<i>Tropheryma whipplei</i> escapes LAPosome and modulates macrophage response in a xenophagy-dependent manner

<i>Tropheryma whipplei</i>, the agent of Whipple's disease, is an intracellular pathogen that replicates in macrophages. The phagocytic and cellular processes leading to the formation of <i>T. whipplei</i> replicative vacuole remain poorly understood. Macrophage microbicidal activity is largely related to macro/autophagy which is also essential for cell homeostasis. Here, we show that <i>T. whipplei</i> uptake by macrophages involved LC3-associated phagocytosis (LAP). Bacteria then escaped into the cytosol from where they were recaptured by xenophagy. We also demonstrate that <i>T. whipplei</i> blocked the autophagic flux to build its replicative compartment. Inhibition of LAP resulted in the decrease of interleukin (IL)-10 secretion and the restoration of the autophagy flux, suggesting that modulation of autophagy during infection alters immune response and promote persistence. Our results provide new insight in the intracellular fate of the bacteria during macrophage infection and suggest the possible involvement of previously unknown virulence factors in <i>T. whipplei</i> infection.

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Publication Details

Journal
Autophagy Reports
Published
2025-03-11
DOI
https://doi.org/10.1080/27694127.2025.2475527
Citations
1
Primary Topic
Whipple's Disease and Interleukins
Type
article
Field-Weighted Citation Impact
1.47

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article

Tropheryma whipplei escapes LAPosome and modulates macrophage response in a xenophagy-dependent manner

Jeffrey Arrindell, Benoît Desnues, Soraya Mezouar, Eloïne Bestion et al.
1 citations
Autophagy Reports
Whipple's Disease and Interleukins
1.47
article

Tropheryma whipplei escapes LAPosome and modulates macrophage response in a xenophagy-dependent manner

Jeffrey Arrindell, Benoît Desnues, Soraya Mezouar, Eloïne Bestion, Emilie Reyne
article en
1 citations

Abstract

<i>Tropheryma whipplei</i>, the agent of Whipple's disease, is an intracellular pathogen that replicates in macrophages. The phagocytic and cellular processes leading to the formation of <i>T. whipplei</i> replicative vacuole remain poorly understood. Macrophage microbicidal activity is largely related to macro/autophagy which is also essential for cell homeostasis. Here, we show that <i>T. whipplei</i> uptake by macrophages involved LC3-associated phagocytosis (LAP). Bacteria then escaped into the cytosol from where they were recaptured by xenophagy. We also demonstrate that <i>T. whipplei</i> blocked the autophagic flux to build its replicative compartment. Inhibition of LAP resulted in the decrease of interleukin (IL)-10 secretion and the restoration of the autophagy flux, suggesting that modulation of autophagy during infection alters immune response and promote persistence. Our results provide new insight in the intracellular fate of the bacteria during macrophage infection and suggest the possible involvement of previously unknown virulence factors in <i>T. whipplei</i> infection.

Autophagy ReportsVol. 4(1)
Centre National de la Recherche Scientifique (FR), Aix-Marseille Université (FR), Méditerranée Infection Foundation (FR), Genoscience Pharma (France) (FR), Phoenix Contact (United States) (US)
Agence Nationale de la Recherche
Zero hunger
Openalex Percentile: Top 22%
Whipple's Disease and Interleukins
1.47
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