Skip to main content

EDITORIAL article

Front. Microbiol., 31 January 2024
Sec. Virology
This article is part of the Research Topic Community Series in Mycoviruses and Related Viruses infecting Fungi, Lower Eukaryotes, Plants and Insects, Volume II View all 6 articles

Editorial: Community series in mycoviruses and related viruses infecting fungi, lower eukaryotes, plants and insects, volume II

  • 1Laboratory of Molecular and Cellular Biology, Graduate School of Agriculture, Tokyo University of Agriculture and Technology, Fuchu, Japan
  • 2Department of Clinical, Pharmaceutical and Biological Science, School of Life and Medical Sciences, University of Hertfordshire, Hatfield, United Kingdom
  • 3Department of Life Sciences, Faculty of Natural Sciences, Imperial College London, London, United Kingdom
  • 4Department of Agricultural Biotechnology, College of Agriculture and Life Sciences, Plant Genomics and Breeding Institute, Research Institute of Agriculture and Life Sciences, Seoul National University, Seoul, Republic of Korea

The Frontiers Community Series in “Mycoviruses and related viruses infecting fungi, lower eukaryotes, plants and insects, volume II” was initiated following the success of the Frontiers Research Topic “Mycoviruses and related viruses infecting fungi, lower eukaryotes, plants and insects.” Unlike the original Research Topic, which accepted submissions through both Frontiers in Microbiology and Frontiers in Plant Pathology, the Community Series was limited to Frontiers in Microbiology and covered exclusively one section: Virology. As a result, most manuscripts in the Community Series focused on viruses infecting insects and human pathogenic fungi, instead of plant pathogens. Our Community Series accommodates 5 high-quality Original Research manuscripts that provide insight into the biology of a range of viruses found in oomycetes and filamentous fungi, including the discovery and characterization of two novel members of the family Polymycoviridae, mycovirus elimination, and numerous host-virus interactions and virus-mediated phenotypes.

Sakuta et al. investigated at the molecular level two members of the family Endornaviridae, Phytophthora endornavirus 2 and 3, found in the plant pathogenic oomycetes Phytophthora rot of asparagus. These endornaviruses were shown to be present in the cells primarily as positive-sense, singe-stranded RNA and have 5′ terminal nick structures approximately 1 kb in length. Full-length cDNA clones of the endornaviruses were introduced into the model yeast Saccharomyces cerevisiae under the control of both constitutive and inducible promoters, and their overexpression resulted in reduced yeast growth. Tagging endornavirus proteins with green fluorescent protein allowed their visualization within yeast cells.

Wang et al. reported the sequence of a new member of the family Polymycoviridae, Metarhizium anisopliae polymycovirus 1, from the insect-pathogenic ascomycete and popular biocontrol agent Metarhizium anisopliae. Polymycovirus infection increases fungal growth, conidiation, and sensitivity to ultraviolet irradiation by altering host gene expression but has no significant effect on virulence. The polymycovirus-mediated phenotypes were not linked to individual polymycoviral proteins.

Teng et al. reported the sequence of a new member of the family Polymycoviridae, Talaromyces amestolkiae polymycovirus 1, the first mycovirus found to infect Talaromyces amestolkiae, an ascomycete ubiquitous in air, soil, food, and plants that is also an opportunistic human pathogen. Polymycovirus infection reduced the production of the characteristic red pigments of T. amestolkiae, while inducing clustering of fungal sclerotia. Transcriptome profiling illustrated that polymycovirus infection results in the downregulation of host genes associated with metabolism.

Jiang et al. investigated the role of RNA interference as an antiviral defense against Aspergillus flavus partitivirus 1 in Aspergillus flavus, an ascomycete known for aflatoxin production. Partitivirus infection depleted sclerotia production and induced expression of genes encoding fungal enzymes, including Dicer, Argonaut, and RNA-dependent RNA polymerases, resulting in virus-derived small RNAs. Deletions of these genes affected viral RNA levels, fungal sporulation, and host sensitivity to cell wall, genotoxic, osmotic, and oxidative stress.

Ikeda et al. explored alternatives for elimination of RNA viruses using antiviral drugs, a process generating virus-infected and virus-free isogenic lines required for further phenotypic comparisons. The nucleoside analog 2′-C-methylcytidine was shown to be active against a wider range of mycoviruses as compared to ribavirin, 2′-C-methyladenosine and 7-Deaza-2′-C-methyladenosine and eliminated members of the families Chrysoviridae, Mitoviridae, Partitiviridae, and Polymycoviridae infecting the human pathogenic ascomycete Aspergillus fumigatus.

As Associate Editors, we would like to take this opportunity to thank and acknowledge all the contributing authors who chose our Community Series in “Mycoviruses and related viruses infecting fungi, lower eukaryotes, plants and insects, volume II” as a vehicle for sharing their exciting work.

Author contributions

HM: Writing – review & editing. IK-L: Writing – original draft. K-HK: Writing – review & editing.

Funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Keywords: mycovirus, Phytophthora, Metarhizium, Talaromyces, Aspergillus, RNA silencing, antiviral drugs

Citation: Moriyama H, Kotta-Loizou I and Kim K-H (2024) Editorial: Community series in mycoviruses and related viruses infecting fungi, lower eukaryotes, plants and insects, volume II. Front. Microbiol. 15:1349526. doi: 10.3389/fmicb.2024.1349526

Received: 04 December 2023; Accepted: 22 January 2024;
Published: 31 January 2024.

Edited and reviewed by: Anna Kramvis, University of the Witwatersrand, South Africa

Copyright © 2024 Moriyama, Kotta-Loizou and Kim. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Ioly Kotta-Loizou, aS5rb3R0YS1sb2l6b3UyJiN4MDAwNDA7aGVydHMuYWMudWs=; aS5rb3R0YS1sb2l6b3UxMyYjeDAwMDQwO2ltcGVyaWFsLmFjLnVr

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.