Author
Listed:
- Sean P. Polster
(The University of Chicago)
- Anukriti Sharma
(The University of Chicago
The University of California San Diego and Scripps Institution of Oceanography)
- Ceylan Tanes
(Children’s Hospital of Philadelphia)
- Alan T. Tang
(University of Pennsylvania)
- Patricia Mericko
(University of Pennsylvania)
- Ying Cao
(The University of Chicago)
- Julián Carrión-Penagos
(The University of Chicago)
- Romuald Girard
(The University of Chicago)
- Janne Koskimäki
(The University of Chicago)
- Dongdong Zhang
(The University of Chicago)
- Agnieszka Stadnik
(The University of Chicago)
- Sharbel G. Romanos
(The University of Chicago)
- Seán B. Lyne
(The University of Chicago)
- Robert Shenkar
(The University of Chicago)
- Kimberly Yan
(Center for Cerebrovascular Research)
- Cornelia Lee
(Angioma Alliance)
- Amy Akers
(Angioma Alliance)
- Leslie Morrison
(1 University of New Mexico)
- Myranda Robinson
(1 University of New Mexico)
- Atif Zafar
(1 University of New Mexico)
- Kyle Bittinger
(Children’s Hospital of Philadelphia)
- Helen Kim
(Center for Cerebrovascular Research)
- Jack A. Gilbert
(The University of Chicago
The University of California San Diego and Scripps Institution of Oceanography)
- Mark L. Kahn
(University of Pennsylvania)
- Le Shen
(The University of Chicago
The University of Chicago)
- Issam A. Awad
(The University of Chicago)
Abstract
Cavernous angiomas (CA) are common vascular anomalies causing brain hemorrhage. Based on mouse studies, roles of gram-negative bacteria and altered intestinal homeostasis have been implicated in CA pathogenesis, and pilot study had suggested potential microbiome differences between non-CA and CA individuals based on 16S rRNA gene sequencing. We here assess microbiome differences in a larger cohort of human subjects with and without CA, and among subjects with different clinical features, and conduct more definitive microbial analyses using metagenomic shotgun sequencing. Relative abundance of distinct bacterial species in CA patients is shown, consistent with postulated permissive microbiome driving CA lesion genesis via lipopolysaccharide signaling, in humans as in mice. Other microbiome differences are related to CA clinical behavior. Weighted combinations of microbiome signatures and plasma inflammatory biomarkers enhance associations with disease severity and hemorrhage. This is the first demonstration of a sensitive and specific diagnostic microbiome in a human neurovascular disease.
Suggested Citation
Sean P. Polster & Anukriti Sharma & Ceylan Tanes & Alan T. Tang & Patricia Mericko & Ying Cao & Julián Carrión-Penagos & Romuald Girard & Janne Koskimäki & Dongdong Zhang & Agnieszka Stadnik & Sharbel, 2020.
"Permissive microbiome characterizes human subjects with a neurovascular disease cavernous angioma,"
Nature Communications, Nature, vol. 11(1), pages 1-11, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-16436-w
DOI: 10.1038/s41467-020-16436-w
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