Fungiculture in termites is associated with a mycolytic gut bacterial community

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Fungiculture in termites is associated with a mycolytic gut bacterial community. / Hu, Haofu; da Costa, Rafael Rodrigues; Pilgaard, Bo; Schiøtt, Morten; Lange, Lene; Poulsen, Michael.

In: mSphere, Vol. 4, No. 3, e00165-19, 2019.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Hu, H, da Costa, RR, Pilgaard, B, Schiøtt, M, Lange, L & Poulsen, M 2019, 'Fungiculture in termites is associated with a mycolytic gut bacterial community', mSphere, vol. 4, no. 3, e00165-19. https://doi.org/10.1128/mSphere.00165-19

APA

Hu, H., da Costa, R. R., Pilgaard, B., Schiøtt, M., Lange, L., & Poulsen, M. (2019). Fungiculture in termites is associated with a mycolytic gut bacterial community. mSphere, 4(3), [e00165-19]. https://doi.org/10.1128/mSphere.00165-19

Vancouver

Hu H, da Costa RR, Pilgaard B, Schiøtt M, Lange L, Poulsen M. Fungiculture in termites is associated with a mycolytic gut bacterial community. mSphere. 2019;4(3). e00165-19. https://doi.org/10.1128/mSphere.00165-19

Author

Hu, Haofu ; da Costa, Rafael Rodrigues ; Pilgaard, Bo ; Schiøtt, Morten ; Lange, Lene ; Poulsen, Michael. / Fungiculture in termites is associated with a mycolytic gut bacterial community. In: mSphere. 2019 ; Vol. 4, No. 3.

Bibtex

@article{41f7add3eb9641b4888de9faccd47763,
title = "Fungiculture in termites is associated with a mycolytic gut bacterial community",
abstract = "Termites forage on a range of substrates, and it has been suggested that diet shapes the composition and function of termite gut bacterial communities. Through comparative analyses of gut metagenomes in nine termite species with distinct diets, we characterize bacterial community compositions and use peptidebased functional annotation method to determine biomass-degrading enzymes and the bacterial taxa that encode them. We find that fungus-growing termite guts have relatively more fungal cell wall-degrading enzyme genes, while wood-feeding termite gut communities have relatively more plant cell wall-degrading enzyme genes. Interestingly, wood-feeding termite gut bacterial genes code for abundant chitinolytic enzymes, suggesting that fungal biomass within the decaying wood likely contributes to gut bacterial or termite host nutrition. Across diets, the dominant biomass-degrading enzymes are predominantly coded for by the most abundant bacterial taxa, suggesting tight links between diet and gut community composition, with the most marked difference being the communities coding for the mycolytic capacity of the fungus-growing termite gut.",
keywords = "Carbohydrate-active enzymes, Cellulase, Chitinase, HiSeq, HotPep, Metagenomics, Peptide-based functional predictions",
author = "Haofu Hu and {da Costa}, {Rafael Rodrigues} and Bo Pilgaard and Morten Schi{\o}tt and Lene Lange and Michael Poulsen",
year = "2019",
doi = "10.1128/mSphere.00165-19",
language = "English",
volume = "4",
journal = "mSphere",
issn = "2379-5042",
publisher = "American Society for Microbiology",
number = "3",

}

RIS

TY - JOUR

T1 - Fungiculture in termites is associated with a mycolytic gut bacterial community

AU - Hu, Haofu

AU - da Costa, Rafael Rodrigues

AU - Pilgaard, Bo

AU - Schiøtt, Morten

AU - Lange, Lene

AU - Poulsen, Michael

PY - 2019

Y1 - 2019

N2 - Termites forage on a range of substrates, and it has been suggested that diet shapes the composition and function of termite gut bacterial communities. Through comparative analyses of gut metagenomes in nine termite species with distinct diets, we characterize bacterial community compositions and use peptidebased functional annotation method to determine biomass-degrading enzymes and the bacterial taxa that encode them. We find that fungus-growing termite guts have relatively more fungal cell wall-degrading enzyme genes, while wood-feeding termite gut communities have relatively more plant cell wall-degrading enzyme genes. Interestingly, wood-feeding termite gut bacterial genes code for abundant chitinolytic enzymes, suggesting that fungal biomass within the decaying wood likely contributes to gut bacterial or termite host nutrition. Across diets, the dominant biomass-degrading enzymes are predominantly coded for by the most abundant bacterial taxa, suggesting tight links between diet and gut community composition, with the most marked difference being the communities coding for the mycolytic capacity of the fungus-growing termite gut.

AB - Termites forage on a range of substrates, and it has been suggested that diet shapes the composition and function of termite gut bacterial communities. Through comparative analyses of gut metagenomes in nine termite species with distinct diets, we characterize bacterial community compositions and use peptidebased functional annotation method to determine biomass-degrading enzymes and the bacterial taxa that encode them. We find that fungus-growing termite guts have relatively more fungal cell wall-degrading enzyme genes, while wood-feeding termite gut communities have relatively more plant cell wall-degrading enzyme genes. Interestingly, wood-feeding termite gut bacterial genes code for abundant chitinolytic enzymes, suggesting that fungal biomass within the decaying wood likely contributes to gut bacterial or termite host nutrition. Across diets, the dominant biomass-degrading enzymes are predominantly coded for by the most abundant bacterial taxa, suggesting tight links between diet and gut community composition, with the most marked difference being the communities coding for the mycolytic capacity of the fungus-growing termite gut.

KW - Carbohydrate-active enzymes

KW - Cellulase

KW - Chitinase

KW - HiSeq

KW - HotPep

KW - Metagenomics

KW - Peptide-based functional predictions

U2 - 10.1128/mSphere.00165-19

DO - 10.1128/mSphere.00165-19

M3 - Journal article

C2 - 31092601

AN - SCOPUS:85066833365

VL - 4

JO - mSphere

JF - mSphere

SN - 2379-5042

IS - 3

M1 - e00165-19

ER -

ID: 225792521