Xu Chuan, Wang Annie, Honnen William, Pinter Abraham, Weston Warren K, Harness Jane A, Narayanan Aarthi, Chang Theresa L
Public Health Research Institute, Rutgers, The State University of New Jersey, New Jersey Medical School, Newark, NJ, USA.
Innovation Pharmaceuticals, Inc., Wakefield, Massachusetts, USA.
EC Microbiol. 2022 Apr;18(4):1-12. Epub 2022 Mar 8.
Brilacidin (PMX-30063), a non-peptide defensin-mimetic small molecule, inhibits SARS-CoV-2 viral infection but the anti-viral mechanism is not defined. Here we determined its effect on the specific step of the viral life cycle. Brilacidin blocked SARS-CoV-2 infection but had no effect after viral entry. Brilacidin inhibited pseudotyped SARS-CoV-2 viruses expressing spike proteins from the P.1 Brazil strain and the B.1.1.7 UK strain. Brilacidin affected viral attachment in hACE2-dependent and independent manners depending on the concentrations. The inhibitory effect on viral entry was not mediated through blocking the binding of either the spike receptor-binding domain or the spike S1 protein to hACE2 proteins. Taken together, brilacidin inhibits SARS-CoV-2 infection by blocking viral entry and is active against SARS-CoV-2 variants.
布里拉西丁(PMX-30063)是一种非肽类防御素模拟小分子,可抑制严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染,但其抗病毒机制尚不清楚。在此,我们确定了其对病毒生命周期特定步骤的影响。布里拉西丁可阻断SARS-CoV-2感染,但在病毒进入后没有作用。布里拉西丁抑制了表达来自巴西P.1毒株和英国B.1.1.7毒株刺突蛋白的假型SARS-CoV-2病毒。根据浓度不同,布里拉西丁以依赖和不依赖人血管紧张素转换酶2(hACE2)的方式影响病毒附着。对病毒进入的抑制作用不是通过阻断刺突受体结合域或刺突S1蛋白与hACE2蛋白的结合来介导的。综上所述,布里拉西丁通过阻断病毒进入来抑制SARS-CoV-2感染,并且对SARS-CoV-2变体具有活性。