Patel Mira C, Pletneva Lioubov M, Boukhvalova Marina S, Vogel Stefanie N, Kajon Adriana E, Blanco Jorge C G
Sigmovir Biosystems, Inc., RockvilleMD, United States.
University of Maryland School of Medicine, BaltimoreMD, United States.
Front Microbiol. 2017 Aug 31;8:1646. doi: 10.3389/fmicb.2017.01646. eCollection 2017.
Human rhinoviruses (HRVs) are the main cause of cold-like illnesses, and currently no vaccine or antiviral therapies against HRVs are available to prevent or mitigate HRV infection. There are more than 150 antigenically heterogeneous HRV serotypes, with ∼90 HRVs belonging to major group species A and B. Development of small animal models that are susceptible to infection with major group HRVs would be beneficial for vaccine research. Previously, we showed that the cotton rat () is semi-permissive to HRV16 (major group, species HRV-A virus) infection, replicating in the upper and lower respiratory tracts with measurable pathology, mucus production, and expression of inflammatory mediators. Herein, we report that intranasal infection of cotton rats with HRV14 (major group, species HRV-B virus) results in isolation of infectious virus from the nose and lung. Similar to HRV16, intramuscular immunization with live HRV14 induces homologous protection that correlated with high levels of serum neutralizing antibodies. Vaccination and challenge experiments with HRV14 and HRV16 to evaluate the development of cross-protective immunity demonstrate that intramuscular immunization with live HRV16 significantly protects animals against HRV14 challenge. Determination of the immunological mechanisms involved in heterologous protection and further characterization of infection with other major HRV serotypes in the cotton rat could enhance the robustness of the model to define heterotypic relationships between this diverse group of viruses and thereby increase its potential for development of a multi-serotype HRV vaccine.
人鼻病毒(HRV)是引起感冒样疾病的主要原因,目前尚无针对HRV的疫苗或抗病毒疗法可用于预防或减轻HRV感染。有超过150种抗原性不同的HRV血清型,其中约90种HRV属于主要的A组和B组病毒种类。开发易受主要组HRV感染的小动物模型将有助于疫苗研究。此前,我们发现棉鼠对HRV16(主要组,HRV-A病毒种类)感染呈半允许状态,在上下呼吸道复制,并伴有可测量的病理变化、黏液产生和炎症介质表达。在此,我们报告用HRV14(主要组,HRV-B病毒种类)鼻内感染棉鼠会导致从鼻腔和肺部分离出感染性病毒。与HRV16相似,用活的HRV14进行肌肉注射免疫可诱导同源保护,这与高水平的血清中和抗体相关。用HRV14和HRV16进行疫苗接种和攻毒实验以评估交叉保护性免疫的发展,结果表明用活的HRV16进行肌肉注射免疫可显著保护动物免受HRV14攻毒。确定棉鼠中异源保护所涉及的免疫机制以及进一步表征其他主要HRV血清型的感染情况,可能会增强该模型的稳健性,以确定这一多样病毒组之间的异型关系,从而增加其开发多血清型HRV疫苗的潜力。