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Alterations of oral microbiota and impact on the gut microbiome in type 1 diabetes mellitus revealed by integrated multi-omic analyses

生物 医学微生物学 组学 微生物生态学 微生物群 肠道菌群 肠道微生物群 微生物学 2型糖尿病 糖尿病 2型糖尿病 基因组 生物信息学 免疫学 遗传学 细菌 基因 内分泌学
作者
Benoît J. Kunath,Oskar Hickl,Pedro Queirós,Camille Martin‐Gallausiaux,Laura Lebrun,Rashi Halder,Cédric C. Laczny,Thomas Schmidt,Matthew R. Hayward,Dörte Becher,Anna Heintz‐Buschart,Carine de Beaufort,Peer Bork,Patrick May,Paul Wilmes
出处
期刊:Microbiome [BioMed Central]
卷期号:10 (1): 243-243 被引量:64
标识
DOI:10.1186/s40168-022-01435-4
摘要

BACKGROUND: Alterations to the gut microbiome have been linked to multiple chronic diseases. However, the drivers of such changes remain largely unknown. The oral cavity acts as a major route of exposure to exogenous factors including pathogens, and processes therein may affect the communities in the subsequent compartments of the gastrointestinal tract. Here, we perform strain-resolved, integrated meta-genomic, transcriptomic, and proteomic analyses of paired saliva and stool samples collected from 35 individuals from eight families with multiple cases of type 1 diabetes mellitus (T1DM). RESULTS: We identified distinct oral microbiota mostly reflecting competition between streptococcal species. More specifically, we found a decreased abundance of the commensal Streptococcus salivarius in the oral cavity of T1DM individuals, which is linked to its apparent competition with the pathobiont Streptococcus mutans. The decrease in S. salivarius in the oral cavity was also associated with its decrease in the gut as well as higher abundances in facultative anaerobes including Enterobacteria. In addition, we found evidence of gut inflammation in T1DM as reflected in the expression profiles of the Enterobacteria as well as in the human gut proteome. Finally, we were able to follow transmitted strain-variants from the oral cavity to the gut at the individual omic levels, highlighting not only the transfer, but also the activity of the transmitted taxa along the gastrointestinal tract. CONCLUSIONS: Alterations of the oral microbiome in the context of T1DM impact the microbial communities in the lower gut, in particular through the reduction of "mouth-to-gut" transfer of Streptococcus salivarius. Our results indicate that the observed oral-cavity-driven gut microbiome changes may contribute towards the inflammatory processes involved in T1DM. Through the integration of multi-omic analyses, we resolve strain-variant "mouth-to-gut" transfer in a disease context. Video Abstract.
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