CHANGES IN ACTIN FILAMENT ARRAYS IN PROTOCORM CELLS OF THE ORCHID SPECIES, SPIRANTHES-SINENSIS, INDUCED BY THE SYMBIOTIC FUNGUS CERATOBASIDIUM-CORNIGERUM
Y. Uetake et Rl. Peterson, CHANGES IN ACTIN FILAMENT ARRAYS IN PROTOCORM CELLS OF THE ORCHID SPECIES, SPIRANTHES-SINENSIS, INDUCED BY THE SYMBIOTIC FUNGUS CERATOBASIDIUM-CORNIGERUM, Canadian journal of botany, 75(10), 1997, pp. 1661-1669
Seeds of the terrestrial orchid, Spiranthes sinensis, were germinated
in vitro in association with the symbiotic fungus, Ceratobasidium corn
igerum. Resulting colonized protocorms were prepared for light microsc
opy, transmission electron microscopy, and fluorescence labelling of a
ctin filaments for examination with laser scanning confocal microscopy
. Fungal hyphae invaded the suspensor end of embryos, formed typical h
yphal coils (pelotons) within parenchyma cells, and then underwent lys
is resulting in degraded hyphal masses. Hyphae and hyphal masses were
enveloped by host-derived membrane. Changes in actin filament arrays a
ccompanied fungal colonization. Uncolonized cells had a network of act
in filaments and actin bundles (cables) located in the cortical region
of the cell cytoplasm; some of these were associated with the nucleus
and amyloplasts. Although actin filament arrays were still present in
protocorm cell cytoplasm during fungal entry and peloton formation, m
ost of the cortical network disappeared and instead actin filaments ra
diated from the periphery of developing pelotons towards the cell wall
. Degraded hyphal masses also had actin filament arrays associated wit
h them, again radiating toward the cell periphery; a network of cortic
al actin filaments reappeared in the protocorm cell cytoplasm at this
stage. Actin filaments did not appear to have a close physical associa
tion with fungal hyphae except in the epidermal hairs that developed f
rom protocorms; this differs from our previous observations on microtu
bules in this system.