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May 29, 2026Plants0 citationsOpen Access

Systematic Screening of Host Interactors for Soybean Mosaic Virus Proteins Identifies Four Soybean (Glycine max) Antiviral Factors

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NNNiu NiuWLWenxia LiZZZikai Zhou

Key Points

  • This research aims to identify soybean proteins that interact with Soybean Mosaic Virus (SMV) and contribute to antiviral resistance.
  • Screened a soybean cDNA library using the yeast two-hybrid method with 10 SMV proteins as baits.
  • Identified 200 positive clones correlating to 147 candidate host proteins.
  • Utilized BiFC and transient expression assays to assess the role of four antiviral factors identified during infection.
  • Four soybean proteins were identified that delay systemic viral spread after SMV infection.
  • Co-expression of GmSTOP1, GmHrBP1, or GmGIP2 partially rebounded SMV accumulation, indicating their role in resistance.
  • GmSiPPase and NIa-Pro co-expression further inhibited viral proliferation.

Abstract

Soybean mosaic virus (SMV) establishes successful infection through the coordinated action of multiple viral proteins, yet how these components are collectively engaged in host processes remains unclear. Using 10 SMV-encoded proteins as baits, we screened a soybean(Glycine max) cDNA library using the yeast two-hybrid (Y2H) method and obtained 200 positive clones corresponding to 147 nonredundant candidate host proteins. Integrative analyses indicated that these interacting proteins were mainly associated with host processes related to photosynthesis and energy metabolism, as well as protein quality control (PQC), and that their promoters were enriched in light- and stress-responsive elements. Photosynthesis-related genes were more strongly perturbed in the susceptible cultivar, whereas PQC-module genes showed overall downregulation in both resistant and susceptible cultivars upon SMV infection. Y2H, Bimolecular Fluorescence Complementation (BiFC), and transient expression assays identified four soybean resistance factors that interact with SMV proteins. These factors delayed systemic spread and continued to restrict viral proliferation after systemic infection was established. Notably, SMV accumulation partially rebounded when viral proteins were co-expressed with GmSTOP1, GmHrBP1, or GmGIP2, while co-expression of GmSiPPase and NIa-Pro further inhibited viral proliferation. In summary, this study maps the host-targeting profile of SMV across multiple viral components and provides clues to the SMV–soybean interaction network and antiviral gene resources in soybean.

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Cite This Study

Niu et al. (2026) studied this question.

synapsesocial.com/papers/6a192e39fab5b468c44172cbhttps://doi.org/10.3390/plants15111650
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