The influence of deoxygenation on Caribbean coral larval settlement and early survival

Deoxygenation is emerging as a major threat to coral reefs where it can have catastrophic effects, including mass coral mortality. Some coral species cannot survive more than a few days of exposure to low oxygen conditions, while others can tolerate deoxygenation for weeks, suggesting that coral tolerance to lowered dissolved oxygen (DO) concentrations is species-specific. However, hypoxia thresholds for corals have not yet been fully defined, and more information is needed to understand if tolerance to deoxygenation is consistent across all life stages. In this study, we tested the influence of severe (1.5 mg L-1 DO) and intermediate (3.5 mg L-1 DO) deoxygenation on larval settlement and survival during the early recruitment life phase of Colpophyllia natans, Orbicella faveolata, and Pseudodiploria strigosa. Exposure to deoxygenation over a 3-day settlement period did not significantly impact larval survival nor settlement rates compared to ambient DO concentrations (6 mg L-1 DO) for all three species. However, recruit survivorship in C. natans and O. faveolata after further exposure to severe deoxygenation was reduced compared to intermediate deoxygenation and control DO conditions. After 45 days of exposure to severe deoxygenation only 2.5 ± 2.5% of the initial O. faveolata had survived the larval and recruit stages compared to 22.5 ± 4.5% in control oxygen conditions. Similarly, C. natans survival was 13.5 ± 6.0% under severe deoxygenation, compared to 41.0 ± 4.4% in the control treatment. In contrast, survival of P. strigosa larvae and recruits was not different under deoxygenation treatments compared to the control, and higher overall, relative to the other species, indicating that P. strigosa is more resilient to severe deoxygenation conditions during its earliest life stages. This study provides unique insights into species-specific variation in the tolerance of coral recruits to deoxygenation with implications for whether this life history stage may be a demographic bottleneck for three ecologically important Caribbean coral species. Given the increasing frequency and severity of deoxygenation events in Caribbean coastal waters, these results are an important contribution to the growing body of research on deoxygenation as a threat to coral reef persistence in the Anthropocene, with implications for conservation and restoration efforts integrating coral recruitment into reef recovery efforts

Finishing the euchromatic sequence of the human genome

The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead

DataSheet_1_The influence of deoxygenation on Caribbean coral larval settlement and early survival.csv

Deoxygenation is emerging as a major threat to coral reefs where it can have catastrophic effects, including mass coral mortality. Some coral species cannot survive more than a few days of exposure to low oxygen conditions, while others can tolerate deoxygenation for weeks, suggesting that coral tolerance to lowered dissolved oxygen (DO) concentrations is species-specific. However, hypoxia thresholds for corals have not yet been fully defined, and more information is needed to understand if tolerance to deoxygenation is consistent across all life stages. In this study, we tested the influence of severe (1.5 mg L-1 DO) and intermediate (3.5 mg L-1 DO) deoxygenation on larval settlement and survival during the early recruitment life phase of Colpophyllia natans, Orbicella faveolata, and Pseudodiploria strigosa. Exposure to deoxygenation over a 3-day settlement period did not significantly impact larval survival nor settlement rates compared to ambient DO concentrations (6 mg L-1 DO) for all three species. However, recruit survivorship in C. natans and O. faveolata after further exposure to severe deoxygenation was reduced compared to intermediate deoxygenation and control DO conditions. After 45 days of exposure to severe deoxygenation only 2.5 ± 2.5% of the initial O. faveolata had survived the larval and recruit stages compared to 22.5 ± 4.5% in control oxygen conditions. Similarly, C. natans survival was 13.5 ± 6.0% under severe deoxygenation, compared to 41.0 ± 4.4% in the control treatment. In contrast, survival of P. strigosa larvae and recruits was not different under deoxygenation treatments compared to the control, and higher overall, relative to the other species, indicating that P. strigosa is more resilient to severe deoxygenation conditions during its earliest life stages. This study provides unique insights into species-specific variation in the tolerance of coral recruits to deoxygenation with implications for whether this life history stage may be a demographic bottleneck for three ecologically important Caribbean coral species. Given the increasing frequency and severity of deoxygenation events in Caribbean coastal waters, these results are an important contribution to the growing body of research on deoxygenation as a threat to coral reef persistence in the Anthropocene, with implications for conservation and restoration efforts integrating coral recruitment into reef recovery efforts.</p

Receptor interacting protein kinase 2-mediated mitophagy regulates inflammasome activation during virus infection

Item does not contain fulltextNOD2 receptor and the cytosolic protein kinase RIPK2 regulate NF-kappaB and MAP kinase signaling during bacterial infections, but the role of this immune axis during viral infections has not been addressed. We demonstrate that Nod2(-/-) and Ripk2(-/-) mice are hypersusceptible to infection with influenza A virus. Ripk2(-/-) cells exhibited defective autophagy of mitochondria (mitophagy), leading to enhanced mitochondrial production of superoxide and accumulation of damaged mitochondria, which resulted in greater activation of the NLRP3 inflammasome and production of IL-18. RIPK2 regulated mitophagy in a kinase-dependent manner by phosphorylating the mitophagy inducer ULK1. Accordingly, Ulk1(-/-) cells exhibited enhanced mitochondrial production of superoxide and activation of caspase-1. These results demonstrate a role for NOD2-RIPK2 signaling in protection against virally triggered immunopathology by negatively regulating activation of the NLRP3 inflammasome and production of IL-18 via ULK1-dependent mitophagy