Cargando…

Phosphorothioate-DNA bacterial diet reduces the ROS levels in C. elegans while improving locomotion and longevity

DNA phosphorothioation (PT) is widely distributed in the human gut microbiome. In this work, PT-diet effect on nematodes was studied with PT-bioengineering bacteria. We found that the ROS level decreased by about 20–50% and the age-related lipofuscin accumulation was reduced by 15–25%. Moreover, the...

Descripción completa

Detalles Bibliográficos
Autores principales: Huang, Qiang, Li, Ruohan, Yi, Tao, Cong, Fengsong, Wang, Dayong, Deng, Zixin, Zhao, Yi-Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8617147/
https://www.ncbi.nlm.nih.gov/pubmed/34824369
http://dx.doi.org/10.1038/s42003-021-02863-y
_version_ 1784604470301163520
author Huang, Qiang
Li, Ruohan
Yi, Tao
Cong, Fengsong
Wang, Dayong
Deng, Zixin
Zhao, Yi-Lei
author_facet Huang, Qiang
Li, Ruohan
Yi, Tao
Cong, Fengsong
Wang, Dayong
Deng, Zixin
Zhao, Yi-Lei
author_sort Huang, Qiang
collection PubMed
description DNA phosphorothioation (PT) is widely distributed in the human gut microbiome. In this work, PT-diet effect on nematodes was studied with PT-bioengineering bacteria. We found that the ROS level decreased by about 20–50% and the age-related lipofuscin accumulation was reduced by 15–25%. Moreover, the PT-feeding worms were more active at all life periods, and more resistant to acute stressors. Intriguingly, their lifespans were prolonged by ~21.7%. Comparative RNA-seq analysis indicated that many gene expressions were dramatically regulated by PT-diet, such as cysteine-rich protein (scl-11/12/13), sulfur-related enzyme (cpr-2), longevity gene (jnk-1) and stress response (sod-3/5, gps-5/6, gst-18/20, hsp-12.6). Both the Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis suggested that neuroactivity pathways were upregulated, while phosphoryl transfer and DNA-repair pathways were down-regulated in good-appetite young worms. The findings pave the way for pro-longevity of multicellular organisms by PT-bacterial interference.
format Online
Article
Text
id pubmed-8617147
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-86171472021-12-10 Phosphorothioate-DNA bacterial diet reduces the ROS levels in C. elegans while improving locomotion and longevity Huang, Qiang Li, Ruohan Yi, Tao Cong, Fengsong Wang, Dayong Deng, Zixin Zhao, Yi-Lei Commun Biol Article DNA phosphorothioation (PT) is widely distributed in the human gut microbiome. In this work, PT-diet effect on nematodes was studied with PT-bioengineering bacteria. We found that the ROS level decreased by about 20–50% and the age-related lipofuscin accumulation was reduced by 15–25%. Moreover, the PT-feeding worms were more active at all life periods, and more resistant to acute stressors. Intriguingly, their lifespans were prolonged by ~21.7%. Comparative RNA-seq analysis indicated that many gene expressions were dramatically regulated by PT-diet, such as cysteine-rich protein (scl-11/12/13), sulfur-related enzyme (cpr-2), longevity gene (jnk-1) and stress response (sod-3/5, gps-5/6, gst-18/20, hsp-12.6). Both the Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis suggested that neuroactivity pathways were upregulated, while phosphoryl transfer and DNA-repair pathways were down-regulated in good-appetite young worms. The findings pave the way for pro-longevity of multicellular organisms by PT-bacterial interference. Nature Publishing Group UK 2021-11-25 /pmc/articles/PMC8617147/ /pubmed/34824369 http://dx.doi.org/10.1038/s42003-021-02863-y Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Huang, Qiang
Li, Ruohan
Yi, Tao
Cong, Fengsong
Wang, Dayong
Deng, Zixin
Zhao, Yi-Lei
Phosphorothioate-DNA bacterial diet reduces the ROS levels in C. elegans while improving locomotion and longevity
title Phosphorothioate-DNA bacterial diet reduces the ROS levels in C. elegans while improving locomotion and longevity
title_full Phosphorothioate-DNA bacterial diet reduces the ROS levels in C. elegans while improving locomotion and longevity
title_fullStr Phosphorothioate-DNA bacterial diet reduces the ROS levels in C. elegans while improving locomotion and longevity
title_full_unstemmed Phosphorothioate-DNA bacterial diet reduces the ROS levels in C. elegans while improving locomotion and longevity
title_short Phosphorothioate-DNA bacterial diet reduces the ROS levels in C. elegans while improving locomotion and longevity
title_sort phosphorothioate-dna bacterial diet reduces the ros levels in c. elegans while improving locomotion and longevity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8617147/
https://www.ncbi.nlm.nih.gov/pubmed/34824369
http://dx.doi.org/10.1038/s42003-021-02863-y
work_keys_str_mv AT huangqiang phosphorothioatednabacterialdietreducestheroslevelsinceleganswhileimprovinglocomotionandlongevity
AT liruohan phosphorothioatednabacterialdietreducestheroslevelsinceleganswhileimprovinglocomotionandlongevity
AT yitao phosphorothioatednabacterialdietreducestheroslevelsinceleganswhileimprovinglocomotionandlongevity
AT congfengsong phosphorothioatednabacterialdietreducestheroslevelsinceleganswhileimprovinglocomotionandlongevity
AT wangdayong phosphorothioatednabacterialdietreducestheroslevelsinceleganswhileimprovinglocomotionandlongevity
AT dengzixin phosphorothioatednabacterialdietreducestheroslevelsinceleganswhileimprovinglocomotionandlongevity
AT zhaoyilei phosphorothioatednabacterialdietreducestheroslevelsinceleganswhileimprovinglocomotionandlongevity