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Molecular Characterization of Potential Microcystin-producing Cyanobacteria in Lake Ontario Embayments and Nearshore Waters

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Date 2007 May 29
PMID 17526791
Citations 14
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Abstract

The distribution and genotypic variation of potential microcystin (MC) producers along the southern and eastern shores of Lake Ontario in 2001 and 2003 were examined using a suite of PCR primers. Cyanobacterial, Microcystis sp., and Microcystis-specific toxin primer sets identified shoreline distribution of cyanobacterial DNA (in 97% of the stations) and MC synthetase genes (in 50% of the stations). Sequence analysis of a partial mcyA amplicon targeting Microcystis, Anabaena, and Planktothrix species indicated that the Microcystis sp. genotype was the dominant MC genotype present and revealed a novel Microcystis-like sequence containing a 6-bp insert. Analysis of the same samples with genus-specific mcyE primers confirmed that the Microcystis sp. genotype was the dominant potential MC producer. Genotype compositions within embayments were relatively homogenous compared to those for shoreline and tributary samples. MC concentrations along the shoreline exhibited both temporal and spatial differences as evidenced by the protein phosphatase inhibition assay, at times exceeding the World Health Organization guideline value for drinking water of 1.0 microg MC-LReq liter(-1). MC genotypes are widespread along the New York State shoreline of Lake Ontario, appear to originate nearshore, and can be carried through the lake via wind and surface water current patterns.

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References
1.
Rouhiainen L, Vakkilainen T, Siemer B, Buikema W, Haselkorn R, Sivonen K . Genes coding for hepatotoxic heptapeptides (microcystins) in the cyanobacterium Anabaena strain 90. Appl Environ Microbiol. 2004; 70(2):686-92. PMC: 348879. DOI: 10.1128/AEM.70.2.686-692.2004. View

2.
Marahiel M, Stachelhaus T, Mootz H . Modular Peptide Synthetases Involved in Nonribosomal Peptide Synthesis. Chem Rev. 2002; 97(7):2651-2674. DOI: 10.1021/cr960029e. View

3.
Boyer G . Cyanobacterial toxins in New York and the lower Great Lakes ecosystems. Adv Exp Med Biol. 2008; 619:153-65. DOI: 10.1007/978-0-387-75865-7_7. View

4.
Urbach E, Robertson D, Chisholm S . Multiple evolutionary origins of prochlorophytes within the cyanobacterial radiation. Nature. 1992; 355(6357):267-70. DOI: 10.1038/355267a0. View

5.
Tillett D, Dittmann E, Erhard M, Von Dohren H, Borner T, Neilan B . Structural organization of microcystin biosynthesis in Microcystis aeruginosa PCC7806: an integrated peptide-polyketide synthetase system. Chem Biol. 2000; 7(10):753-64. DOI: 10.1016/s1074-5521(00)00021-1. View