Phytopathology. 1998 Feb;88(2):129-36. doi: 10.1094/PHYTO.1998.88.2.129.
ABSTRACT A beta-glucuronidase (GUS) reporter gene and a hygromycin B (hygB) phosphotransferase gene were integrated separately into the Trichoderma harzianum strain 1295-22 genome, using biolistic transformation. The mycelial growth and biocontrol ability of the transformed strains did not differ from that of the original strain. The transformed Gus(+)-kanamycin-resistant (Gus(+)Kan(R)) strains were used to monitor growth and interactions with Rhizoctonia solani on creeping bentgrass plants. The hygB-resistant (hygB(R)) strains were used to selectively recover strain 1295-22 from the rhizosphere soil and phylloplane of creeping bentgrass after spray applications. The population levels of two hygB(R) strains and the original strain were very similar for all treatments. All three strains persisted for the duration of the experiment (28 days) in both the rhizosphere soil and on leaves, although population levels declined somewhat over the course of the experiment in unautoclaved soils. In this study, the results demonstrated that hygB(R) strains remained dominant over time when assayed on Trichoderma-selective medium containing hygB. The hygB(R) strains were not displaced by strains that colonized untreated plants. Microscopic observation showed that the Gus(+)Kan(R) strains colonized the rhizoplane, seed coat, and phylloplane of creeping bentgrass. These results supported our earlier observation that strain 1295-22 was rhizosphere and phyllo-plane competent. Interactions between T. harzianum and R. solani were readily observed in situ and changed over time. Two types of reactions were found in these experiments. In the first type, sections of hyphae of R. solani near the hyphae of T. harzianum appeared damaged, and the pathogen appeared necrotic when viewed with a microscope. The second type, observed less frequently than the first type, was typical of myco-parasitism. The findings in this study provide new insight into the interactions between R. solani and T. harzianum, providing a basis for future research.
摘要 分别将β-葡萄糖醛酸酶(GUS)报告基因和潮霉素 B(hygB)磷酸转移酶基因整合到木霉 1295-22 菌株的基因组中,使用弹道转化。转化菌株的菌丝生长和生物防治能力与原始菌株没有差异。转化的 Gus(+)-卡那霉素抗性(Gus(+)Kan(R))菌株被用于监测在匍匐翦股颖植物上的生长和与立枯丝核菌的相互作用。hygB 抗性(hygB(R))菌株被用于在喷雾处理后从匍匐翦股颖的根际土壤和叶表选择性地回收 1295-22 菌株。对于所有处理,两种 hygB(R)菌株和原始菌株的种群水平都非常相似。在未灭菌的土壤中,所有三种菌株在实验期间(28 天)都能在根际土壤和叶片上持续存在,尽管在实验过程中种群水平有所下降。在这项研究中,结果表明,在含有 hygB 的木霉选择培养基上进行测定时,hygB(R)菌株随着时间的推移仍然占据优势。未处理植物上定殖的菌株没有取代 hygB(R)菌株。显微镜观察表明,Gus(+)Kan(R)菌株定殖在匍匐翦股颖的根际、种皮和叶表。这些结果支持了我们之前的观察,即 1295-22 菌株具有根际和叶际定殖能力。在原位很容易观察到木霉和丝核菌之间的相互作用,并随时间而变化。在这些实验中发现了两种类型的反应。在第一种类型中,靠近木霉菌丝的丝核菌菌丝附近的菌丝段看起来受损,当用显微镜观察时,病原体出现坏死。第二种类型比第一种类型观察到的频率低,是典型的菌寄生现象。本研究的结果为丝核菌和木霉之间的相互作用提供了新的认识,为未来的研究提供了依据。