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Introduction to Fungi, Third Edition

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NEMATOPHAGOUS FUNGI<br />

679<br />

Fig 25.5 Dactylellina hap<strong>to</strong>tyla (syn. Dactylaria candida). (a) Conidiophore arising from the substrate, producing a terminal cluster of<br />

septate spindle-shaped conidia. (b) Stalked unicellular knob traps. (c) Non-constricting ring traps. (b,c) <strong>to</strong> same scale.<br />

surface of the ring cells. Since the inner part of<br />

the ring wall rapidly changes shape, it is likely<br />

that there is a slippage of microfibrils making<br />

up the wall. Dowsett et al. (1977) showed that<br />

the inner (luminal) wall of the ring cells in<br />

Drechslerella (Dactylella) brochopaga is thicker than<br />

the outer wall. The luminal wall is initially fourlayered,<br />

but the two external wall layers rupture<br />

during expansion.<br />

The threefold increase in cell volume and the<br />

commensurate increase in surface area, <strong>to</strong>gether<br />

with the process of vacuolation, clearly necessitate<br />

a rapid rearrangement of membrane material<br />

within the cell. Heintz and Pramer (1972)<br />

discovered a labyrinth of membrane-bound<br />

material close <strong>to</strong> the plasma membrane on the<br />

inside of unexpanded ring cells in Drechslerella<br />

(Arthrobotrys) dactyloides. In expanded rings, a<br />

more usual type of plasma membrane organization<br />

was found, suggesting that the membranebound<br />

inclusions had contributed <strong>to</strong> the<br />

formation of the enlarged plasma membrane<br />

(see also Dowsett et al., 1977).<br />

25.1.2 Preda<strong>to</strong>ry fungi belonging <strong>to</strong><br />

Basidiomycota<br />

Nema<strong>to</strong>de-destroying basidiomycetes seem <strong>to</strong><br />

be confined <strong>to</strong> two closely related genera,<br />

Hohenbuehelia and Pleurotus, both belonging <strong>to</strong><br />

the Pleurotaceae in the euagarics clade (p. 541;<br />

Thorn et al., 2000). Both genera contain woodrotting<br />

species forming clamped hyphae.<br />

Hohenbuehelia produces a Nema<strong>to</strong>c<strong>to</strong>nus anamorph<br />

which is of relevance in nema<strong>to</strong>de capture<br />

(Fig. 25.7).<br />

The unusual killing mechanism of Pleurotus<br />

spp. has been described by Barron and<br />

Thorn (1987). Hyphae produce minute unicellular<br />

lollipop-shaped spathulate cells which secrete<br />

droplets of a <strong>to</strong>xin-containing liquid. Various<br />

<strong>to</strong>xins have been identified (p. 682). Nema<strong>to</strong>des<br />

<strong>to</strong>uching such a drop show dramatic symp<strong>to</strong>ms<br />

of a shrinkage of the head region and deformation<br />

of the oesophagus. Onset of symp<strong>to</strong>ms is<br />

within one <strong>to</strong> several minutes and is quickly<br />

followed by lethargy, so that the affected<br />

nema<strong>to</strong>de becomes immobilized close by.<br />

Hyphae of Pleurotus show rapid tropic growth<br />

<strong>to</strong>wards orifices of the paralysed nema<strong>to</strong>de, and<br />

colonization ensues within one <strong>to</strong> several hours<br />

(Fig. 25.7a).<br />

Hohenbuehelia possesses two modes of parasitism.<br />

Hourglass-shaped unicellular mycelial<br />

branches produce a large drop of non-<strong>to</strong>xic glue<br />

by which nema<strong>to</strong>des are trapped in the usual<br />

preda<strong>to</strong>ry way (Fig. 25.7b). In addition, both

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