Colonization with Staphylococcus aureus and Klebsiella pneumoniae causes infections in a Vietnamese intensive care unit. Issue 2 (27th February 2021)

• Record Type: Journal Article
• Authors: Thuy, Duong Bich; Campbell, James; Thuy, Cao Thu; Hoang, Nguyen Van Minh; Voong Vinh, Phat; Nguyen, To Nguyen Thi; Nguyen Ngoc Minh, Chau; Pham, Duy Thanh; Rabaa, Maia A.; Lan, Nguyen Phu Huong; Hao, Nguyen Van; Thwaites, Guy E.; Thwaites, C. Louise; Baker, Stephen; Chau, Nguyen Van Vinh; Chung The, Hao
• Is Part Of: Microbial genomics. Volume 7:Issue 2(2021)
• Publication Date: 2021-02-27
• Subjects: colonization -- hospital-acquired infections -- hypervirulent Klebsiella pneumoniae -- intra-patient diversity -- Staphylococcus aureus; Microbial genomics -- Periodicals; 572.8629
• DOI: 10.1099/mgen.0.000514
• Languages: English
• ISSNs: 2057-5858

Abstract

Abstract : Pre-existing colonization with Staphylococcus aureus or Klebsiella pneumoniae has been found to increase the risk of infection in intensive care patients. We previously conducted a longitudinal study to characterize colonization of these two organisms in patients admitted to intensive care in a hospital in southern Vietnam. Here, using genomic and phylogenetic analyses, we aimed to assess the contribution these colonizing organisms made to infections. We found that in the majority of patients infected with S. aureus or K. pneumoniae, the sequence type of the disease-causing (infecting) isolate was identical to that of corresponding colonizing organisms in the respective patient. Further in-depth analysis revealed that in patients infected by S. aureus ST188 and by K. pneumoniae ST17, ST23, ST25 and ST86, the infecting isolate was closely related to and exhibited limited genetic variation relative to pre-infection colonizing isolates. Multidrug-resistant S. aureus ST188 was identified as the predominant agent of colonization and infection. Colonization and infection by K. pneumoniae were characterized by organisms with limited antimicrobial resistance profiles but extensive repertoires of virulence genes. Our findings augment the understanding of the link between bacterial colonization and infection in a low-resource setting, and could facilitate the development of novel evidence-based approaches to prevent and treat infections in high-risk patients in intensive care.