Ultrastructural and morphological studies on variables affecting Escherichia coli with selected commercial antibiotics

Q1 Immunology and Microbiology
Nur Afrina Muhamad Hendri , Nur Asyura Nor Amdan , Shelly Olevia Dounis , Norzarila Sulaiman Najib , Santhana Raj Louis
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引用次数: 0

Abstract

Background

Many studies reported the effects of antibiotic exposure on E. coli bacterial growth and cell modification. However, scarce descriptive information on ultrastructural effects upon exposure of commercial antibiotics.

Methods

This study described the morphological and ultrastructural alterations caused by selected antibiotics (amoxicillin-clavulanate, ceftriaxone, polymyxin B, colistin, gentamicin, and amikacin) that targeted cell wall, plasma membrane, and cytoplasmic density, and also proteins synthesis. We determined extracellular morphological changes of exposure through scanning electron microscopy (FESEM) and intracellular activities through transmission electron microscopy (TEM) investigation.

Results

FESEM and TEM micrograph of E. coli exposed with selected antibiotics shows ultrastructural changes in beta-lactam class (amoxicillin-clavulanate, ceftriaxone) elongated the cells as the cell wall was altered as it inhibits bacterial cell wall synthesis, polymyxin class (polymyxin B, colistin) had plasmid and curli-fimbriae as it breaking down the plasma/cytoplasmic membrane, and aminoglycoside class (gentamicin, and amikacin) reduced ribosome concentration as it inhibits bacterial protein synthesis by binding to 30 s ribosomes.

Conclusion

Morphological and ultrastructural alterations of E. coli’s mechanism of actions were translated and depicted. This study could be reference for characterization studies for morphological and ultrastructural of E. coli upon exposure to antimicrobial agents.

关于影响大肠埃希氏菌与选定商业抗生素的变量的超微结构和形态学研究
背景许多研究都报道了抗生素暴露对大肠杆菌生长和细胞改造的影响。本研究描述了某些抗生素(阿莫西林-克拉维酸、头孢曲松、多粘菌素 B、大肠杆菌素、庆大霉素和阿米卡星)针对细胞壁、质膜和细胞质密度以及蛋白质合成所引起的形态学和超微结构改变。我们通过扫描电子显微镜(FESEM)和透射电子显微镜(TEM)研究确定了暴露后的细胞外形态变化和细胞内活性。大肠杆菌暴露于某些抗生素后,其超微结构发生了变化:β-内酰胺类(阿莫西林-克拉维酸、头孢曲松)由于抑制了细菌细胞壁的合成而改变了细胞壁,使细胞变长;多粘菌素类(多粘菌素 B、大肠菌素)由于抑制了细菌细胞壁的合成而改变了细胞壁,使细胞变长;多粘菌素类(多粘菌素 B、大肠菌素)由于抑制了细菌细胞壁的合成而改变了细胞壁,使细胞变长、氨基糖苷类(庆大霉素和阿米卡星)通过与 30 s 核糖体结合抑制细菌蛋白质合成,从而降低核糖体浓度。结论 对大肠杆菌作用机制的形态学和超微结构改变进行了翻译和描述。这项研究可作为大肠杆菌接触抗菌剂后形态学和超微结构特征研究的参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell Surface
Cell Surface Immunology and Microbiology-Applied Microbiology and Biotechnology
CiteScore
6.10
自引率
0.00%
发文量
18
审稿时长
49 days
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