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一种短阳离子肽对硕大利什曼原虫(MHRO/IR/75/ER)前鞭毛体和无鞭毛体形式的抗菌活性研究:一项体外研究。

Investigation of the antimicrobial activity of a short cationic peptide against promastigote and amastigote forms of Leishmania major (MHRO/IR/75/ER): An in vitro study.

作者信息

Khalili Sara, Ebrahimzade Elahe, Mohebali Mehdi, Shayan Parviz, Mohammadi-Yeganeh Samira, Moosazadeh Moghaddam Mehrdad, Elikaee Samira, Akhoundi Behnaz, Sharifi-Yazdi Mohammad Kazem

机构信息

Department of Parasitology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran.

Department of Pathobiology, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran.

出版信息

Exp Parasitol. 2019 Jan;196:48-54. doi: 10.1016/j.exppara.2018.11.006. Epub 2018 Nov 26.

Abstract

Cutaneous leishmaniasis is one of the most endemic global health problems in many countries all around the world. Pentavalent antimonial drugs constitute the first line of leishmaniasis treatment; however, resistance to these drugs is a serious problem. Therefore, new therapies with new modes of action are urgently needed. In the current study, we examined antimicrobial activity of CM11 hybrid peptide (WKLFKKILKVL-NH2) against promastigote and amastigote forms of L. major (MHRO/IR/75/ER). In vitro anti-leishmanial activity was identified against L. major by parasite viability and metabolic activity after exposure to different peptide concentration. In the presentt study, we demostrated that different concentrations of CM11 result in dose dependent growth inhibition of Leishmania promastigotes. Furthermore, we demostrated that CM11 peptide has significant anti-leishmanial activities on amastigotes. Our results demonstrated that CM11 antimicrobial peptide may provide an alternative therapeutic approach for L. major treatment.

摘要

皮肤利什曼病是世界上许多国家最流行的全球健康问题之一。五价锑药物是利什曼病治疗的一线用药;然而,对这些药物的耐药性是一个严重问题。因此,迫切需要具有新作用方式的新疗法。在本研究中,我们检测了CM11杂合肽(WKLFKKILKVL-NH2)对硕大利什曼原虫(MHRO/IR/75/ER)前鞭毛体和无鞭毛体形式的抗菌活性。通过暴露于不同肽浓度后寄生虫的活力和代谢活性,确定了对硕大利什曼原虫的体外抗利什曼活性。在本研究中,我们证明不同浓度的CM11导致利什曼原虫前鞭毛体的剂量依赖性生长抑制。此外,我们证明CM11肽对无鞭毛体具有显著的抗利什曼活性。我们的结果表明,CM11抗菌肽可能为硕大利什曼原虫的治疗提供一种替代治疗方法。

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