Mobilization of nuclear antiviral factors by Exportin XPO1 via the actin network inhibits RNA virus replication DOI Creative Commons

Biao Sun,

Cheng‐Yu Wu, Paulina Alatriste González

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown

Опубликована: Дек. 20, 2024

ABSTRACT The intricate interplay between +RNA viruses and their hosts involves the exploitation of host resources to build virus-induced membranous replication organelles (VROs) in cytosol infected cells. Previous genome- proteome-wide approaches have identified numerous nuclear proteins, including restriction factors that affect tomato bushy stunt virus (TBSV). However, it is currently unknown how cells mobilize antiviral proteins tombusviruses manipulate nuclear-cytoplasmic communication. authors discovered XPO1/CRM1 exportin plays a central role TBSV plants. Based on knockdown, chemical inhibition, transient expression vitro experiments, we show XPO1 acts as cellular factor against TBSV. recruited by p33 protein into cytosolic VROs via direct interaction. Blocking nucleocytoplasmic transport function inhibits delivery several resulting dampened effects. co-opted actin network critical for deliver activities. We XPO1-delivered accumulate vir-condensates associated with VROs. Altogether, emerging theme complex: propose vir-condensate serves battleground supremacy controlling infection. It seems balance pro-viral within could be major determining susceptibility. conclude cargos are key players communication during replication. Significance Tomato (TBSV), similar other (+)RNA viruses, replicates exploits organellar membrane surfaces viral represent sites shuttle inhibited conserved interaction nod, which propelled restricted delivered provided inhibitory functions condensates VRO-associated condensate hub implications its

Язык: Английский

Proviral role of ATG2 autophagy related protein in tomato bushy stunt virus replication through bulk phospholipid transfer into the viral replication organelle DOI
Yuanrong Kang,

Judit Pogany,

Peter D. Nagy

и другие.

Molecular Biology of the Cell, Год журнала: 2024, Номер 35(10)

Опубликована: Авг. 7, 2024

Subversion of cellular membranes and membrane proliferation are used by positive-strand RNA viruses to build viral replication organelles (VROs) that support virus replication. The biogenesis the membranous VROs requires major changes in lipid metabolism transfer infected cells. In this work, we show tomato bushy stunt (TBSV) hijacks Atg2 autophagy related protein with bulk activity into via interaction TBSV p33 protein. Deletion yeast knockdown

Язык: Английский

Процитировано

4

Autophagy machinery as exploited by viruses DOI Creative Commons
Christian Münz, Grant R. Campbell, Audrey Esclatine

и другие.

Autophagy Reports, Год журнала: 2025, Номер 4(1)

Опубликована: Март 18, 2025

Viruses adapt and modulate cellular pathways to allow their replication in host cells. The catabolic pathway of macroautophagy, for simplicity referred as autophagy, is no exception. In this review, we discuss anti-viral functions both autophagy select components the machinery, how viruses have evaded them. Some use membrane remodeling ability machinery build compartments cytosol or efficiently egress from cells a non-lytic fashion. remodeled membranes can even be found viral particles envelopes single around virus packages that protect them during spreading transmission. Therefore, studies on regulation by infections reveal beyond lysosomal degradation cytosolic constituents. Furthermore, they also pinpoint molecular interactions with which most manipulated, may relevant develop effective disease treatments based modulation.

Язык: Английский

Процитировано

0

Screening bacterial effectors and human virus proteins in yeast to identify host factors driving tombusvirus RNA recombination: a role for autophagy and membrane phospholipid content DOI Creative Commons

Judit Pogany,

Jun-ichi Inaba, Yuyan Liu

и другие.

Journal of Virology, Год журнала: 2025, Номер unknown

Опубликована: Май 27, 2025

ABSTRACT Recombination in RNA viruses contributes to virus evolution and rapid emergence of new viral variants that helps evade host’s antiviral strategies. Host factors play important but poorly characterized roles recombination. The authors expressed Legionella bacterium effector proteins SARS-CoV-2 human metapneumovirus (HMPV) yeast test their effects on tomato bushy stunt (TBSV) identified 16 effectors, six SARS-CoV-2, two HMPV affecting TBSV recombination likely target shared host with TBSV. Among the targets effectors/viral was autophagy pathway. Inhibition by expression RavZ LegA9 effectors reduced production recombinants plants. Induction rapamycin, via nitrogen starvation or overexpression ATG2 lipid transfer protein, led enhanced Using vitro replicase assembly giant unilamellar vesicles confirmed critical role phosphatidylethanolamine We suggest pro-recombination co-opted is provide abundant phospholipids for replication organelle biogenesis. Overall, this work highlights membrane context regulation show N M2-1 enhance protecting RNAs from Xrn1 5´−3´ exoribonuclease yeast. Altogether, novel strategy using as a cellular system sensor might assist identification functional various bacterial IMPORTANCE Positive-strand (+)RNA replicate cytosol infected cells exploiting resources frequently lead diseases. Virus results generation contribute adaptation hosts. proteins, This approach revealed heterologous TBSV, including In replication. nucleocapsid protein are shown Thus, TBSV/yeast can be used find functions proteins.

Язык: Английский

Процитировано

0

Novel exploitation of autophagy by tombusviruses DOI
Peter D. Nagy,

Judit Pogany,

Yuanrong Kang

и другие.

Virology, Год журнала: 2024, Номер 603, С. 110363 - 110363

Опубликована: Дек. 18, 2024

Язык: Английский

Процитировано

1

Mobilization of nuclear antiviral factors by Exportin XPO1 via the actin network inhibits RNA virus replication DOI Creative Commons

Biao Sun,

Cheng‐Yu Wu, Paulina Alatriste González

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown

Опубликована: Дек. 20, 2024

ABSTRACT The intricate interplay between +RNA viruses and their hosts involves the exploitation of host resources to build virus-induced membranous replication organelles (VROs) in cytosol infected cells. Previous genome- proteome-wide approaches have identified numerous nuclear proteins, including restriction factors that affect tomato bushy stunt virus (TBSV). However, it is currently unknown how cells mobilize antiviral proteins tombusviruses manipulate nuclear-cytoplasmic communication. authors discovered XPO1/CRM1 exportin plays a central role TBSV plants. Based on knockdown, chemical inhibition, transient expression vitro experiments, we show XPO1 acts as cellular factor against TBSV. recruited by p33 protein into cytosolic VROs via direct interaction. Blocking nucleocytoplasmic transport function inhibits delivery several resulting dampened effects. co-opted actin network critical for deliver activities. We XPO1-delivered accumulate vir-condensates associated with VROs. Altogether, emerging theme complex: propose vir-condensate serves battleground supremacy controlling infection. It seems balance pro-viral within could be major determining susceptibility. conclude cargos are key players communication during replication. Significance Tomato (TBSV), similar other (+)RNA viruses, replicates exploits organellar membrane surfaces viral represent sites shuttle inhibited conserved interaction nod, which propelled restricted delivered provided inhibitory functions condensates VRO-associated condensate hub implications its

Язык: Английский

Процитировано

0