Segarra Guillem, Puopolo Gerardo, Porcel-Rodríguez Elena, Giovannini Oscar, Pertot Ilaria
Department of Sustainable Agro-Ecosystems and Bioresources, Research and Innovation Centre, Fondazione Edmund Mach (FEM), Via Edmund Mach 1, 38010 San Michele all'Adige, Trento, Italy.
Department of Sustainable Agro-Ecosystems and Bioresources, Research and Innovation Centre, Fondazione Edmund Mach (FEM), Via Edmund Mach 1, 38010 San Michele all'Adige, Trento, Italy
FEMS Microbiol Lett. 2016 Feb;363(3). doi: 10.1093/femsle/fnv243. Epub 2015 Dec 20.
Survival in the phyllosphere is a critical feature for biofungicides based on non-spore forming bacteria. Moreover, knowledge of their persistence on plants is important to design effective formulations and application techniques. With this scope, the aim of this work was to develop a specific method to monitor the fate in the environment of Lysobacter capsici AZ78, a biocontrol agent of Plasmopara viticola, and to evaluate the contribution of formulation in its persistence on grapevine leaves. A strain-specific primer pair derived from REP-PCR fingerprinting was used in quantitative PCR experiments to track the evolution of L. capsici AZ78 population in vineyards. The population reached between 5 and 6 log10 cells gram of leaf(-1) after application and decreased by more than 100 times in one week. Multiple regression analysis showed that unfavourable temperature was the main environmental factor correlating with the decrease of L. capsici AZ78 persistence on grapevine leaves. Importantly, the use of formulation additives protected L. capsici AZ78 against environmental factors and improved its persistence on the leaves by more than 10 times compared to nude cells. Formulation and the knowledge about the persistence of L. capsici AZ78 in vineyards will be useful to develop commercial biofungicides for foliar application.
对于基于非芽孢形成细菌的生物杀菌剂而言,在叶际环境中的存活能力是一项关键特性。此外,了解它们在植物上的持久性对于设计有效的配方和应用技术至关重要。出于这一目的,本研究旨在开发一种特定方法,用于监测葡萄生单轴霉的生防菌辣椒溶杆菌AZ78在环境中的命运,并评估配方对其在葡萄叶片上持久性的影响。在定量PCR实验中,使用了源自REP-PCR指纹图谱的菌株特异性引物对,以追踪葡萄园中辣椒溶杆菌AZ78种群的演变。施用后,该种群数量达到每克叶片5至6 log10个细胞,一周内减少了100多倍。多元回归分析表明,不利的温度是与辣椒溶杆菌AZ78在葡萄叶片上持久性下降相关的主要环境因素。重要的是,使用配方添加剂可保护辣椒溶杆菌AZ78免受环境因素影响,与裸细胞相比,其在叶片上的持久性提高了10倍以上。辣椒溶杆菌AZ78在葡萄园中的配方及持久性相关知识,将有助于开发用于叶面喷施的商业生物杀菌剂。