DIRECT DNA-PROBE ASSAY FOR NEISSERIA-GONORRHOEAE IN PHARYNGEAL AND RECTAL SPECIMENS

被引:13
作者
LEWIS, JS
FAKILE, O
FOSS, E
LEGARZA, G
LESKYS, A
LOWE, K
POWNING, D
机构
[1] CLARK CTY HLTH DIST,LAS VEGAS,NV 89127
[2] NEVADA STATE HLTH LAB,RENO,NV 89503
关键词
D O I
10.1128/JCM.31.10.2783-2785.1993
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The direct detection of gonococcal DNA in rectal and pharyngeal specimens was evaluated by using a DNA probe-based assay (Gen-Probe, Inc., San Diego, Calif.). Rectal (234) and pharyngeal (608) swab specimens were obtained from 249 men and 372 women attending sexually transmitted disease clinics in Las Vegas and Reno, Nevada. The prevalence of gonococcal infection by culture at the pharyngeal and rectal sites was 2.9% (16 of 548 specimens) in women and 2.7% (8 of 294 specimens) in men. No false-positive reactions were observed among the 234 rectal specimens tested. Two probe-positive, culture-negative specimens were detected among the 361 pharyngeal specimens obtained from women. Both of these samples were confirmed as Neisseria gonorrhoeae by a probe competition assay. The overall correlation of the DNA probe test with pharyngeal and rectal cultures was 99.4% (837 of 842 cultures), with a sensitivity of 87.5% (21 of 24 cultures) and specificity of 99.7% (816 of 818 cultures). The positive and negative predictive values of the DNA assay were 91.3 and 99.8%, respectively. The direct DNA probe assay provides an alternative to culture screening for rectal and/or pharyngeal gonococcal infections.
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页码:2783 / 2785
页数:3
相关论文
共 17 条
[1]  
BROJORGENSEN A, 1973, BRIT J VENER DIS, V49, P491
[2]   EVALUATION OF 8 METHODS FOR IDENTIFICATION OF PATHOGENIC NEISSERIA SPECIES - NEISSERIA-KWIK, RIM-N, GONOBIO-TEST, MINITEK, GONOCHEK-II, GONOGEN, PHADEBACT MONOCLONAL GC OMNI TEST, AND SYVA MICROTRAK TEST [J].
DILLON, JR ;
CARBALLO, M ;
PAUZE, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (03) :493-497
[3]  
GEGG C, 1990, 90TH ANN M AM SOC MI
[4]   USE OF THE GEN-PROBE PACE SYSTEM FOR THE DETECTION OF NEISSERIA-GONORRHOEAE IN UROGENITAL SAMPLES [J].
GRANATO, PA ;
FRANZ, MR .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1990, 13 (03) :217-221
[5]  
HANDSFIELD HH, 1978, CLIN ASPECTS GONOCOC, P57
[6]   API QUADFERM+ WITH RAPID DNASE FOR IDENTIFICATION OF NEISSERIA SPP AND BRANHAMELLA-CATARRHALIS [J].
JANDA, WM ;
ZIGLER, KL ;
BRADNA, JJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 1987, 25 (02) :203-206
[7]  
KELLER R, 1992, 92ND GEN M MICR 1992
[8]  
KINGHORN GR, 1979, BRIT J VENER DIS, V55, P408
[9]   ANORECTAL GONOCOCCAL INFECTION [J].
KLEIN, EJ ;
FISHER, LS ;
CHOW, AW ;
GUZE, LB .
ANNALS OF INTERNAL MEDICINE, 1977, 86 (03) :340-346
[10]   EVALUATION OF CULTURE AND THE GEN-PROBE PACE-2 ASSAY FOR DETECTION OF NEISSERIA-GONORRHOEAE AND CHLAMYDIA-TRACHOMATIS IN ENDOCERVICAL SPECIMENS TRANSPORTED TO A STATE HEALTH LABORATORY [J].
LIMBERGER, RJ ;
BIEGA, R ;
EVANCOE, A ;
MCCARTHY, L ;
SLIVIENSKI, L ;
KIRKWOOD, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 1992, 30 (05) :1162-1166