Further evidence supporting a role for gs signal transduction in severe malaria pathogenesis.

With the functional demonstration of a role in erythrocyte invasion by Plasmodium falciparum parasites, implications in the aetiology of common conditions that prevail in individuals of African origin, and a wealth of pharmacological knowledge, the stimulatory G protein (Gs) signal transduction path...

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Main Authors: Sarah Auburn, Andrew E Fry, Taane G Clark, Susana Campino, Mahamadou Diakite, Angela Green, Anna Richardson, Muminatou Jallow, Fatou Sisay-Joof, Margaret Pinder, Malcolm E Molyneux, Terrie E Taylor, Kasturi Haldar, Kirk A Rockett, Dominic P Kwiatkowski
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-04-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0010017&type=printable
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author Sarah Auburn
Andrew E Fry
Taane G Clark
Susana Campino
Mahamadou Diakite
Angela Green
Anna Richardson
Muminatou Jallow
Fatou Sisay-Joof
Margaret Pinder
Malcolm E Molyneux
Terrie E Taylor
Kasturi Haldar
Kirk A Rockett
Dominic P Kwiatkowski
author_facet Sarah Auburn
Andrew E Fry
Taane G Clark
Susana Campino
Mahamadou Diakite
Angela Green
Anna Richardson
Muminatou Jallow
Fatou Sisay-Joof
Margaret Pinder
Malcolm E Molyneux
Terrie E Taylor
Kasturi Haldar
Kirk A Rockett
Dominic P Kwiatkowski
author_sort Sarah Auburn
collection DOAJ
description With the functional demonstration of a role in erythrocyte invasion by Plasmodium falciparum parasites, implications in the aetiology of common conditions that prevail in individuals of African origin, and a wealth of pharmacological knowledge, the stimulatory G protein (Gs) signal transduction pathway presents an exciting target for anti-malarial drug intervention. Having previously demonstrated a role for the G-alpha-s gene, GNAS, in severe malaria disease, we sought to identify other important components of the Gs pathway. Using meta-analysis across case-control and family trio (affected child and parental controls) studies of severe malaria from The Gambia and Malawi, we sought evidence of association in six Gs pathway candidate genes: adenosine receptor 2A (ADORA2A) and 2B (ADORA2B), beta-adrenergic receptor kinase 1 (ADRBK1), adenylyl cyclase 9 (ADCY9), G protein beta subunit 3 (GNB3), and regulator of G protein signalling 2 (RGS2). Our study amassed a total of 2278 cases and 2364 controls. Allele-based models of association were investigated in all genes, and genotype and haplotype-based models were investigated where significant allelic associations were identified. Although no significant associations were observed in the other genes, several were identified in ADORA2A. The most significant association was observed at the rs9624472 locus, where the G allele (approximately 20% frequency) appeared to confer enhanced risk to severe malaria [OR = 1.22 (1.09-1.37); P = 0.001]. Further investigation of the ADORA2A gene region is required to validate the associations identified here, and to identify and functionally characterize the responsible causal variant(s). Our results provide further evidence supporting a role of the Gs signal transduction pathway in the regulation of severe malaria, and request further exploration of this pathway in future studies.
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spelling doaj-art-c163fefbb2414fcbaa28ffe5e9fe2cda2025-08-20T03:07:40ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-04-0154e1001710.1371/journal.pone.0010017Further evidence supporting a role for gs signal transduction in severe malaria pathogenesis.Sarah AuburnAndrew E FryTaane G ClarkSusana CampinoMahamadou DiakiteAngela GreenAnna RichardsonMuminatou JallowFatou Sisay-JoofMargaret PinderMalcolm E MolyneuxTerrie E TaylorKasturi HaldarKirk A RockettDominic P KwiatkowskiWith the functional demonstration of a role in erythrocyte invasion by Plasmodium falciparum parasites, implications in the aetiology of common conditions that prevail in individuals of African origin, and a wealth of pharmacological knowledge, the stimulatory G protein (Gs) signal transduction pathway presents an exciting target for anti-malarial drug intervention. Having previously demonstrated a role for the G-alpha-s gene, GNAS, in severe malaria disease, we sought to identify other important components of the Gs pathway. Using meta-analysis across case-control and family trio (affected child and parental controls) studies of severe malaria from The Gambia and Malawi, we sought evidence of association in six Gs pathway candidate genes: adenosine receptor 2A (ADORA2A) and 2B (ADORA2B), beta-adrenergic receptor kinase 1 (ADRBK1), adenylyl cyclase 9 (ADCY9), G protein beta subunit 3 (GNB3), and regulator of G protein signalling 2 (RGS2). Our study amassed a total of 2278 cases and 2364 controls. Allele-based models of association were investigated in all genes, and genotype and haplotype-based models were investigated where significant allelic associations were identified. Although no significant associations were observed in the other genes, several were identified in ADORA2A. The most significant association was observed at the rs9624472 locus, where the G allele (approximately 20% frequency) appeared to confer enhanced risk to severe malaria [OR = 1.22 (1.09-1.37); P = 0.001]. Further investigation of the ADORA2A gene region is required to validate the associations identified here, and to identify and functionally characterize the responsible causal variant(s). Our results provide further evidence supporting a role of the Gs signal transduction pathway in the regulation of severe malaria, and request further exploration of this pathway in future studies.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0010017&type=printable
spellingShingle Sarah Auburn
Andrew E Fry
Taane G Clark
Susana Campino
Mahamadou Diakite
Angela Green
Anna Richardson
Muminatou Jallow
Fatou Sisay-Joof
Margaret Pinder
Malcolm E Molyneux
Terrie E Taylor
Kasturi Haldar
Kirk A Rockett
Dominic P Kwiatkowski
Further evidence supporting a role for gs signal transduction in severe malaria pathogenesis.
PLoS ONE
title Further evidence supporting a role for gs signal transduction in severe malaria pathogenesis.
title_full Further evidence supporting a role for gs signal transduction in severe malaria pathogenesis.
title_fullStr Further evidence supporting a role for gs signal transduction in severe malaria pathogenesis.
title_full_unstemmed Further evidence supporting a role for gs signal transduction in severe malaria pathogenesis.
title_short Further evidence supporting a role for gs signal transduction in severe malaria pathogenesis.
title_sort further evidence supporting a role for gs signal transduction in severe malaria pathogenesis
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0010017&type=printable
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