Longitudinal multi-omics of host–microbe dynamics in prediabetes

糖尿病前期 转录组 生物 微生物群 疾病 组学 2型糖尿病 免疫系统 计算生物学 免疫学 生物信息学 糖尿病 医学 遗传学 基因 内科学 内分泌学 基因表达
作者
Wenyu Zhou,M. Reza Sailani,Kévin Contrepois,Yanjiao Zhou,Sara Ahadi,Shana R. Leopold,Martin Jinye Zhang,Varsha Rao,Monika Avina,Tejaswini Mishra,Jethro S. Johnson,Brittany Lee‐McMullen,Songjie Chen,Ahmed A. Metwally,Thi Dong Binh Tran,Hoan Nguyen,Xin Zhou,Brandon Albright,Bo‐Young Hong,Lauren Petersen,Eddy J. Bautista,Blake Hanson,Lei Chen,Daniel Spakowicz,Amir Bahmani,Denis Salins,Benjamin Leopold,Melanie Ashland,Orit Dagan‐Rosenfeld,Shannon Rego,Patricia Limcaoco,Elizabeth Colbert,Candice Allister,Dalia Perelman,Colleen Craig,Eric Wei,Hassan Chaı̈b,Daniel Hornburg,Jessilyn Dunn,Liang Liang,Sophia Miryam Schüssler‐Fiorenza Rose,Kim Kukurba,Brian Piening,Hannes Röst,David Tse,Tracey McLaughlin,Erica Sodergren,George M. Weinstock,M Snyder
出处
期刊:Nature [Nature Portfolio]
卷期号:569 (7758): 663-671 被引量:418
标识
DOI:10.1038/s41586-019-1236-x
摘要

Type 2 diabetes mellitus (T2D) is a growing health problem, but little is known about its early disease stages, its effects on biological processes or the transition to clinical T2D. To understand the earliest stages of T2D better, we obtained samples from 106 healthy individuals and individuals with prediabetes over approximately four years and performed deep profiling of transcriptomes, metabolomes, cytokines, and proteomes, as well as changes in the microbiome. This rich longitudinal data set revealed many insights: first, healthy profiles are distinct among individuals while displaying diverse patterns of intra- and/or inter-personal variability. Second, extensive host and microbial changes occur during respiratory viral infections and immunization, and immunization triggers potentially protective responses that are distinct from responses to respiratory viral infections. Moreover, during respiratory viral infections, insulin-resistant participants respond differently than insulin-sensitive participants. Third, global co-association analyses among the thousands of profiled molecules reveal specific host-microbe interactions that differ between insulin-resistant and insulin-sensitive individuals. Last, we identified early personal molecular signatures in one individual that preceded the onset of T2D, including the inflammation markers interleukin-1 receptor agonist (IL-1RA) and high-sensitivity C-reactive protein (CRP) paired with xenobiotic-induced immune signalling. Our study reveals insights into pathways and responses that differ between glucose-dysregulated and healthy individuals during health and disease and provides an open-access data resource to enable further research into healthy, prediabetic and T2D states.

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