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1.
J Vet Sci ; 18(3): 317-326, 2017 Sep 30.
Artigo em Inglês | MEDLINE | ID: mdl-28057901

RESUMO

Porcine reproductive and respiratory syndrome virus (PRRSV) has a high degree of genetic variation. In this study, we characterized the genetic variation and evolutionary relationships among circulating PRRSV strains in southern China. We analyzed 29 NSP2 strains and 150 ORF5 strains from clinical samples collected in southern China during 2007-2014. The alignment results showed that the nucleotide identity similarities of the two genes among these strains were 80.5%-99.7% and 80.9%-100%, respectively. Phylogenetic analysis based on the NSP2 gene showed that highly pathogenic (HP)-PRRSV was still the dominant virus in southern China from 2013 to 2014. Compared with reference strains CH-1a and VR-2332, the field strain 131101-GD-SHC, which shared high homology with JXA1-P170, had a novel 12 amino acid deletion at position 499-510. Phylogenetic analysis based on the ORF5 gene showed that HP-PRRSV, VR2332-like strains, and QYYZ-like strains were simultaneously circulating in southern China from 2007 to 2014, suggesting that, in recent years, the type 2 PRRSV was more diverse in southern China. In conclusion, mutations in the decoy epitope and primary neutralizing epitope could be markers of viral evolution and used to study evolutionary relationships among PRRSV strains in China.


Assuntos
Variação Genética/genética , Vírus da Síndrome Respiratória e Reprodutiva Suína/genética , Animais , China/epidemiologia , Filogenia , Reação em Cadeia da Polimerase/veterinária , Síndrome Respiratória e Reprodutiva Suína/epidemiologia , Síndrome Respiratória e Reprodutiva Suína/virologia , Alinhamento de Sequência/veterinária , Análise de Sequência de DNA/veterinária , Análise de Sequência de Proteína/veterinária , Suínos
2.
J Vet Sci ; 18(2): 237-243, 2017 Jun 30.
Artigo em Inglês | MEDLINE | ID: mdl-27515262

RESUMO

The spike gene of porcine epidemic diarrhea virus (PEDV) was sequenced from 55 South China field strains isolated from pigs with symptoms of diarrhea. The sequences were compared within the set of field strains as well as with reference strains available in GenBank. Within the 55 South China PEDV field strains, the deduced amino acid sequence identities ranged from 93.8% to 99.9 % and ranged from 90.7% to 99.5% when compared with the foreign reference strains in GenBank. Our phylogenetic analysis showed that 10 of the 55 South China PEDV strains belonged to G1b and 45 belonged to G2b.


Assuntos
Infecções por Coronavirus/veterinária , Genes Virais/genética , Vírus da Diarreia Epidêmica Suína/genética , Doenças dos Suínos/microbiologia , Sequência de Aminoácidos/genética , Animais , China/epidemiologia , Infecções por Coronavirus/virologia , Glicosilação , Filogenia , Alinhamento de Sequência/veterinária , Suínos
3.
J Vet Sci ; 17(3): 369-75, 2016 Sep 30.
Artigo em Inglês | MEDLINE | ID: mdl-26726029

RESUMO

Outbreaks of pseudorabies (PR) have occurred in southern China since late 2011, resulting in significant economic impacts on the swine industry. To identify the cause of PR outbreaks, especially among vaccinated pigs, 11 pseudorabies virus (PRV) field strains were isolated from Guangdong province during 2013-2014. Their major viral genes (gE, TK, gI, PK, gD, 11K, and 28K) were analyzed in this study. Insertions or deletions were observed in gD, gE, gI and PK genes compared with other PRV isolates from all over the world. Furthermore, sequence alignment showed that insertions in gD and gE were unique molecular characteristics of the new prevalent PRV strains in China. Phylogenetic analysis showed that our isolates were clustered in an independent branch together with other strains isolated from China in recent years, and that they showed a closer genetic relationship with earlier isolates from Asia. Our results suggest that these isolates are novel PRV variants with unique molecular signatures.


Assuntos
Surtos de Doenças/veterinária , Herpesvirus Suídeo 1/fisiologia , Pseudorraiva/epidemiologia , Doenças dos Suínos/epidemiologia , Proteínas Virais/genética , Animais , Sequência de Bases , China/epidemiologia , Herpesvirus Suídeo 1/classificação , Herpesvirus Suídeo 1/genética , Filogenia , Pseudorraiva/virologia , Alinhamento de Sequência/veterinária , Suínos , Doenças dos Suínos/virologia , Proteínas Virais/metabolismo
4.
Zhong Xi Yi Jie He Xue Bao ; 4(4): 388-91, 2006 Jul.
Artigo em Chinês | MEDLINE | ID: mdl-16834977

RESUMO

OBJECTIVE: To observe the effects of matrine on proliferation and apoptosis of human renal cell carcinoma cell line GRC-1 in vitro, and to explore its mechanism. METHODS: The human renal cell carcinoma cell line GRC-1 was treated with matrine of different concentrations for 24, 48, 72 and 96 h respectively. The MTT assay was used to evaluate the cytotoxic effects of matrine on GRC-1 cells. The transmission electron microscope and flow cytometry were utilized to observe and detect the apoptosis of GRC-1 cells induced by matrine. The expression levels of Bcl-2 and Bax proteins were evaluated by streptavidin-biotin-peroxidase method. RESULTS: The matrine of different concentrations all have cytotoxic effects on GRC-1 cells, with obvious dose- and time-dependent effects. The apoptosis induced by matrine was confirmed in GRC-1 cells. With intervention of matrine (1.5 g/L) for 12 h, the expression level of Bcl-2 in GRC-1 cells was decreased while the expression level of Bax was increased as compared with those in the untreated group. CONCLUSION: The proliferation-inhibiting effects of matrine on human renal cell carcinoma cell line GRC-1 may be related to down-regulating the ratio of Bcl-2/Bax protein expression and promoting the apoptosis.


Assuntos
Alcaloides/farmacologia , Antineoplásicos Fitogênicos/farmacologia , Carcinoma de Células Renais/tratamento farmacológico , Neoplasias Renais/tratamento farmacológico , Quinolizinas/farmacologia , Apoptose/efeitos dos fármacos , Linhagem Celular Tumoral , Proliferação de Células/efeitos dos fármacos , Regulação para Baixo/efeitos dos fármacos , Humanos , Proteínas Proto-Oncogênicas c-bcl-2 , Proteína X Associada a bcl-2 , Matrinas
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