A novel Amazonian reef biome was discovered, encompassing large rhodolith and sponge beds under low light, low oxygen, and high POC.

Bioeroding sponges of theCliona viridisspecies complex play a large role in carbonate cycling and reef health. In the present study we provide the first record and a description of a Mediterranean lineage ofC. viridis(Schmidt, 1862) in the south-western Atlantic. Specimens were collected in Maricás Archipelago, Rio de Janeiro State in September 2010 by scuba diving at 10–12 m depth and deposited in the Porifera collection of Museu Nacional, Universidade Federal do Rio de Janeiro. Morphologically, the specimens presently examined are very similar to those described in the beta and gamma growth form from the Mediterranean. The Brazilian and Mediterranean specimens share large and irregular papillae over 2 cm in diameter, megasclere tylostyles up to 500 µm long and microsclere spirasters with up to five twists and 34 µm long. A Maximum Likelihood analysis of 28S rDNA ofC. viridis, C. aprica, C. jullieni, C. schmidtiandC. varianswas performed for a genetic identification of the Brazilian specimens. The Brazilian material is phylogenetically closer to the MediterraneanC. viridisthan to the Caribbean and Indian Ocean members of this species complex included in the present analysis. Our results suggest thatC. viridisis a cryptogenic species with a distribution extending from the Mediterranean to the eastern Atlantic and in the SE Brazilian coast or further.

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Background: Given the role of the P2X7 receptor (P2X7R) in inflammatory bowel diseases (IBD), we investigated its role in the development and progression of colitis-associated colorectal cancer (CA-CRC). Methods: CA-CRC was induced in P2X7R+/+ and P2X7R−/− mice with azoxymethane (AOM) combined with dextran sodium sulfate (DSS). In a therapeutic protocol, P2X7R+/+ mice were treated with a P2X7R-selective inhibitor (A740003). Mice were evaluated with follow-up video endoscopy with endoluminal ultrasound biomicroscopy. Colon tissue was analyzed for histological changes, densities of immune cells, expression of transcription factors, cytokines, genes, DNA methylation, and microbiome composition of fecal samples by sequencing for 16S rRNA. Results: The P2X7R+/+ mice displayed more ulcers, tumors, and greater wall thickness, than the P2X7R−/− and the P2X7R+/+ mice treated with A740003. The P2X7R+/+ mice showed increased accumulation of immune cells, production of proinflammatory cytokines, activation of intracellular signaling pathways, and upregulation of NLRP3 and NLRP12 genes, stabilized after the P2X7R-blockade. Microbial changes were observed in the P2X7R−/− and P2X7R+/+-induced mice, partially reversed by the A740003 treatment. Conclusions: Regulatory mechanisms activated downstream of the P2X7R in combination with signals from a dysbiotic microbiota result in the activation of intracellular signaling pathways and the inflammasome, amplifying the inflammatory response and promoting CA-CRC development.

Comprising 56 species, Timea Gray, 1867 belongs to the monotypic family Timeidae Gray, 1867, with both family and genus characterized by the presence of (sub)tylostyles as megascleres, and euasters as microscleres. Two new species are described from the coast of Rio de Janeiro state, Timea berlincki sp. nov. and Timea clandestina sp. nov., the first of which also from São Paulo state (southeastern Brazil). Both are compared to other species based on their morphological and skeletal characters. Records of all species of the genus worldwide are tabulated and discussed, and an identification key for Tropical western Atlantic species of Timea is offered.