Evolutionary immunology to explore original antiviral strategies

Bibliographic Details
Main Author: Imler, Jean-Luc
Publication Date: 2023
Other Authors: Cai, Hua, Meignin, Carine, Martins, Nelson
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10400.14/44131
Summary: Over the past 25 years, the field of evolutionary developmental biology (evo-devo) has used genomics and genetics to gain insight on the developmental mechanisms underlying the evolution of morphological diversity of animals. Evo-devo exploits the key insight that conserved toolkits of development (e.g., Hox genes) are used in animals to produce genetic novelties that provide adaptation to a new environment. Like development, immunity is forged by interactions with the environment, namely the microbial world. Yet, when it comes to the study of immune defence mechanisms in invertebrates, interest primarily focuses on evolutionarily conserved molecules also present in humans. Here, focusing on antiviral immunity, we argue that immune genes not conserved in humans represent an unexplored resource for the discovery of new antiviral strategies. We review recent findings on the cGAS-STING pathway and explain how cyclic dinucleotides produced by cGAS-like receptors may be used to investigate the portfolio of antiviral genes in a broad range of species. This will set the stage for evo-immuno approaches, exploiting the investment in antiviral defences made by metazoans over hundreds million years of evolution.
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spelling Evolutionary immunology to explore original antiviral strategiesInnate immunitySTINGCyclic dinucleotidecGASCBASSOver the past 25 years, the field of evolutionary developmental biology (evo-devo) has used genomics and genetics to gain insight on the developmental mechanisms underlying the evolution of morphological diversity of animals. Evo-devo exploits the key insight that conserved toolkits of development (e.g., Hox genes) are used in animals to produce genetic novelties that provide adaptation to a new environment. Like development, immunity is forged by interactions with the environment, namely the microbial world. Yet, when it comes to the study of immune defence mechanisms in invertebrates, interest primarily focuses on evolutionarily conserved molecules also present in humans. Here, focusing on antiviral immunity, we argue that immune genes not conserved in humans represent an unexplored resource for the discovery of new antiviral strategies. We review recent findings on the cGAS-STING pathway and explain how cyclic dinucleotides produced by cGAS-like receptors may be used to investigate the portfolio of antiviral genes in a broad range of species. This will set the stage for evo-immuno approaches, exploiting the investment in antiviral defences made by metazoans over hundreds million years of evolution.VeritatiImler, Jean-LucCai, HuaMeignin, CarineMartins, Nelson2024-03-06T10:14:50Z2023-12-182023-12-18T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.14/44131eng10.32942/x2dw4tinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-03-13T16:38:53Zoai:repositorio.ucp.pt:10400.14/44131Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T02:22:06.401020Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Evolutionary immunology to explore original antiviral strategies
title Evolutionary immunology to explore original antiviral strategies
spellingShingle Evolutionary immunology to explore original antiviral strategies
Imler, Jean-Luc
Innate immunity
STING
Cyclic dinucleotide
cGAS
CBASS
title_short Evolutionary immunology to explore original antiviral strategies
title_full Evolutionary immunology to explore original antiviral strategies
title_fullStr Evolutionary immunology to explore original antiviral strategies
title_full_unstemmed Evolutionary immunology to explore original antiviral strategies
title_sort Evolutionary immunology to explore original antiviral strategies
author Imler, Jean-Luc
author_facet Imler, Jean-Luc
Cai, Hua
Meignin, Carine
Martins, Nelson
author_role author
author2 Cai, Hua
Meignin, Carine
Martins, Nelson
author2_role author
author
author
dc.contributor.none.fl_str_mv Veritati
dc.contributor.author.fl_str_mv Imler, Jean-Luc
Cai, Hua
Meignin, Carine
Martins, Nelson
dc.subject.por.fl_str_mv Innate immunity
STING
Cyclic dinucleotide
cGAS
CBASS
topic Innate immunity
STING
Cyclic dinucleotide
cGAS
CBASS
description Over the past 25 years, the field of evolutionary developmental biology (evo-devo) has used genomics and genetics to gain insight on the developmental mechanisms underlying the evolution of morphological diversity of animals. Evo-devo exploits the key insight that conserved toolkits of development (e.g., Hox genes) are used in animals to produce genetic novelties that provide adaptation to a new environment. Like development, immunity is forged by interactions with the environment, namely the microbial world. Yet, when it comes to the study of immune defence mechanisms in invertebrates, interest primarily focuses on evolutionarily conserved molecules also present in humans. Here, focusing on antiviral immunity, we argue that immune genes not conserved in humans represent an unexplored resource for the discovery of new antiviral strategies. We review recent findings on the cGAS-STING pathway and explain how cyclic dinucleotides produced by cGAS-like receptors may be used to investigate the portfolio of antiviral genes in a broad range of species. This will set the stage for evo-immuno approaches, exploiting the investment in antiviral defences made by metazoans over hundreds million years of evolution.
publishDate 2023
dc.date.none.fl_str_mv 2023-12-18
2023-12-18T00:00:00Z
2024-03-06T10:14:50Z
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