Establishment of immunomagnetic capture-fluorescent PCR detection method for Campylobacter jejuni.
- Author:
Guang-Ming LIU
1
;
Wen-Jin SU
;
Hui-Nong CAI
;
Ming-Xing XIE
;
Tang LIU
;
Xiao-Li PENG
Author Information
1. Xiamen Entry-Exit Inspection and Quarantine Bureau, Xiamen 361012, China. lgm@xmciq.gov.cn
- Publication Type:Journal Article
- MeSH:
Campylobacter jejuni;
genetics;
isolation & purification;
Fluorescence;
Immunomagnetic Separation;
methods;
Polymerase Chain Reaction;
methods;
Sensitivity and Specificity
- From:
Chinese Journal of Biotechnology
2005;21(2):336-340
- CountryChina
- Language:Chinese
-
Abstract:
In order to develop a rapid method which can check Campylobacter jejuni in animal and poultry foods nicely, an immunomagnetic capture-fluorescent PCR (IMC-FPCR) method was established in this paper. The reported method involves isolation of the target pathogen by immunocapture prior to the fluorescent PCR step, therefore the immunomagnetic-beads for Campylobacter were developed, and two groups of primer/probe, which targeted for the species special sequence of flaA gene and hipO gene for Campylobacter jejuni were designed. The immunomagnetic capture-fluorescent PCR assay amplification of the hipO gene and flaA gene for detection of Campylobacter jejuni was firstly reported in this paper. Result indicated that IMC-FPCR method permits direct detection of the pathogen without an enrichment step and can be performed in approximately 24 h. The assay results are positive for all of the isolates of Campylobacter jejuni (3 isolates, including type strain ATCC 33560 and ATCC8341) with a detection limit of approximately 10 cfu/mL, are negative for Campylobacter coli and several other bacteria. IMC-FPCR assay provide not only a rapid, sensitive method for quantitative detection of Campylobacter jejuni, but also an important method for detecting of Campylobacter jejuni of viable but non-culturerable (VNC) state.
