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  1. Article ; Online: High content quantitative imaging of Mycobacterium tuberculosis responses to acidic microenvironments within human macrophages

    Beren Aylan / Laure Botella / Maximiliano G. Gutierrez / Pierre Santucci

    FEBS Open Bio, Vol 13, Iss 7, Pp 1204-

    2023  Volume 1217

    Abstract: Intracellular pathogens such as Mycobacterium tuberculosis (Mtb) have evolved diverse strategies to counteract macrophage defence mechanisms including phagolysosomal biogenesis. Within macrophages, Mtb initially resides inside membrane‐bound phagosomes ... ...

    Abstract Intracellular pathogens such as Mycobacterium tuberculosis (Mtb) have evolved diverse strategies to counteract macrophage defence mechanisms including phagolysosomal biogenesis. Within macrophages, Mtb initially resides inside membrane‐bound phagosomes that interact with lysosomes and become acidified. The ability of Mtb to control and subvert the fusion between phagosomes and lysosomes plays a key role in the pathogenesis of tuberculosis. Therefore, understanding how pathogens interact with the endolysosomal network and cope with intracellular acidification is important to better understand the disease. Here, we describe in detail the use of fluorescence microscopy‐based approaches to investigate Mtb responses to acidic environments in cellulo. We report high‐content imaging modalities to probe Mtb sensing of external pH or visualise in real‐time Mtb intrabacterial pH within infected human macrophages. We discuss various methodologies with step‐by‐step analyses that enable robust image‐based quantifications. Finally, we highlight the advantages and limitations of these different approaches and discuss potential alternatives that can be applied to further investigate Mtb–host cell interactions. These methods can be adapted to study host–pathogen interactions in different biological systems and experimental settings. Altogether, these approaches represent a valuable tool to further broaden our understanding of the cellular and molecular mechanisms underlying intracellular pathogen survival.
    Keywords bacterial reporters ; endolysosomes ; high‐content fluorescence microscopy ; human‐induced pluripotent stem cell‐derived macrophages ; pH sensing and homeostasis ; Tuberculosis ; Biology (General) ; QH301-705.5
    Subject code 572
    Language English
    Publishing date 2023-07-01T00:00:00Z
    Publisher Wiley
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  2. Article ; Online: Lysosomal damage drives mitochondrial proteome remodelling and reprograms macrophage immunometabolism

    Claudio Bussi / Tiaan Heunis / Enrica Pellegrino / Elliott M. Bernard / Nourdine Bah / Mariana Silva Dos Santos / Pierre Santucci / Beren Aylan / Angela Rodgers / Antony Fearns / Julia Mitschke / Christopher Moore / James I. MacRae / Maria Greco / Thomas Reinheckel / Matthias Trost / Maximiliano G. Gutierrez

    Nature Communications, Vol 13, Iss 1, Pp 1-

    2022  Volume 22

    Abstract: Extensive lysosomal damage can result in cell death but how limited protease leakage affects cytoplasmic organelles in viable cells is not well understood. Here the authors show that limited lysosomal damage leads to changes in the mitochondrial proteome ...

    Abstract Extensive lysosomal damage can result in cell death but how limited protease leakage affects cytoplasmic organelles in viable cells is not well understood. Here the authors show that limited lysosomal damage leads to changes in the mitochondrial proteome and the modulation of macrophage immunometabolism.
    Keywords Science ; Q
    Language English
    Publishing date 2022-11-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: A terpene nucleoside from M. tuberculosis induces lysosomal lipid storage in foamy macrophages

    Melissa Bedard / Sanne van der Niet / Elliott M. Bernard / Gregory Babunovic / Tan-Yun Cheng / Beren Aylan / Anita E. Grootemaat / Sahadevan Raman / Laure Botella / Eri Ishikawa / Mary P. O’Sullivan / Seónadh O’Leary / Jacob A. Mayfield / Jeffrey Buter / Adriaan J. Minnaard / Sarah M. Fortune / Leon O. Murphy / Daniel S. Ory / Joseph Keane /
    Sho Yamasaki / Maximiliano G. Gutierrez / Nicole van der Wel / D. Branch Moody

    The Journal of Clinical Investigation, Vol 133, Iss

    2023  Volume 6

    Abstract: Induction of lipid-laden foamy macrophages is a cellular hallmark of tuberculosis (TB) disease, which involves the transformation of infected phagolysosomes from a site of killing into a nutrient-rich replicative niche. Here, we show that a terpenyl ... ...

    Abstract Induction of lipid-laden foamy macrophages is a cellular hallmark of tuberculosis (TB) disease, which involves the transformation of infected phagolysosomes from a site of killing into a nutrient-rich replicative niche. Here, we show that a terpenyl nucleoside shed from Mycobacterium tuberculosis, 1-tuberculosinyladenosine (1-TbAd), caused lysosomal maturation arrest and autophagy blockade, leading to lipid storage in M1 macrophages. Pure 1-TbAd, or infection with terpenyl nucleoside–producing M. tuberculosis, caused intralysosomal and peribacillary lipid storage patterns that matched both the molecules and subcellular locations known in foamy macrophages. Lipidomics showed that 1-TbAd induced storage of triacylglycerides and cholesterylesters and that 1-TbAd increased M. tuberculosis growth under conditions of restricted lipid access in macrophages. Furthermore, lipidomics identified 1-TbAd–induced lipid substrates that define Gaucher’s disease, Wolman’s disease, and other inborn lysosomal storage diseases. These data identify genetic and molecular causes of M. tuberculosis–induced lysosomal failure, leading to successful testing of an agonist of TRPML1 calcium channels that reverses lipid storage in cells. These data establish the host-directed cellular functions of an orphan effector molecule that promotes survival in macrophages, providing both an upstream cause and detailed picture of lysosome failure in foamy macrophages.
    Keywords Infectious disease ; Microbiology ; Medicine ; R
    Subject code 572
    Language English
    Publishing date 2023-03-01T00:00:00Z
    Publisher American Society for Clinical Investigation
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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