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从印度马哈拉施特拉邦疫情中鉴定并表征一种新型传染性法氏囊病病毒。

Identification and characterization of a novel infectious bursal disease virus from outbreaks in Maharashtra Province of India.

作者信息

Awandkar Sudhakar P, Tembhurne Prabhakar A, Kesharkar Jeevan A, Kurkure Nitin V, Chaudhari Sandeep P, Bonde Sachin W, Ingle Vijay C

机构信息

Department of Veterinary Microbiology, Nagpur Veterinary College, MAFSU, Nagpur - 440 006, Maharashtra, India.

Department of Veterinary Pathology, Nagpur Veterinary College, MAFSU, Nagpur - 440 006, Maharashtra, India.

出版信息

Vet World. 2018 Nov;11(10):1516-1525. doi: 10.14202/vetworld.2018.1516-1525. Epub 2018 Oct 29.

Abstract

AIM

The study was undertaken to isolate infectious bursal disease virus (IBDV) from clinical cases in broiler and cockerel flocks of Maharashtra state, India, and its molecular epidemiological investigation.

MATERIALS AND METHODS

The morbid bursal tissues were collected from flocks suspected for IBD. The samples were subjected for virus adaptation in primary chicken embryo fibroblast (CEF) cells followed by confirmation by reverse transcription polymerase chain reaction (RT-PCR) for partial VP sequence and phylogenetic analysis.

RESULTS

The isolation of IBDV from field samples took seven blind passages for adaptation in CEF. The cytopathic effects included rounding, aggregation, vacuolation, and detachment of the cells. The RT-PCR showed amplification of 627 bp amplicon specific to the primers for VP gene fragment which confirmed successful adaptation and isolation of IBDV using CEF. The nucleotide and deduced amino acids based on phylogeny clustered the current isolate in a distinct clade with classical virulent and antigenic variants. It showed divergence from very virulent (vv) and vaccine strains of Indian origin. The isolate showed unique amino acid substitution at A329V as compared to all other IBDVs. The variation in key amino acids was reported at A222, I242, Q249, Q253, A256, T270, N279, T284, I286, L294, N299, and V329. It shared conserved amino acids at position A222, I242, and Q253 as reported in vvIBDV isolates. However, the amino acids reported at position T270, N279, T284, L294, and N299 are conserved in classic, antigenic variant and attenuated strains of IBDV. The amino acids at positions N279 and T284 indicated that the isolate has key amino acids for cell culture replication.

CONCLUSION

The IBDV field isolate does not reveal the full nucleotide sequence signature of vvIBDV as well as vaccine strains. Hence, we can conclude that it might not belong to vvIBDVs of Indian origin and the vaccine strain used in the region. This may be suggestive of the evolution of the IBDV in the field due to the coexistence of circulating field strains and live attenuated hot strains, resulting into morbidity and mortality, warranting the need for safer protective vaccines, and implementation of stringent biosecurity measures to minimize loss to farmers.

摘要

目的

本研究旨在从印度马哈拉施特拉邦肉鸡和公鸡鸡群的临床病例中分离传染性法氏囊病病毒(IBDV),并对其进行分子流行病学调查。

材料与方法

从疑似患有IBD的鸡群中采集发病的法氏囊组织。将样本在原代鸡胚成纤维细胞(CEF)中进行病毒适应性培养,随后通过逆转录聚合酶链反应(RT-PCR)对部分VP序列进行确认并进行系统发育分析。

结果

从田间样本中分离IBDV在CEF中经过7次盲传才得以适应。细胞病变效应包括细胞变圆、聚集、空泡化和脱落。RT-PCR显示扩增出了针对VP基因片段引物的627 bp扩增子,这证实了使用CEF成功适应并分离出了IBDV。基于系统发育的核苷酸和推导氨基酸将当前分离株聚类到一个与经典强毒株和抗原变异株不同的进化枝中。它与印度来源的超强毒(vv)和疫苗株存在差异。与所有其他IBDV相比,该分离株在A329V处显示出独特的氨基酸替换。在A222、I242、Q249、Q253、A256、T270、N279、T284、I286、L294、N299和V329处报道了关键氨基酸的变异。如在vvIBDV分离株中报道的那样,它在A222、I242和Q253位置共享保守氨基酸。然而,在IBDV的经典株、抗原变异株和弱毒株中,在T270、N279、T284、L294和N299位置报道的氨基酸是保守的。N279和T284位置的氨基酸表明该分离株具有细胞培养复制的关键氨基酸。

结论

IBDV田间分离株未显示出vvIBDV以及疫苗株的完整核苷酸序列特征。因此,我们可以得出结论,它可能不属于印度来源的vvIBDV和该地区使用的疫苗株。这可能暗示由于循环田间毒株和活弱毒热毒株的共存,IBDV在田间发生了进化,导致发病和死亡,这就需要更安全的保护性疫苗,并实施严格的生物安全措施以尽量减少农民的损失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5755/6247889/3d5bc724aba7/VetWorld-11-1516-g001.jpg

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