Comparative Genomics Reveals Prophylactic and Catabolic Capabilities of Actinobacteria within the Fungus-Farming Termite Symbiosis

Research output: Contribution to journalJournal articleResearchpeer-review

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Comparative Genomics Reveals Prophylactic and Catabolic Capabilities of Actinobacteria within the Fungus-Farming Termite Symbiosis. / Murphy, Robert; Benndorf, René; de Beer, Z. Wilhelm; Vollmers, John; Kaster, Anne-Kristin; Beemelmanns, Christine; Poulsen, Michael.

In: mSphere, Vol. 6, No. 2, e01233-20, 03.2021.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Murphy, R, Benndorf, R, de Beer, ZW, Vollmers, J, Kaster, A-K, Beemelmanns, C & Poulsen, M 2021, 'Comparative Genomics Reveals Prophylactic and Catabolic Capabilities of Actinobacteria within the Fungus-Farming Termite Symbiosis', mSphere, vol. 6, no. 2, e01233-20. https://doi.org/10.1128/mSphere.01233-20

APA

Murphy, R., Benndorf, R., de Beer, Z. W., Vollmers, J., Kaster, A-K., Beemelmanns, C., & Poulsen, M. (2021). Comparative Genomics Reveals Prophylactic and Catabolic Capabilities of Actinobacteria within the Fungus-Farming Termite Symbiosis. mSphere, 6(2), [e01233-20]. https://doi.org/10.1128/mSphere.01233-20

Vancouver

Murphy R, Benndorf R, de Beer ZW, Vollmers J, Kaster A-K, Beemelmanns C et al. Comparative Genomics Reveals Prophylactic and Catabolic Capabilities of Actinobacteria within the Fungus-Farming Termite Symbiosis. mSphere. 2021 Mar;6(2). e01233-20. https://doi.org/10.1128/mSphere.01233-20

Author

Murphy, Robert ; Benndorf, René ; de Beer, Z. Wilhelm ; Vollmers, John ; Kaster, Anne-Kristin ; Beemelmanns, Christine ; Poulsen, Michael. / Comparative Genomics Reveals Prophylactic and Catabolic Capabilities of Actinobacteria within the Fungus-Farming Termite Symbiosis. In: mSphere. 2021 ; Vol. 6, No. 2.

Bibtex

@article{fc2fb35de1784267a0de4ccf627ff339,
title = "Comparative Genomics Reveals Prophylactic and Catabolic Capabilities of Actinobacteria within the Fungus-Farming Termite Symbiosis",
abstract = "Actinobacteria, one of the largest bacterial phyla, are ubiquitous in many of Earth{\textquoteright}s ecosystems and often act as defensive symbionts with animal hosts. Members of the phylum have repeatedly been isolated from basidiomycete-cultivating fungus-farming termites that maintain a monoculture fungus crop on macerated dead plant substrate. The proclivity for antimicrobial and enzyme production of Actinobacteria make them likely contributors to plant decomposition and defense in the symbiosis. To test this, we analyzed the prophylactic (biosynthetic gene cluster [BGC]) and metabolic (carbohydrate-active enzyme [CAZy]) potential in 16 (10 existing and six new genomes) termite-associated Actinobacteria and compared these to the soil-dwelling close relatives. Using antiSMASH, we identified 435 BGCs, of which 329 (65 unique) were similar to known compound gene clusters, while 106 were putatively novel, suggesting ample prospects for novel compound discovery. BGCs were identified among all major compound categories, including 26 encoding the production of known antimicrobial compounds, which ranged in activity (antibacterial being most prevalent) and modes of action that might suggest broad defensive potential. Peptide pattern recognition analysis revealed 823 (43 unique) CAZymes coding for enzymes that target key plant and fungal cell wall components (predominantly chitin, cellulose, and hemicellulose), confirming a substantial degradative potential of these bacteria. Comparison of termite-associated and soil-dwelling bacteria indicated no significant difference in either BGC or CAZy potential, suggesting that the farming termite hosts may have coopted these soil-dwelling bacteria due to their metabolic potential but that they have not been subject to genome change associated with symbiosis.",
keywords = "Actinobacteria, Actinomadura, Amycolatopsis, antimicrobial, biosynthetic gene clusters, carbohydrate-active enzymes, Luteimicrobium, Macrotermitinae, Mycolicibacterium, Nocardia, Streptomyces",
author = "Robert Murphy and Ren{\'e} Benndorf and {de Beer}, {Z. Wilhelm} and John Vollmers and Anne-Kristin Kaster and Christine Beemelmanns and Michael Poulsen",
year = "2021",
month = mar,
doi = "10.1128/mSphere.01233-20",
language = "English",
volume = "6",
journal = "mSphere",
issn = "2379-5042",
publisher = "American Society for Microbiology",
number = "2",

