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Differential expression of immunity-related genes in larval Manduca sexta tissues in response to gut and systemic infection
INTRODUCTION: The midgut epithelium functions as tissue for nutrient uptake as well as physical barrier against pathogens. Additionally, it responds to pathogen contact by production and release of various factors including antimicrobial peptides, similar to the systemic innate immune response. Howe...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603244/ https://www.ncbi.nlm.nih.gov/pubmed/37900309 http://dx.doi.org/10.3389/fcimb.2023.1258142 |
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author | von Bredow, Yvette M. Prochazkova, Petra Dvorak, Jiri Skanta, Frantisek Trenczek, Tina E. Bilej, Martin von Bredow, Christoph-Rüdiger |
author_facet | von Bredow, Yvette M. Prochazkova, Petra Dvorak, Jiri Skanta, Frantisek Trenczek, Tina E. Bilej, Martin von Bredow, Christoph-Rüdiger |
author_sort | von Bredow, Yvette M. |
collection | PubMed |
description | INTRODUCTION: The midgut epithelium functions as tissue for nutrient uptake as well as physical barrier against pathogens. Additionally, it responds to pathogen contact by production and release of various factors including antimicrobial peptides, similar to the systemic innate immune response. However, if such a response is restricted to a local stimulus or if it appears in response to a systemic infection, too is a rather underexplored topic in insect immunity. We addressed the role of the midgut and the role of systemic immune tissues in the defense against gut-borne and systemic infections, respectively. METHODS: Manduca sexta larvae were challenged with DAP-type peptidoglycan bacteria – Bacillus thuringiensis for local gut infection and Escherichia coli for systemic stimulation. We compared the immune response to both infection models by measuring mRNA levels of four selected immunity-related genes in midgut, fat body, hematopoietic organs (HOs), and hemocytes, and determined hemolymph antimicrobial activity. Hemocytes and HOs were tested for presence and distribution of lysozyme mRNA and protein. RESULTS: The midgut and circulating hemocytes exhibited a significantly increased level of lysozyme mRNA in response to gut infection but did not significantly alter expression in response to a systemic infection. Conversely, fat body and HOs responded to both infection models by altered mRNA levels of at least one gene monitored. Most, but not all hemocytes and HO cells contain lysozyme mRNA and protein. DISCUSSION: These data suggest that the gut recruits immune-related tissues in response to gut infection whereas systemic infections do not induce a response in the midgut. The experimental approach implies a skewed cross-talk: An intestinal infection triggers immune activity in systemic immune organs, while a systemic infection does not elicit any or only a restricted immune response in the midgut. The HOs, which form and release hemocytes in larval M. sexta, i) synthesize lysozyme, and ii) respond to immune challenges by increased immune gene expression. These findings strongly suggest that they not only provide phagocytes for the cellular immune response but also synthesize humoral immune components. |
format | Online Article Text |
id | pubmed-10603244 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106032442023-10-28 Differential expression of immunity-related genes in larval Manduca sexta tissues in response to gut and systemic infection von Bredow, Yvette M. Prochazkova, Petra Dvorak, Jiri Skanta, Frantisek Trenczek, Tina E. Bilej, Martin von Bredow, Christoph-Rüdiger Front Cell Infect Microbiol Cellular and Infection Microbiology INTRODUCTION: The midgut epithelium functions as tissue for nutrient uptake as well as physical barrier against pathogens. Additionally, it responds to pathogen contact by production and release of various factors including antimicrobial peptides, similar to the systemic innate immune response. However, if such a response is restricted to a local stimulus or if it appears in response to a systemic infection, too is a rather underexplored topic in insect immunity. We addressed the role of the midgut and the role of systemic immune tissues in the defense against gut-borne and systemic infections, respectively. METHODS: Manduca sexta larvae were challenged with DAP-type peptidoglycan bacteria – Bacillus thuringiensis for local gut infection and Escherichia coli for systemic stimulation. We compared the immune response to both infection models by measuring mRNA levels of four selected immunity-related genes in midgut, fat body, hematopoietic organs (HOs), and hemocytes, and determined hemolymph antimicrobial activity. Hemocytes and HOs were tested for presence and distribution of lysozyme mRNA and protein. RESULTS: The midgut and circulating hemocytes exhibited a significantly increased level of lysozyme mRNA in response to gut infection but did not significantly alter expression in response to a systemic infection. Conversely, fat body and HOs responded to both infection models by altered mRNA levels of at least one gene monitored. Most, but not all hemocytes and HO cells contain lysozyme mRNA and protein. DISCUSSION: These data suggest that the gut recruits immune-related tissues in response to gut infection whereas systemic infections do not induce a response in the midgut. The experimental approach implies a skewed cross-talk: An intestinal infection triggers immune activity in systemic immune organs, while a systemic infection does not elicit any or only a restricted immune response in the midgut. The HOs, which form and release hemocytes in larval M. sexta, i) synthesize lysozyme, and ii) respond to immune challenges by increased immune gene expression. These findings strongly suggest that they not only provide phagocytes for the cellular immune response but also synthesize humoral immune components. Frontiers Media S.A. 2023-10-11 /pmc/articles/PMC10603244/ /pubmed/37900309 http://dx.doi.org/10.3389/fcimb.2023.1258142 Text en Copyright © 2023 von Bredow, Prochazkova, Dvorak, Skanta, Trenczek, Bilej and von Bredow https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology von Bredow, Yvette M. Prochazkova, Petra Dvorak, Jiri Skanta, Frantisek Trenczek, Tina E. Bilej, Martin von Bredow, Christoph-Rüdiger Differential expression of immunity-related genes in larval Manduca sexta tissues in response to gut and systemic infection |
title | Differential expression of immunity-related genes in larval Manduca sexta tissues in response to gut and systemic infection |
title_full | Differential expression of immunity-related genes in larval Manduca sexta tissues in response to gut and systemic infection |
title_fullStr | Differential expression of immunity-related genes in larval Manduca sexta tissues in response to gut and systemic infection |
title_full_unstemmed | Differential expression of immunity-related genes in larval Manduca sexta tissues in response to gut and systemic infection |
title_short | Differential expression of immunity-related genes in larval Manduca sexta tissues in response to gut and systemic infection |
title_sort | differential expression of immunity-related genes in larval manduca sexta tissues in response to gut and systemic infection |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603244/ https://www.ncbi.nlm.nih.gov/pubmed/37900309 http://dx.doi.org/10.3389/fcimb.2023.1258142 |
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