Equine Research Institute, Japan Racing Association, 1400-4 Shiba, Shimotsuke, Tochigi 329-0412, Japan.
Equine Research Institute, Japan Racing Association, 1400-4 Shiba, Shimotsuke, Tochigi 329-0412, Japan.
Vet J. 2021 Jun;272:105674. doi: 10.1016/j.tvjl.2021.105674. Epub 2021 Apr 14.
From late 2018 to 2019, equine influenza virus (EIV) strains of Florida sublineage clade 1 (Fc1), which had until then been circulating mainly in the United States, suddenly spread across Europe causing many outbreaks, and Florida sublineage clade 2 (Fc2) strains, which had been circulating mainly in Europe, have not been detected in Europe since 2018. Since 2010, the World Organisation for Animal Health (OIE) has recommended that EIV vaccines contain an Fc1 strain that is like A/equine/South Africa/4/2003 or A/equine/Ohio/2003. Accordingly, Japanese vaccines contain A/equine/Ibaraki/1/2007 as the Fc1 strain. To evaluate the effectiveness of these vaccines against the Fc1 strains detected in Europe in 2019, we performed virus neutralization tests using horse antisera. Challenge viruses used were Irish strain A/equine/Tipperary/1/2019 and two recombinant viruses generated by reverse genetics. Recombinant viruses possessing hemagglutinin (HA) and neuraminidase (NA) derived from A/equine/Tipperary/1/2019 (rA/equine/Tipperary/1/2019) or British strain A/equine/Essex/1/2019 (rA/equine/Essex/1/2019) were generated. Equine antisera against A/equine/South Africa/2003 and A/equine/Ibaraki/2007 were produced by experimental infection. Antibody titers against A/equine/Tipperary/1/2019, rA/equine/Tipperary/1/2019, and rA/equine/Essex/1/2019 were 2.5- to 6.3-fold lower than those against the homologous vaccine strains A/equine/South Africa/4/2003 or A/equine/Ibaraki/2007. These results suggest that the ongoing evolution of the Fc1 viruses may impact on antigenicity and although antibodies against current vaccine strains neutralize the 2019 strains, ongoing surveillance is essential for optimum choice of candidate vaccine strains.
从 2018 年末到 2019 年,在美国流行的佛罗里达亚系 1 分支(Fc1)马流感病毒突然传播到欧洲,引发了许多疫情,而自 2018 年以来,在欧洲流行的佛罗里达亚系 2 分支(Fc2)病毒株则未在欧洲被检测到。自 2010 年以来,世界动物卫生组织(OIE)建议马流感病毒疫苗应包含类似于 A/equine/South Africa/4/2003 或 A/equine/Ohio/2003 的 Fc1 株。因此,日本的疫苗包含 A/equine/Ibaraki/1/2007 作为 Fc1 株。为了评估这些疫苗对 2019 年在欧洲检测到的 Fc1 株的有效性,我们使用马抗血清进行了病毒中和试验。使用的挑战病毒是爱尔兰株 A/equine/Tipperary/1/2019 和通过反向遗传学生成的两种重组病毒。生成了具有源自 A/equine/Tipperary/1/2019 的血凝素(HA)和神经氨酸酶(NA)的重组病毒(rA/equine/Tipperary/1/2019)或源自英国株 A/equine/Essex/1/2019 的重组病毒(rA/equine/Essex/1/2019)。通过实验感染产生了针对 A/equine/South Africa/2003 和 A/equine/Ibaraki/2007 的马抗血清。针对 A/equine/Tipperary/1/2019、rA/equine/Tipperary/1/2019 和 rA/equine/Essex/1/2019 的抗体滴度比针对同源疫苗株 A/equine/South Africa/4/2003 或 A/equine/Ibaraki/2007 的抗体滴度低 2.5 至 6.3 倍。这些结果表明,Fc1 病毒的持续进化可能会影响抗原性,尽管针对当前疫苗株的抗体可以中和 2019 年的株,但持续监测对于选择最佳候选疫苗株至关重要。