Colonization with Staphylococcus aureus and Klebsiella pneumoniae causes infections in a Vietnamese intensive care unit

Author:

Thuy Duong Bich1,Campbell James23,Thuy Cao Thu3,Hoang Nguyen Van Minh3,Voong Vinh Phat3,Nguyen To Nguyen Thi3,Nguyen Ngoc Minh Chau3,Pham Duy Thanh23ORCID,Rabaa Maia A.23ORCID,Lan Nguyen Phu Huong1,Hao Nguyen Van1,Thwaites Guy E.23,Thwaites C. Louise23,Baker Stephen4,Chau Nguyen Van Vinh1ORCID,Chung The Hao3ORCID

Affiliation:

1. The Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam

2. Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, Oxford University, Oxford, UK

3. Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam

4. Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), University of Cambridge, Cambridge, UK

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.

Funder

Wellcome Trust

Publisher

Microbiology Society

Subject

General Medicine

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