Specific detection of hepatitis C virus minus strand RNA in hematopoietic cells - PubMed (original) (raw)
Comparative Study
. 1996 Feb 1;97(3):845-51.
doi: 10.1172/JCI118485.
Affiliations
- PMID: 8609243
- PMCID: PMC507124
- DOI: 10.1172/JCI118485
Comparative Study
Specific detection of hepatitis C virus minus strand RNA in hematopoietic cells
H Lerat et al. J Clin Invest. 1996.
Abstract
The presence of hepatitis C virus (HCV) negative strand RNA in extrahepatic compartments based on PCR detection assays has been suggested in many reports with a very heterologous detection rate (from 0 to 100%). In this study, we have analyzed the presence of HCV negative strand in hepatic (liver biopsies, n = 20) and extrahepatic (sera, n = 32; PBMC, n = 26 and fresh bone marrow cells, n = 8) compartments from infected patients with three different reverse transcriptase (RT)-PCR-based assays using primers located in the 5' noncoding region, with or without a tag selected to display different viral loads (10(5)-3 x 10(7) genomic equivalent/ml or gram) and viral genotypes (n = 5). Using synthetic as well as biological templates, we could document extensive artifactual detection of negative strand RNA, due to self priming and mispriming events, even either 5' noncoding region primer pair was used, whereas both artifacts were dramatically reduced (mispriming) or eliminated (selfpriming) using CAP-based RT-PCR assay. Mispriming artifacts were directly correlated to the titer of positive strand RNA present in the sample. Using the CAP-PCR assay, the presence of HCV negative strand RNA was found in 75% of livers (16:20) and only 8% of PBMC, independent of the genotype involved, but could not be documented in sera (0:32) and fresh bone marrow cells (0:6). These findings suggest that caution regarding the type of RT-PCR assay used and the level of HCV positive strand RNA present in the biological sample analyzed has to be taken to avoid false identification of viral reservoirs. The findings suggest that hematopoietic peripheral cells can support HCV replication, although in a very limited number of carriers.
Similar articles
- Hepatitis C virus replicates in peripheral blood mononuclear cells of patients with occult hepatitis C virus infection.
Castillo I, Rodríguez-Iñigo E, Bartolomé J, de Lucas S, Ortíz-Movilla N, López-Alcorocho JM, Pardo M, Carreño V. Castillo I, et al. Gut. 2005 May;54(5):682-5. doi: 10.1136/gut.2004.057281. Gut. 2005. PMID: 15831916 Free PMC article. - Detection of genomic- and minus-strand of hepatitis C virus RNA in the liver of chronic hepatitis C patients by strand-specific semiquantitative reverse-transcriptase polymerase chain reaction.
Negro F, Krawczynski K, Quadri R, Rubbia-Brandt L, Mondelli M, Zarski JP, Hadengue A. Negro F, et al. Hepatology. 1999 Feb;29(2):536-42. doi: 10.1002/hep.510290223. Hepatology. 1999. PMID: 9918932 - [Polymerase chain reaction--principles and clinical relevance].
Blum HE. Blum HE. Praxis (Bern 1994). 1994 Nov 1;83(44):1230-4. Praxis (Bern 1994). 1994. PMID: 7526433 Review. German. - Hepatitis C virus and the brain.
Fletcher NF, McKeating JA. Fletcher NF, et al. J Viral Hepat. 2012 May;19(5):301-6. doi: 10.1111/j.1365-2893.2012.01591.x. J Viral Hepat. 2012. PMID: 22497808 Review.
Cited by
- Evolution of RNA Viruses: Reasons for the Existence of Separate Plus, Minus, and Double-Strand Replication Strategies.
Park H, Higgs PG. Park H, et al. Viruses. 2024 Jul 5;16(7):1081. doi: 10.3390/v16071081. Viruses. 2024. PMID: 39066243 Free PMC article. - Reverse transcription of plasma-derived HIV-1 RNA generates multiple artifacts through tRNA(Lys-3)-priming.
Hardy J, Demecheleer E, Schauvliege M, Staelens D, Mortier V, Verhofstede C. Hardy J, et al. Microbiol Spectr. 2024 Apr 2;12(4):e0387223. doi: 10.1128/spectrum.03872-23. Epub 2024 Mar 5. Microbiol Spectr. 2024. PMID: 38442427 Free PMC article. - Selective ablation of 3' RNA ends and processive RTs facilitate direct cDNA sequencing of full-length host cell and viral transcripts.
Gallardo CM, Nguyen AT, Routh AL, Torbett BE. Gallardo CM, et al. Nucleic Acids Res. 2022 Sep 23;50(17):e98. doi: 10.1093/nar/gkac516. Nucleic Acids Res. 2022. PMID: 35736235 Free PMC article. - Design, development, and validation of a strand-specific RT-qPCR assay for GI and GII human Noroviruses.
König KMK, Jahun AS, Nayak K, Drumright LN, Zibauer M, Goodfellow I, Hosmillo M. König KMK, et al. Wellcome Open Res. 2021 Sep 23;6:245. doi: 10.12688/wellcomeopenres.17078.1. eCollection 2021. Wellcome Open Res. 2021. PMID: 34708158 Free PMC article. - Direct-acting antivirals ability to clear intestinal HCV-RNA in liver transplant patients.
Pietrosi G, Russelli G, Barbera F, Curcio G, Tuzzolino F, Gallo A, Volpes R, Vizzini G, Conaldi PG. Pietrosi G, et al. Transpl Infect Dis. 2020 Oct;22(5):e13345. doi: 10.1111/tid.13345. Epub 2020 Jun 21. Transpl Infect Dis. 2020. PMID: 32495971 Free PMC article.
References
- Nucleic Acids Res. 1985 Sep 11;13(17):6223-36 - PubMed
- Arch Virol. 1994;134(3-4):293-302 - PubMed
- N Engl J Med. 1989 Nov 30;321(22):1494-500 - PubMed
- Lancet. 1990 Jan 6;335(8680):1-3 - PubMed
- Nucleic Acids Res. 1994 May 25;22(10):1919-20 - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous