TY - JOUR
T1 - Functional replacement of OprJ by OprM in the MexCD-OprJ multidrug efflux system of Pseudomonas aeruginosa
AU - Gotoh, Naomasa
AU - Tsujimoto, Hideto
AU - Nomura, Atsuko
AU - Okamoto, Kiyomi
AU - Tsuda, Masataka
AU - Nishino, Takeshi
N1 - Funding Information:
This research was supported by Grants-in-Aid to N.G. and M.T. for Scientific Research from The Ministry of Education, Science, Sports and Culture of Japan and by the grant to N.G. for `Study of Drug-Resistant Bacteria' funded by The Ministry of Health and Welfare, Japan in 1996.
PY - 1998/8/1
Y1 - 1998/8/1
N2 - For characterization of the MexCD-OprJ efflux system of Pseudomonas aeruginosa involved in resistance to fluoroquinolones and the fourth-generation cephems, we constructed mexC, mexD or oprJ mutants from the nfxB-type PAO strains by insertion mutagenesis. The gene products in the resultant mutants were examined by immunoblot assay using murine and rabbit antibodies developed against purified protein and synthetic oligopeptides. Susceptibility of the mexC (MexC- MexD- OprJ-) and mexD (MexC+ MexD- OprJ-) mutants to fluoroquinolone and the fourth-generation cephems was comparable to that of the wild-type strain PAO1. However, the oprJ mutant (MexC+ MexD+ OprJ-) was still less susceptible than PAO1, since a MexCD-OprM chimera system, which generated from a functional assist of the constitutively expressed OprM, can function in the efflux of the antimicrobial agents in the oprJ mutant. In fact, transformation of the oprJ mutant with an OprM-expression plasmid decreased the former's susceptibility to the levels exhibited by the nfxB mutant without affecting the substrate specificity of MexCD-OprJ. Copyright (C) 1998 Federation of European Microbiological Societies.
AB - For characterization of the MexCD-OprJ efflux system of Pseudomonas aeruginosa involved in resistance to fluoroquinolones and the fourth-generation cephems, we constructed mexC, mexD or oprJ mutants from the nfxB-type PAO strains by insertion mutagenesis. The gene products in the resultant mutants were examined by immunoblot assay using murine and rabbit antibodies developed against purified protein and synthetic oligopeptides. Susceptibility of the mexC (MexC- MexD- OprJ-) and mexD (MexC+ MexD- OprJ-) mutants to fluoroquinolone and the fourth-generation cephems was comparable to that of the wild-type strain PAO1. However, the oprJ mutant (MexC+ MexD+ OprJ-) was still less susceptible than PAO1, since a MexCD-OprM chimera system, which generated from a functional assist of the constitutively expressed OprM, can function in the efflux of the antimicrobial agents in the oprJ mutant. In fact, transformation of the oprJ mutant with an OprM-expression plasmid decreased the former's susceptibility to the levels exhibited by the nfxB mutant without affecting the substrate specificity of MexCD-OprJ. Copyright (C) 1998 Federation of European Microbiological Societies.
KW - Allelic exchange
KW - Immunoblot
KW - Multidrug efflux system
KW - Pseudomonas aeruginosa
KW - Rabbit polyclonal antiserum
KW - Synthetic oligopeptide
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U2 - 10.1016/S0378-1097(98)00250-X
DO - 10.1016/S0378-1097(98)00250-X
M3 - Article
C2 - 9711836
AN - SCOPUS:0032146271
VL - 165
SP - 21
EP - 27
JO - FEMS Microbiology Letters
JF - FEMS Microbiology Letters
SN - 0378-1097
IS - 1
ER -