Comparative genomics of Cylindrospermopsis raciborskii strains with differential toxicities
© Sinha et al.; licensee BioMed Central Ltd. 2014
Received: 16 October 2013
Accepted: 14 January 2014
Published: 29 January 2014
Cylindrospermopsis raciborskii is an invasive filamentous freshwater cyanobacterium, some strains of which produce toxins. Sporadic toxicity may be the result of gene deletion events, the horizontal transfer of toxin biosynthesis gene clusters, or other genomic variables, yet the evolutionary drivers for cyanotoxin production remain a mystery. Through examining the genomes of toxic and non-toxic strains of C. raciborskii, we hoped to gain a better understanding of the degree of similarity between these strains of common geographical origin, and what the primary differences between these strains might be. Additionally, we hoped to ascertain why some cyanobacteria possess the cylindrospermopsin biosynthesis (cyr) gene cluster and produce toxin, while others do not. It has been hypothesised that toxicity or lack thereof might confer a selective advantage to cyanobacteria under certain environmental conditions.
In order to examine the fundamental differences between toxic and non-toxic C. raciborskii strains, we sequenced the genomes of two closely related isolates, CS-506 (CYN+) and CS-509 (CYN-) sourced from different lakes in tropical Queensland, Australia. These genomes were then compared to a third (reference) genome from C. raciborskii CS-505 (CYN+). Genome sizes were similar across all three strains and their G + C contents were almost identical. At least 2,767 genes were shared among all three strains, including the taxonomically important rpoc1, ssuRNA, lsuRNA, cpcA, cpcB, nifB and nifH, which exhibited 99.8-100% nucleotide identity. Strains CS-506 and CS-509 contained at least 176 and 101 strain-specific (or non-homologous) genes, respectively, most of which were associated with DNA repair and modification, nutrient uptake and transport, or adaptive measures such as osmoregulation. However, the only significant genetic difference observed between the two strains was the presence or absence of the cylindrospermopsin biosynthesis gene cluster. Interestingly, we also identified a cryptic secondary metabolite gene cluster in strain CS-509 (CYN-) and a second cryptic cluster common to CS-509 and the reference strain, CS-505 (CYN+).
Our results confirm that the most important factor contributing to toxicity in C. raciborskii is the presence or absence of the cyr gene cluster. We did not identify any other distally encoded genes or gene clusters that correlate with CYN production. The fact that the additional genomic differences between toxic and non-toxic strains were primarily associated with stress and adaptation genes suggests that CYN production may be linked to these physiological processes.
KeywordsCylindrospermopsis raciborskii Cylindrospermopsin Cyanobacteria Comparative genomics
Cyanobacteria are photosynthetic prokaryotes that thrive in a wide variety of habitats. Their occurrence in aquatic environments is of particular interest due to their ability to form dense and potentially toxic blooms under certain environmental conditions [1, 2]. Some of the toxins produced include cyclic hepatotoxic peptides such as microcystin and nodularin , alkaloids such as the cytotoxic cylindrospermopsin (CYN)  and the neurotoxic saxitoxin (STX) , and organophosphates, such as anatoxin-a(s) . These cyanotoxins, produced by over 40 species from 20 genera of cyanobacteria , have adverse health effects on humans and animals, and are a public health and environmental concern .
The toxin CYN first came into recognition following the poisoning of 149 people on Palm Island in 1979 . Since then several animal poisonings have been recorded, including cattle mortalities . Interestingly, several distantly related cyanobacterial species produce CYN, including Aphanizomenon ovalisporum, Raphidiopsis curvata, Oscillatoria sp. PCC 6506 , Anabaena lapponica, Lyngbya wollei, Umezakia natans, Raphidiopsis mediterranea, Anabaena bergii and Cylindrospermopsis raciborskii.
C. raciborskii, a filamentous diazotrophic cyanobacterial species, is a known producer of both cylindrospermopsin and saxitoxin , with the type of toxin produced apparently linked, in part, to geographic distribution. Although STX-producing C. raciborskii strains have been reported in South America , based on the current understanding, the most broadly distributed toxigenic members of this species produce CYN , with CYN producers (CYN+) having been reported in Australia, Asia, and New Zealand . Additionally, C. raciborskii strains containing some cyr and sxt (saxitoxin biosynthesis) genes have also been found in South America, although these strains were found to be non–toxic . There is mounting evidence for the global emergence of C. raciborskii, with the species exhibiting an increasingly cosmopolitan distribution. C. raciborskii was initially identified in tropical climatic regions, however, reports of its occurrence in temperate zones have increased drastically in the last decade [20, 23–25].
Although the production of CYN and STX by cyanobacteria is well characterized and relates primarily to the presence of toxin-specific biosynthetic gene clusters [26, 27], the mechanism for acquisition/loss of toxin gene clusters between and among closely related strains of C. raciborskii or a variety of distantly related cyanobacteria species  is not understood. It is also not known, which, if any, genes associated with the cyr gene cluster might be lost without loss of toxigenicity. Although a representative genome has been published for a toxigenic strain of C. raciborskii there has been no large-scale characterization of the genome of other members of the species, or, specifically between and among toxic and non-toxic strains. Such comparisons may provide insight into how toxin clusters are shared/inherited, whether the differences between being toxic or non-toxic strains relates to a loss (e.g. through gene loss or mutational change) or gain (e.g. through cluster acquisition) of function, and what additional differences may exist between the genomes of toxic and non-toxic Cylindrospermopsis strains.
In the present study we conducted genome-wide comparisons of two closely related, but toxicologically distinct strains, CS-506 (CYN+) and CS-509 (CYN-), of C. raciborskii isolated from the same geographical region of Queensland, Australia and compared these with the published genome of the CYN+C. raciborskii CS-505 . A primary aim of this study was to elucidate the minimal set of genes required for CYN production and explore whether or not this genomic locus extends beyond the cyr cluster. We also hoped to ascertain if toxin production influences the overall physiology of CS-506, by examining the putative metabolic roles of strain-specific genes. Our results are discussed within the context of the evolution and ecophysiology of these closely related cyanobacterial strains.
Cyanobacterial strains and culturing
C. raciborskii strains CS-506 and CS-509 were originally isolated from the Queensland waterbodies Solomon Dam (8.7242°S 146.594°E) in 1996 and Lake Julius (20.1315°S 139.723°E) in 1995, respectively. Detailed toxin and morphotype analyses of strains CS-506 and CS-505 were conducted in a previous study in which they were referred to as ‘form 1’ and ‘form 2’, respectively . For the present study, strains were obtained from the Australian National Algae Culture Collection (ANACC), CSIRO Marine and Atmospheric Research, Hobart, Tasmania. Non-axenic cultures of these strains were grown in 250 ml culture flasks in Jaworski medium (JM)  at 25°C, under a light intensity of 25–30 μmol photons m-2 s-1 with a 12 h light/dark cycle.
