Faculty of Veterinary Medicine, Universiti Putra Malaysia, Serdang, Selangor, Malaysia.
Institute of Bioscience, Universiti Putra Malaysia, Serdang, Selangor, Malaysia.
PLoS One. 2019 Dec 31;14(12):e0225863. doi: 10.1371/journal.pone.0225863. eCollection 2019.
Fowl adenovirus (FAdV) is the causative agent of inclusion body hepatitis (IBH) in chickens with significant economic losses due to high mortality and poor production. It was objectives of the study to attenuate and determine the molecular characteristic of FAdV isolate (UPM1137) of Malaysia passages in primary chicken embryo liver (CEL) cells. The cytopathic effect (CPE) was recorded and the present of the virus was detected by polymerase chain reaction (PCR). Nucleotide and amino acid changes were determined and a phylogenetic tree was constructed. The pathogenicity and immunogenicity of the virus at passage 35 (CEL35) with virus titre of 106.7TCID50/mL was determined in day old specific pathogen free (SPF) chicks via oral or subcutaneous route of inoculation. The study demonstrated that the FAdV isolate was successfully propagated and attenuated in CEL cells up to 35th consecutive passages (CEL35) with delayed of CPE formation within 48 to 72 post inoculation (pi) from CEL20 onwards. The virus caused typical CPE with basophilic intranuclear inclusion bodies, refractile and clumping of cells. The virus is belong to serotype 8b with substitution of amino acid at position 44, 133 and 185 in L1 loop of hexon gene and in knob of fiber gene at position 348 and 360 at CEL35. It is non-pathogenic, but immunogenic in SPF chickens. It was concluded that the FAdV isolate was successfully attenuated in CEL cells with molecular changes in major capsid proteins which affect its infectivity in cell culture and SPF chickens.
禽腺病毒(FAdV)是导致鸡包涵体肝炎(IBH)的病原体,由于高死亡率和生产性能下降,给养鸡业造成了巨大的经济损失。本研究的目的是在原代鸡胚肝细胞(CEL)中对马来西亚分离株(UPM1137)进行减毒,并确定其分子特征。通过聚合酶链反应(PCR)记录细胞病变效应(CPE)并检测病毒的存在。确定核苷酸和氨基酸的变化,并构建系统发育树。通过口服或皮下途径接种,在 1 日龄无特定病原体(SPF)雏鸡中测定第 35 代(CEL35)病毒的毒力(106.7TCID50/mL)的致病性和免疫原性。研究表明,该 FAdV 分离株在 CEL 细胞中成功传代和减毒,在 CEL20 代后连续传代 35 代(CEL35),接种后 48 至 72 小时内 CPE 形成延迟。病毒引起典型的 CPE,具有嗜碱性核内包涵体、折光性和细胞聚集。该病毒属于血清型 8b,在 L1 环的六邻体基因和纤维基因的 knob 中,在位置 44、133 和 185 处的氨基酸发生取代,在 CEL35 处的位置 348 和 360 处发生取代。它是非致病性的,但在 SPF 鸡中具有免疫原性。结论是,该 FAdV 分离株在 CEL 细胞中成功减毒,主要衣壳蛋白发生分子变化,影响其在细胞培养和 SPF 鸡中的感染力。