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首页> 外文期刊>Shahid Beheshti University of Medical Sciences >Enrichment of Acanthamoeba Culture Medium Using TYIS 33 Medium: a Step toward a Successful Axenic Cultivation
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Enrichment of Acanthamoeba Culture Medium Using TYIS 33 Medium: a Step toward a Successful Axenic Cultivation

机译:使用TYIS 33培养基富集棘阿米巴培养基:迈向成功的无菌培养的一步

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Background: Acanthamoeba-related disease have a poor prognosis according to many previous studies. Thus researches regarding biochemical and molecular aspects of this organism are a high priority. To this end achieving high amount of amoebae in culture is the first step for such studies. The main aim of the present research was to address the usage of TYI-S-33 (Tripticase, Yeast extract, iron-serum) medium as an enrichment component for achieving high and fast growth of trophozoites in agar culture medium within 24 hours. M aterials and Methods: Overall, 10 Acanthamoeba strains were cultured, cloned and genotyped and the cultures were then enriched with addition of TYI-S-33 medium. Amoebae growth was then monitored daily. Ten plates also were used without addition of TYI-S-33 medium. R es ults: The result of the present research revealed that addition of TYI-S-33 medium is a promising approach for obtaining 100% trophozoites within 24 hours of culture. Conclusion: To the best of our knowledge this is the first report of successful achieving high amount of trophozoites within short time that able researchers to arrange molecular and biochemical assays
机译:背景:根据许多先前的研究,棘阿米巴相关疾病的预后较差。因此,关于该生物的生化和分子方面的研究是高度优先的。为此,在培养中获得大量的变形虫是此类研究的第一步。本研究的主要目的是解决使用TYI-S-33(海藻糖酶,酵母提取物,铁-血清)培养基作为富集成分的问题,以便在琼脂培养基中24小时内实现滋养体的快速快速生长。材料与方法:总体上,培养,克隆和基因分型了10种棘阿米巴菌株,然后通过添加TYI-S-33培养基富集培养物。然后每天监测变形虫的生长。在不添加TYI-S-33培养基的情况下也使用了十个板。结果:本研究的结果表明,添加TYI-S-33培养基是在培养24小时内获得100%滋养体的有前途的方法。结论:据我们所知,这是首次在短时间内成功获得大量滋养体的报告,这使研究人员能够进行分子和生化分析

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