Mehrotra Isha, Serena Gloria, Cetinbas Murat, Kenyon Victoria, Martin Victoria M, Harshman Stephanie G, Zomorrodi Ali R, Sadreyev Ruslan I, Fasano Alessio, Leonard Maureen M
Center for Celiac Research and Treatment, MassGeneral Hospital for Children, Yawkey Center for Outpatient Care, Suite 6B, 32 Fruit Street, Boston, MA 02114, USA.
Mucosal Immunology and Biology Research Center, MassGeneral Hospital for Children, Jackson, 55 Fruit Street, Boston, MA 02114, USA.
Curr Res Microb Sci. 2021 Aug 30;2:100069. doi: 10.1016/j.crmicr.2021.100069. eCollection 2021 Dec.
Celiac Disease (CD) is an autoimmune disorder triggered by gluten ingestion that can develop in genetically predisposed individuals. Alterations in the gut microbiota have been suggested to contribute to development of autoimmune conditions including CD. Recent work suggests the existence of a blood microbiota. Evidence that alterations in the blood microbiota potentially influence the development of chronic immune based diseases is increasing. However, there is no published literature regarding the blood microbiota in children, including those with CD. This study aimed to characterize the diversity and taxonomic composition of the blood microbiota of children with CD compared to controls. Whole blood samples were collected from children with active CD, CD in remission, and control subjects and 16S rRNA sequencing was utilized to analyze the blood microbiota. We found 16s rRNA present throughout all pediatric blood samples, providing evidence for the presence of a pediatric blood microbiota. We found significant differences in beta diversity and in abundance of certain taxa (Campylobacterales order, Odoribacteraceae and Helicobacteraceae families, genus and species, and species) between subjects with active CD and controls. These taxa have been previously reported to be associated with immune response and gut-inflammatory diseases. We did not find significant differences between subjects with active and remission CD or between remission CD and controls. Conclusions: We provide evidence for a pediatric blood microbiota and identified higher beta diversity and alterations in the composition of blood microbiota in subjects with active CD compared to controls.
乳糜泻(CD)是一种由摄入麸质引发的自身免疫性疾病,可在具有遗传易感性的个体中发生。肠道微生物群的改变被认为与包括CD在内的自身免疫性疾病的发展有关。最近的研究表明存在血液微生物群。血液微生物群改变可能影响慢性免疫性疾病发展的证据越来越多。然而,关于儿童血液微生物群,包括患有CD的儿童,尚无已发表的文献。本研究旨在描述患有CD的儿童与对照组相比血液微生物群的多样性和分类组成。从患有活动性CD的儿童、缓解期CD儿童和对照受试者中采集全血样本,并利用16S rRNA测序分析血液微生物群。我们在所有儿科血液样本中均发现了16S rRNA,为儿科血液微生物群的存在提供了证据。我们发现,活动性CD受试者与对照组之间在β多样性以及某些分类群(弯曲杆菌目、气味杆菌科和螺杆菌科、属和种,以及种)的丰度上存在显著差异。这些分类群此前已被报道与免疫反应和肠道炎症性疾病有关。我们未发现活动性CD受试者与缓解期CD受试者之间或缓解期CD受试者与对照组之间存在显著差异。结论:我们为儿科血液微生物群提供了证据,并发现与对照组相比,活动性CD受试者的血液微生物群具有更高的β多样性和组成改变。