11 research outputs found
Wear Tribo-Performances of Laser Cladding Colmonoy-6 and Stellite-6 Micron Layers on Stainless Steel 304 Using Yb:YAG Disk Laser
Molecular basis for phosphospecific recognition of histone H3 tails by Survivin paralogues at inner centromeres
The structure of hSurvivin bound to the histone H3 tail phosphorylated on Thr-3 was solved to determine how the CPC reads the histone code. Many eukaryotes have two Survivin paralogues. A major difference between them is that class A is pH sensitive in H3T3ph binding, whereas class B is relatively pH insensitive but has lower affinity for H3T3ph
Variation in Antiviral Protection Mediated by Different Wolbachia Strains in Drosophila simulans
Drosophila C virus (DCV) is a natural pathogen of Drosophila and a useful model for studying antiviral defences. The Drosophila host is also commonly infected with the widespread endosymbiotic bacteria Wolbachia pipientis. When DCV coinfects Wolbachia-infected D. melanogaster, virus particles accumulate more slowly and virus induced mortality is substantially delayed. Considering that Wolbachia is estimated to infect up to two-thirds of all insect species, the observed protective effects of Wolbachia may extend to a range of both beneficial and pest insects, including insects that vector important viral diseases of humans, animals and plants. Currently, Wolbachia-mediated antiviral protection has only been described from a limited number of very closely related strains that infect D. melanogaster. We used D. simulans and its naturally occurring Wolbachia infections to test the generality of the Wolbachia-mediated antiviral protection. We generated paired D. simulans lines either uninfected or infected with five different Wolbachia strains. Each paired fly line was challenged with DCV and Flock House virus. Significant antiviral protection was seen for some but not all of the Wolbachia strain-fly line combinations tested. In some cases, protection from virus-induced mortality was associated with a delay in virus accumulation, but some Wolbachia-infected flies were tolerant to high titres of DCV. The Wolbachia strains that did protect occurred at comparatively high density within the flies and were most closely related to the D. melanogaster Wolbachia strain wMel. These results indicate that Wolbachia-mediated antiviral protection is not ubiquitous, a finding that is important for understanding the distribution of Wolbachia and virus in natural insect populations