Multiple horizontally-transmitted quinlone

Multiple horizontally-transmitted quinlone resistance genes were detected among E. coli from Accra We used PCR to screen for qnrA, qnrB, qnrS and qepA genes SB202190 cell line and confirmed all amplicons by sequencing. Of the 40 strains evaluated twelve carried one horizontally acquired quinolone resistance gene. These were qnrB1 (2 isolates), qnrB2 (1 isolate), qnrS1 (7 isolates) and qepA (2 isolates). In two isolates, without mutations in gyrA and parC QRDRs, horizontally-acquired resistance genes could account for the resistance seen. However, in the vast majority of cases, horizontally acquired resistance was seen in combination

with QRDR mutations. Quinolone-resistant E. coli from Accra are over-represented among multi-locus sequence type 10 We hypothesized that clonal expansion might account, at least in part, for the rise in resistance seen in the course of the study. To test this hypothesis, we subjected all the 40 QREC isolates to multi-locus sequence typing by the scheme of Wirth et al [19] and deposited their AZD3965 chemical structure allelic profiles in the database at http://​www.​mlst.​net. We identified 30 Sequence Types (STs) among 40 QREC isolates from Ghana (0.75 STs per strain). As shown in Figure 2, quinolone resistance is seen in diverse lineages that have been detected in Ghana. STs that were recovered more than once among the QREC included

ST10 (9 isolates) as well as STs101, 156, 227, 648 and 1466 (2 isolates each) (Table 1). Although there were 10 QREC STs that were identified for the first time in this study (reflecting the low proportion of strains from West Africa in the PLX-4720 concentration database), Ribose-5-phosphate isomerase only one of these (1466) was seen more than once among QREC (Figure 2, Table 1). Three others were related to STs that were also seen among QREC – ST1471 was a single-locus variant of ST206, and STs1286 and 1467 were respectively single- and double-locus variants of ST10. Horizontally-transmitted quinlone resistance determinants were

expectedly detected in strains belonging to multiple STs. However qnrS1 alleles were in all but two cases detected among strains belonging to the ST10 complex. Figure 2 eBURST output for 165 E. coli isolates in the http://​www.​mlst.​net database that were isolated in Ghana, including 48 isolates sequence-typed in this study. Each ST is marked as a dot or node. The size of the node is proportional to the number of isolates contained in that ST. Blue nodes represent predicted founder STs and sub-founders are indicated in yellow. All other STs marked as black dots. STs annotated in green are comprised of quinolone-resistant strains only and those written in pink contain quinolone-sensitive and quinolone-resistant isolates. Nine of the 40 QREC isolates obtained in this study belonged to ST10, in contrast to 10 of 125 other E. coli from Ghana in the database (p = 0.02, Fisher’s exact test). Moreover six other QREC isolates were single- or double- locus variants of ST10.

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