Commonwealth Scientific & Industrial Research Organization (CSIRO), Land & Water, P.O. Box 2583, Brisbane, QLD, 4001, Australia.
WHO Collaborating Centre for Reference and Research on Influenza, VIDRL, at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia.
Metabolomics. 2019 Mar 1;15(3):33. doi: 10.1007/s11306-019-1499-0.
Influenza is a highly contagious respiratory disease that causes high global morbidity and mortality each year. The dynamics of an influenza infection on the host metabolism, and how metabolism is altered in response to neuraminidase inhibitor drug therapy, is still in its infancy but of great importance.
We aim to investigate the suitability of ferret nasal wash samples for metabolomics-based analysis and characterization of influenza infections and oseltamivir treatment.
Virological and metabolic analyses were performed on nasal wash samples collected from ferrets treated with oseltamivir or a placebo. Untargeted metabolomics was performed using a gas chromatography coupled with mass spectrometery (GC-MS) based protocol that comprised a retention time (RT) locked method and the use of a commercial metabolomics library.
Ferret activity was reduced at 2-3 days post infection, which coincided with the highest influenza viral titre. The metabolomics data indicated a shift in metabolism during various stages of infection. The neuraminidase inhibitor oseltamivir created considerable downregulation of energy center metabolites (glucose, sucrose, glycine and glutamine), which generated high levels of branched amino acids. This further increased branched amino acid degradation and deregulation via glycerate-type intermediates and biosynthesis of fatty acids in oseltamivir-treated animals where abrogated weight loss was observed.
Metabolomics was used to profile influenza infection and antiviral drug treatment in ferrets. This has the potential to provide indicators for the early diagnosis of influenza infection and assess the effectiveness of drug therapies.
流感是一种高度传染性的呼吸道疾病,每年在全球范围内导致高发病率和死亡率。流感感染对宿主代谢的动态影响,以及代谢如何对神经氨酸酶抑制剂药物治疗产生变化,仍处于起步阶段,但非常重要。
我们旨在研究雪貂鼻冲洗样本是否适合基于代谢组学的流感感染和奥司他韦治疗分析和表征。
对接受奥司他韦或安慰剂治疗的雪貂的鼻冲洗样本进行病毒学和代谢分析。使用气相色谱与质谱联用(GC-MS)的非靶向代谢组学方法进行分析,该方法包括保留时间(RT)锁定方法和使用商业代谢组学库。
雪貂在感染后 2-3 天活动减少,这与流感病毒滴度最高的时间一致。代谢组学数据表明,在感染的不同阶段代谢发生了变化。神经氨酸酶抑制剂奥司他韦对能量中心代谢物(葡萄糖、蔗糖、甘氨酸和谷氨酰胺)产生了显著的下调作用,导致支链氨基酸水平升高。在奥司他韦治疗的动物中,这种情况进一步增加了支链氨基酸的降解和通过甘油酸型中间产物的失调以及脂肪酸的生物合成,导致体重减轻被阻断。
代谢组学用于 profiling 流感感染和抗病毒药物治疗雪貂。这有可能为流感感染的早期诊断和评估药物治疗的效果提供指标。