Reduced Aeration Affects the Expression of the NorB Efflux Pump of Staphylococcus aureus by Posttranslational Modification of MgrA

被引:30
|
作者
Que Chi Truong-Bolduc [1 ,2 ]
Hsing, Liao Chun [1 ,2 ]
Villet, Regis [1 ,2 ]
Bolduc, Gilles R. [3 ]
Estabrooks, Zoe [3 ]
Taguezem, G. Florent [3 ]
Hooper, David C. [1 ,2 ]
机构
[1] Massachusetts Gen Hosp, Div Infect Dis & Med Serv, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Massasoit Community Coll, Brockton, MA USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
OXIDATION-SENSING MECHANISM; ANAEROBIC GENE-EXPRESSION; SYNDROME TOXIN 1; GLOBAL REGULATOR; SERINE-PROTEASE; CARBON-DIOXIDE; OXYGEN; ACID; MOXIFLOXACIN; VIRULENCE;
D O I
10.1128/JB.06503-11
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We previously showed that at acid pH, the transcription of norB, encoding the NorB efflux pump, increases due to a reduction in the phosphorylation level of MgrA, which in turn leads to a reduction in bacterial killing by moxifloxacin, a substrate of the NorB efflux pump. In this study, we demonstrated that reduced oxygen levels did not affect the transcript levels of mgrA but modified the dimerization of the MgrA protein, which remained mostly in its monomeric form. Under reduced aeration, we also observed a 21.7-fold increase in the norB transcript levels after 60 min of growth that contributed to a 4-fold increase in the MICs of moxifloxacin and sparfloxacin for Staphylococcus aureus RN6390. The relative proportions of MgrA in monomeric and dimeric forms were altered by treatment with H2O2, but incubation of purified MgrA with extracts of cells grown under reduced but not normal aeration prevented MgrA from being converted to its dimeric DNA-binding form. This modification was associated with cleavage of a fragment of the dimerization domain of MgrA without change in MgrA phosphorylation and an increase in transcript levels of genes encoding serine proteases in cells incubated at reduced aeration. Taken together, these data suggest that modification of MgrA by proteases underlies the reversal of its repression of norB and increased resistance to NorB substrates in response to reduced-aeration conditions, illustrating a third mechanism of posttranslational modification, in addition to oxidation and phosphorylation, that modulates the regulatory activities of MgrA.
引用
收藏
页码:1823 / 1834
页数:12
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