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多药外排泵MexCD - OprJ和MexEF - OprN的过表达与铜绿假单胞菌III型分泌的减少有关。

Overexpression of the multidrug efflux pumps MexCD-OprJ and MexEF-OprN is associated with a reduction of type III secretion in Pseudomonas aeruginosa.

作者信息

Linares Juan F, López Juan A, Camafeita Emilio, Albar Juan P, Rojo Fernando, Martínez Jose L

机构信息

Departamento de Biotecnología Microbiana, Centro Nacional de Biotecnología, CSIC, Campus Universidad Autónoma de Madrid, Cantoblanco, 28049 Madrid, Spain.

出版信息

J Bacteriol. 2005 Feb;187(4):1384-91. doi: 10.1128/JB.187.4.1384-1391.2005.

Abstract

The Pseudomonas aeruginosa genome contains several different multidrug resistance (MDR) efflux pumps. Overproduction of these pumps reduces susceptibility to a variety of antibiotics. Some recently published works have analyzed the effect of the overproduction of MDR efflux pumps on bacterial virulence. Here we have studied the effect of overproduction of the efflux pumps MexAB-OprM, MexCD-OprJ, MexEF-OprN, and MexXY on type III secretion (T3S) in P. aeruginosa. The type III secretion system (T3SS) is used by P. aeruginosa to deliver toxins directly into the cytoplasm of the host cell. Our data indicate that overexpression of either MexCD-OprJ or MexEF-OprN is associated with the impairment of T3S in P. aeruginosa. No effect on overexpression of either MexAB-OprM or MexXY was detected. The observed defect in T3S was due to a lack of expression of genes belonging to the T3SS regulon. Transcription of this regulon is activated by ExsA in response to environmental signals. Overexpression of this transcriptional regulator complemented the defect in T3S observed in the MexCD-OprJ- and MexEF-OprN-overproducing strains. Taken together, these results suggest that overproduction of either MexCD-OprJ or MexEF-OprN is associated with a reduction in the transcription of the T3SS regulon due to the lack of expression of the exsA gene, encoding the master regulator of the system. The relevance of potential metabolic and quorum-sensing imbalances due to overexpression of MDR pumps associated with this phenotype is also discussed.

摘要

铜绿假单胞菌基因组包含几种不同的多药耐药(MDR)外排泵。这些泵的过量产生会降低对多种抗生素的敏感性。最近一些已发表的研究分析了MDR外排泵过量产生对细菌毒力的影响。在此,我们研究了外排泵MexAB - OprM、MexCD - OprJ、MexEF - OprN和MexXY的过量产生对铜绿假单胞菌III型分泌(T3S)的影响。III型分泌系统(T3SS)被铜绿假单胞菌用于将毒素直接输送到宿主细胞的细胞质中。我们的数据表明,MexCD - OprJ或MexEF - OprN的过表达与铜绿假单胞菌中T3S的受损有关。未检测到MexAB - OprM或MexXY过表达有任何影响。观察到的T3S缺陷是由于属于T3SS调控子的基因缺乏表达。该调控子的转录由ExsA响应环境信号激活。这种转录调节因子的过表达弥补了在MexCD - OprJ和MexEF - OprN过量产生菌株中观察到的T3S缺陷。综上所述,这些结果表明,MexCD - OprJ或MexEF - OprN的过量产生与T3SS调控子转录减少有关,这是由于编码该系统主调节因子的exsA基因缺乏表达所致。还讨论了与该表型相关的MDR泵过表达导致的潜在代谢和群体感应失衡的相关性。

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本文引用的文献

1
Expression of Pseudomonas aeruginosa exoS is controlled by quorum sensing and RpoS.
Microbiology (Reading). 2004 Apr;150(Pt 4):843-851. doi: 10.1099/mic.0.26703-0.
2
Effect of metabolic imbalance on expression of type III secretion genes in Pseudomonas aeruginosa.
Infect Immun. 2004 Mar;72(3):1383-90. doi: 10.1128/IAI.72.3.1383-1390.2004.
3
Overexpression of the multidrug efflux pump SmeDEF impairs Stenotrophomonas maltophilia physiology.
J Antimicrob Chemother. 2004 Mar;53(3):432-4. doi: 10.1093/jac/dkh074. Epub 2004 Jan 22.
4
Contribution of the MexXY multidrug transporter to aminoglycoside resistance in Pseudomonas aeruginosa clinical isolates.
Antimicrob Agents Chemother. 2003 Oct;47(10):3202-7. doi: 10.1128/AAC.47.10.3202-3207.2003.
5
The mechanism of action of the Pseudomonas aeruginosa-encoded type III cytotoxin, ExoU.
EMBO J. 2003 Jun 16;22(12):2959-69. doi: 10.1093/emboj/cdg290.
6
ExsD is a negative regulator of the Pseudomonas aeruginosa type III secretion regulon.
Mol Microbiol. 2002 Nov;46(4):1123-33. doi: 10.1046/j.1365-2958.2002.03228.x.
7
Fitness of in vitro selected Pseudomonas aeruginosa nalB and nfxB multidrug resistant mutants.
J Antimicrob Chemother. 2002 Nov;50(5):657-64. doi: 10.1093/jac/dkf185.
9
Characterization of a new efflux pump, MexGHI-OpmD, from Pseudomonas aeruginosa that confers resistance to vanadium.
Microbiology (Reading). 2002 Aug;148(Pt 8):2371-2381. doi: 10.1099/00221287-148-8-2371.

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