Bacterial and fungal growth on fungal necromass and its diverse components : Shared profiles and divergent constraints revealed by high-throughput phenotyping
(2025) In Functional Ecology 39(9). p.2268-2283- Abstract
While fungal necromass is increasingly recognized as a major source of persistent carbon (C) in soils, the relative functional roles of bacteria and fungi in decomposing necromass are not fully resolved, and the processes that select for necromass decomposer communities from the broader soil microbial community are an emerging area of interest. In this study, we characterized the growth of 52 bacterial and 83 fungal strains isolated from necromass and soil on 22 C substrates, including different necromass phenotypes, fungal cell wall polymers, dimers and monomers. We found that the isolation habitat of the strains used in this experiment (necromass vs. soil) had no effect on the substrates they were able to use. Isolates from both... (More)
While fungal necromass is increasingly recognized as a major source of persistent carbon (C) in soils, the relative functional roles of bacteria and fungi in decomposing necromass are not fully resolved, and the processes that select for necromass decomposer communities from the broader soil microbial community are an emerging area of interest. In this study, we characterized the growth of 52 bacterial and 83 fungal strains isolated from necromass and soil on 22 C substrates, including different necromass phenotypes, fungal cell wall polymers, dimers and monomers. We found that the isolation habitat of the strains used in this experiment (necromass vs. soil) had no effect on the substrates they were able to use. Isolates from both microbial domains were able to grow on different labile carbon substrates, polymers and necromass phenotypes. However, fungal growth was most limited by necromass melanin content, while bacterial growth was more limited by the abundance of cell wall polysaccharides. Additionally, overall differences in substrate use between bacteria and fungi were most pronounced on polymer substrates. Collectively, our results suggest that there is substantial functional overlap in necromass substrate use across microbial domains, but some notable differences in bacterial and fungal utilization of cell wall polymers, which can function as a direct energy source or a means of accessing other compounds within necromass. Future studies assessing bacteria and fungi decomposing necromass together rather than in isolation will help to uncover potential physical and chemical interactions within and between these two domains during the decay of this important source of persistent soil C. Read the free Plain Language Summary for this article on the Journal blog.
(Less)
- author
- Narayanan, Achala ; Maillard, François LU ; Beatty, Briana H. ; Novak, Jessica K. ; Gardner, Jeffrey G. ; Schilling, Jonathan S. ; Pett-Ridge, Jennifer and Kennedy, Peter G.
- organization
- publishing date
- 2025-09
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- dead fungal biomass, decomposition, functional diversity, phenotypes, soil microbes, substrate use
- in
- Functional Ecology
- volume
- 39
- issue
- 9
- pages
- 16 pages
- publisher
- Wiley-Blackwell
- external identifiers
-
- scopus:105012116933
- ISSN
- 0269-8463
- DOI
- 10.1111/1365-2435.70128
- language
- English
- LU publication?
- yes
- id
- 911f1d53-e678-48ec-8fba-1adf7facc950
- date added to LUP
- 2026-01-20 16:05:39
- date last changed
- 2026-01-26 10:17:43
@article{911f1d53-e678-48ec-8fba-1adf7facc950,
abstract = {{<p>While fungal necromass is increasingly recognized as a major source of persistent carbon (C) in soils, the relative functional roles of bacteria and fungi in decomposing necromass are not fully resolved, and the processes that select for necromass decomposer communities from the broader soil microbial community are an emerging area of interest. In this study, we characterized the growth of 52 bacterial and 83 fungal strains isolated from necromass and soil on 22 C substrates, including different necromass phenotypes, fungal cell wall polymers, dimers and monomers. We found that the isolation habitat of the strains used in this experiment (necromass vs. soil) had no effect on the substrates they were able to use. Isolates from both microbial domains were able to grow on different labile carbon substrates, polymers and necromass phenotypes. However, fungal growth was most limited by necromass melanin content, while bacterial growth was more limited by the abundance of cell wall polysaccharides. Additionally, overall differences in substrate use between bacteria and fungi were most pronounced on polymer substrates. Collectively, our results suggest that there is substantial functional overlap in necromass substrate use across microbial domains, but some notable differences in bacterial and fungal utilization of cell wall polymers, which can function as a direct energy source or a means of accessing other compounds within necromass. Future studies assessing bacteria and fungi decomposing necromass together rather than in isolation will help to uncover potential physical and chemical interactions within and between these two domains during the decay of this important source of persistent soil C. Read the free Plain Language Summary for this article on the Journal blog.</p>}},
author = {{Narayanan, Achala and Maillard, François and Beatty, Briana H. and Novak, Jessica K. and Gardner, Jeffrey G. and Schilling, Jonathan S. and Pett-Ridge, Jennifer and Kennedy, Peter G.}},
issn = {{0269-8463}},
keywords = {{dead fungal biomass; decomposition; functional diversity; phenotypes; soil microbes; substrate use}},
language = {{eng}},
number = {{9}},
pages = {{2268--2283}},
publisher = {{Wiley-Blackwell}},
series = {{Functional Ecology}},
title = {{Bacterial and fungal growth on fungal necromass and its diverse components : Shared profiles and divergent constraints revealed by high-throughput phenotyping}},
url = {{http://dx.doi.org/10.1111/1365-2435.70128}},
doi = {{10.1111/1365-2435.70128}},
volume = {{39}},
year = {{2025}},
}