many developing countries. High-throughput methods are needed to genotype rotavirus wild-type strains and to identify vaccine strains in stool samples. Quantitative RT-PCR assays (qRT-PCR) offer several advantages including increased sensitivity, higher throughput, and faster turnaround time. Methods. In this study, a one-step multiplex qRT-PCR assay was developed to detect and genotype wild-type strains and vaccine (Rotarix® and RotaTeq®) rotavirus strains along with an internal processing control (Xeno or MS2 RNA). Real-time RT-PCR assays were designed for VP7 (G1, G2, G3, G4, G9, G12) and VP4 (P[4], P[6] and P[8]) genotypes. The multiplex qRT-PCR assay also included previously published NSP3 qRT-PCR for rotavirus detection and Rotarix® NSP2 and RotaTeq® VP6 qRT-PCRs for detection of Rotarix® and RotaTeq® vaccine strains respectively. The multiplex qRT-PCR assay was validated using 853 sequence confirmed stool samples and 24 lab cultured strains of different rotavirus genotypes. By using thermostable rTth polymerase enzyme, dsRNA denaturation, reverse transcription (RT) and amplification (PCR) steps were performed in single tube by uninterrupted thermocycling profile to reduce chances of sample cross contamination and for rapid generation of results. For quantification, standard curves were generated using dsRNA transcripts derived from RVA gene segments. Results. The VP7 qRT-PCRs exhibited 98.8-100% sensitivity, 99.7-100% specificity, 85-95% efficiency and a limit of detection of 4-60 copies per singleplex reaction. The VP7 qRT-PCRs exhibited 81-92% efficiency and limit of detection of 150-600 copies in multiplex reactions. The VP4 qRT-PCRs exhibited 98.8-100% sensitivity, 100% specificity, 86-89% efficiency and a limit of detection of 12-400 copies per singleplex reactions. The VP4 qRT-PCRs exhibited 82-90% efficiency and limit of detection of 120-4000 copies in multiplex reaction. Discussion. The one-step multiplex qRT-PCR assay will facilitate high-throughput rotavirus genotype characterization for monitoring circulating rotavirus wild-type strains causing rotavirus infections, determining the frequency of Rotarix® and RotaTeq® vaccine strains and vaccine-derived reassortants associated with AGE, and help to identify novel rotavirus strains derived by reassortment between vaccine and wild-type strains.

摘要

背景。A组轮状病毒(RVA)感染是全球幼儿急性胃肠炎(AGE)的主要病因。两种减毒活轮状病毒疫苗,即RotaTeq®和Rotarix®的引入,已显著降低了发达国家以及许多发展中国家与RVA相关的AGE和死亡率。需要高通量方法来对轮状病毒野生型菌株进行基因分型,并在粪便样本中鉴定疫苗菌株。定量逆转录聚合酶链反应(qRT-PCR)检测具有多种优势,包括更高的灵敏度、更高的通量以及更快的周转时间。方法。在本研究中,开发了一种一步多重qRT-PCR检测方法,用于检测野生型菌株以及疫苗(Rotarix®和RotaTeq®)轮状病毒菌株并进行基因分型,同时设置内部处理对照(Xeno或MS2 RNA)。针对VP7(G1、G2、G3、G4、G9、G12)和VP(P[4]、P[6]和P[8])基因型设计了实时RT-PCR检测方法。该多重qRT-PCR检测还包括先前发表的用于轮状病毒检测的NSP3 qRT-PCR,以及分别用于检测Rotarix®和RotaTeq®疫苗菌株的Rotarix® NSP2和RotaTeq® VP6 qRT-PCR。使用853份经序列确认的粪便样本和24株不同轮状病毒基因型的实验室培养菌株对该多重qRT-PCR检测进行了验证。通过使用热稳定的rTth聚合酶,在单管中通过不间断的热循环程序进行双链RNA变性、逆转录(RT)和扩增(PCR)步骤,以减少样本交叉污染的机会并快速获得结果。为了进行定量,使用源自RVA基因片段的双链RNA转录本生成标准曲线。结果。VP7 qRT-PCR的灵敏度为98.8 - 100%,特异性为99.7 - 100%,效率为85 - 95%,单重反应的检测限为每反应4 - 60个拷贝。在多重反应中,VP7 qRT-PCR的效率为81 - 92%,检测限为150 - 600个拷贝。VP4 qRT-PCR的灵敏度为98.8 - 100%,特异性为100%,效率为86 - 89%,单重反应的检测限为每反应12 - 400个拷贝。在多重反应中,VP4 qRT-PCR的效率为82 - 90%,检测限为120 - 4000个拷贝。讨论。这种一步多重qRT-PCR检测将有助于进行高通量轮状病毒基因分型,以监测导致轮状病毒感染的循环轮状病毒野生型菌株,确定Rotarix®和RotaTeq®疫苗菌株以及与AGE相关的疫苗衍生重配株的频率,并有助于识别通过疫苗株与野生型菌株重配产生的新型轮状病毒菌株。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e57c/4734446/8502f4535ca7/peerj-04-1560-g001.jpg

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