Distribution of microcystin-producing and non-microcystin-producing Microcystis sp. in European freshwater bodies: detection of microcystins and microcystin genes in individual colonies.

Microcystis is a well-known cyanobacterial genus frequently producing hepatotoxins named microcystins. Toxin production is encoded by microcystin genes (mcy). This study aims (i) to relate the mcy occurrence in individual colonies to the presence of microcystin, (ii) to assess whether morphological characteristics (morphospecies) are related to the occurrence of mcy genes, and (iii) to test whether there are geographical variations in morphospecies specificity and abundance of mcy genes. Individual colonies of nine different European countries were analysed by (1) morphological characteristics, (2) PCR to amplify a gene region within mcyA and mcyB indicative for microcystin biosynthesis, (3) matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry (MALDI-TOF MS) to detect microcystins. Almost one hundred percent of the colonies predicted to produce microcystins by PCR analysis were found to contain microcystins. A high similarity in microcystin variants in the different colonies selected from lakes across Europe was demonstrated. The different morphospecies varied in the frequency with which they contained mcy genes. Most colonies (>75%) of M. aeruginosa and M. botrys contained the mcy genes, whereas < or = 20% of the colonies identified as M. ichthyoblabe and M. viridis gave a PCR product of the mcy genes. No colonies of M. wesenbergii gave a PCR product of either mcy gene. In addition, a positive relationship was found between the size of the colony and the frequency of those containing the mcy genes. It is concluded that the analysis of morphospecies is indicative for microcystin production, although the quantitative analysis of microcystin concentrations in water remains indispensable for hazard control.

[1]  T. Börner,et al.  Abundance of active and inactive microcystin genotypes in populations of the toxic cyanobacterium Planktothrix spp. , 2004, Environmental microbiology.

[2]  J. Vaitomaa,et al.  Phylogenetic evidence for the early evolution of microcystin synthesis. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[3]  K. Sivonen,et al.  PCR-based identification of microcystin-producing genotypes of different cyanobacterial genera , 2003, Archives of Microbiology.

[4]  Kjetill S. Jakobsen,et al.  Natural Variation in the Microcystin Synthetase Operon mcyABC and Impact on Microcystin Production in Microcystis Strains , 2003, Journal of bacteriology.

[5]  I. Chorus,et al.  The Abundance of Microcystin-Producing Genotypes Correlates Positively with Colony Size in Microcystis sp. and Determines Its Microcystin Net Production in Lake Wannsee , 2003, Applied and Environmental Microbiology.

[6]  J. Komárek,et al.  Two common Microcystis species (Chroococcales, Cyanobacteria) from tropical america, including M. panniformis sp. nov. , 2002 .

[7]  J. Komárek,et al.  Review of the European Microcystis morphospecies (Cyanoprokaryotes) from nature. , 2002 .

[8]  M. Erhard,et al.  Applications of MALDI‐TOF MS analysis in cyanotoxin research , 2002, Environmental toxicology.

[9]  M. Erhard,et al.  Determination of Oligopeptide Diversity within a Natural Population of Microcystis spp. (Cyanobacteria) by Typing Single Colonies by Matrix-Assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry , 2001, Applied and Environmental Microbiology.

[10]  T. Rohrlack,et al.  A spontaneous mutant of microcystin biosynthesis: genetic characterization and effect on Daphnia. , 2001, Environmental microbiology.

[11]  K. Harada,et al.  Trace analysis of microcystins in environmental samples. , 2001, Journal of AOAC International.

[12]  B. Neilan,et al.  Detection of Toxigenicity by a Probe for the Microcystin Synthetase A Gene (mcyA) of the Cyanobacterial Genus Microcystis: Comparison of Toxicities with 16S rRNA and Phycocyanin Operon (Phycocyanin Intergenic Spacer) Phylogenies , 2001, Applied and Environmental Microbiology.

[13]  S. Shibata,et al.  A proposal for the unification of five species of the cyanobacterial genus Microcystis Kützing ex Lemmermann 1907 under the rules of the Bacteriological Code. , 2001, International journal of systematic and evolutionary microbiology.

[14]  P. Orr,et al.  Cellular Microcystin Content in N-Limited Microcystis aeruginosa Can Be Predicted from Growth Rate , 2001, Applied and Environmental Microbiology.

