Doctoral Program in Biomedical Sciences, Faculty of Medicine, University of Indonesia, DKI Jakarta, Indonesia.
Animal Health Research and Diagnostic Unit, PT Medika Satwa Laboratoris, Bogor, Indonesia.
Avian Pathol. 2025 Feb;54(1):96-107. doi: 10.1080/03079457.2024.2386315. Epub 2024 Aug 21.
The avian influenza virus is an infectious agent that may cause global health problems in poultry and is potentially zoonotic. In the recent decades, bacterial-derived sialidases have been extensively studied for their ability to inhibit avian influenza virus infections. In this study, the antiviral activity of NanB sialidase from was investigated through analysis using Madin-Darby canine kidney (MDCK) cells. NanB sialidase was purified from to test its toxicity and its ability to hydrolyse its sialic acid receptors on MDCK cells. The H9N2 challenge virus was propagated in MDCK cells until cytopathic effects appeared. Antiviral activity of NanB sialidase was tested using MDCK cells, and then observed based on cell morphology, viral copy number, and expression of apoptosis-mediating genes. NanB sialidase effectively hydrolysed Neu5Acα(2,6)-Gal sialic acid at a dose of 129 mU/ml, while at 258 mU/ml, it caused toxicity to MDCK cells. Antiviral activity of sialidase was evident based on the significant decrease in viral copy number at all doses administered. The increase of p53 and caspase-3 expression was observed in infected cells without sialidase. Our study demonstrates the ability of NanB sialidase to inhibit H9N2 virus replication based on observations of sialic acid hydrolysis, reduction in viral copy number, and expression of apoptosis-related genes. The future application of sialidase may be considered as an antiviral strategy against avian influenza H9N2 virus infections. RESEARCH HIGHLIGHTSNanB sialidase effectively hydrolyses Neu5Acα(2,6)-Gal at a dose of 129 mU/ml.NanB sialidase from can inhibit the entry of H9N2 virus into cells.NanB sialidase of prevents infection-induced cell apoptosis.NanB sialidase reduces the H9N2 viral copy number in MDCK cells.
禽流感病毒是一种传染性病原体,可能会给家禽业带来全球性的健康问题,并且具有潜在的人畜共患性。在最近几十年中,细菌来源的唾液酸酶因其抑制禽流感病毒感染的能力而得到了广泛的研究。在这项研究中,通过使用 Madin-Darby 犬肾 (MDCK) 细胞的分析,研究了 来源的 NanB 唾液酸酶的抗病毒活性。从 中纯化 NanB 唾液酸酶,以测试其毒性及其在 MDCK 细胞上水解唾液酸受体的能力。将 H9N2 挑战病毒在 MDCK 细胞中繁殖,直到出现细胞病变效应。使用 MDCK 细胞测试 NanB 唾液酸酶的抗病毒活性,然后根据细胞形态、病毒拷贝数和凋亡介导基因的表达进行观察。NanB 唾液酸酶在 129 mU/ml 的剂量下有效水解 Neu5Acα(2,6)-Gal 唾液酸,而在 258 mU/ml 的剂量下,它会对 MDCK 细胞产生毒性。在所有给药剂量下,均观察到病毒拷贝数的显著减少,表明唾液酸酶具有抗病毒活性。在没有唾液酸酶的感染细胞中观察到 p53 和 caspase-3 表达增加。我们的研究表明,NanB 唾液酸酶能够抑制 H9N2 病毒的复制,这是基于观察到的唾液酸水解、病毒拷贝数减少和与凋亡相关基因的表达。唾液酸酶的未来应用可以被认为是针对禽流感 H9N2 病毒感染的抗病毒策略。研究亮点NanB 唾液酸酶在 129 mU/ml 的剂量下有效水解 Neu5Acα(2,6)-Gal。来源于 的 NanB 唾液酸酶可以抑制 H9N2 病毒进入细胞。来源于 的 NanB 唾液酸酶可防止感染诱导的细胞凋亡。NanB 唾液酸酶降低 MDCK 细胞中的 H9N2 病毒拷贝数。