Your browser doesn't support javascript.
loading
Broadly reactive real-time reverse transcription-polymerase chain reaction assay for the detection of human sapovirus genotypes.
Oka, Tomoichiro; Iritani, Nobuhiro; Yamamoto, Seiji P; Mori, Kohji; Ogawa, Tomoko; Tatsumi, Chika; Shibata, Shinichiro; Harada, Seiya; Wu, Fang-Tzy.
Affiliation
  • Oka T; Department of Virology II, National Institute of Infectious Diseases, Tokyo, Japan.
  • Iritani N; Division of Microbiology, Osaka Institute of Public Health, Osaka, Japan.
  • Yamamoto SP; Division of Microbiology, Osaka Institute of Public Health, Osaka, Japan.
  • Mori K; Department of Microbiology, Tokyo Metropolitan Institute of Public Health, Tokyo, Japan.
  • Ogawa T; Division of Virology, Chiba Prefectural Institute of Public Health, Chiba, Japan.
  • Tatsumi C; Division of Virology, Shimane Prefectural Institute of Public Health and Environmental Science, Shimane, Japan.
  • Shibata S; Microbiology Department, Nagoya City Public Health Research Institute, Aichi, Japan.
  • Harada S; Department of Microbiology, Kumamoto Prefectural Institute of Public Health and Environmental Science, Kumamoto, Japan.
  • Wu FT; Center for Research, Diagnostics and Vaccine Development, Taiwan Centers for Disease Control, Taipei, Taiwan.
J Med Virol ; 91(3): 370-377, 2019 03.
Article in En | MEDLINE | ID: mdl-30320885
Sapoviruses are associated with acute gastroenteritis. Human sapoviruses are classified into four distinct genogroups (GI, GII, GIV, and GV) based on their capsid gene sequences. A TaqMan probe-based real-time reverse transcription-polymerase chain reaction (RT-PCR) assay that detects the representative strains of these four genogroups is widely used for screening fecal specimens, shellfish, and environmental water samples. However, since the development of this test, more genetically diverse sapovirus strains have been reported, which are not detectable by the previously established assays. In this study, we report the development of a broader-range sapovirus real-time RT-PCR assay. The assay can detect 2.5 × 107 and 2.5 × 10 1 copies of sapovirus and therefore is as sensitive as the previous test. Analysis using clinical stool specimens or synthetic DNA revealed that the new system detected strains representative of all the 18 human sapovirus genotypes: GI.1-7, GII.1-8, GIV.1, and GV.1, 2. No cross-reactivity was observed against other representative common enteric viruses (norovirus, rotavirus, astrovirus, and adenovirus). This new assay will be useful as an improved, broadly reactive, and specific screening tool for human sapoviruses.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: RNA, Viral / Sapovirus / Real-Time Polymerase Chain Reaction Type of study: Diagnostic_studies Limits: Humans Language: En Journal: J Med Virol Year: 2019 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: RNA, Viral / Sapovirus / Real-Time Polymerase Chain Reaction Type of study: Diagnostic_studies Limits: Humans Language: En Journal: J Med Virol Year: 2019 Document type: Article Affiliation country: Country of publication: