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Δ 基因型与流行性肾病的轻度形式有关。

Δ Genotype Is Associated with Mild Form of Nephropathia Epidemica.

机构信息

Openlab "Gene and Cell Technologies", Institute of Fundamental Medicine and Biology Kazan Federal University, Kazan 420008, Republic of Tatarstan, Russian.

Department of Infectious Diseases, Kazan State Medical Academy, Kazan 420012, the Republic of Tatarstan, Russian.

出版信息

Viruses. 2019 Jul 23;11(7):675. doi: 10.3390/v11070675.

DOI:10.3390/v11070675
PMID:31340562
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6669606/
Abstract

Nephropathia Epidemica (NE), a mild form of hemorrhagic fever with renal syndrome (HFRS) and linked to hantavirus infection, is endemic in the Republic of Tatarstan. Several genetic markers of HFRS severity have been identified previously, including human leukocyte antigen (HLA) complexes and nucleotide polymorphism in the tumor necrosis factor alpha () gene. Still, our understanding of the genetic markers of NE severity remains incomplete. The frequency of the C-C chemokine receptor type 5 () gene wild type and gene with 32-base-pair deletion (Δ) genotypes in 98 NE samples and 592 controls was analyzed using PCR. Along with the serum levels of 94 analytes, a lack of differences in the genotype distribution between NE cases and the general population suggests that the genotype does not affect susceptibility to hantavirus infection. However, in NE cases, significant variation in the serum levels of the host matrix metalloproteases between functional homozygous and Δ heterozygous patients was detected. Also, the oliguric phase was longer, while thrombocyte counts were lower in functional homozygous as compared to heterozygous NE cases. Our data, for the first time, presents the potential role of the receptor genotype in NE pathogenesis. Our data suggests that NE pathogenesis in functional homozygous and heterozygous NE patients differs, where homozygous cases may have more disintegration of the extracellular matrix and potentially more severe disease.

摘要

肾综合征出血热(HFRS)是一种温和的出血热,与汉坦病毒感染有关,在鞑靼斯坦共和国流行。以前已经确定了一些 HFRS 严重程度的遗传标记,包括人类白细胞抗原(HLA)复合物和肿瘤坏死因子 alpha () 基因中的核苷酸多态性。尽管如此,我们对 NE 严重程度的遗传标记的了解仍然不完整。使用 PCR 分析了 98 个 NE 样本和 592 个对照中的 C-C 趋化因子受体 5 () 基因野生型和 32 碱基对缺失(Δ)基因型的频率。除了 94 种分析物的血清水平外,NE 病例与一般人群之间的 基因型分布没有差异表明该基因型不影响汉坦病毒感染的易感性。然而,在 NE 病例中,在功能 纯合子和 Δ杂合子患者之间检测到宿主基质金属蛋白酶的血清水平存在显著差异。此外,与杂合子 NE 病例相比,功能性 纯合子的少尿期更长,血小板计数更低。我们的数据首次提出了 受体基因型在 NE 发病机制中的潜在作用。我们的数据表明,功能性 纯合子和杂合子 NE 患者的 NE 发病机制不同,其中纯合子病例可能具有更多的细胞外基质解体,并且可能具有更严重的疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b6/6669606/f02be7e10bbe/viruses-11-00675-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b6/6669606/65f25ed5371d/viruses-11-00675-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b6/6669606/7581d510bcf1/viruses-11-00675-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b6/6669606/9555c513c011/viruses-11-00675-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b6/6669606/a17599ce21b0/viruses-11-00675-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b6/6669606/bcdf14cfa44a/viruses-11-00675-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b6/6669606/f02be7e10bbe/viruses-11-00675-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b6/6669606/65f25ed5371d/viruses-11-00675-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b6/6669606/7581d510bcf1/viruses-11-00675-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b6/6669606/9555c513c011/viruses-11-00675-g003.jpg
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