Beale David J, Shah Rohan, Karpe Avinash V, Hillyer Katie E, McAuley Alexander J, Au Gough G, Marsh Glenn A, Vasan Seshadri S
Land & Water, Commonwealth Scientific and Industrial Research Organisation, Dutton Park, QLD 4102, Australia.
Department of Chemistry and Biotechnology, Faculty of Science, Engineering and Technology, Swinburne University of Technology, Hawthorn, VIC 3122, Australia.
Metabolites. 2021 May 19;11(5):327. doi: 10.3390/metabo11050327.
Coronavirus disease (COVID-19) is a contagious respiratory disease that is causing significant global morbidity and mortality. Understanding the impact of the Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) infection on the host metabolism is still in its infancy but of great importance. Herein, we investigated the metabolic response during viral shedding and post-shedding in an asymptomatic SARS-CoV-2 ferret model (n = 6) challenged with two SARS-CoV-2 isolates. Virological and metabolic analyses were performed on (minimally invasive) collected oral swabs, rectal swabs, and nasal washes. Fragments of SARS-CoV-2 RNA were only found in the nasal wash samples in four of the six ferrets, and in the samples collected 3 to 9 days post-infection (referred to as viral shedding). Central carbon metabolism metabolites were analyzed during viral shedding and post-shedding periods using a dynamic Multiple Reaction Monitoring (dMRM) database and method. Subsequent untargeted metabolomics and lipidomics of the same samples were performed using a Liquid Chromatography Quadrupole Time-of-Flight Mass Spectrometry (LC-QToF-MS) methodology, building upon the identified differentiated central carbon metabolism metabolites. Multivariate analysis of the acquired data identified 29 significant metabolites and three lipids that were subjected to pathway enrichment and impact analysis. The presence of viral shedding coincided with the challenge dose administered and significant changes in the citric acid cycle, purine metabolism, and pentose phosphate pathways, amongst others, in the host nasal wash samples. An elevated immune response in the host was also observed between the two isolates studied. These results support other metabolomic-based findings in clinical observational studies and indicate the utility of metabolomics applied to ferrets for further COVID-19 research that advances early diagnosis of asymptomatic and mild clinical COVID-19 infections, in addition to assessing the effectiveness of new or repurposed drug therapies.
冠状病毒病(COVID-19)是一种具有传染性的呼吸道疾病,正在全球范围内造成严重的发病和死亡。了解严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染对宿主代谢的影响仍处于起步阶段,但非常重要。在此,我们在一个无症状的SARS-CoV-2雪貂模型(n = 6)中,用两种SARS-CoV-2分离株进行挑战,研究了病毒脱落期间和脱落后的代谢反应。对(微创)收集的口腔拭子、直肠拭子和鼻腔灌洗液进行了病毒学和代谢分析。在六只雪貂中的四只的鼻腔灌洗样本中,以及在感染后3至9天收集的样本中(称为病毒脱落),仅发现了SARS-CoV-2 RNA片段。使用动态多反应监测(dMRM)数据库和方法,在病毒脱落期间和脱落后分析中心碳代谢物。基于已鉴定的有差异的中心碳代谢物,使用液相色谱四极杆飞行时间质谱(LC-QToF-MS)方法对相同样本进行后续的非靶向代谢组学和脂质组学分析。对获得的数据进行多变量分析,确定了29种显著代谢物和三种脂质,并对其进行了通路富集和影响分析。病毒脱落的存在与给予的挑战剂量一致,并且宿主鼻腔灌洗样本中的柠檬酸循环、嘌呤代谢和磷酸戊糖途径等发生了显著变化。在所研究的两种分离株之间,还观察到宿主的免疫反应增强。这些结果支持了临床观察研究中其他基于代谢组学的发现,并表明代谢组学应用于雪貂对于进一步开展COVID-19研究具有实用性,这不仅有助于早期诊断无症状和轻度临床COVID-19感染,还能评估新的或重新利用的药物治疗的有效性。