TY - JOUR
T1 - Genetic Ancestry and Natural Selection Drive Population Differences in Immune Responses to Pathogens
AU - Nédélec, Yohann
AU - Sanz, Joaquín
AU - Baharian, Golshid
AU - Szpiech, Zachary A.
AU - Pacis, Alain
AU - Dumaine, Anne
AU - Grenier, Jean Christophe
AU - Freiman, Andrew
AU - Sams, Aaron J.
AU - Hebert, Steven
AU - Pagé Sabourin, Ariane
AU - Luca, Francesca
AU - Blekhman, Ran
AU - Hernandez, Ryan D.
AU - Pique-Regi, Roger
AU - Tung, Jenny
AU - Yotova, Vania
AU - Barreiro, Luis B.
N1 - Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2016/10/20
Y1 - 2016/10/20
N2 - Individuals from different populations vary considerably in their susceptibility to immune-related diseases. To understand how genetic variation and natural selection contribute to these differences, we tested for the effects of African versus European ancestry on the transcriptional response of primary macrophages to live bacterial pathogens. A total of 9.3% of macrophage-expressed genes show ancestry-associated differences in the gene regulatory response to infection, and African ancestry specifically predicts a stronger inflammatory response and reduced intracellular bacterial growth. A large proportion of these differences are under genetic control: for 804 genes, more than 75% of ancestry effects on the immune response can be explained by a single cis- or trans-acting expression quantitative trait locus (eQTL). Finally, we show that genetic effects on the immune response are strongly enriched for recent, population-specific signatures of adaptation. Together, our results demonstrate how historical selective events continue to shape human phenotypic diversity today, including for traits that are key to controlling infection.
AB - Individuals from different populations vary considerably in their susceptibility to immune-related diseases. To understand how genetic variation and natural selection contribute to these differences, we tested for the effects of African versus European ancestry on the transcriptional response of primary macrophages to live bacterial pathogens. A total of 9.3% of macrophage-expressed genes show ancestry-associated differences in the gene regulatory response to infection, and African ancestry specifically predicts a stronger inflammatory response and reduced intracellular bacterial growth. A large proportion of these differences are under genetic control: for 804 genes, more than 75% of ancestry effects on the immune response can be explained by a single cis- or trans-acting expression quantitative trait locus (eQTL). Finally, we show that genetic effects on the immune response are strongly enriched for recent, population-specific signatures of adaptation. Together, our results demonstrate how historical selective events continue to shape human phenotypic diversity today, including for traits that are key to controlling infection.
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U2 - 10.1016/j.cell.2016.09.025
DO - 10.1016/j.cell.2016.09.025
M3 - Article
AN - SCOPUS:84992381901
SN - 0092-8674
VL - 167
SP - 657-669.e21
JO - Cell
JF - Cell
IS - 3
ER -