Analyses of arthropod genomes have shown that the genes in the different innate humoral immune responses are conserved. These genes encode proteins that are involved in immune signalling pathways that recognize pathogens and activate immune responses. These immune responses include phagocytosis, encapsulation of the pathogen, and production of effector molecules for pathogen elimination. So far, most studies have focused on insects leaving other major arthropod groups largely unexplored. Here we annotate the immune related genes of six arachnid genomes and present evidence for a conserved pattern of some immune genes, but also evolutionary changes in the arachnid immune system. Specifically, our results suggest that the family of recognition molecules of Beta-1,3-glucanase-related proteins (βGRPs) and the genes from the immune deficiency (IMD) signalling pathway have been lost in a common ancestor of arachnids. These findings are consistent with previous work suggesting that the humoral immune effector proteins are constitutively produced in arachnids in contrast to insects, where these have to be induced. Further functional studies are needed to verify this. We further show that the full hemolymph clotting cascade found in the horseshoe crab is retrieved in most arachnid genomes. Tetranychus lacks at least one major component, although it is possible that this cascade could still function through recruitment of a different protein. The gel-forming protein in horseshoe crabs, coagulogen, was not recovered in any of the arachnid genomes, however, it is possible that the arachnid clot consists of a related protein, spätzle, that is present in all of the genomes.
Conservation of horseshoe crabs has recently received increasing attention as several populations are in decline. However, scarce information on their distributions in Southeast Asia is impairing conservation efforts. In this study, we sought to improve our understanding of the geographical range and distinct populations of the three Asian horseshoe crabs species in order to identify optimal conservation areas. We mapped the geographic range of Carcinoscorpius rotundicauda, Tachypleus gigas, and T. tridentatus using recent data from field work, literature, Global Biodiversity Information Facility (GBIF), and unpublished data from our scientific network. The data were correlated with 23 different environmental variables of potential ecological importance for horseshoe crabs using the openModeller webservices, including new tidal variables. Ecological niche models were generated using two algorithms, Maximum Entropy and support vector machine, for the three species under present conditions, and projected into a climate change scenario of 2050. The niches of the Asian horseshoe crabs were mostly determined by tidal regime, chlorophyll A concentrations, depth, distance to land, and sea surface temperature. According to our predictions, horseshoe crabs in Southeast Asia are not expected to experience any severe change in extent and distribution of suitable habitat in the future. In order to conserve Asian horseshoe crabs, we suggest establishing Marine Protected Areas at locations where distinct populations and several species occur, such as northern Vietnam, China, Borneo, and southern Japan.
In birds, parasites cause detrimental effects to the individual host, including reduced survival and reproductive output. The level of parasitic infection can vary with a range of factors, including migratory status, body size, sex, and age of hosts, or season. Understanding this baseline variation is important in order to identify the effects of external changes such as climate change on the parasitic load and potential impacts to individuals and populations. In this study, we compared the infection level (prevalence, intensity, and abundance) of gastrointestinal parasites in a total of 457 common eiders ( Somateria mollissima ) from four different sampling locations (Belcher Islands, Cape Dorset, West Greenland and Newfoundland), and explored the effects of migration, sex and age on levels of parasitism. Across all samples, eiders were infected with one nematode genus, two acanthocephalan genera, three genera of cestodes, and three trematode genera. Migratory phase and status alone did not explain the observed variation in infection levels; the expectation that post-migratory eiders would be more parasitized than pre-migratory eiders, due to the energetic cost of migration, did not fit our results. No effect of age was detected, whereas effects of sex and body size were only detected for certain parasitic taxa and was inconsistent with location. Since gastrointestinal helminths are trophically-transmitted, future studies of the regional and temporal variation in the diet of eiders and the associated variation and infestation level of intermediate hosts might further explain the observed variation of the parasitic load in eiders in different regions.
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