Song Sok, Shin Kyu-Sik, Kim Su-Jeong, Joo Yong Yi, Han Bokhee, Park So-Hee, Ku Hyun-Ok, Jeong Wooseog, Park Choi-Kyu
Veterinary Drugs & Biologics Division, Animal and Plant Quarantine Agency, Gimcheon 39660, Gyeongbuk do, Republic of Korea.
College of Veterinary Medicine & Animal Disease Intervention Center, Kyungpook National University, Daegu 41566, Gyeongbuk do, Republic of Korea.
Pathogens. 2025 May 4;14(5):451. doi: 10.3390/pathogens14050451.
African swine fever virus (ASFV) is a highly virulent DNA virus that has spread globally since its introduction into Georgia in 2007, causing substantial economic losses in the swine industry. In the absence of an effective vaccine, chemical disinfection remains a key strategy for disease control. However, in cell-based disinfectant efficacy testing, distinguishing between disinfectant-induced cytotoxicity and virus-induced cytopathic effects (CPEs) remains a major challenge, leading to the potential misinterpretation of results. To address this, we developed a multi-step analytical framework to differentiate CPEs from cytotoxicity using a Vero cell-adapted ASFV strain. Virkon S was tested at three dilutions-375×, 275× (manufacturer-recommended), and 175×-and evaluated through CPE observation, lactate dehydrogenase (LDH) and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assays, and antigen detection via lateral flow immunoassay (p30) and immunofluorescence (p54). Notably, the 375× dilution achieved effective viral inactivation with significantly lower cytotoxicity, demonstrating that this framework can facilitate a more refined determination of disinfectant working dilutions. Furthermore, increased p30 signals after disinfection and the observation of lower cytotoxicity in virus-plus-disinfectant groups compared to disinfectant-only groups highlight the complexity of virus-disinfectant interactions and the potential for misinterpretation. This study provides a standardized and interpretable strategy for assessing ASFV disinfectant efficacy and offers a practical basis for evaluating other enveloped viruses in future disinfection studies.
非洲猪瘟病毒(ASFV)是一种高致病性DNA病毒,自2007年传入格鲁吉亚后已在全球范围内传播,给养猪业造成了巨大经济损失。在缺乏有效疫苗的情况下,化学消毒仍然是疾病控制的关键策略。然而,在基于细胞的消毒剂效力测试中,区分消毒剂诱导的细胞毒性和病毒诱导的细胞病变效应(CPE)仍然是一项重大挑战,可能导致结果的误判。为了解决这一问题,我们开发了一个多步骤分析框架,使用适应Vero细胞的ASFV毒株将CPE与细胞毒性区分开来。对卫可(Virkon S)进行了三种稀释度(375倍、275倍(制造商推荐)和175倍)的测试,并通过CPE观察、乳酸脱氢酶(LDH)和3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)测定以及通过侧向流动免疫测定(p30)和免疫荧光(p54)进行抗原检测来评估。值得注意的是,375倍稀释度实现了有效的病毒灭活,且细胞毒性显著降低,表明该框架可以促进对消毒剂工作稀释度进行更精确的测定。此外,消毒后p30信号增加,以及与仅使用消毒剂的组相比,病毒加消毒剂组中细胞毒性较低,这突出了病毒与消毒剂相互作用的复杂性以及误判的可能性。本研究为评估ASFV消毒剂效力提供了一种标准化且可解释的策略,并为未来消毒研究中评估其他包膜病毒提供了实际依据。