Author(s): Carvalho, A ; Marques, A ; Maciel, P ; Rodrigues, F
Date: 2007
Persistent ID: http://hdl.handle.net/10400.23/364
Origin: Repositório Científico do Hospital de Braga
Project/scholarship: info:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F11837%2F2003/PT; info:eu-repo/grantAgreement/FCT/POCI/61080/PT ;
Subject(s): Polimorfismo Genético; Reacção em Cadeia da Polimerase; Receptor “Toll-like” 4
Toll-like receptors (TLRs) are cellular receptors that mediate recognition of microbial challenges and the subsequent inflammatory response. Genetic variations within these inflammation-associated genes may alter host-pathogen defence mechanisms affecting susceptibility towards infectious diseases. Taking into account the significance of these genes, we developed a simple and rapid method based in the bi-directional PCR amplification of specific alleles (Bi-PASA) for genotyping known sequence variants in TLR4 (Asp299Gly and Thr399Ile) and TLR9 (T-1237C) genes. This method allows genotype determination in a single reaction and is amenable to large-scale analysis. We used Bi-PASA to characterize the distribution of these polymorphisms in the Portuguese population. A total of 388 randomly selected blood donors of Portuguese origin (203 females and 185 males) were genotyped and allele frequencies were determined. Among the tested individuals, 11.1% and 10.8% were heterozygous for Asp299Gly and Thr399Ile, respectively. In what concerns the T-1237C variation in TLR9, the variant allele was present in 19.4% of the individuals tested. Besides confirming the usefulness of the Bi-PASA in polymorphism analysis, the data presented provide valuable information on TLR polymorphisms in the Portuguese population that can be used to stratify risk patients with increased susceptibility to infection.
