Glandorf D C, Verheggen P, Jansen T, Jorritsma J W, Smit E, Leeflang P, Wernars K, Thomashow L S, Laureijs E, Thomas-Oates J E, Bakker P A, van Loon L C
Section of Phytopathology, Institute of Biology, Utrecht University, Utrecht, The Netherlands.
Appl Environ Microbiol. 2001 Aug;67(8):3371-8. doi: 10.1128/AEM.67.8.3371-3378.2001.
We released genetically modified Pseudomonas putida WCS358r into the rhizospheres of wheat plants. The two genetically modified derivatives, genetically modified microorganism (GMM) 2 and GMM 8, carried the phz biosynthetic gene locus of strain P. fluorescens 2-79 and constitutively produced the antifungal compound phenazine-1-carboxylic acid (PCA). In the springs of 1997 and 1998 we sowed wheat seeds treated with either GMM 2, GMM 8, or WCS358r (approximately 10(7) CFU per seed), and measured the numbers, composition, and activities of the rhizosphere microbial populations. During both growing seasons, all three bacterial strains decreased from 10(7) CFU per g of rhizosphere sample to below the limit of detection (10(2) CFU per g) 1 month after harvest of the wheat plants. The phz genes were stably maintained, and PCA was detected in rhizosphere extracts of GMM-treated plants. In 1997, but not in 1998, fungal numbers in the rhizosphere, quantified on 2% malt extract agar (total filamentous fungi) and on Komada's medium (mainly Fusarium spp.), were transiently suppressed in GMM 8-treated plants. We also analyzed the effects of the GMMs on the rhizosphere fungi by using amplified ribosomal DNA restriction analysis. Introduction of any of the three bacterial strains transiently changed the composition of the rhizosphere fungal microflora. However, in both 1997 and 1998, GMM-induced effects were distinct from those of WCS358r and lasted for 40 days in 1997 and for 89 days after sowing in 1998, whereas effects induced by WCS358r were detectable for 12 (1997) or 40 (1998) days. None of the strains affected the metabolic activity of the soil microbial population (substrate-induced respiration), soil nitrification potential, cellulose decomposition, plant height, or plant yield. The results indicate that application of GMMs engineered to have improved antifungal activity can exert nontarget effects on the natural fungal microflora.
我们将基因改造的恶臭假单胞菌WCS358r释放到小麦植株的根际。两种基因改造衍生物,即基因改造微生物(GMM)2和GMM 8,携带荧光假单胞菌2-79菌株的phz生物合成基因座,并组成型产生抗真菌化合物吩嗪-1-羧酸(PCA)。在1997年和1998年春季,我们播种了用GMM 2、GMM 8或WCS358r处理过的小麦种子(每粒种子约10⁷CFU),并测量了根际微生物群落的数量、组成和活性。在两个生长季节中,收获小麦植株1个月后,所有三种细菌菌株的数量均从每克根际样品10⁷CFU降至检测限以下(每克10²CFU)。phz基因得以稳定维持,并且在经GMM处理的植株的根际提取物中检测到了PCA。在1997年,而非1998年,在GMM 8处理的植株中,根际真菌数量(在2%麦芽提取物琼脂上定量的总丝状真菌以及在小田培养基上定量的主要镰刀菌属真菌)被短暂抑制。我们还通过扩增核糖体DNA限制性分析来分析GMM对根际真菌的影响。引入这三种细菌菌株中的任何一种都会短暂改变根际真菌微生物区系的组成。然而,在1997年和1998年,GMM诱导的影响均与WCS358r诱导的影响不同,在1997年持续40天,在1998年播种后持续89天,而WCS358r诱导的影响在1997年可检测到12天,在1998年可检测到40天。这些菌株均未影响土壤微生物群落的代谢活性(底物诱导呼吸)、土壤硝化潜力、纤维素分解、株高或作物产量。结果表明,应用经设计具有增强抗真菌活性的GMM可对天然真菌微生物区系产生非靶标影响。