首页> 美国卫生研究院文献>Elsevier Public Health Emergency Collection >Bovine coronaviruses associated with enteric and respiratory diseases in Canadian dairy cattle display different reactivities to anti-HE monoclonal antibodies and distinct amino acid changes in their HE S and ns4.9 protein
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Bovine coronaviruses associated with enteric and respiratory diseases in Canadian dairy cattle display different reactivities to anti-HE monoclonal antibodies and distinct amino acid changes in their HE S and ns4.9 protein

机译:与加拿大奶牛肠道和呼吸系统疾病相关的牛冠状病毒对抗HE单克隆抗体表现出不同的反应性其HES和ns4.9蛋白的氨基酸发生明显变化

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摘要

Bovine coronavirus isolates associated with recent outbreaks of respiratory disease in Ontario and Quebec dairy farms were compared to reference strains known to be responsible for neonatal calf diarrhea (NCD) or winter dysentery (WD) of adult cattle. In respect to their hemagglutinating properties and their higher RDE activities with rat erythrocytes, WDBCoV strains differed from NCDBCoV strains and respiratory bovine coronaviruses RBCoV strains. Serologically, three MAbs directed to the HE glycoprotein of the WDBCoV strain BCQ.2590 recognized two serogroups amongst NCDBCoV strains by hemagglutination inhibition, whereas only one of the MAbs failed to react toward three of the four RBCoV isolates tested. Sequencing analysis of the S (S1 portion), HE, ORF4 and ORF5 genes of BCoV isolates associated with different clinical syndromes indicated that neither insertions or deletions could explain their distinct tropism. For the HE glycoprotein, a total of 15 amino acids (aa) substitutions were identified by comparing field isolates to the prototype Mebus strain. Two specific proline substitutions were identified for virulent strains being located in the signal peptides (aa 5) and aa position 367; one specific aa change was revealed at position 66 for RBCoV field isolates. Analysis of the S1 portion of the S glycoprotein revealed a total of eight aa changes specific to enteropathogenic (EBCoV) strains and eight aa changes specific to RBCoV strains. For all BCoV isolates studied, the region located between the S and M genes (ORF4) apparently encodes for two non-structural (ns) proteins of 4.9 and 4.8 kDa. A specific non-sense mutation was identified for the nucleotide at position 88 of the putative 4.9 kDa protein gene of RBCoV isolates resulting in 29 rather that 43 aa residues. The ORF5, which encodes a 12.7 ns protein and the 9.5 kDa E protein, was highly conserved amongst the BCoV field isolates.
机译:将与安大略省和魁北克奶牛场最近爆发的呼吸道疾病有关的牛冠状病毒分离株与已知可引起成年牛的新生小牛腹泻(NCD)或冬季痢疾(WD)的参考菌株进行了比较。关于它们的血凝特性和对大鼠红细胞的较高RDE活性,WDBCoV菌株不同于NCDBCoV菌株和呼吸牛冠状病毒RBCoV菌株。血清学上,针对WDBCoV菌株BCQ.2590的HE糖蛋白的3个单克隆抗体通过血凝抑制识别NCDBCoV菌株中的2个血清群,而只有1个单克隆抗体对所测试的4个RBCoV分离株中的3个没有反应。对与不同临床症状相关的BCoV分离株的S(S1部分),HE,ORF4和ORF5基因进行测序分析表明,插入或缺失均不能解释其独特的向性。对于HE糖蛋白,通过将田间分离株与原型Mebus菌株进行比较,鉴定出总共15个氨基酸(aa)取代。对于位于信号肽(aa 5)和aa 367位的强毒株,鉴定了两个特定的脯氨酸取代。 RBCoV场分离株的第66位揭示了一个特定的氨基酸变化。对S糖蛋白的S1部分的分析揭示了总共八个针对肠致病性(EBCoV)菌株的aa变化和八个针对RBCoV菌株的aa变化。对于所有研究的BCoV分离株,位于S和M基因之间的区域(ORF4)显然编码两个4.9和4.8 kDa的非结构(ns)蛋白。对于RBCoV分离株的推定的4.9kDa蛋白质基因的88位核苷酸上的核苷酸,鉴定出特异性的无义突变,产生29个氨基酸残基而不是43个氨基酸残基。编码12.7 ns蛋白和9.5 kDa E蛋白的ORF5在BCoV场分离株中高度保守。

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