Evidence map›Paper›PMID 32130883›Full record

ArticleCell metabolism2020

Bacteria Boost Mammalian Host NAD Metabolism by Engaging the Deamidated Biosynthesis Pathway.

Igor Shats, Jason G Williams, Juan Liu, Mikhail V Makarov, Xiaoyue Wu, Fred B Lih, Leesa J Deterding, Chaemin Lim, Xiaojiang Xu, Thomas A Randall and 10 more

Open access · greenAbstract read
In one paragraph

Article in Cell metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 160 papers.

0numbers the graph read from it
0cells of the map it votes in
160citing papers in PubMed
14.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

160 citing papers in PubMed, 231 citations in OpenAlex.

  1. Trial
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  6. Trial
  7. Gut microbes · 2026
    Article
  8. Gut · 2026
    Article
  9. Article
  10. Article
  11. A vitamin BScience advances · 2026
    Article
  12. Article
  13. Tracing NADCell reports · 2026
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

100 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 4 institutions in 2 countries.

Igor ShatsSignal Transduction Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA. Electronic address: igor.shats@nih.gov.
Jason G WilliamsMass Spectrometry Research and Support Group, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Juan LiuDepartment of Pharmacology and Cancer Biology, Duke University School of Medicine, Durham, NC 27710, USA.
Mikhail V MakarovMitchell Cancer Institute, University of South Alabama, Mobile, AL 36606, USA.
Xiaoyue WuSignal Transduction Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA; Department of Nutrition and Food Hygiene, School of Public Health, Nanjing Medical University, Nanjing 211166, China.
Fred B LihMass Spectrometry Research and Support Group, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Leesa J DeterdingMass Spectrometry Research and Support Group, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Chaemin LimCenter for Nanotechnology in Drug Delivery, University of North Carolina, Chapel Hill, NC 27514, USA.
Xiaojiang XuIntegrative Bioinformatics, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Thomas A RandallIntegrative Bioinformatics, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Ethan LeeSignal Transduction Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Wenling LiBiostatistics and Computational Biology, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Wei FanSignal Transduction Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Jian-Liang LiIntegrative Bioinformatics, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Marina SokolskyCenter for Nanotechnology in Drug Delivery, University of North Carolina, Chapel Hill, NC 27514, USA.
Alexander V KabanovCenter for Nanotechnology in Drug Delivery, University of North Carolina, Chapel Hill, NC 27514, USA.
Leping LiBiostatistics and Computational Biology, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Marie E MigaudMitchell Cancer Institute, University of South Alabama, Mobile, AL 36606, USA.
Jason W LocasaleDepartment of Pharmacology and Cancer Biology, Duke University School of Medicine, Durham, NC 27710, USA.
Xiaoling LiSignal Transduction Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA. Electronic address: lix3@niehs.nih.gov.
National Institute of Environmental Health Sciences · USUniversity of North Carolina at Chapel Hill · USDuke University · USUniversity of South Alabama · US

Funding

Sirtuins and nuclear receptors in aging and age-associated diseasesZIAES102205 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI LI, XIAOLING · 2009 to 2025
$42.4M
BioinformaticsZIAES101765 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI LI, LEPING · 2009 to 2025
$21.0M
Mass Spectrometry QuantitationZICES103005 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI WILLIAMS, JASON · 2018 to 2025
$9.2M
Intramural NIH HHS ZIA ES102205
6 · The paper itself

Abstract

Nicotinamide adenine dinucleotide (NAD), a cofactor for hundreds of metabolic reactions in all cell types, plays an essential role in metabolism, DNA repair, and aging. However, how NAD metabolism is impacted by the environment remains unclear. Here, we report an unexpected trans-kingdom cooperation between bacteria and mammalian cells wherein bacteria contribute to host NAD biosynthesis. Bacteria confer resistance to inhibitors of NAMPT, the rate-limiting enzyme in the amidated NAD salvage pathway, in cancer cells and xenograft tumors. Mechanistically, a microbial nicotinamidase (PncA) that converts nicotinamide to nicotinic acid, a precursor in the alternative deamidated NAD salvage pathway, is necessary and sufficient for this protective effect. Using stable isotope tracing and microbiota-depleted mice, we demonstrate that this bacteria-mediated deamidation contributes substantially to the NAD-boosting effect of oral nicotinamide and nicotinamide riboside supplementation in several tissues. Collectively, our findings reveal an important role of bacteria-enabled deamidated pathway in host NAD metabolism.

Indexed as

Biosynthetic PathwaysAdministration, OralAmidesAnimalsCell Line, TumorCytokinesEnergy MetabolismFemaleGastrointestinal MicrobiomeHumansMaleMammalsMetabolomeMice, Inbred C57BLMycoplasmaNADAmidesCytokinesNADNiacinamideNicotinamidasenicotinamide-beta-ribosideNicotinamide MononucleotideNicotinamide Phosphoribosyltransferasenicotinamide phosphoribosyltransferase, humanPyridinium Compoundscancer cellsdeamidated NAD synthesisgerm-free micehost-microbe interactionmicrobial nicotinamidasemycoplasmaNAMPT inhibitorsnicotinic acidoral nicotinamide riboside supplementation

Identifiers

PMID32130883
PMCPMC7194078
OpenAlexW3010636379

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.