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Jiancheng Chen, Shuhei Yamada, Yoshiki Hama, Ajaya Kumar Shetty, Takanari Kobayashi, Hiroshi Oda, Kosuke Seiki, Eunmi Kim, Takashi Kimura, Naonori Takahashi, Kazuya I. In this study, the lineage of rabies virus RABV in Zambia was determined by phylogenetic analysis of the nucleoprotein N and glycoprotein G gene sequences. Conclusion: Population genetic analyses of Theileria parva from Isoka and Petauke districts showed a low level of genotype exchange between the districts, but a high level of genetic diversity within each district population, implying genetic and geographic sub-structuring between the districts. Equine MHC class I clone 3. All rights reserved. Methods: RNA samples were obtained from the spleens of fruit bats collected from four locations in Indonesia. We histopathologically examined the lungs of these mice. Phylogenetic analysis showed that it was a novel member of the family Polyomaviridae, and thus the virus was tentatively named mastomys polyomavirus.{/INSERTKEYS}{/PARAGRAPH} To identify the MHC class I molecule region that is responsible for EHV-1 entry, domain exchange and site-directed mutagenesis experiments were performed, in which parts of the extracellular region of hamster MHC class I clone C5 were replaced with corresponding sequences from equine MHC class I clone A Substitution of alanine for glutamine at position QA within the alpha 2 domain of the MHC class I molecule enabled hamster MHC class I C5 to mediate EHV-1 entry into cells. The aim of this study was to detect the presence of paramyxovirus RNA in fruit bats from Indonesia. Sucrose gradient sedimentation and cesium chloride gradient ultracentrifugation analyses revealed that the particles of virus lacking agnoprotein assemble into irregularly sized virions, and that agnoprotein alters the efficiency of formation of VP1 virus-like particles. C Elsevier B. Experiments on anticoagulant activity indicated that the shrimp HS exhibited significant anti-thrombin activity, but less than the commercial heparin. When analyzed separately, linkage disequilibrium was observed in Kanyelele and Kalembe areas in Isoka district, Isoka district overall and in Petauke district. This virus was tentatively named vervet monkey PyV 1 VmPyV1 as a novel PyV. Therefore, it is important to understand the mechanism of neuronal apoptosis caused by this virus to develop strategies to control its pathogenicity. Structurally the shrimp HS was more heterogenous than heparin, although it is still highly sulfated. Viral antigen was detected in the neuronal cytoplasm of the cells exhibiting neuronal apoptosis. This viral genome contained potential ORFs for the capsid proteins, VP1, VP2 and VP3, and early proteins, small t antigen and large T antigen. Phylogenetic analysis of the N gene showed two phylogenetic clusters in Zambia belonging to the Africa 1b lineage present in eastern and southern Africa. Exploratory laparotomy showed bilateral, segmentally distended uterine horns with unilateral uterine horn torsion. We designed primers for reverse transcription loop-mediated isothermal amplification RT-LAMP assay from the consensus sequence of the N gene in an attempt to improve the molecular diagnosis of RABV in Zambia. Further, viral antigen-positive cells were observed at 9 dpi in the aged mice, but not in the young ones. Soluble CS-E sCS-E derived from squid cartilage inhibited JEV infection in African green monkey kidney-derived Vero cells and baby hamster kidney-derived BHK cells by interfering with viral attachment. These results suggest that the amino acid residue at position of the MHC class I molecule is involved in the efficiency of EHV-1 entry. Immunohistochemical examination revealed that viral antigen-positive bronchiolar and alveolar epithelial cell numbers at 3 dpi were significantly higher in young mice than in the aged ones. Our histopathological and in vitro studies suggest that accumulation of ubiquitinated proteins in neuronal cells might be associated with neuronal apoptosis caused by WNV infection. J Am Anim Hosp Assoc ; DOI Young mice inoculated with influenza virus showed body weight loss at 4 days post-infection dpi , meanwhile body weight decrease started from 9 dpi in the aged mice. Hence, the HS preparation from shrimp heads, an industrial waste, is a prospective agent for a variety of clinical applications. We detected seven PyV genome