用于登革热病毒诊断和研究的实验室检测:现在和未来

Juan Samuel Sulca Herencia
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引用次数: 4

摘要

登革热是一个重大的公共卫生问题。已确定四种登革热病毒血清型;然而,由于存在许多病毒、细菌和寄生虫,产生相同的临床表现,出现在同一地理区域,甚至产生合并感染,因此诊断困难。因此,确定一个人是否已经、曾经或正在感染登革热病毒是非常重要的。为此,已经开发了直接和间接的实验室测试,以确定通常检测抗体反应的病毒或其结构的一部分。这些技术用于诊断、流行病学研究、监测、评估和生产疫苗和抗病毒药物等。它们的范围从使用细胞培养、动物模型、昆虫接种和血清学测试,到使用检测分子测试和遗传物质定量,本章将对此进行描述,并简要说明该方法、其优缺点及其在登革热研究中的应用。分子技术等等。使用试管,6-96孔培养板和其他工具来维持与细胞培养物的结合。改进的壳瓶技术可以回收更多的YFV、SLV、WNV、ILHV、GCV、OROV、MAYV和DENV分离株。该技术遵循与标准方法相同的步骤,但在接种细胞后,将培养物离心至1800至2200 rpm之间。该技术也可用于分离登革热病毒共感染。然而,对VEE的分离效果似乎不太好[19-22]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Laboratory Tests Used in the Diagnostic and Research of Dengue Virus: Present and Future
Dengue is a significant public health problem. There are four dengue virus serotypes identified; however, its diagnosis is difficult due to the existence of many viruses, bac -teria, and parasites producing the same clinical presentation, being present in the same geographical area and even producing coinfections. Therefore, determining whether a person has, had, or is infected with dengue virus is of great importance. In order to do so, direct and indirect laboratory tests have been developed to identify the virus or part of its structure that generally detects the antibody response. These techniques are used for diagnosis, epidemiological studies, monitoring, assessment and production of vaccines and antivirals, etc. They range from the use of cell cultures, animal models, inoculation by insects, and serology tests to the use of detection molecular tests and quantification of genetic material that are described in this chapter herein, a brief explanation of this methodology, its strengths and weaknesses, and its application in the dengue research. molecular techniques, and others. tubes, 6–96 well culture plates, and oth ers are used in order to sustain the binding to cell cultures. A modified shell vial technique allows the recovery of a higher number of YFV, SLV, WNV, ILHV, GCV, OROV, MAYV and DENV isolations. This technique follows the same steps as a standard method, but after inoculating cells, the cultures are centrifuged to velocities between 1800 and 2200 rpm. This technique can also be used to isolate DENV coinfections. However, it seems not to have good results for VEE isolation [19–22].
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