Emergence of KPC-3- and OXA-181-producing ST13 and ST17 Klebsiella pneumoniae in Portugal: genomic insights on national and international dissemination

Author:

Elias Rita1,Spadar Anton2,Hendrickx Antoni P A3ORCID,Bonnin Remy A4ORCID,Dortet Laurent4ORCID,Pinto Margarida5,Phelan Jody E2ORCID,Portugal Isabel1,Campino Susana2ORCID,da Silva Gabriela Jorge6,Clark Taane G2ORCID,Duarte Aida78,Perdigão João1

Affiliation:

1. Research Institute for Medicines (iMed.ULisboa), Faculdade de Farmácia, Universidade de Lisboa , Lisboa , Portugal

2. Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine , London , UK

3. Infectious Diseases Research, Diagnostics and laboratory Surveillance (IDS), Centre for Infectious Disease Control Netherlands (CIb), National Institute for Public Health and the Environment (RIVM) , Bilthoven , The Netherlands

4. Paris-Saclay University, INSERM UMR1154, National Reference Center for Antimicrobial Resistance , Le Kremlin-Bicêtre , France

5. Laboratório de Microbiologia, Serviço de Patologia Clínica, Centro Hospitalar Universitário Lisboa Central , Lisboa , Portugal

6. Faculty of Pharmacy and Center for Neurosciences and Cell Biology, University of Coimbra , Coimbra , Portugal

7. Departamento de Farmácia, Farmacologia e Tecnologias em Saúde, Faculdade de Farmácia, Universidade de Lisboa , Lisboa , Portugal

8. Centro de Investigação Interdisciplinar Egas Moniz, Instituto Universitário Egas Moniz , Monte da Caparica , Portugal

Abstract

Abstract Background Carbapenem-resistant Klebsiella pneumoniae (CRKP) strains are of particular concern, especially strains with mobilizable carbapenemase genes such as blaKPC, blaNDM or blaOXA-48, given that carbapenems are usually the last line drugs in the β-lactam class and, resistance to this sub-class is associated with increased mortality and frequently co-occurs with resistance to other antimicrobial classes. Objectives To characterize the genomic diversity and international dissemination of CRKP strains from tertiary care hospitals in Lisbon, Portugal. Methods Twenty CRKP isolates obtained from different patients were subjected to WGS for species confirmation, typing, drug resistance gene detection and phylogenetic reconstruction. Two additional genomic datasets were included for comparative purposes: 26 isolates (ST13, ST17 and ST231) from our collection and 64 internationally available genomic assemblies (ST13). Results By imposing a 21 SNP cut-off on pairwise comparisons we identified two genomic clusters (GCs): ST13/GC1 (n = 11), all bearing blaKPC-3, and ST17/GC2 (n = 4) harbouring blaOXA-181 and blaCTX-M-15 genes. The inclusion of the additional datasets allowed the expansion of GC1/ST13/KPC-3 to 23 isolates, all exclusively from Portugal, France and the Netherlands. The phylogenetic tree reinforced the importance of the GC1/KPC-3-producing clones along with their rapid emergence and expansion across these countries. The data obtained suggest that the ST13 branch emerged over a decade ago and only more recently did it underpin a stronger pulse of transmission in the studied population. Conclusions This study identifies an emerging OXA-181/ST17-producing strain in Portugal and highlights the ongoing international dissemination of a KPC-3/ST13-producing clone from Portugal.

Funder

Fundação para a Ciência e Tecnologia

FCT

Bloomsbury Set, Medical Research Council UK

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

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