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The role of the granuloma in expansion and dissemination of early tuberculous infection.

TitleThe role of the granuloma in expansion and dissemination of early tuberculous infection.
Publication TypeJournal Article
Year of Publication2009
AuthorsJ Davis, M, Ramakrishnan, L
JournalCell
Volume136
Issue1
Pagination37-49
Date Published2009 Jan 9
ISSN1097-4172
KeywordsAnimals, Apoptosis, Chemotaxis, Granuloma, Host-Pathogen Interactions, Humans, Macrophages, Mycobacterium Infections, Mycobacterium Infections, Nontuberculous, Mycobacterium marinum, Mycobacterium tuberculosis, Phagocytosis, Tuberculosis, Virulence Factors, Zebrafish
Abstract

Granulomas, organized aggregates of immune cells, form in response to persistent stimuli and are hallmarks of tuberculosis. Tuberculous granulomas have long been considered host-protective structures formed to contain infection. However, work in zebrafish infected with Mycobacterium marinum suggests that granulomas contribute to early bacterial growth. Here we use quantitative intravital microscopy to reveal distinct steps of granuloma formation and assess their consequence for infection. Intracellular mycobacteria use the ESX-1/RD1 virulence locus to induce recruitment of new macrophages to, and their rapid movement within, nascent granulomas. This motility enables multiple arriving macrophages to efficiently find and phagocytose infected macrophages undergoing apoptosis, leading to rapid, iterative expansion of infected macrophages and thereby bacterial numbers. The primary granuloma then seeds secondary granulomas via egress of infected macrophages. Our direct observations provide insight into how pathogenic mycobacteria exploit the granuloma during the innate immune phase for local expansion and systemic dissemination.

DOI10.1016/j.cell.2008.11.014
Alternate JournalCell
PubMed ID19135887
PubMed Central IDPMC3134310
Grant ListR01 AI036396-19 / AI / NIAID NIH HHS / United States
R01 AI054503-09 / AI / NIAID NIH HHS / United States
R01 AI36396 / AI / NIAID NIH HHS / United States
R01 AI54503 / AI / NIAID NIH HHS / United States