Wijerathne Sandani V T, Pandit Rachana, Ipinmoroti Ayodeji O, Crenshaw Brennetta J, Matthews Qiana L
Microbiology Program, Alabama State University, Montgomery, AL, United States.
Department of Biological Sciences, College of Science, Technology, Engineering, and Mathematics, Alabama State University, Montgomery, AL, United States.
Front Vet Sci. 2024 Jul 18;11:1388438. doi: 10.3389/fvets.2024.1388438. eCollection 2024.
Coronavirus (CoV) has become a public health crisis that causes numerous illnesses in humans and certain animals. Studies have identified the small, lipid-bound structures called extracellular vesicles (EVs) as the mechanism through which viruses can enter host cells, spread, and evade the host's immune defenses. EVs are able to package and carry numerous viral compounds, including proteins, genetic substances, lipids, and receptor proteins. We proposed that the coronavirus could alter EV production and content, as well as influence EV biogenesis and composition in host cells.
In the current research, Crandell-Rees feline kidney (CRFK) cells were infected with feline coronavirus (FCoV) in an exosome-free media at a multiplicity of infection (MOI) of 2,500 infectious units (IFU) at 48 h and 72 h time points. Cell viability was analyzed and found to be significantly decreased by 9% (48 h) and 15% (72 h) due to FCoV infection. EVs were isolated by ultracentrifugation, and the surface morphology of isolated EVs was analyzed via Scanning Electron Microscope (SEM).
NanoSight particle tracking analysis (NTA) confirmed that the mean particle sizes of control EVs were 131.9 nm and 126.6 nm, while FCoV infected-derived EVs were 143.4 nm and 120.9 nm at 48 and 72 h, respectively. Total DNA, RNA, and protein levels were determined in isolated EVs at both incubation time points; however, total protein was significantly increased at 48 h. Expression of specific protein markers such as TMPRSS2, ACE2, Alix, TSG101, CDs (29, 47, 63), TLRs (3, 6, 7), TNF-α, and others were altered in infection-derived EVs when compared to control-derived EVs after FCoV infection.
Our findings suggested that FCoV infection could alter the EV production and composition in host cells, which affects the infection progression and disease evolution. One purpose of studying EVs in various animal coronaviruses that are in close contact with humans is to provide significant information about disease development, transmission, and adaptation. Hence, this study suggests that EVs could provide diagnostic and therapeutic applications in animal CoVs, and such understanding could provide information to prevent future coronavirus outbreaks.
冠状病毒(CoV)已成为一场公共卫生危机,在人类和某些动物中引发众多疾病。研究已确定被称为细胞外囊泡(EVs)的小型脂质结合结构是病毒进入宿主细胞、传播并逃避宿主免疫防御的机制。细胞外囊泡能够包裹并携带多种病毒成分,包括蛋白质、遗传物质、脂质和受体蛋白。我们提出冠状病毒可能会改变细胞外囊泡的产生和内容物,以及影响宿主细胞中细胞外囊泡的生物发生和组成。
在当前研究中,将克兰德尔 - 里斯猫肾(CRFK)细胞在无外泌体培养基中以感染复数(MOI)为2500个感染单位(IFU)感染猫冠状病毒(FCoV),分别在48小时和72小时时间点进行。分析细胞活力,发现由于FCoV感染,细胞活力在48小时时显著降低9%,在72小时时显著降低15%。通过超速离心分离细胞外囊泡,并通过扫描电子显微镜(SEM)分析分离出的细胞外囊泡的表面形态。
纳米可视颗粒追踪分析(NTA)证实,对照细胞外囊泡的平均粒径在48小时和72小时分别为131.9纳米和126.6纳米,而FCoV感染衍生的细胞外囊泡在48小时和72小时分别为143.4纳米和120.9纳米。在两个孵育时间点测定分离出的细胞外囊泡中的总DNA、RNA和蛋白质水平;然而,在48小时时总蛋白质显著增加。与FCoV感染后的对照衍生细胞外囊泡相比,感染衍生细胞外囊泡中特定蛋白质标志物如跨膜丝氨酸蛋白酶2(TMPRSS2)、血管紧张素转换酶2(ACE2)、肿瘤易感基因101(TSG101)、CDs(29, 47, 63)、Toll样受体(TLRs)(3, 6, 7)、肿瘤坏死因子-α(TNF-α)等的表达发生了改变。
我们的研究结果表明,FCoV感染可改变宿主细胞中细胞外囊泡的产生和组成,这会影响感染进程和疾病演变。研究与人类密切接触的各种动物冠状病毒中的细胞外囊泡的一个目的是提供有关疾病发展、传播和适应性的重要信息。因此,本研究表明细胞外囊泡可在动物冠状病毒中提供诊断和治疗应用,这种认识可为预防未来冠状病毒爆发提供信息。