At Panguana, a study in the upper Amazon basin, 7 different aquatic breeding sites of anurans were investigated from Nov. 1, 1981 to Oct. 31, 1982. Rainfall in this area is seasonal. Only 20% of the total annual precipitation was maesured during the dry period, which lasted from mid-March until mid-September 1982. The reproductive periods of the species were highly affected by the rainfall distribution. Calling males and/or gravid females of 46 species were found during the study period. 37.0% of the anuran species were exclusively, and 43.5% predominantly, active during the rainy season. Plots of 100 m were established at 6 aquatic sites in primary rainforest. A total of 2126 frogs was counted; 93.2% of these were made during the rainy season. A maximum of 378 individuals were found during one check in the plot at the permanent pond. At this site high concentrations of individuals and large choruses were found at the beginning of the rainy season. As soon as favourable temporary aquatic sites were established, reproductive activities decreased at the permanent pond and increased at temporary breeding sites.

Hemolysis drives susceptibility to bacterial infections and predicts poor outcome from sepsis. These detrimental effects are commonly considered to be a consequence of heme-iron serving as a nutrient for bacteria. We employed a Gram-negative sepsis model and found that elevated heme levels impaired the control of bacterial proliferation independently of heme-iron acquisition by pathogens. Heme strongly inhibited phagocytosis and the migration of human and mouse phagocytes by disrupting actin cytoskeletal dynamics via activation of the GTP-binding Rho family protein Cdc42 by the guanine nucleotide exchange factor DOCK8. A chemical screening approach revealed that quinine effectively prevented heme effects on the cytoskeleton, restored phagocytosis and improved survival in sepsis. These mechanistic insights provide potential therapeutic targets for patients with sepsis or hemolytic disorders.

Toll-like receptor 7 (TLR7) triggers antiviral immune responses by recognizing viral single-stranded RNA in endosomes, but the biosynthetic pathway of human TLR7 (hTLR7) remains unclear. Here, we show that hTLR7 is proteolytically processed and that the C-terminal fragment selectively accumulates in endocytic compartments. hTLR7 processing occurred at neutral pH and was dependent on furin-like proprotein convertases (PCs). Furthermore, TLR7 processing was required for its functional response to TLR7 agonists such as R837 or influenza virus. Notably, proinflammatory and differentiation stimuli increased the expression of furin-like PCs in immune cells, suggesting a positive feedback mechanism for TLR7 processing during infection. Because self-RNA can under certain conditions activate TLR7 and trigger autoimmunity, our results identify furin-like PCs as a possible target to attenuate TLR7-dependent autoimmunity and other immune pathologies.