An inactivated influenza D virus vaccine protects guinea pigs from infections and contact transmission caused by homologous challenge.

IF 4 3区 医学 Q2 VIROLOGY
Zhipeng Dong, Pengyang Lu, Yue Feng, Hongbo Gao, Wentao Wan, Tiecheng Wang, Xianzhu Xia, Weiyang Sun, Yuwei Gao
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Abstract

Influenza D virus (IDV) was first isolated from pigs in 2011 which caused the bovine respiratory disease and economic losses. This study aimed to develop an inactivated vaccine to protect against IDV using guinea pigs as an animal model. Vaccinated guinea pigs exhibited seroconversion with hemagglutination inhibition titers ranging from 1: 320 to 1: 640 and neutralizing antibody levels reaching 1: 2560 after booster immunity. In the vaccinated guinea pigs, viral titers were detected in the nasal lavage fluids from days one to seven, showing a significant difference from the control group. Peak viral shedding of approximately 106 TCID50/mL was measured in the nasal turbinate and nasal washes from days one to five. In contact transmission experiments, non-vaccinated guinea pigs that lived with the infection group were more likely to become infected than those in the vaccinated group. These results demonstrate that the inactivated IDV vaccine protected guinea pigs from contact transmission caused by homologous challenge. Our study provides a new choice for developing IDV vaccines to protect animals from IDV infections.

一种灭活的D型流感病毒疫苗保护豚鼠免受同源攻击引起的感染和接触传播。
2011年首次从猪中分离出D型流感病毒(IDV),造成牛呼吸道疾病和经济损失。本研究旨在以豚鼠为动物模型,研制一种预防IDV的灭活疫苗。接种疫苗的豚鼠在增强免疫后表现出血凝抑制滴度为1:320至1:640的血清转化,中和抗体水平达到1:25 60。在接种疫苗的豚鼠中,从第1天到第7天在鼻灌洗液中检测到病毒滴度,与对照组有显著差异。从第1天到第5天,在鼻鼻甲和鼻洗液中测量到约106 TCID50/mL的峰值病毒脱落。在接触传播实验中,与感染组生活在一起的未接种疫苗的豚鼠比接种疫苗组的豚鼠更容易被感染。这些结果表明,灭活疫苗可以保护豚鼠免受同源攻击引起的接触传播。本研究为研制IDV疫苗保护动物免受IDV感染提供了新的选择。
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来源期刊
Virology Journal
Virology Journal 医学-病毒学
CiteScore
7.40
自引率
2.10%
发文量
186
审稿时长
1 months
期刊介绍: Virology Journal is an open access, peer reviewed journal that considers articles on all aspects of virology, including research on the viruses of animals, plants and microbes. The journal welcomes basic research as well as pre-clinical and clinical studies of novel diagnostic tools, vaccines and anti-viral therapies. The Editorial policy of Virology Journal is to publish all research which is assessed by peer reviewers to be a coherent and sound addition to the scientific literature, and puts less emphasis on interest levels or perceived impact.
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