}

RIS

TY - JOUR

T1 - Comparative Genomics Reveals Prophylactic and Catabolic Capabilities of Actinobacteria within the Fungus-Farming Termite Symbiosis

AU - Murphy, Robert

AU - Benndorf, René

AU - de Beer, Z. Wilhelm

AU - Vollmers, John

AU - Kaster, Anne-Kristin

AU - Beemelmanns, Christine

AU - Poulsen, Michael

PY - 2021/3

Y1 - 2021/3

N2 - Actinobacteria, one of the largest bacterial phyla, are ubiquitous in many of Earth’s ecosystems and often act as defensive symbionts with animal hosts. Members of the phylum have repeatedly been isolated from basidiomycete-cultivating fungus-farming termites that maintain a monoculture fungus crop on macerated dead plant substrate. The proclivity for antimicrobial and enzyme production of Actinobacteria make them likely contributors to plant decomposition and defense in the symbiosis. To test this, we analyzed the prophylactic (biosynthetic gene cluster [BGC]) and metabolic (carbohydrate-active enzyme [CAZy]) potential in 16 (10 existing and six new genomes) termite-associated Actinobacteria and compared these to the soil-dwelling close relatives. Using antiSMASH, we identified 435 BGCs, of which 329 (65 unique) were similar to known compound gene clusters, while 106 were putatively novel, suggesting ample prospects for novel compound discovery. BGCs were identified among all major compound categories, including 26 encoding the production of known antimicrobial compounds, which ranged in activity (antibacterial being most prevalent) and modes of action that might suggest broad defensive potential. Peptide pattern recognition analysis revealed 823 (43 unique) CAZymes coding for enzymes that target key plant and fungal cell wall components (predominantly chitin, cellulose, and hemicellulose), confirming a substantial degradative potential of these bacteria. Comparison of termite-associated and soil-dwelling bacteria indicated no significant difference in either BGC or CAZy potential, suggesting that the farming termite hosts may have coopted these soil-dwelling bacteria due to their metabolic potential but that they have not been subject to genome change associated with symbiosis.

AB - Actinobacteria, one of the largest bacterial phyla, are ubiquitous in many of Earth’s ecosystems and often act as defensive symbionts with animal hosts. Members of the phylum have repeatedly been isolated from basidiomycete-cultivating fungus-farming termites that maintain a monoculture fungus crop on macerated dead plant substrate. The proclivity for antimicrobial and enzyme production of Actinobacteria make them likely contributors to plant decomposition and defense in the symbiosis. To test this, we analyzed the prophylactic (biosynthetic gene cluster [BGC]) and metabolic (carbohydrate-active enzyme [CAZy]) potential in 16 (10 existing and six new genomes) termite-associated Actinobacteria and compared these to the soil-dwelling close relatives. Using antiSMASH, we identified 435 BGCs, of which 329 (65 unique) were similar to known compound gene clusters, while 106 were putatively novel, suggesting ample prospects for novel compound discovery. BGCs were identified among all major compound categories, including 26 encoding the production of known antimicrobial compounds, which ranged in activity (antibacterial being most prevalent) and modes of action that might suggest broad defensive potential. Peptide pattern recognition analysis revealed 823 (43 unique) CAZymes coding for enzymes that target key plant and fungal cell wall components (predominantly chitin, cellulose, and hemicellulose), confirming a substantial degradative potential of these bacteria. Comparison of termite-associated and soil-dwelling bacteria indicated no significant difference in either BGC or CAZy potential, suggesting that the farming termite hosts may have coopted these soil-dwelling bacteria due to their metabolic potential but that they have not been subject to genome change associated with symbiosis.

KW - Actinobacteria

KW - Actinomadura

KW - Amycolatopsis

KW - antimicrobial

KW - biosynthetic gene clusters

KW - carbohydrate-active enzymes

KW - Luteimicrobium

KW - Macrotermitinae

KW - Mycolicibacterium

KW - Nocardia

KW - Streptomyces

U2 - 10.1128/mSphere.01233-20

DO - 10.1128/mSphere.01233-20

M3 - Journal article

C2 - 33658277

AN - SCOPUS:85102246520

VL - 6

JO - mSphere

JF - mSphere

SN - 2379-5042

IS - 2

M1 - e01233-20

ER -

ID: 258540244