Extended-spectrum β-lactamase-producing ST131 has become widespread worldwide. This study aims to characterize the virulome, resistome, and population structure of ST131 isolates from clinical blood samples in Hungary. A total of 30 C2/H30Rx and 33 C1-M27 ST131 isolates were selected for Illumina MiSeq sequencing and 30 isolates for MinION sequencing, followed by hybrid de novo assembly. Five C2/H30Rx and one C1-M27 cluster were identified. C1-M27 isolates harbored the F1:A2:B20 plasmid in 93.9% of cases. Long-read sequencing revealed that was on plasmids. Among the C2/H30Rx isolates, only six isolates carried the C2-associated F2:A1:B- plasmid type. Of 19 hybrid-assembled C2/H30Rx genomes, the gene was located on plasmid only in one isolate, while in the other isolates, IS1 or IS-mediated chromosomal integration of was detected in unique variations. In one isolate a part of F2:A1:B- plasmid integrated into the chromosome. These results suggest that CTX-M-15-producing C2/H30Rx and CTX-M-27-producing C1-M27 subclades may have emerged and spread in different ways in Hungary. While was carried mainly on the C1/H30R-associated F1:A2:B20 plasmid, the IncF-like plasmids of C2/H30Rx or its composite transposons have been incorporated into the chromosome through convergent evolutionary processes.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11047377PMC
http://dx.doi.org/10.3390/antibiotics13040363DOI Listing

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Extended-spectrum β-lactamase-producing ST131 has become widespread worldwide. This study aims to characterize the virulome, resistome, and population structure of ST131 isolates from clinical blood samples in Hungary. A total of 30 C2/H30Rx and 33 C1-M27 ST131 isolates were selected for Illumina MiSeq sequencing and 30 isolates for MinION sequencing, followed by hybrid de novo assembly.

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Article Synopsis
  • Escherichia coli sequence type 131 (ST131) is a global, drug-resistant pathogen with diverse subclones distinguished by specific genetic markers and resistance traits.
  • Researchers developed a multiplex PCR assay using a combination of 36 primers to detect and classify ST131 into 15 molecular subsets, outperforming current detection methods.
  • A command-line tool called ST131Typer was also created for those using whole genome sequencing, providing rapid and accurate subtyping for epidemiological studies and clinical applications.
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