Validation of an automated real-time PCR protocol for detection and quantitation of HIV and HCV genomes in semen

• Published in: Journal of virological methods 2006-10, Vol.137 (1), p.156-159
• Main Authors: Pasquier, Christophe, Souyris, Corinne, Moinard, Nathalie, Bujan, Louis, Izopet, Jacques
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; Fundamental and applied biological sciences. Psychology; Genome, Viral; HCV; Hepacivirus - genetics; Hepacivirus - isolation & purification; Hepatitis C - virology; Hepatitis C virus; HIV; HIV - genetics; HIV - isolation & purification; HIV Infections - virology; Human immunodeficiency virus; Humans; Male; Microbiology; Polymerase Chain Reaction - methods; Real-time PCR; RNA, Viral - analysis; RNA, Viral - genetics; Semen; Semen - virology; Sensitivity and Specificity; Techniques used in virology; Virology
• ISSN: 0166-0934; 1879-0984
• DOI: 10.1016/j.jviromet.2006.05.023

The ability to detect and quantify HIV and HCV genomes is important for checking spermatozoid preparation protocols also known as “sperm washing”. But no commercial assay is available. A method was developed for detecting HIV and HCV in semen fractions using the COBAS Ampliprep™ and COBAS Taqman™ instruments. It will detect fewer than 200 copies of HIV RNA per ml of semen plasma and fewer than 200 copies/3 × 10 6 semen cells. The sensitivity for HCV is similar at more than 200 IU/ml and below 200 IU/3 × 10 6 semen cells. No inhibitor of PCR amplification was detected. This automated protocol permits a convenient, standardized testing for HIV and HCV in semen. The performance is the same as that of the previous generation of automated assays but the cost and operating time are both reduced.