All of the MboI sensitive strains had hrgA, not hpyIIIR. The presence of hrgA appears to have predictive

value for virulence in cagA-positive strains from Asia, because in Asia, hrgA was more prevalent among gastric cancer patients than among non-cancer patients.46 Another example of pathogenicity correlated with R-M systems is the R-M methylase HpyIM, which is growth-phase regulated in vitro, and whose expression varies dramatically in vivo.47 Moreover, Bjorkholm et al. showed that R-M systems regulate the in vivo expression of microbial genes that affect host responses to H. pylori infection.48 Neither gene, hpyIIIR or hrgA, is essential, but because no strain that lacks or contains both genes NVP-AUY922 ic50 has been identified thus far, it is hypothesized that there is selection for the presence of either gene. By homologous recombination involving flanking sequences, hrgA and hpyIIIR could be replaced by one another in the hpyIII locus, and there was simultaneous replacement of several flanking genes.21 We reconstructed the evolutionary history of Ulixertinib molecular weight the locus containing either hpyIIIR or hrgA (Fig. 2). Type II restriction and modification genes

are paired, and whereas cells with a modification gene can survive without the cognate restriction gene, cells with a functional restriction gene cannot survive without an intact and active modification gene. Thus, it must be assumed that hpyIIIR and hpyIIIM were once present together in the H. pylori chromosome and that in certain strains hpyIIIR was subsequently replaced by hrgA. Therefore, in the most recent common ancestor of the H. pylori strains studied, an hpyIII R-M system likely was introduced

downstream of fabD and 上海皓元医药股份有限公司 transfer RNA (tRNA) Ser3, resulting in a type A strain. Insertion of foreign DNA often occurs at tRNA loci.49 Strains with the insertion appear to have completely replaced the bacterial population lacking this R-M system, because no strains could be detected without the insertion. We interpret the presence of hrgA upstream of hpyIIIM (type B strains) as the result of horizontal introduction in one or more ancestral strains, whereby hpyIIIR was replaced, after which hrgA spread by horizontal transformation in the H. pylori population.21 These findings, combined with the hpyIM/iceA2 locus discovered previously, suggest that the two most strongly conserved methylase genes of H. pylori, hpyIIIM and hpyIM, are both preceded by alternative genes that compete for presence at their loci, and furthermore, these genes may relate to H. pylori pathogenicity. All H. pylori strains possess their own unique complement of active R-M systems. Bacteria use R-M systems as a defense against invasion by foreign DNA, but most of the other roles of H. pylori R-M systems are not clear.