Figure 1 Electrophoretic plasmid profiles of representative strains of the Typhimurium ST213 genotype. The diversity of plasmid sizes exhibited by strains carrying or lacking bla CMY-2 is shown. Lanes 1 and 9 show the E. coli reference plasmid pAR060302 [6], which was used as a selleck compound 160-kb-size marker and as a positive control in the hybridization

experiments. Lane 5 shows the plasmid profile of E. coli strain E2348/69 used as other size marker (100 and 6 kb) and as a negative control in the hybridization experiments. Lanes 2 to 4 display the plasmid profiles of bla CMY-2-positive strains belonging to the IncA/C plasmid type I (see Results): YURES 03-7, YUHS 05-78 and YUHS 03-19, respectively. Lanes 6 https://www.selleckchem.com/products/epz-6438.html and 7 show the plasmid profiles of bla CMY-2-negative strains of plasmid type I: SLRES 02-108 and MIPUS 03-27, respectively, GSK2879552 supplier and lane 8 shows the plasmid profile

of a representative strain of plasmid type II: SORAPUS 04-29. The IncA/C plasmids are indicated by an asterisk at the right side of the bands. PCR replicon typing was performed for incompatibility groups that had been reported to be associated with either pSTV or bla CMY-2, such as IncFII, IncFIB, IncA/C, IncHI2 and IncI1 [14, 15, 21, 22]. All 36 isolates that carried bla CMY-2 were positive for the IncA/C group and negative for the other Inc groups. Unexpectedly, among the 32 ST213 isolates lacking bla CMY-2, 23 were positive for the IncA/C group. Additionally, the IncHI2 and IncI1 groups were detected in three and two isolates, respectively. Thirteen bla CMY-2-negative and IncA/C-positive isolates were selected to represent different sources, states and years of isolation for further analysis, and compared them with the bla CMY-2-positive isolates (hereafter referred to as CMY- and CMY+, respectively). Alkaline lysis profiles and PFGE S1-digestion gels of plasmids from strains in our collection were hybridized with bla CMY-2 and repA/C probes; all of the CMY+ isolates yielded signals in the same plasmids, confirming that bla CMY-2 is carried in large

IncA/C plasmids (100 to 160 kb). In contrast, only the repA/C probe hybridized in the CMY- isolates, again targeting Phospholipase D1 large plasmids (100 to 160 kb) (Figure 2). Consistent with their low copy number [9, 12, 15], the IncA/C plasmids yielded faint bands in the ethidium bromide-stained gels, especially those larger than 100 kb (Figure 1), but they were unambiguously detected in the hybridization experiments. Figure 2 Dendrogram depicting the genetic relationships between the IncA/C plasmids based on Pst I fingerprints. The dendrogram was constructed with the UPGMA algorithm using Dice coefficients with a 1.0% band position tolerance. The two main groups (designated as types I and II) are separated by a dotted line (similarity index <50%). The five clusters formed at similarity index values >80% are indicated by the letters a to e.