Literature DB >> 9353746

Multiantibiotic resistance caused by active drug extrusion in Pseudomonas aeruginosa and other gram-negative bacteria.

T Nakae1.   

Abstract

All living organisms have been exposed to noxious compounds throughout their long evolutionary history and those surviving have evolved to fabricate devices that detoxicate and extrude these life threatening substances. It is likely, therefore, that all viable organisms, from bacteria to mammals, are equipped with active extrusion machinery. When bacteria are attacked by antibiotics, they use these tactics to combat the drugs and to develop resistance. Drugs extrusion machinery in Gram-negative bacteria is complex, consisting of the inner membrane transporter which acts as an energy-dependent extrusion pump; a binding protein which presumably connect both membranes; and the outer membrane exit channel. The extrusion pump assemblies are often encoded by chromosomal genes and might be expressed by mutation(s) or induced in the presence of drug(s).

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Year:  1997        PMID: 9353746

Source DB:  PubMed          Journal:  Microbiologia        ISSN: 0213-4101


  9 in total

1.  Mutation in the sdeS gene promotes expression of the sdeAB efflux pump genes and multidrug resistance in Serratia marcescens.

Authors:  Hideaki Maseda; Yumiko Hashida; Akihiro Shirai; Takeshi Omasa; Taiji Nakae
Journal:  Antimicrob Agents Chemother       Date:  2011-03-21       Impact factor: 5.191

2.  Study on Staphylococcus aureus strain HPC-250 for associated antibacterial property.

Authors:  G Bhuvaneswari; P Padmanabhan; Atya Kapley; Hemant J Purohit
Journal:  Curr Microbiol       Date:  2005-10-05       Impact factor: 2.188

3.  Study of the multidrug membrane transporter of single living Pseudomonas aeruginosa cells using size-dependent plasmonic nanoparticle optical probes.

Authors:  Prakash D Nallathamby; Kerry J Lee; Tanvi Desai; Xiao-Hong Nancy Xu
Journal:  Biochemistry       Date:  2010-07-20       Impact factor: 3.162

4.  Design and study of the efflux function of the EGFP fused MexAB-OprM membrane transporter in Pseudomonas aeruginosa using fluorescence spectroscopy.

Authors:  Feng Ding; Kerry J Lee; Ardeschir Vahedi-Faridi; Hiroshi Yoneyama; Christopher J Osgood; Xiao-Hong Nancy Xu
Journal:  Analyst       Date:  2014-04-29       Impact factor: 4.616

5.  NB2001, a novel antibacterial agent with broad-spectrum activity and enhanced potency against beta-lactamase-producing strains.

Authors:  Qing Li; Jean Y Lee; Rosario Castillo; Mark S Hixon; Catherine Pujol; Venkata Ramana Doppalapudi; H Michael Shepard; Geoffrey M Wahl; Thomas J Lobl; Ming Fai Chan
Journal:  Antimicrob Agents Chemother       Date:  2002-05       Impact factor: 5.191

6.  Mutational upregulation of a resistance-nodulation-cell division-type multidrug efflux pump, SdeAB, upon exposure to a biocide, cetylpyridinium chloride, and antibiotic resistance in Serratia marcescens.

Authors:  Hideaki Maseda; Yumiko Hashida; Rumi Konaka; Akihiro Shirai; Hiroki Kourai
Journal:  Antimicrob Agents Chemother       Date:  2009-09-14       Impact factor: 5.191

7.  Resistance of Pseudomonas aeruginosa to imipenem induced by eluates from siliconized latex urinary catheters is related to outer membrane protein alterations.

Authors:  L Martínez-Martínez; A Pascual; M C Conejo; L Picabea; E J Perea
Journal:  Antimicrob Agents Chemother       Date:  1999-02       Impact factor: 5.191

8.  Energy-dependent accumulation of fluoroquinolones in quinolone-resistant Klebsiella pneumoniae strains.

Authors:  L Martínez-Martínez; I García; S Ballesta; V J Benedí; S Hernández-Allés; A Pascual
Journal:  Antimicrob Agents Chemother       Date:  1998-07       Impact factor: 5.191

Review 9.  Lung infections associated with cystic fibrosis.

Authors:  Jeffrey B Lyczak; Carolyn L Cannon; Gerald B Pier
Journal:  Clin Microbiol Rev       Date:  2002-04       Impact factor: 26.132

  9 in total

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