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1.
Virus Genes ; 52(4): 484-94, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27059239

ABSTRACT

G protein-coupled receptors (GPCRs) are known as seven transmembrane domain receptors and consequently can mediate diverse biological functions via regulation of their subcellular localization. Crucian carp herpesvirus (CaHV) was recently isolated from infected fish with acute gill hemorrhage. CaHV GPCR of 349 amino acids (aa) was identified based on amino acid identity. A series of variants with truncation/deletion/substitution mutation in the C-terminal (aa 315-349) were constructed and expressed in fathead minnow (FHM) cells. The roles of three key C-terminal regions in subcellular localization of CaHV GPCR were determined. Lysine-315 (K-315) directed the aggregation of the protein preferentially at the nuclear side. Predicted N-myristoylation site (GGGWTR, aa 335-340) was responsible for punctate distribution in periplasm or throughout the cytoplasm. Predicted phosphorylation site (SSR, aa 327-329) and GGGWTR together determined the punctate distribution in cytoplasm. Detection of organelles localization by specific markers showed that the protein retaining K-315 colocalized with the Golgi apparatus. These experiments provided first evidence that different mutations of CaHV GPCR C-terminals have different affects on the subcellular localization of fish herpesvirus-encoded GPCRs. The study provided valuable information and new insights into the precise interactions between herpesvirus and fish cells, and could also provide useful targets for antiviral agents in aquaculture.


Subject(s)
Carps/virology , Herpesviridae/genetics , Mutation/genetics , Receptors, G-Protein-Coupled/genetics , Viral Proteins/genetics , Amino Acid Sequence , Animals , Base Sequence , Cytoplasm/virology , Fish Diseases/virology , Golgi Apparatus/virology , Herpesviridae Infections/virology
2.
Arch Virol ; 160(1): 365-9, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25287130

ABSTRACT

The complete genome sequence of a novel duck orthoreovirus, designated DRV strain TH11(DRV-TH11), was determined and characterized. The DRV-TH11 genome is comprised of 23,417 bp and its genome organization is more similar to that of avian orthoreoviruses (ARVs) of chicken origin than other reoviruses. The results of comparative sequence analysis and dendrograms based on the µB- and σC-encoding genes indicated that TH11 may be derived from the reassortment of ARVs and classic Muscovy duck reovirus (MDRV). A possible recombinant event was identified using the SimPlot program, and it occurred in the M2 segment. The results indicated that reassortment and mutation play a role in the evolution of duck reovirus.


Subject(s)
Ducks , Orthoreovirus, Avian/isolation & purification , Poultry Diseases/virology , Reoviridae Infections/veterinary , Animals , China/epidemiology , Orthoreovirus, Avian/genetics , Phylogeny , Poultry Diseases/epidemiology , Reoviridae Infections/epidemiology , Reoviridae Infections/virology
3.
Bing Du Xue Bao ; 30(4): 463-9, 2014 Jul.
Article in Chinese | MEDLINE | ID: mdl-25272604

ABSTRACT

Both sides of the picornavirus genome have 5'-untranslated region (5'UTR) and 3'- untranslated region (3'UTR). This study demontrated that both the 5'-and 3'-UTR can form complex structures, such as stem-loop, clover and pseudoknot structure, These structures play an important role in the regulaton of the replication and translation of the viruses. This article reviewed the progress of research on the structure and function of picornavirus' 3'-UTR over recent years.


Subject(s)
3' Untranslated Regions , Picornaviridae Infections/virology , Picornaviridae/chemistry , RNA, Viral/chemistry , RNA, Viral/metabolism , Animals , Humans , Nucleic Acid Conformation , Picornaviridae/genetics , Picornaviridae/metabolism , RNA, Viral/genetics
4.
Avian Pathol ; 38(2): 129-34, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19322711

ABSTRACT

In order to define clearly the conditions leading to the outcome of acute duck hepatitis B virus (DHBV) infection, 1-day-old Pekin ducklings were infected with DHBV by different routes and given different doses of inoculum. Groups of 24 ducklings were inoculated either intravenously via the vena cruralis, or intraperitoneally with pooled serum containing either 1.6 x 10(7) or 1.6 x 10(4) DHBV genomes. One control duck from each group was inoculated with an equal volume of normal duck serum. A sensitive and reproducible real-time polymerase chain reaction assay based on TaqMan technology was developed for the detection and quantitation of DHBV DNA in the serum and liver. DHBAg was observed in the hepatocytes by immunohistochemistry. Histological changes in the liver tissue were also observed. The results demonstrate that ducklings at each time point and in all groups developed detectable viraemia. In each group, DHBV DNA in the liver was at a lower level than in serum and the peak DNA titre was found in serum earlier than in the liver. In the low-dose groups it was always at a lower level than in the high-dose groups. The DHBV replication levels appeared to be directly related to the number of DHBAg-positive hepatocytes. The variation trends of DHBAg-positive hepatocytes were similar in the high-dose groups. Histological changes were associated with liver viral DNA levels. We suggest that this dose and route of inoculation can be used as a model to study acute DHBV infections.


