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Introduction to Fungi, Third Edition

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PYTHIALES<br />

113<br />

Fig 5.27 <strong>Fungi</strong>cides against P. infestans. (a) The dithiocarbamate maneb which is active against Oomycota and Eumycota. (b) The<br />

isothiocyanate radical released by metabolism of dithiocarbamates by fungal hyphae. (c) The phenylamide metalaxyl which is active<br />

only against Oomycota. (d) Aluminium ethyl phosphonate (fosetyl-Al). (e) Cyazofamid, a new fungicide specific against Oomycota.<br />

(f) Famoxadone, a new fungicide active against Oomycota and Eumycota.<br />

Phy<strong>to</strong>phthora spp. (Erwin & Ribeiro, 1996).<br />

Phenylamides are now protected by being used<br />

in a cocktail, e.g. with the less-specific dithiocarbamates,<br />

and tailor-made application regimes<br />

are recommended for each year and each region<br />

(Staub, 1991).<br />

The phosphonates are a different type of<br />

fungicide against Phy<strong>to</strong>phthora spp. Fosetyl Al<br />

(aluminium ethyl phosphonate; Fig. 5.27d) is<br />

readily taken up by plants in which it is broken<br />

down <strong>to</strong> release phosphorous acid (¼ phosphonate),<br />

which seems <strong>to</strong> be the active principle<br />

(Griffith et al., 1992). Fosetyl Al as well as phosphorous<br />

acid can move downwards through the<br />

phloem and upwards in the xylem, showing<br />

similar transport characteristics as sucrose<br />

(Ouimette & Coffey, 1990; Erwin & Ribeiro,<br />

1996). The mode of action of phosphonates is<br />

not known but is likely <strong>to</strong> be complex, with a<br />

stimula<strong>to</strong>ry effect also on the host plant immune<br />

system (Molina et al., 1998). Although active<br />

only against pota<strong>to</strong> tuber blight but not foliar<br />

blight caused by P. infestans (L. R. Cooke & Little,<br />

2002), phosphonates are effective against a wide<br />

range of root-infecting Phy<strong>to</strong>phthora spp. and<br />

even show good curative properties (Erwin &<br />

Ribeiro, 1996).<br />

A useful introduction <strong>to</strong> current fungicides<br />

and their modes of action has been provided<br />

by Uesugi (1998). Because of the enormous<br />

economic significance of P. infestans and other<br />

Oomycota, new fungicide candidates are continually<br />

being developed and introduced in<strong>to</strong> the<br />

market. Two recent examples are cyazofamid<br />

(Fig. 5.27e) and famoxadone (Fig. 5.27f). Both<br />

inhibit mi<strong>to</strong>chondrial respiration. However,<br />

whilst the former is specific against Oomycota<br />

(Sternberg et al., 2001), famoxadone inhibits<br />

both Oomycota and Eumycota (Mitani et al.,<br />

2002). Its molecular target is different from<br />

that of cyazofamid but probably the same as<br />

that of the strobilurins (see Figs. 13.15e,f),<br />

as indicated by the development of crossresistance<br />

in fungal pathogens against famoxadone<br />

and strobilurins.<br />

Disease forecast<br />

To avoid unnecessary spraying and <strong>to</strong> ensure<br />

that timely spray applications are made, it has<br />

proven possible <strong>to</strong> provide forecasts of the<br />

incidence of pota<strong>to</strong> blight epidemics for certain<br />

countries. Beaumont (1947) analysed the incidence<br />

of blight epidemics in south Devon<br />

(England) and established that a ‘temperature<br />

humidity rule’ controls the relationship between<br />

blight epidemics and weather. After a certain<br />

date (which varies with the locality) and assuming<br />

that inoculum on volunteer plants is always

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