DNA extraction and quality control
To harvest cells, dense 250 ml cultures were filtered onto 3 μm pore size nitrocellulose membranes and washed with 2 volumes of JM to reduce contaminating bacteria to undetectable levels by 16S PCR (see below). High molecular weight DNA was extracted as previously described . Briefly, cells were lysed with lysozyme and treated with proteinase K. The resulting lysate was then treated with 20% sodium dodecyl sulphate and cetyl trimethylammonium bromide and extracted with phenol/chloroform. DNA was precipitated with 2 volumes of ethanol, and 0.1 volume of 3 M sodium acetate then washed twice with 70% ethanol. Each sample was incubated at 4°C for 12–24 h to allow RNA degradation to occur and DNA quality was assessed spectrophotometrically and by gel electrophoresis. Only high molecular weight pure DNA samples were used for sequencing. DNA samples with a 260/280 nm absorbance ratio of 1.8-2.0, and a 260/230 nm absorbance ratio of 1.8–2.0 were considered pure.
The DNA samples were further quality-checked by amplification of the 16S rRNA gene by PCR. Primers specifically targeting the cyanobacterial 16S rRNA gene (27FL/809R), and bacterial 16S rRNA gene (27FL/1494R)  were used to this end. PCR was performed using the following conditions: initial denaturation at 94°C for 2 min, followed by 30 cycles of denaturation at 94°C for 30 s, annealing at 55°C for 30 s, extension at 72°C for 1 min, then a final extension at 72°C for 30 s. The resulting amplicons were sequenced using the BigDye Terminator kit (Invitrogen) and analyzed using Bioedit . DNA samples that yielded pure C. raciborskii 16S rRNA gene sequences were finally submitted for genome sequencing. These steps ensured that all C. raciborskii DNA samples used for genome sequencing were free from contaminating heterotrophic bacterial DNA.
Genome sequencing and comparative analyses
Paired-end indexed libraries were prepared from purified DNA fragments of approximately 320 bp in length. Genome sequencing was performed using the Genome Analyzer IIx sequencing platform and TruSeq SBS v4 GA kit. The raw reads generated were 100 bp in length. Raw read quality was visualized using FastQC software (Babraham Bioinformatics) with default settings. All raw reads were filtered for quality (mean phred > 20) and end-trimmed (10 bp at 5' and 3') using custom Perl scripts. Paired-reads passing these quality filters were used to estimate the genome size for each strain using the program khmerfreq  using kmer = 17 and then assembled using SOAPdenovo software  with different kmer lengths (57–64), with the final assembly selected based on overall assembly size, number of contigs and contig size.
The optimal assemblies for C. raciborskii CS-506 and CS-509 were annotated using homology-based (Integrated Microbial Genomes (IMG)  and Rapid Annotations Subsystems Technology (RAST) ) and predictive modeling (Glimmer , Genemarks ) approaches. We used the published genome of the CYN-producing C. raciborskii strain CS-505 , also isolated from Solomon Dam, Queensland, Australia, as a reference genome for comparative assessment of these annotation methods. Glimmer 3 and Genemarks vastly overestimated gene number, when compared to the previously published reference genome for C. raciborskii strain CS-505. For ease of annotation, and to be consistent with the prediction of CS-505 genes, RAST was used for the final analysis. NRPS-PKS predictor  and antiSMASH  software were used to identify non-ribosomal peptide synthetase (NRPS) and polyketide synthase (PKS) domains. Additionally, further annotation of genes encoding hypothetical proteins was conducted using the program InterProScan  or the pfam database .
Following annotation of each genome, we conducted pair-wise comparisons of the gene-sets predicted for each strain using BLASTn . Genes were considered common to two taxa in pair-wise comparisons if reciprocal BLAST hits had (a) an e-value ≤ 1*10-5, (b) ≥ 90% nucleotide identity and (c) a difference between query and alignment length of ≤ 20 bp. Genes not meeting these criteria in any pair-wise comparison were considered strain-specific. To ensure that genes 'missing' from each strain based on these BLASTn comparisons were not absent due to gaps in the assembly or misannotation, we mapped the filtered reads from both CS-506 and CS-509 to the published CS-505 sequence using the program SOAPAligner . The bioinformatic prediction of these strain-specific genes was further tested using PCR for a subset of sequences (n = 13; Additional file 1). Briefly, primers targeting genes that were absent from only one of the three C. raciborskii strains, CS-505, CS-506 or CS-509, were designed using primer-BLAST (NCBI). PCR was performed using the following conditions: initial denaturation at 94°C for 2 min, followed by 30 cycles of denaturation at 94°C for 30 s, annealing at 59°C for 30 s, extension at 72°C for 1 min, and a final extension at 72°C for 30 s. Suitable positive and negative controls were used in all PCR experiments and approximately 20 ng of template DNA was used in each reaction. Amplicons were visualized using an agarose gel electrophoresis unit. 1% agarose in TAE gels were stained in ethidium bromide and subsequently viewed using a UV transilluminator. Amplification of an expected size PCR product was used to confirm the presence of a gene.
Structural and overall nucleotide variation between and among C. raciborskii CS-505, CS-506 and CS-509 genomes was assessed at the whole genomic level by comparative alignment using the '-nucmer' (−−maxmatch) and 'dnadiff' packages of the program Mummer 3 . Specific nucleotide variation between and among protein-encoding genes and within non-coding regions was assessed by comparative alignment of each genome using the Smith-Waterman alignment algorithm of the program Burrows-Wheeler Aligner (BWA: ). Genes common to all three C. raciborskii strains were each aligned as orthologous clusters using Muscle  and the alignments assessed for synonymous, non-synonymous and indel mutations. To ensure only high-confidence single nucleotide polymorphisms (SNPs) were included in our analysis, we mapped the raw reads for each sample to its respective assembly (using Bowtie2)  and filtered the initial SNP calls using the Neighbor-Quality Scoring method  in which only SNPs covered to a depth ≥ 5 with reads having a phred mapping quality of ≥ 20 and flanked to the 5' and 3' by at least 3 bases with a phred mapping quality of ≥ 15 were retained for subsequent analysis. Read mapping quality was assessed using Samtools v 0.1.19 . Using these SNP data, various population genetic metrics ( e.g. segregating sites, synonymous and non-synonymous SNPs per bp) were calculated using custom-perl scripts.
The data sets supporting the results presented in this manuscript are available in the following repository: Integrated Microbial Genomes [IMG] repository, unique persistent identifier 12992 and 12991 and NCBI short read archive under accession numbers: SRR1042336 and SRR1041118 for C. raciborskii strains CS-506 and CS-509, respectively.
