Evidence map›Paper›PMID 26748856›Full record

ArticleCurrent biology : CB2016

period-Regulated Feeding Behavior and TOR Signaling Modulate Survival of Infection.

Victoria W Allen, Reed M O'Connor, Matthew Ulgherait, Clarice G Zhou, Elizabeth F Stone, Vanessa M Hill, Keith R Murphy, Julie C Canman, William W Ja, Mimi M Shirasu-Hiza

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Infection and immunity · 2023
    Review
  4. Review
  5. Article
  6. Methodological tools to study species of the genus Burkholderia.Applied microbiology and biotechnology · 2021
    Review
  7. Article
  8. Article
  9. Time after time: circadian clock regulation of intestinal stem cells.Cellular and molecular life sciences : CMLS · 2020
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. AThe Journal of cell biology · 2017
    Article
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Victoria W AllenDepartment of Genetics and Development, Columbia University Medical Center, New York, NY 10032, USA.
Reed M O'ConnorDepartment of Genetics and Development, Columbia University Medical Center, New York, NY 10032, USA.
Matthew UlgheraitDepartment of Genetics and Development, Columbia University Medical Center, New York, NY 10032, USA.
Clarice G ZhouDepartment of Genetics and Development, Columbia University Medical Center, New York, NY 10032, USA.
Elizabeth F StoneDepartment of Genetics and Development, Columbia University Medical Center, New York, NY 10032, USA.
Vanessa M HillDepartment of Genetics and Development, Columbia University Medical Center, New York, NY 10032, USA.
Keith R MurphyDepartment of Metabolism and Aging, Scripps Research Institute, Jupiter, FL 33458, USA.
Julie C CanmanDepartment of Pathology and Cell Biology, Columbia University Medical Center, New York, NY 10032, USA.
William W JaDepartment of Metabolism and Aging, Scripps Research Institute, Jupiter, FL 33458, USA.
Mimi M Shirasu-HizaDepartment of Genetics and Development, Columbia University Medical Center, New York, NY 10032, USA. Electronic address: ms4095@cumc.columbia.edu.
Columbia University Irving Medical Center · USScripps Research Institute · US

Funding

Circadian-Regulated Aging PhysiologiesR01AG045842 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Michele M Shirasu-Hiza · 2013 to 2026
$5.1M
Cell type-variation of cytokinesisR01GM117407 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CANMAN, JULIE C · 2016 to 2023
$2.9M
IR-LAMP: Optigenetic technology to spatially manipulate protein function in vivoDP2OD008773 · OD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CANMAN, JULIE C · 2011 to 2011
$2.4M
Circadian regulation of phagocytosisR01GM105775 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SHIRASU-HIZA, MICHELE M · 2013 to 2017
$1.6M
Drosophila feeding behavior: New tools for the genetic dissection of prandiologyR21DK092735 · NIDDK · SCRIPPS FLORIDA · PI JA, WILLIAM W · 2011 to 2012
$545k
Phagocytosis is misregulated in a Drosophila model of Fragile X syndromeF31NS080673 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI STONE, ELIZABETH FREDA · 2013 to 2014
$70k
NIA NIH HHS R01 AG045842NIDDK NIH HHS R21 DK092735NIDDK NIH HHS R21DK092735NIGMS NIH HHS R01 GM105775NIGMS NIH HHS R01GM105775NIGMS NIH HHS R01 GM117407NIH HHS DP2 OD008773NIH HHS DP2OD008773NINDS NIH HHS F31 NS080673NINDS NIH HHS F31NS080673
6 · The paper itself

Abstract

Most metazoans undergo dynamic, circadian-regulated changes in behavior and physiology. Currently, it is unknown how circadian-regulated behavior impacts immunity against infection. Two broad categories of defense against bacterial infection are resistance, control of microbial growth, and tolerance, control of the pathogenic effects of infection. Our study of behaviorally arrhythmic Drosophila circadian period mutants identified a novel link between nutrient intake and tolerance of infection with B. cepacia, a bacterial pathogen of rising importance in hospital-acquired infections. We found that infection tolerance in wild-type animals is stimulated by acute exposure to dietary glucose and amino acids. Glucose-stimulated tolerance was induced by feeding or direct injection; injections revealed a narrow window for glucose-stimulated tolerance. In contrast, amino acids stimulated tolerance only when ingested. We investigated the role of a known amino-acid-sensing pathway, the TOR (Target of Rapamycin) pathway, in immunity. TORC1 is circadian regulated and inhibition of TORC1 decreased resistance, as in vertebrates. Surprisingly, inhibition of the less well-characterized TOR complex 2 (TORC2) dramatically increased survival, through both resistance and tolerance mechanisms. This work suggests that dietary intake on the day of infection by B. cepacia can make a significant difference in long-term survival. We further demonstrate that TOR signaling mediates both resistance and tolerance of infection and identify TORC2 as a novel potential therapeutic target for increasing survival of infection.

Indexed as

Feeding BehaviorSignal TransductionAmino AcidsAnimalsDrosophila melanogasterDrosophila ProteinsMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2Multiprotein ComplexesPeriod Circadian ProteinsPhosphorylationSirolimusTOR Serine-Threonine KinasesAmino AcidsDrosophila ProteinsMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2Multiprotein ComplexesPeriod Circadian ProteinsPER protein, DrosophilaSirolimusTOR Serine-Threonine Kinasesamino acidsBurkholderia cepaciacircadiandietDrosophilafeedingglucoseimmunityinfectionperiod mutantresistanceRictortoleranceTORTORC1TORC2

Identifiers

PMID26748856
PMCPMC4729625
OpenAlexW2196866214

What OpenQuestion holds

Textmetadata
LicenceTDM
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.