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Diseases, pathogens and parasites of Undaria pinnatifida

Diseases, pathogens and parasites of Undaria pinnatifida

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filiformis, P. lanceolata, Pterocladiella capillacea <strong>and</strong> Schizymenia dubyi (Cantacuzene 1930;<br />

Apt 1988b; Apt & Gibor 1989; Rheinheimer 1992; Ashen & G<strong>of</strong>f 1996, 1998, 2000).<br />

A number <strong>of</strong> bacterial diseases <strong>of</strong> Porphyra have been reported, particularly in relation to<br />

farmed Porphyra, including “green spot rotting-like deterioration” (Ryokuhan-byo) <strong>of</strong><br />

Porphyra yezoensis (Nakao et al. 1972), "filament bacterial felt" disease (agent not specified)<br />

(Song et al. 1993), <strong>and</strong> "white wasting disease"/ white spot"/ "Gijishirogusare-sho" (Tsukidate<br />

1971, 1977). Tsukidate (1983) examined the symbiotic relationship between Porphyra species<br />

<strong>and</strong> attached bacteria that occurred in conjunction with white rot, the disease which has<br />

caused the most serious damage to the Porphyra cultivation industry in Japan. Anaaki-disease<br />

causes severe damage to the red alga Porphyra yezoensis; Hayashi et al. (1984) identified the<br />

agent as Vibrio fischeri <strong>and</strong> reported on how it attaches to host thalli (Porphyra sp.), digests<br />

host cells <strong>and</strong> makes holes in the thalli. Sunairi et al. (1995) reported Flavobacterium sp. to<br />

be the causative agent <strong>of</strong> Anaaki-disease, as a result <strong>of</strong> several repeated single-colony<br />

isolations <strong>and</strong> infection experiments. In order to ascertain the role <strong>of</strong> bacteria in the process <strong>of</strong><br />

rotting or decaying <strong>of</strong> cultured laver, Fujita et al. (1972) examined 24 strains <strong>of</strong> bacteria<br />

isolated from diseased fronds <strong>of</strong> Porphyra yezoensis, including species <strong>of</strong> Pseudomonas,<br />

Vibrio, Beneckea.<br />

Weinberger et al. (1994) quantified the bacterial epiphytes <strong>of</strong> Gracilaria conferta <strong>and</strong> found<br />

that saprophytic bacteria reached 350 times <strong>and</strong> agar degraders 25,000 times higher numbers<br />

per gram <strong>of</strong> wet weight on tissues infected with the “white tips disease”, as compared to<br />

healthy tissues. Jaffray & Coyne (1996) developed an in situ assay to detect bacterial<br />

<strong>pathogens</strong> <strong>of</strong> the red alga Gracilaria gracilis responsible for causing lesions, thallus<br />

bleaching, <strong>and</strong> Jaffray et al. (1997) examined bacterial epiphytes on Gracilaria gracilis. The<br />

cause for the “white canopy disease” or “colourless disease” described from Gracilaria<br />

tenuistipitata cultivated in Vietnam is not known (Phap & Thuan 2002) although it is<br />

probably similar to “ice-ice disease” in farmed Eucheuma/Kappaphycus species.<br />

Uyenco et al. (1977) isolated strains <strong>of</strong> Pseudomonas, Flavobacterium, <strong>and</strong> Actinobacterium<br />

associated with "ice-ice disease" in diseased Eucheuma striatum. The symptoms <strong>of</strong> this<br />

disease include the presence <strong>of</strong> a white powdery growth on the thallus which causes loss <strong>of</strong><br />

pigments, <strong>and</strong> the gradual consumption <strong>and</strong> subsequent fragmentation <strong>of</strong> the host. Largo et al.<br />

(1995a), found that pathogenic bacteria identified as Vibrio sp. <strong>and</strong> Cytophaga sp. promoted<br />

ice-ice disease in stressed host branches in the carrageenan-producing red algae Kappaphycus<br />

alvarezii <strong>and</strong> Eucheuma denticulatum. Largo et al. (1999) examined the time-dependent<br />

attachment mechanism <strong>of</strong> bacterial <strong>pathogens</strong> during ice-ice infection in Kappaphycus<br />

alvarezii.<br />

Ghirardelli (1998) reported on small sheathed Cyanophyta that occur in the cell walls <strong>of</strong> live<br />

<strong>and</strong> dead crustose rhodophytes, collected in the lower intertidal zone in the Gulf <strong>of</strong> Trieste<br />

(Northern Adriatic Sea, Italy). Pectonema terebrans is a cyanobacterium that grows in the<br />

calcified cell walls <strong>of</strong> coralline algae in Italy, such as Hydrolithon sp., Lithophyllum sp.,<br />

Sporolithon sp. <strong>and</strong> Titanoderma sp., <strong>and</strong> it leaves characteristic holes behind <strong>and</strong> thus can be<br />

identified even in ancient host material (Ghirardelli 1998). The endophytic cyanobacterium<br />

Pleurocapsa sp. is associated with galls <strong>and</strong> the “deformative disease” in Chilean Mazzaella<br />

laminarioides (Correa et al. 1993, 1997, 2000; Sanchez et al. 1996; Buschmann et al. 1997;<br />

Faugeron et al. 2000). Pleurocapsa triggers the development <strong>of</strong> tumours that can result in<br />

major changes in frond morphology <strong>and</strong> texture <strong>and</strong> negatively affect the number <strong>of</strong> spores,<br />

settlement rates, germination success <strong>and</strong> <strong>of</strong>fspring survival (Correa et al. 2000).<br />

An unspecified bacterium is the cause <strong>of</strong> “Coralline Lethal Orange Disease” (CLOD) in the<br />

crustose coralline alga Hydrolithon onkodes from central west Pacific. CLOD is characterised<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> • 21

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