DEFENSE-RELATED REACTIONS OF SEEDLING ROOTS OF NORWAY SPRUCE TO INFECTION BY HETEROBASIDION-ANNOSUM (FR.) BREF

Citation
Fo. Asiegbu et al., DEFENSE-RELATED REACTIONS OF SEEDLING ROOTS OF NORWAY SPRUCE TO INFECTION BY HETEROBASIDION-ANNOSUM (FR.) BREF, Physiological and molecular plant pathology, 45(1), 1994, pp. 1-19
Citations number
34
Categorie Soggetti
Plant Sciences
ISSN journal
08855765
Volume
45
Issue
1
Year of publication
1994
Pages
1 - 19
Database
ISI
SICI code
0885-5765(1994)45:1<1:DROSRO>2.0.ZU;2-B
Abstract
Norway spruce seedlings were cultivated in sterile conditions. Roots w ere infected with a concentration series of germinating conidiospores of Heterobasidion annosum (10(1)-10(6) ml(-1)). In other experiments, roots were treated with either mycelial preparations of H. annosum, ot her wood inhabiting fungi, with protein fractions of culture filtrates of H. annosum, or with chemical elicitors. Successive steps observed during infection were necrosis, formation of phenolics and increasing lignification of cortex and endodermis, colonization of meristem and f inally of the stele. High spore concentrations caused necrosis and inv asion within 48-72 h; these processes were delayed at low spore concen trations. Lyophilized culture filtrates of H. annosum caused a greater hypersensitive response than protein fractions but less than NaCl, Po lygalacturonic acid or ethephon. Mycelial homogenate from nine other w ood inhabiting fungi (saprophytes/parasites) induced a hypersensitive response to various extents but this was not correlated to their degre e of cross-reactivity with a polyclonal antibody to H. annosum [enzyme -linked immunosorbent assay (ELISA)]. Peroxidase activity increased (t wo-threefold) in roots infected with H. annosum and one acidic isozyme was considered responsible for the increase in peroxidase. Using immu nohistochemical and enzyme staining, peroxidase was found mainly in th e cortical/endodermal regions of roots. Cytochemical labelling using a nti-peroxidase and immunogold demonstrated increased peroxidase activi ty in cell walls, papillae and uninvaded middle lamellar cell corners of infected roots.