The peptidoglycan recognition proteins PGRPLA and PGRPLB regulate Anopheles immunity to bacteria and affect infection by Plasmodium
File(s)452797.pdf (655.03 KB)
Published version
Author(s)
Type
Journal Article
Abstract
Peptidoglycan recognition proteins (PGRPs) form a family of
immune regulators that is conserved
from insects to mammals. In the malaria vector mosquito
Anopheles
coluzzii
, the peptidoglycan
receptor PGRPLC activates the Imd pathway limiting both t
he microbiota load and
Plasmodium
infection. Here, we carried out an RNAi screen to examine the rol
e of all seven
Anopheles
PGRPs in
infections with
Plasmodium berghei
and
Plasmodium falciparum
. We show that, in addition to
PGRPLC, PGRPLA and PGRPS2/S3 also participate in antiparas
itic 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, respective
ly. Our data demonstrate that PGRPs
are important regulators of the mosquito epithelial immunity and vector comp
etence.
immune regulators that is conserved
from insects to mammals. In the malaria vector mosquito
Anopheles
coluzzii
, the peptidoglycan
receptor PGRPLC activates the Imd pathway limiting both t
he microbiota load and
Plasmodium
infection. Here, we carried out an RNAi screen to examine the rol
e of all seven
Anopheles
PGRPs in
infections with
Plasmodium berghei
and
Plasmodium falciparum
. We show that, in addition to
PGRPLC, PGRPLA and PGRPS2/S3 also participate in antiparas
itic 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, respective
ly. Our data demonstrate that PGRPs
are important regulators of the mosquito epithelial immunity and vector comp
etence.
Date Issued
2017-05-12
Date Acceptance
2016-10-24
Citation
Journal of Innate Immunity, 2017, 9 (4), pp.333-342
ISSN
1662-8128
Publisher
Karger Publishers
Start Page
333
End Page
342
Journal / Book Title
Journal of Innate Immunity
Volume
9
Issue
4
Copyright Statement
© 2017 The Author(s) Published by S. Karger AG, Basel. Th is article is licensed under the Creative Commons AttributionNonCommercial-NoDerivatives
4.0 International License (CC BYNC-ND)
(http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes as well as any distribution of modifi ed material requires written permission.
4.0 International License (CC BYNC-ND)
(http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes as well as any distribution of modifi ed material requires written permission.
Sponsor
National Institutes of Health
Commission of the European Communities
Biotechnology and Biological Sciences Research Council (BBSRC)
Grant Number
5 P01 AI044220-07
223736
BB/k009338/1
Subjects
Anopheles
Antimicrobial peptides
Bacteria
Drosophila
Immune-deficiency pathway
Microbiota
Peptidoglycan recognition protein
Plasmodium
11 Medical And Health Sciences
Publication Status
Published