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Immune system responses and fitness costs associated with consumption of bacteria in larvae of Trichoplusia ni

BACKGROUND: Insects helped pioneer, and persist as model organisms for, the study of specific aspects of immunity. Although they lack an adaptive immune system, insects possess an innate immune system that recognizes and destroys intruding microorganisms. Its operation under natural conditions has n...

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Autores principales: Freitak, Dalial, Wheat, Christopher W, Heckel, David G, Vogel, Heiko
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2235825/
https://www.ncbi.nlm.nih.gov/pubmed/18154650
http://dx.doi.org/10.1186/1741-7007-5-56
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author Freitak, Dalial
Wheat, Christopher W
Heckel, David G
Vogel, Heiko
author_facet Freitak, Dalial
Wheat, Christopher W
Heckel, David G
Vogel, Heiko
author_sort Freitak, Dalial
collection PubMed
description BACKGROUND: Insects helped pioneer, and persist as model organisms for, the study of specific aspects of immunity. Although they lack an adaptive immune system, insects possess an innate immune system that recognizes and destroys intruding microorganisms. Its operation under natural conditions has not been well studied, as most studies have introduced microbes to laboratory-reared insects via artificial mechanical wounding. One of the most common routes of natural exposure and infection, however, is via food; thus, the role of dietary microbial communities in herbivorous insect immune system evolution invites study. Here, we examine the immune system response and consequences of exposing a lepidopteran agricultural pest to non-infectious microorganisms via simple oral consumption. RESULTS: Immune system response was compared between Trichoplusia ni larvae reared on diets with or without non-pathogenic bacteria (Escherichia coli and Micrococcus luteus). Two major immune response-related enzymatic activities responded to diets differently – phenoloxidase activity was inhibited in the bacteria-fed larvae, whereas general antibacterial activity was enhanced. Eight proteins were highly expressed in the hemolymph of the bacteria fed larvae, among them immune response related proteins arylphorin, apolipophorin III and gloverin. Expression response among 25 putative immune response-related genes were assayed via RT-qPCR. Seven showed more than fivefold up regulation in the presence of bacterial diet, with 22 in total being differentially expressed, among them apolipophorin III, cecropin, gallerimycin, gloverin, lysozyme, and phenoloxidase inhibiting enzyme. Finally, potential life-history trade-offs were studied, with pupation time and pupal mass being negatively affected in bacteria fed larvae. CONCLUSION: The presence of bacteria in food, even if non-pathogenic, can trigger an immune response cascade with life history tradeoffs. Trichoplusia ni larvae are able to detect and respond to environmental microbes encountered in the diet, possibly even using midgut epithelial tissue as a sensing organ. Potential benefits of this immune system priming may outweigh the observed tradeoffs, as priming based on environmentally sensed bacterial may decrease risk of serious infection. These results show that food plant microbial communities represent a dynamic and unstudied part of the coevolutionary interactions between plants and their insect herbivores.
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spelling pubmed-22358252008-02-09 Immune system responses and fitness costs associated with consumption of bacteria in larvae of Trichoplusia ni Freitak, Dalial Wheat, Christopher W Heckel, David G Vogel, Heiko BMC Biol Research Article BACKGROUND: Insects helped pioneer, and persist as model organisms for, the study of specific aspects of immunity. Although they lack an adaptive immune system, insects possess an innate immune system that recognizes and destroys intruding microorganisms. Its operation under natural conditions has not been well studied, as most studies have introduced microbes to laboratory-reared insects via artificial mechanical wounding. One of the most common routes of natural exposure and infection, however, is via food; thus, the role of dietary microbial communities in herbivorous insect immune system evolution invites study. Here, we examine the immune system response and consequences of exposing a lepidopteran agricultural pest to non-infectious microorganisms via simple oral consumption. RESULTS: Immune system response was compared between Trichoplusia ni larvae reared on diets with or without non-pathogenic bacteria (Escherichia coli and Micrococcus luteus). Two major immune response-related enzymatic activities responded to diets differently – phenoloxidase activity was inhibited in the bacteria-fed larvae, whereas general antibacterial activity was enhanced. Eight proteins were highly expressed in the hemolymph of the bacteria fed larvae, among them immune response related proteins arylphorin, apolipophorin III and gloverin. Expression response among 25 putative immune response-related genes were assayed via RT-qPCR. Seven showed more than fivefold up regulation in the presence of bacterial diet, with 22 in total being differentially expressed, among them apolipophorin III, cecropin, gallerimycin, gloverin, lysozyme, and phenoloxidase inhibiting enzyme. Finally, potential life-history trade-offs were studied, with pupation time and pupal mass being negatively affected in bacteria fed larvae. CONCLUSION: The presence of bacteria in food, even if non-pathogenic, can trigger an immune response cascade with life history tradeoffs. Trichoplusia ni larvae are able to detect and respond to environmental microbes encountered in the diet, possibly even using midgut epithelial tissue as a sensing organ. Potential benefits of this immune system priming may outweigh the observed tradeoffs, as priming based on environmentally sensed bacterial may decrease risk of serious infection. These results show that food plant microbial communities represent a dynamic and unstudied part of the coevolutionary interactions between plants and their insect herbivores. BioMed Central 2007-12-21 /pmc/articles/PMC2235825/ /pubmed/18154650 http://dx.doi.org/10.1186/1741-7007-5-56 Text en Copyright © 2007 Freitak et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Freitak, Dalial
Wheat, Christopher W
Heckel, David G
Vogel, Heiko
Immune system responses and fitness costs associated with consumption of bacteria in larvae of Trichoplusia ni
title Immune system responses and fitness costs associated with consumption of bacteria in larvae of Trichoplusia ni
title_full Immune system responses and fitness costs associated with consumption of bacteria in larvae of Trichoplusia ni
title_fullStr Immune system responses and fitness costs associated with consumption of bacteria in larvae of Trichoplusia ni
title_full_unstemmed Immune system responses and fitness costs associated with consumption of bacteria in larvae of Trichoplusia ni
title_short Immune system responses and fitness costs associated with consumption of bacteria in larvae of Trichoplusia ni
title_sort immune system responses and fitness costs associated with consumption of bacteria in larvae of trichoplusia ni
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2235825/
https://www.ncbi.nlm.nih.gov/pubmed/18154650
http://dx.doi.org/10.1186/1741-7007-5-56
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