Results and discussion
Genome assembly statistics of the three strains
C. raciborskii strain
G + C content (%)
Largest scaffold (bp)
Scaffolds > 10 kb
Scaffolds > 40 kb
Scaffolds > 100 kb
Genes with functional annotations (%)
CS-505 and CS-509, contrary to their different toxic phenotypes, were also significantly more similar in sequence than CS-505 and CS-506, with 8,200 SNPs (72.8% in coding regions) and 13,405 SNPs (75.8% in coding regions) observed between the genomes of these pairs respectively. Based on multiple pair-wise alignment of the three C. raciborskii genomes, we established an orthologous relationship among all three strains for 2,917 of the 3,418 protein coding genes annotated for CS-505 . Comparative alignment of these assemblies revealed 99.5% nucleotide identity (representing 3,599,169 alignable bases) among all three strains (Additional file 3). For these orthologous genes, we detected 9,460 (3.3 per kb) and 4,766 (1.8 per kb) SNPs between CS-505 and CS-506 and between CS-505 and CS-509, respectively, relating to a mean nt identity of 99.6 and 99.8%, respectively. Notably, among the genes found to be identical among all three strains were rpoc1 (RNA polymerase subunit), cpcA and cpcB (phycocyanin alpha and beta subunits) and nifB and nifH (nitrogen fixation proteins), all of which are widely utilized for phylogenetic analyses of cyanobacteria. In a separate analysis, we also noted 99.8% sequence identity among ssuRNA and lsuRNA (small and large subunits of ribosomal RNA). Hence, although these loci have proven useful for the molecular classification of cyanobacteria to the species level, our results suggest that they are not useful for differentiating C. raciborskii strains. Some of the more variable genes under low mutational selective pressure based on the accumulation of coding (i.e., non-synonymous) to non-coding (i.e., synonymous) SNPs for both CS-506 and CS-509 that may be worthy of further exploration as intra-specific markers for Cylindrospermopsis are a putative Random Associated Mysterious Protein (RAMP) superfamily protein, CRC_01868 (3.7 and 4.1% nt variability for CS-506 and CS-509, respectively), a hemolysin A homolog, CRC_02719 (3.4 and 4.9% variability) and a HAD-superfamily hydrolase, CRC_00377 (3.4 and 2.1% variability).
Interestingly, a large proportion of the differences between CS-506 and CS-509 in the shared, orthologous genes related to non-synonymous (NS) mutations, with these being more than twice as common in the former (n = 5,971 SNPs) than the latter (n = 2,419) relative to CS-505. By contrast, synonymous (S) SNPs in these orthologous genes were relatively equal in number between the two strains (2,495 and 2,054 for CS-506 and CS-509, respectively). The higher rate of NS SNPs in these genes between CS-506 and CS-505 in comparison to CS-509 and CS-505 may be suggestive of significant differences in the ecological niches of or selective pressures on CS-505 and CS-506 despite their shared toxic phenotype and the close proximity of their geographic origin.
Conservation among C. raciborskii predicted metabolomes
The genes shared between/among all three C. raciborskii strains included those associated with key metabolic pathways, such as photosynthesis, nitrogen and phosphorus metabolism. Many of these pathways appear to be highly conserved across the three C. raciborskii strains and are also similar to primary metabolic pathways identified in other species of cyanobacteria [52–54]. Although all core genes required for photosynthesis in cyanobacteria  were present in each C. raciborskii strain, these genes were distributed among eight distinct operons (e.g. psaAB, psbCD, petCA, petBD, atpIHGFDAC, coxBAC, chlDHI and chlNBL). This arrangement of photosynthesis genes as eight separate operons is also found in other cyanobacteria, including Nostoc punctiforme ATCC 29133 , Raphidiopsis curvata, and Raphidiopsis mediterranea but distinct from related, non-cyanobacterial species, such as Rhodobacter sphaeroides, which organize their photosynthesis genes into a single operon . It is possible that one long continuous photosynthesis gene cluster is ancestral in the bacteria, with subsequent genomic re-arrangement into separate operons occurring more recently in some taxa.
Nitrogen metabolism genes, including those for nitrogen fixation, ammonium, nitrate and nitrite assimilation and heterocyst development were also conserved among CS-505, CS-506, and CS-509. These genes clustered into several distinct operons, including those for nitrogenase (nifB, fdxN, nifS, nifU, nifH, nifD, nifK, ORF, nifE, nifN, nifX, ORF, ORF, nifW, hesA, hesB, fdxH), and nitrite/nitrate uptake and reduction (nirA, nrtA, nrtB, nrtC, nrtD, narB). Such operons have been described in other cyanobacteria, including N. punctiforme ATCC 29133, Anabaena PCC 7120, A. variabilis ATCC 29413 , and A. variabilis PCC 7120 .
We also observed the presence of an identical set of phosphorus metabolism genes, displaying high synteny in all three strains. These comprise the pho regulon (phoU, phoR, phoB, pstA, pstB, pstC and pstS), inorganic phosphatase, transhydrogenases (subunits alpha and beta) and alkaline phosphatases, and are required for phosphorus metabolism . The genes pstA, pstC and pstB form one cluster while the histidine kinase phoR and the transcriptional regulator phoB form another. A similar arrangement of phosphorus metabolism genes has been observed in the genomes of Microcystis aeruginosa PCC 7806  and Raphidiopsis mediterranea.
Substantial differences in transporters among C. raciborskii strains
ABC transporters facilitate the translocation of ions or macromolecules across biological membranes, including the export of substances toxic to the cell . Relative to CS-506 and CS-509, CS-505 was enriched for genes involved in transport, export, and nutrient uptake. The CS-505 genome encodes for a large number of ATP Binding Cassette (ABC) transport-related genes, comprising 4.1% of its total genome. In contrast, ABC-transporter genes comprised only 2.3 and 2.4% of the total genes in CS-506 and CS-509, respectively. The enrichment of ABC transporters in CS-505 was mainly limited to those responsible for the transport of glycerophospholipids [34, 60], with 24 of these genes present exclusively within this strain. The strain-specific nature of these specialized ABC transporters suggests a specific ecological adaptation that is not explicitly linked to CYN production, but may relate to membrane structure and permeability. The number of ABC transporters in other cyanobacteria was found to be significantly lower, for example in Nostoc punctiforme ATCC 29133, ABC transporters comprise only 0.03% of the genome . Similarly, RAST analyses revealed that in M. aeruginosa ABC transporters comprise a mere 0.002% of the genome . Other transport-related genes identified in our study strains include amino acid, N-acetylglucosamine related, energy-coupling bacterial, and tripartite ATP-independent periplasmic (TRAP) transporters, all of which were found in consistent, but low, numbers (<1%).
The presence of strain-specific genes and proteins has been observed in other cyanobacterial genomes and proteomes. For example, a comparative proteomic analysis of six toxic and non-toxic Microcystis aeruginosa strains reported a large diversity in the protein expression profiles of each strain, with a significant proportion of the identified proteins appearing to be strain-specific. The study found that strains of M. aeruginosa species differ in adaptation-related processes, rather than metabolic ones. Additionally, no protein produced exclusively by toxic or non-toxic strains was found, including the Mcy proteins responsible for microcystin biosynthesis . The observed proteome diversity led to the conclusion that M. aeruginosa strains are ecotypes adapted to survival in a particular environmental niche rather than phylogenetically distinct subgroups. Likewise, our data suggests that strains CS-505, CS-506 and CS-509 are ecotypes adapted to specific ecological niches that exist within the same broader geographic location.
