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Host plant and population source drive diversity of microbial gut communities in two polyphagous insects

Symbioses between insects and microbes are ubiquitous, but vary greatly in terms of function, transmission mechanism, and location in the insect. Lepidoptera (butterflies and moths) are one of the largest and most economically important insect orders; yet, in many cases, the ecology and functions of...

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Autores principales: Jones, Asher G., Mason, Charles J., Felton, Gary W., Hoover, Kelli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391413/
https://www.ncbi.nlm.nih.gov/pubmed/30808905
http://dx.doi.org/10.1038/s41598-019-39163-9
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author Jones, Asher G.
Mason, Charles J.
Felton, Gary W.
Hoover, Kelli
author_facet Jones, Asher G.
Mason, Charles J.
Felton, Gary W.
Hoover, Kelli
author_sort Jones, Asher G.
collection PubMed
description Symbioses between insects and microbes are ubiquitous, but vary greatly in terms of function, transmission mechanism, and location in the insect. Lepidoptera (butterflies and moths) are one of the largest and most economically important insect orders; yet, in many cases, the ecology and functions of their gut microbiomes are unresolved. We used high-throughput sequencing to determine factors that influence gut microbiomes of field-collected fall armyworm (Spodoptera frugiperda) and corn earworm (Helicoverpa zea). Fall armyworm midgut bacterial communities differed from those of corn earworm collected from the same host plant species at the same site. However, corn earworm bacterial communities differed between collection sites. Subsequent experiments using fall armyworm evaluating the influence of egg source and diet indicated that that host plant had a greater impact on gut communities. We also observed differences between regurgitant (foregut) and midgut bacterial communities of the same insect host, suggesting differential colonization. Our findings indicate that host plant is a major driver shaping gut microbiota, but differences in insect physiology, gut region, and local factors can also contribute to variation in microbiomes. Additional studies are needed to assess the mechanisms that affect variation in insect microbiomes, as well as the ecological implications of this variability in caterpillars.
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spelling pubmed-63914132019-02-28 Host plant and population source drive diversity of microbial gut communities in two polyphagous insects Jones, Asher G. Mason, Charles J. Felton, Gary W. Hoover, Kelli Sci Rep Article Symbioses between insects and microbes are ubiquitous, but vary greatly in terms of function, transmission mechanism, and location in the insect. Lepidoptera (butterflies and moths) are one of the largest and most economically important insect orders; yet, in many cases, the ecology and functions of their gut microbiomes are unresolved. We used high-throughput sequencing to determine factors that influence gut microbiomes of field-collected fall armyworm (Spodoptera frugiperda) and corn earworm (Helicoverpa zea). Fall armyworm midgut bacterial communities differed from those of corn earworm collected from the same host plant species at the same site. However, corn earworm bacterial communities differed between collection sites. Subsequent experiments using fall armyworm evaluating the influence of egg source and diet indicated that that host plant had a greater impact on gut communities. We also observed differences between regurgitant (foregut) and midgut bacterial communities of the same insect host, suggesting differential colonization. Our findings indicate that host plant is a major driver shaping gut microbiota, but differences in insect physiology, gut region, and local factors can also contribute to variation in microbiomes. Additional studies are needed to assess the mechanisms that affect variation in insect microbiomes, as well as the ecological implications of this variability in caterpillars. Nature Publishing Group UK 2019-02-26 /pmc/articles/PMC6391413/ /pubmed/30808905 http://dx.doi.org/10.1038/s41598-019-39163-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Jones, Asher G.
Mason, Charles J.
Felton, Gary W.
Hoover, Kelli
Host plant and population source drive diversity of microbial gut communities in two polyphagous insects
title Host plant and population source drive diversity of microbial gut communities in two polyphagous insects
title_full Host plant and population source drive diversity of microbial gut communities in two polyphagous insects
title_fullStr Host plant and population source drive diversity of microbial gut communities in two polyphagous insects
title_full_unstemmed Host plant and population source drive diversity of microbial gut communities in two polyphagous insects
title_short Host plant and population source drive diversity of microbial gut communities in two polyphagous insects
title_sort host plant and population source drive diversity of microbial gut communities in two polyphagous insects
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391413/
https://www.ncbi.nlm.nih.gov/pubmed/30808905
http://dx.doi.org/10.1038/s41598-019-39163-9
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