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Structure and dynamics of Toll immunoreceptor activation in the mosquito Aedes aegypti

Aedes aegypti has evolved to become an efficient vector for arboviruses but the mechanisms of host-pathogen tolerance are unknown. Immunoreceptor Toll and its ligand Spaetzle have undergone duplication which may allow neofunctionalization and adaptation. Here we present cryo-EM structures and biophy...

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Autores principales: Saucereau, Yoann, Wilson, Thomas H., Tang, Matthew C. K., Moncrieffe, Martin C., Hardwick, Steven W., Chirgadze, Dimitri Y., Soares, Sandro G., Marcaida, Maria Jose, Gay, Nicholas J., Gangloff, Monique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427763/
https://www.ncbi.nlm.nih.gov/pubmed/36042238
http://dx.doi.org/10.1038/s41467-022-32690-6
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author Saucereau, Yoann
Wilson, Thomas H.
Tang, Matthew C. K.
Moncrieffe, Martin C.
Hardwick, Steven W.
Chirgadze, Dimitri Y.
Soares, Sandro G.
Marcaida, Maria Jose
Gay, Nicholas J.
Gangloff, Monique
author_facet Saucereau, Yoann
Wilson, Thomas H.
Tang, Matthew C. K.
Moncrieffe, Martin C.
Hardwick, Steven W.
Chirgadze, Dimitri Y.
Soares, Sandro G.
Marcaida, Maria Jose
Gay, Nicholas J.
Gangloff, Monique
author_sort Saucereau, Yoann
collection PubMed
description Aedes aegypti has evolved to become an efficient vector for arboviruses but the mechanisms of host-pathogen tolerance are unknown. Immunoreceptor Toll and its ligand Spaetzle have undergone duplication which may allow neofunctionalization and adaptation. Here we present cryo-EM structures and biophysical characterisation of low affinity Toll5A complexes that display transient but specific interactions with Spaetzle1C, forming asymmetric complexes, with only one ligand clearly resolved. Loop structures of Spaetzle1C and Toll5A intercalate, temporarily bridging the receptor C-termini to promote signalling. By contrast unbound receptors form head-to-head homodimers that keep the juxtamembrane regions far apart in an inactive conformation. Interestingly the transcriptional signature of Spaetzle1C differs from other Spaetzle cytokines and controls genes involved in innate immunity, metabolism and tissue regeneration. Taken together our results explain how upregulation of Spaetzle1C in the midgut and Toll5A in the salivary gland shape the concomitant immune response.
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spelling pubmed-94277632022-09-01 Structure and dynamics of Toll immunoreceptor activation in the mosquito Aedes aegypti Saucereau, Yoann Wilson, Thomas H. Tang, Matthew C. K. Moncrieffe, Martin C. Hardwick, Steven W. Chirgadze, Dimitri Y. Soares, Sandro G. Marcaida, Maria Jose Gay, Nicholas J. Gangloff, Monique Nat Commun Article Aedes aegypti has evolved to become an efficient vector for arboviruses but the mechanisms of host-pathogen tolerance are unknown. Immunoreceptor Toll and its ligand Spaetzle have undergone duplication which may allow neofunctionalization and adaptation. Here we present cryo-EM structures and biophysical characterisation of low affinity Toll5A complexes that display transient but specific interactions with Spaetzle1C, forming asymmetric complexes, with only one ligand clearly resolved. Loop structures of Spaetzle1C and Toll5A intercalate, temporarily bridging the receptor C-termini to promote signalling. By contrast unbound receptors form head-to-head homodimers that keep the juxtamembrane regions far apart in an inactive conformation. Interestingly the transcriptional signature of Spaetzle1C differs from other Spaetzle cytokines and controls genes involved in innate immunity, metabolism and tissue regeneration. Taken together our results explain how upregulation of Spaetzle1C in the midgut and Toll5A in the salivary gland shape the concomitant immune response. Nature Publishing Group UK 2022-08-30 /pmc/articles/PMC9427763/ /pubmed/36042238 http://dx.doi.org/10.1038/s41467-022-32690-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Saucereau, Yoann
Wilson, Thomas H.
Tang, Matthew C. K.
Moncrieffe, Martin C.
Hardwick, Steven W.
Chirgadze, Dimitri Y.
Soares, Sandro G.
Marcaida, Maria Jose
Gay, Nicholas J.
Gangloff, Monique
Structure and dynamics of Toll immunoreceptor activation in the mosquito Aedes aegypti
title Structure and dynamics of Toll immunoreceptor activation in the mosquito Aedes aegypti
title_full Structure and dynamics of Toll immunoreceptor activation in the mosquito Aedes aegypti
title_fullStr Structure and dynamics of Toll immunoreceptor activation in the mosquito Aedes aegypti
title_full_unstemmed Structure and dynamics of Toll immunoreceptor activation in the mosquito Aedes aegypti
title_short Structure and dynamics of Toll immunoreceptor activation in the mosquito Aedes aegypti
title_sort structure and dynamics of toll immunoreceptor activation in the mosquito aedes aegypti
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427763/
https://www.ncbi.nlm.nih.gov/pubmed/36042238
http://dx.doi.org/10.1038/s41467-022-32690-6
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