Comparison of an industry-derived LCx Chlamydia pneumoniae PCR research kit to in-house assays performed in five laboratories

被引:26
作者
Chernesky, M [1 ]
Smieja, M
Schachter, J
Summersgill, J
Schindler, L
Solomon, N
Campbell, K
Campbell, L
Cappuccio, A
Gaydos, C
Chong, S
Moncada, J
Phillips, J
Jang, D
Wood, BJ
Petrich, A
Hammerschlag, M
Cerney, M
Mahony, J
机构
[1] McMaster Univ, St Josephs Healthcare, Hamilton, ON L8N 4A6, Canada
[2] Univ Calif San Francisco, San Francisco, CA 94143 USA
[3] Univ Louisville, Louisville, KY 40292 USA
[4] Abbott Labs, Abbott Pk, IL 60064 USA
[5] Univ Washington, Seattle, WA 98195 USA
[6] Johns Hopkins Univ, Baltimore, MD 21218 USA
[7] SUNY Hlth Sci Ctr, Brooklyn, NY 11203 USA
关键词
D O I
10.1128/JCM.40.7.2357-2362.2002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In a multicenter comparison of PCR assays utilizing 120 quantitated samples of 16 Chlamydia pneumoniae isolates, an LCx research-use-only (RUO) PCR developed by Abbott Laboratories demonstrated 100% sensitivity on 48 samples with >1 copy of DNA per mul of specimen. The sensitivities of five in-house PCR assays ranged from 54 to 94% for the same samples. All six assays showed decreased sensitivities as the DNA copy numbers of the samples decreased. Overall, sensitivities ranged from 68% for the LCx PCR assay to 29% for one of the in-house tests. The LCx RUO PCR and three of the five in-house PCR tests reported no false positives with the 24 negative samples. Increasing the number of replicates tested increased the sensitivities of all of the assays, including the LCx PCR. The LCx RUO assay showed high reproducibility for a single technologist and between technologists, with a kappa agreement of 0.77. The within-center agreements of the five in-house PCR tests varied from 0.19 to 0.74 on two challenges of 60 specimens I month apart. The LCx C. pneumoniae RUO PCR shows excellent potential for use in clinical studies, which could enable standardization of results in the field.
引用
收藏
页码:2357 / 2362
页数:6
相关论文
共 26 条
[21]   Circulating nucleic acids of Chlamydia pneumoniae and cytomegalovirus in patients undergoing coronary angiography [J].
Smieja, M ;
Chong, S ;
Natarajan, M ;
Petrich, A ;
Rainen, L ;
Mahony, JB .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (02) :596-600
[22]   DETECTION OF CHLAMYDIA-PNEUMONIAE USING A GENERAL CHLAMYDIA POLYMERASE CHAIN-REACTION WITH SPECIES DIFFERENTIATION AFTER HYBRIDIZATION [J].
TJHIE, HTJ ;
ROOSENDAAL, R ;
WALBOOMERS, JMM ;
THEUNISSEN, JJH ;
SANG, RRMTL ;
MEIJER, CJLM ;
MACLAREN, DM ;
VANDENBRULE, AJC .
JOURNAL OF MICROBIOLOGICAL METHODS, 1993, 18 (02) :137-150
[23]   DETECTION OF CHLAMYDIA-PNEUMONIAE AND CHLAMYDIA-PSITTACI IN SPUTUM SAMPLES BY PCR [J].
TONG, CYW ;
SILLIS, M .
JOURNAL OF CLINICAL PATHOLOGY, 1993, 46 (04) :313-317
[24]   DETECTION OF MYCOPLASMA CONTAMINATION IN CELL-CULTURES BY A MYCOPLASMA GROUP-SPECIFIC PCR [J].
VANKUPPEVELD, FJM ;
JOHANSSON, KE ;
GALAMA, JMD ;
KISSING, J ;
BOLSKE, G ;
VANDERLOGT, JTM ;
MELCHERS, WJG .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1994, 60 (01) :149-152
[25]   GENETIC DIVERSITY AND IDENTIFICATION OF HUMAN INFECTION BY AMPLIFICATION OF THE CHLAMYDIAL 60-KILODALTON CYSTEINE-RICH OUTER-MEMBRANE PROTEIN GENE [J].
WATSON, MW ;
LAMBDEN, PR ;
CLARKE, IN .
JOURNAL OF CLINICAL MICROBIOLOGY, 1991, 29 (06) :1188-1193
[26]   Development of a simplified polymerase chain reaction-enzyme immunoassay for the detection of Chlamydia pneumoniae [J].
Wilson, PA ;
Phipps, J ;
Samuel, D ;
Saunders, NA .
JOURNAL OF APPLIED BACTERIOLOGY, 1996, 80 (04) :431-438