4.6 Article

The plant protein NbP3IP directs degradation ofRice stripe virusp3 silencing suppressor protein to limit virus infection through interaction with the autophagy-related protein NbATG8

期刊

NEW PHYTOLOGIST
卷 229, 期 2, 页码 1036-1051

出版社

WILEY
DOI: 10.1111/nph.16917

关键词

ATG8; autophagy; p3; P3IP; Rice stripe virus(RSV)

资金

  1. National Natural Science Foundation of China [31772239]
  2. national key research and development program of China [2017YFA0503401]
  3. National Transgenic Science and Technology Program [2016ZX08001-002]
  4. Rural & Environment Science & Analytical Services Division of the Scottish Government
  5. International Science & Technology Cooperation Program of China [2015DFA30700]
  6. K.C.Wong Magna Fund of Ningbo University

向作者/读者索取更多资源

A newly identified plant protein, NbP3IP, has been shown to degrade the silencing suppressor protein p3 of RSV through the autophagy pathway, thereby inhibiting RSV infection. The interaction of NbP3IP with autophagy proteins suggests a potential role in selective autophagosomal cargo receptor activity. This study provides evidence that autophagy can play an antiviral role against negative-strand RNA viruses by antagonizing p3 of RSV.
In plants, autophagy is involved in responses to viral infection. However, the role of host factors in mediating autophagy to suppress viruses is poorly understood. A previously uncharacterized plant protein, NbP3IP, was shown to interact with p3, an RNA-silencing suppressor protein encoded byRice stripe virus(RSV), a negative-strand RNA virus. The potential roles of NbP3IP in RSV infection were examined. NbP3IP degraded p3 through the autophagy pathway, thereby affecting the silencing suppression activity of p3. Transgenic overexpression of NbP3IP conferred resistance to RSV infection inNicotiana benthamiana. RSV infection was promoted in ATG5- or ATG7-silenced plants and was inhibited in GAPC-silenced plants where autophagy was activated, confirming the role of autophagy in suppressing RSV infection. NbP3IP interacted with NbATG8f, indicating a potential selective autophagosomal cargo receptor role for P3IP. Additionally, the rice NbP3IP homolog (OsP3IP) also mediated p3 degradation and interacted with OsATG8b and p3. Through identification of the involvement of P3IP in the autophagy-mediated degradation of RSV p3, we reveal a new mechanism to antagonize the infection of RSV, and thereby provide the first evidence that autophagy can play an antiviral role against negative-strand RNA viruses.

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