Literature DB >> 2116213

Enterically-transmitted non-A, non-B hepatitis.

D W Bradley1.   

Abstract

More than 50% of acute viral hepatitis occurring in some developing countries appears to be unrelated to infection by HAV or HBV and accumulating evidence suggests that a high proportion of this non-A, non-B hepatitis (NANB) is enterically transmitted. Epidemics or outbreaks of enterically-transmitted NANB (ET-NANB) have been documented in the Soviet Union, Nepal, Burma, Pakistan, India, Borneo, Somalia, Sudan, Ivory Coast, Algeria, and Mexico. These outbreaks primarily affect young to middle-age adults and are often associated with a high mortality rate in infected pregnant women, approaching 20% in most reported epidemics. Several investigators have reported finding 27 to 34 nm virus-like particles (VLPs) in stools of acutely infected cases. Stools containing these small, non-enveloped VLPs have been shown to cause NANB in experimentally infected cynomolgus macaques, African green monkeys, chimpanzees, rhesus monkeys, and Saguinus mystax monkeys (tamarins). Infected primates have been shown to seroconvert to 27-34 nm VLPs recovered from stools of cases occurring in the Soviet Union, India, Nepal, Burma, Pakistan and/or Mexico, suggesting that ET-NANB is caused by one virus or class of serologically related viruses. The morphological features and physicochemical properties of one candidate virus are very similar to those of some human caliciviruses, a group of viruses that is normally associated with outbreaks of severe diarrhoea.

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Year:  1990        PMID: 2116213     DOI: 10.1093/oxfordjournals.bmb.a072409

Source DB:  PubMed          Journal:  Br Med Bull        ISSN: 0007-1420            Impact factor:   4.291


  40 in total

Review 1.  Hepatitis E virus.

Authors:  A J Zuckerman
Journal:  BMJ       Date:  1990-06-09

Review 2.  Sexually transmitted hepatitis: a review.

Authors:  R J Gilson
Journal:  Genitourin Med       Date:  1992-04

3.  The ORF3 protein of hepatitis E virus is a phosphoprotein that associates with the cytoskeleton.

Authors:  M Zafrullah; M H Ozdener; S K Panda; S Jameel
Journal:  J Virol       Date:  1997-12       Impact factor: 5.103

4.  The 41-amino-acid C-terminal region of the hepatitis E virus ORF3 protein interacts with bikunin, a kunitz-type serine protease inhibitor.

Authors:  Shweta Tyagi; Milan Surjit; Sunil K Lal
Journal:  J Virol       Date:  2005-09       Impact factor: 5.103

Review 5.  Calicivirus emergence from ocean reservoirs: zoonotic and interspecies movements.

Authors:  A W Smith; D E Skilling; N Cherry; J H Mead; D O Matson
Journal:  Emerg Infect Dis       Date:  1998 Jan-Mar       Impact factor: 6.883

6.  The role of hepatitis E virus in acute sporadic non-A, non-B hepatitis.

Authors:  I Köksal; K Aydin; B Kardes; H Turgut; F Murt
Journal:  Infection       Date:  1994 Nov-Dec       Impact factor: 3.553

7.  Detection of hepatitis E virus in raw and treated wastewater with the polymerase chain reaction.

Authors:  N Jothikumar; K Aparna; S Kamatchiammal; R Paulmurugan; S Saravanadevi; P Khanna
Journal:  Appl Environ Microbiol       Date:  1993-08       Impact factor: 4.792

8.  Self-association and mapping of the interaction domain of hepatitis E virus ORF3 protein.

Authors:  S Tyagi; S Jameel; S K Lal
Journal:  J Virol       Date:  2001-03       Impact factor: 5.103

9.  The ORF2 protein of hepatitis E virus binds the 5' region of viral RNA.

Authors:  Milan Surjit; Shahid Jameel; Sunil K Lal
Journal:  J Virol       Date:  2004-01       Impact factor: 5.103

10.  Expression in animal cells and characterization of the hepatitis E virus structural proteins.

Authors:  S Jameel; M Zafrullah; M H Ozdener; S K Panda
Journal:  J Virol       Date:  1996-01       Impact factor: 5.103

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