Cargando…

Host Bias in Diet-Source Microbiome Transmission in Wild Cohabitating Herbivores: New Knowledge for the Evolution of Herbivory and Plant Defense

It is commonly understood that dietary nutrition will influence the composition and function of the animal gut microbiome. However, the transmission of organisms from the diet-source microbiome to the animal gut microbiome in the natural environment remains poorly understood, and elucidating this pr...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhu, Lifeng, Zhang, Yongyong, Cui, Xinyuan, Zhu, Yudong, Dai, Qinlong, Chen, Hua, Liu, Guoqi, Yao, Ran, Yang, Zhisong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552726/
https://www.ncbi.nlm.nih.gov/pubmed/34406815
http://dx.doi.org/10.1128/spectrum.00756-21
_version_ 1784591440405331968
author Zhu, Lifeng
Zhang, Yongyong
Cui, Xinyuan
Zhu, Yudong
Dai, Qinlong
Chen, Hua
Liu, Guoqi
Yao, Ran
Yang, Zhisong
author_facet Zhu, Lifeng
Zhang, Yongyong
Cui, Xinyuan
Zhu, Yudong
Dai, Qinlong
Chen, Hua
Liu, Guoqi
Yao, Ran
Yang, Zhisong
author_sort Zhu, Lifeng
collection PubMed
description It is commonly understood that dietary nutrition will influence the composition and function of the animal gut microbiome. However, the transmission of organisms from the diet-source microbiome to the animal gut microbiome in the natural environment remains poorly understood, and elucidating this process may help in understanding the evolution of herbivores and plant defenses. Here, we investigated diet-source microbiome transmission across a range of herbivores (insects and mammals) living in both captive and wild environments. We discovered a host bias among cohabitating herbivores (leaf-eating insects and deer), where a significant portion of the herbivorous insect gut microbiome may originate from the diet, while in deer, only a tiny fraction of the gut microbiome is of dietary origin. We speculated that the putative difference in the oxygenation level in the host digestion systems would lead to these host biases in plant-source (diet) microbiome transmission due to the oxygenation living condition of the dietary plant’s symbiotic microbiome. IMPORTANCE We discovered a host bias among cohabitating herbivores (leaf-eating insects and deer), where a significant portion of the herbivorous insect gut microbiome may originate from the diet, while in deer, only a tiny fraction of the gut microbiome is of dietary origin. We speculated that the putative difference in the oxygenation level in the host digestion systems would lead to these host biases in plant-source (diet) microbiome transmission due to the oxygenation living condition of the dietary plant's symbiotic microbiome. This study shed new light on the coevolution of herbivory and plant defense.
format Online
Article
Text
id pubmed-8552726
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-85527262021-11-08 Host Bias in Diet-Source Microbiome Transmission in Wild Cohabitating Herbivores: New Knowledge for the Evolution of Herbivory and Plant Defense Zhu, Lifeng Zhang, Yongyong Cui, Xinyuan Zhu, Yudong Dai, Qinlong Chen, Hua Liu, Guoqi Yao, Ran Yang, Zhisong Microbiol Spectr Research Article It is commonly understood that dietary nutrition will influence the composition and function of the animal gut microbiome. However, the transmission of organisms from the diet-source microbiome to the animal gut microbiome in the natural environment remains poorly understood, and elucidating this process may help in understanding the evolution of herbivores and plant defenses. Here, we investigated diet-source microbiome transmission across a range of herbivores (insects and mammals) living in both captive and wild environments. We discovered a host bias among cohabitating herbivores (leaf-eating insects and deer), where a significant portion of the herbivorous insect gut microbiome may originate from the diet, while in deer, only a tiny fraction of the gut microbiome is of dietary origin. We speculated that the putative difference in the oxygenation level in the host digestion systems would lead to these host biases in plant-source (diet) microbiome transmission due to the oxygenation living condition of the dietary plant’s symbiotic microbiome. IMPORTANCE We discovered a host bias among cohabitating herbivores (leaf-eating insects and deer), where a significant portion of the herbivorous insect gut microbiome may originate from the diet, while in deer, only a tiny fraction of the gut microbiome is of dietary origin. We speculated that the putative difference in the oxygenation level in the host digestion systems would lead to these host biases in plant-source (diet) microbiome transmission due to the oxygenation living condition of the dietary plant's symbiotic microbiome. This study shed new light on the coevolution of herbivory and plant defense. American Society for Microbiology 2021-08-18 /pmc/articles/PMC8552726/ /pubmed/34406815 http://dx.doi.org/10.1128/spectrum.00756-21 Text en Copyright © 2021 Zhu et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Zhu, Lifeng
Zhang, Yongyong
Cui, Xinyuan
Zhu, Yudong
Dai, Qinlong
Chen, Hua
Liu, Guoqi
Yao, Ran
Yang, Zhisong
Host Bias in Diet-Source Microbiome Transmission in Wild Cohabitating Herbivores: New Knowledge for the Evolution of Herbivory and Plant Defense
title Host Bias in Diet-Source Microbiome Transmission in Wild Cohabitating Herbivores: New Knowledge for the Evolution of Herbivory and Plant Defense
title_full Host Bias in Diet-Source Microbiome Transmission in Wild Cohabitating Herbivores: New Knowledge for the Evolution of Herbivory and Plant Defense
title_fullStr Host Bias in Diet-Source Microbiome Transmission in Wild Cohabitating Herbivores: New Knowledge for the Evolution of Herbivory and Plant Defense
title_full_unstemmed Host Bias in Diet-Source Microbiome Transmission in Wild Cohabitating Herbivores: New Knowledge for the Evolution of Herbivory and Plant Defense
title_short Host Bias in Diet-Source Microbiome Transmission in Wild Cohabitating Herbivores: New Knowledge for the Evolution of Herbivory and Plant Defense
title_sort host bias in diet-source microbiome transmission in wild cohabitating herbivores: new knowledge for the evolution of herbivory and plant defense
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552726/
https://www.ncbi.nlm.nih.gov/pubmed/34406815
http://dx.doi.org/10.1128/spectrum.00756-21
work_keys_str_mv AT zhulifeng hostbiasindietsourcemicrobiometransmissioninwildcohabitatingherbivoresnewknowledgefortheevolutionofherbivoryandplantdefense
AT zhangyongyong hostbiasindietsourcemicrobiometransmissioninwildcohabitatingherbivoresnewknowledgefortheevolutionofherbivoryandplantdefense
AT cuixinyuan hostbiasindietsourcemicrobiometransmissioninwildcohabitatingherbivoresnewknowledgefortheevolutionofherbivoryandplantdefense
AT zhuyudong hostbiasindietsourcemicrobiometransmissioninwildcohabitatingherbivoresnewknowledgefortheevolutionofherbivoryandplantdefense
AT daiqinlong hostbiasindietsourcemicrobiometransmissioninwildcohabitatingherbivoresnewknowledgefortheevolutionofherbivoryandplantdefense
AT chenhua hostbiasindietsourcemicrobiometransmissioninwildcohabitatingherbivoresnewknowledgefortheevolutionofherbivoryandplantdefense
AT liuguoqi hostbiasindietsourcemicrobiometransmissioninwildcohabitatingherbivoresnewknowledgefortheevolutionofherbivoryandplantdefense
AT yaoran hostbiasindietsourcemicrobiometransmissioninwildcohabitatingherbivoresnewknowledgefortheevolutionofherbivoryandplantdefense
AT yangzhisong hostbiasindietsourcemicrobiometransmissioninwildcohabitatingherbivoresnewknowledgefortheevolutionofherbivoryandplantdefense