Diet-induced mechanical stress promotes immune and metabolic alterations in the<i> Drosophila melanogaster </i>digestive tract

<p dir="ltr">A fundamental query in <u>immunology </u>is how cells recognize danger in the tissue milieu. For many years, standpoints were mainly centered around damaged cells or structures of invading<u> pathogens</u>, like <u>lipopolysaccharide</u&g...

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Main Author: Abeer Qush (21383261) (author)
Other Authors: Hadi M. Yassine (4675846) (author), Asad Zeidan (8879705) (author), Layla Kamareddine (121079) (author)
Published: 2025
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author Abeer Qush (21383261)
author2 Hadi M. Yassine (4675846)
Asad Zeidan (8879705)
Layla Kamareddine (121079)
author2_role author
author
author
author_facet Abeer Qush (21383261)
Hadi M. Yassine (4675846)
Asad Zeidan (8879705)
Layla Kamareddine (121079)
author_role author
dc.creator.none.fl_str_mv Abeer Qush (21383261)
Hadi M. Yassine (4675846)
Asad Zeidan (8879705)
Layla Kamareddine (121079)
dc.date.none.fl_str_mv 2025-07-01T00:00:00Z
dc.identifier.none.fl_str_mv 10.1016/j.jip.2025.108348
dc.relation.none.fl_str_mv https://figshare.com/articles/journal_contribution/Diet-induced_mechanical_stress_promotes_immune_and_metabolic_alterations_in_the_i_Drosophila_melanogaster_i_digestive_tract/30454505
dc.rights.none.fl_str_mv CC BY 4.0
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Biomedical and clinical sciences
Immunology
Medical biochemistry and metabolomics
Indigestible fiber
Mechanical stress
Gut homeostasis
Innate immunity
Metabolism
Drosophila melanogaster
dc.title.none.fl_str_mv Diet-induced mechanical stress promotes immune and metabolic alterations in the<i> Drosophila melanogaster </i>digestive tract
dc.type.none.fl_str_mv Text
Journal contribution
info:eu-repo/semantics/publishedVersion
text
contribution to journal
description <p dir="ltr">A fundamental query in <u>immunology </u>is how cells recognize danger in the tissue milieu. For many years, standpoints were mainly centered around damaged cells or structures of invading<u> pathogens</u>, like <u>lipopolysaccharide</u>, being the initiators of danger signals to activate immunity. Today, rising evidence presents “biophysical signals” as potential regulators of <u>immune cell</u> functions too. This emerging notion of the ability of tissue <u>mechanotransduction</u> to tune the immunological system appears to likewise exist in other body system, among which is the metabolic system, where startling connection between <u>mechanotransduction</u> and enzymesknown to regulate metabolism have been also reported. Being continuously subjected to mechanical forces, and owing to its multifaceted role in not only absorbing and digesting nutrients, but also in supporting important immunological defense strategies as well as metabolic responses, attention has been lately given to organs making up the gastrointestinal (GI) tract, predominantly the intestine, with growing interest in unravelling the impact of <u>mechanotransduction</u> on the intestinal environment is on the rise. As such, we investigated in this study the impact of mechanical stress introduced by ingesting diet containing the indigestible fiber <u>methylcellulose </u>(MC) on gut immune and metabolic activities using the <u>Drosophila melanogaster</u> model organism. Our findings reveal that feeding on MC-containing diet causes consequential alterations in the fly gut environment manifested by enlargement of the midgut diameter, remodeling of the <u>microbiota </u>community, <u>activation of immune responses</u>, differential regulation of the <i>tachykinin</i> (<i>Tk</i>)<i> peptide </i><i>hormone</i> expression and modulation of lipometabolism. Particularly, we show that feeding on MC-containing diet promotes a marked increase in the relative abundance of Leuconostocaceae/Leuconostoc, microbiota-dependent Reactive Oxygen Species (ROS) production, IMD pathway activation, and IMD-dependent elevation in <i>Tk</i> expression. We also demonstrate that maintaining flies on MC-containing diet for several days leads to a reduction in body weight and in systemic glucose and <u>triacylglycerol</u> levels and modulates <u>lipid droplets</u> accumulation and storage in the gut and fat body. Taken together, these findings provide novel insight into the effect of diet induced-mechanical forces on the intestinal physiology and pathology.</p><h2>Other Information</h2><p dir="ltr">Published in: Journal of Invertebrate Pathology<br>License: <a href="http://creativecommons.org/licenses/by/4.0/" target="_blank">http://creativecommons.org/licenses/by/4.0/</a><br>See article on publisher's website: <a href="https://dx.doi.org/10.1016/j.jip.2025.108348" target="_blank">https://dx.doi.org/10.1016/j.jip.2025.108348</a></p>
eu_rights_str_mv openAccess
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identifier_str_mv 10.1016/j.jip.2025.108348
network_acronym_str Manara2
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oai_identifier_str oai:figshare.com:article/30454505
publishDate 2025
