Literature DB >> 28494453

The Peptidoglycan Recognition Proteins PGRPLA and PGRPLB Regulate Anopheles Immunity to Bacteria and Affect Infection by Plasmodium.

Mathilde Gendrin1, Fanny Turlure, Faye H Rodgers, Anna Cohuet, Isabelle Morlais, George K Christophides.   

Abstract

Peptidoglycan recognition proteins (PGRPs) form a family of immune regulators that is conserved from insects to mammals. In the malaria vector mosquito Anophelescoluzzii, the peptidoglycan receptor PGRPLC activates the immune-deficiency (Imd) pathway limiting both the microbiota load and Plasmodium infection. Here, we carried out an RNA interference screen to examine the role of all 7 Anopheles PGRPs in infections with Plasmodium berghei and P. falciparum. We show that, in addition to PGRPLC, PGRPLA and PGRPS2/PGRPS3 also participate in antiparasitic defenses, and that PGRPLB promotes mosquito permissiveness to P. falciparum. We also demonstrate that following a mosquito blood feeding, which promotes growth of the gut microbiota, PGRPLA and PGRPLB positively and negatively regulate the activation of the Imd pathway, respectively. Our data demonstrate that PGRPs are important regulators of the mosquito epithelial immunity and vector competence.
© 2017 The Author(s) Published by S. Karger AG, Basel.

Entities:  

Keywords:  Anopheles; Antimicrobial peptides; Bacteria; Drosophila; Immune-deficiency pathway; Microbiota; Peptidoglycan recognition protein; Plasmodium

Mesh:

Substances:

Year:  2017        PMID: 28494453      PMCID: PMC5569699          DOI: 10.1159/000452797

Source DB:  PubMed          Journal:  J Innate Immun        ISSN: 1662-811X            Impact factor:   7.349


  25 in total

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4.  PGRP-LC and PGRP-LE have essential yet distinct functions in the drosophila immune response to monomeric DAP-type peptidoglycan.

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5.  Anopheles gambiae PGRPLC-mediated defense against bacteria modulates infections with malaria parasites.

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6.  A Plasmodium berghei reference line that constitutively expresses GFP at a high level throughout the complete life cycle.

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4.  Insulin-like peptide 3 stimulates hemocytes to proliferate in anautogenous and facultatively autogenous mosquitoes.

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Review 8.  The tripartite interactions between the mosquito, its microbiota and Plasmodium.

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9.  PGRP-LD mediates A. stephensi vector competency by regulating homeostasis of microbiota-induced peritrophic matrix synthesis.

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Review 10.  The mosquito holobiont: fresh insight into mosquito-microbiota interactions.

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