Zimmermann Matthias R, Knauer Torsten, Furch Alexandra C U
Department of Plant Physiology, Faculty of Biological Science, Matthias-Schleiden-Institute for Genetics, Bioinformatics and Molecular Botany, Friedrich-Schiller-University Jena, Jena, Germany.
Max-Planck Institute for Chemical Ecology, Jena, Germany.
Methods Mol Biol. 2019;1875:291-299. doi: 10.1007/978-1-4939-8837-2_21.
Phytoplasmas colonize specifically the phloem sieve elements (SEs) of plants and influence effectively the plant physiology. To study and understand the interaction of phytoplasmas and host plants an access to the cellular, microscale volume of SEs is demanded. Different methods are suitable to collect phloem sap of phytoplasma-infected plants. The two most common methods are the EDTA-facilitated exudation and the stylectomy. For the EDTA-facilitated method, the cut end of a leaf is placed into an EDTA solution. The EDTA prevents and avoids the Ca dependent (re-) occlusion of SEs by binding Ca ions and the mass flow of SEs is restarted which results in an outflow of the SE content into the EDTA bathing solution. The advantage is on the one hand a simple application and secondly, feasible for all plant species.The stylectomy method requires piercing-sucking insects like any aphids. During phloem-sap ingestion, the stylet is severed by a microcautery device or a laser from the insect body. Due to the high turgor pressure of the SEs the phloem sap is forced out through the remaining stylet and can be collected with a glass capillary, for example. The stylectomy delivers pure phloem sap, however, the collected volumes are in the range of nano liters and the temporal and staff costs are tremendous. A third method is the spontaneous exudation in phytoplasma-infected apple trees providing only in springtime large volumes of vascular sap after cutting along the bark. For the spontaneous exudation the proportion of phloem sap is unclear. Thus, this third method still needs a closer examination in prospective surveys.
植原体专门定殖于植物的韧皮部筛管分子(SEs)中,并有效影响植物生理。为了研究和理解植原体与寄主植物之间的相互作用,需要获取细胞尺度的微体积SEs。有多种方法适用于收集感染植原体植物的韧皮部汁液。两种最常用的方法是EDTA促进渗出法和口针切除法。对于EDTA促进法,将叶片的切口端放入EDTA溶液中。EDTA通过结合钙离子来防止和避免SEs因钙依赖而(重新)堵塞,SEs的质量流得以重新启动,从而导致SEs内容物流出到EDTA浴液中。其优点一方面是应用简单,另一方面对所有植物物种都可行。口针切除法需要像蚜虫这样的刺吸式昆虫。在摄取韧皮部汁液期间,用微烧灼装置或激光将昆虫身体上的口针切断。由于SEs的高膨压,韧皮部汁液会通过剩余的口针被挤出,例如可以用玻璃毛细管收集。口针切除法能得到纯净的韧皮部汁液,然而,收集到的体积在纳升范围内,而且时间和人力成本巨大。第三种方法是感染植原体的苹果树的自然渗出,仅在春季沿树皮切割后能提供大量维管汁液。对于自然渗出,韧皮部汁液的比例尚不清楚。因此,这种第三种方法仍需要在未来的调查中进行更深入的研究。