Expression of a structural protein of the mycovirus FgV-ch9 negatively affects the transcript level of a novel symptom alleviation factor and causes virus-infection like symptoms in Fusarium graminearum
Infections of fungi by mycoviruses are often symptomless but sometimes also fatal as they perturb sporulation, growth, and, if applicable, virulence of the fungal host. Hypovirulence-inducing mycoviruses, therefore, represent a powerful mean to defeat fungal epidemics on crop plants. Infection with...
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Published in | Journal of virology Vol. 92; no. 17 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Society for Microbiology
01.09.2018
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Subjects | |
Online Access | Get full text |
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Summary: | Infections of fungi by mycoviruses are often symptomless but sometimes also fatal as they perturb sporulation, growth, and, if applicable, virulence of the fungal host. Hypovirulence-inducing mycoviruses, therefore, represent a powerful mean to defeat fungal epidemics on crop plants. Infection with Fusarium graminearum virus China 9 (FgV-ch9), a dsRNA chrysovirus-like mycovirus, debilitates
, the causal agent of Fusarium Head Blight. In search for potential symptom alleviation or aggravation factors in
, we consecutively infected a custom-made
mutant collection with FgV-ch9 and found a mutant with constantly elevated expression of a gene coding for a putative mRNA-binding protein that did not show any disease symptoms despite harboring high amounts of virus. Deletion of this gene, named virus response 1 (
), resulted in phenotypes identical to those observed in the virus-infected wild type with respect to growth, reproduction, and virulence. Similarly, the viral structural protein coded on segment 3 (P3) caused virus-infection like symptoms when expressed in the wild-type but not in the
-overexpression mutant. Gene expression analysis revealed a drastic downregulation of
in the presence of virus and in mutants expressing P3. We conclude that symptom development and severity correlate with gene expression levels of
This was confirmed by comparative transcriptome analysis showing a large transcriptional overlap between the virus-infected wild type, the
deletion mutant and the P3-expressing mutant. Hence,
represents a fundamental host factor for the expression of virus-related symptoms and helps to understand the underlying mechanism of hypovirulence.
Virus infections of phytopathogenic fungi occasionally impair growth, reproduction, and virulence, a phenomenon referred to as hypovirulence. Hypovirulence-inducing mycoviruses, therefore, represent a powerful mean to defeat fungal epidemics on crop plants. However, the poor understanding of the molecular basis of hypovirulence induction limits their application. Using the devastating fungal pathogen on cereal crops,
, we identified an mRNA binding protein (named virus response 1,
) which is involved in symptom expression. Downregulation of
in the virus-infected fungus and
deletion evoke virus-infection like symptoms while constitutive expression overrules the cytopathic effects of the virus infection. Intriguingly, the presence of a specific viral structural protein is sufficient to trigger the fungal response,
downregulation, and symptom development similar to virus infection. The advancements in understanding fungal infection and response may aid biological pest control approaches using mycoviruses or viral proteins to prevent future Fusarium epidemics. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Citation Bormann J, Heinze C, Blum C, Mentges M, Brockmann A, Alder A, Landt SK, Josephson B, Indenbirken D, Spohn M, Plitzko B, Loesgen S, Freitag M, Schäfer W. 2018. Expression of a structural protein of the mycovirus FgV-ch9 negatively affects the transcript level of a novel symptom alleviation factor and causes virus infection-like symptoms in Fusarium graminearum. J Virol 92:e00326-18. https://doi.org/10.1128/JVI.00326-18. J.B. and C.H. contributed equally to this work. Present address: Jörg Bormann, University Bremen, Department for Cell Biology, Bremen, Germany. |
ISSN: | 0022-538X 1098-5514 |
DOI: | 10.1128/jvi.00326-18 |