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Inherent constraints on a polyfunctional tissue lead to a reproduction-immunity tradeoff

BACKGROUND: Single tissues can have multiple functions, which can result in constraints, impaired function, and tradeoffs. The insect fat body performs remarkably diverse functions including metabolic control, reproductive provisioning, and systemic immune responses. How polyfunctional tissues simul...

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Detalles Bibliográficos
Autores principales: Gupta, Vanika, Frank, Ashley M., Matolka, Nick, Lazzaro, Brian P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9161490/
https://www.ncbi.nlm.nih.gov/pubmed/35655304
http://dx.doi.org/10.1186/s12915-022-01328-w
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author Gupta, Vanika
Frank, Ashley M.
Matolka, Nick
Lazzaro, Brian P.
author_facet Gupta, Vanika
Frank, Ashley M.
Matolka, Nick
Lazzaro, Brian P.
author_sort Gupta, Vanika
collection PubMed
description BACKGROUND: Single tissues can have multiple functions, which can result in constraints, impaired function, and tradeoffs. The insect fat body performs remarkably diverse functions including metabolic control, reproductive provisioning, and systemic immune responses. How polyfunctional tissues simultaneously execute multiple distinct physiological functions is generally unknown. Immunity and reproduction are observed to trade off in many organisms but the mechanistic basis for this tradeoff is also typically not known. Here we investigate constraints and trade-offs in the polyfunctional insect fat body. RESULTS: Using single-nucleus sequencing, we determined that the Drosophila melanogaster fat body executes diverse basal functions with heterogenous cellular subpopulations. The size and identity of these subpopulations are remarkably stable between virgin and mated flies, as well as before and after infection. However, as an emergency function, the immune response engages the entire tissue and all cellular subpopulations produce induce expression of defense genes. We found that reproductively active females who were given bacterial infection exhibited signatures of ER stress and impaired capacity to synthesize new protein in response to infection, including decreased capacity to produce antimicrobial peptides. Transient provision of a reversible translation inhibitor to mated females prior to infection rescued general protein synthesis, specific production of antimicrobial peptides, and survival of infection. CONCLUSIONS: The commonly observed tradeoff between reproduction and immunity appears to be driven, in D. melanogaster, by a failure of the fat body to be able to handle simultaneous protein translation demands of reproductive provisioning and immune defense. We suggest that inherent cellular limitations in tissues that perform multiple functions may provide a general explanation for the wide prevalence of physiological and evolutionary tradeoffs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01328-w.
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spelling pubmed-91614902022-06-03 Inherent constraints on a polyfunctional tissue lead to a reproduction-immunity tradeoff Gupta, Vanika Frank, Ashley M. Matolka, Nick Lazzaro, Brian P. BMC Biol Research Article BACKGROUND: Single tissues can have multiple functions, which can result in constraints, impaired function, and tradeoffs. The insect fat body performs remarkably diverse functions including metabolic control, reproductive provisioning, and systemic immune responses. How polyfunctional tissues simultaneously execute multiple distinct physiological functions is generally unknown. Immunity and reproduction are observed to trade off in many organisms but the mechanistic basis for this tradeoff is also typically not known. Here we investigate constraints and trade-offs in the polyfunctional insect fat body. RESULTS: Using single-nucleus sequencing, we determined that the Drosophila melanogaster fat body executes diverse basal functions with heterogenous cellular subpopulations. The size and identity of these subpopulations are remarkably stable between virgin and mated flies, as well as before and after infection. However, as an emergency function, the immune response engages the entire tissue and all cellular subpopulations produce induce expression of defense genes. We found that reproductively active females who were given bacterial infection exhibited signatures of ER stress and impaired capacity to synthesize new protein in response to infection, including decreased capacity to produce antimicrobial peptides. Transient provision of a reversible translation inhibitor to mated females prior to infection rescued general protein synthesis, specific production of antimicrobial peptides, and survival of infection. CONCLUSIONS: The commonly observed tradeoff between reproduction and immunity appears to be driven, in D. melanogaster, by a failure of the fat body to be able to handle simultaneous protein translation demands of reproductive provisioning and immune defense. We suggest that inherent cellular limitations in tissues that perform multiple functions may provide a general explanation for the wide prevalence of physiological and evolutionary tradeoffs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01328-w. BioMed Central 2022-06-02 /pmc/articles/PMC9161490/ /pubmed/35655304 http://dx.doi.org/10.1186/s12915-022-01328-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Gupta, Vanika
Frank, Ashley M.
Matolka, Nick
Lazzaro, Brian P.
Inherent constraints on a polyfunctional tissue lead to a reproduction-immunity tradeoff
title Inherent constraints on a polyfunctional tissue lead to a reproduction-immunity tradeoff
title_full Inherent constraints on a polyfunctional tissue lead to a reproduction-immunity tradeoff
title_fullStr Inherent constraints on a polyfunctional tissue lead to a reproduction-immunity tradeoff
title_full_unstemmed Inherent constraints on a polyfunctional tissue lead to a reproduction-immunity tradeoff
title_short Inherent constraints on a polyfunctional tissue lead to a reproduction-immunity tradeoff
title_sort inherent constraints on a polyfunctional tissue lead to a reproduction-immunity tradeoff
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9161490/
https://www.ncbi.nlm.nih.gov/pubmed/35655304
http://dx.doi.org/10.1186/s12915-022-01328-w
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