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低剂量生物除草剂有利于朊病毒在体内聚集和繁殖。

Low doses of bioherbicide favour prion aggregation and propagation in vivo.

机构信息

MMDN, University Montpellier, EPHE, INSERM, U1198- EiAlz team, PSL Research University, Montpellier, F-34095, France.

Ann Romney Center for Neurologic Diseases, Brigham and Women's hospital, Harvard Medical School, Boston, MA, USA.

出版信息

Sci Rep. 2018 May 23;8(1):8023. doi: 10.1038/s41598-018-25966-9.

DOI:10.1038/s41598-018-25966-9
PMID:29795181
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5966510/
Abstract

Public concerns over the use of synthetic pesticides are growing since many studies have shown their impact on human health. A new environmental movement in occidental countries promoting an organic agriculture favours the rebirth of botanical pesticides. These products confer an effective alternative to chemical pesticides such as glyphosate. Among the biopesticides, the α-terthienyls found in the roots of Tagetes species, are powerful broad-spectrum pesticides. We found that an α-terthienyl analogue with herbicidal properties, called A6, triggers resistant SDS oligomers of the pathogenic prion protein PrP (rSDS-PrP) in cells. Our main question is to determine if we can induce those rSDS-PrP oligomers in vitro and in vivo, and their impact on prion aggregation and propagation. Using wild-type mice challenged with prions, we showed that A6 accelerates or slows down prion disease depending on the concentration used. At 5 mg/kg, A6 is worsening the pathology with a faster accumulation of PrP, reminiscent to soluble toxic rSDS-PrP oligomers. In contrast, at 10 and 20 mg/kg of A6, prion disease occurred later, with less PrP deposits and with rSDS-PrP oligomers in the brain reminiscent to non-toxic aggregates. Our results are bringing new openings regarding the impact of biopesticides in prion and prion-like diseases.

摘要

公众对合成农药使用的担忧日益增加,因为许多研究表明它们会对人类健康造成影响。西方国家兴起的一场新的环保运动提倡有机农业,这有利于植物性农药的复兴。这些产品为化学农药(如草甘膦)提供了有效的替代品。在生物农药中,在万寿菊属植物根部发现的α-噻吩基是一种强大的广谱杀虫剂。我们发现一种具有除草特性的α-噻吩基类似物 A6,可在细胞中引发致病性朊病毒蛋白 PrP(rSDS-PrP)的抗性 SDS 低聚物。我们的主要问题是确定我们是否可以在体外和体内诱导这些 rSDS-PrP 低聚物,以及它们对朊病毒聚集和传播的影响。使用受到朊病毒挑战的野生型小鼠,我们表明 A6 可以根据使用的浓度加速或减缓朊病毒疾病的发展。在 5mg/kg 时,A6 通过更快地积累 PrP 使病理学恶化,这与可溶性有毒 rSDS-PrP 低聚物相似。相比之下,在 A6 的 10 和 20mg/kg 时,朊病毒疾病发生得更晚,大脑中的 PrP 沉积物更少,并且存在 rSDS-PrP 低聚物,这与非毒性聚集物相似。我们的研究结果为生物农药在朊病毒和朊病毒样疾病中的影响带来了新的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/813d/5966510/7ab0652e53cf/41598_2018_25966_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/813d/5966510/a8da6e9490e5/41598_2018_25966_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/813d/5966510/28a2b81bfdb4/41598_2018_25966_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/813d/5966510/d28eed1fb5e8/41598_2018_25966_Fig3_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/813d/5966510/8b90089cd8b7/41598_2018_25966_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/813d/5966510/66b517506ff1/41598_2018_25966_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/813d/5966510/7ab0652e53cf/41598_2018_25966_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/813d/5966510/a8da6e9490e5/41598_2018_25966_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/813d/5966510/28a2b81bfdb4/41598_2018_25966_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/813d/5966510/d28eed1fb5e8/41598_2018_25966_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/813d/5966510/8638c857a6b1/41598_2018_25966_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/813d/5966510/8b90089cd8b7/41598_2018_25966_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/813d/5966510/66b517506ff1/41598_2018_25966_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/813d/5966510/7ab0652e53cf/41598_2018_25966_Fig7_HTML.jpg

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