Journal
PLANT PATHOLOGY
Volume 64, Issue 5, Pages 1076-1084Publisher
WILEY-BLACKWELL
DOI: 10.1111/ppa.12355
Keywords
anatomy; Citrullus lanatus; defence gene expression; Fusarium oxysporum f. sp niveum; green fluorescent protein
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Funding
- National Industrial Technology System for Watermelon Melon (CARS)
- Jiangsu Provincial Major Support Program for Agricultural [BE2012323]
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Fusarium oxysporum f. sp. niveum (FON) is the causal pathogen of fusarium wilt in watermelon. Understanding the interactions of watermelon seedlings and FON is of scientific and practical importance for disease control. The colonization dynamics of a susceptible watermelon cultivar, Sumi 1 (SM 1), were visualized using a green fluorescent protein (GFP)-expressing strain of FON race 1 (FON 1-GFP). Within 2 days post-inoculation (dpi), hyphae adhered to and grew on epidermal cells. At 3 dpi, hyphae crossed the epidermis, penetrated into the cortex and progressed through parenchymal cell borders reaching the xylem vessels at 7 dpi. Growth of hyphae was restricted to the xylem vessels even in the colonized lower hypocotyl. The responses of SM 1 seedlings to infection were analysed. In the roots of SM 1, infected xylem vessels were plugged with gums and tyloses and some occluded vessels were shed from the root vascular tissue. Parenchyma cells surrounding the vascular cylinder showed wall thickening and cell disintegration, which eventually formed cavities. Hypocotyls of most SM 1 plants were also infected. Vascular tissues were densely colonized by hyphae until the vascular bundle became hollow and plants withered. Moreover, the expression patterns of six defence-related genes in roots of SM 1 were analysed using real-time quantitative PCR. Transcript levels of plant defensin-like genes ClPDF2.1 and ClPDF2.4, phenylalanine ammonia lyase (PAL), chitinase (CHI) and ascorbate peroxidase (APX) were significantly induced in SM 1 roots during FON 1 infection, while polyphenoloxidase (PPO) did not show significant responses to FON 1 infection.
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