pseudotuberculosis [23] and Y. enterocolitica [24]. Therefore, data presented in Y. pestis biovar Microtus can be generally applied to the above three pathogenic yersiniae. A single CRP-dependent promoter transcribed for the sycO-ypkA-yopJ operon, but two CRP-binding sites (site 1 and site 2) were detected within its promoter region. A CRP box-like sequence (TAGATATCACC) was found in site 1 rather than in site 2. It was speculated that site 2 was a non-specific or non-functional CRP-binding site. Further reporter fusion experiments and/or in vitro transcription assays, using the sycO promoter-proximate regions with different mutations/deletions

within sites 1 and 2, should be done to elucidate the roles of site 1 and site 2 in CRP-mediated regulation of sycO-ypkA-yopJ. CRP and T3SS The crp mutation caused a reduced secretion of YOP proteins in both Y. enterocolitica [5] and Y. pestis [9] grown under calcium-depleted conditions. learn more This indicated that CRP is a positive Adriamycin chemical structure regulator for the YOP secretion by Y. pestis. It is well known that the YOP secretion phenotype is only observable under calcium depleted conditions. Herein, the direct and

negative regulation of sycO-ypkA-yopJ by CRP was observed at transcriptional level under calcium-rich conditions. How CRP controls T3SS is essentially unclear yet. It needs to investigate the mRNA/protein pools of T3SS that are regulated by CRP under calcium depleted or rich conditions and upon cell contact, and to answer whether CRP has a regulatory action on T3SS in general or on SycO, YpkA and YopJ specifically. CRP and virulence

The crp deletion attenuated Y. pestis much more greatly by subcutaneous route of infection in relative to an intravenous inoculation, and a reduced in vivo growth phenotype of the crp mutant was observed [4]. CRP seemed more important for the infection at the subcutaneous site and in the lymph other than the later systemic infection, while the reduced in vivo growth of the crp mutant should contribute to its attenuation by intravenous infection. The crp disruption led to a great defect of pla expression [4]. Since Pla specifically Temsirolimus solubility dmso promoted Y. pestis dissemination from peripheral infection routes, the defect of pla expression in the crp mutant will contribute to the huge loss of virulence of this mutant strain after subcutaneous infection. Expression of Pla, Pst, F1 antigen and T3SS are dependent on CRP, and this regulator appears to control a wide set of virulence-related factors in Y. pestis [4]. All the above CRP-regulated genes are harbored in plasmids that are required through horizontal gene transfer. Either the CRP protein itself or the mechanism of CRP-promoter DNA association is extremely conserved between E. coli and Y. pestis. Therefore, the above laterally acquired genes have evolved to integrate themselves into the ‘ancestral’ CRP regulatory cascade.