Beyond the genomes of Fulvia fulva (syn. Cladosporium fulvum) and Dothistroma septosporum: New insights into how these fungal pathogens interact with their host plants

Author:

Mesarich Carl H.12ORCID,Barnes Irene3ORCID,Bradley Ellie L.1ORCID,de la Rosa Silvia1,de Wit Pierre J. G. M.4,Guo Yanan25ORCID,Griffiths Scott A.67,Hamelin Richard C.89,Joosten Matthieu H. A. J.4ORCID,Lu Mengmeng10ORCID,McCarthy Hannah M.5ORCID,Schol Christiaan R.411ORCID,Stergiopoulos Ioannis12ORCID,Tarallo Mariana5,Zaccaron Alex Z.12ORCID,Bradshaw Rosie E.25ORCID

Affiliation:

1. Laboratory of Molecular Plant Pathology, School of Agriculture and Environment Massey University Palmerston North New Zealand

2. Bioprotection Aotearoa Massey University Palmerston North New Zealand

3. Department of Biochemistry, Genetics and Microbiology, Forestry and Agricultural Biotechnology Institute University of Pretoria Pretoria South Africa

4. Laboratory of Phytopathology Wageningen University Wageningen Netherlands

5. Laboratory of Molecular Plant Pathology, School of Natural Sciences Massey University Palmerston North New Zealand

6. Lazarus Bio Ltd Llanelli UK

7. Hydro Industries Ltd Llanelli UK

8. Department of Forest and Conservation Sciences University of British Columbia Vancouver British Columbia Canada

9. Institut de Biologie Intégrative et des Systèmes Université Laval Québec City Québec Canada

10. Department of Biological Sciences University of Calgary Calgary Alberta Canada

11. Plant Breeding Wageningen University & Research Wageningen Netherlands

12. Department of Plant Pathology University of California Davis Davis California USA

Abstract

AbstractFulvia fulva and Dothistroma septosporum are closely related apoplastic pathogens with similar lifestyles but different hosts: F. fulva is a pathogen of tomato, whilst D. septosporum is a pathogen of pine trees. In 2012, the first genome sequences of these pathogens were published, with F. fulva and D. septosporum having highly fragmented and near‐complete assemblies, respectively. Since then, significant advances have been made in unravelling their genome architectures. For instance, the genome of F. fulva has now been assembled into 14 chromosomes, 13 of which have synteny with the 14 chromosomes of D. septosporum, suggesting these pathogens are even more closely related than originally thought. Considerable advances have also been made in the identification and functional characterization of virulence factors (e.g., effector proteins and secondary metabolites) from these pathogens, thereby providing new insights into how they promote host colonization or activate plant defence responses. For example, it has now been established that effector proteins from both F. fulva and D. septosporum interact with cell‐surface immune receptors and co‐receptors to activate the plant immune system. Progress has also been made in understanding how F. fulva and D. septosporum have evolved with their host plants, whilst intensive research into pandemics of Dothistroma needle blight in the Northern Hemisphere has shed light on the origins, migration, and genetic diversity of the global D. septosporum population. In this review, we specifically summarize advances made in our understanding of the F. fulva–tomato and D. septosporum–pine pathosystems over the last 10 years.

Publisher

Wiley

Subject

Plant Science,Soil Science,Agronomy and Crop Science,Molecular Biology

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