A comparative cell wall analysis of Trichoderma spp. confirms a conserved polysaccharide scaffold and suggests an important role for chitosan in mycoparasitism
Trichoderma species are emerging model fungi for the development of biocontrol agents and are used in industrial biotechnology as efficient enzyme producers. Fungal cell walls are complex structures that differ in carbohydrate, protein, and enzyme composition across taxa. Here, we present a chemical...
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Published in | Microbiology spectrum Vol. 12; no. 8; p. e0349523 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Society for Microbiology
06.08.2024
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Subjects | |
Online Access | Get full text |
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Summary: | Trichoderma
species are emerging model fungi for the development of biocontrol agents and are used in industrial biotechnology as efficient enzyme producers. Fungal cell walls are complex structures that differ in carbohydrate, protein, and enzyme composition across taxa. Here, we present a chemical characterization of the cell walls of two
Trichoderma
spp., namely the predominantly saprotrophic
Trichoderma reesei
and the mycoparasite
Trichoderma atroviride
. Chemical profiling revealed that
Trichoderma
spp. remodel their cell wall to adapt to particular lifestyles, with dynamic changes during vegetative development. Importantly, we found that chitosan accumulation during mycoparasitism of a fungal host emerged as a sophisticated strategy underpinning an effective attack. These insights shed light on the molecular mechanisms that allow mycoparasites to overcome host defenses and can be exploited to improve the application of
T. atroviride
in biological pest control. Moreover, our results provide valuable information for targeting the fungal cell wall for therapeutic purposes. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 The authors declare no conflict of interest. Present address: College of Medicine & Public Health, Flinders University, Bedford Park, Australia Lisa Kappel and Long Yu contributed equally to this article. Author order was determined both alphabetically and in order of increasing seniority. Present address: Division of Glycoscience, KTH Royal Institute of Technology, AlbaNova University Centre, Stockholm, Sweden |
ISSN: | 2165-0497 2165-0497 |
DOI: | 10.1128/spectrum.03495-23 |