Detection of Campylobacter spp. in chicken fecal samples by real-time PCR

被引:164
作者
Lund, M [1 ]
Nordentoft, S [1 ]
Pedersen, K [1 ]
Madsen, M [1 ]
机构
[1] Danish Inst Food & Vet Res, DFVF, DK-2800 Aarhus N, Denmark
关键词
D O I
10.1128/JCM.42.11.5125-5132.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A real-time PCR assay for detecting thermophilic Campylobacter spp. directly in chicken feces has been developed. DNA was isolated from fecal material by using magnetic beads followed by PCR with a prealiquoted PCR mixture, which had been stored at -18degreesC. Campylobacter could be detected in less than 4 h, with a detection limit of 100 to 150 CFU/ml, in a fecal suspension. A bacterial internal control was added before DNA extraction to control both DNA isolation and the presence of PCR inhibitors in the samples. The assay was performed on 111 swab samples from a Danish surveillance program and compared to conventional culturing using selective enrichment. There was no statistically significant difference in performance between real-time PCR and culture by selective enrichment, and the diagnostic specificity was 0.96 with an agreement of 0.92. Therefore, the assay should be useful for screening poultry flocks for the presence of Campylobacter.
引用
收藏
页码:5125 / 5132
页数:8
相关论文
共 55 条
[1]   A one-year study of campylobacter carriage by individual Danish broiler chickens as the basis for selection of Campylobacter spp. strains for a chicken infection model [J].
Bang, DD ;
Nielsen, EM ;
Knudsen, K ;
Madsen, M .
EPIDEMIOLOGY AND INFECTION, 2003, 130 (02) :323-333
[2]   Thermophilic Campylobacter spp. in turkey samples:: evaluation of two automated enzyme immunoassays and conventional microbiological techniques [J].
Borck, B ;
Stryhn, H ;
Ersboll, AK ;
Pedersen, K .
JOURNAL OF APPLIED MICROBIOLOGY, 2002, 92 (03) :574-582
[3]   Rapid detection of Campylobacter jejuni in chicken rinse water by melting-peak analysis of amplicons in real-time polymerase chain reaction [J].
Cheng, ZH ;
Griffiths, MW .
JOURNAL OF FOOD PROTECTION, 2003, 66 (08) :1343-1352
[4]   Campylobacter contamination in French chicken production from farm to consumers.: Use of a PCR assay for detection and identification of Campylobacter jejuni and Camp. coli [J].
Denis, M ;
Refrégier-Petton, J ;
Laisney, MJ ;
Ermel, G ;
Salvat, G .
JOURNAL OF APPLIED MICROBIOLOGY, 2001, 91 (02) :255-267
[5]   Comparison of real-time, quantitative PCR with molecular beacons to nested PCR and culture methods for detection of Mycobacterium avium subsp paratuberculosis in bovine fecal samples [J].
Fang, Y ;
Wu, WH ;
Pepper, JL ;
Larsen, JL ;
Marras, SAE ;
Nelson, EA ;
Epperson, WB ;
Christopher-Hennings, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (01) :287-291
[6]   Development and evaluation of a broad-range PCR-ELISA assay with Borrelia burgdorferi and Streptococcus pneumoniae as model organisms for reactive arthritis and bacterial meningitis [J].
Fischer-Romero, C ;
Lüthy-Hottenstein, J ;
Altwegg, M .
JOURNAL OF MICROBIOLOGICAL METHODS, 2000, 40 (01) :79-88
[7]  
Gibello A, 1999, APPL ENVIRON MICROB, V65, P346
[8]   Development of a triplex PCR assay for the specific detection of Campylobacter jejuni, Salmonella spp., and Escherichia coli O157:H7 [J].
Gilbert, C ;
Winters, D ;
O'Leary, A ;
Slavik, M .
MOLECULAR AND CELLULAR PROBES, 2003, 17 (04) :135-138
[9]   Specific identification of the enteropathogens Campylobacter jejuni and Campylobacter coli by using a PCR test based on the ceuE gene encoding a putative virulence determinant [J].
Gonzalez, I ;
Grant, KA ;
Richardson, PT ;
Park, SF ;
Collins, MD .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (03) :759-763
[10]   Quantitation of viral DNA by real-time PCR applying duplex amplification, internal standardization, and two-color fluorescence detection [J].
Gruber, F ;
Falkner, FG ;
Dorner, F ;
Hämmerle, T .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2001, 67 (06) :2837-2839