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No evidence for trans-generational immune priming in Drosophila melanogaster
Most organisms are under constant and repeated exposure to pathogens, leading to perpetual natural selection for more effective ways to fight-off infections. This could include the evolution of memory-based immunity to increase protection from repeatedly-encountered pathogens both within and across...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10343036/ https://www.ncbi.nlm.nih.gov/pubmed/37440541 http://dx.doi.org/10.1371/journal.pone.0288342 |
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author | Radhika, R. Lazzaro, Brian P. |
author_facet | Radhika, R. Lazzaro, Brian P. |
author_sort | Radhika, R. |
collection | PubMed |
description | Most organisms are under constant and repeated exposure to pathogens, leading to perpetual natural selection for more effective ways to fight-off infections. This could include the evolution of memory-based immunity to increase protection from repeatedly-encountered pathogens both within and across generations. There is mixed evidence for intra- and trans-generational priming in non-vertebrates, which lack the antibody-mediated acquired immunity characteristic of vertebrates. In this work, we tested for trans-generational immune priming in adult offspring of the fruit fly, Drosophila melanogaster, after maternal challenge with 10 different bacterial pathogens. We focused on natural opportunistic pathogens of Drosophila spanning a range of virulence from 10% to 100% host mortality. We infected mothers via septic injury and tested for enhanced resistance to infection in their adult offspring, measured as the ability to suppress bacterial proliferation and survive infection. We categorized the mothers into four classes for each bacterium tested: those that survived infection, those that succumbed to infection, sterile-injury controls, and uninjured controls. We found no evidence for trans-generational priming by any class of mother in response to any of the bacteria. |
format | Online Article Text |
id | pubmed-10343036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-103430362023-07-14 No evidence for trans-generational immune priming in Drosophila melanogaster Radhika, R. Lazzaro, Brian P. PLoS One Research Article Most organisms are under constant and repeated exposure to pathogens, leading to perpetual natural selection for more effective ways to fight-off infections. This could include the evolution of memory-based immunity to increase protection from repeatedly-encountered pathogens both within and across generations. There is mixed evidence for intra- and trans-generational priming in non-vertebrates, which lack the antibody-mediated acquired immunity characteristic of vertebrates. In this work, we tested for trans-generational immune priming in adult offspring of the fruit fly, Drosophila melanogaster, after maternal challenge with 10 different bacterial pathogens. We focused on natural opportunistic pathogens of Drosophila spanning a range of virulence from 10% to 100% host mortality. We infected mothers via septic injury and tested for enhanced resistance to infection in their adult offspring, measured as the ability to suppress bacterial proliferation and survive infection. We categorized the mothers into four classes for each bacterium tested: those that survived infection, those that succumbed to infection, sterile-injury controls, and uninjured controls. We found no evidence for trans-generational priming by any class of mother in response to any of the bacteria. Public Library of Science 2023-07-13 /pmc/articles/PMC10343036/ /pubmed/37440541 http://dx.doi.org/10.1371/journal.pone.0288342 Text en © 2023 Radhika, Lazzaro 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 use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Radhika, R. Lazzaro, Brian P. No evidence for trans-generational immune priming in Drosophila melanogaster |
title | No evidence for trans-generational immune priming in Drosophila melanogaster |
title_full | No evidence for trans-generational immune priming in Drosophila melanogaster |
title_fullStr | No evidence for trans-generational immune priming in Drosophila melanogaster |
title_full_unstemmed | No evidence for trans-generational immune priming in Drosophila melanogaster |
title_short | No evidence for trans-generational immune priming in Drosophila melanogaster |
title_sort | no evidence for trans-generational immune priming in drosophila melanogaster |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10343036/ https://www.ncbi.nlm.nih.gov/pubmed/37440541 http://dx.doi.org/10.1371/journal.pone.0288342 |
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