Comparison of three commercially available amplification assays, AMP CT, LCx, and COBAS AMPLICOR, for detection of Chlamydia trachomatis in first-void urine

被引:74
作者
Goessens, WHF [1 ]
Mouton, JW [1 ]
vanderMeijden, WI [1 ]
Deelen, S [1 ]
vanRijsoortVos, TH [1 ]
Toom, NLD [1 ]
Verbrugh, HA [1 ]
Verkooyen, RP [1 ]
机构
[1] UNIV ROTTERDAM HOSP, DEPT DERMATOVENEREOL, NL-3015 GD ROTTERDAM, NETHERLANDS
关键词
D O I
10.1128/JCM.35.10.2628-2633.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We compared the Gen-Probe transcription-mediated amplification assay (AMP CT), the Abbott LCx assay, and the Roche COBAS AMPLICOR assay for the defection of Chlamydia trachomatis in a mixed population in urine samples. First-void urine, urethral specimens, and cervical specimens in females were obtained from 1,000 patients (544 males and 456 females) visiting the outpatient sexually transmitted disease clinic of our hospital, The prevalence of C. trachomatis infection was 7.7% as determined by tissue culture of urethral and cervical specimens, The sensitivities of LCx, COBAS AMPLICOR, and AMP CT compared to cell culture were 79, 86, and 78%, respectively. Sensitivity and specificity were recalculated by using a new ''gold standard'', i.e., a sample was considered to be true. positive if two or more techniques yielded positive results. Specimens positive only by cell culture or positive in only one commercial amplification technique were retested by a previously described in-house PCR, After discordance analysis the sensitivities of LCx, COBAS AMPLICOR, and AMP CT were 84, 93, and 85%, respectively. Specificity exceeded 99% for all three assays. With each method the sensitivity was lower for urine samples from females compared to urine Samples from malts. By application of this new gold standard, existing differences between methods are highlighted; future evaluations of new techniques should be validated against two or more amplification assays.
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页码:2628 / 2633
页数:6
相关论文
共 31 条
[1]   LABORATORY DIAGNOSIS OF HUMAN CHLAMYDIAL INFECTIONS [J].
BARNES, RC .
CLINICAL MICROBIOLOGY REVIEWS, 1989, 2 (02) :119-136
[2]   DETECTION OF CHLAMYDIA-TRACHOMATIS IN URINE SPECIMENS FROM WOMEN BY LIGASE CHAIN-REACTION [J].
BASSIRI, M ;
HU, HY ;
DOMEIKA, MA ;
BURCZAK, J ;
SVENSSON, LO ;
LEE, HH ;
MARDH, PA .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (04) :898-900
[3]   DIAGNOSIS OF CHLAMYDIA-TRACHOMATIS URETHRITIS IN MEN BY POLYMERASE CHAIN-REACTION ASSAY OF 1ST-CATCH URINE [J].
BAUWENS, JE ;
CLARK, AM ;
LOEFFELHOLZ, MJ ;
HERMAN, SA ;
STAMM, WE .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (11) :3013-3016
[4]   CENTERS FOR DISEASE-CONTROL GUIDELINES FOR PREVENTION AND CONTROL OF CHLAMYDIA-TRACHOMATIS INFECTIONS - SUMMARY AND COMMENTARY [J].
BELL, TA ;
GRAYSTON, JT .
ANNALS OF INTERNAL MEDICINE, 1986, 104 (04) :524-526
[5]   AN EVALUATION OF THE POLYMERASE CHAIN-REACTION AMPLICOR CHLAMYDIA-TRACHOMATIS IN MALE URINE AND FEMALE UROGENITAL SPECIMENS [J].
BIANCHI, A ;
SCIEUX, C ;
BRUNAT, N ;
VEXIAU, D ;
KERMANACH, M ;
PEZIN, P ;
JANIER, M ;
MOREL, P ;
LAGRANGE, PH .
SEXUALLY TRANSMITTED DISEASES, 1994, 21 (04) :196-200
[6]   RAPID AND SIMPLE METHOD FOR PURIFICATION OF NUCLEIC-ACIDS [J].
BOOM, R ;
SOL, CJA ;
SALIMANS, MMM ;
JANSEN, CL ;
WERTHEIMVANDILLEN, PME ;
VANDERNOORDAA, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (03) :495-503
[7]  
BRADLEY MG, 1985, GENITOURIN MED, V61, P371
[8]   DIAGNOSIS OF CHLAMYDIA-TRACHOMATIS INFECTIONS IN MEN AND WOMEN BY TESTING FIRST-VOID URINE BY LIGASE CHAIN-REACTION [J].
CHERNESKY, MA ;
JANG, D ;
LEE, H ;
BURCZAK, JD ;
HU, H ;
SELLORS, J ;
TOMAZICALLEN, SJ ;
MAHONY, JB .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (11) :2682-2685
[9]   DIAGNOSIS OF CHLAMYDIA-TRACHOMATIS URETHRAL INFECTION IN SYMPTOMATIC AND ASYMPTOMATIC MEN BY TESTING FIRST-VOID URINE IN A LIGASE CHAIN-REACTION ASSAY [J].
CHERNESKY, MA ;
LEE, H ;
SCHACHTER, J ;
BURCZAK, JD ;
STAMM, WE ;
MCCORMACK, WM ;
QUINN, TC .
JOURNAL OF INFECTIOUS DISEASES, 1994, 170 (05) :1308-1311
[10]  
*CTR DIS CONTR, 1985, MMWR-MORBID MORTAL W, V35, P535