Literature DB >> 8046390

Human enteric Caliciviridae: a new prevalent small round-structured virus group defined by RNA-dependent RNA polymerase and capsid diversity.

S M Green1, K E Dingle, P R Lambden, E O Caul, C R Ashley, I N Clarke.   

Abstract

Sequence comparison of the RNA-dependent RNA polymerases of small round-structured viruses (SRSVs) from 10 recent U.K. outbreaks of gastroenteritis revealed significant genetic variation. Computer analyses indicated that these viruses can be divided into two discrete groups. SRSV group I contains the previously characterized antigenic type 1 Norwalk and type 3 Southampton viruses. The amino acid sequences of the RNA polymerase, capsid and ORF3 of these two viruses are relatively similar (about 92%, 69% and 72% amino acid identity, respectively). A representative member of group II SRSVs, Bristol virus, was subjected to a detailed genetic analysis. Bristol virus is a recent antigenic type 2 isolate from a U.K. hospital outbreak of gastroenteritis. Using a single clinical sample the 3'-terminal 3881 nucleotide cDNA sequence [excluding the poly(A) tail] of this virus was determined. Analysis of the sequence revealed significant differences from those of group I viruses with the RNA polymerase region, capsid and ORF3 showing only about 62%, 43% and 30% amino acid identity respectively with the equivalent proteins of the Norwalk and Southampton viruses. These data suggest that the morphologically identical SRSVs belong to at least two genetically distinct groups.

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Year:  1994        PMID: 8046390     DOI: 10.1099/0022-1317-75-8-1883

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  34 in total

1.  Outbreaks of gastroenteritis caused by SRSVs from 1987 to 1992 in Kyushu, Japan: four outbreaks associated with oyster consumption.

Authors:  R Otsu
Journal:  Eur J Epidemiol       Date:  1999-02       Impact factor: 8.082

2.  Broadly reactive and highly sensitive assay for Norwalk-like viruses based on real-time quantitative reverse transcription-PCR.

Authors:  Tsutomu Kageyama; Shigeyuki Kojima; Michiyo Shinohara; Kazue Uchida; Shuetsu Fukushi; Fuminori B Hoshino; Naokazu Takeda; Kazuhiko Katayama
Journal:  J Clin Microbiol       Date:  2003-04       Impact factor: 5.948

3.  Study of Norwalk virus and Mexico virus infections at Ga-Rankuwa Hospital, Ga-Rankuwa, South Africa.

Authors:  T K Smit; A D Steele; I Peenze; X Jiang; M K Estes
Journal:  J Clin Microbiol       Date:  1997-09       Impact factor: 5.948

4.  Molecular surveillance of enterovirus and norwalk-like virus in oysters relocated to a municipal-sewage-impacted gulf estuary.

Authors:  Y Carol Shieh; Ralph S Baric; Jacquelina W Woods; Kevin R Calci
Journal:  Appl Environ Microbiol       Date:  2003-12       Impact factor: 4.792

5.  Detection, quantitation, and phylogenetic analysis of noroviruses in Japanese oysters.

Authors:  Tomoko Nishida; Hirokazu Kimura; Mika Saitoh; Michiyo Shinohara; Masahiko Kato; Shinji Fukuda; Tetsuya Munemura; Toshiyuki Mikami; Ayumi Kawamoto; Miho Akiyama; Yumiko Kato; Kanako Nishi; Kunihisa Kozawa; Osamu Nishio
Journal:  Appl Environ Microbiol       Date:  2003-10       Impact factor: 4.792

6.  Detection of noroviruses in tap water in Japan by means of a new method for concentrating enteric viruses in large volumes of freshwater.

Authors:  Eiji Haramoto; Hiroyuki Katayama; Shinichiro Ohgaki
Journal:  Appl Environ Microbiol       Date:  2004-04       Impact factor: 4.792

7.  Reverse transcription-booster PCR for detection of noroviruses in shellfish.

Authors:  Dario De Medici; Luciana Croci; Elisabetta Suffredini; Laura Toti
Journal:  Appl Environ Microbiol       Date:  2004-10       Impact factor: 4.792

8.  Virological, serological, and clinical features of an outbreak of acute gastroenteritis due to recombinant genogroup II norovirus in an infant home.

Authors:  Takeshi Tsugawa; Kazuko Numata-Kinoshita; Shinjiro Honma; Shuji Nakata; Masatoshi Tatsumi; Yoshiyuki Sakai; Katsuro Natori; Naokazu Takeda; Shinichi Kobayashi; Hiroyuki Tsutsumi
Journal:  J Clin Microbiol       Date:  2006-01       Impact factor: 5.948

9.  A one-tube method of reverse transcription-PCR to efficiently amplify a 3-kilobase region from the RNA polymerase gene to the poly(A) tail of small round-structured viruses (Norwalk-like viruses).

Authors:  T Ando; S S Monroe; J S Noel; R I Glass
Journal:  J Clin Microbiol       Date:  1997-03       Impact factor: 5.948

10.  Polyprotein processing in Southampton virus: identification of 3C-like protease cleavage sites by in vitro mutagenesis.

Authors:  B Liu; I N Clarke; P R Lambden
Journal:  J Virol       Date:  1996-04       Impact factor: 5.103

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