Department of Agricultural Biology, Jeonbuk National University, Jeonju, Korea.
Department of Microbiology and Cell Science, University of Florida, Gainesville, Florida, USA.
J Basic Microbiol. 2021 Jul;61(7):642-651. doi: 10.1002/jobm.202100049. Epub 2021 May 13.
The species of Beauveria bassiana is widely used for the management of agricultural insect pests. In this study, we integrated egfp-double-stranded RNA (dsRNA) to a previously generated egfp-expressing B. bassiana transformant (Bb-egfp#3) using a protoplast integration method. The Bb-egfp#3 protoplast was mixed with the dsRNA under PEG/CaCl conditions and liquid-cultured in Sabouraud dextrose broth for 5 days. A control culture followed the same procedure without dsRNA. Bb-egfp#3/egfp-dsRNA cultures showed very low fungal growth (OD = 0.2) compared to the control culture, Bb-egfp#3 only (OD = 1.1). Screening of possible transformants on Sabouraud dextrose agar revealed a transformant T3, without egfp signal. T3 was confirmed as B. bassiana through sequencing of conserved genes and insect bioassays. Interestingly, the genomic egfp fragment of T3 was disrupted, and the egfp signal was not detected over four subcultures, which was also confirmed by RNA-seq of Bb-egfp#3 and T3. This study provides an interesting observation that protoplast integration with dsRNA could possibly generate significantly reduced gene expression in B. bassiana and it is stable across several generations.
球孢白僵菌的物种被广泛用于农业害虫的管理。在这项研究中,我们使用原生质体整合方法将 egfp-双链 RNA(dsRNA)整合到之前生成的 egfp 表达的球孢白僵菌转化体(Bb-egfp#3)中。将 Bb-egfp#3 原生质体与 dsRNA 在 PEG/CaCl 条件下混合,并在萨氏葡萄糖肉汤中液体培养 5 天。对照培养遵循相同的程序,但不使用 dsRNA。与对照培养物(Bb-egfp#3 仅为 0.2)相比,Bb-egfp#3/egfp-dsRNA 培养物的真菌生长非常低(OD=0.2)。在萨氏葡萄糖琼脂上筛选可能的转化体显示出一个没有 egfp 信号的转化体 T3。通过对保守基因的测序和昆虫生物测定,T3 被确认为球孢白僵菌。有趣的是,T3 的基因组 egfp 片段被破坏,并且在四个亚培养物中都没有检测到 egfp 信号,这也通过 Bb-egfp#3 和 T3 的 RNA-seq 得到了证实。这项研究提供了一个有趣的观察结果,即原生质体与 dsRNA 的整合可能会导致球孢白僵菌中的基因表达显著降低,并且在几代中都是稳定的。