Abstract

Hypervirulent Klebsiella pneumoniae (hvKp) is a significant cause of severe invasive infections in Vietnam, yet data on its epidemiology, population structure and dynamics are scarce. We screened hvKp isolates from patients with bloodstream infections (BSIs) at a tertiary infectious diseases hospital in Vietnam and healthy individuals, followed by whole genome sequencing and plasmid analysis. Among 700 BSI-causing Kp strains, 100 (14.3%) were hvKp. Thirteen hvKp isolates were identified from 350 rectal swabs of healthy adults; none from 500 rectal swabs of healthy children. The hvKp isolates were genetically diverse, encompassing 17 sequence types (STs), predominantly ST23, ST86 and ST65. Among the 113 hvKp isolates, 14 (12.6%) carried at least one antimicrobial resistance (AMR) gene, largely mediated by IncFII, IncR, and IncA/C plasmids. Notably, the acquisition of AMR conjugative plasmids facilitated horizontal transfer of the non-conjugative virulence plasmid between K. pneumoniae strains. Phylogenetic analysis demonstrated hvKp isolates from BSIs and human carriage clustered together, suggesting a significant role of intestinal carriage in hvKp transmission. Enhanced surveillance is crucial to understand the factors driving intestinal carriage and hvKp transmission dynamics for informing preventive measures. Furthermore, we advocate the clinical use of our molecular assay for diagnosing hvKp infections to guide effective management.

Hypervirulent Klebsiella pneumoniae (hvKp) is a significant cause of severe community-acquired infection, primarily in Asia. Here, the authors characterise the genetic profile, phylogenetic structure, and plasmid features of hvKp in Vietnam.

Details

Title
Genomic insights unveil the plasmid transfer mechanism and epidemiology of hypervirulent Klebsiella pneumoniae in Vietnam
Author
Nguyen, Quynh 1 ; Nguyen, Yen Thi Phuong 1 ; Ha, Tuyen Thanh 1 ; Tran, Dung Thi Ngoc 1 ; Voong, Phat Vinh 1 ; Chau, Vinh 1   VIAFID ORCID Logo  ; Nguyen, Phuong Luong Nha 2 ; Le, Ngan Thi Quynh 2 ; Nguyen, Lan Phu Huong 2 ; Nguyen, To Thi Nguyen 1 ; Trinh, Tan Van 1 ; Carrique-Mas, Juan J. 3 ; Baker, Stephen 4   VIAFID ORCID Logo  ; Thwaites, Guy 3   VIAFID ORCID Logo  ; Rabaa, Maia A. 3 ; Choisy, Marc 3 ; Chung, Hao The 1   VIAFID ORCID Logo  ; Pham, Duy Thanh 3   VIAFID ORCID Logo 

 Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam (GRID:grid.412433.3) (ISNI:0000 0004 0429 6814) 
 Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam (GRID:grid.414273.7) (ISNI:0000 0004 0621 021X) 
 Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam (GRID:grid.412433.3) (ISNI:0000 0004 0429 6814); University of Oxford, Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, Oxford, UK (GRID:grid.4991.5) (ISNI:0000 0004 1936 8948) 
 University of Cambridge, Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID) Department of Medicine, Cambridge, UK (GRID:grid.5335.0) (ISNI:0000 0001 2188 5934) 
Pages
4187
Publication year
2024
Publication date
2024
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3056070392
Copyright
© The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.