학술논문
Genome-wide association study identifies human genetic variants associated with fatal outcome from Lassa fever
Document Type
Original Paper
Author
Kotliar, Dylan; Raju, Siddharth; Tabrizi, Shervin; Odia, Ikponmwosa; Goba, Augustine; Momoh, Mambu; Sandi, John Demby; Nair, Parvathy; Phelan, Eric; Tariyal, Ridhi; Eromon, Philomena E.; Mehta, Samar; Robles-Sikisaka, Refugio; Siddle, Katherine J.; Stremlau, Matt; Jalloh, Simbirie; Gire, Stephen K.; Winnicki, Sarah; Chak, Bridget; Schaffner, Stephen F.; Pauthner, Matthias; Karlsson, Elinor K.; Chapin, Sarah R.; Kennedy, Sharon G.; Branco, Luis M.; Kanneh, Lansana; Vitti, Joseph J.; Broodie, Nisha; Gladden-Young, Adrianne; Omoniwa, Omowunmi; Jiang, Pan-Pan; Yozwiak, Nathan; Heuklom, Shannon; Moses, Lina M.; Akpede, George O.; Asogun, Danny A.; Rubins, Kathleen; Kales, Susan; Happi, Anise N.; Iruolagbe, Christopher O.; Dic-Ijiewere, Mercy; Iraoyah, Kelly; Osazuwa, Omoregie O.; Okonkwo, Alexander K.; Kunz, Stefan; McCormick, Joseph B.; Khan, S. Humarr; Honko, Anna N.; Lander, Eric S.; Oldstone, Michael B. A.; Hensley, Lisa; Folarin, Onikepe A.; Okogbenin, Sylvanus A.; Günther, Stephan; Ollila, Hanna M.; Tewhey, Ryan; Okokhere, Peter O.; Schieffelin, John S.; Andersen, Kristian G.; Reilly, Steven K.; Grant, Donald S.; Garry, Robert F.; Barnes, Kayla G.; Happi, Christian T.; Sabeti, Pardis C.
Source
Nature Microbiology. 9(3):751-762
Subject
Language
English
ISSN
2058-5276
Abstract
Infection with Lassa virus (LASV) can cause Lassa fever, a haemorrhagic illness with an estimated fatality rate of 29.7%, but causes no or mild symptoms in many individuals. Here, to investigate whether human genetic variation underlies the heterogeneity of LASV infection, we carried out genome-wide association studies (GWAS) as well as seroprevalence surveys, human leukocyte antigen typing and high-throughput variant functional characterization assays. We analysed Lassa fever susceptibility and fatal outcomes in 533 cases of Lassa fever and 1,986 population controls recruited over a 7 year period in Nigeria and Sierra Leone. We detected genome-wide significant variant associations with Lassa fever fatal outcomes near GRM7 and LIF in the Nigerian cohort. We also show that a haplotype bearing signatures of positive selection and overlapping LARGE1, a required LASV entry factor, is associated with decreased risk of Lassa fever in the Nigerian cohort but not in the Sierra Leone cohort. Overall, we identified variants and genes that may impact the risk of severe Lassa fever, demonstrating how GWAS can provide insight into viral pathogenesis.
GWAS in difficult-to-recruit populations identifies variants associated with Lassa fever outcome and susceptibility at loci proximal to LIF, GRM7 and LARGE1.
GWAS in difficult-to-recruit populations identifies variants associated with Lassa fever outcome and susceptibility at loci proximal to LIF, GRM7 and LARGE1.