fragments in DNA samples using a nested broadspectrum PCR method, and identified five full-length viral genomes using an inverse PCR method. We detected VP1 protein expression in the transfected HEKT cells by immunocytochemical and immunoblot analyses. It has been reported that WNV replication directly induces neuronal injury, followed by neuronal cell death proven as apoptosis. We analysed DNA samples from the spleens and kidneys n each of yellow baboons and vervet monkeys VMs n each. It was found that mature virions of agnoprotein-negative JCV are irregularly shaped. These results show the paradoxical effects of sCS-E on JEV infection in different cell types and indicate that potential use of sCS-E as an antiviral agent against JEV infection should be approached with caution considering its effects in the neuron, the major target of JEV. To obtain a better understanding of the mechanisms of WNV-induced neuronal apoptosis, we evaluated the accumulation of ubiquitinated proteins in the WNV-infected neuronal cells. To examine whether the VmPyV1 genome could produce viral proteins in cultured cells, the whole genome was transfected into HEKT cells. Accumulation of ubiquitinated abnormal proteins has been reported to be associated with neuronal apoptosis in some pathological conditions. The molecular mass of the shrimp HS preparation was determined to be Notably, the shrimp HS had a greater inhibitory effect against infections by dengue virus type 2 as well as Japanese encephalitis virus than heparin. The results showed that rM2ss23 bound to both Aichi and PR8 M2 proteins expressed on the cell surface. Microsatellite analysis was then performed on all Theileria parva positive samples for PCR using a panel of 9 microsatellite markers. JCV encodes early proteins large T antigen, small T antigen, and T' antigen and four late proteins agnoprotein, and three viral capsid proteins, VP1, VP2, and VP3. These findings provide detailed insights into the age-specific course of infection in young and aged populations with associated differences in lung pathology. The sub-structuring observed, along with the lack of panmixia in the populations, could have been due to low transmission levels at the time of sampling. In the current study, a novel function for JCV agnoprotein in the morphogenesis of JC virion particles was identified. Comparison with other PyVs revealed that VmPyV1, like chimpanzee PyV, had a longer VP1 ORF. Substitution of alanine for threonine at position TA enabled MHC class I 3. Methods: Cattle blood samples were collected for genetic analysis of Theileria parva from Isoka and Petauke districts in Zambia. While one cluster exclusively comprised Zambian strains, the other was more heterogeneous regarding the RABV origins and included strains from Tanzania, Mozambique and Zambia. Therefore, the RI-LAMP assay presented in this study may prove to be useful for routine diagnosis of rabies in Zambia. It is a major constraint to the development of the livestock industry in some parts of eastern, central and southern Africa. Moreover, T cell and macrophage accumulation in the lungs was significantly higher in the young mice than in the aged mice at 9 dpi. An in vitro binding assay and immunocytochemistry revealed that agnoprotein binds to glutathione S-transferase fusion proteins of VP1 and that some fractions of agnoprotein colocalize with VP1 in the nucleus. In contrast, sCS-E enhanced viral infection in the mouse neuroblastoma cell line Neuro-2a, despite the fact that viral attachment to Neuro-2a cells was inhibited by sCS-E. Notably, ubiquitinated proteins were detected in WNV-infected neuronal cells. Diffuse and severe bronchointerstitial pneumonia characterized by the accumulation of polymorphonuclear leukocytes PMNs was observed in young mice at 6 dpi. EHV-1 utilizes equine MHC class I molecules as entry receptors. However, the Isoka population was less diverse than the Petauke population. Thus, we identified a novel PyV genome from VM spleen. The specificity and reproducibility of the RI-LAMP assay was confirmed with actual clinical specimens. Conclusions: This study indicates the presence of novel paramyxoviruses among fruit bat populations in Indonesia. C Elsevier Inc. Histopathological changes in the aged mice were milder than those in the young mice. Phylogenetic analysis of virally encoded proteins revealed that four PyVs were closely related to either African green