Toxic strain-specific genes
Although the cyr cluster was missing from CS-509, a single cyr gene, cyrO was present between the hyp genes. The precise function of CyrO remains to be determined as does its relationship to the cyr cluster. CyrO has low homology to WD repeat proteins, which have diverse regulatory signal transduction roles as well as to ATPases associated with diverse activities (AAA) family proteins which participate in chaperone like functions such as the assembly, operation and disassembly of protein complexes . The G + C content of cyrO was found to be 43, consistent with the cyr gene cluster, and higher than the flanking genes, suggesting that it may have been acquired by horizontal gene transfer or has moved from a high GC region of the genome. In contrast to its location in the C. raciborskii genome, cyrO in Raphidiopsis curvata D9 is separate from and distally located to the cyr gene cluster . Likewise, no clear orthologs of this gene were found in CYN-producing Aphanizomenon sp. 10E6 . The absence of cyrO from the cyr gene cluster or genomes of other CYN-producing species, suggests that this putative CYN regulatory protein may have an alternative function, or at least is not essential for CYN-production.
Although the presence of the complete cyr gene cluster was the most obvious toxic strain-specific trait identified in this study, a few other genes were common to CS-505 and CS-506, but absent from CS-509. These included genes putatively involved in transport and protein processing. The production of cyanotoxins is energetically expensive to the cell therefore the expression of additional ABC transporters may facilitate the uptake of nutrients required by toxic strains. Single genes responsible for cell division, cell wall capsule biosynthesis, and DNA repair were also found. Another gene, whose function in cyanobacteria has not yet been defined, was also found to be specific to the toxic strains. This gene was homologous to vanadium dependent bromopeptidases (VBPOs), which play a role in the hydrogen peroxide-dependent oxidization of halides in eukaryotes . VBPOs can also act as antioxidants, removing hydrogen peroxide, a byproduct of photosynthesis detrimental to cells. In cyanobacteria, VBPOs are thought to be associated with organic compounds that infer allelopathic attributes  and therefore selective advantages to toxic strains.
Potential mechanism for transfer, acquisition and/or loss of the cyr cluster
A recent study comparing over twenty strains of non-toxic, STX and CYN-producing C. raciborskii, found no correlation between phylogeny and toxicity . Stucken et al. 2010 suggested that the absence of toxicity in some strains of C. raciborskii was due to the absence or loss of the cyr cluster, rather than to point mutations or partial deletions . Our results support this hypothesis and suggest that cyr genes were acquired by horizontal transfer in CS-505 and CS-506, and lost in toto from the CS-509 genome.
Evidence of acquired toxicity via horizontal gene transfer (HGT) and its subsequent loss has been documented for other species of cyanobacteria. For example a recent study  hypothesized that saxitoxin production was either gained independently via HGT in STX-producing strains, or that it was gained by a common ancestor, and lost after several generations from non-STX producers. Genomic analysis of STX-producing Anabaena circinalis ACBU02 and a non-STX-producing ACFR02 showed that the latter strain contained four of the 26 sxt biosynthetic pathway genes, advocating the occurrence of genetic deletion. Another study examining the loss of microcystin production in Plankothrix species found that certain non-toxic strains had lost up to 90% of the mcy gene cluster . These strains, however, still contained the genes flanking the mcy gene cluster along with remnants of the transposable regions.
Presence of novel metabolite clusters
The cryptic NRPS1 gene cluster identified in the non-toxic C. raciborskii strain CS-509 (ORF 2370–2375) is 7,000 bp long and encompasses 6 ORFs, including a 4,209 bp NRPS, a hypothetical protein (ORF 2373), a major family facilitator (MFS_1 gene, ORF 2372), and a sterol desaturase (ORF 2374). An incomplete NRPS1 cluster was also identified in the reference strain CS-505. However, in this cluster, the NRPS gene exists as a truncated (600 bp) fragment and the MFS_1 gene is missing. Sequence-based analyses suggest that the NRPS and MFS_1 genes in the CS-509 NRPS1 cluster were acquired via HGT from a common ancestor of Anabaena variabilis ATCC 29413 and Cyanothece sp., which possess genes with 82% and 86% similarity to NRPS and MFS_1, respectively. The peptide sequence of NRPS1 is also 92% similar to an NRPS in Raphidiopsis brookii D9, the function of which is unknown. The R. brookii D9 NRPS, however, possesses an additional thiolation domain, putatively required for the production of a dipeptide.
The second cryptic cluster identified in this study, NRPS2 occurs in the straight morphotypes, CS-505 and CS-509, but not in the coiled strain CS-506. NRPS2 is approximately 25 kb in length and comprises 8 ORFs (numbered 2680–2687 in CS-505 and 727–734 in CS-509), including a probable hydroxylase and an acyl carrier protein reductase. This cluster is present in the same location in both CS-505 and CS-509 and is flanked by identical genes in both genomes. AntiSMASH analysis suggests that the NRPS2 cluster is involved in the biosynthesis of an octapeptide, which could possibly be the unidentified C. raciborskii toxin reported by Falconer et al. 1999 . However, further experimentation, including mutagenesis of the biosynthesis genes or heterologous expression of the complete cluster, combined with chemo-analytical studies are required to verify this.
Genetic divergence and plasticity
We observed numerous instances of genome duplication in the three study strains, often in multiloci positions. These ranged from photosynthesis-related genes in CS-509 to a unique transposase gene, present as ORFs 10 and 487 in CS-506. Further, two identical gene clusters, each comprising five genes encoding hypothetical proteins, which bear >20% nucleotide similarity to kinases and a gene encoding a DUF324 protein of unknown function, were also found in the CS-509 genome. The genes that constitute these twin gene clusters also show a high degree of similarity (92%) to a cluster of hypothetical proteins in Cyanothece sp. PCC 7424.
Nasvall et al. 2012 proposed and subsequently validated the innovation-amplification-divergence (IAD) model, based on a study conducted on over 3,000 generations of the bacterium Salmonella enterica. This theory proffers that genes initially amplify to a higher copy number, following which, one of the extra copies suffer mutations. This eventually leads to divergence of the strain from its co-strains. It is possible that the same phenomenon is in play here, and the different strains of C. raciborskii are gradually diverging through gene duplication, mutation and deletion events.
Further, the highly plastic nature of the C. raciborskii genomes is highlighted by the presence of transposase genes, which are found in close proximity to genes with G + C contents highly deviant from the average G + C content of the C. raciborskii genomes. Additionally, G + C rich genes were found amidst genes of lower G + C content. This along with the presence of strain-specific genes and integrases reiterates the polymorphic nature of the C. raciborskii genome. Numerous other instances, such as the varying G + C content of the cyr gene cluster compared to the flanking hyp gene cluster and the presence of transposase genes adjacent to CRISPR arrays, advocate construction of these genomes via HGT events.
