Key points are not available for this paper at this time.
ABSTRACT Escherichia coli ST131 is a multidrug-resistant lineage associated with the global spread of extended-spectrum β-lactamase-producing organisms. Particularly, ST131 clade C1 is the most predominant clade in Japan, harboring bla CTX-M-14 at a high frequency. However, the process of resistance gene acquisition and spread remains unclear. Here, we performed whole-genome sequencing of 19 E. coli strains belonging to 12 STs and 12 fimH types collected between 1997 and 2016. Additionally, we analyzed the full-length genome sequences of 96 ST131- H 30 clade C0 and C1 strains, including those obtained from this study and those registered in public databases, to understand how ST131 clade C1 acquired and spread bla CTX-M-14 . We detected conjugative IncFII plasmids and IncB/O/K/Z plasmids carrying bla CTX-M-14 in diverse genetic lineages of E. coli strains from the 1990s to the 2010s, suggesting that these plasmids played an important role in the spread of bla CTX-M-14 . Molecular phylogenetic and molecular clock analyses of the 96 ST131- H 30 clade C0 and C1 strains identified 8 subclades. Strains harboring bla CTX-M-14 were clustered in subclades 4 and 5, and it was inferred that clade C1 acquired bla CTX-M-14 around 1993. All 34 strains belonging to subclade 5 possessed bla CTX-M-14 with IS Ecp1 upstream at the same chromosomal position, indicating their common ancestor acquired bla CTX-M-14 in a single IS Ecp1 -mediated transposition event during the early formation of the subclade around 1999. Therefore, both the horizontal transfer of plasmids carrying bla CTX-M-14 to diverse genetic lineages and chromosomal integration in the predominant genetic lineage have contributed to the spread of bla CTX-M-14 .
Komori et al. (Mon,) studied this question.