Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, 17493 Greifswald - Insel Riems, Germany.
Department of Experimental Animal Facilities and Biorisk Management, Friedrich-Loeffler-Institut, 17493 Greifswald - Insel Riems, Germany.
Viruses. 2020 Feb 19;12(2):232. doi: 10.3390/v12020232.
In 2012 and 2013, the genomic sequences of two novel influenza A virus (IAV) subtypes, designated H17N10 and H18N11, were identified via next-generation sequencing in the feces of the little yellow-shouldered fruit bat () and the flat-faced fruit-eating bat (), respectively. The pathogenesis caused by these viruses in their respective host species is currently insufficiently understood, which is primarily due to the inability to obtain and keep these bat species under appropriate environmental and biosafety conditions. Seba's short-tailed bats (), in contrast, are close relatives and a natural H18N11 reservoir species, with the advantage of established animal husbandry conditions in academic research. To study viral pathogenesis in more detail, we here oro-nasally inoculated Seba's short-tailed bats with the bat IAV H18N11 subtype. Following inoculation, bats appeared clinically healthy, but the histologic examination of tissues revealed a mild necrotizing rhinitis. Consistently, IAV-matrix protein and H18-RNA positive cells were seen in lesioned respiratory and olfactory nasal epithelia, as well as in intestinal tissues. A RT-qPCR analysis confirmed viral replication in the conchae and intestines as well as the presence of viral RNA in the excreted feces, without horizontal transmission to naïve contact animals. Moreover, all inoculated animals seroconverted with low titers of neutralizing antibodies.
在 2012 年和 2013 年,通过下一代测序技术分别在小黄肩果蝠和扁脸果蝠的粪便中鉴定出了两种新型甲型流感病毒(IAV)亚型,分别命名为 H17N10 和 H18N11。这些病毒在各自宿主物种中引起的发病机制目前了解不足,这主要是由于无法在适当的环境和生物安全条件下获得和保存这些蝙蝠物种。相比之下,短尾果蝠是近亲,也是自然的 H18N11 储存物种,具有在学术研究中建立动物养殖条件的优势。为了更详细地研究病毒发病机制,我们在这里通过鼻内接种将蝙蝠 IAV H18N11 亚型接种到短尾果蝠中。接种后,蝙蝠表现出临床健康,但组织学检查显示轻度坏死性鼻炎。一致地,在受损的呼吸和嗅觉鼻上皮以及肠道组织中,观察到 IAV-基质蛋白和 H18-RNA 阳性细胞。RT-qPCR 分析证实了鼻甲和肠道中的病毒复制以及粪便中存在病毒 RNA,没有向未接触的接触动物进行水平传播。此外,所有接种动物均发生血清转化,中和抗体滴度较低。