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Proof‐of‐principle demonstration of endogenous circadian system and circadian misalignment effects on human oral microbiota
Author(s) -
Chellappa Sarah L.,
Engen Phillip A.,
Naqib Ankur,
Qian Jingyi,
Vujovic Nina,
Rahman Nishath,
Green Stefan J.,
Garaulet Marta,
Keshavarzian Ali,
Scheer Frank A. J. L.
Publication year - 2022
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fj.202101153r
Subject(s) - circadian rhythm , biology , endogeny , circadian clock , microbiome , saliva , gut flora , physiology , medicine , endocrinology , bioinformatics , immunology , biochemistry
Circadian misalignment—the misalignment between the central circadian “clock” and behavioral and environmental cycles (including sleep/wake, fasting/eating, dark/light)—results in adverse cardiovascular and metabolic effects. Potential underlying mechanisms for these adverse effects include alterations in the orogastrointestinal microbiota. However, it remains unknown whether human oral microbiota has endogenous circadian rhythms (i.e., independent of sleep/wake, fasting/eating, and dark/light cycles) and whether circadian misalignment influences oral microbiota community composition. Healthy young individuals [27.3 ± 2.3 years (18–35 years), 4 men and 2 women, body‐mass index range: 18–28 kg/m 2 ] were enrolled in a stringently controlled 14‐day circadian laboratory protocol. This included a 32‐h constant routine (CR) protocol (endogenous circadian baseline assessment), a forced desynchrony protocol with four 28‐h “days” under ~3 lx to induce circadian misalignment, and a post‐misalignment 40‐h CR protocol. Microbiota assessments were performed on saliva samples collected every 4 h throughout both CR protocols. Total DNA was extracted and processed using high‐throughput 16S ribosomal RNA gene amplicon sequencing. The relative abundance of specific oral microbiota populations, i.e., one of the five dominant phyla, and three of the fourteen dominant genera, exhibited significant endogenous circadian rhythms. Importantly, circadian misalignment dramatically altered the oral microbiota landscape, such that four of the five dominant phyla and eight of the fourteen dominant genera exhibited significant circadian misalignment effects. Moreover, circadian misalignment significantly affected the metagenome functional content of oral microbiota (inferred gene content analysis), as indicated by changes in specific functional pathways associated with metabolic control and immunity. Collectively, our proof‐of‐concept study provides evidence for endogenous circadian rhythms in human oral microbiota and show that even relatively short‐term experimental circadian misalignment can dramatically affect microbiota community composition and functional pathways involved in metabolism and immune function. These proof‐of‐principle findings have translational relevance to individuals typically exposed to circadian misalignment, including night shift workers and frequent flyers.