Rapid Detection of Campylobacter jejuni, Campylobacter coli, and Campylobacter lari in Fresh Chicken Meat and By-Products in Bangkok, Thailand, Using Modified Multiplex PCR

被引:18
作者
Saiyudthong, S. [1 ]
Phusri, K. [2 ]
Buates, S. [2 ]
机构
[1] Kasetsart Univ, Inst Food Res & Prod Dev, Bangkok, Thailand
[2] Mahidol Univ, Fac Sci, Dept Microbiol, Bangkok 10400, Thailand
关键词
THERMOPHILIC CAMPYLOBACTER; SPECIES-LEVEL; C-LARI; IDENTIFICATION; PREVALENCE; DIFFERENTIATION; ASSAY; CONTAMINATION; UPSALIENSIS; SPP;
D O I
10.4315/0362-028X.JFP-14-415
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A multiplex PCR assay for simultaneous detection and differentiation of Campylobacter jejuni, Campylobacter coli, and Campylobacter lari was developed and validated to assess the occurrence of these bacteria in fresh chicken meat and by-products in Bangkok, Thailand, by using a new combination of four previously published PCR primers for C. jejuni, C. coli, C. lari, and a universal 16S rDNA gene as an internal control. The specificity was determined by using 13 strains of other bacteria. With pure culture DNA, the detection limit was 0.017 ng/PCR for C. jejuni and C. coli and was 0.016 ng/PCR for C. lari. It can detect 10 CPU of C. jejuni, C. coli, and C. lari in 2 g of chicken meat within a 16-h enrichment time. Our multiplex PCR assay was applied for identification of Campylobacter spp. in 122 supermarket samples and 108 fresh market samples. Of the 230 samples evaluated by multiplex PCR, 54.0, 3.3, and 10.7% of supermarket samples were positive for C. jejuni, C. coli, and mixed C. jejuni and C. coli, respectively, and 56.5 and 33.3% of fresh market samples were positive for C. jejuni and mixed C. jejuni and C. coli, respectively. No sample was positive for C. lari. Fresh market samples had significantly higher C. jejuni and C. coli contamination than those from supermarkets (relative risk: 1.3; P = 0.0001). Compared with the culture method (a gold standard), the sensitivity, specificity, positive predictive value, negative predictive value, and diagnostic accuracy of multiplex PCR were 97.7, 86.8, 96.1, 92.0, and 95.2%, respectively. No significant difference was observed between results from two methods (P = 0.55). Therefore, the established multiplex PCR was not only rapid and easy to perform but had a high sensitivity and specificity to distinguish between C. jejuni, C. coli, and C. lari, even in samples containing mixed contamination. Our study indicated that fresh chicken meat and by-products from fresh markets were significantly less hygienic than those. from supermarkets.
引用
收藏
页码:1363 / 1369
页数:7
相关论文
共 29 条
[1]   Detection of thermophilic Campylobacter from sparrows by multiplex PCR:: The role of sparrows as a source of contamination of broilers with Camplylobacter [J].
Chuma, T ;
Hashimoto, S ;
Okamoto, K .
JOURNAL OF VETERINARY MEDICAL SCIENCE, 2000, 62 (12) :1291-1295
[2]   A rapid DNA isolation procedure for the identification of Campylobacter jejuni by the polymerase chain reaction [J].
Englen, MD ;
Kelley, LC .
LETTERS IN APPLIED MICROBIOLOGY, 2000, 31 (06) :421-426
[3]  
Evans S., 2008, POULTRY DIS, P181
[4]   Risk factors for sporadic Campylobacter infection in the United States:: A case-control study in FoodNet sites [J].
Friedman, CR ;
Hoekstra, RM ;
Samuel, M ;
Marcus, R ;
Bender, J ;
Shiferaw, B ;
Reddy, S ;
Ahuja, SD ;
Helfrick, DL ;
Hardnett, F ;
Carter, M ;
Anderson, B ;
Tauxe, RV .
CLINICAL INFECTIOUS DISEASES, 2004, 38 :S285-S296
[5]   Genomic Characterization of Campylobacter jejuni Strain M1 [J].
Friis, Carsten ;
Wassenaar, Trudy M. ;
Javed, Muhammad A. ;
Snipen, Lars ;
Lagesen, Karin ;
Hallin, Peter F. ;
Newell, Diane G. ;
Toszeghy, Monique ;
Ridley, Anne ;
Manning, Georgina ;
Ussery, David W. .
PLOS ONE, 2010, 5 (08)
[6]   Prevalence of Campylobacter in Wild Birds of the Mid-Atlantic Region, USA [J].
Keller, Judith I. ;
Shriver, W. Gregory ;
Waldenstrom, Jonas ;
Griekspoor, Petra ;
Olsen, Bjorn .
JOURNAL OF WILDLIFE DISEASES, 2011, 47 (03) :750-754
[7]   Pathogenesis of enteric infection by Campylobacter [J].
Ketley, JM .
MICROBIOLOGY-UK, 1997, 143 :5-21
[8]   Development of a novel triplex PCR assay for the detection and differentiation of thermophilic species of Campylobacter using 16S-23S rDNA internal transcribed spacer (ITS) region [J].
Khan, I. U. H. ;
Edge, T. A. .
JOURNAL OF APPLIED MICROBIOLOGY, 2007, 103 (06) :2561-2569
[9]   Prevalence and Characterization of Campylobacter spp. Isolated from Domestic and Imported Poultry Meat in Korea, 2004-2008 [J].
Kim, Hae Ji ;
Kim, Jong Hyun ;
Kim, Young Ihl ;
Choi, Jung Su ;
Park, Mi Young ;
Nam, Hyang-Mi ;
Jung, Suk-Chan ;
Kwon, Jin Wook ;
Lee, Chul Hyun ;
Kim, Yong Hwan ;
Ku, Bok Kyung ;
Lee, Young Ju .
FOODBORNE PATHOGENS AND DISEASE, 2010, 7 (10) :1203-1209
[10]   PCR detection, identification to species level, and fingerprinting of Campylobacter jejuni and Campylobacter coli direct from diarrheic samples [J].
Linton, D ;
Lawson, AJ ;
Owen, RJ ;
Stanley, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (10) :2568-2572