2009Laboratory MedicineRequires access

Detection of Campylobacter jejuni by real-time fluorescent PCR

Bing Zhao

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Abstract

Objective To explore a rapid,sensitivety and specific method for examining Campylobacter jejuni(C.jejuni).Methods According to C.jejuni sequences from Ganbank,the specific primers and probe were designed on the basis of conserved gene region and a TaqMan real-time fluorescent polymerase chain reaction(PCR) was established.The specificity,sensitivity and repeatability of the assay were also studied.Results C.jejuni was amplified by real-time fluorescent PCR successfully while all non-C.jejuni bacterial species did not generate any signal.The assay had high sensitivity and repeatability,and the low detecting limit was 10 cfu /mL.Conclusions The real-time fluorescent PCR is a rapid,specific and sensitive method for quantifying C.jejuni,thus it has high practical value of application.

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What this paper is about

Objective To explore a rapid,sensitivety and specific method for examining Campylobacter jejuni(C.jejuni).Methods According to C.jejuni sequences from Ganbank,the specific primers and probe were designed on the basis of conserved gene region and a TaqMan real-time fluorescent polymerase chain reaction(PCR) was established.The specificity,sensitivity and repeatability of the assay were also studied.Results C.jejuni was amplified by real-time fluorescent PCR successfully while all non-C.jejuni bacterial species did not generate any signal.The assay had high sensitivity and repeatability,and the low detecting limit was 10 cfu /mL.Conclusions The real-time fluorescent PCR is a rapid,specific and sensitive method for quantifying C.jejuni,thus it has high practical value of application.

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Available abstract

Objective To explore a rapid,sensitivety and specific method for examining Campylobacter jejuni(C.jejuni).Methods According to C.jejuni sequences from Ganbank,the specific primers and probe were designed on the basis of conserved gene region and a TaqMan real-time fluorescent polymerase chain reaction(PCR) was established.The specificity,sensitivity and repeatability of the assay were also studied.Results C.jejuni was amplified by real-time fluorescent PCR successfully while all non-C.jejuni bacterial species did not generate any signal.The assay had high sensitivity and repeatability,and the low detecting limit was 10 cfu /mL.Conclusions The real-time fluorescent PCR is a rapid,specific and sensitive method for quantifying C.jejuni,thus it has high practical value of application.

Key concepts: Campylobacter jejuni, TaqMan, Repeatability, Real-time polymerase chain reaction, Polymerase chain reaction, Biology, Fluorescence, Detection limit

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