Detection of mutations in Salmonella enterica, gyrA, gyrB, parC and parE genes by denaturing high performance liquid chromatography (DHPLC) using standard HPLC instrumentation

Journal of Antimicrobial Chemotherapy

Volumn 56, Issue 4, 2005, Pages 619-623

  Randall, L P ^a   Coldham, N G ^a   Woodward, M J ^a  

^a VETERINARY LABORATORIES AGENCY   (United Kingdom)

Author keywords

Ciprofloxacin; Fluoroquinolones; Resistance; S. enterica

Indexed keywords

BACTERIAL DNA; CIPROFLOXACIN; DNA POLYMERASE; DNA TOPOISOMERASE (ATP HYDROLYSING) A; DNA TOPOISOMERASE (ATP HYDROLYSING) B; DOUBLE STRANDED DNA; QUINOLONE DERIVATIVE;

ANTIBIOTIC SENSITIVITY; ARTICLE; BACTERIAL GENE; BACTERIAL STRAIN; CHROMATOGRAPHY; CONTROLLED STUDY; DENATURING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; GENE MUTATION; GENE SEQUENCE; INTERMETHOD COMPARISON; MINIMUM INHIBITORY CONCENTRATION; NONHUMAN; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; SALMONELLA ENTERICA; SALMONELLA TYPHIMURIUM; SEQUENCE ANALYSIS; SEROTYPE; SINGLE NUCLEOTIDE POLYMORPHISM; STRAIN DIFFERENCE; VALIDATION PROCESS; WILD TYPE;

AMINO ACID SUBSTITUTION; ANTI-BACTERIAL AGENTS; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; DNA GYRASE; DNA MUTATIONAL ANALYSIS; DNA TOPOISOMERASE IV; MUTATION; REPRODUCIBILITY OF RESULTS; SALMONELLA ENTERICA; TEMPERATURE;

EID: 27144521399     PISSN: 03057453     EISSN: 14602091     Source Type: Journal    
DOI: 10.1093/jac/dki293     Document Type: Article

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