Cell biology and molecular ecology of Francisella tularensis
Article first published online: 27 OCT 2009
© 2009 Blackwell Publishing Ltd
Volume 12, Issue 2, pages 129–139, February 2010
How to Cite
Santic, M., Al-Khodor, S. and Abu Kwaik, Y. (2010), Cell biology and molecular ecology of Francisella tularensis. Cellular Microbiology, 12: 129–139. doi: 10.1111/j.1462-5822.2009.01400.x
- Issue published online: 12 JAN 2010
- Article first published online: 27 OCT 2009
- Received 24 August, 2009; revised 9 October, 2009; accepted 12 October, 2009.
Francisella tularensis is a highly infectious intracellular bacterium that causes the fulminating disease tularemia, which can be transmitted between mammals by arthorpod vectors. Genomic studies have shown that the F. tularensis has been undergoing genomic decay with the most virulent strains having the lowest number of functional genes. Entry of F. tularensis into macrophages is mediated by looping phagocytosis and is associated with signalling through Syk tyrosine kinase. Within macrophages and arthropod-derived cells, the Francisella-containing phagosome matures transiently into an acidified late endosome-like phagosome with limited fusion to lysosomes followed by rapid bacterial escape into the cytosol within 30–60 min, and bacterial proliferation within the cytosol. The Francisella pathogenicity island, which potentially encodes a putative type VI secretion system, is essential for phagosome biogenesis and bacterial escape into the cytosol within macrophages and arthropod-derived cells. Initial sensing of F. tularensis in the cytosol triggers IRF-3-dependent IFN-β secretion, type I IFNR-dependent signalling, activation of the inflammasome mediated by caspase-1, and a pro-inflammatory response, which is suppressed by triggering of SHIP. The past few years have witnessed a quantum leap in our understanding of various aspects of this organism and this review will discuss these remarkable advances.