Description of a multiplex Bordetella pertussis and Bordetella parapertussis LightCycler® PCR assay with inhibition control

被引:31
作者
Cloud, JL [1 ]
Hymas, WC
Turlak, A
Croft, A
Reischl, U
Daly, JA
Carroll, KC
机构
[1] ARUP, Inst Clin & Expt Pathol, Salt Lake City, UT USA
[2] ARUP Labs, Salt Lake City, UT USA
[3] Univ Utah, Dept Pathol, Salt Lake City, UT USA
[4] Inst Med Microbiol & Hyg, Regensburg, Germany
[5] Primary Childrens Med Ctr, Salt Lake City, UT 84103 USA
关键词
D O I
10.1016/S0732-8893(03)00045-2
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
While culture for Bordetella species is highly specific, sensitivity is extremely variable due to patient age, immunization status, antibiotic treatment, and specimen transport conditions. We evaluated a real-time multiplex PCR assay as an alternative to culture for the detection and differentiation of Bordetella pertussis and Bordetella parapertussis. The PCR conditions allowed the simultaneous detection of one B. pertussis organism and five B. parapertussis organisms per reaction. An inhibition control was incorporated into the assay. Of 163 total samples evaluated, 37 of 38 samples positive by either culture or direct fluorescent antibody testing (DFA) were also positive by PCR (97% sensitivity). Of 125 culture- or DFA-negative samples, 101 were also negative by PCR (81% specificity). The described multiplex assay is a rapid, sensitive, contamination-limiting, real-time PCR assay that controls for inhibition. The assay performs well using liquid or swab samples and from dried material on slides. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:189 / 195
页数:7
相关论文
共 17 条
[1]   The seroepidemiology of Bordetella pertussis infections: A study of persons ages 1-65 years [J].
Cattaneo, LA ;
Reed, GW ;
Haase, DH ;
Wills, MJ ;
Edwards, KM .
JOURNAL OF INFECTIOUS DISEASES, 1996, 173 (05) :1256-1259
[2]   Impact of nasopharyngeal swab types on detection of Bordetella pertussis by PCR and culture [J].
Cloud, JL ;
Hymas, W ;
Carroll, KC .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (10) :3838-3840
[3]   FREQUENCY OF UNRECOGNIZED BORDETELLA-PERTUSSIS INFECTIONS IN ADULTS [J].
DEVILLE, JG ;
CHERRY, JD ;
CHRISTENSON, PD ;
PINEDA, E ;
LEACH, CT ;
KUHLS, TL ;
VIKER, S .
CLINICAL INFECTIOUS DISEASES, 1995, 21 (03) :639-642
[4]   Clinical validation of a polymerase chain reaction assay for the diagnosis of pertussis by comparison with serology, culture, and symptoms during a large pertussis vaccine efficacy trial [J].
Heininger, U ;
Schmidt-Schläper, G ;
Cherry, JD ;
Stehr, K .
PEDIATRICS, 2000, 105 (03) :E31
[5]   SERIOUS PERTUSSIS OVERLOOKED IN INFANTS [J].
HEININGER, U ;
STEHR, K ;
CHERRY, JD .
EUROPEAN JOURNAL OF PEDIATRICS, 1992, 151 (05) :342-343
[6]   Neonatal pertussis [J].
Hoppe, JE .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2000, 19 (03) :244-247
[7]   Comparison of PCR, culture, and direct fluorescent-antibody testing for detection of Bordetella pertussis [J].
Loeffelholz, MJ ;
Thompson, CJ ;
Long, KS ;
Gilchrist, MJR .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (09) :2872-2876
[8]  
Loeffelholz MJ, 2000, J CLIN MICROBIOL, V38, P467
[9]  
Mazengia E, 2000, J CLIN MICROBIOL, V38, P2330
[10]   Real-time PCR assay targeting IS481 of Bordetella pertussis and molecular basis for detecting Bordetella holmesii [J].
Reischl, U ;
Lehn, N ;
Sanden, GN ;
Loeffelholz, MJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (05) :1963-1966