埃塞俄比亚裂谷中部和中部地区鸡新城疫病毒的分子检测和特征描述。

IF 1.7 Q2 VETERINARY SCIENCES
Veterinary medicine (Auckland, N.Z.) Pub Date : 2024-05-08 eCollection Date: 2024-01-01 DOI:10.2147/VMRR.S442787
Esubalew Endale Alemu, Bayeta Senbata, Melaku Sombo, Chala Guyassa, Dawit Hailu Alemayehu, Eleni Kidane, Adane Mihret, Andargachew Mulu, Hunduma Dinka
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引用次数: 0

摘要

背景:新城疫(ND)是一种高度传染性家禽疾病,在全球范围内造成重大经济损失。该病由新城疫病毒(NDV)引起,病毒株的早期检测和鉴定至关重要。了解某些地区流行的 NDV 株基因型有助于设计有效的疫苗来控制该疾病。在这方面,有关埃塞俄比亚裂谷中部和中部地区鸡只中 NDV 株系的信息很少。因此,本研究的目的是检测埃塞俄比亚裂谷中部和中部地区鸡只的 NDV 株基因型并确定其特征,同时检验该 NDV 株基因型是否与研究地区目前使用的疫苗株相匹配:方法:共采集了 98 份样本:方法:共收集了 98 份样本:78 份(气管和泄殖腔)拭子(来自 5 个鸡池)和 20 份组织样本。通过 qRT-PCR 扩增病毒矩阵(M)基因的保守区,检测 NDV 株系。为确定 NDV 株系的基因型,对 M 基因阳性样本进行了针对融合(F)基因区域的常规 PCR 扩增,并通过 Sanger 方法进行了测序:13.26% 的检测样本对研究地区的 NDV 株系呈阳性,差异有统计学意义(PC):目前的研究表明,存在与目前使用的疫苗株不同的 NDV 株基因型。尽管需要在国家层面对多个分离株进行大规模的特征描述,但本研究为野外 NDV 株系基因型与该国目前使用的 ND 疫苗株系之间存在差异提供了基础信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular Detection and Characterization of Newcastle Disease Virus from Chickens in Mid-Rift Valley and Central Part of Ethiopia.

Background: Newcastle disease (ND) is a highly infectious poultry disease that causes major economic losses worldwide. The disease is caused by Newcastle Disease Virus (NDV) and early detection and identification of the viral strain is essential. Having knowledge of the NDV strain genotype that circulates in some regions would help in designing an effective vaccine to control the disease. In this regard, there is little information on NDV strain in chickens in mid Rift Valley and the central part of Ethiopia. Therefore, the purpose of this study was to detect and characterize NDV strain genotype from chickens in mid-Rift Valley and the central part of Ethiopia and test whether this NDV strain genotype matches the vaccine strain currently used in the study area.

Methods: A total of 98 samples: 78 (tracheal and cloacal) swabs from chicken pools of five and 20 tissue samples were collected. To detect NDV strain, conserved region of the virus Matrix (M) gene was amplified by qRT-PCR. To characterize NDV strain genotypes, M-gene positive samples were specifically re-amplified by conventional PCR targeting the Fusion (F) gene region and sequenced by Sanger method.

Results: 13.26% of tested samples were positive for NDV strain in the study area with statistically significant difference (P<0.05) among the study sites. Further characterization of the F genes from NDV strain isolates by phylogenetic analysis indicated that one field isolate clustered with genotype VII whereas three of the isolates clustered to genotype I, II, and III. The isolate of the current NDV strain vaccine in use in the study area clustered with genotype II.

Conclusion: The current study indicates the existence of different NDV strain genotype from that of the vaccine strain currently used. Even though large-scale characterization of several isolates is required at national level, the current study laid baseline information for the existence of variations between field NDV strain genotype and vaccine strain currently used against ND in the country.

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