Post-PCR sterilization : development and application to an HIV-1 diagnostic assay

• Published in: Nucleic acids research Vol. 19; no. 1; pp. 109 - 116
• Main Authors: ISAACS, S. T, TESSMAN, J. W, METCHETTE, K. C, HEARST, J. E, CIMINO, G. D
• Format: Journal Article
• Language: English
• Published: Oxford Oxford University Press 11.01.1991
• Subjects: AIDS/HIV; Base Sequence; Biological and medical sciences; Biotechnology; DNA, Viral - analysis; Fundamental and applied biological sciences. Psychology; Furocoumarins - chemistry; Genetic engineering; Genetic technics; HIV Seropositivity - diagnosis; HIV-1 - genetics; Human immunodeficiency virus 1; Humans; In vitro gene amplification. Pcr technique; Methods. Procedures. Technologies; Molecular Sequence Data; Photochemistry; Polymerase Chain Reaction - methods; Virus; Human; HIV-1 virus; Photochemical method; Sterilization; Retroviridae; Lentivirinae; Artefact; Human immunodeficiency virus; Diagnosis
• ISSN: 0305-1048; 1362-4962
• DOI: 10.1093/nar/19.1.109

We have developed an effective post-PCR sterilization process and have applied the procedure to a diagnostic assay for HIV-1. The method, which is based on isopsoralen photochemistry, satisfies both the inactivation and hybridization requirements of a practical sterilization process. The key feature of the technique is the use of isopsoralen compounds which form covalent photochemical adducts with DNA. These covalent adducts prevent subsequent extension of previously amplified sequences (amplicons) by Taq polymerase. Isopsoralens have minimal inhibitory effect on the PCR, are activated by long wavelength ultraviolet light, provide sufficient numbers of covalent adducts to impart effective sterilization, modify the amplified sequence such that it remains single-stranded, and have little effect on subsequent hybridization. The sterilization procedure can be applied to a closed system and is suitable for use with commonly used detection formats. The photochemical sterilization protocol we have devised is an effective and pragmatic method for eliminating the amplicon carryover problem associated with the PCR. While the work described here is limited to HIV-1, proper use of the technique will relieve the concern associated with carryover for a wide variety of amplicons, especially in the clinical setting.