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Common aquatic pollutants modify hemocyte immune responses in Biomphalaria glabrata

Disruptions to reproductive health in wildlife species inhabiting polluted environments is often found to occur alongside compromised immunity. However, research on impacts of aquatic pollution on freshwater mollusc immune responses is limited despite their importance as vectors of disease (Schistos...

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Autores principales: Lynch, Adam E., Noble, Leslie R., Jones, Catherine S., Routledge, Edwin J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9493456/
https://www.ncbi.nlm.nih.gov/pubmed/36159819
http://dx.doi.org/10.3389/fimmu.2022.839746
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author Lynch, Adam E.
Noble, Leslie R.
Jones, Catherine S.
Routledge, Edwin J.
author_facet Lynch, Adam E.
Noble, Leslie R.
Jones, Catherine S.
Routledge, Edwin J.
author_sort Lynch, Adam E.
collection PubMed
description Disruptions to reproductive health in wildlife species inhabiting polluted environments is often found to occur alongside compromised immunity. However, research on impacts of aquatic pollution on freshwater mollusc immune responses is limited despite their importance as vectors of disease (Schistosomiasis) in humans, cattle and wild mammals. We developed an in vitro ‘tool-kit’ of well-characterized quantitative immune tests using Biomphalaria glabrata hemocytes. We exposed hemocytes to environmentally-relevant concentrations of common aquatic pollutants (17β-estradiol, Bisphenol-A and p,p’-DDE) and measured key innate immune responses including motility, phagocytosis and encapsulation. Additionally, we tested an extract of a typical domestic tertiary treated effluent as representative of a ‘real-world’ mixture of chemicals. Encapsulation responses were stimulated by p,p’-DDE at low doses but were suppressed at higher doses. Concentrations of BPA (above 200 ng/L) and p,p’-DDE (above 500 ng/L) significantly inhibited phagocytosis compared to controls, whilst hemocyte motility was reduced by all test chemicals and the effluent extract in a dose-dependent manner. All responses occurred at chemical concentrations considered to be below the cytotoxic thresholds of hemocytes. This is the first time a suite of in vitro tests has been developed specifically in B. glabrata with the purpose of investigating the impacts of chemical pollutants and an effluent extract on immunity. Our findings indicate that common aquatic pollutants alter innate immune responses in B. glabrata, suggesting that pollutants may be a critical, yet overlooked, factor impacting disease by modulating the dynamics of parasite transmission between molluscs and humans.
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spelling pubmed-94934562022-09-23 Common aquatic pollutants modify hemocyte immune responses in Biomphalaria glabrata Lynch, Adam E. Noble, Leslie R. Jones, Catherine S. Routledge, Edwin J. Front Immunol Immunology Disruptions to reproductive health in wildlife species inhabiting polluted environments is often found to occur alongside compromised immunity. However, research on impacts of aquatic pollution on freshwater mollusc immune responses is limited despite their importance as vectors of disease (Schistosomiasis) in humans, cattle and wild mammals. We developed an in vitro ‘tool-kit’ of well-characterized quantitative immune tests using Biomphalaria glabrata hemocytes. We exposed hemocytes to environmentally-relevant concentrations of common aquatic pollutants (17β-estradiol, Bisphenol-A and p,p’-DDE) and measured key innate immune responses including motility, phagocytosis and encapsulation. Additionally, we tested an extract of a typical domestic tertiary treated effluent as representative of a ‘real-world’ mixture of chemicals. Encapsulation responses were stimulated by p,p’-DDE at low doses but were suppressed at higher doses. Concentrations of BPA (above 200 ng/L) and p,p’-DDE (above 500 ng/L) significantly inhibited phagocytosis compared to controls, whilst hemocyte motility was reduced by all test chemicals and the effluent extract in a dose-dependent manner. All responses occurred at chemical concentrations considered to be below the cytotoxic thresholds of hemocytes. This is the first time a suite of in vitro tests has been developed specifically in B. glabrata with the purpose of investigating the impacts of chemical pollutants and an effluent extract on immunity. Our findings indicate that common aquatic pollutants alter innate immune responses in B. glabrata, suggesting that pollutants may be a critical, yet overlooked, factor impacting disease by modulating the dynamics of parasite transmission between molluscs and humans. Frontiers Media S.A. 2022-09-08 /pmc/articles/PMC9493456/ /pubmed/36159819 http://dx.doi.org/10.3389/fimmu.2022.839746 Text en Copyright © 2022 Lynch, Noble, Jones and Routledge https://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
Lynch, Adam E.
Noble, Leslie R.
Jones, Catherine S.
Routledge, Edwin J.
Common aquatic pollutants modify hemocyte immune responses in Biomphalaria glabrata
title Common aquatic pollutants modify hemocyte immune responses in Biomphalaria glabrata
title_full Common aquatic pollutants modify hemocyte immune responses in Biomphalaria glabrata
title_fullStr Common aquatic pollutants modify hemocyte immune responses in Biomphalaria glabrata
title_full_unstemmed Common aquatic pollutants modify hemocyte immune responses in Biomphalaria glabrata
title_short Common aquatic pollutants modify hemocyte immune responses in Biomphalaria glabrata
title_sort common aquatic pollutants modify hemocyte immune responses in biomphalaria glabrata
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9493456/
https://www.ncbi.nlm.nih.gov/pubmed/36159819
http://dx.doi.org/10.3389/fimmu.2022.839746
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