@article{0b77e964ce2f4d85b1f47b5469553fdd,
title = "Respiratory carriage of hypervirulent Klebsiella pneumoniae by indigenous populations of Malaysia",
abstract = "Klebsiella pneumoniae is a Gram-negative Enterobacteriaceae that is classified by the World Health Organisation (WHO) as a Priority One ESKAPE pathogen. South and Southeast Asian countries are regions where both healthcare associated infections (HAI) and community acquired infections (CAI) due to extended-spectrum β-lactamase (ESBL)-producing and carbapenem-resistant K. pneumoniae (CRKp) are of concern. As K. pneumoniae can also exist as a harmless commensal, the spread of resistance genotypes requires epidemiological vigilance. However there has been no significant study of carriage isolates from healthy individuals, particularly in Southeast Asia, and specially Malaysia. Here we describe the genomic analysis of respiratory isolates of K. pneumoniae obtained from Orang Ulu and Orang Asli communities in Malaysian Borneo and Peninsular Malaysia respectively. The majority of isolates were K. pneumoniae species complex (KpSC) 1 K. pneumoniae (n = 53, 89.8\%). Four Klebsiella variicola subsp. variicola (KpSC3) and two Klebsiella quasipneumoniae subsp. similipneumoniae (KpSC4) were also found. It was discovered that 30.2\% (n = 16) of the KpSC1 isolates were ST23, 11.3\% (n = 6) were of ST65, 7.5\% (n = 4) were ST13, and 13.2\% (n = 7) were ST86. Only eight of the KpSC1 isolates encoded ESBL, but importantly not carbapenemase. Thirteen of the KpSC1 isolates carried yersiniabactin, colibactin and aerobactin, all of which harboured the rmpADC locus and are therefore characterised as hypervirulent. Co-carriage of multiple strains was minimal. In conclusion, most isolates were KpSC1, ST23, one of the most common sequence types and previously found in cases of K. pneumoniae infection. A proportion were hypervirulent (hvKp) however antibiotic resistance was low.",
keywords = "Antimicrobial resistance, ESBL, Hypervirulent, Klebsiella pneumoniae, Malaysia",
author = "Souradeep Das and Pandey, \{Anish K.\} and Morris, \{Denise E.\} and Rebecca Anderson and Victor Lim and Wie, \{Chong Chun\} and Yap, \{Ivan Kok Seng\} and Alattraqchi, \{Ahmed Ghazi\} and Hafis Simin and Ramle Abdullah and Yeo, \{Chew Chieng\} and Clarke, \{Stuart C.\} and Cleary, \{David W.\}",
note = "Funding Information: Sequencing was performed by the Environmental Sequencing Facility at the University of Southampton to whom we are grateful. We would like to thank the Department of Orang Asli Affairs and Development (JAKOA). Additionally, the authors would especially like to thank the communities who partook for their support and participation in this study. Funding Information: This work was funded by a Newton Fund Institutional Links award to Prof Stuart C. Clarke and Prof Mohd Nor Norazmi [grant number 172686537], an International Medical University grant awarded to Dr Chong Chun Wie and Dr Ivan Kok Seng Yap (BP I-01/12 (09) 2015), and two University of Southampton HEFCE Newton Fund Official Development Assistance (ODA) awards, one each to Prof Stuart C. Clarke and Dr David W. Cleary. Dr Cleary was supported by the National Institute for Health Research through the NIHR Southampton Biomedical Research Centre. Funding Information: DWC was a post-doctoral researcher on projects funded by Pfizer and GSK between April 2014 and October 2017. SCC acts as principal investigator on studies conducted on behalf of University Hospital Southampton NHS Foundation Trust/University of Southampton that are sponsored by vaccine manufacturers but receives no personal payments from them. SCC has participated in advisory boards for vaccine manufacturers but receives no personal payments for this work. SCC has received financial assistance from vaccine manufacturers to attend conferences. All grants and honoraria are paid into accounts within the respective NHS Trusts or Universities, or to independent charities. All other authors have no conflicts of interest. Publisher Copyright: {\textcopyright} The Author(s) 2024.",
year = "2024",
month = dec,
doi = "10.1186/s12864-024-10276-4",
language = "English",
volume = "25",
journal = "BMC Genomics",
issn = "1471-2164",
publisher = "Springer",
number = "1",
}