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Phylogenetic analysis of Dengue virus 1 isolated from South Minas Gerais Brazil

机译:从巴西南米纳斯吉拉斯州分离出的登革热病毒1的系统发育分析

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摘要

Dengue is a major worldwide public health problem, especially in the tropical and subtropical regions of the world. Primary infection with a single Dengue virus serotype causes a mild, self-limiting febrile illness called dengue fever. However, a subset of patients who experience secondary infection with a different serotype can progress to a more severe form of the disease, called dengue hemorrhagic fever. The four Dengue virus serotypes (1–4) are antigenically and genetically distinct and each serotype is composed of multiple genotypes. In this study we isolated one Dengue virus 1 serotype, named BR/Alfenas/2012, from a patient with dengue hemorrhagic fever in Alfenas, South Minas Gerais, Brazil and molecular identification was performed based on the analysis of NS5 gene. Swiss mice were infected with this isolate to verify its potential to induce histopathological alterations characteristic of dengue. Liver histopathological analysis of infected animals showed the presence of inflammatory infiltrates, hepatic steatosis, as well as edema, hemorrhage and necrosis focal points. Phylogenetic and evolutionary analyses based on the envelope gene provided evidence that the isolate BR/Alfenas/2012 belongs to genotype V, lineage I and it is probably derived from isolates of Rio de Janeiro, Brazil. The isolate BR/Alfenas/2012 showed two unique amino acids substitutions (SER222THRE and PHE306SER) when compared to other Brazilian isolates from the same genotype/lineage. Molecular models were generated for the envelope protein indicating that the amino acid alteration PHE 306 SER could contribute to a different folding in this region located within the domain III. Further genetic and animal model studies using BR/Alfenas/2012 and other isolates belonging to the same lineage/genotype could help determine the relation of these genetic alterations and dengue hemorrhagic fever in a susceptible population.
机译:登革热是全球主要的公共卫生问题,尤其是在世界热带和亚热带地区。单一登革热病毒血清型的初次感染会引起一种轻度,自限性的发热疾病,称为登革热。但是,经历不同血清型继发感染的一部分患者会发展为更严重的疾病形式,称为登革出血热。四种登革热病毒血清型(1-4)在抗原和遗传上截然不同,每种血清型均由多种基因型组成。在这项研究中,我们从巴西南米纳斯吉拉斯州阿尔菲纳斯的一名患有登革出血热的患者中分离出了一种名为BR / Alfenas / 2012的登革热病毒1型血清型,并根据NS5基因的分析进行了分子鉴定。瑞士小鼠感染了这种分离株,以验证其诱发登革热组织病理学改变的潜力。感染动物的肝脏组织病理学分析显示存在炎性浸润,肝脂肪变性以及水肿,出血和坏死灶。基于包膜基因的系统发育和进化分析提供了证据,证明分离株BR / Alfenas / 2012属于基因型V,谱系I,它可能来自巴西里约热内卢的分离株。与来自相同基因型/谱系的其他巴西分离株相比,BR / Alfenas / 2012分离株表现出两个独特的氨基酸取代(SER222THRE和PHE306SER)。为包膜蛋白生成了分子模型,表明氨基酸改变PHE 306 SER可能有助于位于结构域III内该区域的不同折叠。使用BR / Alfenas / 2012和其他属于同一谱系/基因型的分离株进行进一步的遗传和动物模型研究,可以帮助确定易感人群中这些遗传变异与登革出血热的关系。

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