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一种基于四氮唑盐XTT的用于检测曼氏血吸虫活力的高通量比色测定法。

A high-throughput colorimetric assay for detection of Schistosoma mansoni viability based on the tetrazolium salt XTT.

作者信息

Aguiar Pedro Henrique Nascimento, Fernandes Núbia Monteiro Gonçalves Soares, Zani Carlos Leomar, Mourão Marina Moraes

机构信息

Laboratório de Helmintologia e Malacologia Médica, René Rachou Research Center, FIOCRUZ, Belo Horizonte, Minas Gerais, Brazil.

Laboratório de Química dos Produtos Naturais, René Rachou Research Center, FIOCRUZ, Belo Horizonte, Minas Gerais, Brazil.

出版信息

Parasit Vectors. 2017 Jun 21;10(1):300. doi: 10.1186/s13071-017-2240-3.

Abstract

BACKGROUND

Schistosoma mansoni is a trematode parasite that causes schistosomiasis, one of the most prevalent neglected tropical diseases, leading to the loss of 2.6 million disability-adjusted life years. Praziquantel is the only drug available, and new drugs are required. The most common strategy in schistosomiasis drug discovery is the use of the schistosomula larval-stage for a pre-screen in drug sensitivity assays. However, assessing schistosomula viability by microscopy has always been a limitation to the throughput of such assays. Hence, the development of validated, robust high-throughput in vitro assays for Schistosoma with simple readouts is needed. Here, we present a simple and affordable alternative to assess schistosomula viability. The method employed is based on the hydrosoluble tetrazolium salt XTT which has been widely used in other organisms but has never been used to drug screen in schistosomes.

RESULTS

We showed that schistosomula reduce XTT salt to a coloured formazan product and that absorbance levels reflected the viability and parasites number. This XTT viability assay was validated for high throughput screening of compounds in schistosomula, and dose-response curves of compounds could be reproduced.

CONCLUSIONS

We conclude that the XTT viability assay could be applied for the screening of large compounds collections in S. mansoni and accelerate the identification of novel antischistosomal compounds.

摘要

背景

曼氏血吸虫是一种吸虫寄生虫,可导致血吸虫病,这是最普遍的被忽视的热带疾病之一,导致260万个伤残调整生命年的损失。吡喹酮是唯一可用的药物,因此需要新药。血吸虫病药物发现中最常见的策略是在药物敏感性试验中使用血吸虫幼虫期进行预筛选。然而,通过显微镜评估血吸虫幼虫的活力一直是此类试验通量的限制因素。因此,需要开发经过验证的、强大的高通量体外血吸虫检测方法,并具有简单的读数。在此,我们提出一种简单且经济实惠的方法来评估血吸虫幼虫的活力。所采用的方法基于水溶性四唑盐XTT,该盐已在其他生物体中广泛使用,但从未用于血吸虫的药物筛选。

结果

我们发现血吸虫幼虫可将XTT盐还原为有色的甲臜产物,吸光度水平反映了活力和寄生虫数量。这种XTT活力测定法经过验证,可用于高通量筛选血吸虫幼虫中的化合物,并可重现化合物的剂量反应曲线。

结论

我们得出结论,XTT活力测定法可用于筛选曼氏血吸虫中的大量化合物库,并加速新型抗血吸虫化合物的鉴定。

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