a unique role for the host escrt proteins in replication of tomato bushy stunt virus宿主escrt蛋白质的独特作用在番茄浓密的阻碍病毒的复制.pdfVIP
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a unique role for the host escrt proteins in replication of tomato bushy stunt virus宿主escrt蛋白质的独特作用在番茄浓密的阻碍病毒的复制
A Unique Role for the Host ESCRT Proteins in Replication
of Tomato bushy stunt virus
Daniel Barajas, Yi Jiang, Peter D. Nagy*
Department of Plant Pathology, University of Kentucky, Lexington, Kentucky, United States of America
Abstract
Plus-stranded RNA viruses replicate in infected cells by assembling viral replicase complexes consisting of viral- and host-
coded proteins. Previous genome-wide screens with Tomato bushy stunt tombusvirus (TBSV) in a yeast model host revealed
the involvement of seven ESCRT (endosomal sorting complexes required for transport) proteins in viral replication. In this
paper, we show that the expression of dominant negative Vps23p, Vps24p, Snf7p, and Vps4p ESCRT factors inhibited virus
replication in the plant host, suggesting that tombusviruses co-opt selected ESCRT proteins for the assembly of the viral
replicase complex. We also show that TBSV p33 replication protein interacts with Vps23p ESCRT-I and Bro1p accessory
ESCRT factors. The interaction with p33 leads to the recruitment of Vps23p to the peroxisomes, the sites of TBSV replication.
The viral replicase showed reduced activity and the minus-stranded viral RNA in the replicase became more accessible to
ribonuclease when derived from vps23D or vps24D yeast, suggesting that the protection of the viral RNA is compromised
within the replicase complex assembled in the absence of ESCRT proteins. The recruitment of ESCRT proteins is needed for
the precise assembly of the replicase complex, which might help the virus evade recognition by the host defense
surveillance system and/or prevent viral RNA destruction by the gene silencing machinery.
Citation: Barajas D, Jiang Y, Nagy PD (2009) A Unique Role for the Host ESCRT Proteins in Replication of Tomato bushy stunt virus. PLoS Pathog 5(12): e1000705.
doi:10.1371/journal.ppat.1000705
Editor: Ja
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