Other cyanobacteria also display evidence of genome plasticity. For example 6.8% of the Microcystis aeruginosa PCC 7806 genome encodes putative transposases as well as a large number of atypical genes not found in other cyanobacteria . Similarly, a large proportion of the Nostoc punctiforme ATCC 29133 genome encodes unique proteins (29%), insertion sites and multilocus repeat sequences .
Genes associated with morphological variation between CS-505, CS-506 and CS-509
In addition to differing in toxin-production, CS-505, CS-506 and CS-509 differ in physical morphology; CS-505 and CS-509 are straight, while CS-506 has a coiled trichome . The differing morphologies may be associated with different survival strategies. For example coiled CS-506 have been observed to dominate over straight CS-505 in environmental blooms, likely in relation to the preference among predators, such as Daphnia, for straight, rather than coiled morphotypes . To better understand the genetics underpinning cell morphology in this species, we examined the three C. raciborskii genomes for the presence of morphotype-specific genes. Around 200 genes were common to the straight morphotypes (CS-505, CS-509) but absent from the coiled strain (CS-506). As expected, numerous genes related to cell wall and capsule biosynthesis were exclusive to the straight morphotypes. These include genes responsible for the biosynthesis of capsular and extracellular polysaccharide and murein hydrolases, which play a role in the regulation of cell wall growth in bacteria . Additionally, while the Mre gene that is responsible for cell shape in bacteria was found in all three strains, we observed a total of five SNPs in the gene sequences, three of which were common to the straight morphotypes. The inactivation of the Mre gene in Anabaena sp. PCC 7120 has previously been shown to convert the rod-like shape of the cell to a spherical form . While, further experimentation is required to validate whether the Mre genes in the coiled C. raciborskii strains are active or not, or whether the presence of the SNPs in the straight morphotypes affects the translation of these genes in some way, it is possible that this gene plays a role in C. raciborskii morphology. We also found several genes exclusive to the straight morphotypes, many of which are putatively involved in cell division, transport, DNA repair, recombination and stress response. Whether or not these genes play a role in cell morphology remains to be determined.
Our results suggest that CS-505, CS-506 and CS-509 represent distinct ecotypes of C. raciborskii, with subtle genetic differences resulting from the niche selective pressures of their specific but geographically similar environments.
This is the first example of genome comparison between closely related toxic and non-toxic C. raciborskii strains. As expected, the genomes of these strains were very similar. However, subtle genomic differences alluding to the adaptability of the species were identified. Moreover, numerous examples of strain-specific genes, genes with disparate G + C contents, duplicated and/or rearranged genes, as well as transposases and integrases were observed. Taken together, these results underpin the plasticity of the C. raciborskii genome and its potential to evolve in the face of selective pressures. This ability to adapt may help explain the recent invasion of C. raciborskii from tropical to temperate climates around the globe.
Most significantly, we demonstrated that toxicity in this species is dependent on possession of the cyr gene cluster, as no other candidate secondary metabolite gene clusters were positively correlated with toxicity. While previous attempts to mutate and thus confirm the role of cyr genes have been unsuccessful, we can now conclude with a high degree of certainty that the cyr cluster is in fact responsible for CYN biosynthesis. Additionally, the non-toxic CS-509 strain lacked the complete suite of cyr genes, but possessed a unique cryptic secondary metabolite gene cluster, NRPS1, the function of which is unknown.
The description of two closely related, but toxigenically different C. raciborskii genomes can be considered a starting point for further molecular studies into the regulation of CYN production and its native role in this species. For example, transcriptomic and proteomic analyses examining the effects of chemophysical parameters, such as light, nutrients, and trace elements, on toxic and non-toxic strains can provide insight into the environmental drivers for toxin production. Since the occurrence of this potentially toxic cyanobacterium is on the rise due to increased eutrophication and global warming [24, 72], it is imperative to gain a better understanding of the various aspects of its physiology and the integral role played by CYN production. This will further facilitate better prediction and management of harmful cyanobacterial blooms.
This work has been supported by an Australian Research Council grant: LP0989475.
- Rouhiainen L, Sivonen K, Buikema WJ, Haselkorn R: Characterization of toxin-producing cyanobacteria by using an oligonucleotide probe containing a tandemly repeated heptamer. J Bacteriol. 1995, 177 (20): 6021-6026.PubMed CentralPubMedGoogle Scholar
- Santos PVF, Lopes IC, Diculescu VC, Oliveira-Brett AM: DNA – cyanobacterial hepatotoxins Microcystin-LR and Nodularin interaction: electrochemical evaluation. Electroanalysis. 2012, 24 (3): 547-553. 10.1002/elan.201100516.View ArticleGoogle Scholar
- Carmichael W, Krishnamurthy T, Beasley V, Min-Juan Y, Bunner DL, Moore RE, Eloff JN, Rinehart K, Falconer I, Runnegar M, Gorham P, Skulberg OM, Harada KI, Watanabe M: Naming of cyclic heptapeptide toxins of cyanobacteria (blue-green algae). Toxicon. 1988, 26 (11): 971-973. 10.1016/0041-0101(88)90195-X.PubMedView ArticleGoogle Scholar
