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A novel locus of resistance to severe malaria in a region of ancient balancing selection

Auburn, Sarah and Malaria Genomic Epidemiology Network (2015). A novel locus of resistance to severe malaria in a region of ancient balancing selection. Nature,526(7572):253-257.

Document type: Journal Article
Citation counts: Altmetric Score Altmetric Score is 283
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IRMA ID 10444xPUB72
Title A novel locus of resistance to severe malaria in a region of ancient balancing selection
Author Auburn, Sarah
Malaria Genomic Epidemiology Network
Journal Name Nature
Publication Date 2015
Volume Number 526
Issue Number 7572
ISSN 0028-0836   (check CDU catalogue open catalogue search in new window)
Start Page 253
End Page 257
Total Pages 5
Place of Publication United Kingdom
Publisher Nature Publishing Group
Field of Research MEDICAL AND HEALTH SCIENCES
HERDC Category C1 - Journal Article (DIISR)
Abstract The high prevalence of sickle haemoglobin in Africa shows that malaria has been a major force for human evolutionary selection, but surprisingly few other polymorphisms have been proven to confer resistance to malaria in large epidemiological studies1, 2, 3. To address this problem, we conducted a multi-centre genome-wide association study (GWAS) of life-threatening Plasmodium falciparum infection (severe malaria) in over 11,000 African children, with replication data in a further 14,000 individuals. Here we report a novel malaria resistance locus close to a cluster of genes encoding glycophorins that are receptors for erythrocyte invasion by P. falciparum. We identify a haplotype at this locus that provides 33% protection against severe malaria (odds ratio = 0.67, 95% confidence interval = 0.60–0.76, P value = 9.5 × 10−11) and is linked to polymorphisms that have previously been shown to have features of ancient balancing selection, on the basis of haplotype sharing between humans and chimpanzees4. Taken together with previous observations on the malaria-protective role of blood group O1, 2, 3, 5, these data reveal that two of the strongest GWAS signals for severe malaria lie in or close to genes encoding the glycosylated surface coat of the erythrocyte cell membrane, both within regions of the genome where it appears that evolution has maintained diversity for millions of years. These findings provide new insights into the host–parasite interactions that are critical in determining the outcome of malaria infection.
Keywords Genome-wide association studies
Genetic variation
Parasite host response
DOI http://dx.doi.org/10.1038/nature15390   (check subscription with CDU E-Gateway service for CDU Staff and Students  check subscription with CDU E-Gateway in new window)
 
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