Begomovirus-Host Interactions: Viral Proteins Orchestrating Intra and Intercellular Transport of Viral DNA While Suppressing Host Defense Mechanisms

Viruses. 2023 Jul 21;15(7):1593. doi: 10.3390/v15071593.

Abstract

Begomoviruses, which belong to the Geminiviridae family, are intracellular parasites transmitted by whiteflies to dicotyledonous plants thatsignificantly damage agronomically relevant crops. These nucleus-replicating DNA viruses move intracellularly from the nucleus to the cytoplasm and then, like other plant viruses, cause disease by spreading systemically throughout the plant. The transport proteins of begomoviruses play a crucial role in recruiting host components for the movement of viral DNA within and between cells, while exhibiting functions that suppress the host's immune defense. Pioneering studies on species of the Begomovirus genus have identified specific viral transport proteins involved in intracellular transport, cell-to-cell movement, and systemic spread. Recent research has primarily focused on viral movement proteins and their interactions with the cellular host transport machinery, which has significantly expanded understanding on viral infection pathways. This review focuses on three components within this context: (i) the role of viral transport proteins, specifically movement proteins (MPs) and nuclear shuttle proteins (NSPs), (ii) their ability to recruit host factors for intra- and intercellular viral movement, and (iii) the suppression of antiviral immunity, with a particular emphasis on bipartite begomoviral movement proteins.

Keywords: begomoviruses; intracellular virus movement; movement protein; nuclear shuttle protein; suppression of antiviral signaling; virus–host interactions.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Begomovirus* / genetics
  • Carrier Proteins / metabolism
  • DNA, Viral / genetics
  • Defense Mechanisms
  • Plant Diseases
  • Viral Proteins / genetics

Substances

  • DNA, Viral
  • Viral Proteins
  • Carrier Proteins

Grants and funding

This work was partially funded by CAPES finance code 001, CNPq (Grant 403819/2021-0 to E.P.B./F.), FAPEMIG (Grant RED 00205-22 and Grant CBB—APQ-01282-17 to E.P.B.F.), and the National Institute of Science and Technology in Plant–Pest interactions. S.S.B. is a recipient of a CNPq graduate fellowship and F.A.S. is a post-doctoral fellow from CAPES.