Structural characteristics and antiviral activity of multiple peptides derived from MDV glycoproteins B and H

<p>Abstract</p> <p>Background</p> <p>Marek's disease virus (MDV), which is widely considered to be a natural model of virus-induced lymphoma, has the potential to cause tremendous losses in the poultry industry. To investigate the structural basis of MDV membrane fusion and to identify new viral targets for inhibition, we examined the domains of the MDV glycoproteins gH and gB.</p> <p>Results</p> <p>Four peptides derived from the MDV glycoprotein gH (gHH1, gHH2, gHH3, and gHH5) and one peptide derived from gB (gBH1) could efficiently inhibit plaque formation in primary chicken embryo fibroblast cells (CEFs) with 50% inhibitory concentrations (IC₅₀) of below 12 μM. These peptides were also significantly able to reduce lesion formation on chorioallantoic membranes (CAMs) of infected chicken embryos at a concentration of 0.5 mM in 60 μl of solution. The HR2 peptide from Newcastle disease virus (NDVHR2) exerted effects on MDV specifically at the stage of virus entry (i.e., in a cell pre-treatment assay and an embryo co-treatment assay), suggesting cross-inhibitory effects of NDV HR2 on MDV infection. None of the peptides exhibited cytotoxic effects at the concentrations tested. Structural characteristics of the five peptides were examined further.</p> <p>Conclusions</p> <p>The five MDV-derived peptides demonstrated potent antiviral activity, not only in plaque formation assays in vitro, but also in lesion formation assays in vivo. The present study examining the antiviral activity of these MDV peptides, which are useful as small-molecule antiviral inhibitors, provides information about the MDV entry mechanism.</p

Biodiversity of Reef-Building, Scleractinian Corals

Zooxanthellate scleractinian corals are moderately well-known for shallow reef habitats, but not for mesophotic depths (>30 m) that are relatively difficult to access. Mesophotic habitats are light-limited, with different hydrodynamics and sedimentation processes, which result in growth forms that are often difficult to classify using traditional schemes based largely on shallow reef specimens. We analyzed published data and museum records, using specimen-based records to minimize classification issues, finding 53 mesophotic species in the western Atlantic Ocean (85% of total species) and 338 in the Indo-Pacific (45%). Only four species were recorded exclusively below 30 m depth, while the great majority were common shallow reef taxa. Over 96% of western Atlantic and 82% of Indo-Pacific genera and most coral lineages were represented below 30 m depth. In the Indo-Pacific, species and genus richness varied widely between regions and were significantly correlated with shallow reef species richness. Overall, species richness decreased steadily with increasing depth, with little evidence for distinct faunal boundaries: 157 species occurred >= 60 m and 31 deeper than 100 m, with species occurrence only moderately related to phylogeny. Our knowledge of mesophotic biodiversity is rapidly changing as more regions are documented and new molecular techniques suggest taxonomic revisions and resolve deepwater cryptic species. We conclude that mesophotic scleractinian fauna are largely a subset of shallow scleractinian fauna, comprising a significant proportion of coral species and most genera, with the potential to play a significant role in lineage preservation and the future of coral reefs