生物
核酶
核糖核酸
核糖核酸酶
ADP核糖基化
转移RNA
细胞生物学
微生物学
分泌物
酶
生物化学
基因
NAD+激酶
作者
Nathan P. Bullen,David Sychantha,Stephanie S. Thang,Peter H. Culviner,Marta Rudzite,Shehryar Ahmad,Vraj S. Shah,Alain Filloux,Gerd Prehna,John C. Whitney
出处
期刊:Molecular Cell
[Elsevier BV]
日期:2022-09-01
卷期号:82 (18): 3484-3498.e11
被引量:40
标识
DOI:10.1016/j.molcel.2022.08.015
摘要
ADP-ribosyltransferases (ARTs) were among the first identified bacterial virulence factors. Canonical ART toxins are delivered into host cells where they modify essential proteins, thereby inactivating cellular processes and promoting pathogenesis. Our understanding of ARTs has since expanded beyond protein-targeting toxins to include antibiotic inactivation and DNA damage repair. Here, we report the discovery of RhsP2 as an ART toxin delivered between competing bacteria by a type VI secretion system of Pseudomonas aeruginosa. A structure of RhsP2 reveals that it resembles protein-targeting ARTs such as diphtheria toxin. Remarkably, however, RhsP2 ADP-ribosylates 2'-hydroxyl groups of double-stranded RNA, and thus, its activity is highly promiscuous with identified cellular targets including the tRNA pool and the RNA-processing ribozyme, ribonuclease P. Consequently, cell death arises from the inhibition of translation and disruption of tRNA processing. Overall, our data demonstrate a previously undescribed mechanism of bacterial antagonism and uncover an unprecedented activity catalyzed by ART enzymes.
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