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Moynihan, M.

Publications and source records attributed to Moynihan, M..

2 recordsLinked to original sources

Bloom-forming bacteria heavily invest in anti-phage defense

Bacterial blooms are characterized by unusually high cell densities and exceptionally low diversity and can profoundly alter ecosystem function and services. Bacteriophages have long been considered an important cause of mortality in blooms, acting as a mechanism for control. Here, we characterize the viral ecology of a long-lasting estuarine bloom of green sulfur bacteria (Chlorobiota). We combined direct cell and viral counts with metagenomic and metaproteomic data to characterize host and phage activity at different time points. The abundance of virus-like particles (VLPs) decreased at high cell densities, suggesting reduced lytic infection rates. The dominant organism, GSB-TRL01 (genus Prosthecochloris), apparently contained a large conjugative plasmid encoding five different anti-phage defense systems. The organism's genome encoded 13 additional defense systems. Compared to the average of five defense systems per microbial genome, this enrichment suggests robust anti-phage defense capabilities. Proteins from ten different defense systems on GSB-TRL01's genome and four systems from the conjugative plasmid were expressed in the proteome. This suggests that GSB-TRL01 invests heavily in anti-phage defense, leading to reduced lysis at high cell densities and allowing blooms to persist for weeks to months. To determine whether this ability is widespread among bloom forming organisms, we compared genomes of putative bloomers to those of non-blooming organisms. We found that bloomer genomes were significantly enriched with anti-phage defense systems. This challenges traditional paradigms of phage ecology in bloom-forming systems and suggests that microbes adapted to high-density growth may have evolved mechanisms to reduce their susceptibility to phage attack.

microbiology↗

Dietary copper exposure decreases splenic MMC coverage but does not cause splenic disorganization or damage.

Exposure to copper, one of the prevalent contaminants in aquatic environments, has wide-ranging adverse immunological effects. However, it is unclear if copper induced immune changes are due to alterations in lymphoid tissues or the result of direct immune cell toxicity. Therefore, to understand the mechanistic action of copper immunomodulation, we utilized an emerging immunotoxicologic model, threespine stickleback fish (Gasterosteus aculeatus). We exposed stickleback fish to dietary copper for a period of 14 days and examined its effect on the spleen, including histopathologic changes in splenic architecture and resident melanomacrophage centers (MMC) populations. We found that dietary copper exposure decreases splenic MMC coverage, suggesting copper is suppressing this phagocyte population. We found no histopathological differences between control and copper groups. Quantification of splenic compartments demonstrated that there is no significant difference in red or white pulp between the control and copper groups, suggesting that reduced MMC coverage is not due to the expansion of other splenic regions. Overall, results from this study suggest that copper toxicity leads to melanomacrophage suppression without damaging or altering the splenic secondary immune tissue structure. Future studies should examine the effect of copper on melanomacrophage viability, development, and function to better understand the mechanism behind MMC reduction. Impact statementThis study demonstrates that dietary copper reduces splenic MMCs but does not cause histopathological damage or alter other compartments of spleen, including the red and white pulp, suggesting that copper-induced immune modulation is the result of direct melanomacrophage toxicity and not due to secondary immune tissue damage. MMC assays could be a useful tool for monitoring heavy metal and other contaminant exposures in aquatic organisms.

immunology↗