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Introduction to Fungi, Third Edition

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NEMATOPHAGOUS FUNGI<br />

681<br />

Fig 25.7 Nema<strong>to</strong>de-trapping Basidiomycota. (a) Growth of Pleurotus hyphae <strong>to</strong>wards buccal cavities of two nema<strong>to</strong>des killed<br />

at za distance by secreted <strong>to</strong>xins. (b d) Nema<strong>to</strong>c<strong>to</strong>nus state of Hohenbuehelia. (b) Hourglass-shaped cell producing an adhesive.<br />

(c) Production of an awl-shaped conidium from a hypha bearing clamp connections. (d) Conidia attached <strong>to</strong> the cuticle of a dead<br />

nema<strong>to</strong>de by a sticky knob at the tip of a bent neck. Infection has given rise <strong>to</strong> trophic hyphae. (b,c) <strong>to</strong> same scale.<br />

are obligate parasites without a free-living<br />

saprotrophic phase. In some species, the conidia<br />

attach themselves <strong>to</strong> the cuticle of the host and,<br />

on germination, penetrate in<strong>to</strong> the body cavity,<br />

eventually filling it with hyphae. Drechmeria<br />

coniospora (Figs. 25.8a c) has conical conidia<br />

which, at maturity, bear a globose, adhesive<br />

knob at the narrow end. Such conidia readily<br />

adhere <strong>to</strong> the cuticle of a nema<strong>to</strong>de which<br />

brushes past them, and they become preferentially<br />

attached <strong>to</strong> the buccal end of nema<strong>to</strong>des<br />

(Jansson et al., 1985). In some other forms, infection<br />

follows ingestion of a conidium. When the<br />

crescent-shaped conidia of Harposporium anguillulae<br />

are ingested, the pointed end of the spore<br />

becomes lodged in the wall of the oesophagus<br />

and, upon germination, penetrates the body<br />

cavity from within (Aschner & Kohn, 1958). The<br />

conidiophores emerging from the dead host bear<br />

sessile, subglobose phialides (Figs. 25.8d,e). The<br />

mycelium within the host may form chlamydospores<br />

which presumably survive in the soil when<br />

the body of the nema<strong>to</strong>de decays.<br />

Little is known about the taxonomic position<br />

of endoparasitic fungi. Several genera contain<br />

members parasitizing soil invertebrates other<br />

than nema<strong>to</strong>des. For instance, the teleomorph of<br />

Harposporium, Podocrella (syn. Atricordyceps), is<br />

related <strong>to</strong> the insect-parasitic genus Cordyceps in<br />

the Clavicipitaceae (see p. 360). There are also<br />

numerous examples of lower fungi adopting<br />

an endoparasitic mode of life, such as Catenaria<br />

anguillulae (Chytridiomycota) and Myzocytium<br />

spp. (Oomycota) which infect nema<strong>to</strong>des by<br />

means of zoospores, or Hap<strong>to</strong>glossa which<br />

produces the spectacular gun cells shown in<br />

Fig. 3.9.<br />

Although endoparasitic fungi can sometimes<br />

be observed on soil-sprinkle plates, a more<br />

efficient technique for their detection is the<br />

Baermann funnel. A conical funnel is fitted with<br />

rubber tubing at its base, and the opening is<br />

sealed with a clamp. The funnel is lined with<br />

tissue paper or filter paper; the soil sample is<br />

filled in<strong>to</strong> the funnel and submerged in water.<br />

Nema<strong>to</strong>des will migrate through the filter paper

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