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Direct detection of hepatitis C virus (HCV) RNA from whole blood, and comparison with HCV RNA in plasma and peripheral blood mononuclear cells

โœ Scribed by Warren N. Schmidt; Donna Klinzman; Douglas R. Labrecque; Donald E. Macfarlane; Jack T. Stapleton


Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
854 KB
Volume
47
Category
Article
ISSN
0146-6615

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โœฆ Synopsis


Abstract

Hepatitis C virus (HCV) requires reverse transcriptaseโ€polymerase chain reaction (RTโ€PCR) or branched DNA signal amplification assays to be detected in patient samples. Although conventional methods of RNA isolation are employed for samples of serum, plasma, and peripheral blood mononuclear cells (PBMCs), whole blood is generally considered an unsuitable source of RNA because of abundant RNases and polyโ€merase inhibitors. Using a cationic surfactant, Catrimoxโ€14, we adapted a procedure for RNA isolation from whole blood, plasma, and PBMCs that yields RNA template suitable for HCV RTโ€PCR. RNA isolation required less than 2 hr, and HCV sequences were easily detected in sample volumes of 50 ฮผl whole blood or plasma, and in less than 1 ร— l0^4^ PBMC. Following the addition of blood to Catrimox, HCV RNA was stable in the mixture when incubated for at least 7 days at room temperature prior to RNA extraction. Comparison of whole blood HCV RNA and plasma HCV RNA from individuals with chronic hepatitis suggests that HCV RNA can be more reliably detected in whole blood. Three of 15 HCV antibody positive patients (20%) had HCV RNA present in whole blood but simultaneously obtained plasma samples were negative. Two of five HCV antibody negative individuals with chronic hepatitis contained HCV RNA in whole blood, yet one of these patient's plasma was negative for viral RNA. The Catrimoxโ€I4 method of RNA purification is useful for detecting HCV RNA in whole blood and blood subfractions, and provides a practical method of measuring plasma and PBMC HCV RNA from clinical specimens. ยฉ 1995 WiIeyโ€Liss, Inc.


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