Multiplex PCR assay for Cylindrospermopsis raciborskii and cylindrospermopsin-producing cyanobacteria

dc.contributor.authorFerguson, K.M.
dc.contributor.authorSaint, C.
dc.date.issued2003
dc.description.abstractWater bodies are routinely monitored for the presence of potentially toxic cyanobacteria; however, the methodology for confirming toxicity is currently complex and expensive. Here we describe the application of gene-based technology to rapidly identify cylindrospermopsin-producing cyanobacteria, specifically, Cylindrospermopsis raciborskii. A multiplex polymerase chain reaction (PCR) test was developed that simultaneously identified polyketide synthase (pks) and peptide synthetase (ps) determinants associated with cylindrospermopsin production and distinguished C. raciborskii from other cylindrospermopsin-producing cyanobacteria of the species Anabaena bergii and Aphanizomenon ovalisporum, by targeting the rpoC1 gene. Twenty-one C. raciborskii, 5 A. bergii, 10 Aph. ovalisporum isolates and 3 environmental samples all yielded PCR results consistent with their toxicological status, as assessed by high-performance liquid chromatography coupled to mass spectrometry or matrix-assisted laser desorption ionization-time-of-flight mass spectrometry, and C. raciborskii was always correctly identified. The PCR test is a rapid, reliable, and economical way of assessing the toxic potential of cyanobacterial blooms formed by these organisms.
dc.identifier.citationEnvironmental Toxicology, 2003; 18(2):120-125
dc.identifier.doi10.1002/tox.10108
dc.identifier.issn1520-4081
dc.identifier.issn1522-7278
dc.identifier.urihttps://hdl.handle.net/1959.8/87251
dc.language.isoen
dc.publisherJohn Wiley and Sons
dc.rightsCopyright status unknown
dc.source.urihttps://doi.org/10.1002/tox.10108
dc.subjecttoxicology
dc.subjectcylindrospermopsis raciborskii
dc.subjectcylindrospermopsin-producing
dc.subjectcyanobacteria
dc.titleMultiplex PCR assay for Cylindrospermopsis raciborskii and cylindrospermopsin-producing cyanobacteria
dc.typeJournal article
pubs.publication-statusPublished
ror.mmsid9915913486301831

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