[15]  E. Dittmann,et al.  Diversity of Microcystin Genes within a Population of the Toxic Cyanobacterium Microcystis spp. in Lake Wannsee (Berlin, Germany) , 2001, Microbial Ecology.

[16]  E. Dittmann,et al.  Structural organization of microcystin biosynthesis in Microcystis aeruginosa PCC7806: an integrated peptide-polyketide synthetase system. , 2000, Chemistry & biology.

[17]  S. Suda,et al.  Morphological variability of colonies of Microcystis morphospecies in culture. , 2000, The Journal of general and applied microbiology.

[18]  Lise,et al.  LIVER FAILURE AND DEATH AFTER EXPOSURE TO MICROCYSTINS AT A HEMODIALYSIS CENTER IN BRAZIL LIVER FAILURE AND DEATH AFTER EXPOSURE TO MICROCYSTINS AT A HEMODIALYSIS CENTER IN BRAZIL , 2000 .

[19]  M. Asayama,et al.  Genetic analysis of the peptide synthetase genes for a cyclic heptapeptide microcystin in Microcystis spp. , 1999, Journal of biochemistry.

[20]  H. Rönicke,et al.  Characterization and diversity of microcystins in natural blooms and strains of the genera Microcystis and Planktothrix from German freshwaters , 1999 .

[21]  J. Bartram,et al.  HUMAN HEALTH ASPECTS , 1999 .

[22]  Jamie Bartram,et al.  Toxic Cyanobacteria in Water: a Guide to Their Public Health Consequences, Monitoring and Management Chapter 2. Cyanobacteria in the Environment 2.1 Nature and Diversity 2.1.1 Systematics , 2022 .

[23]  P. Orr,et al.  Relationship between microcystin production and cell division rates in nitrogen‐limited Microcystis aeruginosa cultures , 1998 .

[24]  Mohamed A. Marahiel,et al.  Modular Peptide Synthetases Involved in Nonribosomal Peptide Synthesis. , 1997, Chemical reviews.

[25]  E. Dittmann,et al.  Insertional mutagenesis of a peptide synthetase gene that is responsible for hepatotoxin production in the cyanobacterium Microcystis aeruginosa PCC 7806 , 1997, Molecular microbiology.

[26]  K. Sivonen,et al.  Variation of microcystins, cyanobacterial hepatotoxins, in Anabaena spp. as a function of growth stimuli , 1997, Applied and environmental microbiology.

[27]  D. Jacobs,et al.  Genetic diversity and phylogeny of toxic cyanobacteria determined by DNA polymorphisms within the phycocyanin locus , 1995, Applied and environmental microbiology.

[28]  K. Sivonen,et al.  Isolation and identification of 12 microcystins from four strains and two bloom samples of Microcystis spp.: structure of a new hepatotoxin. , 1994, Toxicon : official journal of the International Society on Toxinology.

[29]  W. Carmichael,et al.  Cyanobacteria secondary metabolites--the cyanotoxins. , 1992, The Journal of applied bacteriology.

[30]  Y. Watanabe,et al.  Release of heptapeptide toxin (microcystin) during the decomposition process of Microcystis aeruginosa. , 1992, Natural toxins.

[31]  K. Rinehart,et al.  Nodularin, microcystin, and the configuration of Adda , 1988 .

[32]  F. Jüttner,et al.  Occurrence of isopropylthio compounds in the aquatic ecosystem (Lake Neusiedl, Austria) as a chemical marker for Microcystis flos-aquae , 1988 .

[33]  R. Rippka Isolation and purification of cyanobacteria. , 1988, Methods in enzymology.

[34]  H. Ettl,et al.  Süsswasserflora von Mitteleuropa , 1985 .

[35]  D. L. Parker IMPROVED PROCEDURES FOR THE CLONING AND PURIFICATION OF MICROCYSTIS CULTURES (CYANOPHYTA) 1 , 1982 .

[36]  C. Reynolds,et al.  On the Annual Cycle of the Blue-Green Alga Microcystis Aeruginosa Kutz. Emend. Elenkin , 1981 .

[37]  J. Waterbury,et al.  Generic assignments, strain histories, and properties of pure cultures of cyanobacteria , 1979 .