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
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