A requirement for septins and the autophagy receptor p62 in the proliferation of intracellular Shigella

التفاصيل البيبلوغرافية
العنوان: A requirement for septins and the autophagy receptor p62 in the proliferation of intracellular Shigella
المؤلفون: Lobato‐Márquez, Damián, Krokowski, Sina, Sirianni, Andrea, Larrouy‐Maumus, Gerald, Mostowy, Serge
المساهمون: Wellcome Trust, Lister Institute of Preventive Medicine, Commission of the European Communities, Medical Research Council (MRC)
المصدر: Cytoskeleton (Hoboken, N.j.)
Cytoskeleton
مصطلحات موضوعية: autophagy, COMPLETION, Short Report, EFFECTOR, macromolecular substances, GLYCOLYTIC-ENZYMES, 0601 Biochemistry and Cell Biology, ACTIN, CARBON METABOLISM, Humans, septin, Cell Proliferation, Science & Technology, fungi, cytoskeleton, 1103 Clinical Sciences, Cell Biology, DEGRADATION, TRANSPORT, MICROTUBULES, Shigella, biological phenomena, cell phenomena, and immunity, PHOSPHOFRUCTOKINASE, ALDOLASE, Life Sciences & Biomedicine, metabolism, Septins, HeLa Cells
الوصف: Shigella flexneri, a Gram‐negative enteroinvasive pathogen, causes inflammatory destruction of the human intestinal epithelium. During infection of epithelial cells, Shigella escape from the phagosome to the cytosol, where they reroute host cell glycolysis to obtain nutrients for proliferation. Septins, a poorly understood component of the cytoskeleton, can entrap cytosolic Shigella targeted to autophagy in cage‐like structures to restrict bacterial proliferation. Although bacterial entrapment by septin caging has been the subject of intense investigation, the role of septins and the autophagy machinery in the proliferation of noncaged Shigella is mostly unknown. Here, we found that intracellular Shigella fail to efficiently proliferate in SEPT2‐, SEPT7‐, or p62/SQSTM1‐depleted cells. Consistent with a failure to proliferate, single cell analysis of bacteria not entrapped in septin cages showed that the number of metabolically active Shigella in septin‐ or p62‐depleted cells is reduced. Targeted metabolomic analysis revealed that host cell glycolysis is dysregulated in septin‐depleted cells, suggesting a key role for septins in modulation of glycolysis. Together, these results suggest that septins and the autophagy machinery may regulate metabolic pathways that promote the proliferation of intracellular Shigella not entrapped in septin cages.
وصف الملف: application/pdf
اللغة: English
تدمد: 1949-3592
1949-3584
DOI: 10.1002/cm.21453
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ec6a8be78fc4106c6625401ea7117e45Test
حقوق: OPEN
رقم الانضمام: edsair.pmid.dedup....ec6a8be78fc4106c6625401ea7117e45
قاعدة البيانات: OpenAIRE
الوصف
تدمد:19493592
19493584
DOI:10.1002/cm.21453