Non-specific PCR products using rat-derived Pneumocystis carinii dihydrofolate reductase gene-specific primers in DNA amplification of human respiratory samples

被引:11
作者
Ortona, E
Margutti, P
DeLuca, A
Peters, SE
Wakefield, AE
Tamburrini, E
Mencarini, P
Visconti, E
Siracusano, A
机构
[1] CATHOLIC UNIV ROME,INST CLIN INFECT DIS,ROME,ITALY
[2] UNIV LONDON QUEEN MARY & WESTFIELD COLL,SCH BIOL SCI,LONDON E1 4NS,ENGLAND
[3] JOHN RADCLIFFE HOSP,INST MOLEC MED,DEPT PAEDIAT,MOL INFECT DIS GRP,OXFORD OX3 9DU,ENGLAND
基金
英国医学研究理事会;
关键词
Pneumocystis carinii; DHFR; PCR; DNA sequence;
D O I
10.1006/mcpr.1996.0026
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
DNA amplification using dihydrofolate reductase (DHFR) primers in bronchoalveolar lavage fluids (BALFs) from patients with Pneumocystis carinii (PC) pneumonia yielded low sensitivity and specificity. Amplified products of BALFs from an AIDS patient without PC pneumonia and five patients with PC pneumonia were cloned and sequenced. All samples showed the same sequence without any homology with DHFR cDNA of rat PC, or with any DHFR sequences in databases at the DNA or amino acid level. The data demonstrate that these DHFR primers amplify a non-specific region of DNA with a sequence unrelated to the human PC DHFR gene both in PC positive and in PC negative samples. This finding precludes the use of these DHFR primers for the diagnosis of PC pneumonia in respiratory specimens. (C) 1996 Academic Press Limited
引用
收藏
页码:187 / 190
页数:4
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