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采用蚊虫接种技术分离和滴定登革病毒。

Isolation and titration of dengue viruses by the mosquito inoculation technique.

作者信息

Choy Milly M, Gubler Duane J

机构信息

Emerging Infectious Diseases Program, Duke-NUS Graduate Medical School, 8 College Road, Singapore, 169857, Singapore.

出版信息

Methods Mol Biol. 2014;1138:15-25. doi: 10.1007/978-1-4939-0348-1_2.

Abstract

Mosquito inoculation is a highly sensitive technique for isolation and titration of dengue virus (DENV) from sera, human tissues, wild animals, or mosquitoes. It has been under utilized since it was described 40 years ago because most dengue laboratories do not have access to an insectary to rear mosquitoes. This technique requires good eye-hand coordination while doing manipulation under a stereoscopic microscope, and extensive practice is needed to become proficient at inoculating mosquitoes. Following inoculation, mosquitoes are held for 10 days to allow dengue virus to replicate and disseminate to tissues throughout the mosquitoes. They are then harvested and examined for the presence of viral antigens in head tissue by either immunofluorescence assay (IFA) or PCR (polymerase chain reaction). The mosquito infectious dose 50 (MID50) is calculated using the method of Reed and Muench to quantitate the virus. This method can be used for other arboviruses as well as for dengue.

摘要

蚊媒接种是一种从血清、人体组织、野生动物或蚊子中分离和滴定登革病毒(DENV)的高度敏感技术。自40年前被描述以来,该技术一直未得到充分利用,因为大多数登革热实验室无法使用昆虫饲养室来饲养蚊子。这项技术在立体显微镜下进行操作时需要良好的眼手协调能力,并且需要大量练习才能熟练接种蚊子。接种后,将蚊子饲养10天,以使登革病毒复制并扩散到蚊子的各个组织中。然后将它们收集起来,通过免疫荧光测定法(IFA)或聚合酶链反应(PCR)检测头部组织中是否存在病毒抗原。使用里德-孟奇方法计算蚊媒感染剂量50(MID50)以定量病毒。该方法可用于其他虫媒病毒以及登革病毒。

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