Literature DB >> 1874920

A simple and rapid method for detecting human immunodeficiency virus by PCR.

K M Gibson1, K A McLean, J P Clewley.   

Abstract

A simple, sensitive and specific method using the polymerase chain reaction (PCR) for amplification of human immunodeficiency virus type 1 (HIV-1) is described. The method involves minimal manipulations. Peripheral blood mononuclear cells (PBMC) were prepared by a rapid Ficoll-Paque gradient method. Lymphocytes were lysed in PCR buffer containing Proteinase K and detergents, and subjected to amplification under stringent conditions, using two primer pairs. Amplified DNA sequences were hybridized with a 3'-end labelled probe, electrophoresed on agarose gels and visualised by ethidium bromide staining. Identification of amplified HIV-1 proviral DNA sequences was confirmed by autoradiography. HIV-1 sequences were amplified in all samples from 103 HIV-1 seropositive individuals, but not in 40 HIV-1 seronegative controls. The absence of contamination may be attributable in part to minimisation of manipulations before amplification.

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Year:  1991        PMID: 1874920     DOI: 10.1016/0166-0934(91)90058-8

Source DB:  PubMed          Journal:  J Virol Methods        ISSN: 0166-0934            Impact factor:   2.014


  3 in total

1.  Performance of the Amplicor human immunodeficiency virus type 1 PCR and analysis of specimens with false-negative results.

Authors:  K L Barlow; J H Tosswill; J V Parry; J P Clewley
Journal:  J Clin Microbiol       Date:  1997-11       Impact factor: 5.948

2.  Detection of Trypanosoma cruzi in blood specimens of chronic chagasic patients by polymerase chain reaction amplification of kinetoplast minicircle DNA: comparison with serology and xenodiagnosis.

Authors:  H A Avila; J B Pereira; O Thiemann; E De Paiva; W DeGrave; C M Morel; L Simpson
Journal:  J Clin Microbiol       Date:  1993-09       Impact factor: 5.948

3.  Low human immunodeficiency virus type 1 (HIV-1) DNA burden as a major cause for failure to detect HIV-1 DNA in clinical specimens by PCR.

Authors:  M Zazzi; L Romano; M Catucci; A De Milito; P Almi; A Gonnelli; M Rubino; P E Valensin
Journal:  J Clin Microbiol       Date:  1995-01       Impact factor: 5.948

  3 in total

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