Saliva microbiota differs between children with low and high sedentary screen times

Q1 Medicine
Elina Engberg , Sajan C. Raju , Rejane A.O. Figueiredo , Elisabete Weiderpass , Trine B. Rounge , Heli Viljakainen
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引用次数: 1

Abstract

This study examined whether the diversity, composition and functional capacity of the saliva microbiota differed between children with low and high sedentary screen times. We analyzed the saliva microbiota using 16S rRNA (V3–V4) sequencing from 193 children with low and 183 children with high TV/screen viewing times while sitting. Microbiota diversity was higher among children with low screen times compared to children with high screen times. Furthermore, microbiota composition differed between the screen time groups. In addition, we identified ten differentially abundant taxonomic groups, including Veillonella, Prevotella and Streptococcus, and five differentially present metabolic pathways between the screen time groups. Children with high screen times exhibited a higher capacity to synthesize the fatigue- and activity-related amino acids ornithine and arginine. To conclude, children with high sedentary screen (sitting) times exhibited a lower diversity and a different composition and functionality of the microbiota compared to children with low screen times.

久坐屏幕时间较短和较长儿童的唾液微生物群不同
这项研究调查了久坐屏幕时间较短和较长儿童的唾液微生物群的多样性、组成和功能能力是否存在差异。我们使用16S rRNA (V3-V4)测序分析了193名坐着看电视/屏幕时间少的儿童和183名坐着看电视/屏幕时间多的儿童的唾液微生物群。与高屏幕时间的儿童相比,低屏幕时间的儿童的微生物群多样性更高。此外,屏幕时间组之间的微生物群组成也存在差异。此外,我们确定了10个差异丰富的分类类群,包括细络菌、普雷沃氏菌和链球菌,以及5个不同的代谢途径。高屏幕时间的儿童表现出更高的合成疲劳和活动相关氨基酸鸟氨酸和精氨酸的能力。综上所述,与屏幕时间较短的儿童相比,久坐屏幕(坐着)时间较长的儿童表现出较低的微生物群多样性和不同的组成和功能。
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来源期刊
Human Microbiome Journal
Human Microbiome Journal Medicine-Infectious Diseases
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期刊介绍: The innumerable microbes living in and on our bodies are known to affect human wellbeing, but our knowledge of their role is still at the very early stages of understanding. Human Microbiome is a new open access journal dedicated to research on the impact of the microbiome on human health and disease. The journal will publish original research, reviews, comments, human microbe descriptions and genome, and letters. Topics covered will include: the repertoire of human-associated microbes, therapeutic intervention, pathophysiology, experimental models, physiological, geographical, and pathological changes, and technical reports; genomic, metabolomic, transcriptomic, and culturomic approaches are welcome.
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