MICROPLATE-BASED DNA HYBRIDIZATION ASSAYS FOR DETECTION OF HUMAN RETROVIRAL GENE-SEQUENCES

被引:16
作者
DYSTER, LM
ABBOTT, L
BRYZGORNIA, V
POIESZ, BJ
PAPSIDERO, LD
机构
[1] CELLULAR PROD INC,BUFFALO,NY 14202
[2] SUNY HLTH SCI CTR,SYRACUSE,NY 13210
关键词
D O I
10.1128/JCM.32.2.547-550.1994
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Nonisotopic, microwell-based DNA hybridization assays for the specific detection of human immunodeficiency virus type 1 (HTV-1) gag, human T-cell lymphotropic virus type I (HTLV-I) pol, and HTLV-II pol DNA sequences were evaluated. The performances of these detection kits (Gene Detective enzyme oligonucleotide assays; Cellular Products, Inc., Buffalo, N.Y.) were assessed by using clinical samples whose infection status were established by amplification by PCR and then liquid hybridization detection by using virus-specific probes. Peripheral blood mononuclear cell lysates from 59 HIV-1-, 35 HTLV-I-, and 19 HTLV-II-infected individuals and from 15 healthy blood donors were used as substrates for PCR amplification. The results of the study demonstrated a clinical sensitivity of 100%. In addition, the enzyme oligonucleotide assays were able to detect 1 to 10 proviral copies subsequent to PCR amplification, indicating an analytical sensitivity comparable to that of liquid hybridization.
引用
收藏
页码:547 / 550
页数:4
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