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Magnaporthe oryzae chrysovirus 1 strain D confers growth inhibition to the host fungus and exhibits multiform viral structural proteins.
- Source :
-
Virology [Virology] 2019 Sep; Vol. 535, pp. 241-254. Date of Electronic Publication: 2019 Jul 15. - Publication Year :
- 2019
-
Abstract
- A Japanese isolate of Magnaporthe oryzae is infected by Magnaporthe oryzae chrysovirus 1-D (MoCV1-D), which is classified in cluster II of the family Chrysoviridae. The genome of MoCV1-D consists of five dsRNAs. dsRNAs 1-4 show high identity with those of related MoCV1 viruses, whereas dsRNA5 shows relatively low identity and is sometimes deleted during virus propagation. MoCV1-D causes growth inhibition of its host fungus, and the protein encoded by its dsRNA4 impairs cell growth when expressed in yeast cells. It also causes abnormal pigmentation and colony albinization, and we showed that these phenotypes are associated with reduced accumulation of the melanin biosynthesis intermediate scylatone. MoCV1-D exhibits multiform viral structural proteins during prolonged culture. The original host isolate is co-infected with MoCV1-D, a victorivirus, and a partitivirus, and these mycoviruses are detected in cell-free supernatant fractions after prolonged liquid culturing. Hyphal fusion experiments demonstrated that MoCV1-D is transmissible via anastomosis.<br /> (Copyright © 2019 Elsevier Inc. All rights reserved.)
- Subjects :
- Ascomycota metabolism
Fungal Viruses genetics
Melanins biosynthesis
Protein Isoforms genetics
Protein Isoforms metabolism
RNA Viruses genetics
RNA, Double-Stranded genetics
Viral Structural Proteins genetics
Ascomycota growth & development
Ascomycota virology
Fungal Viruses growth & development
RNA Viruses growth & development
RNA, Viral genetics
Viral Structural Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1096-0341
- Volume :
- 535
- Database :
- MEDLINE
- Journal :
- Virology
- Publication Type :
- Academic Journal
- Accession number :
- 31344549
- Full Text :
- https://doi.org/10.1016/j.virol.2019.07.014