| Literature DB >> 29563200 |
Yuki Higashimoto1, Masaru Ihira2, Yu Miyazaki1, Ayumi Kuboshiki1, Sayaka Yoshinaga1, Hiroyuki Hiramatsu3, Ryota Suzuki3, Masafumi Miyata4, Hiroki Miura4, Satoshi Komoto5, Jun Yukitake1, Koki Taniguchi5, Yoshiki Kawamura6, Tetsushi Yoshikawa4.
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.Entities:
Keywords: RotaTeq; genotype; human rotavirus; real-time RT-PCR; rotavirus vaccine; shedding
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Year: 2018 PMID: 29563200 PMCID: PMC5971533 DOI: 10.1128/JCM.00035-18
Source DB: PubMed Journal: J Clin Microbiol ISSN: 0095-1137 Impact factor: 5.948