TY - JOUR
T1 - Geographical distribution of complement receptor type 1 variants and their associated disease risk
AU - Sandri, Thaisa Lucas
AU - Adukpo, Selorme
AU - Giang, Dao Phuong
AU - Nguetse, Christian N.
AU - Andrade, Fabiana Antunes
AU - Van Tong, Hoang
AU - Toan, Nguyen Linh
AU - Song, Le Huu
AU - Elumalai, Preetham
AU - Thangaraj, Kumarasamy
AU - Valluri, Vijaya Lakshmi
AU - Ntoumi, Francine
AU - Meyer, Christian G.
AU - De Messias Reason, Iara Jose
AU - Kremsner, Peter G.
AU - Velavan, Thirumalaisamy P.
N1 - Publisher Copyright:
© 2017 Lucas Sandri et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2017/5
Y1 - 2017/5
N2 - Background Pathogens exert selective pressure which may lead to substantial changes in host immune responses. The human complement receptor type 1 (CR1) is an innate immune recognition glycoprotein that regulates the activation of the complement pathway and removes opsonized immune complexes. CR1 genetic variants in exon 29 have been associated with expression levels, C1q or C3b binding and increased susceptibility to several infectious diseases. Five distinct CR1 nucleotide substitutions determine the Knops blood group phenotypes, namely Kna/b, McCa/b, Sl1/Sl2, Sl4/Sl5 and KCAM+/-. Methods CR1 variants were genotyped by direct sequencing in a cohort of 441 healthy individuals from Brazil, Vietnam, India, Republic of Congo and Ghana. Results The distribution of the CR1 alleles, genotypes and haplotypes differed significantly among geographical settings (p0.001). CR1 variants rs17047660A/G (McCa/b) and rs17047661A/G (Sl1/Sl2) were exclusively observed to be polymorphic in African populations compared to the groups from Asia and South-America, strongly suggesting that these two SNPs may be subjected to selection. This is further substantiated by a high linkage disequilibrium between the two variants in the Congolese and Ghanaian populations. A total of nine CR1 haplotypes were observed. The CR1-AGAATA haplotype was found more frequently among the Brazilian and Vietnamese study groups; the CR1-AGAATG haplotype was frequent in the Indian and Vietnamese populations, while the CR1-AGAGTG haplotype was frequent among Congolese and Ghanaian individuals. Conclusion The African populations included in this study might have a selective advantage conferred to immune genes involved in pathogen recognition and signaling, possibly contributing to disease susceptibility or resistance.
AB - Background Pathogens exert selective pressure which may lead to substantial changes in host immune responses. The human complement receptor type 1 (CR1) is an innate immune recognition glycoprotein that regulates the activation of the complement pathway and removes opsonized immune complexes. CR1 genetic variants in exon 29 have been associated with expression levels, C1q or C3b binding and increased susceptibility to several infectious diseases. Five distinct CR1 nucleotide substitutions determine the Knops blood group phenotypes, namely Kna/b, McCa/b, Sl1/Sl2, Sl4/Sl5 and KCAM+/-. Methods CR1 variants were genotyped by direct sequencing in a cohort of 441 healthy individuals from Brazil, Vietnam, India, Republic of Congo and Ghana. Results The distribution of the CR1 alleles, genotypes and haplotypes differed significantly among geographical settings (p0.001). CR1 variants rs17047660A/G (McCa/b) and rs17047661A/G (Sl1/Sl2) were exclusively observed to be polymorphic in African populations compared to the groups from Asia and South-America, strongly suggesting that these two SNPs may be subjected to selection. This is further substantiated by a high linkage disequilibrium between the two variants in the Congolese and Ghanaian populations. A total of nine CR1 haplotypes were observed. The CR1-AGAATA haplotype was found more frequently among the Brazilian and Vietnamese study groups; the CR1-AGAATG haplotype was frequent in the Indian and Vietnamese populations, while the CR1-AGAGTG haplotype was frequent among Congolese and Ghanaian individuals. Conclusion The African populations included in this study might have a selective advantage conferred to immune genes involved in pathogen recognition and signaling, possibly contributing to disease susceptibility or resistance.
UR - http://www.scopus.com/inward/record.url?scp=85019901467&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0175973
DO - 10.1371/journal.pone.0175973
M3 - Article
C2 - 28520715
AN - SCOPUS:85019901467
SN - 1932-6203
VL - 12
JO - PLoS ONE
JF - PLoS ONE
IS - 5
M1 - e0175973
ER -