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添加0.5％或1％的S-H混合物或其滤液于PDA中,都可促进香蕉黄叶病菌菌丝生长和产胞,而直接添加S-H混合物比其滤液的效果好。添加1％S-H混合物于抑病土或导病土,都会显著的促进厚膜胞子发芽,但发芽管很快融解,亦会促进菌丝的融解,并抑制新厚膜孢子的形成,病原菌在添加S-H混合物土壤中的存活能力亦显著降低。导病土添加1％S-H混合物后,其大分生胞子转变为厚膜胞子的百分率显著减少。又添加S-H混合物的土壤,其细菌与放射菌的族群密度很快增加,经一周后,其族群密度又渐减少。
The addition of 0.5% or 1% S-H mixture or its filtrate in the PDA promoted the mycelial growth and cell production of D. banana, while the direct addition of S-H mixture was more effective than the filtrate. The addition of 1% SH mixture in the soil-deterrent soil or conductive soil significantly promoted the germination of the thick film sprout, but the germination tube melted quickly and also promoted the thawing of the mycelium and inhibited the formation of new thick film spores. The viability of soil in SH blends also decreased significantly. After the addition of 1% S-H mixture in guide soil, the percentage of anaplasma to transmembrane change to thick film was significantly reduced. In the soil with S-H mixture added, the population density of bacteria and actinomycetes rapidly increased. After one week, the population density decreased again.