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重症监护病房发生脓毒症和感染性休克患者的肠道微生物群分类。

Classification of the Gut Microbiota of Patients in Intensive Care Units During Development of Sepsis and Septic Shock.

机构信息

Department of Critical Care Medicine, Peking Union Medical College Hospital, Beijing 100730, China.

Key Laboratory of Molecular Biophysics of the Ministry of Education, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, China.

出版信息

Genomics Proteomics Bioinformatics. 2020 Dec;18(6):696-707. doi: 10.1016/j.gpb.2020.06.011. Epub 2021 Feb 17.

DOI:10.1016/j.gpb.2020.06.011
PMID:33607294
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8377022/
Abstract

The gut microbiota of intensive care unit (ICU) patients displays extreme dysbiosis associated with increased susceptibility to organ failure, sepsis, and septic shock. However, such dysbiosis is difficult to characterize owing to the high dimensional complexity of the gut microbiota. We tested whether the concept of enterotype can be applied to the gut microbiota of ICU patients to describe the dysbiosis. We collected 131 fecal samples from 64 ICU patients diagnosed with sepsis or septic shock and performed 16S rRNA gene sequencing to dissect their gut microbiota compositions. During the development of sepsis or septic shock and during various medical treatments, the ICU patients always exhibited two dysbiotic microbiota patterns, or ICU-enterotypes, which could not be explained by host properties such as age, sex, and body mass index, or external stressors such as infection site and antibiotic use. ICU-enterotype I (ICU E1) comprised predominantly Bacteroides and an unclassified genus of Enterobacteriaceae, while ICU-enterotype II (ICU E2) comprised predominantly Enterococcus. Among more critically ill patients with Acute Physiology and Chronic Health Evaluation II (APACHE II) scores > 18, septic shock was more likely to occur with ICU E1 (P = 0.041). Additionally, ICU E1 was correlated with high serum lactate levels (P = 0.007). Therefore, different patterns of dysbiosis were correlated with different clinical outcomes, suggesting that ICU-enterotypes should be diagnosed as independent clinical indices. Thus, the microbial-based human index classifier we propose is precise and effective for timely monitoring of ICU-enterotypes of individual patients. This work is a first step toward precision medicine for septic patients based on their gut microbiota profiles.

摘要

重症监护病房(ICU)患者的肠道微生物群表现出极度的生态失调,与器官衰竭、败血症和感染性休克的易感性增加有关。然而,由于肠道微生物群的高维复杂性,这种生态失调很难被描述。我们测试了是否可以将肠型的概念应用于 ICU 患者的肠道微生物群来描述这种生态失调。我们收集了 64 名被诊断为败血症或感染性休克的 ICU 患者的 131 份粪便样本,并进行了 16S rRNA 基因测序,以剖析他们的肠道微生物群落组成。在败血症或感染性休克的发展过程中以及在各种医疗治疗过程中,ICU 患者总是表现出两种失调的微生物群模式,或 ICU 肠型,这不能用宿主特性(如年龄、性别和体重指数)或外部应激源(如感染部位和抗生素使用)来解释。ICU 肠型 I(ICU E1)主要由拟杆菌和未分类的肠杆菌科组成,而 ICU 肠型 II(ICU E2)主要由肠球菌组成。在急性生理学和慢性健康评估 II(APACHE II)评分>18 的更危重患者中,ICU E1 更可能发生感染性休克(P=0.041)。此外,ICU E1 与高血清乳酸水平相关(P=0.007)。因此,不同的失调模式与不同的临床结局相关,表明 ICU 肠型应作为独立的临床指标进行诊断。因此,我们提出的基于微生物的人类指数分类器对于及时监测个体患者的 ICU 肠型是精确和有效的。这项工作是基于肠道微生物群谱为败血症患者制定精准医学的第一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e631/8377022/8b2fb2a08e7b/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e631/8377022/afa7a27c47a8/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e631/8377022/2f42fd418b6c/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e631/8377022/5d2596e05f7c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e631/8377022/8b2fb2a08e7b/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e631/8377022/afa7a27c47a8/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e631/8377022/2f42fd418b6c/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e631/8377022/5d2596e05f7c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e631/8377022/8b2fb2a08e7b/gr4.jpg

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