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马来西亚生物反应器适应性超强传染性法氏囊病病毒分离株的传播及分子特征分析

Propagation and Molecular Characterization of Bioreactor Adapted Very Virulent Infectious Bursal Disease Virus Isolates of Malaysia.

作者信息

Lawal Nafi'u, Hair-Bejo Mohd, Arshad Siti Suri, Omar Abdul Rahman, Ideris Aini

机构信息

Department of Veterinary Pathology and Microbiology, Faculty of Veterinary Medicine, Universiti Putra Malaysia (UPM), 43400 Serdang, Selangor, Malaysia.

Department of Veterinary Microbiology, Faculty of Veterinary Medicine, Usmanu Danfodiyo University, Sokoto (UDUS), 2346 Sokoto, Nigeria.

出版信息

J Pathog. 2018 Sep 2;2018:1068758. doi: 10.1155/2018/1068758. eCollection 2018.

Abstract

Two Malaysian very virulent infectious bursal disease virus (vvIBDV) strains UPM0081 (also known as B00/81) and UPM190 (also known as UPM04/190) isolated from local IBD outbreaks in 2000 and 2004, respectively, were separately passaged for 12 consecutive times in 11-day-old specific pathogen free (SPF) chicken embryonated eggs (CEE) via the chorioallantoic membrane (CAM) route. The CEE passage 8 (EP8) isolates were passaged once in BGM-70 cell line yielding UPM0081EP8BGMP1 and UPM190EP8BGMP1, while the EP12 isolates were passaged 15 times in BGM-70 cell line yielding UPM0081EP12BGMP15 and UPM190EP12BGMP15 using T25 tissue culture flask. These isolates were all propagated once in bioreactor using cytodex 1 as microcarrier at 3 g per liter (3 g/L) yielding UPM0081EP8BGMP1BP1, UPM190EP8BGMP1BP1, UPM0081EP12BGMP15BP1, and UPM190EP12BGMP15BP1 isolates. The viruses were harvested at 3 days after inoculation, following the appearance of cytopathic effects (CPE) characterized by detachment from the microcarrier using standard protocol and filtered using 0.2 m syringe filter. The filtrates were positive for IBDV by RT-PCR and immunofluorescence. Sequence and phylogenetic tree analysis indicated that the isolates were of the vvIBDV strains and were not different from the flask propagated parental viruses.

摘要

分别从2000年和2004年当地传染性法氏囊病(IBD)疫情中分离出的两株马来西亚超强毒传染性法氏囊病病毒(vvIBDV)毒株UPM0081(也称为B00/81)和UPM190(也称为UPM04/190),通过绒毛尿囊膜(CAM)途径在11日龄无特定病原体(SPF)鸡胚(CEE)中连续传代12次。CEE传代8(EP8)分离株在BGM-70细胞系中传代一次,得到UPM0081EP8BGMP1和UPM190EP8BGMP1,而EP12分离株在BGM-70细胞系中使用T25组织培养瓶传代15次,得到UPM0081EP12BGMP15和UPM190EP12BGMP15。这些分离株均以每升3克(3 g/L)的细胞葡聚糖1作为微载体在生物反应器中传代一次,得到UPM0081EP8BGMP1BP1、UPM190EP8BGMP1BP1、UPM0081EP12BGMP15BP1和UPM190EP12BGMP15BP1分离株。接种后3天,在出现以从微载体上脱离为特征的细胞病变效应(CPE)后,按照标准方案收获病毒,并使用0.2μm注射器滤器过滤。通过RT-PCR和免疫荧光检测,滤液中IBDV呈阳性。序列和系统发育树分析表明,这些分离株属于vvIBDV毒株,与在培养瓶中传代的亲本病毒没有差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248d/6139196/41cf6b9ece3e/JPATH2018-1068758.001.jpg

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