Francisella tularensis is a highly virulent gram-negative intracellular bacterium that causes the zoonotic disease tularemia. Essential for its virulence is the ability to multiply within host cells, in particular monocytic cells. The bacterium has developed intricate means to subvert host immune mechanisms and thereby facilitate its intracellular survival by preventing phagolysosomal fusion followed by escape into the cytosol, where it multiplies. Moreover, it targets and manipulates numerous host cell signaling pathways, thereby ameliorating the otherwise bactericidal capacity. Many of the underlying molecular mechanisms still remain unknown but key elements, directly or indirectly responsible for many of the aforementioned mechanisms, rely on the expression of proteins encoded by the Francisella pathogenicity island (FPI), suggested to constitute a type VI secretion system. We here describe the current knowledge regarding the components of the FPI and the roles that have been ascribed to them.
Francisella tularensis harbors genes with similarity to genes encoding components of a type VI secretion system (T6SS) recently identified in several gram-negative bacteria. These genes include iglA and iglB encoding IglA and IglB, homologues of which are conserved in most T6SSs. We used a yeast two-hybrid system to study the interaction of the Igl proteins of F. tularensis LVS. We identified a region of IglA, encompassing residues 33 to 132, necessary for efficient binding to IglB, as well as for IglAB protein stability and intramacrophage growth. In particular, residues 103 to 122, overlapping a highly conserved ␣-helix, played an absolutely essential role. Point mutations within this domain caused modest defects in IglA-IglB binding in the yeast Saccharomyces cerevisiae but markedly impaired intramacrophage replication and phagosomal escape, resulting in severe attenuation of LVS in mice. Thus, IglA-IglB complex formation is clearly crucial for Francisella pathogenicity. This interaction may be universal to type VI secretion, since IglAB homologues of Yersinia pseudotuberculosis, Pseudomonas aeruginosa, Vibrio cholerae, Salmonella enterica serovar Typhimurium, and Escherichia coli were also shown to interact in yeast, and the interaction was dependent on preservation of the same ␣-helix. Heterologous interactions between nonnative IglAB proteins further supported the notion of a conserved binding site. Thus, IglA-IglB complex formation is clearly crucial for Francisella pathogenicity, and the same interaction is conserved in other human pathogens.Francisella tularensis is a gram-negative facultative intracellular bacterial pathogen capable of causing a severe disease, tularemia, in many mammalian species (22). Human infections are caused mainly by two subspecies, the more virulent organism F. tularensis subsp. tularensis (type A) found predominantly in North America and the less virulent organism F. tularensis subsp. holarctica (type B) found in North America, Europe, and Asia (34, 43). While little is known about the molecular mechanisms of Francisella pathogenesis, a key strategy appears to be its ability to survive and replicate within macrophages (42,46). Francisella-containing vacuoles have been reported to evade phagosome-lysosome fusion, followed by bacterial escape into the cytoplasm (8, 16). Several genes necessary for intramacrophage survival, as well as growth within the amoeba Acanthamoeba castellanii, a putative natural reservoir of F. tularensis, have been identified. Many of these genes, including the members of the iglABCD operon, are located in a 34-kb Francisella pathogenicity island (FPI) (reviewed in reference 31), and they are regulated by the global regulator MglA (4, 23). Almost all of the proteins of the FPI are essentially conserved across subspecies. Studies have shown that IglC and IglD are required for F. tularensis to replicate within the cytosol of macrophages (24, 37). While IglC was shown to be essential for bacterial escape from the phagosome into the cytoplasm (24, 38), the r...
