Associations between host microbiome and in fl ammation suggest role for host microbiome in driving COVID-19 disease severity

被引:2
|
作者
MacCann, Rachel [1 ,2 ,3 ]
Ghosh, Tarini Shankar [4 ]
Leon, Alejandro Abner Garcia [3 ]
Li, Junhui [4 ]
Negi, Riya [3 ]
Gaillard, Colette [3 ]
Saini, Gurvin [3 ]
Tinago, Willard [3 ]
Feeney, Eoin R. [1 ,2 ]
Yousif, Obada [5 ]
Cotter, Aoife G. [3 ,6 ]
de Barra, Eoghan [7 ,8 ]
Sadlier, Corinna [9 ]
Doran, Peter [10 ]
Landay, Alan [11 ]
O'Toole, Paul W. [4 ]
Mallon, Patrick W. [1 ,2 ,3 ]
机构
[1] Univ Coll Dublin, Sch Med, Dublin 4, Ireland
[2] St Vincents Univ Hosp, Dept Infect Dis, Elm Pk, Dublin 4, Ireland
[3] Univ Coll Dublin, Ctr Expt Pathogen Host Res CEPHR, Dublin 4, Ireland
[4] APC Microbiome Ireland, Cork, Ireland
[5] Wexford Gen Hosp, Endocrinol Dept, Carricklawn, Wexford, Ireland
[6] Mater Misericordiae Univ Hosp, Dept Infect Dis, Eccles St, Dublin 7, Ireland
[7] Beaumont Hosp, Dept Infect Dis, Dublin 9, Ireland
[8] Royal Coll Surgeons Ireland, Dept Int Hlth & Trop Med, Dublin, Ireland
[9] Cork Univ Hosp, Dept Infect Dis, Cork, Cork, Ireland
[10] Univ Galway, Clin Trials Inst, Galway, Ireland
[11] Rush Univ, Dept Internal Med, Chicago, IL USA
基金
爱尔兰科学基金会; 英国惠康基金;
关键词
SARS-CoV-2; COVID-19; Inflammation; Microbiome; GUT; HEALTH; AXIS;
D O I
10.1016/j.micinf.2023.105247
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Systemic inflammation and innate immune activation are associated with COVID-19 disease severity. Knowledge gaps remain in the relationships between microbiome, inflammation and COVID-19 disease severity. To better characterise these associations, we performed 16SrDNA analysis of stool samples in COVID-19 subjects to explore diversity and taxanomic composition. We correlated these to host inflammatory profiles, derived from soluble plasma biomarkers measured by bead -based fluorescence and electrochemiluminescence immunoassays. Associations of microbial diversity and inflammatory biomarkers on maximal COVID-19 severity (mild, moderate v severe/critical) was explored using logistic regression and weighted gene correlation network analysis (WGCNA). Of 79 subjects, 58% were male and 88% were Caucasian with 36% experiencing mild disease, 22% moderate disease and 40% critical/severe COVID-19. Hierarchical clustering and principal component analysis (PCo) revealed distinct inflammatory clusters that were found to correlate with 4 modules of microbiome profiles. Modules 3 and 4 were associated with both older age and severe/critical disease outcomes. These modules were enriched in pathogenic and inflammatory bacteria that mapped to a pro -inflammatory biomarker cluster. In contrast, module 1 exhibited enrichment of anti-inflammatory bacteria, was associated with younger age and mild/moderate disease outcomes and mapped to a less -inflamed biomarker cluster. This study provides further insights into links between host microbiome, inflammatory responses to SARS-CoV-2 infection and clinical COVID-19 disease severity, suggesting a role for the microbiome in shaping distinct host inflammatory responses to infection. (c) 2023 The Author(s). Published by Elsevier Masson SAS on behalf of Institut Pasteur. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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页数:9
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