Chaaithanya Itta Krishna, Muruganandam Nagarajan, Surya Palani, Anwesh Maile, Alagarasu Kalichamy, Vijayachari Paluru
1 Regional Medical Research Centre (ICMR) , Port Blair, Andaman and Nicobar Islands, India .
2 Regional Medical Research Centre (ICMR) , Nehru Nagar, Belgaum, Karnataka, India .
DNA Cell Biol. 2016 Jan;35(1):44-50. doi: 10.1089/dna.2015.2819. Epub 2015 Sep 23.
Biology and pathogenesis of chikungunya virus (CHIKV) are not clearly established. Host factors play an important role in determining the progression and severity of the disease. Polymorphisms in the promoter region of CD209 gene (rs735239, rs4804803, rs2287886) and OAS1 (rs1131454 and rs10774671), OAS2 (rs15895 and rs1732778), and OAS3 (rs2285932 and rs2072136) genes were investigated in 100 patients with CHIKV infection and 101 healthy controls to find out the association of these polymorphisms with CHIKV infection. To evaluate the association of OAS and CD209 gene polymorphisms with the presence or absence of disease symptoms in CHIKV-infected patients. DNA was extracted and typed using polymerase chain reaction followed by restriction fragment length polymorphism methods. Results revealed that the allele and genotype frequencies of OAS1, OAS3, and OAS2 gene polymorphisms were not different between healthy controls and CHIKV patients. The frequency of CD209 gene G/G genotype of rs4804803 was significantly higher in CHIKV patients compared to healthy controls (p = 0.046). The present study suggests that rs4804803 GG genotype of CD209 gene is associated with susceptibility to CHIKV infection. To conclude, the present preliminary study suggests that OAS gene cluster and CD209 gene polymorphisms influence the risk of developing clinical symptoms in CHIKV-infected patients. Further follow-up studies with a large number of samples are needed to assess the role of these genes in association with post-sequela symptoms observed in CHIKV patients. A detailed research is required in these directions to understand the biology behind CHIKV infection and disease severity.
基孔肯雅病毒(CHIKV)的生物学特性和发病机制尚未明确。宿主因素在决定疾病的进展和严重程度方面起着重要作用。对100例CHIKV感染患者和101例健康对照者进行了CD209基因(rs735239、rs4804803、rs2287886)以及OAS1(rs1131454和rs10774671)、OAS2(rs15895和rs1732778)和OAS3(rs2285932和rs2072136)基因启动子区域多态性的研究,以确定这些多态性与CHIKV感染的关联。为了评估OAS和CD209基因多态性与CHIKV感染患者疾病症状有无的关联。采用聚合酶链反应结合限制性片段长度多态性方法提取DNA并进行分型。结果显示,健康对照者和CHIKV患者之间OAS1、OAS3和OAS2基因多态性的等位基因和基因型频率没有差异。与健康对照者相比,CHIKV患者中rs4804803的CD209基因G/G基因型频率显著更高(p = 0.046)。本研究表明,CD209基因的rs4804803 GG基因型与CHIKV感染易感性相关。总之,本初步研究表明,OAS基因簇和CD209基因多态性影响CHIKV感染患者出现临床症状的风险。需要进一步进行大量样本的随访研究,以评估这些基因在CHIKV患者观察到的后遗症症状中的作用。需要在这些方向上进行详细研究,以了解CHIKV感染和疾病严重程度背后的生物学机制。