Watt Michelle, Hugenholtz Philip, White Rosemary, Vinall Kerry
CSIRO Plant Industry, GPO Box 1600, Canberra, ACT 2601, Australia.
Environ Microbiol. 2006 May;8(5):871-84. doi: 10.1111/j.1462-2920.2005.00973.x.
Native bacteria, Pseudomonas and filamentous bacteria were quantified and localized on wheat roots grown in the field using fluorescence in situ hybridization (FISH). Seminal roots were sampled through the season from unploughed soil in a conservation farming system. Such soils are spatially heterogeneous, and many roots grow slowly through hard soil with cracks and pores containing dead roots remnant from previous crops. Root and rhizosphere morphology, and contact with soil particles were preserved, and autofluorescence was avoided by observing sections in the far-red with Cy5 and Cy5.5 fluorochromes. Spatial analyses showed that bacteria were embedded in a stable matrix (biofilm) within 11 microm of the root surface (range 2-30 microm) and were clustered on 40% of roots. Half the clusters co-located with axial grooves between epidermal cells, soil particles, cap cells or root hairs; the other half were not associated with visible features. Across all wheat roots, although variable, bacteria averaged 15.4 x 10(5) cells per mm(3) rhizosphere, and of these, Pseudomonas and filaments comprised 10% and 4%, respectively, with minor effects of sample time, and no effect of plant age. Root caps were most heavily colonized by bacteria along roots, and elongation zones least heavily colonized. Pseudomonas varied little with root development and were 17% of bacteria on the elongation zone. Filamentous bacteria were not found on the elongation zone. The most significant factor to rhizosphere populations along a wheat root, however, was contact with dead root remnants, where Pseudomonas were reduced but filaments increased to 57% of bacteria (P < 0.001). This corresponded with analyses of root remnants showing they were heavily colonized by bacteria, with 48% filaments (P < 0.001) and 1.4%Pseudomonas (P = 0.014). Efforts to manage rhizosphere bacteria for sustainable agricultural systems should continue to focus on root cap and mucilage chemistry, and remnant roots as sources of beneficial bacteria.
利用荧光原位杂交(FISH)技术对田间种植的小麦根系上的原生细菌、假单胞菌和丝状细菌进行了定量和定位分析。在保护性耕作系统中,从未耕土壤中采集了整个生长季的种子根。这类土壤在空间上具有异质性,许多根系在坚硬的土壤中生长缓慢,土壤中有裂缝和孔隙,还残留着前茬作物的死根。根系和根际形态以及与土壤颗粒的接触得以保留,通过使用Cy5和Cy5.5荧光染料在远红光下观察切片,避免了自发荧光的干扰。空间分析表明,细菌嵌入在根表面11微米范围内(范围为2 - 30微米)的稳定基质(生物膜)中,并且在40%的根系上呈簇状分布。一半的簇与表皮细胞之间的轴向凹槽、土壤颗粒、根冠细胞或根毛共定位;另一半与可见特征无关。在所有小麦根系中,尽管细菌数量存在差异,但根际平均每立方毫米有15.4×10⁵个细胞,其中假单胞菌和丝状细菌分别占10%和4%,采样时间影响较小,植株年龄无影响。沿着根系,根冠被细菌定殖的程度最高,伸长区最低。假单胞菌数量随根系发育变化不大,在伸长区占细菌总数的17%。在伸长区未发现丝状细菌。然而,沿小麦根系根际菌群的最重要因素是与死根残余物的接触,在此处假单胞菌数量减少,但丝状细菌增加到细菌总数的57%(P < 0.001)。这与对根残余物的分析结果一致,表明它们被大量细菌定殖,其中48%为丝状细菌(P < 0.001),1.4%为假单胞菌(P = 0.014)。为可持续农业系统管理根际细菌的工作应继续关注根冠和黏液化学,以及作为有益细菌来源的残余根。