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基因和 基因中的功能性单核苷酸多态性影响印度马哈拉施特拉邦感染甲型流感(H1N1)pdm09 病毒患者的疾病严重程度。

Functional Single-Nucleotide Polymorphisms in the and Genes Influence Disease Severity in Influenza A (H1N1)pdm09 Virus-Infected Patients from Maharashtra, India.

机构信息

ICMR-National Institute of Virology, Pune, India.

Jehangir Hospital Research Center, Pune, India.

出版信息

Viral Immunol. 2022 May;35(4):303-309. doi: 10.1089/vim.2021.0179. Epub 2022 Feb 22.

DOI:10.1089/vim.2021.0179
PMID:35196173
Abstract

The clinical outcome in influenza A (H1N1)pdm09 virus-infected subjects is determined by several factors, including host genetics. In the present study, single-nucleotide polymorphisms (SNPs) in the , and genes were investigated in influenza A (H1N1)pdm09 virus-infected subjects to find out their association with disease severity. Influenza A (H1N1)pdm09 virus-infected subjects with severe disease ( = 86) and mild disease ( = 293) from western India were included in the study. The SNPs were investigated by PCR-based methods. The results revealed a higher frequency of rs5743313 T/T genotype [odds ratio (OR) with 95% confidence interval (CI) 2.55 (1.08-6.04)  = 0.039] and two-locus haplotype rs3775291-rs3775290 T-A [OR with 95% CI 7.94 (2.05-30.68)] in severe cases. Lower frequency of the mutant allele of rs1800450 [OR with 95% CI 0.51 (0.27-0.87),  = 0.01] and two-locus haplotype rs3775291-rs3775290 T-G [OR with 95% CI 0.48 (0.27-0.85)] was observed in severe cases compared with cases with mild disease. Higher frequency of two-locus haplotype rs3775291-rs3775290 T-A was observed in severe cases [OR with 95% CI 7.9 (2.0-30.7)]. The allele and genotype frequencies of other SNPs were not different between the study categories. The results suggest that the functional SNPs in and are associated with severe disease in influenza A (H1N1)pdm09 virus-infected subjects.

摘要

甲型流感病毒(H1N1)pdm09 感染患者的临床结局受多种因素影响,包括宿主遗传因素。本研究旨在探讨甲型流感病毒(H1N1)pdm09 感染患者中 、 和 基因的单核苷酸多态性(SNP)与疾病严重程度的关系。本研究纳入了来自印度西部的甲型流感病毒(H1N1)pdm09 感染患者,其中重症患者(n=86)和轻症患者(n=293)。采用基于 PCR 的方法检测 SNP。结果显示,重症患者中 rs5743313 T/T 基因型的频率较高(比值比[OR]及其 95%置信区间[CI]为 2.55[1.08-6.04],P=0.039),rs3775291-rs3775290 二联体 haplotype T-A 的频率也较高(OR 及其 95%CI 为 7.94[2.05-30.68],P=0.004)。与轻症患者相比,重症患者中 rs1800450 突变等位基因的频率较低(OR 及其 95%CI 为 0.51[0.27-0.87],P=0.01),rs3775291-rs3775290 二联体 haplotype T-G 的频率也较低(OR 及其 95%CI 为 0.48[0.27-0.85],P=0.01)。重症患者中 rs3775291-rs3775290 二联体 haplotype T-A 的频率较高(OR 及其 95%CI 为 7.9[2.0-30.7],P=0.004)。其他 SNP 的等位基因和基因型频率在不同研究组间无差异。研究结果表明,甲型流感病毒(H1N1)pdm09 感染患者中 和 基因的功能性 SNP 与疾病严重程度相关。

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