Wildlife Reservoirs of Canine Distemper Virus Resulted in a Major Outbreak in Danish Farmed Mink (<em>Neovison vison</em>)

A major outbreak of canine distemper virus (CDV) in Danish farmed mink (Neovison vison) started in the late summer period of 2012. At the same time, a high number of diseased and dead wildlife species such as foxes, raccoon dogs, and ferrets were observed. To track the origin of the outbreak virus full-length sequencing of the receptor binding surface protein hemagglutinin (H) was performed on 26 CDV's collected from mink and 10 CDV's collected from wildlife species. Subsequent phylogenetic analyses showed that the virus circulating in the mink farms and wildlife were highly identical with an identity at the nucleotide level of 99.45% to 100%. The sequences could be grouped by single nucleotide polymorphisms according to geographical distribution of mink farms and wildlife. The signaling lymphocytic activation molecule (SLAM) receptor binding region in most viruses from both mink and wildlife contained G at position 530 and Y at position 549; however, three mink viruses had an Y549H substitution. The outbreak viruses clustered phylogenetically in the European lineage and were highly identical to wildlife viruses from Germany and Hungary (99.29% – 99.62%). The study furthermore revealed that fleas (Ceratophyllus sciurorum) contained CDV and that vertical transmission of CDV occurred in a wild ferret. The study provides evidence that wildlife species, such as foxes, play an important role in the transmission of CDV to farmed mink and that the virus may be maintained in the wild animal reservoir between outbreaks

Preparation of Hydrogen Permeable Membrane Using Nanoparticles Electrophoresis Technique

Hydrogen perm-selective membranes composed of Pd nanoparticles were investigated. The nanoparticles were prepared by ultrasonic reduction from PdII ions, and then deposited on a substrate disc with electrophoresis technique. These electrophoretic membranes have shown high performance of perm-selectivity for H2 with separation factor α = 3.85, under room temperature

Traveling up the fishways, Descending and Ascending Migration of Satsukimasu (Sea-run-form Amago Salmon)

In the springs of 1994 and 1995, surveys were conducted to confirm the state of the fishways at Nagaragawa Estuary Barrage and confirmed that Satsukimasu (Sea-run-form Amago Salmon) travel up the fishways. Amago smolts with marking were also released during November and December of 1994, the state of descending and the state of ascending were surveyed. However, few marked fish could be confirmed so it was difficult to adequately clarify the effect of Estuary Barrage descending and ascending characteristics of Satsukimasu in the current survey

In silico experiments of bone remodeling explore metabolic diseases and their drug treatment

骨再構築(リモデリング)のシミュレーション実験基盤を開発 --骨疾患と薬物治療の効果の予測を目指して--. 京都大学プレスリリース. 2020-03-10.Bone structure and function are maintained by well-regulated bone metabolism and remodeling. Although the underlying molecular and cellular mechanisms are now being understood, physiological and pathological states of bone are still difficult to predict due to the complexity of intercellular signaling. We have now developed a novel in silico experimental platform, V-Bone, to integratively explore bone remodeling by linking complex microscopic molecular/cellular interactions to macroscopic tissue/organ adaptations. Mechano-biochemical couplings modeled in V-Bone relate bone adaptation to mechanical loading and reproduce metabolic bone diseases such as osteoporosis and osteopetrosis. V-Bone also enables in silico perturbation on a specific signaling molecule to observe bone metabolic dynamics over time. We also demonstrate that this platform provides a powerful way to predict in silico therapeutic effects of drugs against metabolic bone diseases. We anticipate that these in silico experiments will substantially accelerate research into bone metabolism and remodeling

In silico tools predict effects of drugs on bone remodelling.

status: publishe