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应用基因型特异性实时 RT-PCR 检测方法监测五型 Rotateq 疫苗病毒的脱落情况。

Monitoring Shedding of Five Genotypes of RotaTeq Vaccine Viruses by Genotype-Specific Real-Time Reverse Transcription-PCR Assays.

机构信息

Faculty of Medical Technology, Fujita Health University School of Health Sciences, Toyoake, Aichi, Japan.

Faculty of Clinical Engineering, Fujita Health University School of Health Sciences, Toyoake, Aichi, Japan.

出版信息

J Clin Microbiol. 2018 May 25;56(6). doi: 10.1128/JCM.00035-18. Print 2018 Jun.

Abstract

RotaTeq (RV5) is a widely used live attenuated pentavalent rotavirus (RV) vaccine. Although fecal shedding of RV vaccine strains persists for long time periods, it is unclear how each vaccine strain replicates in intestinal tissue and is excreted in stool. To examine this issue, we established RV5 genotype-specific real-time reverse transcription-PCR (RT-PCR) assays. Five real-time RT-PCR assays were designed for the VP7 gene in genotypes G1, G2, G3, G4, and G6. All assays exhibited excellent linearity, and the detection limit was 1 infectious unit (IU)/reaction for G2, G4, and G6 and 10 IUs/reaction for G1 and G3. No cross-reactivity was observed among G genotypes. The inter- and intra-assay coefficients of variation were less than 3%. The assays were used to examine 129 stool samples collected from eight infants who received RV5. In cases 1 and 2, who received three rounds of vaccination, RV shedding decreased gradually with the number of vaccinations. G1 and G6 shedding appeared to be predominant in comparison to shedding of the other genotypes. Patterns of fecal shedding of the five genotypes of vaccine viruses differed between the eight vaccine recipients. RV5 genotype-specific real-time RT-PCR assays will be useful to study the molecular biology of RV5 replication in infants and experimental animals.

摘要

Rotateq (RV5) 是一种广泛使用的减毒五价轮状病毒 (RV) 疫苗。尽管 RV 疫苗株的粪便排出持续很长时间,但不清楚每种疫苗株如何在肠道组织中复制并在粪便中排出。为了研究这个问题,我们建立了 RV5 基因型特异性实时逆转录 PCR (RT-PCR) 检测方法。针对基因型 G1、G2、G3、G4 和 G6 的 VP7 基因设计了 5 种实时 RT-PCR 检测方法。所有检测方法均表现出优异的线性,检测限为 G2、G4 和 G6 的 1 个感染单位 (IU)/反应,G1 和 G3 的 10 IU/反应。G 基因型之间无交叉反应。组内和组间变异系数均小于 3%。该检测方法用于检测 8 名接受 RV5 疫苗接种的婴儿的 129 份粪便样本。在接受三轮疫苗接种的病例 1 和 2 中,随着接种次数的增加,RV 排出逐渐减少。与其他基因型相比,G1 和 G6 的排出似乎更为明显。8 名疫苗接种者的五种疫苗病毒基因型的粪便排出模式不同。RV5 基因型特异性实时 RT-PCR 检测方法将有助于研究 RV5 在婴儿和实验动物中的复制分子生物学。

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