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Horizontally Acquired Cellulases Assist the Expansion of Dietary Range in Pristionchus Nematodes

Horizontal gene transfer (HGT) enables the acquisition of novel traits via non-Mendelian inheritance of genetic material. HGT plays a prominent role in the evolution of prokaryotes, whereas in animals, HGT is rare and its functional significance is often uncertain. Here, we investigate horizontally...

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Autores principales: Han, Ziduan, Sieriebriennikov, Bogdan, Susoy, Vladislav, Lo, Wen-Sui, Igreja, Catia, Dong, Chuanfu, Berasategui, Aileen, Witte, Hanh, Sommer, Ralf J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8826503/
https://www.ncbi.nlm.nih.gov/pubmed/34978575
http://dx.doi.org/10.1093/molbev/msab370
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author Han, Ziduan
Sieriebriennikov, Bogdan
Susoy, Vladislav
Lo, Wen-Sui
Igreja, Catia
Dong, Chuanfu
Berasategui, Aileen
Witte, Hanh
Sommer, Ralf J
author_facet Han, Ziduan
Sieriebriennikov, Bogdan
Susoy, Vladislav
Lo, Wen-Sui
Igreja, Catia
Dong, Chuanfu
Berasategui, Aileen
Witte, Hanh
Sommer, Ralf J
author_sort Han, Ziduan
collection PubMed
description Horizontal gene transfer (HGT) enables the acquisition of novel traits via non-Mendelian inheritance of genetic material. HGT plays a prominent role in the evolution of prokaryotes, whereas in animals, HGT is rare and its functional significance is often uncertain. Here, we investigate horizontally acquired cellulase genes in the free-living nematode model organism Pristionchus pacificus. We show that these cellulase genes 1) are likely of eukaryotic origin, 2) are expressed, 3) have protein products that are secreted and functional, and 4) result in endo-cellulase activity. Using CRISPR/Cas9, we generated an octuple cellulase mutant, which lacks all eight cellulase genes and cellulase activity altogether. Nonetheless, this cellulase-null mutant is viable and therefore allows a detailed analysis of a gene family that was horizontally acquired. We show that the octuple cellulase mutant has associated fitness costs with reduced fecundity and slower developmental speed. Furthermore, by using various Escherichia coli K-12 strains as a model for cellulosic biofilms, we demonstrate that cellulases facilitate the procurement of nutrients from bacterial biofilms. Together, our analysis of cellulases in Pristionchus provides comprehensive evidence from biochemistry, genetics, and phylogeny, which supports the integration of horizontally acquired genes into the complex life history strategy of this soil nematode.
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spelling pubmed-88265032022-02-09 Horizontally Acquired Cellulases Assist the Expansion of Dietary Range in Pristionchus Nematodes Han, Ziduan Sieriebriennikov, Bogdan Susoy, Vladislav Lo, Wen-Sui Igreja, Catia Dong, Chuanfu Berasategui, Aileen Witte, Hanh Sommer, Ralf J Mol Biol Evol Discoveries Horizontal gene transfer (HGT) enables the acquisition of novel traits via non-Mendelian inheritance of genetic material. HGT plays a prominent role in the evolution of prokaryotes, whereas in animals, HGT is rare and its functional significance is often uncertain. Here, we investigate horizontally acquired cellulase genes in the free-living nematode model organism Pristionchus pacificus. We show that these cellulase genes 1) are likely of eukaryotic origin, 2) are expressed, 3) have protein products that are secreted and functional, and 4) result in endo-cellulase activity. Using CRISPR/Cas9, we generated an octuple cellulase mutant, which lacks all eight cellulase genes and cellulase activity altogether. Nonetheless, this cellulase-null mutant is viable and therefore allows a detailed analysis of a gene family that was horizontally acquired. We show that the octuple cellulase mutant has associated fitness costs with reduced fecundity and slower developmental speed. Furthermore, by using various Escherichia coli K-12 strains as a model for cellulosic biofilms, we demonstrate that cellulases facilitate the procurement of nutrients from bacterial biofilms. Together, our analysis of cellulases in Pristionchus provides comprehensive evidence from biochemistry, genetics, and phylogeny, which supports the integration of horizontally acquired genes into the complex life history strategy of this soil nematode. Oxford University Press 2022-01-03 /pmc/articles/PMC8826503/ /pubmed/34978575 http://dx.doi.org/10.1093/molbev/msab370 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Discoveries
Han, Ziduan
Sieriebriennikov, Bogdan
Susoy, Vladislav
Lo, Wen-Sui
Igreja, Catia
Dong, Chuanfu
Berasategui, Aileen
Witte, Hanh
Sommer, Ralf J
Horizontally Acquired Cellulases Assist the Expansion of Dietary Range in Pristionchus Nematodes
title Horizontally Acquired Cellulases Assist the Expansion of Dietary Range in Pristionchus Nematodes
title_full Horizontally Acquired Cellulases Assist the Expansion of Dietary Range in Pristionchus Nematodes
title_fullStr Horizontally Acquired Cellulases Assist the Expansion of Dietary Range in Pristionchus Nematodes
title_full_unstemmed Horizontally Acquired Cellulases Assist the Expansion of Dietary Range in Pristionchus Nematodes
title_short Horizontally Acquired Cellulases Assist the Expansion of Dietary Range in Pristionchus Nematodes
title_sort horizontally acquired cellulases assist the expansion of dietary range in pristionchus nematodes
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8826503/
https://www.ncbi.nlm.nih.gov/pubmed/34978575
http://dx.doi.org/10.1093/molbev/msab370
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