Pikuła Anna, Domańska-Blicharz Katarzyna, Cepulis Rytis, Śmietanka Krzysztof
Department of Poultry Diseases, National Veterinary Research Institute, 24-100 Pulawy, Poland.
MSD Animal Health, 08124 Vilnius, Lithuania.
J Vet Res. 2017 Dec 6;61(2):145-149. doi: 10.1515/jvetres-2017-0018. eCollection 2017 Jun.
Infectious bursal disease virus (IBDV) is a causative agent of immunosuppressive disorder resulting in significant losses to the world poultry industry. This study describes the molecular characterisation of an atypical IBDV from a field outbreak that occurred in vaccinated chicken flocks in Latvia in 2011.
Ten bursae of Fabricius from each flock were collected for laboratory examination. Virus isolation was performed in embryonated eggs and CEF culture. The RT-PCR aimed at hypervariable domain of VP2 gene combined with sequencing was performed for detection and identification of IBDV.
The molecular examinations confirmed the IBDV infection. The analysis of the amino acid sequence revealed that the strain possessed four amino acids at VP2 protein (222A, 256I, 294I, and 299S), indicating a genetic relatedness to a very virulent IBDV. However, some unique or rare amino acid substitutions (219L, 220F, 254D, 279N, and 280T) were also detected.
The obtained results demonstrate the occurrence of IBDV with a high mutation rate within the hypervariable domain of VP2 peptide, and highlight the necessity of implementation of IBDV surveillance in Eastern European poultry industry to determine whether this strain is an exception or a new wave of IBDV with new genetic features emerged in the field.
传染性法氏囊病病毒(IBDV)是一种导致免疫抑制性疾病的病原体,给全球家禽业造成了重大损失。本研究描述了2011年在拉脱维亚接种疫苗的鸡群中发生的一次野外疫情中一株非典型IBDV的分子特征。
从每个鸡群中收集10个法氏囊进行实验室检查。在鸡胚和鸡胚成纤维细胞(CEF)培养物中进行病毒分离。针对VP2基因高变区进行逆转录聚合酶链反应(RT-PCR)并结合测序,用于检测和鉴定IBDV。
分子检查证实了IBDV感染。氨基酸序列分析表明,该毒株在VP2蛋白上有四个氨基酸(222A、256I、294I和299S),表明与超强毒IBDV存在遗传相关性。然而,还检测到一些独特或罕见的氨基酸替代(219L、220F、254D、279N和280T)。
所得结果表明在VP2肽高变区内存在高突变率的IBDV,并强调了在东欧家禽业实施IBDV监测的必要性,以确定该毒株是一个例外还是在该领域出现的具有新遗传特征的IBDV新毒株。