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Novel penA mutations identified in Neisseria gonorrhoeae with decreased susceptibility to ceftriaxone isolated between 2000 and 2014 in Japan.

Authors :
Kensaku Seike
Mitsuru Yasuda
Kyoko Hatazaki
Kosuke Mizutani
Kazuya Yuhara
Yasuhisa Ito
Yoshinori Fujimoto
Shin Ito
Tomohiro Tsuchiya
Shigeaki Yokoi
Masahiro Nakano
Takashi Deguchi
Seike, Kensaku
Yasuda, Mitsuru
Hatazaki, Kyoko
Mizutani, Kosuke
Yuhara, Kazuya
Ito, Yasuhisa
Fujimoto, Yoshinori
Ito, Shin
Source :
Journal of Antimicrobial Chemotherapy (JAC). Sep2016, Vol. 71 Issue 9, p2466-2470. 5p.
Publication Year :
2016

Abstract

<bold>Objectives: </bold>We examined four clinical strains of Neisseria gonorrhoeae (GU030113, GU110095, GU110332 and GU110362) isolated between 2000 and 2014 in Japan, exhibiting ceftriaxone MICs of 0.5 mg/L, for mutations of the genes associated with penicillin resistance.<bold>Methods: </bold>The penA, mtrR, porB1b (penB), ponA and pilQ genes of the strains were sequenced. PBP2s of the strains were aligned to the PBP2s associated with decreased susceptibility to oral cephalosporins, and PBP2s of previously reported strains with decreased susceptibility to ceftriaxone.<bold>Results: </bold>GU030113 had PBP2 pattern X with an additional substitution of A502T. GU110095 had PBP2 pattern XXVII. GU110332 had PBP2 pattern XXXIV with an additional substitution of P552S. GU110362 had PBP2 composed of pattern X (amino acid positions 1-291) and pattern V (amino acid positions 292-576). GU030113, GU110095 and GU110332 had deletion of A in the mtrR promoter, G120K and A121D or A121N in PorB1b and L421P in PBP1. GU110362 had A40D in the repressor of MtrR and L421P in PBP1. The strains did not have mutations of pilQ1 and pilQ2.<bold>Conclusions: </bold>Addition of A502T to PBP2 pattern X in GU030113 and of P552S to PBP2 pattern XXXIV in GU110332 would possibly contribute to decreased susceptibility to ceftriaxone. In GU110095 and GU110362, it was suggested that, in addition to their altered PBP2s, the enhanced efflux pump, reduced permeability in the outer membrane, another altered target of β-lactams and/or other mechanisms not identified in the present study might contribute to decreased susceptibility. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03057453
Volume :
71
Issue :
9
Database :
Academic Search Index
Journal :
Journal of Antimicrobial Chemotherapy (JAC)
Publication Type :
Academic Journal
Accession number :
117666572
Full Text :
https://doi.org/10.1093/jac/dkw161