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Virulence. 2018 Jan 1;9(1):402-413. doi: 10.1080/21505594.2017.1405190.

The entomopathogenic fungus Metarhizium robertsii communicates with the insect host Galleria mellonella during infection.

Author information

1
a Fraunhofer Institute for Molecular Biology and Applied Ecology , Department of Bioresources , Giessen , Germany.
2
b Institute for Insect Biotechnology, Justus-Liebig University of Giessen , Giessen , Germany.

Abstract

Parasitic fungi are the only pathogens that can infect insect hosts directly through their proteinaceous exoskeleton. Penetration of the cuticle requires the release of fungal enzymes, including proteinases, which act as virulence factors. Insects can sense fungal infections and activate innate immune responses, including the synthesis of antifungal peptides and proteinase inhibitors that neutralize the incoming proteinases. This well-studied host response is epigenetically regulated by histone acetylation/deacetylation. Here we show that entomopathogenic fungi can in turn sense the presence of insect-derived antifungal peptides and proteinase inhibitors, and respond by inducing the synthesis of chymotrypsin-like proteinases and metalloproteinases that degrade the host-derived defense molecules. The rapidity of this response is dependent on the virulence of the fungal strain. We confirmed the specificity of the pathogen response to host-derived defense molecules by LC/MS and RT-PCR analysis, and correlated this process with the epigenetic regulation of histone acetylation/deacetylation. This cascade of responses reveals that the coevolution of pathogens and hosts can involve a complex series of attacks and counterattacks based on communication between the invading fungal pathogen and its insect host. The resolution of this process determines whether or not pathogenesis is successful.

KEYWORDS:

Metarhizium robertsii; antifungal peptides; epigenetics; fungal pathogenesis; fungi; galleria mellonella; insects; protease inhibitors

PMID:
29166834
PMCID:
PMC5955202
DOI:
10.1080/21505594.2017.1405190
[Indexed for MEDLINE]
Free PMC Article

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