Development of a Loop-Mediated Isothermal Amplification Assay for Rapid, Sensitive Detection of Campylobacter jejuni in Cattle Farm Samples

被引:29
|
作者
Dong, Hee-Jin [1 ,2 ]
Cho, Ae-Ri [1 ,2 ]
Hahn, Tae-Wook [3 ,4 ]
Cho, Seongbeom [1 ,2 ]
机构
[1] Seoul Natl Univ, PLUS Program Creat Vet Sci Res BK21, Res Inst Vet Sci, Seoul 151742, South Korea
[2] Seoul Natl Univ, Coll Vet Med, Seoul 151742, South Korea
[3] Kangwon Natl Univ, Dept Vet Med, Coll Vet Med, Chunchon 200701, South Korea
[4] Kangwon Natl Univ, Inst Vet Sci, Chunchon 200701, South Korea
基金
新加坡国家研究基金会;
关键词
MOLECULAR EPIDEMIOLOGY; COLI; PREVALENCE; POULTRY; SPP; RAW; PCR; PATHOGENS; SURVIVAL; PRIMERS;
D O I
10.4315/0362-028X.JFP-14-056
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
Campylobacter jejuni is a leading cause of bacterial foodborne disease worldwide. The detection of this organism in cattle and their environment is important for the control of C. jejuni transmission and the prevention of campylobacteriosis. Here, we describe the development of a rapid and sensitive method for the detection of C. jejuni in naturally contaminated cattle farm samples, based on real-time loop-mediated isothermal amplification (LAMP) of the hipO gene. The LAMP assay was specific (100% inclusivity and exclusivity for 84 C. jejuni and 41 non-C. jejuni strains, respectively), sensitive (detection limit of 100 fg/mu l), and quantifiable (R-2 = 0.9133). The sensitivity of the LAMP assay was then evaluated for its application to the naturally contaminated cattle farm samples. C. jejuni strains were isolated from 51 (20.7%) of 246 cattle farm samples, and the presence of the hipO gene was tested using the LAMP assay. Amplification of the hipO gene by LAMP within 30 min (mean = 10.8 min) in all C. jejuni isolates (n = 51) demonstrated its rapidity and accuracy. Next, template DNA was prepared from a total of 186 enrichment broth cultures of cattle farm samples either by boiling or using a commercial kit, and the sensitivity of detection of C. jejuni was compared between the LAMP and PCR assays. In DNA samples prepared by boiling, the higher sensitivity of the LAMP assay (84.4%) compared with the PCR assay (35.5%) indicates that it is less susceptible to the existence of inhibitors in sample material. In DNA samples prepared using a commercial kit, both the LAMP and PCR assays showed 100% sensitivity. We anticipate that the use of this rapid, sensitive, and simple LAMP assay, which is the first of its kind for the identification and screening of C. jejuni in cattle farm samples, may play an important role in the prevention of C. jejuni contamination in the food chain, thereby reducing the risk of human campylobacteriosis.
引用
收藏
页码:1593 / 1598
页数:6
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