White James F, Torres Mónica S, Somu Mohini P, Johnson Holly, Irizarry Ivelisse, Chen Qiang, Zhang Ning, Walsh Emily, Tadych Mariusz, Bergen Marshall
Department of Plant Biology and Pathology, Rutgers University, New Brunswick, New Jersey.
Microsc Res Tech. 2014 Aug;77(8):566-73. doi: 10.1002/jemt.22375. Epub 2014 May 13.
Visualization of bacteria in living plant cells and tissues is often problematic due to lack of stains that pass through living plant cell membranes and selectively stain bacterial cells. In this article, we report the use of 3,3'-diaminobenzidine tetrachloride (DAB) to stain hydrogen peroxide associated with bacterial invasion of eukaryotic cells. Tissues were counterstained with aniline blue/lactophenol to stain protein in bacterial cells. Using this staining method to visualize intracellular bacterial (Burkholderia gladioli) colonization of seedling roots of switch grass (Panicum virgatum), we compared bacterial free seedling roots and those inoculated with the bacterium. To further assess application of the technique in multiple species of vascular plants, we examined vascular plants for seedling root colonization by naturally occurring seed-transmitted bacteria. Colonization by bacteria was only observed to occur within epidermal (including root hairs) and cortical cells of root tissues, suggesting that bacteria may not be penetrating deeply into root tissues. DAB/peroxidase with counter stain aniline blue/lactophenol was effective in penetration of root cells to selectively stain bacteria. Furthermore, this stain combination permitted the visualization of the bacterial lysis process. Before any evidence of H2 O2 staining, intracellular bacteria were seen to stain blue for protein content with aniline blue/lactophenol. After H2 O2 staining became evident, bacteria were often swollen, without internal staining by aniline blue/lactophenol; this suggests loss of protein content. This staining method was effective for seedling root tissues; however, it was not effective at staining bacteria in shoot tissues due to poor penetration.
由于缺乏能穿透活植物细胞膜并选择性地对细菌细胞进行染色的染料,在活植物细胞和组织中观察细菌往往存在问题。在本文中,我们报告了使用四氯化3,3'-二氨基联苯胺(DAB)对与真核细胞细菌入侵相关的过氧化氢进行染色。组织用苯胺蓝/乳酸酚进行复染,以对细菌细胞中的蛋白质进行染色。使用这种染色方法来观察柳枝稷(Panicum virgatum)幼苗根中细胞内细菌(唐菖蒲伯克霍尔德菌)的定殖情况,我们比较了无菌幼苗根和接种了该细菌的幼苗根。为了进一步评估该技术在多种维管植物中的应用,我们检测了维管植物中由自然传播种子的细菌引起的幼苗根定殖情况。仅在根组织的表皮(包括根毛)和皮层细胞中观察到细菌定殖,这表明细菌可能没有深入穿透根组织。DAB/过氧化物酶与苯胺蓝/乳酸酚复染有效地穿透根细胞以选择性地对细菌进行染色。此外,这种染色组合能够观察到细菌的裂解过程。在出现任何过氧化氢染色迹象之前,细胞内细菌用苯胺蓝/乳酸酚染色显示蛋白质含量为蓝色。过氧化氢染色明显后,细菌常常肿胀,不再被苯胺蓝/乳酸酚进行内部染色;这表明蛋白质含量丧失。这种染色方法对幼苗根组织有效;然而,由于穿透性差,它对茎组织中的细菌染色无效。