IMPROVED PCR SENSITIVITY FOR DIRECT GENOTYPING OF CHLAMYDIA-TRACHOMATIS SEROVARS BY USING A NESTED PCR

被引:87
作者
LAN, J
OSSEWAARDE, JM
WALBOOMERS, JMM
MEIJER, CJLM
VANDENBRULE, AJC
机构
[1] FREE UNIV AMSTERDAM HOSP,DEPT PATHOL,MOLEC PATHOL SECT,1081 HV AMSTERDAM,NETHERLANDS
[2] NATL INST PUBL HLTH & ENVIRONM PROTECT,VIROL LAB,3720 BA BILTHOVEN,NETHERLANDS
关键词
D O I
10.1128/JCM.32.2.528-530.1994
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Successful amplification of omp1 DNA by PCR is crucial in the genotyping of Chlamydia trachomatis when directly performed with clinical samples (J. Lan, J. M. M. Walboomers, R. Roosendaal, G. J. van Doornum, D. M. McLaren, C. J. L. M. Meijer, and A. J. C. van den Brule, J. Clin. Microbiol. 31:1060-1065, 1993). Several primers Banking the four variable domains of the omp1 gene were selected and tested for sensitivity in several nested PCRs with serial dilutions of serovar G. The optimal sensitivity obtained was 0.1 to 0.01 inclusion-forming units, similar to that obtained in the C. trachomatis plasmid PCR. With this approach, any C. trachomatis PCR-positive sample can be typed.
引用
收藏
页码:528 / 530
页数:3
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