State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.
Key Laboratory of Plant Pathology of Ministry of Agriculture, College of Plant Protection, China Agricultural University, Beijing, 100193, China.
Mol Plant Pathol. 2019 Apr;20(4):471-484. doi: 10.1111/mpp.12768. Epub 2019 Jan 9.
Despite the fact that venom allergen-like proteins (VAPs) have been identified in many animal- and plant-parasitic nematodes, studies on VAPs in Heterodera avenae, which is an important phytonematode, are still in their infancy. Here, we isolated, cloned and characterized two VAPs, named HaVAP1 and HaVAP2, from H. avenae. The two encoded proteins, HaVAP1 and HaVAP2, harbour an SCP-like domain each, but share only 38% identity with each other. HaVAP1 and HaVAP2 are expressed in subventral and dorsal oesophageal glands, respectively. HaVAP1 is expressed mainly at the early stages, whereas HaVAP2 accumulates principally at the late stages. Both HaVAP1 and HaVAP2 are secreted when expressed in Nicotiana benthamiana leaves, but HaVAP1 is delivered into chloroplasts, whereas HaVAP2 is translocated to the nucleus without signal peptides. Knocking down HaVAP1 increased the virulence of H. avenae. In contrast, silencing of HaVAP2 hampered the parasitism of H. avenae. Both HaVAP1 and HaVAP2 suppressed the cell death induced by BAX in N. benthamiana leaves. Moreover, HaVAP2 physically interacted with a CYPRO4-like protein (HvCLP) of Hordeum vulgare in the nucleus of the plant. It is reasonable to speculate that the changes in the transcript of HvCLP are associated with HaVAP2 during the parasitism of H. avenae. All results obtained in this study show that both HaVAP1 and HaVAP2 are involved in the parasitism of H. avenae, but they possess different functions, broadening our understanding of the parasitic mechanism of H. avenae.
尽管毒液过敏原样蛋白 (VAPs) 已在许多动物和植物寄生线虫中被鉴定出来,但对于重要的植物寄生线虫禾谷孢囊线虫 (Heterodera avenae) 中的 VAPs 研究仍处于起步阶段。在这里,我们从禾谷孢囊线虫中分离、克隆和鉴定了两个 VAPs,分别命名为 HaVAP1 和 HaVAP2。这两个编码蛋白,HaVAP1 和 HaVAP2,各自都含有一个 SCP 样结构域,但彼此之间只有 38%的同源性。HaVAP1 和 HaVAP2 分别在亚腹和背食道腺中表达。HaVAP1 主要在早期表达,而 HaVAP2 主要在晚期积累。当在 Nicotiana benthamiana 叶片中表达时,HaVAP1 和 HaVAP2 都被分泌,但 HaVAP1 被递送到叶绿体中,而 HaVAP2 没有信号肽就被转运到细胞核中。敲低 HaVAP1 增加了禾谷孢囊线虫的毒力。相比之下,沉默 HaVAP2 阻碍了禾谷孢囊线虫的寄生。HaVAP1 和 HaVAP2 都抑制了 BAX 在 N. benthamiana 叶片中诱导的细胞死亡。此外,HaVAP2 在植物细胞核中与大麦 CYPRO4 样蛋白 (HvCLP) 发生物理相互作用。可以合理地推测,HvCLP 的转录变化与禾谷孢囊线虫寄生过程中 HaVAP2 的变化有关。本研究获得的所有结果表明,HaVAP1 和 HaVAP2 都参与了禾谷孢囊线虫的寄生,但它们具有不同的功能,这拓宽了我们对禾谷孢囊线虫寄生机制的理解。