Rabbit hemorrhagic disease virus type 2 epidemic in a rabbit colony in Japan. [PDF]
Twenty-three of 42 European rabbits (Oryctolagus cuniculus), belonging to the same rabbit colony, died in March 2020 (55% mortality) in Chiba prefecture, Japan. The disease course was extremely acute without indicators of death or hemorrhage. Necropsy revealed liver swelling, discoloration, cloudiness and fragility, and pulmonary edema. Histologically,
Fukui H +4 more
europepmc +3 more sources
Ecosystem Effects of Variant Rabbit Hemorrhagic Disease Virus, Iberian Peninsula
Letter to the Editor. The Aragón monitoring scheme is run by the Fish and Game Department, Government of Aragón. M.D.M. was supported by a JAE-DOC contract (Programa Junta para la Ampliación de Estudios), funded by CSIC and the European Social Fund. C.F. was supported by a Post-Doctoral Fellowship funded by NSERC, Government of Canada.
Miguel Delibes-Mateos +4 more
doaj +4 more sources
Down the Rabbit Hole: Domestic Rabbit Owners’ Perceptions of Rabbit Hemorrhagic Disease Virus 2
Rabbit hemorrhagic disease virus 2 (RHDV2) is a highly contagious pathogen that infects wild and domestic rabbits and hares (lagomorphs). Globally, RHDV2 has resulted in substantial economic losses for commercial rabbit trade and caused wild lagomorph population declines.
H. Shapiro, M. Ruder, E. Pienaar
semanticscholar +4 more sources
Origin and Phylodynamics of Rabbit Hemorrhagic Disease Virus [PDF]
ABSTRACT To determine the origin, phylogenetic relationships, and evolutionary dynamics of rabbit hemorrhagic disease virus (RHDV), we examined 210 partial and complete capsid gene nucleotide sequences. Using a Bayesian Markov chain Monte Carlo approach, we estimated that these sequences evolved at a rate of 3.9 × 10 −
Peter J, Kerr +2 more
openaire +2 more sources
Hemagglutination and Antigenic Comparison of Rabbit Hemorrhagic Disease Virus.
The hemagglutinating activity and serological properties of three strains of rabbit hemorrhagic disease virus, Chinese, Korean and Shizuoka, which was first isolated in Japan, were examined by hemagglutination (HA) and cross hemagglutination inhibition (HI) test with human erythrocytes.
Toru Mizoguchi +2 more
openalex +4 more sources
Abstract Objective Trigeminal postherpetic neuralgia (PHN) is often refractory to treatment. Pulsed radiofrequency (PRF) neuromodulation can help in preventing PHN after herpes zoster. This study aimed to compare the efficacy and safety of two different PRF modes on gasserian ganglion neuromodulation in elderly patients with acute/subacute trigeminal ...
Cheng‐Fu Wan, Tao Song
wiley +1 more source
Vesivirus 2117 capsids more closely resemble sapovirus and lagovirus particles than other known vesivirus structures [PDF]
Vesivirus 2117 is an adventitious agent that in 2009, was identified as a contaminant of CHO cells propagated in bioreactors at a pharmaceutical manufacturing plant belonging to Genzyme.
Bhella, David +8 more
core +1 more source
Identification and characterization of the virus causing rabbit hemorrhagic disease [PDF]
Liver tissue from animals that died of rabbit hemorrhagic disease (RHD) was used to identify the causative agent. After extraction of liver homogenates and sucrose density gradient ultracentrifugation, distinct bands were obtained. The respective gradient fractions reacted positively in an enzyme-linked immunosorbent assay as well as in ...
V F, Ohlinger +4 more
openaire +2 more sources
An isolated epizootic of hemorrhagic-like fever in cats caused by a novel and highly virulent strain of feline calicivirus. [PDF]
An isolated epizootic of a highly fatal feline calicivirus (FCV) infection, manifested in its severest form by a systemic hemorrhagic-like fever, occurred over a 1-month period among six cats owned by two different employees and a client of a private ...
Elliott, JB +4 more
core +1 more source
Capsid gene divergence in rabbit hemorrhagic disease virus
The emergence and rapid global spread of rabbit hemorrhagic disease virus (RHDV) remains enigmatic despite two decades of study, largely due to the difficulties associated with modelling substitution processes of the RNA genome for phylogenetic inference. We used maximum-likelihood and Bayesian methods to investigate rates of molecular evolution in the
Kinnear, Mark, Linde, Celeste
openaire +3 more sources

