1 Department of Entomology & Plant Pathology, Oklahoma State University, Stillwater, OK 74078, U.S.A.
2 Departamento de Ciencias de la Vida y la Agricultura, Universidad de las Fuerzas Armadas-ESPE, Av. General Rumiñahui s/n, Sangolquí, Pichincha, Ecuador.
Mol Plant Microbe Interact. 2016 Oct;29(10):750-766. doi: 10.1094/MPMI-07-16-0147-R. Epub 2016 Oct 24.
The inositol requiring enzyme (IRE1) is an endoplasmic reticulum (ER) stress sensor. When activated, it splices the bZIP60 mRNA, producing a truncated transcription factor that upregulates genes involved in the unfolded protein response. Bax inhibitor 1 (BI-1) is another ER stress sensor that regulates cell death in response to environmental assaults. The potyvirus 6K2 and potexvirus TGB3 proteins are known to reside in the ER, serving, respectively, as anchors for the viral replicase and movement protein complex. This study used green fluorescent protein (GFP)-tagged Turnip mosaic virus (TuMV), Plantago asiatica mosaic virus (PlAMV), Potato virus Y (PVY), and Potato virus X (PVX) to determine that the IRE1/bZIP60 pathway and BI-1 machinery are induced early in virus infection in Arabidopsis thaliana, Nicotiana benthamiana, and Solanum tuberosum. Agrodelivery of only the potyvirus 6K2 or TGB3 genes into plant cells activated bZIP60 and BI-1 expression in Arabidopsis thaliana, N. benthamiana, and S. tuberosum. Homozygous ire1a-2, ire1b-4, and ire1a-2/ire1b-4 mutant Arabidopsis plants were inoculated with TuMV-GFP or PlAMV-GFP. PlAMV accumulates to a higher level in ire1a-2 or ire1a-2/ire1b-4 mutant plants than in ire1b-4 or wild-type plants. TuMV-GFP accumulates to a higher level in ire1a-2, ire1b-4, or ire1a-2/ire1b-4 compared with wild-type plants, suggesting that both isoforms contribute to TuMV-GFP infection. Gene silencing was used to knock down bZIP60 and BI-1 expression in N. benthamiana. PVX-GFP and PVY-GFP accumulation was significantly elevated in these silenced plants compared with control plants. This study demonstrates that two ER stress pathways, namely IRE1/bZIP60 and the BI-1 pathway, limit systemic accumulation of potyvirus and potexvirus infection. Silencing BI-1 expression also resulted in systemic necrosis. These data suggest that ER stress-activated pathways, led by IRE1 and BI-1, respond to invading potyvirus and potexviruses to restrict virus infection and enable physiological changes enabling plants to tolerate virus assault.
肌醇需求酶(IRE1)是内质网(ER)应激传感器。当被激活时,它剪接 bZIP60 mRNA,产生一种截断的转录因子,上调参与未折叠蛋白反应的基因。Bax 抑制剂 1(BI-1)是另一种 ER 应激传感器,可响应环境攻击调节细胞死亡。已知马铃薯 Y 病毒(PVY)和马铃薯 X 病毒(PVX)的 6K2 和 TGB3 蛋白分别作为病毒复制酶和运动蛋白复合物的锚定物存在于内质网中。本研究使用绿色荧光蛋白(GFP)标记的芜菁花叶病毒(TuMV)、车前草花叶病毒(PlAMV)、马铃薯 Y 病毒(PVY)和马铃薯 X 病毒(PVX),确定 IRE1/bZIP60 途径和 BI-1 机制在拟南芥、烟草原生质体和马铃薯感染病毒早期被诱导。将马铃薯 Y 病毒 6K2 或 TGB3 基因仅通过农杆菌介导转入植物细胞,激活了 bZIP60 和 BI-1 在拟南芥、烟草原生质体和马铃薯中的表达。用 TuMV-GFP 或 PlAMV-GFP 接种 ire1a-2、ire1b-4 和 ire1a-2/ire1b-4 双突变拟南芥植物。PlAMV 在 ire1a-2 或 ire1a-2/ire1b-4 突变体植物中的积累水平高于 ire1b-4 或野生型植物。TuMV-GFP 在 ire1a-2、ire1b-4 或 ire1a-2/ire1b-4 中的积累水平高于野生型植物,表明两种同工酶均有助于 TuMV-GFP 感染。通过基因沉默敲低烟草原生质体中的 bZIP60 和 BI-1 表达。与对照植物相比,沉默植物中 PVX-GFP 和 PVY-GFP 的积累显著升高。本研究表明,两种内质网应激途径,即 IRE1/bZIP60 和 BI-1 途径,限制了马铃薯 Y 病毒和车前草花叶病毒感染的系统性积累。沉默 BI-1 表达也导致系统性坏死。这些数据表明,由 IRE1 和 BI-1 引发的内质网应激激活途径,对入侵的马铃薯 Y 病毒和车前草花叶病毒作出反应,限制病毒感染,并使植物发生生理变化,从而耐受病毒攻击。