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KSF103 甲醇提取物抗登革病毒 2 型的抗病毒活性。

Antiviral Activities of KSF 103 Methanolic Extracts against Dengue Virus Type-2.

机构信息

Institute of Biological Sciences, Faculty of Science, Universiti Malaya, Kuala Lumpur 50603, Wilayah Persekutuan Kuala Lumpur, Malaysia.

Tropical Infectious Diseases Research and Education Centre (TIDREC), Universiti Malaya, Level 2, High Impact Research (HIR) Building, Kuala Lumpur 50603, Wilayah Persekutuan Kuala Lumpur, Malaysia.

出版信息

Viruses. 2023 Aug 20;15(8):1773. doi: 10.3390/v15081773.

DOI:10.3390/v15081773
PMID:37632115
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10459629/
Abstract

Dengue has long been a serious health burden to the global community, especially for those living in the tropics. Despite the availability of vaccines, effective treatment for the infection is still needed and currently remains absent. In the present study, the antiviral properties of the sp. KSF 103 methanolic extract ( KSF 103 ME), which consists of a number of potential antiviral compounds, were investigated against dengue virus serotype 2 (DENV-2). The effects of this extract against DENV-2 replication were determined using the quantitative Real Time-Polymerase Chain Reaction (qRT-PCR). Findings from the study suggested that the KSF 103 ME showed maximum inhibitory properties toward the virus during the virus entry stage at concentrations of more than 12.5 µg/mL. Minimal antiviral activities were observed at other virus replication stages; adsorption (42% reduction at 50 µg/mL), post-adsorption (67.6% reduction at 50 µg/mL), prophylactic treatment (68.4% and 87.7% reductions at 50 µg/mL and 25 µg/mL, respectively), and direct virucidal assay (48% and 56.8% reductions at 50 µg/mL and 25 µg/mL, respectively). The KSF 103 ME inhibited dengue virus replication with a 50% inhibitory concentration (IC) value of 20.3 µg/mL and an International System of Units (SI) value of 38.9. The KSF 103 ME showed potent antiviral properties against dengue virus (DENV) during the entry stage. Further studies will be needed to deduce the antiviral mechanisms of the KSF 103 ME against DENV.

摘要

登革热长期以来一直是全球社区的严重健康负担,尤其是对生活在热带地区的人来说。尽管有疫苗可用,但仍需要有效的治疗方法,而目前这种方法仍然不存在。在本研究中,研究了由多种潜在抗病毒化合物组成的 sp. KSF 103 甲醇提取物 (KSF 103 ME) 对登革热病毒血清型 2 (DENV-2) 的抗病毒特性。使用定量实时聚合酶链反应 (qRT-PCR) 测定了该提取物对 DENV-2 复制的影响。研究结果表明,在病毒进入阶段,KSF 103 ME 在浓度高于 12.5 µg/mL 时对病毒表现出最大的抑制特性。在其他病毒复制阶段观察到最小的抗病毒活性;吸附(50 µg/mL 时减少 42%)、吸附后(50 µg/mL 时减少 67.6%)、预防治疗(50 µg/mL 和 25 µg/mL 时分别减少 68.4%和 87.7%)和直接病毒杀灭测定(50 µg/mL 和 25 µg/mL 时分别减少 48%和 56.8%)。KSF 103 ME 抑制登革热病毒复制的 50%抑制浓度 (IC) 值为 20.3 µg/mL,国际单位制 (SI) 值为 38.9。KSF 103 ME 在进入阶段对登革热病毒 (DENV) 表现出强大的抗病毒特性。需要进一步研究来推断 KSF 103 ME 对 DENV 的抗病毒机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/affa/10459629/cb5d4c7bfd57/viruses-15-01773-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/affa/10459629/bf74de9d9081/viruses-15-01773-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/affa/10459629/246fdb9ebbd4/viruses-15-01773-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/affa/10459629/16186fb83f13/viruses-15-01773-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/affa/10459629/2ae7a23e05cc/viruses-15-01773-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/affa/10459629/80b5e9eb0c97/viruses-15-01773-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/affa/10459629/cb5d4c7bfd57/viruses-15-01773-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/affa/10459629/bf74de9d9081/viruses-15-01773-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/affa/10459629/246fdb9ebbd4/viruses-15-01773-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/affa/10459629/16186fb83f13/viruses-15-01773-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/affa/10459629/4a93b6905bd0/viruses-15-01773-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/affa/10459629/2ae7a23e05cc/viruses-15-01773-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/affa/10459629/80b5e9eb0c97/viruses-15-01773-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/affa/10459629/cb5d4c7bfd57/viruses-15-01773-g007.jpg

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本文引用的文献

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Insecticidal activities of Streptomyces sp. KSF103 ethyl acetate extract against medically important mosquitoes and non-target organisms.
KSF103 链霉菌乙酸乙酯提取物对医学重要蚊虫和非靶标生物的杀虫活性。
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Potential Role of Flavivirus NS2B-NS3 Proteases in Viral Pathogenesis and Anti-flavivirus Drug Discovery Employing Animal Cells and Models: A Review.黄病毒 NS2B-NS3 蛋白酶在病毒发病机制和利用动物细胞及模型的抗黄病毒药物研发中的潜在作用:综述。
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