Inan Cihan, Muratoglu Hacer, Arif Basil M, Demirbag Zihni
Department of Biology, Faculty of Sciences, Karadeniz Technical University, Trabzon, Turkey.
Department of Molecular Biology and Genetics, Faculty of Sciences, Karadeniz Technical University, Trabzon, Turkey.
Virus Genes. 2018 Jun;54(3):438-445. doi: 10.1007/s11262-018-1561-4. Epub 2018 Apr 17.
Amsacta moorei entomopoxvirus (AMEV) infects certain lepidopteran and orthopteran insects and is the most studied member of the genus Betaentomopoxvirus. It has been considered as a potential vector for gene therapy, a vector to express exogenous proteins and a biological control agent. One of its open reading frames, amv248, encodes a putative glycosyltransferase and is the only known attachment protein conserved in AMEV and chordopoxviruses. The ORF was successfully expressed and the protein was shown to bind soluble heparin, both in silico and in vitro. Our results also showed that, while viral infection was inhibited by soluble glycosaminoglycans (GAGs), GAG-deficient cells were more resistant to the virus. Finally, we revealed that amv248 encodes an active heparin-binding glycosyltransferase which is likely to have a key role in the initiation of infection by AMEV.
摩尔伊氏昆虫痘病毒(AMEV)感染某些鳞翅目和直翅目昆虫,是β昆虫痘病毒属中研究最多的成员。它被认为是基因治疗的潜在载体、表达外源蛋白的载体和生物防治剂。其一个开放阅读框amv248编码一种推定的糖基转移酶,是AMEV和脊索痘病毒中唯一已知的保守附着蛋白。该开放阅读框成功表达,并且该蛋白在计算机模拟和体外实验中均显示能结合可溶性肝素。我们的结果还表明,虽然可溶性糖胺聚糖(GAGs)可抑制病毒感染,但缺乏GAG的细胞对该病毒更具抗性。最后,我们揭示amv248编码一种活性肝素结合糖基转移酶,它可能在AMEV感染起始过程中起关键作用。