The traC-dsbC junction (PCR G) of the CMY

LDC000067 solubility dmso island (Figure 4) was found in all the plasmids mentioned above and in the recently described integrating conjugative element ICEPmiJpn1 Selleckchem CBL0137 of Proteus mirabilis [GenBank:AB525688]. The finding that traC-dsbC is present in pIP1202, pYR1, pP91278, pP99-018, pMRV150 and pRA1, which lack the CMY island, revealed that this gene cluster is part of a conserved core region of these closely related IncA/C plasmids. However, this region did not match with any other plasmids in the database, and it was not amplified in the CMY- plasmids of ST213 (Figure 2). Therefore, to assess the insertion of the right CMY junction, a second marker was used: PCR D spanning from sugE to the hypothetical protein 0093 (Figure 4). The complete traVA-tnpA right junction (PCR A and B) of the CMY island

was identical to that of the E. coli and Newport plasmids, but only traVA (PCR B) was present in the other CMY- IncA/C reference plasmids. This result indicates that this marker is the left CMY island junction. Interestingly, the ST213 CMY- plasmids did not amplify the traVA region, indicating that the region around the CMY island is not present in these plasmids. R-7 and R-8 were found to be present in all the IncA/C reference plasmids, with the only exception being peH4H, which lacks R-7. The mer region was detected only in the E. coli pAR060302 and Newport plasmids; however, it was found to be related to other mer operons present in several selleck chemicals llc plasmids such as pRMH760 (Klebsiella pneumoniae). Characterization of the CMY region When we started this Mannose-binding protein-associated serine protease study, the only completely sequenced plasmid carrying bla CMY-2 was that of the Newport strain [GenBank:NC_009140] [8]. PCR mapping experiments were performed to compare the CMY region of our

Typhimurium isolates with that of Newport pSN254 (Figure 4 and Additional file 1, Table S1). To determine if the bla CMY-2 gene is present as an inverted repeat element as in pSN245, we performed PCR H and I, which we expected to produce bands of around 3.2 and 2.3 kb, respectively, based on the in silico prediction. The Newport strain SN11 was used as a positive control for these amplifications. No bands were obtained with our Typhimurium isolates, consistent with the notion that our isolates possess only a single bla CMY-2 gene. We designed a set of primer pairs to amplify overlapping fragments covering the complete CMY region and to obtain the nucleotide sequence of one of our isolates, YUHS 07-18, which is the most recent strain in our collection and which displays Xba I and Pst I fingerprints prevalent in the ST213 population.