Evidence map›Paper›PMID 19829691›Full record

ArticlePloS one2009

The Imd pathway is involved in antiviral immune responses in Drosophila.

Alexandre Costa, Eric Jan, Peter Sarnow, David Schneider

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 137 papers.

0numbers the graph read from it
0cells of the map it votes in
137citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

137 citing papers in PubMed, 261 citations in OpenAlex.

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

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

4 authors at 1 institution in 1 country.

Alexandre CostaDepartment of Microbiology and Immunology, Stanford University, Stanford, California, USA.
Eric Jan
Peter Sarnow
David Schneider
Stanford University · US

Funding

Adaptation in the Drosophila innate immune responseR01AI069164 · NIAID · STANFORD UNIVERSITY · PI SCHNEIDER, DAVID S. · 2007 to 2011
$1.6M
NIAID NIH HHS 1R01 AI 060164NIAID NIH HHS R01 AI069164
6 · The paper itself

Abstract

Cricket Paralysis virus (CrPV) is a member of the Dicistroviridae family of RNA viruses, which infect a broad range of insect hosts, including the fruit fly Drosophila melanogaster. Drosophila has emerged as an effective system for studying innate immunity because of its powerful genetic techniques and the high degree of gene and pathway conservation. Intra-abdominal injection of CrPV into adult flies causes a lethal infection that provides a robust assay for the identification of mutants with altered sensitivity to viral infection. To gain insight into the interactions between viruses and the innate immune system, we injected wild type flies with CrPV and observed that antimicrobial peptides (AMPs) were not induced and hemocytes were depleted in the course of infection. To investigate the contribution of conserved immune signaling pathways to antiviral innate immune responses, CrPV was injected into isogenic mutants of the Immune Deficiency (Imd) pathway, which resembles the mammalian Tumor Necrosis Factor Receptor (TNFR) pathway. Loss-of-function mutations in several Imd pathway genes displayed increased sensitivity to CrPV infection and higher CrPV loads. Our data show that antiviral innate immune responses in flies infected with CrPV depend upon hemocytes and signaling through the Imd pathway.

Indexed as

AnimalsAntiviral AgentsBacteriaDiaminopimelic AcidDicistroviridaeDrosophila melanogasterGryllidaeHemocytesMaleMultigene FamilyMutationPeptidoglycanProtein Structure, TertiaryReceptors, Tumor Necrosis FactorSignal TransductionAntiviral AgentsDiaminopimelic AcidPeptidoglycanReceptors, Tumor Necrosis Factor

Identifiers

PMID19829691
PMCPMC2758544
OpenAlexW2025476226

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.