Laboratory of Epidemiology and Veterinary Microbiology LR 11 IPT 03, Institut Pasteur of Tunis, University of Tunis El Manar, 13 place Pasteur, BP74 Tunis Belvedere 1002, Tunisia.
Poult Sci. 2019 Oct 1;98(10):4338-4345. doi: 10.3382/ps/pez384.
Avian infectious bronchitis virus (IBV) is responsible of significant economic losses for poultry industry around the world, through evolution of its pathogenicity, inadequacy of vaccines, and virus evasion. Such evasion is related to the unstable nature of its RNA, in particular the S glycoprotein encoding gene, which raises great challenges with regard to the control of the disease, along with the lack of proof reading mechanisms of the RNA polymerase. The emergence of new variants might be a reason for the endemic outbreaks that are being reported in Tunisia, in addition to poor vaccination techniques and ineffective prophylactic programs. In the present study, partial nucleotide sequences of the S1 glycoprotein gene and the 3'-untranslated region (UTR) of 2 Tunisian isolates, TN1011/16 and TN1012/16, identified in 2016, were determined. Specific mutations were found in S1 gene as well as in 3'UTR region. Phylogenetic analysis of the S1 nucleotide sequences showed that both isolates are closely related to the Algerian strains, and formed a common cluster within the genotype I. In addition, these isolates were non-recombinant ones, confirming that they are unique variants. Based on their S1 gene sequences, TN1011/16 and TN1012/16 strains were distant from the H120 vaccine strain, commercially used in Tunisia along with the variant vaccine 793B type (4/91). A comparison between nucleotide sequences of their 3'UTR region and S1 gene showed a difference in IBV classification. The obtained results have confirmed that the IBVsequence continues to drift and brings valuable information in relation with its evolution, vaccine development and better control of the disease.
禽传染性支气管炎病毒(IBV)通过其致病性的演变、疫苗的不足以及病毒的逃逸,给全世界的家禽业造成了巨大的经济损失。这种逃逸与它的 RNA 的不稳定性质有关,特别是编码 S 糖蛋白的基因,这给疾病的控制带来了巨大的挑战,同时也缺乏 RNA 聚合酶的校对机制。新变种的出现可能是突尼斯报告的地方性爆发的原因之一,此外还有疫苗接种技术差和预防性计划无效等原因。在本研究中,测定了 2016 年鉴定的 2 株突尼斯分离株 TN1011/16 和 TN1012/16 的 S1 糖蛋白基因和 3'UTR 区的部分核苷酸序列。在 S1 基因和 3'UTR 区发现了特定的突变。S1 核苷酸序列的系统发育分析表明,这两种分离株与阿尔及利亚株密切相关,并且在 I 型内形成了一个共同的簇。此外,这些分离株是非重组的,证实它们是独特的变种。基于它们的 S1 基因序列,TN1011/16 和 TN1012/16 株与在突尼斯商业使用的 H120 疫苗株以及变体疫苗 793B 型(4/91)相距甚远。它们 3'UTR 区和 S1 基因核苷酸序列的比较显示出 IBV 分类的差异。获得的结果证实了 IBV 序列的持续漂移,并为其进化、疫苗开发和更好地控制疾病提供了有价值的信息。