Virology Department, Animal and Plant Health Agency (APHA-Weybridge), Addlestone, Surrey, KT15 3NB, UK.
Present address: Worldwide Influenza Centre, The Francis Crick Institute, Midland Road, London, NW1 1AT, UK.
J Gen Virol. 2024 Sep;105(9). doi: 10.1099/jgv.0.002022.
Direct and indirect transmission of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been attributed to virus survival in droplets, bioaerosols and on fomites including skin and surfaces. Survival of SARS-CoV-2 variants of concern (Alpha, Beta, Gamma, and Delta) on the skin and virus transference following rounds of skin-to-skin contact were assessed on porcine skin as a surrogate for human skin. SARS-CoV-2 variants were detectable on skin by RT-qPCR after 72 h at biologically relevant temperatures (35.2 °C) with viral RNA (vRNA) detected after ten successive skin-to-skin contacts. Skin-to-skin virus transmission to establish infection in ferrets as a model for mild/asymptomatic SARS-CoV-2 infection in mustelids and humans was also investigated and compared to intranasal ferret inoculation. Naïve ferrets exposed to Delta variant SARS-CoV-2 in a 'wet' or 'dry' form on porcine skin resulted in robust infection with shedding detectable for up to 14 days post-exposure, at comparable viral loads to ferrets inoculated intranasally. Transmission of SARS-CoV-2 to naïve ferrets in direct contact with infected ferrets was achieved, with environmental contamination detected from ferret fur swabs and air samples. Genetic substitutions were identified in bioaerosol samples acquired following single contact passage in ferrets, including Spike, ORF1ab, and ORF3a protein sequences, suggesting a utility for monitoring host adaptation and virus evolution via air sampling. The longevity of SARS-CoV-2 variants survival directly on the skin and skin-to-skin transference, enabling subsequent infection via the skin to oro-nasal contact route, could represent a pathway for SARS-CoV-2 infection with implications to public and veterinary health.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的直接和间接传播归因于病毒在飞沫、生物气溶胶和包括皮肤和表面在内的污染物中的存活。在作为人体皮肤替代物的猪皮上评估了关切的 SARS-CoV-2 变体(Alpha、Beta、Gamma 和 Delta)在皮肤上的存活以及经过多轮皮肤接触后的病毒转移。在具有生物学相关性的温度(35.2°C)下,SARS-CoV-2 变体在 72 小时后可通过 RT-qPCR 在皮肤上检测到,并且在连续 10 次皮肤接触后可检测到病毒 RNA(vRNA)。还研究了皮肤到皮肤的病毒传播以在雪貂中建立感染,作为雪貂和人类轻度/无症状 SARS-CoV-2 感染的模型,并与鼻腔内雪貂接种进行了比较。在猪皮上以“湿”或“干”形式暴露于 Delta 变体 SARS-CoV-2 的天真雪貂导致了强烈的感染,可检测到长达 14 天的排毒,病毒载量与鼻腔内接种的雪貂相当。通过与感染雪貂的直接接触,将 SARS-CoV-2 传播给天真的雪貂,从雪貂的皮毛拭子和空气样本中检测到环境污染。在雪貂中进行单次接触传代后获得的生物气溶胶样本中鉴定出了遗传替换,包括 Spike、ORF1ab 和 ORF3a 蛋白序列,这表明通过空气采样监测宿主适应和病毒进化具有一定的作用。SARS-CoV-2 变体在皮肤上的直接存活时间长,并且通过皮肤接触传播,能够通过皮肤到口鼻腔接触途径导致感染,这可能代表了 SARS-CoV-2 感染的一种途径,对公共和兽医健康具有重要意义。