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Skin bacterial richness and diversity in intensive care unit patients with severe pneumonia.
Lu, Sifen; Zhang, Wengeng; Li, Xiaojin; Xian, Jinghong; Hu, Ya; Zhou, Yongzhao.
Affiliation
  • Lu S; Precision Medicine Key Laboratory of Sichuan Province and Precision Medicine Center, West China Hospital, Sichuan University, Chengdu, China.
  • Zhang W; Precision Medicine Key Laboratory of Sichuan Province and Precision Medicine Center, West China Hospital, Sichuan University, Chengdu, China.
  • Li X; Department of Critical Care Medicine, West China Hospital, Sichuan University, Chengdu 610041, China.
  • Xian J; Department of Clinical Research Management, West China Hospital, Sichuan University, Chengdu 610041, China.
  • Hu Y; Center of Infectious Diseases, West China Hospital, Sichuan University, Chengdu, China. Electronic address: huya@wchscu.cn.
  • Zhou Y; Department of Respiratory and Critical Care Medicine, Frontier Science Center of Disease Molecular Network, West China Hospital, Sichuan University, Chengdu, China. Electronic address: yongzhaozhou001@wchscu.cn.
Int J Infect Dis ; 121: 75-84, 2022 Aug.
Article in En | MEDLINE | ID: mdl-35533832
ABSTRACT

OBJECTIVES:

Patients with severe pneumonia admitted to the intensive care unit (ICU) have a high risk of mortality, and the microbiome is likely to affect the outcome of such patients. However, the composition of the skin microbiota of ICU patients with severe pneumonia remains unclear. In this study, on the basis of 16S ribosomal ribonucleic acid sequencing, we explored the difference in skin bacterial richness and diversity between the ICU patient group (PG) with severe pneumonia and the healthy control group (CG).

METHODS:

The diversity index and taxonomic distribution of skin bacteria were analyzed using the Quantitative Insights Into Microbial Ecology (QIIME) bioinformatics pipeline. Blood, endotracheal aspirate, and bronchoalveolar lavage fluid samples were collected from the same PG subjects for culture.

RESULTS:

Compared with the CG, the diversity of skin bacteria in the PG decreased significantly. Staphylococcus, Acinetobacter, Stenotrophomonas, Enterococcus, Halomonas, and Brevibacillus were differentially abundant in the PG, and most of these bacteria were also identified in the cultures of upper respiratory tract samples of the same PG.

CONCLUSION:

We provide evidence that healthcare-associated infection in ICU patients with severe pneumonia is strongly associated with skin microbiota, which necessitates the prevention and control of skin bacterial pathogens for these patients.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pneumonia / Microbiota Limits: Humans Language: En Journal: Int J Infect Dis Journal subject: DOENCAS TRANSMISSIVEIS Year: 2022 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pneumonia / Microbiota Limits: Humans Language: En Journal: Int J Infect Dis Journal subject: DOENCAS TRANSMISSIVEIS Year: 2022 Document type: Article Affiliation country: