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Unique combined penA/mtrR/porB mutations and NG-MAST strain types associated with ceftriaxone and cefixime MIC increases in a 'susceptible' Neisseria gonorrhoeae population
被引:28
|作者:
Thakur, S. D.
[1
]
Starnino, S.
[2
]
Horsman, G. B.
[3
]
Levett, P. N.
[3
]
Dillon, J. R.
[1
,2
]
机构:
[1] Univ Saskatchewan, Dept Microbiol & Immunol, Saskatoon, SK, Canada
[2] Univ Saskatchewan, Vaccine & Infect Dis Org, Int Vaccine Ctr, Saskatoon, SK, Canada
[3] Saskatchewan Dis Control Lab, Regina, SK, Canada
关键词:
gonorrhoea;
antimicrobial resistance mechanisms;
extended-spectrum cephalosporins;
PENICILLIN-BINDING PROTEIN-2;
MTRE EFFLUX PUMP;
REDUCED SUSCEPTIBILITY;
ANTIMICROBIAL RESISTANCE;
LEVEL RESISTANCE;
PENA;
GENE;
CEPHALOSPORINS;
IDENTIFICATION;
MECHANISM;
D O I:
10.1093/jac/dkt543
中图分类号:
R51 [传染病];
学科分类号:
100401 ;
摘要:
To determine which mutations in penA, mtrR and porB are implicated in increasing minimum MICs of ceftriaxone and cefixime in a susceptible gonococcal population and to ascertain associations with gonococcal strain types (STs). One hundred and forty-six Neisseria gonorrhoeae isolates formed two extended-spectrum cephalosporin susceptibility groups: group 1 isolates with cefixime and ceftriaxone MICs of 0.0005-0.016 mg/L; and group 2 isolates with cefixime MICs of 0.03-0.125 mg/L (naEuroS=aEuroS24) and ceftriaxone MICs of 0.03-0.06 mg/L (naEuroS=aEuroS23). Mutation patterns in penicillin-binding protein 2 (PBP2; penA), multiple transfer resistance repressor (MtrR; mtrR) and porin B (PorB; porB) were ascertained by DNA sequence and bioinformatic analysis. STs were determined using N. gonorrhoeae multiantigen sequence typing (NG-MAST). Most isolates carried PBP2 mutation pattern IX (D345a, F504L, A510V, A516G and P551L; 50/146, 34.2%), a G45D substitution in MtrR (37.7%) and a wild-type (WT) sequence for PorB (43.2%). Group 2 gonococcal isolates were significantly associated with: penA pattern IX; dual mutations in the promoter (A-) and DNA dimerization domain (H105Y) of MtrR; and G120K;A121D substitutions in PorB. There were 50 combined penA/mtrR/porB mutation patterns, with corresponding patterns I/WT/WT and IX/G45D/G120K;A121D predominating. Gonococci susceptible to ceftriaxone and cefixime were significantly associated with NG-MAST ST 25 (33/36; 92%) and the combined penA/mtrR/porB mutation pattern I/WT/WT. No combined mutation pattern or specific ST was associated with elevated ceftriaxone MICs. NG-MAST ST 3654 was significantly associated with the pattern IX/G45D/G120K;A121D and cefixime group 2 isolates. Specific single or combined mutation patterns in penA, mtrR and porB and specific STs were associated with differences in susceptibility to ceftriaxone and cefixime.
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页码:1510 / 1516
页数:7
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