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Journal of Clinical Microbiology, Mar 1995, 641-647, Vol 33, No. 3
F Pane, S Butto, ML Gobbo, M Franco, C Butteroni, L Pastore, G Maiorano, M Foggia, PT Cataldo and A Guarino
We used a colorimetric polymerase chain reaction (PCR)-based assay in kit
form to detect directly human immunodeficiency virus type 1 (HIV-1)
proviral gag sequences in peripheral blood cells from 68 healthy blood
donors, 51 subjects at risk for HIV infection, 122 patients with HIV-1
infection, 11 patients with indeterminate Western blot (immunoblot)
results, 4 blood donors HIV-1 positive by enzyme immunoassay, and 13
children born to HIV-1-seropositive mothers. The results obtained in the
blood donors and HIV-1-infected patients demonstrated the high degree of
diagnostic specificity and sensitivity of the PCR method. HIV- 1 infection
was excluded in 10 of the 11 patients with indeterminate Western blot
results and in all four enzyme immunoassay-positive blood donors. A
diagnosis of HIV infection was ruled out by negative PCR results in 5 of 13
children from seropositive mothers, which excluded vertical transmission of
the infection in these cases; these children were younger than 3 months and
had positive serological results. Two at- risk patients with negative
serological results had positive PCR results. All results were confirmed by
conventional PCR. In conclusion, colorimetric PCR, which is commercially
available in kit form, is an easy and reliable technique that can be used
to detect proviral HIV-1 genomes in blood cells, and despite the
limitations owing to HIV genome variability, it is useful in the clinical
setting for the diagnosis of HIV infection in selected categories of
patients.
Copyright © 1995 by the American Society for Microbiology. All rights reserved.
Direct detection of proviral gag segment of human immunodeficiency virus in peripheral blood lymphocytes by colorimetric PCR assay as a clinical laboratory tool applied to different at-risk populations
CEINGE-Biotecnologie Avanzate, Universita di Napoli Federico II, Italy.
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