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Author(s)
Luciana Mecatti Elias1, Maria Estela Silva-Stenico2, Danillo Oliveira Alvarenga2, Janaina Rigonato2, Marli Fátima Fiore2, Simone Possedente de Lira1*
Affiliation(s)
1Department of Exact Sciences, Escola Superior de Agricultura “Luiz de Queiroz”, Universidade de Sao Paulo, Piracicaba, Brazil.
2Centro de Energia Nuclear na Agricultura, Universidade de Sao Paulo, Piracicaba, Brazil.
2Centro de Energia Nuclear na Agricultura, Universidade de Sao Paulo, Piracicaba, Brazil.
ABSTRACT
The
genetic diversity and the potential toxicity of bloom-forming
cyanobacteria were studied in four lagoons located in the state of Sao
Paulo (Campinas, Limeira and Piracicaba cities). Bloom samples were
collected on the water surface and cyanobacterial communities were
evaluated using DGGE fingerprinting and 16S rDNA clone library. The
amplification of genes encoding secondary metabolites such as
microcystin (mcy), anatoxin (ana), cylindrospermopsin (cyr), saxitoxin (sxt), cyanopeptolin (mcn) and aeruginosin (aer)
was performed and their production analyzed by LC-MS. The comparison of
DGGE banding pattern among the different water samples suggested that
some operational taxonomic units (OTUs) in these locations were
predominant over others. The 16S rDNA clone libraries sequences matched
with nine different known cyanobacterial genera available in NCBI,
identified as Anabaena, Brasilonema, Cylindrospermopsis, Limnococcus, Microcystis, Nostoc, Pseudanabaena, Synechococcus and Woronichinia. The lagoons ESALQ2, Taquaral and Limeira had more than 80% of the cyanobacterial community assigned to the genus Microcystis.
Genes encoding aeruginosin, cyanopeptolin and microcystin synthetases
and saxitoxin synthase were amplified, and LC-MS/MS confirmed the
production of aeruginosin, cyanopeptolin and microcystin. Rapid and
sensitive methods for the detection of these secondary metabolites,
especially toxins, using chemical and molecular tools together, can be
used for a faster diagnostic of toxic cyanobacterial blooms.
Cite this paper
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