- Ohtani C, Ikuko MRE, Runnegar M: Cylindrospermopsin: a potent hepatotoxin from the blue-green alga Cylindrospermopsis raciborskii. J Am Chem Soc. 1992, 114 (20): 7941-7942. 10.1021/ja00046a067.View ArticleGoogle Scholar
- Schantz EJ, Ghazarossian VE, Schnoes HK, Strong FM, Springer JP, Pezzanite JO, Clardy J: Structure of saxitoxin. J Am Chem Soc. 1975, 97 (5): 1238-1239. 10.1021/ja00838a045.PubMedView ArticleGoogle Scholar
- Hyde EG, Carmichael WW: Anatoxin-A(S), a naturally occurring organophosphate, is an irreversible active site-directed inhibitor of acetylcholinesterase. J Biochem Toxicol. 1991, 6 (3): 195-201. 10.1002/jbt.2570060305.PubMedView ArticleGoogle Scholar
- Neilan BA, Dittmann E, Rouhiainen L, Bass RA, Schaub V, Sivonen K, Borner T: Nonribosomal peptide synthesis and toxigenicity of cyanobacteria. J Bacteriol. 1999, 181 (13): 4089-4097.PubMed CentralPubMedGoogle Scholar
- Griffiths DJ, Saker ML: The Palm Island mystery disease 20 years on: a review of research on the cyanotoxin cylindrospermopsin. Environ Toxicol. 2003, 18 (2): 78-93. 10.1002/tox.10103.PubMedView ArticleGoogle Scholar
- Saker ML, Eaglesham GK: The accumulation of cylindrospermopsin from the cyanobacterium Cylindrospermopsis raciborskii in tissues of the Redclaw crayfish Cherax quadricarinatus. Toxicon. 1999, 37 (7): 1065-1077. 10.1016/S0041-0101(98)00240-2.PubMedView ArticleGoogle Scholar
- Banker R, Carmeli S, Hadas O, Teltsch B, Porat R, Sukenik A: Identification of cylindrospermopsin in Aphanizomenon ovalisporum (Cyanophyceae) isolated from lake Kinneret. Israel. J Phycol. 1997, 33 (4): 613-616. 10.1111/j.0022-3646.1997.00613.x.View ArticleGoogle Scholar
- Li R, Carmichael WW, Brittain S, Eaglesham GK, Shaw GR, Liu Y, Watanabe MM: First report of the cyanotoxins cylindrospermopsin and deoxycylindrospermopsin from Raphidiopsis curvata (cyanobacteria). J Phycol. 2001, 37 (6): 1121-1126. 10.1046/j.1529-8817.2001.01075.x.View ArticleGoogle Scholar
- Mazmouz R, Chapuis-Hugon F, Mann S, Pichon V, Mejean A, Ploux O: Biosynthesis of cylindrospermopsin and 7-epicylindrospermopsin in Oscillatoria sp. strain PCC 6506: identification of the cyr gene cluster and toxin analysis. Appl Environ Microbiol. 2010, 76 (15): 4943-10.1128/AEM.00717-10.PubMed CentralPubMedView ArticleGoogle Scholar
- Spoof L, Berg KA, Rapala J, Lahti K, Lepist L, Metcalf JS, Codd GA, Meriluoto J: First observation of cylindrospermopsin in Anabaena lapponica isolated from the boreal environment (Finland). Environ Toxicol. 2006, 21 (6): 552-560. 10.1002/tox.20216.PubMedView ArticleGoogle Scholar
- Seifert M, McGregor G, Eaglesham G, Wickramasinghe W, Shaw G: First evidence for the production of cylindrospermopsin and deoxy-cylindrospermopsin by the freshwater benthic cyanobacterium, Lyngbya wollei (Farlow ex Gomont) Speziale and Dyck. Harmful Algae. 2007, 6 (1): 73-80. 10.1016/j.hal.2006.07.001.View ArticleGoogle Scholar
- Terao K, Ohmori S, Igarashi K, Ohtani I, Watanabe MF, Harada KI, Ito E, Watanabe M: Electron microscopic studies on experimental poisoning in mice induced by cylindrospermopsin isolated from blue-green alga Umezakia natans. Toxicon. 1994, 32 (7): 833-843. 10.1016/0041-0101(94)90008-6.PubMedView ArticleGoogle Scholar
- McGregor GB, Sendall BC, Hunt LT, Eaglesham GK: Report of the cyanotoxins cylindrospermopsin and deoxy-cylindrospermopsin from Raphidiopsis mediterranea Skuja (Cyanobacteria/Nostocales). Harmful Algae. 2011, 10: 402-410. 10.1016/j.hal.2011.02.002.View ArticleGoogle Scholar
- Schembri MA, Neilan BA, Saint CP: Identification of genes implicated in toxin production in the cyanobacterium Cylindrospermopsis raciborskii. Environ Toxicol. 2001, 16 (5): 413-421. 10.1002/tox.1051.PubMedView ArticleGoogle Scholar
- Hawkins PR, Runnegar MT, Jackson AR, Falconer IR: Severe hepatotoxicity caused by the tropical cyanobacterium (blue-green alga) Cylindrospermopsis raciborskii (Woloszynska) Seenaya and Subba Raju isolated from a domestic water supply reservoir. Appl Environ Microbiol. 1985, 50 (5): 1292-1295.PubMed CentralPubMedGoogle Scholar
- Stucken K, John U, Cembella A, Murillo AA, Soto-Liebe K, Fuentes-Valdvas JJ, Friedel M, Plominsky AM, Vassquez M, Glockner G: The smallest known genomes of multicellular and toxic cyanobacteria: comparison, minimal gene sets for linked traits and the evolutionary implications. PLoS ONE. 2010, 5 (2): e9235-10.1371/journal.pone.0009235.PubMed CentralPubMedView ArticleGoogle Scholar
- Padisak J: Cylindrospermopsis raciborskii (Woloszynska) Seenayya et Subba Raju, an expanding, highly adaptive cyanobacterium: worldwide distribution and review of its ecology. Arch Hydrobiol. 1997, 107: 563-593.Google Scholar
- Wood SA, Stirling DJ: First identification of the cylindrospermopsin-producing cyanobacterium Cylindrospermopsis raciborskii in New Zealand. NZ J Mar Freshw Res. 2003, 37 (4): 821-828. 10.1080/00288330.2003.9517211.View ArticleGoogle Scholar
- Hoff-Risseti C, Dorr FA, Schaker PDC, Pinto E, Werner VR: et al.: Cylindrospermopsin and saxitoxin synthetase genes in Cylindrospermopsis raciborskii strains from Brazilian freshwater. PLoS ONE. 2013, 8 (8): 74238-10.1371/journal.pone.0074238.View ArticleGoogle Scholar
- Sinha R, Pearson LA, Davis TW, Burford MA, Orr PT, Neilan BA: Increased incidence of Cylindrospermopsis raciborskii in temperate zones, Is climate change responsible?. Water Res. 2012, 46 (5): 1408-1419. 10.1016/j.watres.2011.12.019.PubMedView ArticleGoogle Scholar
- Wiedner C, Rucker J, Bruggemann R, Nixdorf B: Climate change affects timing and size of populations of an invasive cyanobacterium in temperate regions. Oecologia. 2007, 152 (3): 473-484. 10.1007/s00442-007-0683-5.PubMedView ArticleGoogle Scholar
