Proof‐of‐principle demonstration of endogenous circadian system and circadian misalignment effects on human oral microbiota
Proof‐of‐principle demonstration of endogenous circadian system and circadian misalignment effects on human oral microbiota
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/m2] 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.
Chellappa, Sarah L.
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Engen, Phillip A.
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Naqib, Ankur
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Qian, Jingyi
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Vujovic, Nina
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Rahman, Nishath
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Green, Stefan J.
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Garaulet, Marta
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Keshavarzian, Ali
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Scheer, Frank A. J. L.
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Chellappa, Sarah L.
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Engen, Phillip A.
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Naqib, Ankur
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Qian, Jingyi
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Vujovic, Nina
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Rahman, Nishath
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Green, Stefan J.
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Garaulet, Marta
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Keshavarzian, Ali
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Scheer, Frank A. J. L.
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Chellappa, Sarah L., Engen, Phillip A., Naqib, Ankur, Qian, Jingyi, Vujovic, Nina, Rahman, Nishath, Green, Stefan J., Garaulet, Marta, Keshavarzian, Ali and Scheer, Frank A. J. L.
(2021)
Proof‐of‐principle demonstration of endogenous circadian system and circadian misalignment effects on human oral microbiota.
The FASEB Journal.
(doi:10.1096/fj.202101153R).
Abstract
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/m2] 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.
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Accepted/In Press date: 1 November 2021
e-pub ahead of print date: 3 December 2021
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Local EPrints ID: 479535
URI: http://eprints.soton.ac.uk/id/eprint/479535
ISSN: 0892-6638
PURE UUID: 4dbe3f24-00bc-45af-80db-c8824e27bfc8
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Date deposited: 26 Jul 2023 16:30
Last modified: 17 Mar 2024 04:20
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Contributors
Author:
Sarah L. Chellappa
Author:
Phillip A. Engen
Author:
Ankur Naqib
Author:
Jingyi Qian
Author:
Nina Vujovic
Author:
Nishath Rahman
Author:
Stefan J. Green
Author:
Marta Garaulet
Author:
Ali Keshavarzian
Author:
Frank A. J. L. Scheer
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