A real-time PCR assay was developed to identify ciprofloxacin-resistant Campylobacter jejuni. Ciprofloxacin resistance in C. jejuni has been associated with a C→T nucleotide point mutation occurring at the 86 codon of the gyrA gene. Other nucleotide substitutions have been identified in proximity to or at the same codon in the gyrA gene, but their role in ciprofloxacin resistance is still unknown. The LightCycler assay is based on the fluorescence resonance energy transfer technology using melting peak analysis of two fluorescent probes hybridized on PCR amplicons. This assay was used to detect the 86-codon mutation conferring ciprofloxacin resistance, as well as other nucleotides substitutions occurring within the same site in the gyrA gene. This gyrA mutation assay allows a rapid and reproducible screening method of ciprofloxacin resistant strains and was applied to C. jejuni strains isolated in Italy in 2000. © 2004 Elsevier Ltd. All rights reserved.

Identification of ciprofloxacin-resistant Campylobacter jejuni and analysis of the gyrA gene by the LightCycler mutation assay / Dionisi, Am; Luzzi, I; Carattoli, A.. - In: MOLECULAR AND CELLULAR PROBES. - ISSN 0890-8508. - 18:4(2004), pp. 255-261. [10.1016/j.mcp.2004.02.001]

Identification of ciprofloxacin-resistant Campylobacter jejuni and analysis of the gyrA gene by the LightCycler mutation assay

Carattoli A.
2004

Abstract

A real-time PCR assay was developed to identify ciprofloxacin-resistant Campylobacter jejuni. Ciprofloxacin resistance in C. jejuni has been associated with a C→T nucleotide point mutation occurring at the 86 codon of the gyrA gene. Other nucleotide substitutions have been identified in proximity to or at the same codon in the gyrA gene, but their role in ciprofloxacin resistance is still unknown. The LightCycler assay is based on the fluorescence resonance energy transfer technology using melting peak analysis of two fluorescent probes hybridized on PCR amplicons. This assay was used to detect the 86-codon mutation conferring ciprofloxacin resistance, as well as other nucleotides substitutions occurring within the same site in the gyrA gene. This gyrA mutation assay allows a rapid and reproducible screening method of ciprofloxacin resistant strains and was applied to C. jejuni strains isolated in Italy in 2000. © 2004 Elsevier Ltd. All rights reserved.
2004
ciprofloxacin; fluorescent dye, amplicon; analytic method; antibiotic resistance; article; bacterial gene; bacterial genetics; bacterial strain; bacterium identification; bacterium isolation; bioassay; Campylobacter jejuni; codon; controlled study; fluorescence resonance energy transfer; gene mutation; genetic analysis; gyra gene; mutational analysis; nonhuman; nucleotide sequence; priority journal; real time polymerase chain reaction; reproducibility, Base Sequence; Campylobacter jejuni; Ciprofloxacin; DNA Gyrase; Drug Resistance, Microbial; Fluorescence Resonance Energy Transfer; Fluorescent Dyes; Gene Expression Regulation, Bacterial; Molecular Sequence Data; Point Mutation, Campylobacter; Campylobacter jejuni
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Identification of ciprofloxacin-resistant Campylobacter jejuni and analysis of the gyrA gene by the LightCycler mutation assay / Dionisi, Am; Luzzi, I; Carattoli, A.. - In: MOLECULAR AND CELLULAR PROBES. - ISSN 0890-8508. - 18:4(2004), pp. 255-261. [10.1016/j.mcp.2004.02.001]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1284935
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