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Published in: Virology Journal 1/2014

Open Access 01-12-2014 | Short report

Genetic heterogeneity of hepatitis C virus cell entry receptors seems to have no influence on selection of virus variants

Authors: Maren Lipskoch, Manfred Wiese, Joerg Timm, Michael Roggendorf, Sergei Viazov

Published in: Virology Journal | Issue 1/2014

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Abstract

Background

No information is available on the possible influence of the genetic heterogeneity of major hepatitis C virus (HCV) cell receptors on selection of virus variants.

Findings

Anti-D globulin preparations contaminated with the HCV strain AD78 caused hepatitis C infection in more than 3000 women in East Germany in 1978. Analysis of the core to NS2 gene sequences of this strain in several globulin batches revealed the presence of three closely related but distinct virus variants of the same strain. Apparently even distribution of these three virus variants was observed in 91 patients infected with the AD78 strain. None of these patients was infected with more than one virus variant, suggesting a selection mechanism of a particular virus variant in each patient. To verify the hypothesis that heterogeneity of HCV cell receptors might influence the virus variant selection, single-nucleotide polymorphisms (SNPs) in low-density lipoprotein receptor (LDLR), occludin (OCLN), and scavenger receptor B1 (SCARB1) genes in AD patients were analyzed. No evident correlation between receptor polymorphisms and presence of a particular virus variant was noted.

Conclusion

SNPs of HCV cell entry receptors have no influence on virus selection in patients infected with an inoculum containing different virus variants.
Appendix
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Metadata
Title
Genetic heterogeneity of hepatitis C virus cell entry receptors seems to have no influence on selection of virus variants
Authors
Maren Lipskoch
Manfred Wiese
Joerg Timm
Michael Roggendorf
Sergei Viazov
Publication date
01-12-2014
Publisher
BioMed Central
Published in
Virology Journal / Issue 1/2014
Electronic ISSN: 1743-422X
DOI
https://doi.org/10.1186/1743-422X-11-50

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