Abstract
Annual Review of Microbiology
Vol. 60:
167-185
(Volume publication date October 2006)
(doi:10.1146/annurev.micro.60.080805.142126)
First published online as a Review in Advance on May 10, 2006Francisella tularensis: Taxonomy, Genetics, and Immunopathogenesis of a Potential Agent of Biowarfare Molly K. McLendon,1,2 Michael A. Apicella,1,2 and Lee-Ann H. Allen1,2,31Inflammation Program and the Departments of 2Microbiology and 3Internal Medicine, University of Iowa and the VA Medical Center, Iowa City, Iowa 52242; email: molly-mclendon@uiowa.edu, michael-apicella@uiowa.edu, lee-ann-allen@uiowa.edu Abstract Tularemia is a zoonosis of humans caused by infection with the facultative intracellular bacterium Francisella tularensis. Interest in F. tularensis has increased markedly in the past few years because of its potential use as an agent of bioterrorism. Five subspecies of this organism are found in the Northern hemisphere, but only F. tularensis subsp. tularensis and subsp. holarctica cause disease in humans. This review summarizes what is known about the pathogenesis of tularemia with a focus on bacterial surface components such as lipopolysaccharide and capsule as well as information obtained from the F. tularensis subsp. tularensis SCHU S4 genome. In particular, the mechanisms of action of recently identified virulence factors are discussed in the context of bacterial replication in macrophages and manipulation of the host inflammatory response. Throughout this report, shared and unique features of F. tularensis subsp. tularensis, subsp. holarctica, and subsp. novicida are discussed. Acronyms CFU: colony-forming unit D-GalNacAN: 2-acetamido-2-deoxy-2-galacturonamide Igl: intracellular growth locus iNOS: inducible nitric oxide synthase MDM: human monocyte-derived macrophage Mgl: macrophage growth locus MOI: multiplicity of infection PMN: polymorphonuclear leukocyte, neutrophil SCHU S4: genome strain of F. tularensis subsp. tularensis TLR: Toll-like receptor Terms and Definitions Capsule: a sugar-rich structure on the surface of some bacteria that can inhibit phagocytosis or prevent killing by serum complement Francisella pathogenicity island (FPI): a distinct region of the genome containing genes that encode virulence factors Lipopolysaccharide (LPS, or endotoxin): the major surface component of gram-negative bacteria Live vaccine strain (LVS): an attenuated strain of F. tularensis subsp. holarctica previously used as a live vaccine Opsonize: binding of opsonins (serum complement factors and/or antibodies) to the surface of microbes to facilitate phagocytosis Pathogen: a microorganism that causes disease Phagocytosis: a specialized form of endocytosis that allows macrophages and neutrophils to engulf microorganisms Virulence factor: a component of a microorganism that is important for its ability to damage a host and cause disease Most recent citing papers (via CrossRef)Intracellular pathogenic bacteria and fungi — a case of convergent evolution? Nature Reviews Microbiology (2009) Effective host response to
Francisella tularensis
requires functional mast cells Future Microbiology 3(5):503-506 (2008) Generation and Characterization of an Attenuated Mutant in a Response Regulator Gene of
Francisella tularensis
Live Vaccine Strain (LVS) DNA and Cell Biology 27(7):387-403 (2008) Characterization of the Francisella tularensis subsp. novicida type IV pilus Microbiology 154(7):2139-2150 (2008) Drosophila melanogaster as a model for elucidating the pathogenicity of Francisella tularensis Cellular Microbiology 10(6):1327-1338 (2008)
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