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多药耐药转运蛋白 AbcA 分泌金黄色葡萄球菌细胞溶解毒素。

Multidrug-Resistance Transporter AbcA Secretes Staphylococcus aureus Cytolytic Toxins.

机构信息

Laboratory of Microbiology, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Japan.

出版信息

J Infect Dis. 2016 Jan 15;213(2):295-304. doi: 10.1093/infdis/jiv376. Epub 2015 Jul 9.

Abstract

Phenol-soluble modulins (PSMs) are Staphylococcus aureus cytolytic toxins that lyse erythrocytes and neutrophils and have important functions in the S. aureus infectious process. The molecular mechanisms of PSM secretion, however, are not well understood. Here we report that knockout of the multidrug-resistance ABC transporter AbcA, which contributes to S. aureus resistance against antibiotics and chemicals, diminished the secreted amount of PSM, leading to the accumulation of PSM in the intracellular fraction. The amount of PSM in the culture supernatants of the abcA knockout mutants was restored by introduction of the wild-type abcA gene, whereas it was not completely restored by introduction of mutant abcA genes encoding AbcA mutant proteins carrying amino acid substitutions in the adenosine triphosphate binding motifs. The abcA knockout mutant exhibited attenuated virulence in a mouse systemic infection model. These findings suggest that the multidrug resistance transporter AbcA secretes PSMs and contributes to S. aureus virulence.

摘要

酚可溶性调节素(PSMs)是金黄色葡萄球菌溶细胞毒素,可裂解红细胞和中性粒细胞,并在金黄色葡萄球菌感染过程中具有重要功能。然而,PSM 分泌的分子机制尚不清楚。在这里,我们报告多药耐药 ABC 转运蛋白 AbcA 的敲除减少了 PSM 的分泌量,导致 PSM 在细胞内部分积累,而 AbcA 对抗生素和化学物质的耐药性有助于金黄色葡萄球菌。abcA 敲除突变体培养上清液中的 PSM 量通过引入野生型 abcA 基因得以恢复,而通过引入编码在三磷酸腺苷结合基序中携带氨基酸取代的 AbcA 突变蛋白的突变 abcA 基因则不能完全恢复。abcA 敲除突变体在小鼠全身感染模型中表现出毒力减弱。这些发现表明多药耐药转运蛋白 AbcA 分泌 PSMs 并有助于金黄色葡萄球菌的毒力。

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