Viable protoplast isolation, organelle visualization and transformation of the globally distributed plant pathogen Phytophthora cinnamomi.

Autor: Kharel A; School of Life and Environmental Sciences, Deakin University, Geelong Waurn Ponds Campus, Waurn Ponds, VIC, 3216, Australia., Rookes J; School of Life and Environmental Sciences, Deakin University, Geelong Waurn Ponds Campus, Waurn Ponds, VIC, 3216, Australia., Ziemann M; School of Life and Environmental Sciences, Deakin University, Geelong Waurn Ponds Campus, Waurn Ponds, VIC, 3216, Australia.; Burnet Institute, Melbourne, Australia., Cahill D; School of Life and Environmental Sciences, Deakin University, Geelong Waurn Ponds Campus, Waurn Ponds, VIC, 3216, Australia. david.cahill@deakin.edu.au.
Jazyk: angličtina
Zdroj: Protoplasma [Protoplasma] 2024 Sep; Vol. 261 (5), pp. 1073-1092. Date of Electronic Publication: 2024 May 04.
DOI: 10.1007/s00709-024-01953-y
Abstrakt: Phytophthora cinnamomi is an oomycete plant pathogen with a host range of almost 5000 plant species worldwide and therefore poses a serious threat to biodiversity. Omics technology has provided significant progress in our understanding of oomycete biology, however, transformation studies of Phytophthora for gene functionalisation are still in their infancy. Only a limited number of Phytophthora species have been successfully transformed and gene edited to elucidate the role of particular genes. There is a need to escalate our efforts to understand molecular processes, gene regulation and infection mechanisms of the pathogen to enable us to develop new disease management strategies. The primary obstacle hindering the advancement of transformation studies in Phytophthora is their challenging and unique nature, coupled with our limited comprehension of why they remain such an intractable system to work with. In this study, we have identified some of the key factors associated with the recalcitrant nature of P. cinnamomi. We have incorporated fluorescence microscopy and flow cytometry along with the organelle-specific dyes, fluorescein diacetate, Hoechst 33342 and MitoTracker™ Red CMXRos, to assess P. cinnamomi-derived protoplast populations. This approach has also provided valuable insights into the broader cell biology of Phytophthora. Furthermore, we have optimized the crucial steps that allow transformation of P. cinnamomi and have generated transformed isolates that express a cyan fluorescent protein, with a transformation efficiency of 19.5%. We therefore provide a platform for these methodologies to be applied for the transformation of other Phytophthora species and pave the way for future gene functionalisation studies.
(© 2024. The Author(s).)
Databáze: MEDLINE
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