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reported to be toxic (Sivonen et al ., 1990a). Oksanen et al. (2004) concluded that Nostoc sp. strain-IO-
102I is distantly related to Nostoc sp. strain-152 but closely related to Nostoc punctiforme PCC 73102
and other symbiotic strains. It is quite intriguing to note that 95% of the genera of cyanobacteria
belonging to the fi ve taxonomic groups revealed a common neurotoxic amino acid termed as β-N-
methylamino-L-alanine (Cox et al ., 2005).
Classifi cation: The cyanobacterial toxins are classifi ed either on the basis of their chemical properties
or symptoms of toxicity (Gorham and Carmichael, 1988; Codd, 1995, 2000; Briand et al ., 2003; Haider
et al ., 2003). On the basis of their chemical structure cyanobacterial toxins are divided into (1) cyclic
peptides (2) alkaloids and (3) lipopolysaccharides in order of their decreasing toxicity. On the basis
of their toxicity symptoms, the cyanobacterial toxins are classifi ed as (1) hepatotoxins (2) neurotoxins
and (3) dermatotoxins. The latter classifi cation is followed in this text.
1) Hepatotoxins : Microcystins (MCs), nodularin and cylindrospermopsin (CYN) are the three
hepatotoxins produced by different cyanobacteria. MCs are produced by the freshwater bloom-
forming, unicellular and colonial Microcystis species, mainly M . aeruginosa that is worldwide
in its distribution (Fig. 1 A). Three other species of Microcystis that produce MCs are M . botrys ,
M . viridis and M . wesenbergii (Fig. 1 B, C and D). Filamentous forms of Anabaena (Fig. 1 E),
Anabaenopsis , Aphanizomenon (Fig. 2 A-E), Phormidium , Planktothrix (Fig. 1 F) and Nostoc also produce
MCs, besides the terrestrial genus Hapalosiphon . As many as 90 variants of MCs have so far been
recorded which show variations in the degree of methylation, hydroxylation, epimerization, peptide
sequence and toxicity (Rinehart et al ., 1988; Codd, 1995, 2000; Sivonen, 1996; Dow and Swoboda, 2000;
Kaeberinck and Neilan, 2001; Pearson et al. , 2010). Nodularins are produced by Nodularia spumigena
(Fig. 3) whereas CYN is produced by Cylindrospermopsis (Fig. 4 A), Raphidiopsis (Fig. 4B) and certain
other fi lamentous forms. MCs are cyclic heptapeptides while nodularins are cyclic pentapeptides.
CYN is an alkaloid.
The target tissue in animals including man is liver. The symptoms of poisoning by MCs in
human beings range from weakness, loss of appetite, vomiting, diarrhea and cancer. It is because
of their carcinogenic nature, a lot of attention has been given to MC related research (Ueno et al .,
1996; Zhou et al ., 2002).
2) Neurotoxins : Anatoxins and STXs that are alkaloid in nature are included here. Several freshwater
bloom-forming algae Anabaena fl os-aquae (anatoxins a,b,c) and Aphanizomenon fl os-aquae (Fig. 2 B),
Oscillatoria ( O . mougeotii ) and Cylindrospermopsis are known to produce anatoxins (Mitrovic et al .,
2004). STXs are toxins generally found in the dinofl agellates that cause paralytic shellfi sh poisoning
and these toxins fi nd their way into human beings when the shellfi sh is consumed. More than 30
STXs are produced by the freshwater cyanobacteria. Other cyanobacteria such as Lyngbya majuscula
and O . mougeotii are also known to produce STXs (Ferreira et al ., 2001). Anatoxins and STXs mainly
act upon the nervous system and also affect skin, liver and gastro-intestinal region. The occurrence
of cyanobacterial neurotoxins, their chemical properties, mode of action and biosynthetic pathways
have been reviewed (Aráoz et al ., 2010).
3) Dermatotoxins : Species of Lyngbya (Fig. 5), Oscillatoria and Schizothrix have been reported
to be responsible for the commonly observed severe dermatitis in swimmers. Severe oral and
gastrointestinal infl ammation also has been noted in certain cases of ingestion. The toxins of Lyngbya,
i.e. aplysiotoxins and debromoaplysiotoxins are tumor promoters . O. nigroviridis and Schizothrix
calcicola also produce debromoaplysiotoxins along with other two such toxins (Chorus and Bartram,
1999).
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