Bais Harsh Pal, Fall Ray, Vivanco Jorge M
Department of Horticulture and Landscape Architecture, Colorado State University, Fort Collins, Colorado 80523-1173, USA.
Plant Physiol. 2004 Jan;134(1):307-19. doi: 10.1104/pp.103.028712. Epub 2003 Dec 18.
Relatively little is known about the exact mechanisms used by Bacillus subtilis in its behavior as a biocontrol agent on plants. Here, we report the development of a sensitive plant infection model demonstrating that the bacterial pathogen Pseudomonas syringae pv tomato DC3000 is capable of infecting Arabidopsis roots both in vitro and in soil. Using this infection model, we demonstrated the biocontrol ability of a wild-type B. subtilis strain 6051 against P. syringae. Arabidopsis root surfaces treated with B. subtilis were analyzed with confocal scanning laser microscopy to reveal a three-dimensional B. subtilis biofilm. It is known that formation of biofilms by B. subtilis is a complex process that includes secretion of surfactin, a lipopeptide antimicrobial agent. To determine the role of surfactin in biocontrol by B. subtilis, we tested a mutant strain, M1, with a deletion in a surfactin synthase gene and, thus, deficient in surfactin production. B. subtilis M1 was ineffective as a biocontrol agent against P. syringae infectivity in Arabidopsis and also failed to form robust biofilms on either roots or inert surfaces. The antibacterial activity of surfactin against P. syringae was determined in both broth and agar cultures and also by live-dead staining methods. Although the minimum inhibitory concentrations determined were relatively high (25 microg mL(-1)), the levels of the lipopeptide in roots colonized by B. subtilis are likely to be sufficient to kill P. syringae. Our results collectively indicate that upon root colonization, B. subtilis 6051 forms a stable, extensive biofilm and secretes surfactin, which act together to protect plants against attack by pathogenic bacteria.
关于枯草芽孢杆菌作为植物生物防治剂所采用的确切机制,人们了解得相对较少。在此,我们报告了一种灵敏的植物感染模型的建立,该模型表明细菌病原体丁香假单胞菌番茄致病变种DC3000能够在体外和土壤中感染拟南芥根。利用这个感染模型,我们证明了野生型枯草芽孢杆菌菌株6051对丁香假单胞菌的生物防治能力。用共聚焦扫描激光显微镜分析经枯草芽孢杆菌处理的拟南芥根表面,以揭示三维的枯草芽孢杆菌生物膜。已知枯草芽孢杆菌形成生物膜是一个复杂的过程,包括分泌表面活性素,一种脂肽类抗菌剂。为了确定表面活性素在枯草芽孢杆菌生物防治中的作用,我们测试了一个突变菌株M1,其表面活性素合成酶基因缺失,因此缺乏表面活性素的产生。枯草芽孢杆菌M1作为抗丁香假单胞菌感染拟南芥的生物防治剂无效,并且在根或惰性表面上也未能形成强大的生物膜。在肉汤和琼脂培养物中以及通过死活染色方法测定了表面活性素对丁香假单胞菌的抗菌活性。尽管所确定的最低抑菌浓度相对较高(25微克/毫升),但在被枯草芽孢杆菌定殖的根中脂肽的水平可能足以杀死丁香假单胞菌。我们的结果共同表明,在根定殖后,枯草芽孢杆菌6051形成稳定、广泛的生物膜并分泌表面活性素,它们共同作用以保护植物免受病原菌的攻击。