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初始表达水平 nimA 对脆弱拟杆菌抵抗甲硝唑的保护作用具有决定性意义。

Initial expression levels of nimA are decisive for protection against metronidazole in Bacteroides fragilis.

机构信息

Institute for Specific Prophylaxis and Tropical Medicine Center for Pathophysiology, Infectiology, and Immunology, Medical University of Vienna, Kinderspitalgasse 15, A-1090, Vienna, Austria.

Institute of Medical Microbiology, Faculty of Medicine, University of Szeged, 10 Dóm Square, H-6720, Szeged, Hungary.

出版信息

Anaerobe. 2022 Oct;77:102630. doi: 10.1016/j.anaerobe.2022.102630. Epub 2022 Aug 24.

Abstract

OBJECTIVES

In the genus Bacteroides, the nim genes are resistance determinants for metronidazole, a nitroimidazole drug widely used against anaerobic pathogens. The Nim proteins are considered to act as nitroreductases. However, data from several studies suggest that the expression levels of Nim do not increase with increasing resistance which is conflicting with this notion. The impact of Nim protein levels on low-level metronidazole resistance, however, representing the early stage of induced resistance in the laboratory, has not been assessed as yet.

METHODS

The nimA gene was cloned into two different plasmids and introduced into B. fragilis strain 638R. Expression levels of nimA mRNA were measured by RT-qPCR and compared to those in strain 638R harbouring plasmid pI417, the original clinical plasmid harbouring IS element IS1168 with the nimA gene. Further, metronidazole susceptibility was assessed by Etest and the activity of pyruvate:ferredoxin oxidoreductase (PFOR) was measured in all strains after induction of high-level metronidazole resistance.

RESULTS

The level of protection against metronidazole by nimA correleated with the level of expression of nimA mRNA. Further, the activity of PFOR in highly-resistant B. fragilis 638R was only preserved when expression levels of nimA were high.

CONCLUSIONS

Although the development of high-level metronidazole resistance in B. fragilis strains with a nimA gene is not caused by an increase of nimA expression as compared to the less resistant parent strains, nimA expression levels might be of decisive importance in the early stage of resistance development. This has potential implications for metronidazole resistance in clinical isolates.

摘要

目的

在拟杆菌属中,nim 基因是甲硝唑的耐药决定因素,甲硝唑是一种广泛用于抗厌氧病原体的硝基咪唑类药物。Nim 蛋白被认为是硝基还原酶。然而,来自几项研究的数据表明,随着耐药性的增加,Nim 的表达水平并没有增加,这与这一观点相矛盾。然而,尚未评估 Nim 蛋白水平对实验室中诱导耐药早期阶段(即低水平甲硝唑耐药)的影响。

方法

将 nimA 基因克隆到两个不同的质粒中,并引入脆弱拟杆菌 638R 菌株。通过 RT-qPCR 测量 nimA mRNA 的表达水平,并将其与携带质粒 pI417 的 638R 菌株(含有 nimA 基因的原始临床质粒 IS 元素 IS1168)进行比较。此外,通过 Etest 评估甲硝唑的敏感性,并在所有菌株中诱导高水平甲硝唑耐药后测量丙酮酸:铁氧还蛋白氧化还原酶(PFOR)的活性。

结果

nimA 对甲硝唑的保护水平与 nimA mRNA 的表达水平相关。此外,当 nimA 的表达水平较高时,高耐药性脆弱拟杆菌 638R 的 PFOR 活性仅得到保留。

结论

尽管与耐药性较低的亲本菌株相比,带有 nimA 基因的脆弱拟杆菌菌株中高水平甲硝唑耐药的发展并非由于 nimA 表达的增加所致,但 nimA 表达水平可能在耐药性发展的早期阶段具有决定性意义。这对临床分离株中甲硝唑耐药性具有潜在影响。

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