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Thermoneutrality and severe malaria: investigating the effect of warmer environmental temperatures on the inflammatory response and disease progression

INTRODUCTION: Most studies using murine disease models are conducted at housing temperatures (20 – 22°C) that are sub-optimal (ST) for mice, eliciting changes in metabolism and response to disease. Experiments performed at a thermoneutral temperature (TT; 28 – 31°C) have revealed an altered immune r...

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Autores principales: Vialard, Fiorella, Allaeys, Isabelle, Dong, George, Phan, Minh Phuong, Singh, Urvashi, Hébert, Marie Josée, Dieudé, Mélanie, Langlais, David, Boilard, Eric, Labbé, David P., Olivier, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10283000/
https://www.ncbi.nlm.nih.gov/pubmed/37350957
http://dx.doi.org/10.3389/fimmu.2023.1128466
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author Vialard, Fiorella
Allaeys, Isabelle
Dong, George
Phan, Minh Phuong
Singh, Urvashi
Hébert, Marie Josée
Dieudé, Mélanie
Langlais, David
Boilard, Eric
Labbé, David P.
Olivier, Martin
author_facet Vialard, Fiorella
Allaeys, Isabelle
Dong, George
Phan, Minh Phuong
Singh, Urvashi
Hébert, Marie Josée
Dieudé, Mélanie
Langlais, David
Boilard, Eric
Labbé, David P.
Olivier, Martin
author_sort Vialard, Fiorella
collection PubMed
description INTRODUCTION: Most studies using murine disease models are conducted at housing temperatures (20 – 22°C) that are sub-optimal (ST) for mice, eliciting changes in metabolism and response to disease. Experiments performed at a thermoneutral temperature (TT; 28 – 31°C) have revealed an altered immune response to pathogens and experimental treatments in murine disease model that have implications for their translation to clinical research. How such conditions affect the inflammatory response to infection with Plasmodium berghei ANKA (PbA) and disease progression is unknown. We hypothesized that changes in environmental temperature modulate immune cells and modify host response to malaria disease. To test this hypothesis, we conducted experiments to determine: (1) the inflammatory response to malarial agents injection in a peritonitis model and (2) disease progression in PbA-infected mice at TT compared to ST. METHODS: In one study, acclimatized mice were injected intraperitoneally with native hemozoin (nHZ) or Leishmania at TT (28 – 31°C) or ST, and immune cells, cytokine, and extracellular vesicle (EV) profiles were determined from the peritoneal cavity (PEC) fluid. In another study, PbA-infected mice were monitored until end-point (i.e. experimental malaria score ≥4). RESULTS: We found that Leishmania injection resulted in decreased cell recruitment and higher phagocytosis of nHZ in mice housed at TT. We found 398 upregulated and 293 downregulated proinflammatory genes in mice injected with nHZ, at both temperatures. We report the presence of host-derived EVs never reported before in a murine parasitic murine model at both temperatures. We observed metabolic changes in mice housed at TT, but these did not result to noticeable changes in disease progression compared to ST. DISCUSSION: To our knowledge, these experiments are the first to investigate the effect of thermoneutrality on a malaria murine model. We found important metabolic difference in mice housed at TT. Our results offer insights on how thermoneutrality might impact a severe malaria murine model and directions for more targeted investigations.
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spelling pubmed-102830002023-06-22 Thermoneutrality and severe malaria: investigating the effect of warmer environmental temperatures on the inflammatory response and disease progression Vialard, Fiorella Allaeys, Isabelle Dong, George Phan, Minh Phuong Singh, Urvashi Hébert, Marie Josée Dieudé, Mélanie Langlais, David Boilard, Eric Labbé, David P. Olivier, Martin Front Immunol Immunology INTRODUCTION: Most studies using murine disease models are conducted at housing temperatures (20 – 22°C) that are sub-optimal (ST) for mice, eliciting changes in metabolism and response to disease. Experiments performed at a thermoneutral temperature (TT; 28 – 31°C) have revealed an altered immune response to pathogens and experimental treatments in murine disease model that have implications for their translation to clinical research. How such conditions affect the inflammatory response to infection with Plasmodium berghei ANKA (PbA) and disease progression is unknown. We hypothesized that changes in environmental temperature modulate immune cells and modify host response to malaria disease. To test this hypothesis, we conducted experiments to determine: (1) the inflammatory response to malarial agents injection in a peritonitis model and (2) disease progression in PbA-infected mice at TT compared to ST. METHODS: In one study, acclimatized mice were injected intraperitoneally with native hemozoin (nHZ) or Leishmania at TT (28 – 31°C) or ST, and immune cells, cytokine, and extracellular vesicle (EV) profiles were determined from the peritoneal cavity (PEC) fluid. In another study, PbA-infected mice were monitored until end-point (i.e. experimental malaria score ≥4). RESULTS: We found that Leishmania injection resulted in decreased cell recruitment and higher phagocytosis of nHZ in mice housed at TT. We found 398 upregulated and 293 downregulated proinflammatory genes in mice injected with nHZ, at both temperatures. We report the presence of host-derived EVs never reported before in a murine parasitic murine model at both temperatures. We observed metabolic changes in mice housed at TT, but these did not result to noticeable changes in disease progression compared to ST. DISCUSSION: To our knowledge, these experiments are the first to investigate the effect of thermoneutrality on a malaria murine model. We found important metabolic difference in mice housed at TT. Our results offer insights on how thermoneutrality might impact a severe malaria murine model and directions for more targeted investigations. Frontiers Media S.A. 2023-06-07 /pmc/articles/PMC10283000/ /pubmed/37350957 http://dx.doi.org/10.3389/fimmu.2023.1128466 Text en Copyright © 2023 Vialard, Allaeys, Dong, Phan, Singh, Hébert, Dieudé, Langlais, Boilard, Labbé and Olivier 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
Vialard, Fiorella
Allaeys, Isabelle
Dong, George
Phan, Minh Phuong
Singh, Urvashi
Hébert, Marie Josée
Dieudé, Mélanie
Langlais, David
Boilard, Eric
Labbé, David P.
Olivier, Martin
Thermoneutrality and severe malaria: investigating the effect of warmer environmental temperatures on the inflammatory response and disease progression
title Thermoneutrality and severe malaria: investigating the effect of warmer environmental temperatures on the inflammatory response and disease progression
title_full Thermoneutrality and severe malaria: investigating the effect of warmer environmental temperatures on the inflammatory response and disease progression
title_fullStr Thermoneutrality and severe malaria: investigating the effect of warmer environmental temperatures on the inflammatory response and disease progression
title_full_unstemmed Thermoneutrality and severe malaria: investigating the effect of warmer environmental temperatures on the inflammatory response and disease progression
title_short Thermoneutrality and severe malaria: investigating the effect of warmer environmental temperatures on the inflammatory response and disease progression
title_sort thermoneutrality and severe malaria: investigating the effect of warmer environmental temperatures on the inflammatory response and disease progression
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10283000/
https://www.ncbi.nlm.nih.gov/pubmed/37350957
http://dx.doi.org/10.3389/fimmu.2023.1128466
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