Lysosome Fusion Maintains Phagosome Integrity during Fungal Infection.


Journal

Cell host & microbe
ISSN: 1934-6069
Titre abrégé: Cell Host Microbe
Pays: United States
ID NLM: 101302316

Informations de publication

Date de publication:
09 12 2020
Historique:
received: 24 09 2019
revised: 10 08 2020
accepted: 02 09 2020
pubmed: 7 10 2020
medline: 20 7 2021
entrez: 6 10 2020
Statut: ppublish

Résumé

Phagosomes must maintain membrane integrity to exert their microbicidal function. Some microorganisms, however, survive and grow within phagosomes. In such instances, phagosomes must expand to avoid rupture and microbial escape. We studied whether phagosomes regulate their size to preserve integrity during infection with the fungal pathogen Candida albicans. Phagosomes release calcium as C. albicans hyphae elongate, inducing lysosome recruitment and insertion, thereby increasing the phagosomal surface area. As hyphae grow, the expanding phagosome consumes the majority of free lysosomes. Simultaneously, lysosome biosynthesis is stimulated by activation of TFEB, a transcriptional regulator of lysosomal biogenesis. Preventing lysosomal insertion causes phagosomal rupture, NLRP3 inflammasome activation, IL-1β secretion and host-cell death. Whole-genome transcriptomic analysis demonstrate that stress responses elicited in C. albicans upon engulfment are reversed if phagosome expansion is prevented. Our findings reveal a mechanism whereby phagosomes maintain integrity while expanding, ensuring that growing pathogens remain entrapped within this microbicidal compartment.

Identifiants

pubmed: 33022213
pii: S1931-3128(20)30505-9
doi: 10.1016/j.chom.2020.09.004
pii:
doi:

Substances chimiques

Basic Helix-Loop-Helix Leucine Zipper Transcription Factors 0
IL1B protein, mouse 0
Inflammasomes 0
Interleukin-1beta 0
NLR Family, Pyrin Domain-Containing 3 Protein 0
Nlrp3 protein, mouse 0
Tcfeb protein, mouse 0
Calcium SY7Q814VUP

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

798-812.e6

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Interests The authors declare no competing interests.

Auteurs

Johannes Westman (J)

Program in Cell Biology, Peter Gilgan Centre for Research and Learning, the Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.

Glenn F W Walpole (GFW)

Program in Cell Biology, Peter Gilgan Centre for Research and Learning, the Hospital for Sick Children, Toronto, ON M5G 0A4, Canada; Department of Biochemistry, University of Toronto, Toronto, ON M5S 1A8, Canada.

Lydia Kasper (L)

Department Microbial Pathogenicity Mechanisms, Hans Knoell Institute, 07745 Jena, Germany.

Bessie Y Xue (BY)

Department of Biochemistry, University of Toronto, Toronto, ON M5S 1A8, Canada.

Osama Elshafee (O)

Department Microbial Pathogenicity Mechanisms, Hans Knoell Institute, 07745 Jena, Germany.

Bernhard Hube (B)

Department Microbial Pathogenicity Mechanisms, Hans Knoell Institute, 07745 Jena, Germany; Institute of Microbiology, Faculty of Biological Sciences, Friedrich Schiller University, 07743 Jena, Germany.

Sergio Grinstein (S)

Program in Cell Biology, Peter Gilgan Centre for Research and Learning, the Hospital for Sick Children, Toronto, ON M5G 0A4, Canada; Department of Biochemistry, University of Toronto, Toronto, ON M5S 1A8, Canada; Keenan Research Centre of the Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, ON M5C 1N8, Canada. Electronic address: sergio.grinstein@sickkids.ca.

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Classifications MeSH