Evidence map›Paper›PMID 34666189›Full record

ArticleInsect biochemistry and molecular biology2021

Increased insulin signaling in the Anopheles stephensi fat body regulates metabolism and enhances the host response to both bacterial challenge and Plasmodium falciparum infection.

Lewis V Hun, Kong Wai Cheung, Elizabeth Brooks, Rissa Zudekoff, Shirley Luckhart, Michael A Riehle

Open access · greenAbstract read
In one paragraph

Article in Insect biochemistry and molecular biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

9 citing papers in PubMed, 9 citations in OpenAlex.

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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

6 authors at 4 institutions in 1 country.

Lewis V HunDepartment of Entomology, University of California Riverside, Riverside, CA, USA; Department of Entomology, University of Arizona, Tucson, AZ, USA.
Kong Wai CheungDepartment of Medical Microbiology and Immunology, University of California Davis, Davis, CA, USA.
Elizabeth BrooksDepartment of Entomology, University of Arizona, Tucson, AZ, USA.
Rissa ZudekoffDepartment of Entomology, University of Arizona, Tucson, AZ, USA.
Shirley LuckhartDepartrment of Entomology, Plant Pathology and Nematology and Department of Biological Sciences, University of Idaho, Moscow, ID, USA.
Michael A RiehleDepartment of Entomology, University of Arizona, Tucson, AZ, USA. Electronic address: mriehle@ag.arizona.edu.
University of Arizona · USUniversity of California Davis Medical Center · USUniversity of California, Riverside · USUniversity of Idaho · US

Funding

Midgut mitochondrial function as a driver of resistance and fitness in mosquitoesR56AI129420 · NIAID · UNIVERSITY OF ARIZONA · PI LUCKHART, SHIRLEY, RIEHLE, MICHAEL ALLEN · 2018 to 2018
$726k
Midgut mitochondria as the key to fit, Plasmodium-resistant Anopheline mosquitoesR56AI118926 · NIAID · UNIVERSITY OF IDAHO · PI GIULIVI, CECILIA, LUCKHART, SHIRLEY · 2016 to 2016
$707k
Improving Anopheline fitness and resistance through fat body insulin signalingR21AI125823 · NIAID · UNIVERSITY OF ARIZONA · PI RIEHLE, MICHAEL ALLEN · 2016 to 2017
$426k
NIAID NIH HHS R21 AI125823NIAID NIH HHS R56 AI118926NIAID NIH HHS R56 AI129420
6 · The paper itself

Abstract

In vertebrates and invertebrates, the insulin/insulin-like growth factor 1 (IGF1) signaling (IIS) cascade is highly conserved and plays a vital role in many different physiological processes. Among the many tissues that respond to IIS in mosquitoes, the fat body has a central role in metabolism, lifespan, reproduction, and innate immunity. We previously demonstrated that fat body specific expression of active Akt, a key IIS signaling molecule, in adult Anopheles stephensi and Aedes aegypti activated the IIS cascade and extended lifespan. Additionally, we found that transgenic females produced more vitellogenin (Vg) protein than non-transgenic mosquitoes, although this did not translate into increased fecundity. These results prompted us to further examine how IIS impacts immunity, metabolism, growth and development of these transgenic mosquitoes. We observed significant changes in glycogen, trehalose, triglycerides, glucose, and protein in young (3-5 d) transgenic mosquitoes relative to non-transgenic sibling controls, while only triglycerides were significantly changed in older (18 d) transgenic mosquitoes. More importantly, we demonstrated that enhanced fat body IIS decreased both the prevalence and intensity of Plasmodium falciparum infection in transgenic An. stephensi. Additionally, challenging transgenic An. stephensi with Gram-positive and Gram-negative bacteria altered the expression of several antimicrobial peptides (AMPs) and two anti-Plasmodium genes, nitric oxide synthase (NOS) and thioester complement-like protein (TEP1), relative to non-transgenic controls. Increased IIS in the fat body of adult female An. stephensi had little to no impact on body size, growth or development of progeny from transgenic mosquitoes relative to non-transgenic controls. This study both confirms and expands our understanding of the critical roles insulin signaling plays in regulating the diverse functions of the mosquito fat body.

Indexed as

Host-Pathogen InteractionsSignal TransductionAnimalsAnophelesFat BodyFemaleGram-Negative BacteriaGram-Positive BacteriaHost-Parasite InteractionsInsulinPlasmodium falciparumInsulinAnopheles stephensiInnate immunityInsulin signalingMetabolismMosquito

Identifiers

PMID34666189
PMCPMC8647039
OpenAlexW3205362048

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.