Expression of Human Immunodeficiency Virus type 1 (HIV-1) coat protein genes in plants using cotton leaf curl Multan betasatellite-based vector

被引:7
作者
Kachoie, Elham Ataie [1 ]
Behjatnia, Seyed Ali Akbar [2 ]
Kharazmi, Sara [1 ]
机构
[1] Shiraz Univ, Inst Biotechnol, Shiraz, Iran
[2] Shiraz Univ, Plant Virol Res Ctr, Coll Agr, Shiraz, Iran
来源
PLOS ONE | 2018年 / 13卷 / 01期
关键词
HIGH-LEVEL EXPRESSION; TOBACCO-MOSAIC-VIRUS; GEMINIVIRUS VECTORS; TRANSIENT EXPRESSION; VACCINE PRODUCTION; FOREIGN PROTEINS; VIRAL VECTORS; DNA; REPLICATION; SATELLITE;
D O I
10.1371/journal.pone.0190403
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
It has already been demonstrated that a betasatellite associated with cotton leaf curl Multan virus (CLCuMB) can be used as a plant and animal gene delivery vector to plants. To examine the ability of CLCuMB as a tool to transfer coat protein genes of HIV-1 to plants, two recombinant CLCuMB constructs in which the CLCuMB beta C1 ORF was replaced with two HIV-1 genes fractions including a 696 bp DNA fragment related to the HIV-1 p24 gene and a 1501 bp DNA fragment related to the HIV-1 gag gene were constructed. Gag is the HIV-1 coat protein gene and p24 is a component of the particle capsid. Gag and p24 are used for vaccine production. Recombinant constructs were inoculated to Nicotiana glutinosa and N. benthamiana plants in the presence of an Iranian isolate of Tomato yellow leaf curl virus (TYLCV-[Ab]) as a helper virus. PCR analysis of inoculated plants indicated that p24 gene was successfully replicated in inoculated plants, but the gag gene was not. Real-time PCR and ELISA analysis of N. glutinosa and N. benthamiana plants containing the replicative forms of recombinant construct of CLCuMB/p24 indicated that p24 was expressed in these plants. This CLCuMB-based expression system offers the possibility of mass production of recombinant HIV-1 p24 protein in plants.
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页数:18
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