Joubert Dirk A, Slaughter Ana R, Kemp Gabré, Becker John V W, Krooshof Geja H, Bergmann Carl, Benen Jacques, Pretorius Isak S, Vivier Melané A
Department of Viticulture & Oenology, Institute for Wine Biotechnology, Stellenbosch University, Stellenbosch, South Africa.
Transgenic Res. 2006 Dec;15(6):687-702. doi: 10.1007/s11248-006-9019-1. Epub 2006 Oct 27.
Polygalacturonase-inhibiting proteins (PGIPs) selectively inhibit polygalacturonases (PGs) secreted by invading plant pathogenic fungi. PGIPs display differential inhibition towards PGs from different fungi, also towards different isoforms of PGs originating from a specific pathogen. Recently, a PGIP-encoding gene from Vitis vinifera (Vvpgip1) was isolated and characterised. PGIP purified from grapevine was shown to inhibit crude polygalacturonase extracts from Botrytis cinerea, but this inhibitory activity has not yet been linked conclusively to the activity of the Vvpgip1 gene product. Here we use a transgenic over-expression approach to show that the PGIP encoded by the Vvpgip1 gene is active against PGs of B. cinerea and that over-expression of this gene in transgenic tobacco confers a reduced susceptibility to infection by this pathogen. A calculated reduction in disease susceptibility of 47-69% was observed for a homogeneous group of transgenic lines that was statistically clearly separated from untransformed control plants following infection with Botrytis over a 15-day-period. VvPGIP1 was subsequently purified from transgenic tobacco and used to study the specific inhibition profile of individual PGs from Botrytis and Aspergillus. The heterologously expressed and purified VvPGIP1 selectively inhibited PGs from both A. niger and B. cinerea, including BcPG1, a PG from B. cinerea that has previously been shown to be essential for virulence and symptom development. Altogether our data confirm the antifungal nature of the VvPGIP1, and the in vitro inhibition data suggest at least in part, that the VvPGIP1 contributed to the observed reduction in disease symptoms by inhibiting the macerating action of certain Botrytis PGs in planta. The ability to correlate inhibition profiles to individual PGs provides a more comprehensive analysis of PGIPs as antifungal genes with biotechnological potential, and adds to our understanding of the importance of PGIP:PG interactions during disease and symptom development in plants.
多聚半乳糖醛酸酶抑制蛋白(PGIPs)可选择性抑制入侵植物病原真菌分泌的多聚半乳糖醛酸酶(PGs)。PGIPs对来自不同真菌的PGs表现出不同的抑制作用,对源自特定病原体的PGs的不同同工型也有不同抑制作用。最近,从葡萄(Vitis vinifera)中分离并鉴定了一个编码PGIP的基因(Vvpgip1)。从葡萄中纯化得到的PGIP被证明能抑制灰葡萄孢的粗多聚半乳糖醛酸酶提取物,但这种抑制活性尚未与Vvpgip1基因产物的活性建立确凿联系。在此,我们采用转基因过表达方法表明,Vvpgip1基因编码的PGIP对灰葡萄孢的PGs具有活性,并且该基因在转基因烟草中的过表达使植株对该病原体感染的易感性降低。在接种灰葡萄孢15天后,一组同质的转基因株系与未转化的对照植株在统计学上有明显区分,观察到其疾病易感性计算降低了47% - 69%。随后从转基因烟草中纯化出VvPGIP1,并用于研究灰葡萄孢和曲霉中单个PGs的特异性抑制谱。异源表达并纯化的VvPGIP1选择性抑制了黑曲霉和灰葡萄孢的PGs,包括BcPG1,一种先前已证明对致病力和症状发展至关重要的灰葡萄孢PG。我们的数据总体上证实了VvPGIP1的抗真菌特性,体外抑制数据至少部分表明,VvPGIP1通过抑制植物中某些灰葡萄孢PGs的浸解作用,导致了观察到的疾病症状减轻。将抑制谱与单个PGs相关联的能力,为作为具有生物技术潜力的抗真菌基因的PGIPs提供了更全面的分析,并加深了我们对PGIP:PG相互作用在植物疾病和症状发展过程中的重要性的理解。