Evidence map›Paper›PMID 22554890›Full record

ArticleGenetics2012

Age-specific variation in immune response in Drosophila melanogaster has a genetic basis.

Tashauna M Felix, Kimberly A Hughes, Eric A Stone, Jenny M Drnevich, Jeff Leips

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

42 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
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  7. Insulin/IGF-1 signaling promotes immunosuppression via the STAT3 pathway: impact on the aging process and age-related diseases.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2021
    Review
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  16. The Journal of experimental biology · 2018
    Article
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  18. Review
  19. Genetic determinants of susceptibility to silver nanoparticle-induced acute lung inflammation in mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Article
  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

5 authors at 4 institutions in 1 country.

Tashauna M FelixDepartment of Biological Sciences, University of Maryland, Baltimore, MD 21250, USA.
Kimberly A Hughes
Eric A Stone
Jenny M Drnevich
Jeff Leips
University of Maryland, Baltimore · USFlorida State University · USNorth Carolina State University · USUniversity of Illinois Urbana-Champaign · US

Funding

EXPAND PARTICIPATION BY MINORITIES IN BIOMEDICAL SCIENCER25GM055036 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI SUMMERS, MICHAEL FINLEY · 1996 to 2021
$16.9M
Genetic control of quantitative traits associated with the metabolic syndromeR01DK084219 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DE LUCA, MARIA · 2010 to 2013
$1.3M
Nonesterified Fatty Acids and Cardiovascular AgingR03AG023339 · NIA · SPAULDING REHABILITATION HOSPITAL · PI TAYLOR, J ANDREW · 2005 to 2006
$156k
NIA NIH HHS 1R03 AG023339-01NIA NIH HHS R03 AG023339NIDDK NIH HHS 5R01 DK084219-02NIDDK NIH HHS R01 DK084219NIGMS NIH HHS R25 GM055036
6 · The paper itself

Abstract

Immunosenescence, the age-related decline in immune system function, is a general hallmark of aging. While much is known about the cellular and physiological changes that accompany immunosenescence, we know little about the genetic influences on this phenomenon. In this study we combined age-specific measurements of bacterial clearance ability following infection with whole-genome measurements of the transcriptional response to infection and wounding to identify genes that contribute to the natural variation in immunosenescence, using Drosophila melanogaster as a model system. Twenty inbred lines derived from nature were measured for their ability to clear an Escherichia coli infection at 1 and 4 weeks of age. We used microarrays to simultaneously determine genome-wide expression profiles in infected and wounded flies at each age for 12 of these lines. Lines exhibited significant genetically based variation in bacterial clearance at both ages; however, the genetic basis of this variation changed dramatically with age. Variation in gene expression was significantly correlated with bacterial clearance ability only in the older age group. At 4 weeks of age variation in the expression of 247 genes following infection was associated with genetic variation in bacterial clearance. Functional annotation analyses implicate genes involved in energy metabolism including those in the insulin signaling/TOR pathway as having significant associations with bacterial clearance in older individuals. Given the evolutionary conservation of the genes involved in energy metabolism, our results could have important implications for understanding immunosenescence in other organisms, including humans.

Indexed as

AgingAnimalsDrosophila melanogasterEscherichia coliEscherichia coli InfectionsFemaleGenetic VariationGenome, InsectGenotypeImmunityTranscription, GeneticWounds and Injuries

Identifiers

PMID22554890
PMCPMC3389989
OpenAlexW2052968942

What OpenQuestion holds

Textmetadata
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.