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用于淋病奈瑟菌培养确认的单克隆抗体方法与核糖体核糖核酸探针检测的比较。

Comparison of monoclonal antibody methods and a ribosomal ribonucleic acid probe test for Neisseria gonorrhoeae culture confirmation.

作者信息

Janda W M, Wilcoski L M, Mandel K L, Ruther P, Stevens J M

机构信息

Department of Pathology, University of Illinois, Chicago 60612.

出版信息

Eur J Clin Microbiol Infect Dis. 1993 Mar;12(3):177-84. doi: 10.1007/BF01967108.

DOI:10.1007/BF01967108
PMID:7685283
Abstract

Recently, a chemiluminescent nucleic acid probe test that specifically detects the ribosomal ribonucleic acid of Neisseria gonorrhoeae has been released for clinical laboratory use (AccuProbe Neisseria gonorrhoeae). In this study, three coagglutination tests (GonoGen I, Meritec GC, and GC Omni), the GonoGen II immunofiltration method and the Micro Trak Neisseria gonorrhoeae fluorescent monoclonal antibody test were compared with AccuProbe for identification of gonococci. Strains tested (n = 376) included 194 Neisseria gonorrhoeae, 82 Neisseria meningitidis, 32 Neisseria lactamica, 32 Neisseria species, 32 Moraxella catarrhalis, 2 Moraxella spp. and 2 Kingella denitrificans. The GonoGen I, Meritec GC and GC Omni coagglutination tests produced clearly positive results for 93.8%, 92.3% and 95.9% of the gonococci, respectively. The GonoGen II unequivocally identified 91.8% and the MicroTrak fluorescent antibody test identified 90.7% with 2+ or greater fluorescence. AccuProbe identified 100% of the gonococci tested. GonoGen I and GonoGen II were 98% specific, Meritec GC was 99% specific and the specificity of the GC Omni, MicroTrak fluorescent antibody and AccuProbe tests was 100%. While antibody-based tests were reliable when results were clearly interpretable, the AccuProbe was the only confirmatory test that was 100% accurate. Serotyping studies indicate that an array of beta-lactamase positive and negative gonococcal serotypes fail to react with the monoclonal antibody-based tests in general and with the fluorescent antibody test in particular.

摘要

最近,一种专门检测淋病奈瑟菌核糖体核糖核酸的化学发光核酸探针检测法已投放临床实验室使用(AccuProbe淋病奈瑟菌检测法)。在本研究中,将三种协同凝集试验(GonoGen I、Meritec GC和GC Omni)、GonoGen II免疫过滤法以及Micro Trak淋病奈瑟菌荧光单克隆抗体检测法与AccuProbe检测法进行比较,以鉴定淋球菌。所检测的菌株(n = 376)包括194株淋病奈瑟菌、82株脑膜炎奈瑟菌、32株乳糖奈瑟菌、32株其他奈瑟菌属、32株卡他莫拉菌、2株莫拉克斯氏菌属和2株反硝化金氏杆菌。GonoGen I、Meritec GC和GC Omni协同凝集试验分别对93.8%、92.3%和95.9%的淋球菌产生明显阳性结果。GonoGen II明确鉴定出91.8%的淋球菌,MicroTrak荧光抗体检测法鉴定出90.7%荧光强度为2+或更高的淋球菌。AccuProbe鉴定出所检测的100%的淋球菌。GonoGen I和GonoGen II的特异性为98%,Meritec GC的特异性为99%,GC Omni、MicroTrak荧光抗体检测法和AccuProbe检测法的特异性均为100%。虽然基于抗体的检测法在结果易于解释时是可靠的,但AccuProbe是唯一一种100%准确的确诊检测法。血清分型研究表明,一系列β-内酰胺酶阳性和阴性淋球菌血清型通常不与基于单克隆抗体的检测法反应,尤其是不与荧光抗体检测法反应。

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本文引用的文献

1
Gono Gen coagglutination test for confirmation of Neisseria gonorrhoeae.淋菌乳胶凝集试验用于确诊淋病奈瑟菌。
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Evaluation of GonoGen coagglutination test for serodiagnosis of Neisseria gonorrhoeae: identification of problem isolates by auxotyping, serotyping, and with a fluorescent antibody reagent.
用于淋病奈瑟菌血清学诊断的GonoGen协同凝集试验评估:通过辅助分型、血清分型以及荧光抗体试剂鉴定问题菌株
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Serologic confirmation of Neisseria gonorrhoeae by monoclonal antibody-based coagglutination procedures.采用基于单克隆抗体的协同凝集程序对淋病奈瑟菌进行血清学确认。
J Clin Microbiol. 1988 Nov;26(11):2283-6. doi: 10.1128/jcm.26.11.2283-2286.1988.
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Evaluation of a ten-minute chromogenic substrate test for identification of pathogenic Neisseria species and Branhamella catarrhalis.用于鉴定致病性奈瑟菌属菌种和卡他布兰汉菌的十分钟显色底物试验的评估
Eur J Clin Microbiol Infect Dis. 1988 Feb;7(1):25-9. doi: 10.1007/BF01962166.
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Evaluation of eight 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.八种致病性奈瑟菌属菌种鉴定方法的评估:奈瑟菌快速鉴定法、RIM-N、淋菌生物检测法、迷你泰克法、淋菌检测二代法、淋菌基因检测法、法德巴克单克隆淋菌全项检测法以及赛瓦微生物追踪检测法。
J Clin Microbiol. 1988 Mar;26(3):493-7. doi: 10.1128/jcm.26.3.493-497.1988.
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J Clin Microbiol. 1988 Feb;26(2):293-6. doi: 10.1128/jcm.26.2.293-296.1988.
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Fluorescent monoclonal antibody for confirmation of Neisseria gonorrhoeae cultures.用于确认淋病奈瑟菌培养物的荧光单克隆抗体。
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