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spelling Diet-induced mechanical stress promotes immune and metabolic alterations in the<i> Drosophila melanogaster </i>digestive tractAbeer Qush (21383261)Hadi M. Yassine (4675846)Asad Zeidan (8879705)Layla Kamareddine (121079)Biomedical and clinical sciencesImmunologyMedical biochemistry and metabolomicsIndigestible fiberMechanical stressGut homeostasisInnate immunityMetabolismDrosophila melanogaster<p dir="ltr">A fundamental query in <u>immunology </u>is how cells recognize danger in the tissue milieu. For many years, standpoints were mainly centered around damaged cells or structures of invading<u> pathogens</u>, like <u>lipopolysaccharide</u>, being the initiators of danger signals to activate immunity. Today, rising evidence presents “biophysical signals” as potential regulators of <u>immune cell</u> functions too. This emerging notion of the ability of tissue <u>mechanotransduction</u> to tune the immunological system appears to likewise exist in other body system, among which is the metabolic system, where startling connection between <u>mechanotransduction</u> and enzymesknown to regulate metabolism have been also reported. Being continuously subjected to mechanical forces, and owing to its multifaceted role in not only absorbing and digesting nutrients, but also in supporting important immunological defense strategies as well as metabolic responses, attention has been lately given to organs making up the gastrointestinal (GI) tract, predominantly the intestine, with growing interest in unravelling the impact of <u>mechanotransduction</u> on the intestinal environment is on the rise. As such, we investigated in this study the impact of mechanical stress introduced by ingesting diet containing the indigestible fiber <u>methylcellulose </u>(MC) on gut immune and metabolic activities using the <u>Drosophila melanogaster</u> model organism. Our findings reveal that feeding on MC-containing diet causes consequential alterations in the fly gut environment manifested by enlargement of the midgut diameter, remodeling of the <u>microbiota </u>community, <u>activation of immune responses</u>, differential regulation of the <i>tachykinin</i> (<i>Tk</i>)<i> peptide </i><i>hormone</i> expression and modulation of lipometabolism. Particularly, we show that feeding on MC-containing diet promotes a marked increase in the relative abundance of Leuconostocaceae/Leuconostoc, microbiota-dependent Reactive Oxygen Species (ROS) production, IMD pathway activation, and IMD-dependent elevation in <i>Tk</i> expression. We also demonstrate that maintaining flies on MC-containing diet for several days leads to a reduction in body weight and in systemic glucose and <u>triacylglycerol</u> levels and modulates <u>lipid droplets</u> accumulation and storage in the gut and fat body. Taken together, these findings provide novel insight into the effect of diet induced-mechanical forces on the intestinal physiology and pathology.</p><h2>Other Information</h2><p dir="ltr">Published in: Journal of Invertebrate Pathology<br>License: <a href="http://creativecommons.org/licenses/by/4.0/" target="_blank">http://creativecommons.org/licenses/by/4.0/</a><br>See article on publisher's website: <a href="https://dx.doi.org/10.1016/j.jip.2025.108348" target="_blank">https://dx.doi.org/10.1016/j.jip.2025.108348</a></p>2025-07-01T00:00:00ZTextJournal contributioninfo:eu-repo/semantics/publishedVersiontextcontribution to journal10.1016/j.jip.2025.108348https://figshare.com/articles/journal_contribution/Diet-induced_mechanical_stress_promotes_immune_and_metabolic_alterations_in_the_i_Drosophila_melanogaster_i_digestive_tract/30454505CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/304545052025-07-01T00:00:00Z
spellingShingle Diet-induced mechanical stress promotes immune and metabolic alterations in the<i> Drosophila melanogaster </i>digestive tract
Abeer Qush (21383261)
Biomedical and clinical sciences
Immunology
Medical biochemistry and metabolomics
Indigestible fiber
Mechanical stress
Gut homeostasis
Innate immunity
Metabolism
Drosophila melanogaster
status_str publishedVersion
title Diet-induced mechanical stress promotes immune and metabolic alterations in the<i> Drosophila melanogaster </i>digestive tract
title_full Diet-induced mechanical stress promotes immune and metabolic alterations in the<i> Drosophila melanogaster </i>digestive tract
title_fullStr Diet-induced mechanical stress promotes immune and metabolic alterations in the<i> Drosophila melanogaster </i>digestive tract
title_full_unstemmed Diet-induced mechanical stress promotes immune and metabolic alterations in the<i> Drosophila melanogaster </i>digestive tract
title_short Diet-induced mechanical stress promotes immune and metabolic alterations in the<i> Drosophila melanogaster </i>digestive tract
title_sort Diet-induced mechanical stress promotes immune and metabolic alterations in the<i> Drosophila melanogaster </i>digestive tract
topic Biomedical and clinical sciences
Immunology
Medical biochemistry and metabolomics
Indigestible fiber
Mechanical stress
Gut homeostasis
Innate immunity
Metabolism
Drosophila melanogaster