ISEcp1-mediated transposition and homologous recombination can explain the context of blaCTX-M-62 linked to qnrB2

Antimicrobial Agents and Chemotherapy

Volumn 54, Issue 7, 2010, Pages 3039-3042

  Zong, Zhiyong ^a,b   Partridge, Sally R ^a   Iredell, Jonathan R ^a  

^a UNIVERSITY OF SYDNEY   (Australia)

^b SICHUAN UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

BETA LACTAMASE CTX M; BETA LACTAMASE CTX M 3B; BETA LACTAMASE CTX M 62; CEFTAZIDIME; EXTENDED SPECTRUM BETA LACTAMASE; QUINOLONE; SINGLE STRANDED DNA BINDING PROTEIN; UNCLASSIFIED DRUG; ANTIINFECTIVE AGENT;

ANTIBIOTIC SENSITIVITY; ARTICLE; BACTERIAL GENE; BACTERIUM ISOLATION; DNA TRANSPOSITION; GENE DELETION; GENE INSERTION SEQUENCE; GENETIC VARIABILITY; HOMOLOGOUS RECOMBINATION; INSERTION SEQUENCE ECP1; KLEBSIELLA PNEUMONIAE; NONHUMAN; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; QNRB2 GENE; SEQUENCE ANALYSIS; ANTIBIOTIC RESISTANCE; DRUG EFFECTS; GENETIC RECOMBINATION; GENETICS; INTEGRON; MOLECULAR GENETICS; PLASMID;

ANTI-BACTERIAL AGENTS; DRUG RESISTANCE, BACTERIAL; INTEGRONS; KLEBSIELLA PNEUMONIAE; MOLECULAR SEQUENCE DATA; PLASMIDS; RECOMBINATION, GENETIC;

EID: 77953802451     PISSN: 00664804     EISSN: 10986596     Source Type: Journal    
DOI: 10.1128/AAC.00041-10     Document Type: Article

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