Cargando…

Arthropods Under Pressure: Stress Responses and Immunity at the Pathogen-Vector Interface

Understanding what influences the ability of some arthropods to harbor and transmit pathogens may be key for controlling the spread of vector-borne diseases. Arthropod immunity has a central role in dictating vector competence for pathogen acquisition and transmission. Microbial infection elicits im...

Descripción completa

Detalles Bibliográficos
Autores principales: Rosche, Kristin L., Sidak-Loftis, Lindsay C., Hurtado, Joanna, Fisk, Elizabeth A., Shaw, Dana K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7917218/
https://www.ncbi.nlm.nih.gov/pubmed/33659000
http://dx.doi.org/10.3389/fimmu.2020.629777
_version_ 1783657650720866304
author Rosche, Kristin L.
Sidak-Loftis, Lindsay C.
Hurtado, Joanna
Fisk, Elizabeth A.
Shaw, Dana K.
author_facet Rosche, Kristin L.
Sidak-Loftis, Lindsay C.
Hurtado, Joanna
Fisk, Elizabeth A.
Shaw, Dana K.
author_sort Rosche, Kristin L.
collection PubMed
description Understanding what influences the ability of some arthropods to harbor and transmit pathogens may be key for controlling the spread of vector-borne diseases. Arthropod immunity has a central role in dictating vector competence for pathogen acquisition and transmission. Microbial infection elicits immune responses and imparts stress on the host by causing physical damage and nutrient deprivation, which triggers evolutionarily conserved stress response pathways aimed at restoring cellular homeostasis. Recent studies increasingly recognize that eukaryotic stress responses and innate immunity are closely intertwined. Herein, we describe two well-characterized and evolutionarily conserved mechanisms, the Unfolded Protein Response (UPR) and the Integrated Stress Response (ISR), and examine evidence that these stress responses impact immune signaling. We then describe how multiple pathogens, including vector-borne microbes, interface with stress responses in mammals. Owing to the well-conserved nature of the UPR and ISR, we speculate that similar mechanisms may be occurring in arthropod vectors and ultimately impacting vector competence. We conclude this Perspective by positing that novel insights into vector competence will emerge when considering that stress-signaling pathways may be influencing the arthropod immune network.
format Online
Article
Text
id pubmed-7917218
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-79172182021-03-02 Arthropods Under Pressure: Stress Responses and Immunity at the Pathogen-Vector Interface Rosche, Kristin L. Sidak-Loftis, Lindsay C. Hurtado, Joanna Fisk, Elizabeth A. Shaw, Dana K. Front Immunol Immunology Understanding what influences the ability of some arthropods to harbor and transmit pathogens may be key for controlling the spread of vector-borne diseases. Arthropod immunity has a central role in dictating vector competence for pathogen acquisition and transmission. Microbial infection elicits immune responses and imparts stress on the host by causing physical damage and nutrient deprivation, which triggers evolutionarily conserved stress response pathways aimed at restoring cellular homeostasis. Recent studies increasingly recognize that eukaryotic stress responses and innate immunity are closely intertwined. Herein, we describe two well-characterized and evolutionarily conserved mechanisms, the Unfolded Protein Response (UPR) and the Integrated Stress Response (ISR), and examine evidence that these stress responses impact immune signaling. We then describe how multiple pathogens, including vector-borne microbes, interface with stress responses in mammals. Owing to the well-conserved nature of the UPR and ISR, we speculate that similar mechanisms may be occurring in arthropod vectors and ultimately impacting vector competence. We conclude this Perspective by positing that novel insights into vector competence will emerge when considering that stress-signaling pathways may be influencing the arthropod immune network. Frontiers Media S.A. 2021-02-15 /pmc/articles/PMC7917218/ /pubmed/33659000 http://dx.doi.org/10.3389/fimmu.2020.629777 Text en Copyright © 2021 Rosche, Sidak-Loftis, Hurtado, Fisk and Shaw http://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 Immunology
Rosche, Kristin L.
Sidak-Loftis, Lindsay C.
Hurtado, Joanna
Fisk, Elizabeth A.
Shaw, Dana K.
Arthropods Under Pressure: Stress Responses and Immunity at the Pathogen-Vector Interface
title Arthropods Under Pressure: Stress Responses and Immunity at the Pathogen-Vector Interface
title_full Arthropods Under Pressure: Stress Responses and Immunity at the Pathogen-Vector Interface
title_fullStr Arthropods Under Pressure: Stress Responses and Immunity at the Pathogen-Vector Interface
title_full_unstemmed Arthropods Under Pressure: Stress Responses and Immunity at the Pathogen-Vector Interface
title_short Arthropods Under Pressure: Stress Responses and Immunity at the Pathogen-Vector Interface
title_sort arthropods under pressure: stress responses and immunity at the pathogen-vector interface
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7917218/
https://www.ncbi.nlm.nih.gov/pubmed/33659000
http://dx.doi.org/10.3389/fimmu.2020.629777
work_keys_str_mv AT roschekristinl arthropodsunderpressurestressresponsesandimmunityatthepathogenvectorinterface
AT sidakloftislindsayc arthropodsunderpressurestressresponsesandimmunityatthepathogenvectorinterface
AT hurtadojoanna arthropodsunderpressurestressresponsesandimmunityatthepathogenvectorinterface
AT fiskelizabetha arthropodsunderpressurestressresponsesandimmunityatthepathogenvectorinterface
AT shawdanak arthropodsunderpressurestressresponsesandimmunityatthepathogenvectorinterface