Interaction of Al2O3 nanoparticles with Escherichia coli and their cell envelope biomolecules

被引:95
作者
Ansari, M. A. [1 ]
Khan, H. M. [1 ]
Khan, A. A. [2 ]
Cameotra, S. S. [3 ]
Saquib, Q. [4 ]
Musarrat, J. [5 ]
机构
[1] Aligarh Muslim Univ, Jawaharlal Nehru Med Coll & Hosp, Dept Microbiol, Nanotechnol & Antimicrobial Drug Resistance Res L, Aligarh 202002, UP, India
[2] Aligarh Muslim Univ, Jawaharlal Nehru Med Coll & Hosp, Dept Anat, Aligarh 202002, UP, India
[3] CSIR, Inst Microbial Technol IMTECH, Chandigarh, India
[4] King Saud Univ, Coll Sci, Dept Zool, Riyadh 11451, Saudi Arabia
[5] Aligarh Muslim Univ, Fac Agr Sci, Dept Agr Microbiol, Aligarh 202002, UP, India
关键词
PE; Al2O3; NPs; ESBL; HR-TEM; LPS; AT-FTIR; METAL-OXIDE NANOPARTICLES; SPECTRUM BETA-LACTAMASES; ANTIBACTERIAL ACTIVITY; SILVER NANOPARTICLES; KLEBSIELLA-PNEUMONIAE; TOXICITY; ZNO; BACTERIA; RESISTANCE; ALUMINA;
D O I
10.1111/jam.12423
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aims The aim of this study is to investigate the antibacterial activity of aluminium oxide nanoparticles (Al2O3 NPs) against multidrug-resistant clinical isolates of Escherichia coli and their interaction with cell envelope biomolecules. Methods and Results Al2O3 NPs were characterized by scanning electron microscope (SEM), high-resolution transmission electron microscope (HR-TEM) and X-ray diffraction (XRD) analyses. Antibacterial activity and interaction of Al2O3 NPs with E.coli and its surface biomolecules were assessed by spectrophotometry, SEM, HR-TEM and attenuated total reflectance/Fourier transform infrared (ATR-FTIR). Of the 80 isolates tested, about 64 (80%) were found to be extended spectrum beta-lactamase (ESBL) positive and 16 (20%) were non-ESBL producers. Al2O3 NPs at 1000 mu gml(-1) significantly inhibited the bacterial growth. SEM and HR-TEM analyses revealed the attachment of NPs to the surface of cell membrane and also their presence inside the cells due to formation of irregular-shaped pits and perforation on the surfaces of bacterial cells. The intracellular Al2O3 NPs might have interacted with cellular biomolecules and caused adverse effects eventually triggering the cell death. ATR-FTIR studies suggested the interaction of lipopolysaccharide (LPS) and L-alpha-Phosphatidyl-ethanolamine (PE) with Al2O3 NPs. Infrared (IR) spectral changes revealed that the LPS could bind to Al2O3 NPs through hydrogen binding and ligand exchange. The Al2O3 NPs-induced structural changes in phospholipids may lead to the loss of amphiphilic properties, destruction of the membrane and cell leaking. Conclusions The penetration and accumulation of NPs inside the bacterial cell cause pit formation, perforation and disorganization and thus drastically disturb its proper function. The cell surface biomolecular changes revealed by ATR-FTIR spectra provide a better understanding of the cytotoxicity of Al2O3 NPs. Significance and Impact of the Study Al2O3 NPs may serve as broad-spectrum bactericidal agents to control the emergent pathogens regardless of their drug-resistance mechanisms.
引用
收藏
页码:772 / 783
页数:12
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