T he global rise of carbapenem-resistant Enterobacterales (CRE) infections is posing a grave challenge to hospital systems worldwide (1). Carbapenemase genes usually are located on plasmids that can transmit vertically along clonal lineages and horizontally between different strains and species (2). However, the principles governing the transmission of carbapenemase-encoding plasmids in clinically relevant settings are complex and dynamic. Plasmid properties, donor, recipient, and ecologic factors all affect transmission (3,4).Previously, we found a 71,861-bp pKPC2 plasmid, pKPC2_sg1 (GenBank accession no. MN542377), in all 18 carbapenem-resistant hypervirulent Klebsiella pneumoniae isolates available in the Carbapenemase-Producing Enterobacteriaceae in Singapore (CaPES) collection (5,6). (Enterobacteriaceae is the former name of Enterobacterales.) The plasmid sequence was stable and unchanged after moving into different bacterial hosts or when maintained in human hosts for >200 days. This discovery prompted questions about the extent of pKPC2_sg1 dominance in clinical settings in Singapore, and its transmissibility and stability in hypervirulent K. pneumoniae. Using >1,000 CRE isolates collected from the 6 public hospitals in Singapore during 2010-2015, a subset of which was previously described (6), we examined the distribution of different carbapenem-encoding plasmids to investigate the dynamics and dominance of pKPC2.
Materials and Methods
Bacterial Strains, Growth Conditions, and PlasmidsWe analyzed 1,215 CRE isolates for carbapenemase plasmids distribution (Appendix 1 Table ,