Comparison of in-house and commercial sample preparation and PCR amplification systems for detection of human immunodeficiency virus type 1 DNA in blood samples from Tanzanian adults

被引:21
作者
Lyamuya, E
BredbergRaden, U
Albert, J
Grankvist, O
Msangi, V
Kagoma, C
Mhalu, F
Biberfeld, G
机构
[1] SWEDISH INST INFECT DIS CONTROL,S-10521 STOCKHOLM,SWEDEN
[2] UNIV DAR ES SALAAM,MUHIMBILI UNIV COLL HLTH SCI,DEPT MICROBIOL IMMUNOL,DAR ES SALAAM,TANZANIA
[3] KAROLINSKA INST,CTR MICROBIOL & TUMOR BIOL,STOCKHOLM,SWEDEN
[4] UMEA UNIV,DEPT VIROL,UMEA,SWEDEN
关键词
D O I
10.1128/JCM.35.1.278-280.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
This study compared the performance of several in-house nested PCR systems and the Amplicor human immunodeficiency virus type 1 (HIV-1) PCR kit in the detection of HIV-1 DNA in Tanzanian samples prepared by two different methods. All six of the in-house primer sets evaluated had a higher sensitivity for HN DNA detection in samples prepared by the Amplicor PCR sample preparation method than in those prepared by the Ficoll-Isopaque (FIP) density gradient centrifugation method. A sensitivity of 100% was achieved by combining two in-house primer sets. The sensitivity of the standard Amplicor HIV-1 PCR kit was only 59%, whereas a modified Amplicor HIV-1 PCR test had a sensitivity of 98%. Our data show that Tanzanian samples prepared by the Amplicor preparation method are more suitable for HIV-1 PCR testing than samples prepared by the FIP method. The modified, but not the standard, Amplicor HIV-1 PCR kit provides an alternative to the nested in-house PCR technique for the diagnosis of HIV infection.
引用
收藏
页码:278 / 280
页数:3
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