A mycoviral infection drives virulence and ecological fitness of the entomopathogenic fungus Beauveria bassiana

Entomopathogenic ascomycetes are important natural regulators of insect pest populations and an increasingly adopted microbial control option. Fungal virulence in entomopathogenic ascomycetes can be modified by mycoviruses, viruses that infect fungi, whereas the possible role of these viruses on the physical and biochemical properties of the virus-containing fungal strains and on their ecological fitness has remained largely unexplored. Here, utilizing a Beauveria bassiana strain naturally infected with two mycoviruses, Beauveria bassiana partitivirus 2 (BbPV-2) and Beauveria bassiana polymycovirus 1 (BbPmV-1), we found that the mycovirus-containing strain is hypervirulent towards the experimental insect Galleria mellonella and shows major physical and biochemical changes in spore size, isoelectric point, and Pr1 activity, but even more impactful, the mycoviral infection confers a significant environmental- abiotic and biotic stress tolerance to the fungus. Hence, mycovirus infection expanded the temperature range for fungal growth and germination, and improved tolerance to osmotic stress, water stress, and UV-B radiation. Similarly, the antagonistic activity of the mycovirus-containing strain against Trichoderma harzianum was increased as compared to the mycovirus-free one. Taken together, these data suggest for the first time a mycovirus related adaptation of key traits indicators of environmental competence of a beneficial fungus, rendering these mycoviruses as potent tools for entomopathogenic fungal strain selection and development as mycoinsecticides.

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Publication Details

Journal
Journal of Invertebrate Pathology
Published
2024-12-06
DOI
https://doi.org/10.1016/j.jip.2024.108251
Citations
7
Primary Topic
Insect symbiosis and bacterial influences
Type
article
Field-Weighted Citation Impact
3.78

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article

A mycoviral infection drives virulence and ecological fitness of the entomopathogenic fungus Beauveria bassiana

Ioly Kotta‐Loizou, Enrique Quesada‐Moraga, Inmaculada Garrido‐Jurado, Fátima Rueda-Maíllo
7 citations
Journal of Invertebrate Pathology
Insect symbiosis and bacterial influences
3.78
article

A mycoviral infection drives virulence and ecological fitness of the entomopathogenic fungus Beauveria bassiana

Ioly Kotta‐Loizou, Enrique Quesada‐Moraga, Inmaculada Garrido‐Jurado, Fátima Rueda-Maíllo
article en
7 citations

Abstract

Entomopathogenic ascomycetes are important natural regulators of insect pest populations and an increasingly adopted microbial control option. Fungal virulence in entomopathogenic ascomycetes can be modified by mycoviruses, viruses that infect fungi, whereas the possible role of these viruses on the physical and biochemical properties of the virus-containing fungal strains and on their ecological fitness has remained largely unexplored. Here, utilizing a Beauveria bassiana strain naturally infected with two mycoviruses, Beauveria bassiana partitivirus 2 (BbPV-2) and Beauveria bassiana polymycovirus 1 (BbPmV-1), we found that the mycovirus-containing strain is hypervirulent towards the experimental insect Galleria mellonella and shows major physical and biochemical changes in spore size, isoelectric point, and Pr1 activity, but even more impactful, the mycoviral infection confers a significant environmental- abiotic and biotic stress tolerance to the fungus. Hence, mycovirus infection expanded the temperature range for fungal growth and germination, and improved tolerance to osmotic stress, water stress, and UV-B radiation. Similarly, the antagonistic activity of the mycovirus-containing strain against Trichoderma harzianum was increased as compared to the mycovirus-free one. Taken together, these data suggest for the first time a mycovirus related adaptation of key traits indicators of environmental competence of a beneficial fungus, rendering these mycoviruses as potent tools for entomopathogenic fungal strain selection and development as mycoinsecticides.

Journal of Invertebrate PathologyVol. 209
University of Hertfordshire (GB), University of Córdoba (ES)
Ministerio de Ciencia, Innovación y Universidades, Ministerio de Ciencia e Innovación, Agencia Estatal de Investigación
Openalex Percentile: Top 7%
Insect symbiosis and bacterial influences
3.78
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