Introduction. The techniques presented allow a long-term conservation of Cylindrocladium strains to preserve them from major morphological and physiological changes. The principle of the methods applied, key advantages, starting plant material, time required and expected results are presented. Materials and methods. The necessary laboratory materials, and details of the nine steps achieved for the monospore purification of Cylindrocladium strains, their long-term maintenance, and the production of conidia and microsclerotia are described. Results. When revived, purified strains generate actively growing colonies within 48–72 h. Such colonies can then be readily used for conidia or microsclerotia production.

Introduction. This protocol aims at detecting Cylindrocladium spp. in root and soil samples from banana fields and at quantifying the inoculum. The principle of the two methods applied [Root Slice Plating Method (RSPM) and Soil Isolation Method (SIM)], the key advantages of these methods, starting plant and soil materials, the time required and the expected results are presented. Materials and methods. Necessary laboratory materials, and details of the six steps achieved for the use of the two methods are described. Results. When using the RSPM, typical Cylindrocladium colonies are isolated in petri dishes. When using the SIM, typical Cylindrocladium colonies originate from microsclerotia embedded or not in banana root tissue. The inoculum density can be calculated.