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Diseases, pathogens and parasites of Undaria pinnatifida

Diseases, pathogens and parasites of Undaria pinnatifida

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Taxa belonging to the Bigyra, including species <strong>of</strong> Olpidiopsis, Eurychasmidium, Petersenia,<br />

Pontisma have been described from a number <strong>of</strong> hosts (e.g. Sparrow 1934, 1936; Aleem<br />

1950b, c, 1952b; Feldmann & Feldmann 1967; Whittick & South 1972; van der Meer &<br />

Pueschel 1985; Molina 1986; West et al. 2006).<br />

The geographic coverage <strong>of</strong> studies on marine fungi in red algae is very incomplete <strong>and</strong><br />

currently reflects the regions where the key workers have been based. For example, the<br />

studies reporting on Chytridium <strong>and</strong> Rhizophidium species are Sparrow (1936) in the northwest<br />

Atlantic, Aleem (1952b) in Sweden <strong>and</strong> Raghukumar (1987a, b) in India. Similarly, the<br />

only papers focusing on thraustochytrids are Quick (1974) in Florida, USA <strong>and</strong> Raghukumar<br />

(1986b, 1987a, b) <strong>and</strong> Raghukumar et al. (1992) in India.<br />

Other algae<br />

Parasitic red algae<br />

More research has been published on red algal <strong>parasites</strong> than on any other area <strong>of</strong> algal<br />

diseases, <strong>pathogens</strong> <strong>and</strong> <strong>parasites</strong> considered in this study. Red algal <strong>parasites</strong> are quite<br />

common, making up to 15% <strong>of</strong> all named red algal genera, although this figure needs revising<br />

as the last comprehensive review <strong>of</strong> red algal <strong>parasites</strong> was by G<strong>of</strong>f (1982). Red algal<br />

parasitism is the most specific symbiosis between two red algae: parasitic red algae are<br />

symbionts that have a reduced size <strong>and</strong> are either completely colourless or have reduced<br />

pigmentation <strong>and</strong> must rely on their nutrition from their host. In the past two decades a lot has<br />

been learned about the origin <strong>of</strong> red algal <strong>parasites</strong> (G<strong>of</strong>f et al. 1996, 1997, Zuccarello et al.<br />

2004), their development (G<strong>of</strong>f & Coleman 1984, 1985; G<strong>of</strong>f & Zuccarello 1994; Zuccarello<br />

& West 1994a), <strong>and</strong> host specificity (Nonomura & West 1981b; G<strong>of</strong>f & Zuccarello 1994;<br />

G<strong>of</strong>f et al. 1997, Zuccarello & West 1994b, c). However only a very small percentage <strong>of</strong><br />

these parasitic red algae have been studied in any detail beyond their first description.<br />

The host specificity <strong>and</strong> evolutionary studies are especially revealing in the context <strong>of</strong> algal<br />

pathogenicity <strong>and</strong> the effects <strong>of</strong> new interactions. Evolutionary studies have revealed that<br />

many red algal <strong>parasites</strong> are derived directly from their hosts (G<strong>of</strong>f et al. 1996, 1997). This<br />

was able to be understood once the development <strong>of</strong> <strong>parasites</strong> on their hosts was elucidated<br />

(G<strong>of</strong>f & Coleman 1984, 1985; G<strong>of</strong>f & Zuccarello 1994), showing that their unusual<br />

development was very similar to post-fertilisation processes in red algae. Early in their<br />

development, either upon spore germination or soon after, red algal <strong>parasites</strong> transfer into a<br />

host cell the cytoplasm <strong>of</strong> an entire cell, or the complete contents <strong>of</strong> a spore. This<br />

“transforms” the host cell as it now develops as a parasite, presumably under the control <strong>of</strong><br />

the transferred parasite nucleus, producing more parasite nuclei <strong>and</strong> dividing to form new<br />

parasite cells. Finally reproductive structures are formed which eventually will lead to new<br />

infections. These developmental processes are similar to the nuclear transfer <strong>and</strong> subsequent<br />

events that occur during post-fertilisation development in most red algae, <strong>and</strong> thus red algal<br />

parasitism has been hypothesised to have been derived from these post-fertilisation processes<br />

(G<strong>of</strong>f et al. 1996, 1997).<br />

Nuclear transfer places constraints on the host range <strong>of</strong> red algal <strong>parasites</strong>. The majority <strong>of</strong> red<br />

algal <strong>parasites</strong> appear to be host specific, although this could be an artifact <strong>of</strong> naming new<br />

parasite species when <strong>parasites</strong> are found on new hosts. However, when host range has been<br />

tested in culture it has been shown to be quite limited (e.g. G<strong>of</strong>f & Zuccarello 1994).<br />

Occasionally <strong>parasites</strong> can grow on closely related host species (Nonomura & West 1981b;<br />

Zuccarello & West 1994b, c), but <strong>of</strong>ten this alternate host development is reduced <strong>and</strong><br />

reproductive structures are not produced. Thus evidence to date supports a high level <strong>of</strong> host<br />

specificity. However, on an evolutionary time scale this is shown not to be so, as “host<br />

jumps” have been discovered using molecular markers. Parasites <strong>of</strong> the Gigartinales family<br />

MAF Biosecurity New Zeal<strong>and</strong> <strong>Diseases</strong>, <strong>pathogens</strong> <strong>and</strong> <strong>parasites</strong> <strong>of</strong> <strong>Undaria</strong> <strong>pinnatifida</strong> • 23

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