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Gut microbial community supplementation and reduction modulates African armyworm susceptibility to a baculovirus

Gut microbiota stimulates the immune system and inhibits pathogens, and thus, it is critical for disease prevention. Probiotics represent an effective alternative to antibiotics used for the therapy and prevention of bacterial diseases. Probiotic bacteria are commonly used in vertebrates, although t...

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Autores principales: Donkersley, Philip, Rice, Annabel, Graham, Robert I, Wilson, Kenneth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764207/
https://www.ncbi.nlm.nih.gov/pubmed/36473704
http://dx.doi.org/10.1093/femsec/fiac147
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author Donkersley, Philip
Rice, Annabel
Graham, Robert I
Wilson, Kenneth
author_facet Donkersley, Philip
Rice, Annabel
Graham, Robert I
Wilson, Kenneth
author_sort Donkersley, Philip
collection PubMed
description Gut microbiota stimulates the immune system and inhibits pathogens, and thus, it is critical for disease prevention. Probiotics represent an effective alternative to antibiotics used for the therapy and prevention of bacterial diseases. Probiotic bacteria are commonly used in vertebrates, although their use in invertebrates is still rare. We manipulated the gut microbiome of the African Armyworm (Spodoptera exempta Walker) using antibiotics and field-collected frass, in an attempt to understand the interactions of the gut microbiome with the nucleopolyhedrovirus, SpexNPV. We found that S. exempta individuals with supplemented gut microbiome were significantly more resistant to SpexNPV, relative to those with a typical laboratory gut microbiome. Illumina MiSeq sequencing revealed the bacterial phyla in the S. exempta gut belonged to 28 different classes. Individuals with an increased abundance of Lactobacillales had a higher probability of surviving viral infection. In contrast, there was an increased abundance of Enterobacteriales and Pseudomonadales in individuals dying from viral infection, corresponding with decreased abundance of these two Orders in surviving caterpillars, suggesting a potential role for them in modulating the interaction between the host and its pathogen. These results have important implications for laboratory studies testing biopesticides.
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spelling pubmed-97642072022-12-20 Gut microbial community supplementation and reduction modulates African armyworm susceptibility to a baculovirus Donkersley, Philip Rice, Annabel Graham, Robert I Wilson, Kenneth FEMS Microbiol Ecol Research Article Gut microbiota stimulates the immune system and inhibits pathogens, and thus, it is critical for disease prevention. Probiotics represent an effective alternative to antibiotics used for the therapy and prevention of bacterial diseases. Probiotic bacteria are commonly used in vertebrates, although their use in invertebrates is still rare. We manipulated the gut microbiome of the African Armyworm (Spodoptera exempta Walker) using antibiotics and field-collected frass, in an attempt to understand the interactions of the gut microbiome with the nucleopolyhedrovirus, SpexNPV. We found that S. exempta individuals with supplemented gut microbiome were significantly more resistant to SpexNPV, relative to those with a typical laboratory gut microbiome. Illumina MiSeq sequencing revealed the bacterial phyla in the S. exempta gut belonged to 28 different classes. Individuals with an increased abundance of Lactobacillales had a higher probability of surviving viral infection. In contrast, there was an increased abundance of Enterobacteriales and Pseudomonadales in individuals dying from viral infection, corresponding with decreased abundance of these two Orders in surviving caterpillars, suggesting a potential role for them in modulating the interaction between the host and its pathogen. These results have important implications for laboratory studies testing biopesticides. Oxford University Press 2022-12-06 /pmc/articles/PMC9764207/ /pubmed/36473704 http://dx.doi.org/10.1093/femsec/fiac147 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of FEMS. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Donkersley, Philip
Rice, Annabel
Graham, Robert I
Wilson, Kenneth
Gut microbial community supplementation and reduction modulates African armyworm susceptibility to a baculovirus
title Gut microbial community supplementation and reduction modulates African armyworm susceptibility to a baculovirus
title_full Gut microbial community supplementation and reduction modulates African armyworm susceptibility to a baculovirus
title_fullStr Gut microbial community supplementation and reduction modulates African armyworm susceptibility to a baculovirus
title_full_unstemmed Gut microbial community supplementation and reduction modulates African armyworm susceptibility to a baculovirus
title_short Gut microbial community supplementation and reduction modulates African armyworm susceptibility to a baculovirus
title_sort gut microbial community supplementation and reduction modulates african armyworm susceptibility to a baculovirus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764207/
https://www.ncbi.nlm.nih.gov/pubmed/36473704
http://dx.doi.org/10.1093/femsec/fiac147
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