Transmission blocking immunity in the malaria non-vector mosquito Anopheles quadriannulatus species A.

Despite being phylogenetically very close to Anopheles gambiae, the major mosquito vector of human malaria in Africa, Anopheles quadriannulatus is thought to be a non-vector. Understanding the difference between vector and non-vector mosquitoes can facilitate development of novel malaria control str...

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Main Authors: Tibebu Habtewold, Michael Povelones, Andrew M Blagborough, George K Christophides
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-05-01
Series:PLoS Pathogens
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18497855/?tool=EBI
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spelling doaj-4601efad7c8f443c812200ee6df2a1682021-04-21T17:19:49ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742008-05-0145e100007010.1371/journal.ppat.1000070Transmission blocking immunity in the malaria non-vector mosquito Anopheles quadriannulatus species A.Tibebu HabtewoldMichael PovelonesAndrew M BlagboroughGeorge K ChristophidesDespite being phylogenetically very close to Anopheles gambiae, the major mosquito vector of human malaria in Africa, Anopheles quadriannulatus is thought to be a non-vector. Understanding the difference between vector and non-vector mosquitoes can facilitate development of novel malaria control strategies. We demonstrate that An. quadriannulatus is largely resistant to infections by the human parasite Plasmodium falciparum, as well as by the rodent parasite Plasmodium berghei. By using genetics and reverse genetics, we show that resistance is controlled by quantitative heritable traits and manifested by lysis or melanization of ookinetes in the mosquito midgut, as well as by killing of parasites at subsequent stages of their development in the mosquito. Genes encoding two leucine-rich repeat proteins, LRIM1 and LRIM2, and the thioester-containing protein, TEP1, are identified as essential in these immune reactions. Their silencing completely abolishes P. berghei melanization and dramatically increases the number of oocysts, thus transforming An. quadriannulatus into a highly permissive parasite host. We hypothesize that the mosquito immune system is an important cause of natural refractoriness to malaria and that utilization of this innate capacity of mosquitoes could lead to new methods to control transmission of the disease.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18497855/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Tibebu Habtewold
Michael Povelones
Andrew M Blagborough
George K Christophides
spellingShingle Tibebu Habtewold
Michael Povelones
Andrew M Blagborough
George K Christophides
Transmission blocking immunity in the malaria non-vector mosquito Anopheles quadriannulatus species A.
PLoS Pathogens
author_facet Tibebu Habtewold
Michael Povelones
Andrew M Blagborough
George K Christophides
author_sort Tibebu Habtewold
title Transmission blocking immunity in the malaria non-vector mosquito Anopheles quadriannulatus species A.
title_short Transmission blocking immunity in the malaria non-vector mosquito Anopheles quadriannulatus species A.
title_full Transmission blocking immunity in the malaria non-vector mosquito Anopheles quadriannulatus species A.
title_fullStr Transmission blocking immunity in the malaria non-vector mosquito Anopheles quadriannulatus species A.
title_full_unstemmed Transmission blocking immunity in the malaria non-vector mosquito Anopheles quadriannulatus species A.
title_sort transmission blocking immunity in the malaria non-vector mosquito anopheles quadriannulatus species a.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2008-05-01
description Despite being phylogenetically very close to Anopheles gambiae, the major mosquito vector of human malaria in Africa, Anopheles quadriannulatus is thought to be a non-vector. Understanding the difference between vector and non-vector mosquitoes can facilitate development of novel malaria control strategies. We demonstrate that An. quadriannulatus is largely resistant to infections by the human parasite Plasmodium falciparum, as well as by the rodent parasite Plasmodium berghei. By using genetics and reverse genetics, we show that resistance is controlled by quantitative heritable traits and manifested by lysis or melanization of ookinetes in the mosquito midgut, as well as by killing of parasites at subsequent stages of their development in the mosquito. Genes encoding two leucine-rich repeat proteins, LRIM1 and LRIM2, and the thioester-containing protein, TEP1, are identified as essential in these immune reactions. Their silencing completely abolishes P. berghei melanization and dramatically increases the number of oocysts, thus transforming An. quadriannulatus into a highly permissive parasite host. We hypothesize that the mosquito immune system is an important cause of natural refractoriness to malaria and that utilization of this innate capacity of mosquitoes could lead to new methods to control transmission of the disease.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18497855/?tool=EBI
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