TY - JOUR
T1 - Plasmid dynamics driving carbapenemase gene dissemination in healthcare environments
T2 - a nationwide analysis of closed Enterobacterales genomes
AU - Koh, Vanessa
AU - Cabrera, Rodrigo
AU - Sridatta, Prakki Sai Rama
AU - Thevasagayam, Natascha May
AU - Lim, Ze Qin
AU - Marimuthu, Kalisvar
AU - Venkatachalam, Indumathi
AU - Cherng, Benjamin Pei Zhi
AU - Fong, Raymond Kok Choon
AU - Pada, Surinder Kaur
AU - Ooi, Say Tat
AU - Smitasin, Nares
AU - Thoon, Koh Cheng
AU - Hsu, Li Yang
AU - Koh, Tse Hsien
AU - De, Partha Pratim
AU - Tan, Thean Yen
AU - Chan, Douglas
AU - Deepak, Rama Narayana
AU - Tee, Nancy Wen Sim
AU - Gan, Yunn Hwen
AU - Matlock, William
AU - Eyre, David W.
AU - Ang, Michelle
AU - Lin, Raymond Tzer Pin
AU - Teo, Jeanette
AU - Ng, Oon Tek
N1 - Publisher Copyright:
© 2025. The Author(s).
PY - 2025/10/28
Y1 - 2025/10/28
N2 - Plasmid-mediated transmission can account for half of carbapenem-producing Enterobacterales (CPE) dissemination, underscoring the need to identify genetic determinants of plasmid persistence in the hospital setting. From 1,088 CPE isolates detected through nationwide surveillance in Singapore over five years, 1,115 closed carbapenemase-producing plasmids were identified and clustered, of which 92.5% (n = 1031) were grouped into 48 plasmid clusters (PCs). The most common plasmid genotypes were PC1 and PC2. Of 389 isolates carrying blaKPC-2-positive PC1 plasmids and 283 isolates carrying blaNDM-1-positive PC2 plasmids, 236 (60.7%) and 168 (59.4%) putatively acquired the carbapenemase gene via plasmid-mediated horizontal transmission, whereas 153 (39.3%) and 115 (40.6%) putatively acquired the carbapenemase gene via clonal lineage-dependent vertical transmission, respectively. Less abundant plasmids showed distinct inserted genomic regions encoding genes related to heavy metal and formaldehyde detoxification not found in predominant plasmids. Our data suggest that PC1 and PC2 genotypes are better adapted for stable propagation of blaKPC-2 and blaNDM-1, respectively, during inter-patient clonal spread and across multiple species (and sequence types) compared to other genetic settings. We propose that a crucial factor enabling evolutionarily successful carbapenemase plasmid genotypes to achieve hyperendemicity in the population is the maintenance of conserved genomes, thus minimizing fitness costs to their hosts.
AB - Plasmid-mediated transmission can account for half of carbapenem-producing Enterobacterales (CPE) dissemination, underscoring the need to identify genetic determinants of plasmid persistence in the hospital setting. From 1,088 CPE isolates detected through nationwide surveillance in Singapore over five years, 1,115 closed carbapenemase-producing plasmids were identified and clustered, of which 92.5% (n = 1031) were grouped into 48 plasmid clusters (PCs). The most common plasmid genotypes were PC1 and PC2. Of 389 isolates carrying blaKPC-2-positive PC1 plasmids and 283 isolates carrying blaNDM-1-positive PC2 plasmids, 236 (60.7%) and 168 (59.4%) putatively acquired the carbapenemase gene via plasmid-mediated horizontal transmission, whereas 153 (39.3%) and 115 (40.6%) putatively acquired the carbapenemase gene via clonal lineage-dependent vertical transmission, respectively. Less abundant plasmids showed distinct inserted genomic regions encoding genes related to heavy metal and formaldehyde detoxification not found in predominant plasmids. Our data suggest that PC1 and PC2 genotypes are better adapted for stable propagation of blaKPC-2 and blaNDM-1, respectively, during inter-patient clonal spread and across multiple species (and sequence types) compared to other genetic settings. We propose that a crucial factor enabling evolutionarily successful carbapenemase plasmid genotypes to achieve hyperendemicity in the population is the maintenance of conserved genomes, thus minimizing fitness costs to their hosts.
UR - https://www.scopus.com/pages/publications/105020345913
UR - https://www.scopus.com/pages/publications/105020345913#tab=citedBy
U2 - 10.1038/s41467-025-64515-7
DO - 10.1038/s41467-025-64515-7
M3 - Research Article
C2 - 41152242
AN - SCOPUS:105020345913
SN - 2041-1723
VL - 16
SP - 9522
JO - Nature Communications
JF - Nature Communications
IS - 1
ER -