Low level or absent in vivo replication of hepatitis C virus and hepatitis G virus/GB virus C in peripheral blood mononuclear cells
J Mellor, G Haydon, C Blair, W Livingstone and P Simmonds Department of Medical Microbiology, University of Edinburgh, UK. To investigate which subsets of peripheral blood mononuclear cells (PBMCs) are susceptible to infection with hepatitis C virus (HCV) and hepatitis G virus (HGV) or GB virus C (G...
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Published in | Journal of general virology Vol. 79; no. 4; pp. 705 - 714 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
England
Soc General Microbiol
01.04.1998
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Subjects | |
Online Access | Get full text |
ISSN | 0022-1317 1465-2099 |
DOI | 10.1099/0022-1317-79-4-705 |
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Abstract | J Mellor, G Haydon, C Blair, W Livingstone and P Simmonds
Department of Medical Microbiology, University of Edinburgh, UK.
To investigate which subsets of peripheral blood mononuclear cells (PBMCs)
are susceptible to infection with hepatitis C virus (HCV) and hepatitis G
virus (HGV) or GB virus C (GBV-C), a PCR-based assay using tagged primers
in the core region (HCV) and NS3 region (HGV/GBV-C) for the specific
detection of negative strand (replicating) viral RNA sequences was
developed. In liver biopsy samples both positive and negative strands of
HCV RNA were detected, at levels ranging from 3 to 11 x 10(6) RNA copies
per 10(6) cells and 3.7-4.2 x 10(3) copies per 10(6) cells respectively,
while lower frequencies of positive strands of GBV-C/HGV RNA were detected
(from 13 biopsies, the highest frequency was 7.3 x 10(3) per 10(6) cells).
In no samples were negative RNA strands detected. To investigate
extra-hepatic replication of HCV and GBV-C/HGV, CD4+, CD8+ and B
lymphocytes, monocytes and putative dendritic cell populations were
separated from PBMCs from ten study subjects. Detection of positive strand
HCV RNA was largely confined to B lymphocytes (at levels of up to 5 x 10(3)
copies per 10(6) cells), while detection of negative strands was confined
to a single subset (dendritic cells) of one of the study individuals.
Similarly, GBV-C/HGV was detected at low levels in only twelve of twenty
PBMC samples, while negative strands were uniformly absent. The low levels
of HCV and GBV- C/HGV RNA in PBMCs suggest that these cells are at most a
minor reservoir for virus replication. The absence of detectable
replication of GBV-C/HGV suggests that the actual site of GBV-C/HGV
replication remains to be discovered. |
---|---|
AbstractList | To investigate which subsets of peripheral blood mononuclear cells (PBMCs) are susceptible to infection with hepatitis C virus (HCV) and hepatitis G virus (HGV) or GB virus C (GBV-C), a PCR-based assay using tagged primers in the core region (HCV) and NS3 region (HGV/GBV-C) for the specific detection of negative strand (replicating) viral RNA sequences was developed. In liver biopsy samples both positive and negative strands of HCV RNA were detected, at levels ranging from 3 to 11 x 10 super(6) RNA copies per 10 super(6) cells and 3.7-4.2 x 10 super(3) copies per 10 super(6) cells respectively, while lower frequencies of positive strands of GBV-C/HGV RNA were detected (from 13 biopsies, the highest frequency was 7.3 x 10 super(3) per 10 super(6) cells). In no samples were negative RNA strands detected. To investigate extra-hepatic replication of HCV and GBV-C/HGV, CD4 super(+), CD8 super(+) and B lymphocytes, monocytes and putative dendritic cell populations were separated from PBMCs from ten study subjects. Detection of positive strand HCV RNA was largely confined to B lymphocytes (at levels of up to 5 x 10 super(3) copies per 10 super(6) cells), while detection of negative strands was confined to a single subset (dendritic cells) of one of the study individuals. Similarly, GBV-C/HGV was detected at low levels in only twelve of twenty PBMC samples, while negative strands were uniformly absent. The low levels of HCV and GBV-C/HGV RNA in PBMCs suggest that these cells are at most a minor reservoir