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In vivo imaging assay for the convenient evaluation of antiviral compounds against cytomegalovirus in mice.

机译:体内成像测定法,用于方便地评估小鼠抗巨细胞病毒的抗病毒化合物。

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摘要

Evaluation of newly identified antiviral compounds against cytomegalovirus (CMV) in vivo still requires laborious and time-consuming experiments using a large number of animals. In this study, we examined an in vivo imaging assay for the evaluation of antiviral compounds using a recombinant murine CMV expressing EGFP (MCMV-GFP). We found the followings: (1) Fluorescent signals were detectable from 1 day after subcutaneous inoculation of the viruses into the backs of mice, and reached to the peak within 2-4 days. (2) Incubation period required for the signal appearance and peak signal intensities depended on the inoculated dose. (3) Not only BALB/c but also a hairless mouse strain, HR1, can be used for the assay, and no need to shave the HR1 mice added to the convenience of the assay. (4) However, BALB/c mice showed better sensitivity and dose-response to the inoculated virus, and inoculation with 200 PFUs of MCMV-GFP still yielded the signals. (5) Demonstration of the antiviral effect of ganciclovir provided a proof-of-concept. Thus, the in vivo imaging assay can allow the fast and convenient initial evaluation of anti-CMV candidate compounds in animals prior to comprehensive analyses.
机译:在体内评估新发现的抗巨细胞病毒(CMV)的抗病毒化合物仍需要大量动物的费力且费时的实验。在这项研究中,我们使用表达EGFP(MCMV-GFP)的重组鼠CMV检查了体内成像试验,以评估抗病毒化合物。我们发现以下情况:(1)从将病毒皮下接种到小鼠背部后1天开始检测到荧光信号,并在2-4天内达到峰值。 (2)信号出现所需的孵育时间和峰值信号强度取决于接种剂量。 (3)不仅BALB / c,而且无毛小鼠品系HR1都可以用于测定,并且无需剃除为测定方便而添加的HR1小鼠。 (4)然而,BALB / c小鼠对接种病毒表现出更好的敏感性和剂量反应,并且用200 PFU的MCMV-GFP接种仍能产生信号。 (5)更昔洛韦抗病毒作用的证明提供了概念证明。因此,在全面分析之前,体内成像分析可以快速,方便地对动物体内的抗CMV候选化合物进行初步评估。

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