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1.
Arch Virol ; 169(9): 174, 2024 Aug 06.
Artigo em Inglês | MEDLINE | ID: mdl-39107506

RESUMO

In this study, a novel mitovirus, tentatively designated as "Alternaria alternata mitovirus 2" (AaMV2), was isolated from the fungus Alternaria alternata f. sp. mali causing apple leaf blotch disease. The complete genome of AaMV2 is 3,157 nucleotides in length, with an A+U content of 68.10%. The genome has a single large open reading frame (ORF) encoding an RNA-dependent RNA polymerase (RdRp) protein with a molecular mass of 98.10 kDa. BLAST analysis revealed that AaMV2 has the highest sequence identity to Leptosphaeria biglobosa mitovirus 6, with 79.76% and 82.86% identity at the amino acid and nucleotide level, respectively. Phylogenetic analysis suggested that AaMV2 is a new member of the genus Duamitovirus within the family Mitoviridae. This is the first report of the complete genome sequence analysis of a mitovirus in A. alternata.


Assuntos
Alternaria , Micovírus , Genoma Viral , Malus , Fases de Leitura Aberta , Filogenia , Doenças das Plantas , Vírus de RNA , Sequenciamento Completo do Genoma , Alternaria/virologia , Alternaria/genética , Doenças das Plantas/microbiologia , Malus/microbiologia , Malus/virologia , Micovírus/genética , Micovírus/isolamento & purificação , Micovírus/classificação , Vírus de RNA/genética , Vírus de RNA/isolamento & purificação , Proteínas Virais/genética , RNA Viral/genética , RNA Polimerase Dependente de RNA/genética , Composição de Bases , Folhas de Planta/microbiologia , Folhas de Planta/virologia , Sequência de Bases
2.
Front Microbiol ; 15: 1409677, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38846572

RESUMO

Mycoviruses have been found in various fungal species across different taxonomic groups, while no viruses have been reported yet in the fungus Exserohilum rostratum. In this study, a novel orfanplasmovirus, namely Exserohilum rostratum orfanplasmovirus 1 (ErOrfV1), was identified in the Exserohilum rostratum strain JZ1 from maize leaf. The complete genome of ErOrfV1 consists of two positive single-stranded RNA segments, encoding an RNA-dependent RNA polymerase and a hypothetical protein with unknown function, respectively. Phylogenetic analysis revealed that ErOrfV1 clusters with other orfanplasmoviruses, forming a distinct phyletic clade. A new family, Orfanplasmoviridae, is proposed to encompass this newly discovered ErOrfV1 and its associated orfanplasmoviruses. ErOrfV1 exhibits effective vertical transmission through conidia, as evidenced by its 100% presence in over 200 single conidium isolates. Moreover, it can be horizontally transmitted to Exserohilum turcicum. Additionally, the infection of ErOrfV1 is cryptic in E. turcicum because there were no significant differences in mycelial growth rate and colony morphology between ErOrfV1-infected and ErOrfV1-free strains. This study represents the inaugural report of a mycovirus in E. rostratum, as well as the first documentation of the biological and transmission characteristics of orfanplasmovirus. These discoveries significantly contribute to our understanding of orfanplasmovirus.

3.
Zhonghua Nan Ke Xue ; 15(7): 617-20, 2009 Jul.
Artigo em Chinês | MEDLINE | ID: mdl-19694375

RESUMO

OBJECTIVE: To investigate the effect of the mammalian target of rapamycin (mTOR) inhibitor CCI-779 on the chemosensitivity of androgen-independent prostate cancer cell line PC-3. METHODS: Prostate cancer cells PC-3 were cultured and treated with CCI-779, Paclitaxel and combination of the two. Then the inhibitory effects of the three medications on the growth of the PC-3 cells were determined by MTT, and the their cell cycle and apoptosis were detected by flow cytometry. RESULTS: Compared with the control group, the three medications all significantly inhibited the proliferation of the PC-3 cells, and the combined method even enhanced the effect. Flow cytometry showed that CCI-779 and Paclitaxel blocked the cell cycle mainly in the G1/G2 stage, while the combined medication mainly in the G0/G1 stage. Significantly increased apoptosis of the PC-3 cells was observed in the three medication groups as compared with the control group (P < 0.01). CONCLUSION: CCI-779 can inhibit the proliferation of PC-3 cells and enhance the chemosensitivity of prostate cancer.


Assuntos
Antineoplásicos/farmacologia , Inibidores de Proteínas Quinases/farmacologia , Sirolimo/análogos & derivados , Sirolimo/antagonistas & inibidores , Ciclo Celular/efeitos dos fármacos , Linhagem Celular Tumoral , Quimioterapia Combinada , Humanos , Masculino , Paclitaxel/farmacologia , Neoplasias da Próstata/tratamento farmacológico , Sirolimo/farmacologia
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