抗菌肽 TM9 的抗病毒作用和呼吸道冠状病毒感染小鼠模型

Maxim Lebedev, Aaron B. Benjamin, Sathish Kumar, N. Molchanova, Jennifer S. Lin, Kent J. Koster, Julian L. Leibowitz, A. Barron, Jeffrey D. Cirillo
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摘要

SARS-CoV-2 感染可导致 COVID-19 疾病,新的抗病毒药物对改善治疗和控制至关重要。抗菌肽是一种序列特异的寡-N-取代甘氨酸拟肽物,它模仿天然抗菌肽的结构和功能,但对蛋白酶具有抗性。我们展示了一种新型拟肽类化合物(TM9)对冠状病毒--小鼠肝炎病毒(MHV)的抗病毒活性,MHV 是一种与 SARS-CoV-2 的结构和抗病毒敏感性特征密切相关的模型。这种蛋白胨模仿人类柔毛素 LL-37,后者也被证明具有抗菌和抗病毒活性。在这项研究中,TM9 对三种小鼠冠状病毒株都有效,这表明治疗窗口足够大,可以使用 TM9 进行治疗。在使用麦迪逊气溶胶室进行气溶胶暴露 15 分钟后,所有三种 MHV 分离物都会在小鼠体内产生感染,在感染后的 5 天观察期内,所有三种病毒株都能从肺部分离出来,滴度在第 2 天达到峰值。从肝脏、心脏、脾脏、嗅球和大脑中也分离到了 MHV-A59 和 MHV-A59-GFP。这些数据表明,MHV 是冠状病毒在包括大脑在内的多个器官中致病的一种有价值的天然小鼠模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antiviral Effect of Antimicrobial Peptoid TM9 and Murine Model of Respiratory Coronavirus Infection
New antiviral agents are essential to improving treatment and control of SARS-CoV-2 infections that can lead to the disease COVID-19. Antimicrobial peptoids are sequence-specific oligo-N-substituted glycine peptidomimetics that emulate the structure and function of natural antimicrobial peptides but are resistant to proteases. We demonstrate antiviral activity of a new peptoid (TM9) against the coronavirus, murine hepatitis virus (MHV), as a closely related model for the structure and antiviral susceptibility profile of SARS-CoV-2. This peptoid mimics the human cathelicidin LL-37, which has also been shown to have antimicrobial and antiviral activity. In this study, TM9 was effective against three murine coronavirus strains, demonstrating that the therapeutic window is large enough to allow the use of TM9 for treatment. All three isolates of MHV generated infection in mice after 15 min of exposure by aerosol using the Madison aerosol chamber, and all three viral strains could be isolated from the lungs throughout the 5-day observation period post-infection, with the peak titers on day 2. MHV-A59 and MHV-A59-GFP were also isolated from the liver, heart, spleen, olfactory bulbs, and brain. These data demonstrate that MHV serves as a valuable natural murine model of coronavirus pathogenesis in multiple organs, including the brain.
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