Abstract

Coffee Leaf Rust, caused by Hemileia vastatrix, is the most important disease of Arabica coffee (Coffea arabica), which prompts studies aimed at understanding the genetic basis of this pathogen as well as its complex interaction with the host. In this work, 11 genes, putatively involved in signalling, establishment and maintenance of biotrophy (transport and metabolism), were characterised, and their expression profiles during host infection were assessed by RT-qPCR in three compatible coffee-rust interactions comprising two different rust races. The profiles of two chitin deacetylases (CD) and a heterotrimeric G-protein α subunit transcripts suggest that these enzymes are involved in host-pathogen recognition and establishment of biotrophy at early stages of infection, and the late expression of the CD1 gene was also recorded. Different expression profiles were observed for a MAP kinase gene between the two rust races, suggesting that this gene may be involved in the differentiation of infection structures in a race-specific pattern. Two amino acid transporters, an invertase, a hexose transporter and a mannitol dehydrogenase presented expression profiles similar to those reported in other rust fungi, indicating a fairly conserved genetic programme related to host infection in rust fungi. The strong upregulation of a Uromyces fabae rust transferred protein 1 orthologous gene was observed in H. vastatrix in planta structures, suggesting that this gene may also play a role during the establishment and the maintenance of biotrophy in coffee leaves. Overall, our results provide valuable insights to the current understanding of the biotrophic interaction between H. vastatrix – C. arabica at the molecular level and will contribute to a reasoned and sustainable use of resistant genotypes.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.