Legionnaires' disease and its agent Legionella pneumophila (CROSBI ID 34435)
Prilog u knjizi | izvorni znanstveni rad
Podaci o odgovornosti
Biter, Dina M. ; Šantić, Marina ; Abu Kwaik, Yousef ; Molmeret, Maelle
engleski
Legionnaires' disease and its agent Legionella pneumophila
Legionella pneumophila, the agent responsible for Legionnaire's disease, is a facultative intracellular pathogen that can replicate within protozoa and macrophages. Protozoa are considered to play a central role in the pathogenesis and ecology of L. pneumophila. In humans, L. pneumophila reaches the lungs, where it is ingested by alveolar macrophages. Unlike phagosomes containing inert particles or avirulent bacteria, the L. pneumophila containing vacuoles avoid fusion with lysosomes, recruiting rough endoplasmic reticulum and mitochondria. The formation of this specialized vacuole is directed by the type IV secretion system encoded by the dot/icm genes in mammalian and protozoan cells. Killing of mammalian cells by L. pneumophila has been proposed to occur through induction of apoptosis during the early stages of the infection. A rapid induction of necrosis by L. pneumophila also occurs upon entry into the post-exponential phase of growth within both macrophages and protozoa, when the bacteria become cytotoxic. Before the lysis of the mammalian or protozoan plasma membrane, the bacteria egress into the cytoplasm. In vivo, clearence of Legionella from the lungs depends on the host production of IFN-gamma in A/J mice, while in BALB/c mice IFN-gamma is not produced. Intracellular replication of L. pneumophila is inhibited in IFN-gamma-activated mouse and human primary macrophages. Both antigen-specific humoral and cell-mediated immune responses are induced during Legionella infection. Although Legionella-specific antibodies are produced during human or murine infecion, acquired cell-mediated immune response is belived to play a stronger role in Legionella clearence. Both macrophages and DCs are able to present microbial antigens on major histocompatibility class I and class II molecules, which stimulate antigen-specific T-cell response. Identification of antigens and determination of vesicular trafficking mechanisms involved in processing and presentation remain to be understood in greated detail.
Legionella, pneumonia, pathogenesis
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
Podaci o prilogu
111-138-x.
objavljeno
Podaci o knjizi
Community-Acquired Pneumonia
R. Marre ; N. Suttorp ; T. Welte
Basel : Boston : Berlin: Birkhäuser
2007.
978-3-7643-7562-1