for virus replication. The absence of detectable replication of GBV-C/HGV suggests that the actual site of GBV-C/HGV replication remains to be discovered. To investigate which subsets of peripheral blood mononuclear cells (PBMCs) are susceptible to infection with hepatitis C virus (HCV) and hepatitis G virus (HGV) or GB virus C (GBV-C), a PCR-based assay using tagged primers in the core region (HCV) and NS3 region (HGV/GBV-C) for the specific detection of negative strand (replicating) viral RNA sequences was developed. In liver biopsy samples both positive and negative strands of HCV RNA were detected, at levels ranging from 3 to 11 x 10(6) RNA copies per 10(6) cells and 3.7-4.2 x 10(3) copies per 10(6) cells respectively, while lower frequencies of positive strands of GBV-C/HGV RNA were detected (from 13 biopsies, the highest frequency was 7.3 x 10(3) per 10(6) cells). In no samples were negative RNA strands detected. To investigate extra-hepatic replication of HCV and GBV-C/HGV, CD4+, CD8+ and B lymphocytes, monocytes and putative dendritic cell populations were separated from PBMCs from ten study subjects. Detection of positive strand HCV RNA was largely confined to B lymphocytes (at levels of up to 5 x 10(3) copies per 10(6) cells), while detection of negative strands was confined to a single subset (dendritic cells) of one of the study individuals. Similarly, GBV-C/HGV was detected at low levels in only twelve of twenty PBMC samples, while negative strands were uniformly absent. The low levels of HCV and GBV-C/HGV RNA in PBMCs suggest that these cells are at most a minor reservoir for virus replication. The absence of detectable replication of GBV-C/HGV suggests that the actual site of GBV-C/HGV replication remains to be discovered.To investigate which subsets of peripheral blood mononuclear cells (PBMCs) are susceptible to infection with hepatitis C virus (HCV) and hepatitis G virus (HGV) or GB virus C (GBV-C), a PCR-based assay using tagged primers in the core region (HCV) and NS3 region (HGV/GBV-C) for the specific detection of negative strand (replicating) viral RNA sequences was developed. In liver biopsy samples both positive and negative strands of HCV RNA were detected, at levels ranging from 3 to 11 x 10(6) RNA copies per 10(6) cells and 3.7-4.2 x 10(3) copies per 10(6) cells respectively, while lower frequencies of positive strands of GBV-C/HGV RNA were detected (from 13 biopsies, the highest frequency was 7.3 x 10(3) per 10(6) cells). In no samples were negative RNA strands detected. To investigate extra-hepatic replication of HCV and GBV-C/HGV, CD4+, CD8+ and B lymphocytes, monocytes and putative dendritic cell populations were separated from PBMCs from ten study subjects. Detection of positive strand HCV RNA was largely confined to B lymphocytes (at levels of up to 5 x 10(3) copies per 10(6) cells), while detection of negative strands was confined to a single subset (dendritic cells) of one of the study individuals. Similarly, GBV-C/HGV was detected at low levels in only twelve of twenty PBMC samples, while negative strands were uniformly absent. The low levels of HCV and GBV-C/HGV RNA in PBMCs suggest that these cells are at most a minor reservoir for virus replication. The absence of detectable replication of GBV-C/HGV suggests that the actual site of GBV-C/HGV replication remains to be discovered. J Mellor, G Haydon, C Blair, W Livingstone and P Simmonds Department of Medical Microbiology, University of Edinburgh, UK. To investigate which subsets of peripheral blood mononuclear cells (PBMCs) are susceptible to infection with hepatitis C virus (HCV) and hepatitis G virus (HGV) or GB virus C (GBV-C), a PCR-based assay using tagged primers in the core region (HCV) and NS3 region (HGV/GBV-C) for the specific detection of negative strand (replicating) viral RNA sequences was developed. In liver biopsy samples both positive and negative strands of HCV RNA were detected, at levels ranging from 3 to 11 x 10(6) RNA copies per 10(6) cells and 3.7-4.2 x 10(3) copies per 10(6) cells respectively, while lower frequencies of positive strands of GBV-C/HGV RNA were detected (from 13 