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1.
Chinese Journal of Virology ; (6): 1-6, 2013.
Artigo em Chinês | WPRIM | ID: wpr-339983

RESUMO

During 2009-2012, the Nam Dinh virus (NDiv) was detected from the samples of Culex pipiens quinquefasciatus in Shenzhen China. In this study, cell culture,SYBR Green I based real time RT-PCR and RT-PCR were performed to analyze the cell susceptibility and other biological characteristics of the NDiV isolates. The results showed that C6/36 cell line was susceptible to four isolates of Culex pipiens quinquefasciatus. The "S" type amplification curve and specific melting curve were obtained in the realtime fluorescence quantitative RT-PCR based on SYBR Green I for the detection of the NDiV from the mosquito. The target bands from the RdRp gene and partial fragment of ZmHel1 gene were observed using agarose gel electrophoresis. Both the nucleotide and amino acid sequences of four Shenzhen isolates showed more than 99.00% homology with the Vietnam representative NDiV strain (02VN178). Phylogenetic analysis showed that four Shenzhen isolates shared the same evolution branch as the Vietnam representative NDiV strain. This is the first report of NDiV in China.


Assuntos
Animais , China , Culex , Virologia , Nidovirales , Classificação , Genética , Filogenia
2.
Chinese Journal of Virology ; (6): 368-375, 2009.
Artigo em Chinês | WPRIM | ID: wpr-297946

RESUMO

Recently, much work has been devoted to study MD-induced oncogenesis and the genes involved in this process. Among many genes in the MDV genome, several genes such as Meq, RLORF4, RLORF12, and 132bpr have been considered recently associated with virulence of MDV. In this paper, primers of Meq, RLORF4, RLORF12 and 132bpr genes were designed and synthesized, based on the published whole genome sequence of MDV strain GA. The genes of Meq, RLORF4 and RLORF12 from four Chinese epidemic MDV strains highly passaged on chicken embryo fibroblast (CEF), i. e. L-SYp85C, L-MSp75C, L-CZp75C, and L-ZYp75C, as well as their corresponding parent strains, i. e. L-SY, L-MS, L-CZ, and L-ZY, the reference virulent strain J-1 and the vaccine strain 814 were amplified by PCR respectively. Then the PCR products of interest were cloned and sequenced respectively. The results of sequence comparison and analysis of Meq genes in the study indicated that Meq genes from the two strains L-ZYp75C and L-CZp75C contained single nucleotide insertion and deletion. The Meq gene from strain L-ZYp75C contained an extra cytidine (C) insertion at nucleotide position 529 and a single thymidine (T) deletion at nucleotide position 602, resulting in a frameshift mutation. And this frameshift mutation could lead to changes in deduced amino acid sequence from position 177 to 200 of Meq gene. The extra C insertion at nucleotide position 625 in Meq gene of strain L-CZp75C was also predicted to cause frameshift mutation in three overlapping genes (Meq, RLORF6 and 23KD genes). The comparison of nucleotide sequences of RLORF4 genes in the study revealed that the RLORF4 gene of strain L-SYp85C contained a fragment deletion in Open Reading Frame (ORF) from nucleotide position 215 to 265, resulting in 17 amino acids deletions, which were not found in other sequenced strains. Comparison of nucleotide sequences of RLORF12 genes in the study revealed several mutations. The RLORF12 gene of strain L-MSp75C contained a single T deletion at nucleotide position 67 and of 814 vaccine strain a large fragment deletion from nucleotide position 18 to 86, both of the deletions located in Origin of replication site (Ori) of MDV genome. But strain L-ZYp75C possessed an unique "TGTTGGG" deletion in its RLORF12 gene. When the four Chinese epidemic MDV strains were serially passaged on CEF, the number of copies of the 132bp repeats increased from 2 to more than 10 copies. All of above results indicated that deletion and/or insertion mutation occurred in Meq, RLORF4, RLORF12 and 132bpr after serial passage of these four Chinese epidemic MDV strains on CEF.


