铜绿假单胞菌的细菌膜囊泡通过抑制线粒体复合体III激活单磷酸腺苷活化的蛋白激酶信号。

IF 3.8 Q2 MULTIDISCIPLINARY SCIENCES
PNAS nexus Pub Date : 2025-08-19 eCollection Date: 2025-08-01 DOI:10.1093/pnasnexus/pgaf248
Julia Müller, Marcel Kretschmer, Elise Opitsch, Svea Holland, José Manuel Borrero-de Acuña, Dieter Jahn, Meina Neumann-Schaal, Andre Wegner
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引用次数: 0

摘要

细菌膜囊泡(BMVs)由许多致病菌分泌,已知在感染时刺激宿主的各种反应,从而有助于铜绿假单胞菌等细菌性病原体的致病性。虽然bmv对宿主免疫反应的影响已经得到了很好的研究,但它们对细胞代谢和线粒体呼吸的影响却知之甚少。在这里,我们发现铜绿假单胞菌bmv (i)重编程人肺细胞的细胞代谢,(ii)通过(iii)特异性抑制电子传递链的复合物iii对线粒体呼吸产生负面影响,导致(iv)单磷酸腺苷活化蛋白激酶(AMPK)信号的激活,进而导致(v) AMPK依赖性的整体蛋白质合成抑制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Bacterial membrane vesicles of <i>Pseudomonas aeruginosa</i> activate adenosine monophosphate-activated protein kinase signaling through inhibition of mitochondrial complex III.

Bacterial membrane vesicles of <i>Pseudomonas aeruginosa</i> activate adenosine monophosphate-activated protein kinase signaling through inhibition of mitochondrial complex III.

Bacterial membrane vesicles of <i>Pseudomonas aeruginosa</i> activate adenosine monophosphate-activated protein kinase signaling through inhibition of mitochondrial complex III.

Bacterial membrane vesicles of Pseudomonas aeruginosa activate adenosine monophosphate-activated protein kinase signaling through inhibition of mitochondrial complex III.

Bacterial membrane vesicles (BMVs) are secreted by many pathogenic bacteria and known to stimulate various host responses upon infection, thereby contributing to the pathogenicity of bacterial pathogens like Pseudomonas aeruginosa. While the effects of BMVs on host immune responses are well studied, little is known about their impact on cell metabolism and mitochondrial respiration. Here, we show that P. aeruginosa BMVs (i) reprogram cell metabolism of human lung cells, (ii) negatively affect mitochondrial respiration by (iii) specifically inhibiting complex III of the electron transport chain, leading to (iv) the activation of adenosine monophosphate-activated protein kinase (AMPK) signaling, which in turn results in (v) AMPK-dependent inhibition of global protein synthesis.

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