Kulp Adam J, Sun Bo, Ai Teresa, Manning Andrew J, Orench-Rivera Nichole, Schmid Amy K, Kuehn Meta J
Dept. of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, 27710, United States of America.
Dept. of Biology, Duke University, Durham, NC, 27708, United States of America.
PLoS One. 2015 Sep 25;10(9):e0139200. doi: 10.1371/journal.pone.0139200. eCollection 2015.
The production of outer membrane vesicles by Gram-negative bacteria has been well documented; however, the mechanism behind the biogenesis of these vesicles remains unclear. Here a high-throughput experimental method and systems-scale analysis was conducted to determine vesiculation values for the whole genome knockout library of Escherichia coli mutant strains (Keio collection). The resultant dataset quantitatively recapitulates previously observed phenotypes and implicates nearly 150 new genes in the process of vesiculation. Gene functional and biochemical pathway analyses suggest that mutations that truncate outer membrane structures such as lipopolysaccharide and enterobacterial common antigen lead to hypervesiculation, whereas mutants in oxidative stress response pathways result in lower levels. This study expands and refines the current knowledge regarding the cellular pathways required for outer membrane vesiculation in E. coli.
革兰氏阴性菌产生外膜囊泡已有充分记录;然而,这些囊泡生物发生背后的机制仍不清楚。在此,我们采用了一种高通量实验方法和系统规模分析来确定大肠杆菌突变菌株(Keio文库)全基因组敲除文库的囊泡化值。所得数据集定量概括了先前观察到的表型,并表明近150个新基因参与了囊泡化过程。基因功能和生化途径分析表明,截断脂多糖和肠杆菌共同抗原等外膜结构的突变会导致过度囊泡化,而氧化应激反应途径中的突变体则导致较低水平。本研究扩展并完善了目前关于大肠杆菌外膜囊泡化所需细胞途径的知识。