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微需氧寄生虫的药物敏感性检测:半胱氨酸强烈影响甲硝唑和金诺芬(一种新型、有前途的抗菌药物)的疗效。

Drug susceptibility testing in microaerophilic parasites: Cysteine strongly affects the effectivities of metronidazole and auranofin, a novel and promising antimicrobial.

机构信息

Institute of Specific Prophylaxis and Tropical Medicine, Medical University of Vienna, Kinderspitalgasse 15, A-1095 Vienna, Austria.

出版信息

Int J Parasitol Drugs Drug Resist. 2017 Dec;7(3):321-327. doi: 10.1016/j.ijpddr.2017.09.001. Epub 2017 Sep 5.

Abstract

The microaerophilic parasites Entamoeba histolytica, Trichomonas vaginalis, and Giardia lamblia annually cause hundreds of millions of human infections which are treated with antiparasitic drugs. Metronidazole is the most often prescribed drug but also other drugs are in use, and novel drugs with improved characteristics are constantly being developed. One of these novel drugs is auranofin, originally an antirheumatic which has been relabelled for the treatment of parasitic infections. Drug effectivity is arguably the most important criterion for its applicability and is commonly assessed in susceptibility assays using in vitro cultures of a given pathogen. However, drug susceptibility assays can be strongly affected by certain compounds in the growth media. In the case of microaerophilic parasites, cysteine which is added in large amounts as an antioxidant is an obvious candidate because it is highly reactive and known to modulate the toxicity of metronidazole in several microaerophilic parasites. In this study, it was attempted to reduce cysteine concentrations as far as possible without affecting parasite viability by performing drug susceptibility assays under strictly anaerobic conditions in an anaerobic cabinet. Indeed, T. vaginalis and E. histolytica could be grown without any cysteine added and the cysteine concentration necessary to maintain G. lamblia could be reduced to 20%. Susceptibilities to metronidazole were found to be clearly reduced in the presence of cysteine. With auranofin the protective effect of cysteine was extreme, providing protection to concentrations up to 100-fold higher as observed in the absence of cysteine. With three other drugs tested, albendazole, furazolidone and nitazoxanide, all in use against G. lamblia, the effect of cysteine was less pronounced. Oxygen was found to have a less marked impact on metronidazole and auranofin than cysteine but bovine bile which is standardly used in growth media for G. lamblia, displayed a marked synergistic effect with metronidazole.

摘要

微需氧寄生虫溶组织内阿米巴、阴道毛滴虫和蓝氏贾第鞭毛虫每年导致数亿人感染,这些感染都用抗寄生虫药物进行治疗。甲硝唑是最常开的药物,但也有其他药物在使用,并且具有改进特性的新型药物不断被开发。其中一种新型药物是金诺芬,它最初是一种抗风湿药物,后来被重新标记用于治疗寄生虫感染。药物疗效无疑是其适用性的最重要标准,通常在使用特定病原体的体外培养物进行药敏试验中进行评估。然而,药物敏感性试验可能会受到生长培养基中某些化合物的强烈影响。在微需氧寄生虫的情况下,作为抗氧化剂大量添加的半胱氨酸是一个明显的候选物,因为它具有很高的反应性,并且已知在几种微需氧寄生虫中调节甲硝唑的毒性。在这项研究中,通过在厌氧柜中严格厌氧条件下进行药敏试验,尝试尽可能降低胱氨酸浓度而不影响寄生虫活力。事实上,阴道毛滴虫和溶组织内阿米巴可以在不添加任何胱氨酸的情况下生长,并且维持蓝氏贾第鞭毛虫所需的胱氨酸浓度可以降低到 20%。在存在胱氨酸的情况下,甲硝唑的敏感性明显降低。对于金诺芬,胱氨酸的保护作用非常极端,提供了高达 100 倍的保护作用,而在没有胱氨酸的情况下观察到的保护作用。对于测试的另外三种药物,阿苯达唑、呋喃唑酮和硝唑尼特,所有这些药物都用于治疗蓝氏贾第鞭毛虫,胱氨酸的作用不那么明显。与胱氨酸相比,氧气对甲硝唑和金诺芬的影响较小,但牛胆盐是蓝氏贾第鞭毛虫生长培养基中标准使用的物质,与甲硝唑显示出明显的协同作用。

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