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Primed Immune Responses Triggered by Ingested Bacteria Lead to Systemic Infection Tolerance in Silkworms

In the present study, we examined whether microorganisms collaterally ingested by insects with their food activate the innate immune system to confer systemic resistance against subsequent bacterial invasion. Silkworms orally administered heat-killed Pseudomonas aeruginosa cells showed resistance ag...

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Autores principales: Miyashita, Atsushi, Takahashi, Shinji, Ishii, Kenichi, Sekimizu, Kazuhisa, Kaito, Chikara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4479504/
https://www.ncbi.nlm.nih.gov/pubmed/26107254
http://dx.doi.org/10.1371/journal.pone.0130486
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author Miyashita, Atsushi
Takahashi, Shinji
Ishii, Kenichi
Sekimizu, Kazuhisa
Kaito, Chikara
author_facet Miyashita, Atsushi
Takahashi, Shinji
Ishii, Kenichi
Sekimizu, Kazuhisa
Kaito, Chikara
author_sort Miyashita, Atsushi
collection PubMed
description In the present study, we examined whether microorganisms collaterally ingested by insects with their food activate the innate immune system to confer systemic resistance against subsequent bacterial invasion. Silkworms orally administered heat-killed Pseudomonas aeruginosa cells showed resistance against intra-hemolymph infection by P. aeruginosa. Oral administration of peptidoglycans, cell wall components of P. aeruginosa, conferred protective effects against P. aeruginosa infection, whereas oral administration of lipopolysaccharides, bacterial surface components, did not. In silkworms orally administered heat-killed P. aeruginosa cells, P. aeruginosa growth was inhibited in the hemolymph, and mRNA amounts of the antimicrobial peptides cecropin A and moricin were increased in the hemocytes and fat body. Furthermore, the amount of paralytic peptide, an insect cytokine that activates innate immune reactions, was increased in the hemolymph of silkworms orally administered heat-killed P. aeruginosa cells. These findings suggest that insects sense bacteria present in their food by peptidoglycan recognition, which activates systemic immune reactions to defend the insects against a second round of infection.
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spelling pubmed-44795042015-06-29 Primed Immune Responses Triggered by Ingested Bacteria Lead to Systemic Infection Tolerance in Silkworms Miyashita, Atsushi Takahashi, Shinji Ishii, Kenichi Sekimizu, Kazuhisa Kaito, Chikara PLoS One Research Article In the present study, we examined whether microorganisms collaterally ingested by insects with their food activate the innate immune system to confer systemic resistance against subsequent bacterial invasion. Silkworms orally administered heat-killed Pseudomonas aeruginosa cells showed resistance against intra-hemolymph infection by P. aeruginosa. Oral administration of peptidoglycans, cell wall components of P. aeruginosa, conferred protective effects against P. aeruginosa infection, whereas oral administration of lipopolysaccharides, bacterial surface components, did not. In silkworms orally administered heat-killed P. aeruginosa cells, P. aeruginosa growth was inhibited in the hemolymph, and mRNA amounts of the antimicrobial peptides cecropin A and moricin were increased in the hemocytes and fat body. Furthermore, the amount of paralytic peptide, an insect cytokine that activates innate immune reactions, was increased in the hemolymph of silkworms orally administered heat-killed P. aeruginosa cells. These findings suggest that insects sense bacteria present in their food by peptidoglycan recognition, which activates systemic immune reactions to defend the insects against a second round of infection. Public Library of Science 2015-06-24 /pmc/articles/PMC4479504/ /pubmed/26107254 http://dx.doi.org/10.1371/journal.pone.0130486 Text en © 2015 Miyashita et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Miyashita, Atsushi
Takahashi, Shinji
Ishii, Kenichi
Sekimizu, Kazuhisa
Kaito, Chikara
Primed Immune Responses Triggered by Ingested Bacteria Lead to Systemic Infection Tolerance in Silkworms
title Primed Immune Responses Triggered by Ingested Bacteria Lead to Systemic Infection Tolerance in Silkworms
title_full Primed Immune Responses Triggered by Ingested Bacteria Lead to Systemic Infection Tolerance in Silkworms
title_fullStr Primed Immune Responses Triggered by Ingested Bacteria Lead to Systemic Infection Tolerance in Silkworms
title_full_unstemmed Primed Immune Responses Triggered by Ingested Bacteria Lead to Systemic Infection Tolerance in Silkworms
title_short Primed Immune Responses Triggered by Ingested Bacteria Lead to Systemic Infection Tolerance in Silkworms
title_sort primed immune responses triggered by ingested bacteria lead to systemic infection tolerance in silkworms
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4479504/
https://www.ncbi.nlm.nih.gov/pubmed/26107254
http://dx.doi.org/10.1371/journal.pone.0130486
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