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[具体藻类名称]藻类提取物对单纯疱疹病毒1型和2型的抗疱疹活性

Anti-herpetic Activity of and Algae Extracts Against HSV-1 and HSV-2.

作者信息

Castillo Estefanía, Duarte Luisa F, Corrales Nicolas, Álvarez Diana M, Farías Mónica A, Henríquez Adolfo, Smith Patricio C, Agurto-Muñoz Cristian, González Pablo A

机构信息

Millennium Institute on Immunology and Immunotherapy, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.

GIBMAR, Grupo Interdisciplinario de Biotecnología Marina, Centro de Biotecnología, Universidad de Concepción, Concepción, Chile.

出版信息

Front Microbiol. 2020 Sep 11;11:2006. doi: 10.3389/fmicb.2020.02006. eCollection 2020.

DOI:10.3389/fmicb.2020.02006
PMID:33013743
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7516053/
Abstract

Herpes simplex viruses (HSVs) type 1 (HSV-1) and type 2 (HSV-2) are highly prevalent in the human population, and the infections they produce are lifelong with frequent reactivations throughout life. Both viruses produce uncomfortable and sometimes painful lesions in the orofacial and genital areas, as well as herpetic gingivostomatitis, among other clinical manifestations. At present, the most common treatments against HSVs consist of nucleoside analogs that target the viral polymerases. However, such drugs are poorly effective for treating skin lesions, as they only reduce in 1-2 days the duration of the herpetic lesions. Additionally, viral isolates resistant to these drugs can emerge in immunosuppressed individuals, and second-line drugs for such variants are frequently accompanied by adverse effects requiring medical supervision. Thus, novel or improved therapeutic drugs for treating HSV lesions are needed. Here, we assessed the potential antiviral activity of aqueous extracts obtained from two brown macroalgae, namely and against HSVs. Both extracts showed antiviral activity against acyclovir-sensitive and acyclovir-resistant HSV-1 and HSV-2. Our analyses show that there is a significant antiviral activity associated with proteins in the extract, although other compounds also seem to contribute to inhibiting the replication cycle of these viruses. Evaluation of the algae extracts as topical formulations in an animal model of HSV-1 skin infection significantly reduced the severity of the disease more than acyclovir, as well as the duration of the herpetic lesions, when compared to mock-treated animals, with the extract performing best. Taken together, these findings suggest that these algae extracts may be potential phytotherapeutics against HSVs and may be useful for the treatment and reduction of common herpetic manifestations in humans.

摘要

1型单纯疱疹病毒(HSV-1)和2型单纯疱疹病毒(HSV-2)在人群中高度流行,它们所引发的感染会伴随终生,且在一生中频繁复发。这两种病毒都会在口面部和生殖器区域产生令人不适甚至有时疼痛的损伤,以及疱疹性龈口炎等其他临床表现。目前,针对HSV的最常见治疗方法是使用靶向病毒聚合酶的核苷类似物。然而,这类药物对治疗皮肤损伤效果不佳,因为它们只能将疱疹损伤的持续时间缩短1 - 2天。此外,免疫抑制个体中可能会出现对这些药物耐药的病毒分离株,而针对此类变异株的二线药物常常伴有需要医疗监管的不良反应。因此,需要用于治疗HSV损伤的新型或改进型治疗药物。在此,我们评估了从两种褐藻(即[具体名称1]和[具体名称2])中提取的水提取物对HSV的潜在抗病毒活性。两种提取物均显示出对阿昔洛韦敏感和耐药的HSV-1及HSV-2具有抗病毒活性。我们的分析表明,提取物中的蛋白质具有显著的抗病毒活性,尽管其他化合物似乎也有助于抑制这些病毒的复制周期。在HSV-1皮肤感染动物模型中,将藻类提取物作为局部制剂进行评估时,与未处理的动物相比,其显著降低了疾病的严重程度,且疱疹损伤的持续时间也短于阿昔洛韦,其中[具体名称1]提取物表现最佳。综上所述,这些发现表明这些藻类提取物可能是针对HSV的潜在植物疗法,可能有助于治疗和减轻人类常见的疱疹表现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5931/7516053/2c6b30b9611a/fmicb-11-02006-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5931/7516053/c8a531f9ea11/fmicb-11-02006-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5931/7516053/d2e7ebda43fb/fmicb-11-02006-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5931/7516053/2d9bb38e55be/fmicb-11-02006-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5931/7516053/eb8bd15d9065/fmicb-11-02006-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5931/7516053/86552d1808fa/fmicb-11-02006-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5931/7516053/3776d4b9344c/fmicb-11-02006-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5931/7516053/ab12d42c1f88/fmicb-11-02006-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5931/7516053/ebd07902472f/fmicb-11-02006-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5931/7516053/2c6b30b9611a/fmicb-11-02006-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5931/7516053/c8a531f9ea11/fmicb-11-02006-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5931/7516053/d2e7ebda43fb/fmicb-11-02006-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5931/7516053/2d9bb38e55be/fmicb-11-02006-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5931/7516053/eb8bd15d9065/fmicb-11-02006-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5931/7516053/86552d1808fa/fmicb-11-02006-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5931/7516053/3776d4b9344c/fmicb-11-02006-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5931/7516053/ab12d42c1f88/fmicb-11-02006-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5931/7516053/ebd07902472f/fmicb-11-02006-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5931/7516053/2c6b30b9611a/fmicb-11-02006-g009.jpg

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