Subject(s)
Hepatitis B Virus, Duck/isolation & purification , Hepatitis B/veterinary , Hepatitis, Viral, Animal/pathology , Poultry Diseases/virology , Viral Load , Animals , DNA Primers , DNA, Viral/blood , DNA, Viral/isolation & purification , Ducks , Gene Amplification , Genome, Viral , Hepatitis B/pathology , Hepatitis B/virology , Hepatitis B Virus, Duck/genetics , Hepatitis, Viral, Animal/genetics , Hepatitis, Viral, Animal/virology , Hepatocytes/virology , Liver/pathology , Liver/virology , Viremia/blood , Viremia/veterinary
5.
ACS Appl Mater Interfaces ; 1(7): 1525-32, 2009 Jul.
Article in English | MEDLINE | ID: mdl-20355956

ABSTRACT

We have used a very large scale integration process to generate well-defined patterns of polymerized 2-hydroxyethyl methacrylate (HEMA) on patterned Si(100) surfaces. An atom transfer radical polymerization initiator covalently bonded to the patterned surface was employed for the graft polymerization of HEMA to prepare the poly(2-hydroxyethyl methacrylate) (PHEMA) brushes. After immersing wafers presenting lines of these polymers in water and cyclohexane, we observed brush- and mushroom-like regions, respectively, for the PHEMA brushes, with various pattern resolutions. The PHEMA brushes behaved as "tentacles" that captured ferritin complexes from aqueous solution through entanglement between the brushes and the ferritin proteins, whose ferritins were trapped due to the collapsing of the PHEMA. Using high-resolution scanning electron microscopy, we observed patterned ferritin iron cores on the Si surface after thermal removal of the patterned PHEMA brushes and ferritin protein sheaths.


Subject(s)
Ferritins/chemistry , Methacrylates/chemistry , Silicon/chemistry , Water/chemistry , Adsorption , Cyclohexanes/chemistry , Microscopy, Electron, Scanning/methods , Models, Chemical , Proteins/chemistry , Solvents/chemistry , Surface Properties , Time Factors
6.
Acta Pharmacol Sin ; 28(10): 1652-8, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17883953

ABSTRACT

AIM: To study the efficacy of antiviral treatment with PNA for the duck model of HBV (DHBV)-infected ducks. PNA is a 2-amine-9-(2,3-dideoxy-2,3-dihydro-beta-D-arabinofuranosyl)-6-methoxy-9H-purine. METHODS: The Sichuan Mallard ducklings in the hepatitis B virus model were treated with PNA, a new antiviral agent. DHBV DNA from the blood serum and liver tissues were measured at 0, 5, and 10 d during the treatment and at 3 d withdrawal by real-time PCR. The duck hepatitis B surface antigen (DHBsAg) in the liver cells was observed by Immunohistochemistry (IHC). Pathological changes in the liver tissues were also observed. Control group I was administered with distilled water and control group II was administered with 3-thiacytidine. Treatment group I was administered with PNA at a dose of 40 mg/kg and treatment group II was administered perorally (po) with PNA at a dose of 80 mg/kg. Treatment group III was administered with PNA at a dose of 20 mg/kg and treatment group IV was intravenously administered with PNA at a dose of 40 mg/kg. Each group contained 15 ducklings. RESULTS: PNA can significantly lower the DHBV replication levels in serum and liver. Compared with control group II, there were no significant differences in inhibiting efficacy in treatment groups I and III (P>0.05) and there were significant differences in inhibiting efficacy in treatment groups II and IV (P<0.05). Interestingly, significant differences were observed at 3 d withdrawal. The DHBV replication levels in each group slightly increased at 3 d withdrawal, but rebounded slightly in the PNA treatment groups than in control group II (P<0.05). The DHBV replication levels in the treatment groups were lower than in control group I. The DHBV replication levels in sera had a positive relationship with that in the liver, but the DHBV replication levels in the liver was lower than that in sera. Pathological changes in the treatment groups were obviously improved and the changes were associated with liver viral DNA levels. CONCLUSION: The results demonstrate that PNA is a strong inhibitor of DHBV replication in the DHBV-infected duck model.


Subject(s)
Antiviral Agents/pharmacology , Hepadnaviridae Infections/prevention & control , Hepatitis B Virus, Duck/drug effects , Hepatitis, Viral, Animal/prevention & control , Purine Nucleosides/pharmacology , Animals , Antigens, Viral/blood , Antigens, Viral/metabolism , Antiviral Agents/administration & dosage , DNA, Viral/blood , DNA, Viral/metabolism , Disease Models, Animal , Ducks , Hepadnaviridae Infections/pathology , Hepadnaviridae Infections/virology , Hepatitis B Virus, Duck/genetics , Hepatitis B Virus, Duck/immunology , Hepatitis, Viral, Animal/pathology , Hepatitis, Viral, Animal/virology , Immunohistochemistry , Liver/drug effects , Liver/pathology , Liver/virology , Purine Nucleosides/administration & dosage , Virus Replication/drug effects
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