Development of an improved PCR-ICT hybrid assay for direct detection of Legionellae and Legionella pneumophila from cooling tower water specimens

被引:16
作者
Horng, Yu-Tze
Soo, Po-Chi
Shen, Bin-Jon
Hung, Yu-Li
Lo, Kai-Yin
su, Hn-Pi Su
Wei, Jun-Rong
Hsieh, Shang-Chen
Hsueh, Po-Ren
Lai, Hsin-Chih
机构
[1] Natl Taiwan Univ, Coll Med, Dept Clin Lab Sci & Med Biotechnol, Taipei 100, Taiwan
[2] Natl Taiwan Univ Hosp, Dept Lab Med, Taipei, Taiwan
[3] Natl Taiwan Univ, Coll Med, Taipei 10764, Taiwan
[4] Ctr Dis Control, Dept Hlth, Atlanta, GA 30333 USA
关键词
Legionella pneumophila; PCR-ICT; lateral flow;
D O I
10.1016/j.watres.2006.03.033
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A novelly improved polymerase chian reaction and immunochromatography test (PCR-ICT) hybrid assay comprising traditional multiplex-nested PCR and ICT, (a lateral-flow device) was developed for direct detection of Legionella bacteria from environmental cooling tower samples. The partial 16S rDNA (specific for Legionella spp.) and dnaJ (specific for Legionella pneumophila) genes from Legionella chromosome were first specifically amplified by multiplex-nested PCR, respectively, followed by detection using ICT strip. Reading of results was based on presence or absence of the two test lines on the strips. Presence of test line 1 indicated existence of Legionella spp. specific 16S rDNA and identified Legionella spp. Presence of test line 2 further indicated existence of dnaJ and thus specifically identified L. pneumophila. In contrast, for non-Legionellae bacteria no test line formation was observed. Results of direct detection of Legionella bacteria and L. pneumophila from water tower specimens by this assay showed 100% sensitivity, and 96.6% and 100% specificity, respectively compared with traditional culture, biochemical and serological identification methods. The PCR-ICT hybrid assay does not require sophisticated equipment and was proved to be practically useful in rapid and direct Legionellae detection from environmental water samples. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2221 / 2229
页数:9
相关论文
共 39 条
[11]   Comparison of diagnostic sensitivities of three assays (Bartels enzyme immunoassay [EIA], Biotest EIA, and Binax NOW immunochromatographic test) for detection of Legionella pneumophila serogroup 1 antigen in urine [J].
Guerrero, C ;
Toldos, CM ;
Yagüe, G ;
Ramírez, C ;
Rodríguez, T ;
Segovia, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (01) :467-468
[12]   Direct detection of Legionella species from bronchoalveolar lavage and open lung biopsy specimens:: Comparison of LightCycler PCR, in situ hybridization, direct fluorescence antigen detection, and culture [J].
Hayden, RT ;
Uhl, JR ;
Qian, X ;
Hopkins, MK ;
Aubry, MC ;
Limper, AH ;
LLoyd, RV ;
Cockerill, FR .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (07) :2618-2626
[13]   Delay in appropriate therapy of Legionella pneumonia associated with increased mortality [J].
Heath, CH ;
Grove, DI ;
Looke, DFM .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1996, 15 (04) :286-290
[14]   Detection of Legionella pneumophila antigen in urine samples by the BinaxNOW immunochromatographic assay and comparison with both Binax Legionella Urinary Enzyme Immunoassay (EIA) and Biotest Legionella urinary antigen EIA [J].
Helbig, JH ;
Uldum, SA ;
Lück, PC ;
Harrison, TG .
JOURNAL OF MEDICAL MICROBIOLOGY, 2001, 50 (06) :509-516
[15]   Clinical utility of urinary antigen detection for diagnosis of community-acquired, travel-associated, and nosocomial Legionnaires' disease [J].
Helbig, JH ;
Uldum, SA ;
Bernander, S ;
Lück, PC ;
Wewalka, G ;
Abraham, B ;
Gaia, V ;
Harrison, TG .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (02) :838-840
[16]   The LuxR family protein SpnR functions as a negative regulator of N-acylhomoserine lactone-dependent quorum sensing in Serratia marcescens [J].
Horng, YT ;
Deng, SC ;
Daykin, M ;
Soo, PC ;
Wei, JR ;
Luh, KT ;
Ho, SW ;
Swift, S ;
Lai, HC ;
Williams, P .
MOLECULAR MICROBIOLOGY, 2002, 45 (06) :1655-1671
[17]  
Jansà JM, 2002, INT J TUBERC LUNG D, V6, P831
[18]   ENZYME-LINKED IMMUNOASSAY FOR DETECTION OF PCR-AMPLIFIED DNA OF LEGIONELLAE IN BRONCHOALVEOLAR FLUID [J].
JONAS, D ;
ROSENBAUM, A ;
WEYRICH, S ;
BHAKDI, S .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (05) :1247-1252
[19]   Rapid diagnosis of Legionella pneumophila serogroup 1 infection with the Binax enzyme immunoassay urinary antigen test [J].
Kazandjian, D ;
Chiew, R ;
Gilbert, GL .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (04) :954-956
[20]   RAPID DETECTION OF LEGIONELLA SPECIES IN BRONCHOALVEOLAR LAVAGE FLUIDS WITH THE ENVIROAMP LEGIONELLA PCR AMPLIFICATION AND DETECTION KIT [J].
KESSLER, HH ;
REINTHALER, FF ;
PSCHAID, A ;
PIERER, K ;
KLEINHAPPL, B ;
EBER, E ;
MARTH, E .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (12) :3325-3328