biopsies, the highest frequency was 7.3 x 10(3) per 10(6) cells). In no samples were negative RNA strands detected. To investigate extra-hepatic replication of HCV and GBV-C/HGV, CD4+, CD8+ and B lymphocytes, monocytes and putative dendritic cell populations were separated from PBMCs from ten study subjects. Detection of positive strand HCV RNA was largely confined to B lymphocytes (at levels of up to 5 x 10(3) copies per 10(6) cells), while detection of negative strands was confined to a single subset (dendritic cells) of one of the study individuals. Similarly, GBV-C/HGV was detected at low levels in only twelve of twenty PBMC samples, while negative strands were uniformly absent. The low levels of HCV and GBV- C/HGV RNA in PBMCs suggest that these cells are at most a minor reservoir for virus replication. The absence of detectable replication of GBV-C/HGV suggests that the actual site of GBV-C/HGV replication remains to be discovered. To investigate which subsets of peripheral blood mononuclear cells (PBMCs) are susceptible to infection with hepatitis C virus (HCV) and hepatitis G virus (HGV) or GB virus C (GBV-C), a PCR-based assay using tagged primers in the core region (HCV) and NS3 region (HGV/GBV-C) for the specific detection of negative strand (replicating) viral RNA sequences was developed. In liver biopsy samples both positive and negative strands of HCV RNA were detected, at levels ranging from 3 to 11 x 10(6) RNA copies per 10(6) cells and 3.7-4.2 x 10(3) copies per 10(6) cells respectively, while lower frequencies of positive strands of GBV-C/HGV RNA were detected (from 13 biopsies, the highest frequency was 7.3 x 10(3) per 10(6) cells). In no samples were negative RNA strands detected. To investigate extra-hepatic replication of HCV and GBV-C/HGV, CD4+, CD8+ and B lymphocytes, monocytes and putative dendritic cell populations were separated from PBMCs from ten study subjects. Detection of positive strand HCV RNA was largely confined to B lymphocytes (at levels of up to 5 x 10(3) copies per 10(6) cells), while detection of negative strands was confined to a single subset (dendritic cells) of one of the study individuals. Similarly, GBV-C/HGV was detected at low levels in only twelve of twenty PBMC samples, while negative strands were uniformly absent. The low levels of HCV and GBV-C/HGV RNA in PBMCs suggest that these cells are at most a minor reservoir for virus replication. The absence of detectable replication of GBV-C/HGV suggests that the actual site of GBV-C/HGV replication remains to be discovered. |
Author | Mellor, J Livingstone, W Haydon, G Blair, C Simmonds, P |
Author_xml | – sequence: 1 fullname: Mellor, J – sequence: 2 fullname: Haydon, G – sequence: 3 fullname: Blair, C – sequence: 4 fullname: Livingstone, W – sequence: 5 fullname: Simmonds, P |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/9568964$$D View this record in MEDLINE/PubMed |
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Snippet | J Mellor, G Haydon, C Blair, W Livingstone and P Simmonds
Department of Medical Microbiology, University of Edinburgh, UK.
To investigate which subsets of... To investigate which subsets of peripheral blood mononuclear cells (PBMCs) are susceptible to infection with hepatitis C virus (HCV) and hepatitis G virus... |
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SubjectTerms | B-Lymphocytes - virology Base Sequence Dendritic Cells - virology DNA Primers - genetics Flaviviridae - genetics Flaviviridae - pathogenicity Flaviviridae - physiology Hepacivirus - genetics Hepacivirus - pathogenicity Hepacivirus - physiology Hepatitis C - virology Hepatitis, Viral, Human - virology Humans Leukocytes, Mononuclear - virology Liver - virology Monocytes - virology Polymerase Chain Reaction - methods Polymerase Chain Reaction - statistics & numerical data RNA, Viral - analysis RNA, Viral - blood RNA, Viral - genetics Sensitivity and Specificity Viremia - virology Virus Replication |
Title | Low level or absent in vivo replication of hepatitis C virus and hepatitis G virus/GB virus C in peripheral blood mononuclear cells |
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