Department of Microbiology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Mashhad Branch, Razi Vaccine and Serum Research Institute, Agricultural Research, Education and Extension Organization (AREEO), Mashhad, Iran.
Vet Med Sci. 2022 Nov;8(6):2521-2531. doi: 10.1002/vms3.928. Epub 2022 Sep 9.
Newcastle disease (ND) is an economically significant poultry disease worldwide. During field surveillance for ND in 2010 in Iran, a backyard chicken flock showed clinical signs of ND with 100% mortality.
We aimed to characterise genetically, biologically and epidemiologically an exotic virulent ND virus (NDV) detected in Iran.
After observing high mortality, dead birds were sampled and then disposed of by burial, and the chicken house was disinfected. Tissue samples were molecularly tested for NDV. The genetic homogeneity of the isolate RT30/2010 was tested by plaque assay, and then a large virus plaque was used for the second step of plaque purification. Fusion and matrix complete genes were sequenced and used for genotyping and epidemiological tracing. We tested biological pathotypes using mean death time (MDT) and intracerebral pathogenicity index (ICPI) assays.
The isolate formed heterogeneous plaques in chicken embryo fibroblast cells. The second step of plaque purification produced homogeneous and large plaques. Phylogenetic analysis using both genes classified the virus into sub-genotype XIII.2.1. Nucleic acid and amino acid identities of RT30/2010 fusion gene with the closest available isolate SPVC/Karachi/NDV/43 are 97.95% and 98.73%, respectively. Isolate has RRRKRF motif at the fusion cleavage site, and pathogenicity tests showed MDT of 56.4 h and ICPI of 1.85.
This study presents the first detection and characterisation of a velogenic NDV of sub-genotype XIII.2.1 from Iran. Our follow-up surveillance for ND shows that timely virus detection and carcass management have led to the cessation of virus transmission in Iran.
新城疫(ND)是一种在全球范围内对家禽具有重要经济意义的疾病。在 2010 年伊朗对 ND 的田间监测中,一个后院鸡群出现了 ND 的临床症状,死亡率为 100%。
我们旨在对在伊朗检测到的一种外来强毒 ND 病毒进行基因、生物学和流行病学特征分析。
在观察到高死亡率后,对病死禽进行采样,然后进行埋葬处理,并对鸡舍进行消毒。对组织样本进行 ND 病毒的分子检测。通过噬斑试验检测分离株 RT30/2010 的遗传同质性,然后使用大的病毒噬斑进行第二步噬斑纯化。融合和基质完整基因进行测序,并用于基因分型和流行病学溯源。我们使用平均死亡时间(MDT)和脑内致病指数(ICPI)试验测试生物病原型。
分离株在鸡胚成纤维细胞中形成异质噬斑。第二步噬斑纯化产生了同质的大噬斑。使用这两个基因进行的系统发育分析将病毒分为亚基因型 XIII.2.1。RT30/2010 的核苷酸和氨基酸与最接近的现有分离株 SPVC/Karachi/NDV/43 的融合基因的同源性分别为 97.95%和 98.73%。分离株在融合切割位点具有 RRRKRF 基序,致病性试验显示 MDT 为 56.4 小时,ICPI 为 1.85。
本研究首次从伊朗检测到并鉴定了一种属于亚基因型 XIII.2.1 的强毒 ND 病毒。我们对 ND 的后续监测表明,及时的病毒检测和病尸处理已导致伊朗病毒传播的停止。