Heterodimers as the Structural Unit of the T=1 Capsid of the Fungal Double-Stranded RNA Rosellinia necatrix Quadrivirus 1

Author:

Luque Daniel12,Mata Carlos P.1,González-Camacho Fernando2,González José M.1,Gómez-Blanco Josué1,Alfonso Carlos3,Rivas Germán3,Havens Wendy M.4,Kanematsu Satoko5,Suzuki Nobuhiro6,Ghabrial Said A.4,Trus Benes L.7,Castón José R.1

Affiliation:

1. Department of Structure of Macromolecules, Centro Nacional de Biotecnología (CNB-CSIC), Cantoblanco, Madrid, Spain

2. Centro Nacional de Microbiología/ISCIII, Carretera de Majadahonda-Pozuelo, Majadahonda, Madrid, Spain

3. Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas, Madrid, Spain

4. Department of Plant Pathology, University of Kentucky, Lexington, Kentucky, USA

5. Institute of Fruit Tree Science, National Agriculture and Food Research Organization (NARO), Morioka, Iwate, Japan

6. Institute of Plant Science and Resources, Okayama, Japan

7. Imaging Sciences Laboratory, CIT, NIH, Bethesda, Maryland, USA

Abstract

ABSTRACT Most double-stranded RNA (dsRNA) viruses are transcribed and replicated in a specialized icosahedral capsid with a T=1 lattice consisting of 60 asymmetric capsid protein (CP) dimers. These capsids help to organize the viral genome and replicative complex(es). They also act as molecular sieves that isolate the virus genome from host defense mechanisms and allow the passage of nucleotides and viral transcripts. Rosellinia necatrix quadrivirus 1 (RnQV1), the type species of the family Quadriviridae , is a dsRNA fungal virus with a multipartite genome consisting of four monocistronic segments (segments 1 to 4). dsRNA-2 and dsRNA-4 encode two CPs (P2 and P4, respectively), which coassemble into ∼450-Å-diameter capsids. We used three-dimensional cryo-electron microscopy combined with complementary biophysical techniques to determine the structures of RnQV1 virion strains W1075 and W1118. RnQV1 has a quadripartite genome, and the capsid is based on a single-shelled T=1 lattice built of P2-P4 dimers. Whereas the RnQV1-W1118 capsid is built of full-length CP, P2 and P4 of RnQV1-W1075 are cleaved into several polypeptides, maintaining the capsid structural organization. RnQV1 heterodimers have a quaternary organization similar to that of homodimers of reoviruses and other dsRNA mycoviruses. The RnQV1 capsid is the first T=1 capsid with a heterodimer as an asymmetric unit reported to date and follows the architectural principle for dsRNA viruses that a 120-subunit capsid is a conserved assembly that supports dsRNA replication and organization. IMPORTANCE Given their importance to health, members of the family Reoviridae are the basis of most structural and functional studies and provide much of our knowledge of dsRNA viruses. Analysis of bacterial, protozoal, and fungal dsRNA viruses has improved our understanding of their structure, function, and evolution, as well. Here, we studied a dsRNA virus that infects the fungus Rosellinia necatrix , an ascomycete that is pathogenic to a wide range of plants. Using three-dimensional cryo-electron microscopy and analytical ultracentrifugation analysis, we determined the structure and stoichiometry of Rosellinia necatrix quadrivirus 1 (RnQV1). The RnQV1 capsid is a T=1 capsid with 60 heterodimers as the asymmetric units. The large amount of genetic information used by RnQV1 to construct a simple T=1 capsid is probably related to the numerous virus-host and virus-virus interactions that it must face in its life cycle, which lacks an extracellular phase.

Funder

Spanish Ministry of Economy and Competitively

Spanish Ministry of Economy and Competitivity

Comunidad Autónoma de Madrid

Intramural Research Program of the NIH

Ministry of Education, Culture, Science, Sports and Technology (MEXT) of Japan

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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