Assuntos
Animais , Embrião de Galinha , Sequência de Aminoácidos , Células Cultivadas , Galinhas , Análise Mutacional de DNA , Fibroblastos , Doença de Marek , Genética , Virologia , Dados de Sequência Molecular , Mutação , Fases de Leitura Aberta , Genética , Homologia de Sequência de Aminoácidos , Proteínas Virais , Química , Genética
3.
Chinese Journal of Virology ; (6): 117-125, 2008.
Artigo em Chinês | WPRIM | ID: wpr-334837

RESUMO

Earlier studies have determined that the repeat regions of oncogenic serotype 1 MDV (Marek's disease virus) encode a basic leucine zipper protein, Meq, which structurally resembles the Jun/Fos family of transcriptional activators. Meq has been suggested as the MDV-associated oncogene. In this paper, based on the published sequence of Meq gene of GA strain of MDV, a pair of primers were designed and synthesized. Meq gene ORF (Open reading frame) of the four Chinese local MDV isolates, the reference strain J-1 and the vaccine strain 814 were amplified by using polymerase chain reaction(PCR). Then the PCR products were cloned and sequenced respectively. The results of sequence comparison indicated that the sequences of Meq gene in different strains are relatively conserved and homology of the amino acid sequences is 96.5%-99.7%. The proline-rich repeats of Meq gene of four MDV isolates have site mutations, and it is related to MDV's virulence. Two unique site mutations appear in Meq gene of Chinese local MDV isolates, but they aren't present in Meq gene of the published MDV strains from abroad and the early domestic strains. It seems that some regularities exist between such mutations in four Chinese local MDV isolates and the virulence of MDV, but the regularities need further research.


Assuntos
Animais , Sequência de Aminoácidos , Sequência de Bases , Galinhas , Clonagem Molecular , Herpesvirus Galináceo 2 , Genética , Dados de Sequência Molecular , Mutação , Proteínas Oncogênicas Virais , Genética
4.
Journal of Korean Neuropsychiatric Association ; : 219-228, 2004.
Artigo em Coreano | WPRIM | ID: wpr-13403

RESUMO

OBJECTIVES: This study was to investigate the mental health status and quality of life of Korean-Chinese workers, who are residing illegally in Korea. METHODS: Total 147 illegal status Korean-Chinese workers completed to the questionnaire for demographic data, Korean version of Symptom Check List-90-Revision (SCL-90-R) and Korean version of World Health Organization Quality of Life Scale (WHOQOL-BREF). RESULTS: The results of this study showed that general mental health was relatively poor and the quality of life was relatively poorer among Korean-Chinese. Mental health and quality of life were worse among those who accompanied spouses, had no religion, had less income, and those who experienced unjust treatments such as delayed payment, violence and industrial accidents. There were significant correlations between scores of all categories of SCL-90-R and scores of domains of physical health, social relationship and environment in WHOQOL-BREF. CONCLUSION: These results suggest that Korean-Chinese laborers in illegal status in Korea need improved treatment neleved from delayed payment, social violence and industrial accidents and with extended medical service and better residential environment.


Assuntos
Humanos , Acidentes de Trabalho , Coreia (Geográfico) , Saúde Mental , Qualidade de Vida , Inquéritos e Questionários , Cônjuges , Violência , Organização Mundial da Saúde
5.
Microbiology ; (12)1992.
Artigo em Chinês | WPRIM | ID: wpr-685881

RESUMO

Three-dimensional structure model of azoreductase AZR of Rhodobacter sphaeroides was con- structed using homology modeling method. It is a flavodoxin adopting ?/? structure. Structure alignment of two different types of flavin-dependent azoreductases revealed that they possessed high similarity. Based on sequence and structure analysis, site-directed mutagenesis of K109H and K109A were performed. The opti- mal pH values are pH 6 and pH 9 for K109H and K109A mutant protein, respectively. The optimal tempera- ture (30℃) is not affected by mutagenesis. Positively charged residues at position 109 is necessary for the binding of methyl red, while K109H is not a conserved mutagenesis for the binding of NADPH. K109 may only be involved in the binding of the 2’-phosphate group of NADPH and have no effect on the binding of NADH.

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