Evidence map›Paper›PMID 26165161›Full record

ArticleDevelopmental and comparative immunology2015

Plasmodium falciparum suppresses the host immune response by inducing the synthesis of insulin-like peptides (ILPs) in the mosquito Anopheles stephensi.

Jose E Pietri, Eduardo J Pietri, Rashaun Potts, Michael A Riehle, Shirley Luckhart

Abstract read
In one paragraph

Article in Developmental and comparative immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

22 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
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  4. Review
  5. Novel systems to study vector-pathogen interactions in malaria.Frontiers in cellular and infection microbiology · 2023
    Review
  6. Viruses · 2022
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  13. Review
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  16. Review
  17. Article
  18. Article
  19. Immunity, host physiology, and behaviour in infected vectors.Current opinion in insect science · 2017
    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

5 authors at 3 institutions in 1 country.

Jose E PietriDepartment of Medical Microbiology and Immunology, 3437 Tupper Hall, One Shields Avenue, School of Medicine, University of California, Davis, CA 95616, USA. Electronic address: jepietri@ucdavis.edu.
Eduardo J PietriDepartment of Medical Microbiology and Immunology, 3437 Tupper Hall, One Shields Avenue, School of Medicine, University of California, Davis, CA 95616, USA. Electronic address: ejpietri@ucdavis.edu.
Rashaun PottsDepartment of Medical Microbiology and Immunology, 3437 Tupper Hall, One Shields Avenue, School of Medicine, University of California, Davis, CA 95616, USA. Electronic address: rapotts@ucdavis.edu.
Michael A RiehleDepartment of Entomology, 410 Forbes, College of Agriculture and Life Sciences, University of Arizona, Tucson, AZ 85721, USA. Electronic address: mriehle@ag.arizona.edu.
Shirley LuckhartDepartment of Medical Microbiology and Immunology, 3437 Tupper Hall, One Shields Avenue, School of Medicine, University of California, Davis, CA 95616, USA. Electronic address: sluckhart@ucdavis.edu.
University of California, Davis · USUniversity of California System · USUniversity of Arizona · US

Funding

Systems biology approach to MAPK regulation of malaria infection in A. stephensiR01AI080799 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LUCKHART, SHIRLEY, VODOVOTZ, YORAM · 2009 to 2013
$3.4M
Insulin, IGF and Insulin Signaling: effects on Anopheles lifespan and immunityR01AI073745 · NIAID · UNIVERSITY OF ARIZONA · PI RIEHLE, MICHAEL ALLEN · 2008 to 2012
$2.5M
Harnessing midgut mitochondrial dynamics to enhance Anopheline mosquito fitnessR56AI107263 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LUCKHART, SHIRLEY, RIEHLE, MICHAEL ALLEN · 2014 to 2014
$775k
Endogenous insulin-like peptides and control of malaria infection in the mosquitoF31AI100589 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI PIETRI, JOSE ENRIQUE · 2012 to 2014
$108k
NIAID NIH HHS AI073745NIAID NIH HHS AI080799NIAID NIH HHS AI107263NIAID NIH HHS F31 AI100589NIAID NIH HHS F31-NRSA AI100589NIAID NIH HHS R01 AI073745NIAID NIH HHS R01 AI080799NIAID NIH HHS R56 AI107263
6 · The paper itself

Abstract

The insulin-like peptides (ILPs) and their respective signaling and regulatory pathways are highly conserved across phyla. In invertebrates, ILPs regulate diverse physiological processes, including metabolism, reproduction, behavior, and immunity. We previously reported that blood feeding alone induced minimal changes in ILP expression in Anopheles stephensi. However, ingestion of a blood meal containing human insulin or Plasmodium falciparum, which can mimic insulin signaling, leads to significant increases in ILP expression in the head and midgut, suggesting a potential role for AsILPs in the regulation of P. falciparum sporogonic development. Here, we show that soluble P. falciparum products, but not LPS or zymosan, directly induced AsILP expression in immortalized A. stephensi cells in vitro. Further, AsILP expression is dependent on signaling by the mitogen-activated protein kinase kinase/extracellular signal-regulated kinase (MEK/ERK) and phosphatidylinositol 3'-kinase (PI3K)/Akt branches of the insulin/insulin-like growth factor signaling (IIS) pathway. Inhibition of P. falciparum-induced ILPs in vivo decreased parasite development through kinetically distinct effects on mosquito innate immune responses. Specifically, knockdown of AsILP4 induced early expression of immune effector genes (1-6 h after infection), a pattern associated with significantly reduced parasite abundance prior to invasion of the midgut epithelium. In contrast, knockdown of AsILP3 increased later expression of the same genes (24 h after infection), a pattern that was associated with significantly reduced oocyst development. These data suggest that P. falciparum parasites alter the expression of mosquito AsILPs to dampen the immune response and facilitate their development in the mosquito vector.

Indexed as

AnimalsAnophelesExtracellular Signal-Regulated MAP KinasesInsect HormonesInsect ProteinsInsulinIntercellular Signaling Peptides and ProteinsMalaria, FalciparumMAP Kinase Signaling SystemMitogen-Activated Protein Kinase KinasesPeptide HormonesPhosphatidylinositol 3-KinasePlasmodium falciparumProto-Oncogene Proteins c-aktSomatomedinsExtracellular Signal-Regulated MAP KinasesInsect HormonesInsect ProteinsInsulinIntercellular Signaling Peptides and ProteinsMitogen-Activated Protein Kinase KinasesPeptide HormonesPhosphatidylinositol 3-KinaseProto-Oncogene Proteins c-aktSomatomedinsAnophelesImmunityInsulinInsulin-like peptideMalariaMosquitoNF-κBPlasmodium

Identifiers

PMID26165161
PMCPMC4536081
OpenAlexW909462797

What OpenQuestion holds

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Registered trials

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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.