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利用阴道毛滴虫临床分离株评估基因表达与甲硝唑耐药性的相关性。

Use of Trichomonas vaginalis clinical isolates to evaluate correlation of gene expression and metronidazole resistance.

作者信息

Mead J R, Fernadez M, Romagnoli P A, Secor W E

机构信息

Veterans Affairs Medical Center, Decatur, Georgia 30033, USA.

出版信息

J Parasitol. 2006 Feb;92(1):196-9. doi: 10.1645/GE-616R.1.

Abstract

We investigated whether variations in gene expression of enzymes associated with anaerobic resistance of laboratory-derived strains of Trichomonas vaginalis could be detected in a group of 28 clinical isolates with variations in metronidazole sensitivity. We compared isolates by real-time PCR because this method allows for highly sensitive quantification of mRNA and for evaluation of several genes simultaneously. We found that PFOR gene A mRNA levels were highly correlated with PFOR gene B levels, as well as the D subunit of malic enzyme and ferrodoxin. Ferrodoxin mRNA expression was also significantly correlated with that of malic enzyme and hydrogenase. However, when we evaluated relationships between these enzymes and resistance to metronidazole, we found no significant correlations between aerobic or anaerobic in vitro sensitivity to drug and mRNA levels of any of the enzymes tested. Similarly, using a Student's t-test, no significant differences in enzyme mRNA levels were observed between isolates separated by metronidazole resistance or susceptibility. The lack of correlation between gene expression and resistance or susceptibility could be the result of differences in expression at the protein level or because other biochemical pathways or genes are involved in the resistance observed in clinical settings.

摘要

我们研究了在一组28株甲硝唑敏感性存在差异的临床分离株中,是否能检测到与实验室衍生的阴道毛滴虫菌株厌氧抗性相关的酶的基因表达变化。我们通过实时PCR对分离株进行比较,因为该方法能够对mRNA进行高度灵敏的定量分析,并且可以同时评估多个基因。我们发现,PFOR基因A的mRNA水平与PFOR基因B的水平高度相关,与苹果酸酶的D亚基和铁氧化还原蛋白的水平也高度相关。铁氧化还原蛋白的mRNA表达也与苹果酸酶和氢化酶的表达显著相关。然而,当我们评估这些酶与甲硝唑抗性之间的关系时,我们发现对药物的需氧或厌氧体外敏感性与所测试的任何一种酶的mRNA水平之间均无显著相关性。同样,使用学生t检验,在根据甲硝唑抗性或敏感性分开的分离株之间,未观察到酶mRNA水平有显著差异。基因表达与抗性或敏感性之间缺乏相关性,可能是由于蛋白质水平表达的差异,或者是因为在临床环境中观察到的抗性涉及其他生化途径或基因。

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