Department of Virology I, National Institute of Infectious Diseases, Tokyo, Japan.
Department of Pathology, National Institute of Infectious Diseases, Tokyo, Japan.
J Virol. 2022 Apr 13;96(7):e0004922. doi: 10.1128/jvi.00049-22. Epub 2022 Mar 23.
Heartland bandavirus (HRTV), which is an emerging tick-borne virus first identified in Missouri in 2009, causes fever, fatigue, decreased appetite, headache, nausea, diarrhea, and muscle or joint pain in humans. HRTV is genetically close to Dabie bandavirus, which is the causative agent of severe fever with thrombocytopenia syndrome (SFTS) in humans and is known as SFTS virus (SFTSV). The generation of infectious HRTV entirely from cloned cDNAs has not yet been reported. The absence of a reverse genetics system for HRTV has delayed efforts to understand its pathogenesis and to generate vaccines and antiviral drugs. Here, we developed a reverse genetics system for HRTV, which employs an RNA polymerase I-mediated expression system. A recombinant nonstructural protein (NSs)-knockout HRTV (rHRTV-NSsKO) was generated. We found that NSs interrupted signaling associated with innate immunity in HRTV-infected cells. The rHRTV-NSsKO was highly attenuated, indicated by the apparent absence of symptoms in a mouse model of HRTV infection. Moreover, mice immunized with rHRTV-NSsKO survived a lethal dose of HRTV. These findings suggest that NSs is a virulence factor of HRTV and that rHRTV-NSsKO could be a vaccine candidate for HRTV. Heartland bandavirus (HRTV) is a tick-borne virus identified in the United States in 2009. HRTV causes fever, fatigue, decreased appetite, headache, nausea, diarrhea, and muscle or joint pain in humans. FDA-approved vaccines and antiviral drugs are unavailable. The lack of a reverse genetics system hampers efforts to develop such antiviral therapeutics. Here, we developed a reverse genetics system for HRTV that led to the generation of a recombinant nonstructural protein (NSs)-knockout HRTV (rHRTV-NSsKO). We found that NSs interrupted signaling associated with innate immunity in HRTV-infected cells. Furthermore, rHRTV-NSsKO was highly attenuated and immunogenic in a mouse model. These findings suggest that NSs is a virulence factor of HRTV and that rHRTV-NSsKO could be a vaccine candidate for HRTV.
心域病毒(HRTV)是一种新兴的蜱传病毒,于 2009 年在美国密苏里州首次发现,可引起人类发热、疲劳、食欲不振、头痛、恶心、腹泻以及肌肉或关节疼痛。HRTV 在遗传学上与导致人类严重发热伴血小板减少综合征(SFTS)的大别山病毒密切相关,被称为 SFTS 病毒(SFTSV)。目前尚未有从克隆 cDNA 中完全产生感染性 HRTV 的报道。由于缺乏 HRTV 的反向遗传学系统,阻碍了对其发病机制的研究以及疫苗和抗病毒药物的研发。在此,我们开发了一种 HRTV 的反向遗传学系统,该系统采用 RNA 聚合酶 I 介导的表达系统。生成了重组非结构蛋白(NSs)缺失的 HRTV(rHRTV-NSsKO)。我们发现 NSs 中断了 HRTV 感染细胞中与固有免疫相关的信号转导。rHRTV-NSsKO 高度减毒,在 HRTV 感染的小鼠模型中明显无症状。此外,用 rHRTV-NSsKO 免疫的小鼠可耐受致死剂量的 HRTV。这些发现表明 NSs 是 HRTV 的毒力因子,rHRTV-NSsKO 可能是 HRTV 的候选疫苗。
心域病毒(HRTV)是 2009 年在美国发现的一种蜱传病毒。HRTV 可引起人类发热、疲劳、食欲不振、头痛、恶心、腹泻以及肌肉或关节疼痛。目前尚无 FDA 批准的疫苗和抗病毒药物。缺乏反向遗传学系统阻碍了此类抗病毒治疗药物的研发。在此,我们开发了一种 HRTV 的反向遗传学系统,由此产生了重组非结构蛋白(NSs)缺失的 HRTV(rHRTV-NSsKO)。我们发现 NSs 中断了 HRTV 感染细胞中与固有免疫相关的信号转导。此外,rHRTV-NSsKO 在小鼠模型中高度减毒并具有免疫原性。这些发现表明 NSs 是 HRTV 的毒力因子,rHRTV-NSsKO 可能是 HRTV 的候选疫苗。