- Briand JF, Leboulanger C, Humbert JF, Bernard C, Dufour P: Cylindrospermopsis raciborskii (cyanobacteria) invasion at mid-latitudes: selection, wide physiological tolerance or global warming?. J Phycol. 2004, 40 (2): 231e238-View ArticleGoogle Scholar
- Mihali TK, Kellmann R, Muenchhoff J, Barrow KD, Neilan BA: Characterization of the gene cluster responsible for Cylindrospermopsin biosynthesis. Appl Environ Microbiol. 2008, 74 (3): 716-722. 10.1128/AEM.01988-07.PubMed CentralPubMedView ArticleGoogle Scholar
- Kellmann R, Mihali TK, Jeon YJ, Pickford R, Pomati F, Neilan BA: Biosynthetic intermediate analysis and functional homology reveal a saxitoxin gene cluster in cyanobacteria. Appl Environ Microbiol. 2008, 74 (13): 4044-4053. 10.1128/AEM.00353-08.PubMed CentralPubMedView ArticleGoogle Scholar
- Stucken K, Murillo AA, Soto-Liebe K, Fuentes-Valdes JJ, Mendez MA, Vasquez M: Toxicity phenotype does not correlate with phylogeny of Cylindrospermopsis raciborskii strains. Syst Appl Microbiol. 2009, 32 (1): 37-48. 10.1016/j.syapm.2008.10.002.PubMedView ArticleGoogle Scholar
- Saker ML, Neilan BA, Griffiths DJ: Two morphological forms of Cylindrospermopsis raciborskii (cyanobacteria) isolated from Solomon Dam, Palm Island. Queensland. J Phycol. 1999, 35 (3): 599-606.View ArticleGoogle Scholar
- Hu B, Yang G, Zhao W, Zhang Y, Zhao J: MreB is important for cell shape but not for chromosome segregation of the filamentous cyanobacterium Anabaena sp. Mol Microbiol. 2007, 63 (6): 1640-1652. 10.1111/j.1365-2958.2007.05618.x.PubMedView ArticleGoogle Scholar
- Morin N, Vallaeys T, Hendrick L, Natalie L, Wilmotte A: An efficient DNA isolation protocol for filamentous cyanobacteria of the genus Arthrospira. J Microbiol Methods. 2010, 80 (2): 148-154. 10.1016/j.mimet.2009.11.012.PubMedView ArticleGoogle Scholar
- Vollmer W, Joris B, Charlier P, Foster S: Bacterial peptidoglycan (murein) hydrolases. FEMS Microbiol Rev. 2008, 32 (2): 259-286. 10.1111/j.1574-6976.2007.00099.x.PubMedView ArticleGoogle Scholar
- Tillett D, Dittmann E, Erhard M, Von-Dohren H, Borner T, Neilan BA: Structural organization of microcystin biosynthesis in Microcystis aeruginosa PCC7806: an integrated peptide-polyketide synthetase system. Chem Biol. 2000, 7 (10): 753-764. 10.1016/S1074-5521(00)00021-1.PubMedView ArticleGoogle Scholar
- Ishida K, Welker M, Christiansen G, Cadel-Six S, Bouchier C, Dittmann E, Hertweck C, Tandeau de Marsac N: Plasticity and evolution of Aeruginosin biosynthesis in cyanobacteria. Appl Environ Microbiol. 2009, 75 (7): 2017-2026. 10.1128/AEM.02258-08.PubMed CentralPubMedView ArticleGoogle Scholar
- Markowitz V, Korzeniewski F, Palaniappan K, Szeto E, Werner G, Padki A, Zhao X, Dubchak I, Hugenholtz P, Anderson I, et al: The integrated microbial genomes (IMG) system. Nucleic Acids Res. 2006, 34: 344-348. 10.1093/nar/gkj024.View ArticleGoogle Scholar
- Aziz R, Bartels D, Best A, DeJongh M, Disz T, Edwards R, Formsma K, Gerdes S, Glass E, Kubal M: The RAST Server: rapid annotations using subsystems technology. BMC genomics. 2008, 9 (1): 75-10.1186/1471-2164-9-75.PubMed CentralPubMedView ArticleGoogle Scholar
- Delcher A, Harmon D, Kasif S, White O, Salzberg S: Improved microbial gene identification with GLIMMER. Nucleic Acids Res. 1999, 27 (23): 4636-4641. 10.1093/nar/27.23.4636.PubMed CentralPubMedView ArticleGoogle Scholar
- Besemer J, Borodovsky M: GeneMark: web software for gene finding in prokaryotes, eukaryotes and viruses. Nucleic Acids Res. 2005, 33 (2): 451-454. 10.1093/nar/gki186.View ArticleGoogle Scholar
- Ansari M: NRPS-PKS: a knowledge-based resource for analysis of NRPS/PKS megasynthases. Nucleic Acids Res. 2004, 32 (2): 405-View ArticleGoogle Scholar
- Medema MH, Blin K, Cimermancic P, DeJager V, Zakrzewski P, Fischbach MA, Weber T, Takano E, Breitling R: antiSMASH: rapid identification, annotation and analysis of secondary metabolite biosynthesis gene clusters in bacterial and fungal genome sequences. Nucleic Acids Res. 2011, 39: 339-346. 10.1093/nar/gkr466.View ArticleGoogle Scholar
- Quevillon E, Silventoinen V, Pillai S, Harte N, Mulder N, Apweiler R, Lopez R: InterProScan: protein domains identifier. Nucleic Acids Res. 2005, 33: W116-W120. 10.1093/nar/gki442.PubMed CentralPubMedView ArticleGoogle Scholar
- Punta M, Coggill PC, Eberhardt RY, Mistry J, Tate J, Boursnell C, Pang N, Forslund K, Ceric G, Clements J, et al: The Pfam protein families database. Nucleic Acids Res. 2012, 40 (D1): D290-D301. 10.1093/nar/gkr1065.PubMed CentralPubMedView ArticleGoogle Scholar
- Altschul SF, et al: Basic local alignment search tool. J Mol Biol. 1990, 215: 403-410.PubMedView ArticleGoogle Scholar
- Li R, Li Y, Kristiansen K, Wang J: SOAP: short oligonucleotide alignment program. Bioinformatics. 2008, 24 (5): 713-10.1093/bioinformatics/btn025.PubMedView ArticleGoogle Scholar
- Delcher A, Salzberg SL, Phillippy AM: Using MUMmer to identify similar regions in large sequence sets. Curr Protoc Bioinformatics. 2003, 10 (3): Chapter 10, unit 10.3.Google Scholar
- Li H, Durbin R: Fast and accurate long-read alignment with Burrows-Wheeler transform. Bioinformatics. 2010, 26 (5): 589-595. 10.1093/bioinformatics/btp698.PubMed CentralPubMedView ArticleGoogle Scholar
- Edgar RC: MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acid Res. 2004, 32 (5): 1792-1797. 10.1093/nar/gkh340.PubMed CentralPubMedView ArticleGoogle Scholar
- Langmead B, Salzberg SL: Fast gapped-read alignment with Bowtie 2. Nat Methods. 2012, 9: 357-359. 10.1038/nmeth.1923.PubMed CentralPubMedView ArticleGoogle Scholar
- Volkman SK: A genome-wide map of diversity in Plasmodium falciparum. Nature Genet. 2007, 39: 113-119. 10.1038/ng1930.PubMedView ArticleGoogle Scholar
- Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, Marth G, Abecasis G, Durbin R, 1000 Genome Project Data Processing Subgroup: The Sequence alignment/map (SAM) format and SAMtools. Bioinformatics. 2009, 25 (16): 2078-2079. 10.1093/bioinformatics/btp352.PubMed CentralPubMedView ArticleGoogle Scholar
- Aziz R, Bartels D, Best A, DeJongh M, Disz T, et al: The RAST server: Rapid annotations using subsystems technology. BMC Genomics. 2008, 9 (1): 75-10.1186/1471-2164-9-75.PubMed CentralPubMedView ArticleGoogle Scholar
- Shi T, Bibby TS, Jiang L, Irwin AJ, Falkowski PG: Protein interactions limit the rate of evolution of photosynthetic genes in cyanobacteria. Mol Biol Evol. 2005, 22 (11): 2179-2189. 10.1093/molbev/msi216.PubMedView ArticleGoogle Scholar
- Meeks J, Elhai J, Thiel T, Potts M, Larimer F, Lamerdin J, Predki P, Atlas R: An overview of the genome of Nostoc punctiforme, a multicellular, symbiotic cyanobacterium. Photosynth Res. 2001, 70 (1): 85-106. 10.1023/A:1013840025518.PubMedView ArticleGoogle Scholar
- Su Z, Olman V, Xu Y: Computational prediction of Pho regulons in cyanobacteria. BMC Genomics. 2007, 8: 156-158. 10.1186/1471-2164-8-156.PubMed CentralPubMedView ArticleGoogle Scholar
- Naylor GW, Addlesee HA, Gibson LCD, Hunter CN: The photosynthesis gene cluster of Rhodobacter sphaeroides. Photosynth Res. 1999, 62 (2): 121-139.View ArticleGoogle Scholar
- Thiel T, Lyons E, Erker J: Characterization of genes for a second Mo-dependent nitrogenase in the cyanobacterium Anabaena variabilis. J Bacteriol. 1997, 179 (16): 5222-5225.PubMed CentralPubMedGoogle Scholar
- Herrero A, Muro-Pastor AM, Flores E: Nitrogen control in cyanobacteria. J Bacteriol. 2001, 183 (2): 411-425. 10.1128/JB.183.2.411-425.2001.PubMed CentralPubMedView ArticleGoogle Scholar
- Frangeul L, Quillardet P, Castets AM, et al: Highly plastic genome of Microcystis aeruginosa PCC 7806, a ubiquitous toxic freshwater cyanobacterium. BMC Genomics. 2008, 9: 274-10.1186/1471-2164-9-274.PubMed CentralPubMedView ArticleGoogle Scholar
- Rounge TB, Rohrlack T, Tooming-Klunderud A, Kristensen T, Jakobsen KS: Comparison of cyanopeptolin genes in Planktothrix, Microcystis, and Anabaena Strains: Evidence for independent evolution within each genus. Appl Environ Microbiol. 2007, 73 (22): 7322-7330. 10.1128/AEM.01475-07.PubMed CentralPubMedView ArticleGoogle Scholar
- Tanaka M, Moriya Y, Goto S, Kanehisa M: Analysis of a lipid biosynthesis protein family and phospholipid structural variations. Jap Soc Bioinformatics. 2010, 22: 191-201.Google Scholar
- Hu B, Yang G, Zhao W, Zhang Y, Zhao J: MreB is important for cell shape but not for chromosome segregation of the filamentous cyanobacterium Anabaena sp. PCC 7120. Mol Microbiol. 2007, 63 (6): 640-652.View ArticleGoogle Scholar
- Alexova R, Haynes PA, Ferrari BC, Neilan BA: Comparative protein expression in different strains of the bloom-forming cyanobacterium Microcystis aeruginosa. Mol cell proteomics. 2011, 10 (9): 3749-3765.View ArticleGoogle Scholar
- Jiang Y, Xiao P, Yu G, Sano T, Pan Q, Li R: Molecular basis and phylogenetic implications for deoxy-cylindrospermopsin biosynthesis in Raphidiopsis curvata (cyanobacteria). Appl Environ Microbiol. 2012, 78 (7): 2256-2263. 10.1128/AEM.07321-11.PubMed CentralPubMedView ArticleGoogle Scholar
- Stuken A, Campbell RJ, Quesada A, Sukenik A, Dadheech PK, Wiedner C: Genetic and morphologic characterization of four putative cylindrospermopsin producing species of the cyanobacterial genera Anabaena and Aphanizomenon. J Plankton Res. 2009, 31 (5): 465-480. 10.1093/plankt/fbp011.View ArticleGoogle Scholar
- Tamagnini P, Leitão E, Oliveira P, Ferreira D, Pinto F, Harris DJ, Heidorn T, Lindblad P: Cyanobacterial hydrogenases: diversity, regulation and applications. FEMS Microbiol Rev. 2007, 31 (6): 692-720. 10.1111/j.1574-6976.2007.00085.x.PubMedView ArticleGoogle Scholar
- Stuken A, Jakobsen KS: The cylindrospermopsin gene cluster of Aphanizomenon sp. strain 10E6: organization and recombination. Microbiol. 2010, 156 (8): 2438-2451. 10.1099/mic.0.036988-0.View ArticleGoogle Scholar
- Johnson TL, Palenik B, Brahamsha B: Characterization of a functional vanadium-dependent bromoperoxidase in the marine cyanobacterium Synechococcus Sp. CC93111. J Phycol. 2011, 47 (4): 792-801. 10.1111/j.1529-8817.2011.01007.x.View ArticleGoogle Scholar
- Moustafa A, Loram JE, Hackett JD, Anderson DM, Plumley FG, Bhattacharya D: Origin of Saxitoxin biosynthetic genes in cyanobacteria. PLoS ONE. 2009, 4 (6): e5758-10.1371/journal.pone.0005758.PubMed CentralPubMedView ArticleGoogle Scholar
- Christiansen G, Molitor C, Philmus B, Kurmayer R: Nontoxic strains of cyanobacteria are the result of major gene deletion events induced by a transposable element. Mol Biol Evol. 2008, 25 (8): 1695-1704. 10.1093/molbev/msn120.PubMed CentralPubMedView ArticleGoogle Scholar
- Neilan BA, Pearson LA, Moffitt MC, Mihali TK, Kaebernick M, Kellmann R, Pomati F: The genetics and genomics of cyanobacterial toxicity. In: Cyanobacterial Harmful Algal Blooms: State of the Science and Research Needs, Chapter 17. Adv Exp Med Biol. 2008, 619: 417-452. 10.1007/978-0-387-75865-7_17.PubMedView ArticleGoogle Scholar
- Falconer IR, Hardy SJ, Humpage AR, Froscio SM, Tozer GJ, Hawkins PR: Hepatic and renal toxicity of the blue–green alga (cyanobacterium) Cylindrospermopsis raciborskii in male Swiss albino mice. Environ Toxicol. 1999, 14 (1): 143-150. 10.1002/(SICI)1522-7278(199902)14:1<143::AID-TOX18>3.0.CO;2-H.View ArticleGoogle Scholar
- Paerl HW, Fulton RS: Ecology of harmful cyanobacteria. Ecology of Harmful Algae. Edited by: Graneli E, Turner JT. 2006, Berlin Heidelberg: Springer, 95-109.View ArticleGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.