首页> 外文OA文献 >Novel Receptor Specificity of Avian Gammacoronaviruses That Cause Enteritis
【2h】

Novel Receptor Specificity of Avian Gammacoronaviruses That Cause Enteritis

机译:引起肠炎的禽伽马冠状病毒的新型受体特异性

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Viruses exploit molecules on the target membrane as receptors for attachment and entry into host cells. Thus, receptor expression patterns can define viral tissue tropism and might to some extent predict the susceptibility of a host to a particular virus. Previously, others and we have shown that respiratory pathogens of the genus Gammacoronavirus, including chicken infectious bronchitis virus (IBV), require specific alpha2,3-linked sialylated glycans for attachment and entry. Here, we studied determinants of binding of enterotropic avian gammacoronaviruses, including turkey coronavirus (TCoV), guineafowl coronavirus (GfCoV), and quail coronavirus (QCoV), which are evolutionarily distant from respiratory avian coronaviruses based on the viral attachment protein spike (S1). We profiled the binding of recombinantly expressed S1 proteins of TCoV, GfCoV, and QCoV to tissues of their respective hosts. Protein histochemistry showed that the tissue binding specificity of S1 proteins of turkey, quail, and guineafowl CoVs was limited to intestinal tissues of each particular host, in accordance with the reported pathogenicity of these viruses in vivo. Glycan array analyses revealed that, in contrast to the S1 protein of IBV, S1 proteins of enteric gammacoronaviruses recognize a unique set of nonsialylated type 2 poly-N-acetyl-lactosamines. Lectin histochemistry as well as tissue binding patterns of TCoV S1 further indicated that these complex N-glycans are prominently expressed on the intestinal tract of various avian species. In conclusion, our data demonstrate not only that enteric gammacoronaviruses recognize a novel glycan receptor but also that enterotropism may be correlated with the high specificity of spike proteins for such glycans expressed in the intestines of the avian host. IMPORTANCE: Avian coronaviruses are economically important viruses for the poultry industry. While infectious bronchitis virus (IBV), a respiratory pathogen of chickens, is rather well known, other viruses of the genus Gammacoronavirus, including those causing enteric disease, are hardly studied. In turkey, guineafowl, and quail, coronaviruses have been reported to be the major causative agent of enteric diseases. Specifically, turkey coronavirus outbreaks have been reported in North America, Europe, and Australia for several decades. Recently, a gammacoronavirus was isolated from guineafowl with fulminating disease. To date, it is not clear why these avian coronaviruses are enteropathogenic, whereas other closely related avian coronaviruses like IBV cause respiratory disease. A comprehensive understanding of the tropism and pathogenicity of these viruses explained by their receptor specificity and receptor expression on tissues was therefore needed. Here, we identify a novel glycan receptor for enteric avian coronaviruses, which will further support the development of vaccines.
机译:病毒利用靶膜上的分子作为受体附着并进入宿主细胞。因此,受体表达模式可以定义病毒组织的向性,并可能在某种程度上预测宿主对特定病毒的敏感性。以前,其他人和我们已经表明,γ冠状病毒属的呼吸道病原体,包括鸡传染性支气管炎病毒(IBV),需要特定的与α2,3连接的唾液酸化聚糖才能附着和进入。在这里,我们研究了肠溶性肠道丙种冠状病毒的结合决定因素,包括火鸡冠状病毒(TCoV),豚鼠冠状病毒(GfCoV)和鹌鹑冠状病毒(QCoV),它们基于病毒附着蛋白的尖峰(S1)与呼吸道禽冠状病毒进化距离较远。我们介绍了重组表达的TCoV,GfCoV和QCoV的S1蛋白与它们各自宿主组织的结合。蛋白质组织化学表明,根据已报道的这些病毒在体内的致病性,火鸡,鹌鹑和豚鼠CoV的S1蛋白的组织结合特异性仅限于每个特定宿主的肠道组织。聚糖阵列分析显示,与IBV的S1蛋白相反,肠道γ冠状病毒的S1蛋白可识别一组独特的非唾液酸化2型聚N-乙酰基-乳糖胺。凝集素的组织化学以及TCoV S1的组织结合模式进一步表明,这些复杂的N-聚糖在各种禽类的肠道中显着表达。总之,我们的数据不仅表明肠丙种冠状病毒能够识别一种新的聚糖受体,而且肠溶性可能与这种禽类肠道中表达的聚糖的突突蛋白的高特异性相关。重要信息:禽冠状病毒是家禽业的重要经济病毒。尽管鸡呼吸道病原体传染性支气管炎病毒(IBV)是众所周知的,但几乎没有研究过γ冠状病毒属的其他病毒,包括引起肠道疾病的病毒。据报道,在火鸡,珍珠鸡和鹌鹑中,冠状病毒是肠道疾病的主要病原体。具体而言,在北美,欧洲和澳大利亚已有数十年的报道报道了土耳其冠状病毒的爆发。最近,从具有暴发性疾病的豚鼠中分离出了γ-冠状病毒。迄今为止,尚不清楚为什么这些禽冠状病毒是肠致病性的,而其他紧密相关的禽冠状病毒如IBV会引起呼吸系统疾病。因此,需要对这些病毒的向性和致病性有一个全面的了解,以它们在组织中的受体特异性和受体表达来解释。在这里,我们确定了肠道禽冠状病毒的新型聚糖受体,它将进一步支持疫苗的开发。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号