UGSpace Repository

Geographical distribution of complement receptor type 1 variants and their associated disease risk

Show simple item record

dc.contributor.author Sandri, T.L.
dc.contributor.author Adukpo, S.
dc.contributor.author Giang, D.P.
dc.contributor.author Nguetse, C.N.
dc.contributor.author Andrade, F.A.
dc.contributor.author Van Tong, H.
dc.contributor.author Toan, N.L.
dc.contributor.author Song, L.H.
dc.contributor.author Elumalai, P.
dc.contributor.author Thangaraj, K.
dc.contributor.author Valluri, V.L.
dc.contributor.author Ntoumi, F.
dc.contributor.author Meyer, C.G.
dc.contributor.author De Messias Reason, I.J.
dc.contributor.author Kremsner, P.G.
dc.contributor.author Velavan, T.P.
dc.date.accessioned 2017-10-25T17:05:40Z
dc.date.available 2017-10-25T17:05:40Z
dc.date.issued 2017
dc.identifier.other 10.1371/journal.pone.0175973
dc.identifier.uri http://ugspace.ug.edu.gh/handle/123456789/22173
dc.description.abstract 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. © 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. en_US
dc.language.iso en en_US
dc.publisher Public Library of Science en_US
dc.title Geographical distribution of complement receptor type 1 variants and their associated disease risk en_US
dc.type Article en_US


Files in this item

This item appears in the following Collection(s)

  • Electron Microscopy Department [77]
    The main research focus of the Electron Microscopy and Histopathology Department in the past 20 years has been in the areas of enteric diarrhoeas with special emphasis on rotavirus. Through its diarrhoea surveillance studies, the Department has helped to firmly establish rotaviruses as a major cause of diarrhoea in children, and document the circulation of unusual rotavirus genotypes in Ghana. The Department has also recently expanded its diagnostic repertoire to include the identification and characterization of noroviruses, astroviruses, and other enteric viruses.

Show simple item record

Search UGSpace


Browse

My Account