23 research outputs found
Microcystin aids in cold temperature acclimation: Differences between a toxic Microcystis wildtype and non-toxic mutant
For Microcystis aeruginosa PCC 7806, temperature decreases from 26 °C to 19 °C double the microcystin quota per cell during growth in continuous culture. Here we tested whether this increase in microcystin provided M. aeruginosa PCC 7806 with a fitness advantage during colder-temperature growth by comparing cell concentration, cellular physiology, reactive oxygen species damage, and the transcriptomics-inferred metabolism to a non-toxigenic mutant strain M. aeruginosa PCC 7806 ÎmcyB. Photo-physiological data combined with transcriptomic data revealed metabolic changes in the mutant strain during growth at 19 °C, which included increased electron sinks and non-photochemical quenching. Increased gene expression was observed for a glutathione-dependent peroxiredoxin during cold treatment, suggesting compensatory mechanisms to defend against reactive oxygen species are employed in the absence of microcystin in the mutant. Our observations highlight the potential selective advantages of a longer-term defensive strategy in management of oxidative stress (i.e., making microcystin) vs the shorter-term proactive strategy of producing cellular components to actively dissipate or degrade oxidative stress agents
Crime prediction using hotel reviews?
Abstract
Can hotel reviews be used as a proxy for predicting crime hotspots? Domain knowledge indicates that hotels are crime attractors, and therefore, hotel guests might be reliable âhuman crime sensorsâ. In order to assess this heuristic, we propose a novel method by mapping actual crime events into hotel reviews from London, using spatial clustering and sentiment feedback. Preliminary findings indicate that sentiment scores from hotel reviews are inversely correlated with crime intensity. Hotels with positive reviews are more likely to be adjacent to crime hotspots, and vice versa. One possible explanation for this counterintuitive finding that the review data are not mapped against specific crime types, and thus the crime data capture mostly police visibility on the site. More research and domain knowledge are needed to establish the strength of hotel reviews as a proxy for crime prediction
Spatial and Temporal Variation in Paralytic Shellfish Toxin Production by Benthic Microseira (Lyngbya) wollei in a Freshwater New York Lake
Butterfield Lake is a mesotrophic lake in New York State where residents and pets have experienced unexplained health issues. Microseira wollei (basionym Lyngbya wollei) was found at two of 15 sites in Butterfield Lake and analyzed for microcystins, anatoxins, cylindrospermopsins, and paralytic shellfish poisoning toxins (PSTs). Only PSTs and trace levels of anatoxin-a were detected in these samples. This is the first published report of PSTs within a New York State lake. To evaluate the environmental and temporal drivers leading to the observed toxicity, PST content at the two sites was examined in detail. There were distinct differences in the total PST content, filament nutrient, filament chlorophyll, and relationship to environmental drivers between the sites, as well as distinct differences in the total PST content measured using different analytical techniques. A multivariate model containing site, temperature, and filament chlorophyll explained 85% of the variation in PSTs observed over the growing season. This work emphasizes the importance of proper site selection and choice of analytical technique in the development of monitoring programs to protect lake users from the occurrence of benthic cyanobacteria toxins
Microcystin aids in photo-acclimation during prolonged cold stress treatment in Microcystis aeruginosa strain PCC7806
Microcystis aeruginosa PCC7806 has been shown to increase toxin production in response to prolonged cold stress. To test whether this increase in toxin production is a beneficial adaptation that aids in cold fitness, the non-toxic mutant Microcystis aeruginosa PCC 7806 ÎmcyB was grown in duplicate chemostat cultures alongside chemostats containing the wildtype isolate. Strains reached steady-state at 26â, then were subjected to an 11-day shift to 19â, followed by a reversion back to 26â. Throughout the experimental period, samples were collected to measure cell abundance, excitation pressure, effective quantum yield, microcystin production, reactive oxygen species (ROS) formation, and for RNA-seq analyses. During the 19â period, the mutant experienced elevated excitation pressure and ROS formation relative to the wildtype strain. Microcystin quota doubled in the wildtype strain by day 7 of the 19â treatment, followed by decreased effective quantum yields 24 h later. This was not observed in the mutant strains. Both mutant and wildtype populations began to recover after 8 days at 19â. Microcystin did not aid in growth recovery during cold stress, although it seemed to play a part in the photo-acclimatory process based on excitation pressure and quantum yield readings
Episodic Decrease in Temperature Increases mcy Gene Transcription and Cellular Microcystin in Continuous Cultures of Microcystis aeruginosa PCC 7806
Microcystins produced during harmful cyanobacterial blooms are a public health concern. Although patterns are emerging, the environmental cues that stimulate production of microcystin remain confusing, hindering our ability to predict fluctuations in bloom toxicity. In earlier work, growth at cool temperatures relative to optimum (18°C vs. 26°C) was confirmed to increase microcystin quota in batch cultures of Microcystis aeruginosa NIES-843. Here, we tested this response in M. aeruginosa PCC 7806 using continuous cultures to examine temporal dynamics and using RNA-sequencing to investigate the physiological nature of the response. A temperature reduction from 26 to 19°C increased microcystin quota âŒ2-fold, from an average of âŒ464 ag ÎŒmâ3 cell volume to âŒ891 ag ÎŒmâ3 over a 7â9 d period. Reverting the temperature to 26°C returned the cellular microcystin quota to âŒ489 ag ÎŒmâ3. Long periods (31â42 d) at 19°C did not increase or decrease microcystin quota beyond that observed at 7â9 d. Nitrogen concentration had little effect on the overall response. RNA sequencing indicated that the decrease in temperature to 19°C induced a classic cold-stress response in M. aeruginosa PCC 7806, but this operated on a different timescale than the increased microcystin production. Microcystin quota showed a strong 48- to 72-h time-lag correlation to mcy gene expression, but no correlation to concurrent mcy expression. This work confirms an effect of temperature on microcystin quota and extends our understanding of the physiological nature of the response