02449naa a2200229 a 450000100080000000500110000800800410001910000170006024500870007726000090016452018120017365300290198565300260201465300210204065300230206170000250208470000200210970000190212970000140214870000130216277300440217519009452013-03-01       2011    bl uuuu     u00u1 u    #d1 aMUNIZ, C. R.  aColonization of cashew plants by Lasiodiplodia theobromaebmicroscopical features.  c2011  aLasiodiplodia theobromae is a phytopathogenic fungus causing gummosis, a threatening disease for cashew plants in Brazil. In an attempt to investigate the ultrastructural features of the pathogen colonization and its response to immunofluorescence labeling, light, confocal and electron microscope studies were conducted on different severity scale patterns of diseased plants. Lasiodiplodia-antisera was checked for cross reactivity against common cashew plants fungi. Optical microscopy analysis revealed a longitudinally sectioned hyphae located within the xylem vessels, showing an extensive hyphal development in the secondary xylem tissue. SEM images demonstrated that the fungus was found in some asymptomatic samples, particularly within the xylem vessels as confirmed by the optical images. Symptomatic sample images showed an extensive distribution of the fungus along the secondary xylem, within the vessels, infecting xylem parenchyma. A closer look in the secondary xylem parenchyma reveals a heavy and profuse invasion of the cells with a distinguishable cell wall disintegration and fully hyphae dispersal. There was no reactivity of Lasiodiplodia-antisera against mycelial extracts of Colletotrichum gloeosporioides, Phomopsis anardii and Pestalotiopsis guepinii. Following incubation of sections with the polyclonal antisera, the hyphae were intensely and regularly labeled. Rays, vessels and parenchyma cells were the preferred pathway for L. theobromae colonization. Artificial infection provides the information that the vascular cylinder is undoubtedly employed and used by the fungus for hyphae distribution. Immunofluorescence assay employed in situ was applied and the polyclonal antisera produced was able to recognize the fungus and proved to be a sensitive technique to detect it.  aAnacardium occidentale L  aCell wall degradation  aEndophytic fungi  aImmunofluorescence1 aFREIRE, F. das C. O.1 aVIANA, F. M. P.1 aCARDOSO, J. E.1 aCOOKE, P.1 aWOOD, D.  tMicrongv. 42, n. 5, p. 419-428 , 2011.