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Neilan, B. A.

Publications and source records attributed to Neilan, B. A..

3 recordsLinked to original sources

Markers of biosynthetic innovation in the Cyanobacteria

Cyanobacteria are a rich source of specialised metabolites of ecological, biomedical and industrial significance, yet discovery of novel compounds is constrained by rediscovery and uneven taxonomic exploration. Diversification of specialised metabolism constitutes a key evolutionary innovation associated with ecological expansion. Further, understanding how biosynthetic capacity is distributed across cyanobacterial lineages and environments is critical for guiding natural product discovery. We therefore analysed 939 cyanobacterial genomes spanning 11 orders and five habitat types to identify taxonomic and ecological hotspots of biosynthetic potential. We evaluated several indicators of biosynthetic innovation, including singleton BGCs and specialized enzymes and assessed the distribution of cyanobacterial toxin BGCs. Conserved terpene and ribosomally synthesised and post-translationally modified peptide (RiPP) clusters dominated, accounting for >50% of identified BGCs. These two classes exhibited high sequence conservation, averaging 16.41 and 28.10 similarity links per BGC, respectively. Conversely, NRPS and polyketide synthase clusters were less common (18.5% and 2.5% of total BGCs, respectively) but displayed considerable sequence diversity, with a mean of 1.9 and 0.79 links per BGC, respectively. Enzymes associated with potentially novel chemistries were rare, with halogenases and cytochrome P450s present in 4.9% and 1.27% of BGCs, respectively, whereas amidinotransferases were detected in only 0.42% of BGCs. Symbiotic, terrestrial and thermal spring cyanobacteria, particularly Nostocales, showed elevated biosynthetic potential, whereas marine Synechococcales genomes showed comparatively low biosynthetic potential. Putative toxin BGCs were enriched in freshwater Nostocales, Chroococcales and Oscillatoriales. These findings link phylogeny, ecology and genomic features to prioritise taxa, habitats and biosynthetic pathways for future natural product discovery.

genomics↗

Comparative genomics of Dolichospermum circinale strains with differential paralytic shellfish toxin profiles

The cyanobacterium Dolichospermum circinale is a known producer of the neurotoxin saxitoxin and its analogues, collectively known as the paralytic shellfish toxins (PSTs). PSTs vary in potency, and the reported toxin profiles of D. circinale blooms vary in the quantities of individual PSTs, with the regulation of these profiles being poorly understood. In this study, we present the genomes of four D. circinale strains (ACBU01, ACMB03, ACMB13 and FSS-124) with unique PST profiles and perform genome-wide comparisons and specific analysis of the PST-producing biosynthetic gene cluster (sxt) to understand the variability in PST quotas. A reassessment of the previously published D. circinale AWQC131C genome was also performed to collate genomic variation between all strains. Analysis at the nucleotide and amino acid sequence level revealed that toxic strains maintain high genome-wide similarities, corroborated by the analysis of the pan- and variable genomes of each strain. Specifically, the sxt gene sequences were 99-100% identical across all strains. Novel tailoring (sxtSUL, sxtDIOX) and transport (sxtM4) genes were identified within the sxt cluster that were not reported previously in D. circinale. Taken together, these results indicate that the genetic machinery involved in PST production is conserved in this species, suggesting that the regulation of PST biosynthesis in D. circinale does not occur at the genomic level.

microbiology↗

Perfluorooctane sulfonate affects proliferation and differentiation of pluripotent human teratocarcinoma cells

Perfluorinated compounds have raised concern due to their potential association with detrimental postnatal outcomes in animals and humans. We tested the effects of perfluorooctane sulfonate (PFOS) on a human pluripotent teratocarcinoma (known as NCCIT) cells as an in vitro prototype for developmental toxicity in mammals. NCCIT contains stem-cells able to differentiate into endoderm, mesoderm and ectoderm. We tested our cell model using a teratogenic compound, retinoic acid (RA), a cytotoxin, nocodazole (ND), and PFOS. We assayed cells proliferation, morphology and expression of stem cell and germ layer marker genes. PFOS reduced NCCIT cell proliferation in a concentration-dependent manner and induced morphological changes in cell cultures that resembled ectodermal phenotypes. A tendency towards a differentiated state in NCCIT was confirmed by real-time gene expression. PFOS triggered up-regulation of the gene nestin, indicative of ectodermal lineage differentiation, and interfered with the expression of the pluripotency stem-cell marker TERT. PFOS produced effects on both cells proliferation and differentiation, although not as severe as those observed for RA and ND, at levels that fall within the range of concentrations found in animal and human plasma. We discuss our findings in the context of possible interference of PFOS with the processes governing the early development of mammalian tissues.

pharmacology and toxicology↗