monkey PyV or simian agent The obtained entire genome of this virus was bp and had large T- and small t-antigens, and VP1 and VP2 ORFs. These results suggest that there may be a correlation between the relatively low level of infiltration of PMNs, macrophages, and T lymphocytes and the delayed body weight loss and longer lasting infections observed in the lungs of the aged mice. Yasuko Orba, Shintaro Kobayashi, Ichiro Nakamura, Akihiro Ishii, Bernard M. While the antibody did not prevent virus entry into cells, it significantly inhibited plaque formation by the Aichi strain in a dose-dependent manner when infected cells were cultured in the presence of the antibody. In addition, gel filtration analysis of formation of VP1-pentamers revealed that agnoprotein enhances formation of these pentamers by interacting with VP1. By contrast, the growth of PR8 H1N1 was not affected by the antibody. However, hamster MHC class I molecules on EHVsusceptible CHO-K1 cells play no role in EHV-1 entry. In Zambia, theileriosis causes losses of up to 10, cattle annually. A lot of cellular stresses prevent cellular protein quality control mechanisms, resulting in the accumulation of ubiquitinated abnormal proteins. Results: Semi-nested reverse transcription PCR detected five previously unidentified paramyxoviruses from six fruit bats. In addition, accumulation of ubiquitinated proteins was markedly enhanced in mouse neuroblastoma, Neuro-2a cells after WNV infection. We have observed that WNV infection caused massive neuronal injury in the brains of mice. This enhancement effect in Neuro-2a cells seemed to be related to increased viral RNA replication and was also observed in a rat infection model in which intracerebral coadministration of sCS-E with JEV in day-old rats resulted in higher brain viral loads than in rats infected without sCS-E administration. Microsatellite data was analyzed using microsatellite toolkit, GenAlEx ver. To the authors' knowledge, this is the first report of uterine horn torsion in conjunction with segmental aplasia of the uterine horn in a bitch. The present findings suggest that JCV agnoprotein plays a role, similar to that of SV40 agnoprotein, in facilitating virion assembly. Conversely, substitution of glutamine for alanine at position AQ in equine MHC class I A68 resulted in loss of EHV-1 receptor function. Petauke district had a higher multiplicity of infection than Isoka district. All samples were screened by semi-nested broad spectrum reverse transcription PCR targeting the paramyxovirus polymerase L genes. Phylogenetic analysis of the G gene revealed similar RABV strains in different hosts and regions of Zambia. A previously unknown polyomavirus genome was identified in a sample from a multimammate mouse Mastomys species and the entire viral genome of bp was :subsequently sequenced. Results: The combined percentage of positive samples in both districts determined by PCR using the p gene primers was We analyzed the population genetic structure of Theileria parva from a total of 61 samples 33 from Isoka and 28 from Petauke using a panel of 9 microsatellite markers encompassing the 4 chromosomes of Theileria parva. Hang'ombe, Aaron S. These results suggest that rM2ss23 prevents virus release from infected cells and further suggest that the mechanisms underlying the virus budding mediates by HA and M2 proteins might differ between the Aichi and PR8 strains. The purpose of this study was to evaluate the possible roles of the E-disaccharide units GlcA beta Gal-NAc 4,6-O-disulfate of chondroitin sulfate CS , a GAG involved in neuritogenesis and neuronal migration, in Japanese encephalitis virus JEV infection. Ovariohysterectomy was performed, and bilateral segmental aplasia of the uterine horns with the development of unilateral uterine horn torsion was diagnosed histopathologically. Linkage disequilibrium was observed when populations from both districts were treated as a single population. Phylogenetic analysis showed that these virus sequences were related to henipavirus or rubulavirus. Because radiographic and ultrasonographic findings revealed the presence of markedly enlarged bilateral uterine horns filled with fluid in the caudal abdomen, a tentative diagnosis of either pyometra or hydrometra with uterine horn torsion was made. {PARAGRAPH}{INSERTKEYS}Hiroki Yamaguchi, Shintaro Kobayashi, Akihiro Ishii, Hirohito Ogawa, Ichiro Nakamura, Ladslav Moonga, Bernard M.