Literature DB >> 34666189

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 Hun1, Kong Wai Cheung2, Elizabeth Brooks3, Rissa Zudekoff3, Shirley Luckhart4, Michael A Riehle5.   

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.
Copyright © 2021 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Anopheles stephensi; Innate immunity; Insulin signaling; Metabolism; Mosquito

Mesh:

Substances:

Year:  2021        PMID: 34666189      PMCID: PMC8647039          DOI: 10.1016/j.ibmb.2021.103669

Source DB:  PubMed          Journal:  Insect Biochem Mol Biol        ISSN: 0965-1748            Impact factor:   4.714


  78 in total

1.  Akt and FOXO dysregulation contribute to infection-induced wasting in Drosophila.

Authors:  Marc S Dionne; Linh N Pham; Mimi Shirasu-Hiza; David S Schneider
Journal:  Curr Biol       Date:  2006-10-24       Impact factor: 10.834

2.  Induction of nitric oxide synthase in Anopheles stephensi by Plasmodium falciparum: mechanism of signaling and the role of parasite glycosylphosphatidylinositols.

Authors:  Junghwa Lim; D Channe Gowda; Gowdahalli Krishnegowda; Shirley Luckhart
Journal:  Infect Immun       Date:  2005-05       Impact factor: 3.441

3.  Identification of the first insulin-like peptide in the disease vector Rhodnius prolixus: Involvement in metabolic homeostasis of lipids and carbohydrates.

Authors:  Marina S Defferrari; Ian Orchard; Angela B Lange
Journal:  Insect Biochem Mol Biol       Date:  2015-12-29       Impact factor: 4.714

4.  Activating transcription factor 3 regulates immune and metabolic homeostasis.

Authors:  Jan Rynes; Colin D Donohoe; Peter Frommolt; Susanne Brodesser; Marek Jindra; Mirka Uhlirova
Journal:  Mol Cell Biol       Date:  2012-07-30       Impact factor: 4.272

Review 5.  Insulin-Like Peptide Signaling in Mosquitoes: The Road Behind and the Road Ahead.

Authors:  Arvind Sharma; Andrew B Nuss; Monika Gulia-Nuss
Journal:  Front Endocrinol (Lausanne)       Date:  2019-03-22       Impact factor: 5.555

6.  A Drosophila insulin-like peptide promotes growth during nonfeeding states.

Authors:  Maija Slaidina; Rénald Delanoue; Sebastian Gronke; Linda Partridge; Pierre Léopold
Journal:  Dev Cell       Date:  2009-12       Impact factor: 12.270

7.  Sustained activation of Akt elicits mitochondrial dysfunction to block Plasmodium falciparum infection in the mosquito host.

Authors:  Shirley Luckhart; Cecilia Giulivi; Anna L Drexler; Yevgeniya Antonova-Koch; Danielle Sakaguchi; Eleonora Napoli; Sarah Wong; Mark S Price; Richard Eigenheer; Brett S Phinney; Nazzy Pakpour; Jose E Pietri; Kong Cheung; Martha Georgis; Michael Riehle
Journal:  PLoS Pathog       Date:  2013-02-28       Impact factor: 6.823

8.  Conserved mosquito/parasite interactions affect development of Plasmodium falciparum in Africa.

Authors:  Antonio M Mendes; Timm Schlegelmilch; Anna Cohuet; Parfait Awono-Ambene; Maria De Iorio; Didier Fontenille; Isabelle Morlais; George K Christophides; Fotis C Kafatos; Dina Vlachou
Journal:  PLoS Pathog       Date:  2008-05-16       Impact factor: 6.823

9.  The insulin receptor substrate Chico regulates antibacterial immune function in Drosophila.

Authors:  Sarah McCormack; Shruti Yadav; Upasana Shokal; Eric Kenney; Dustin Cooper; Ioannis Eleftherianos
Journal:  Immun Ageing       Date:  2016-05-01       Impact factor: 6.400

10.  A new malaria vector in Africa: Predicting the expansion range of Anopheles stephensi and identifying the urban populations at risk.

Authors:  M E Sinka; S Pironon; N C Massey; J Longbottom; J Hemingway; C L Moyes; K J Willis
Journal:  Proc Natl Acad Sci U S A       Date:  2020-09-14       Impact factor: 11.205

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