The most recently discovered secretion pathway in Gram-negative bacteria, the type VI secretion system (T6SS), is present in many species and is considered important for the survival of non-O1 non-O139 Vibrio cholerae in aquatic environments. Until now, it was not known whether there is a functionally active T6SS in wild-type V. cholerae O1 strains, the cause of cholera disease in humans. Here, we demonstrate the presence of a functionally active T6SS in wild-type V. cholerae O1 strains, as evidenced by the secretion of the T6SS substrate Hcp, which required several gene products encoded within the putative vas gene cluster. Our analyses showed that the T6SS of wild-type V. cholerae O1 strain A1552 was functionally activated when the bacteria were grown under high-osmolarity conditions. The T6SS was also active when the bacteria were grown under low temperature (23°C), suggesting that the system may be important for the survival of the bacterium in the environment. A test of the interbacterial virulence of V. cholerae strain A1552 against an Escherichia coli K-12 strain showed that it was strongly enhanced under high osmolarity and that it depended on the hcp genes. Interestingly, we found that the newly recognized osmoregulatory protein OscR plays a role in the regulation of T6SS gene expression and secretion of Hcp from V. cholerae O1 strains.T he severe diarrheal disease cholera is caused by Vibrio cholerae bacteria of serogroups O1 and O139 that carry the ctxAB and tcp genes, encoding cholera toxin and toxin-coregulated pili, respectively (22). These bacteria have been the cause of seven pandemics since 1817 (12,38,42). Non-O1, non-O139 V. cholerae (NOVC) constitutes a large group of V. cholerae bacteria found as environmental isolates. Typically, they lack the ctx and tcp genes and do not cause cholera but have recently been emerging as potential extraintestinal pathogens. NOVC isolates possess a protein secretion system, the type VI secretion system (T6SS), which appears to play an important role in the bacterium's environmental survival by promoting killing of predator organisms, like amoebas (37).The T6SS is present in several Gram-negative bacterial species ranging from environmental to pathogenic bacteria and is involved in a variety of cellular processes (3-5, 10, 13, 43). It can secrete certain effector proteins into the extracellular milieu and/or translocate them into the eukaryotic host cell cytoplasm (31,32,36,37). Intriguingly, a role for T6SS in interbacterial competition was recently described in Pseudomonas aeruginosa, Burkholderia thailandensis, and a NOVC isolate (19,24,44). Although little is known about the contribution of the T6SS to virulence in general, expression of T6SS loci is precisely modulated to adapt T6SS production to the specific needs of and conditions encountered by individual bacteria (3, 4). Two T6SS-associated proteins, hemolysin-coregulated protein (Hcp) and valine-glycine repeat protein G (VgrG), have recently been characterized in NOVC isolates and in P. aeruginosa (1...
The Gram-negative bacterium Francisella tularensis is the causative agent of tularemia, a disease intimately associated with the multiplication of the bacterium within host macrophages. This in turn requires the expression of Francisella pathogenicity island (FPI) genes, believed to encode a type VI secretion system. While the exact functions of many of the components have yet to be revealed, some have been found to contribute to the ability of Francisella to cause systemic infection in mice as well as to prevent phagolysosomal fusion and facilitate escape into the host cytosol. Upon reaching this compartment, the bacterium rapidly multiplies, inhibits activation of the inflammasome, and ultimately causes apoptosis of the host cell. In this study, we analyzed the contribution of the FPI-encoded proteins IglG, IglI, and PdpE to the aforementioned processes in F. tularensis LVS. The ⌬pdpE mutant behaved similarly to the parental strain in all investigated assays. In contrast, ⌬iglG and ⌬iglI mutants, although they were efficiently replicating in J774A.1 cells, both exhibited delayed phagosomal escape, conferred a delayed activation of the inflammasome, and exhibited reduced cytopathogenicity as well as marked attenuation in the mouse model. Thus, IglG and IglI play key roles for modulation of the intracellular host response and also for the virulence of F. tularensis.
Gram-negative bacteria have evolved sophisticated secretion machineries specialized for the secretion of macromolecules important for their life cycles. The Type VI secretion system (T6SS) is the most widely spread bacterial secretion machinery and is encoded by large, variable gene clusters, often found to be essential for virulence. The latter is true for the atypical T6SS encoded by the Francisella pathogenicity island (FPI) of the highly pathogenic, intracellular bacterium Francisella tularensis. We here undertook a comprehensive analysis of the intramacrophage secretion of the 17 FPI proteins of the live vaccine strain, LVS, of F. tularensis. All were expressed as fusions to the TEM β-lactamase and cleavage of the fluorescent substrate CCF2-AM, a direct consequence of the delivery of the proteins into the macrophage cytosol, was followed over time. The FPI proteins IglE, IglC, VgrG, IglI, PdpE, PdpA, IglJ and IglF were all secreted, which was dependent on the core components DotU, VgrG, and IglC, as well as IglG. In contrast, the method was not directly applicable on F. novicida U112, since it showed very intense native β-lactamase secretion due to FTN_1072. Its role was proven by ectopic expression in trans in LVS. We did not observe secretion of any of the LVS substrates VgrG, IglJ, IglF or IglI, when tested in a FTN_1072 deficient strain of F. novicida, whereas IglE, IglC, PdpA and even more so PdpE were all secreted. This suggests that there may be fundamental differences in the T6S mechanism among the Francisella subspecies. The findings further corroborate the unusual nature of the T6SS of F. tularensis since almost all of the identified substrates are unique to the species.
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