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Introduction to Fungi, Third Edition

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HYPOCREALES<br />

343<br />

Fig12.18 Canker caused by Nectria galligena<br />

on the twig of an old apple tree.<br />

readily distinguished from conidial pustules by<br />

their bright red colour and their granular<br />

appearance. The pustules are regarded as perithecial<br />

stromata, bearing as many as 30 perithecia.<br />

Ripe perithecia contain numerous<br />

club-shaped asci, each with eight two-celled<br />

hyaline ascospores (Fig. 12.20c). These are somewhat<br />

unusual in being multinucleate (El-Ani,<br />

1971). There is no obvious apical apparatus <strong>to</strong> the<br />

ascus (Strickmann & Chadefaud, 1961).<br />

Perithecial development begins by the formation<br />

of ascogonial primordia beneath the surface<br />

of the conidial pustule. The details of development<br />

are as described on p. 337. An important<br />

feature is the development of apical paraphyses<br />

which grow downwards from the upper part of<br />

the perithecial cavity. As the asci develop from<br />

ascogenous hyphae lining the base of the<br />

perithecial cavity, they grow upwards through<br />

the mass of apical paraphyses, which are difficult<br />

<strong>to</strong> find in mature perithecia (Strickmann &<br />

Chadefaud, 1961).<br />

Other species of Nectria differ from N. cinnabarina<br />

in a number of ways. In many, the perithecia<br />

are not grouped <strong>to</strong>gether on a stroma, but<br />

occur singly (e.g. in N. galligena). The asci of some<br />

species, e.g. N. mammoidea, have a well-defined<br />

apical apparatus (Fig. 12.21a).<br />

12.4.3 Fusarium (Nectriaceae)<br />

Fusarium-type conidia are known in several<br />

species of Nectria and also in the related genus<br />

Gibberella (Samuels et al., 2001). For many<br />

Fusarium species a teleomorph has not yet been<br />

found. The number of species recognized by<br />

morphological characters in pure culture varies<br />

from one authority <strong>to</strong> another. Booth (1971)<br />

included 44 species and 7 varieties; Gerlach and<br />

Nirenberg (1982) included 73 species and 26<br />

varieties, while Nelson et al. (1983) distinguished<br />

30 species. However, using molecular techniques<br />

a large number of species which cannot be<br />

distinguished by morphological characters are<br />

now being defined (O’Donnell, 1996), and a<br />

publically accessible database of diagnostic DNA<br />

sequences has been established as an aid <strong>to</strong> identification<br />

(Geiser et al., 2004). Species of Fusarium<br />

are cosmopolitan in soils from the permafrost of<br />

the Arctic <strong>to</strong> sand in the Sahara desert (Booth,<br />

1971). They are particularly common in cultivated<br />

soil and are associated with a wide range of<br />

plant diseases as indicated in Table 12.3 (Nelson<br />

et al., 1981). Some species are also known <strong>to</strong><br />

cause diseases of humans such as onychomycosis<br />

(nail infections), kera<strong>to</strong>mycosis of the cornea,<br />

ulcers, necroses, skin infections and fatal infections<br />

of internal organs, especially in immunocompromised<br />

patients (Joffe, 1986; de Hoog et al.,<br />

2000a).<br />

A characteristic feature in the asexual reproduction<br />

of Fusarium is the development from<br />

phialides of fusoid, transversely septate macroconidia<br />

with a basal contracted foot cell<br />

(Fig. 12.22b). Microconidia, also formed from<br />

phialides, develop in some species. On plant<br />

hosts macroconidia often accumulate in<br />

orange pink sporodochia (Plate 5e, Fig. 12.22a).<br />

Macroconidia may be dispersed by rain splash

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