Nebraska Center for Virology, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.
School of Biological Sciences, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.
J Virol. 2018 May 14;92(11). doi: 10.1128/JVI.00110-18. Print 2018 Jun 1.
Two lineages of influenza D virus (IDV) have been found to infect cattle and promote bovine respiratory disease complex, one of the most commonly diagnosed causes of morbidity and mortality within the cattle industry. Furthermore, IDV can infect other economically important domestic livestock, including pigs, and has the potential to infect humans, which necessitates the need for an efficacious vaccine. In this study, we designed a DNA vaccine expressing consensus hemagglutinin-esterase fusion (HEF) protein (FluD-Vax) and tested its protective efficacy against two lineages of IDV (D/OK and D/660) in guinea pigs. Animals that received FluD-Vax ( = 12) developed appreciable titers of neutralizing antibodies against IDV lineage representatives, D/OK and D/660. Importantly, vaccinated animals were protected against intranasal challenge with IDV [3 × 10 50% tissue culture infective dose(s) (TCID)] D/OK ( = 6) or D/600 ( = 6), based on the absence of viral RNA in necropsied tissues (5 and 7 days postchallenge) using quantitative reverse transcription-PCR and hybridization. In contrast, animals that received a sham DNA vaccine ( = 12) had no detectable neutralizing antibodies against IDV, and viral RNA was readily detectable in respiratory tract tissues after intranasal challenge (3 × 10 TCID) with IDV D/OK ( = 6) or D/660 ( = 6). Using a TUNEL (terminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling) assay, we found that IDV D/OK and D/600 infections induced apoptosis in epithelial cells lining alveoli and bronchioles, as well as nonepithelial cells in lung tissues. Our results demonstrate for the first time that the consensus IDV HEF DNA vaccine can elicit complete protection against infection from two lineages of IDV in the guinea pig model. Influenza D virus (IDV) infection has been associated with bovine respiratory disease complex, one of the most devastating diseases of the cattle population. Moreover, with broad host range and high environmental stability, IDV has the potential to further gain virulence or even infect humans. An efficacious vaccine is needed to prevent infection and stop potential cross-species transmission. In this study, we designed a DNA vaccine encoding the consensus hemagglutinin-esterase fusion (HEF) protein of two lineages of IDV (D/OK and D/660) and tested its efficacy in a guinea pig model. Our results showed that the consensus DNA vaccine elicited high-titer neutralizing antibodies and achieved sterilizing protection against two lineage-representative IDV intranasal infections. To our knowledge, this is the first study showing that a DNA vaccine expressing consensus HEF is efficacious in preventing different lineages of IDV infections.
两种流感 D 病毒(IDV)谱系已被发现可感染牛并促进牛呼吸道疾病综合征,这是牛群中最常见的发病和死亡原因之一。此外,IDV 还可以感染其他具有重要经济意义的家畜,包括猪,并有可能感染人类,因此需要有效的疫苗。在这项研究中,我们设计了一种表达共识血凝素-酯酶融合(HEF)蛋白的 DNA 疫苗(FluD-Vax),并在豚鼠中测试了其针对两种 IDV 谱系(D/OK 和 D/660)的保护效力。接受 FluD-Vax 疫苗接种的动物(n = 12)针对 IDV 谱系代表物 D/OK 和 D/660 产生了可观的中和抗体滴度。重要的是,接种疫苗的动物在鼻腔内挑战 3×1050%组织培养感染剂量(TCID)D/OK(n = 6)或 D/660(n = 6)时得到了保护,这是基于定量逆转录-PCR 和杂交检测到尸检组织中没有病毒 RNA(感染后 5 天和 7 天)。相比之下,接受假 DNA 疫苗接种的动物(n = 12)针对 IDV 没有检测到中和抗体,并且在用 IDV D/OK(n = 6)或 D/660(n = 6)进行鼻腔内挑战后,呼吸道组织中很容易检测到病毒 RNA。使用 TUNEL(末端脱氧核苷酸转移酶介导的 dUTP-生物素缺口末端标记)检测,我们发现 IDV D/OK 和 D/600 感染诱导了肺泡和细支气管上皮细胞以及肺组织中非上皮细胞的细胞凋亡。我们的结果首次证明,共识 IDV HEF DNA 疫苗可在豚鼠模型中针对两种 IDV 谱系引发完全保护。流感 D 病毒(IDV)感染与牛呼吸道疾病综合征有关,这是牛群中最具破坏性的疾病之一。此外,由于其宿主范围广泛且环境稳定性高,IDV 有可能进一步获得毒力甚至感染人类。需要一种有效的疫苗来预防感染并阻止潜在的跨物种传播。在这项研究中,我们设计了一种编码两种 IDV(D/OK 和 D/660)共识血凝素-酯酶融合(HEF)蛋白的 DNA 疫苗,并在豚鼠模型中测试了其功效。我们的结果表明,共识 DNA 疫苗引发了高滴度的中和抗体,并对两种代表 IDV 的鼻腔内感染实现了杀菌保护。据我们所知,这是第一项表明表达共识 HEF 的 DNA 疫苗可有效预防不同 IDV 谱系感染的研究。