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The P3N-PIPO Protein Encoded by Wheat Yellow Mosaic Virus Is a Pathogenicity Determinant and Promotes Its Pathogenicity through Interaction with NbRLK6 in . | LitMetric

The P3N-PIPO Protein Encoded by Wheat Yellow Mosaic Virus Is a Pathogenicity Determinant and Promotes Its Pathogenicity through Interaction with NbRLK6 in .

Viruses

State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-Products, Key Laboratory of Biotechnology in Plant Protection of Ministry of Agriculture and Zhejiang Province, Institute of Plant Virology, Ningbo University, Ningbo 315211, China.

Published: September 2022

AI Article Synopsis

  • The wheat yellow mosaic virus (WYMV) has a protein called P3N-PIPO, which is important for the movement and severity of the disease it causes, similar to other potyviruses.
  • Research demonstrated that the presence of the P3N-PIPO protein in a potato virus X (PVX) vector led to more severe disease symptoms and increased virus levels in infected plants compared to a PVX without this protein.
  • Additionally, scientists identified proteins that interact with P3N-PIPO, including a receptor-like kinase, and found that reducing the expression of P3N-PIPO led to milder symptoms and less virus accumulation in plants.

Article Abstract

Similarly to other potyvirids, the bymovirus wheat yellow mosaic virus (WYMV) encodes a P3N-PIPO protein that is expressed by frameshifting occurring within the open reading frame of the P3 protein. P3N-PIPO is known to be essential for the cell-to-cell movement of several potyviruses, but this has not yet been confirmed for the WYMV. Here, we show that the WYMV P3N-PIPO protein influences disease symptom formation. Infection of plants with a potato virus X (PVX)-based vector carrying the WYMV P3N-PIPO gene induced more severe disease symptoms and resulted in higher virus accumulation levels than did infection with PVX lacking the P3N-PIPO gene. P3N-PIPO-interacting proteins were identified through co-immunoprecipitation (Co-IP) coupled with LC-MS/MS (mass spectrometry), and the interaction between P3N-PIPO and the receptor-like kinase NbRLK6 was further verified by Co-IP and bimolecular fluorescence complementation (BiFC) of transiently-expressed proteins. Furthermore, our investigation showed that the disease symptom severity and accumulation level of PVX-P3N-PIPO were decreased in plants when expression was reduced by tobacco rattle virus-induced gene silencing.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9607425PMC
http://dx.doi.org/10.3390/v14102171DOI Listing

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