Of particular note is the production of IgG2a antibodies which are known to play an important role in the rapid clearance of Salmonellae through complement activation and the promotion of phagocytosis by macrophages Temozolomide nmr [31], [32] and [33]. Immunisation with both SL3261 and SL1344 atp caused splenomegaly as evidenced by increased spleen weights compared to unimmunised controls. However, the increase in spleen weight was significantly reduced in mice immunised with SL1344 atp versus SL3261. This was further examined via histopathological analysis of H&E-stained spleen sections. Consistent with the differences in spleen weights

following immunisation, SL1344 atp immunised mice showed reduced inflammation and reactogenicity compared to mice immunised with SL3261. This reduction in splenomegaly following SL1344 atp immunisation may be a potential benefit of immunisation with SL1344 atp. The ability to infect host macrophages and survive within them is a key process in Salmonella infection and mutants impaired in this property are typically attenuated in the mouse model [34]. The ability of SL1344 atp to infect and grow within

RAW cells was not impaired compared to SL1344. The attenuated growth in vivo of SL1344 atp is therefore not due to an inherent defect in the infection of and growth within host macrophages. This agrees with previous data showing ABT-199 price various Salmonellaatp mutants had no significant deficiency in intracellular survival [29] and [30]. However, this finding does not exclude the possibility of a defect in this property being manifested specifically in vivo where conditions are likely to be very different from those in vitro. Understanding the components of the immune system required to control infection and generate protection following immunisation with live attenuated vaccine strains is of interest as it may offer the potential to enhance immunogenicity and reduce reactogenicity.

It also has significance for the use of these strains in immunocompromised hosts. Therefore, IFNγR1−/− and gp91 phox −/− counterparts along with their wild type C57BL/6 mice were infected Urease with SL1344 atp. These gene knock-out mice are of particular interest as they represent immune defects found in humans. Genetic deficiencies in the NADPH oxidase system (phox) manifest as chronic granulamatous disease [35], while deficiencies in IFNγ activity lead to increased susceptibility to bacterial and fungal infections, particularly with mycobacteria [36] and [37]. Both NADPH oxidase and IFNγ were required to control SL1344 atp infection with bacterial counts in livers and spleens significantly higher in the absence of these host defence mechanisms. A similar effect was seen in mice infected with SL3261. These data are perhaps not surprising given the central role of both NADPH oxidase and IFNγ in the control of S. Typhimurium infection in mice [38], [39] and [40].