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Overexpression of the mexC–mexD–oprJ efflux operon in nfxB‐type multidrug‐resistant strains of Pseudomonas aeruginosa

Poole, Keith, Gotoh, Naomasa, Tsujimoto, Hideto, Zhao, Qixun, Wada, Akihisa, Yamasaki, Tetsuo, Neshat, Shadi, Yamagishi, Jun‐ichi, Li, Xian‐Zhi, Nishino, Takeshi·1996·Molecular Microbiology

Abstract

OprJ, overproduced in nfxB multidrug‐resistant strains of Pseudomonas aeruginosa, and OprK, overproduced in the multidrug‐resistant strain K385, were demonstrated to be immunologically cross‐reactive using an OprJ‐specific monoclonal antibody. Treatment of the purified proteins with trypsin or chymotrypsin yielded virtually indistinguishable digestion patterns, and the N‐terminal sequence of two trypsin fragments was identical for both proteins, indicating that OprJ and OprK share identity. The N‐terminal amino acid sequences were used to facilitate cloning of the oprJ gene on a 5kbp Kpn I fragment and a 10kbp Bam HI fragment. Nucleotide sequencing of portions of these fragments revealed that oprJ was the terminal gene in a putative three‐gene operon, The predicted mexC–mexD–oprJ gene products exhibit homology to the MexA–MexB–OprM components of the multidrug‐resistance efflux pump of P. aeruginosa (43–46% identity). Consistent with an implied role for mexC–mexD–oprJ in drug efflux, the mexC–mexD–oprJ‐hyperexpressing strain K385 showed reduced accumulation of a variety of antibiotics as compared with its parent strain, and this drug ‘exclusion’ was abrogated by energy inhibitors. The mexC and oprJ products are putative lipoproteins of a molecular mass of 40707 and 51742Da, respectively, while mexD was predicted to encode a protein of 111936Da. Sequencing upstream of mexC revealed the presence of the nfxB gene transcribed divergently from the efflux genes. Overproduction of OprJ and the attendant multiple‐antibiotic resistance of strain K385 was shown to result from a point mutation in nfxB, resulting in a H87→R change in the predicted NfxB polypeptide. OprJ overproduction and multidrug resistance in K385 was reversed by the cloned nfxB gene, suggesting that nfxB encodes a repressor of mexC–mexD–oprJ expression. Consistent with this, the cloned nfxB gene repressed synthesis of a mexC–lacZ fusion in Escherichia coli. nfxB also repressed expression of a nfxB–lacZ fusion, indicating that NfxB negatively regulates its own expression. These data indicate that the multidrug resistance of nfxB strains is due to overexpression of an efflux operon, mexC–mexD–oprJ, encoding components of a second efflux pump in P. aeruginosa.

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Metadata

Authors
Poole, K., Gotoh, N., Tsujimoto, H., Zhao, Q., Wada, A., Yamasaki, T., Neshat, S., Yamagishi, J., Li, X., & Nishino, T.
Venue
Molecular Microbiology
Publisher
Wiley
Published
1996-08
Volume
21
Issue
4
Pages
713-725
ISSN
  • 0950-382X (ISSN-L)
  • 1365-2958
OpenAlex
W2007889243
Cited by
443
References
0
FWCI
13.80
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Overexpression of the mexC–mexD–oprJ efflux operon in nfxB‐type multidrug‐resistant strains of Pseudomonas aeruginosa. https://app.cochat.ai/papers/10.1046/j.1365-2958.1996.281397.x
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Poole, K., Gotoh, N., Tsujimoto, H., Zhao, Q., Wada, A., Yamasaki, T., Neshat, S., Yamagishi, J., Li, X., & Nishino, T. (1996). Overexpression of the mexC–mexD–oprJ efflux operon in nfxB‐type multidrug‐resistant strains of Pseudomonas aeruginosa. Molecular Microbiology. https://doi.org/10.1046/j.1365-2958.1996.281397.x

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