Comparison of PCR nucleic acid hybridization and EIA for the detection of Chlamydia trachomatis in different populations in a regional centre

被引:4
|
作者
Farrell, DJ
Haran, MV
Park, BW
机构
[1] TOOWOOMBA GEN HOSP,SEXUAL HLTH CLIN,TOOWOOMBA,QLD 4350,AUSTRALIA
[2] TOOWOOMBA GEN HOSP,DEPT OBSTET & GYNAECOL,TOOWOOMBA,QLD 4350,AUSTRALIA
[3] TOOWOOMBA GEN HOSP,PUBL HLTH CLIN,TOOWOOMBA,QLD 4350,AUSTRALIA
关键词
Chlamydia trachomatis; PCR; Amplicor(TM); VIDAS(TM); IDEIA(TM);
D O I
10.1080/00313029600169583
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Culture on McCoy cell monolayers has been accepted as the reference method for the detection of Chlamydia trachomatis. Recent studies have shown that polymerase chain reaction (PCR)/nucleic acid hybridization based methods have increased sensitivity over culture while still retaining specificity. In situations where organism viability is of concern, due to factors such as transportation delays, culture is inappropriate. Regional laboratories therefore have not been able to utilize the reference method and have been forced to use less reliable methods. The aims of our study were to assess the feasibility of performing PCR to diagnose infections due to C. trachomatis in a regional laboratory using a new commercial kit - AmplicorTM (Roche Molecular Systems, Branchburg, NJ) and to compare the current enzyme-immunoassay (EIA) based-methods used in our laboratory (VIDASTM [bioMerieux Vitek, Hazelwood MO] and IDEIATM [Novo Nordisk Diagnostics, Cambridge, UK]) against PCR. Thirteen positive AmplicorTM specimens were found in 267 urine specimens collected from asymptomatic adolescent males and females. All 13 were confirmed positive using major outer membrane protein gene PCR (MOMP). VIDASTM and IDEIATM showed 100% correlation to each other but only detected 5/13 positives. Of 140 consecutive patients attending the regional sexual health clinic, 13 were AmplicorTM positive, 11/13 MOMP positive and 10/13 positive by VIDASTM. Five of 254 patients attending the hospital antenatal clinic were positive by AmplicorTM, all being confirmed by MOMP. No PCR inhibition was detected in a random sample of 100 varied negative AmplicorTM tests using a modification of the AmplicorTM kit. No contamination was experienced. The AmplicorTM kit was shown to be suitable for use in the routine clinical laboratory with minimal disruption to workflow. For regional laboratories this kit should provide more accurate results than EIA based methods, particularly in the detection of asymptomatic persons.
引用
收藏
页码:74 / 79
页数:6
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