TY - JOUR
T1 - Eco-friendly drugs induce cellular changes in colistin-resistant bacteria
AU - Al-Khattaf, Fatimah Saleh
AU - Aloufi, Abeer Salem
AU - Moglad, Ehssan
AU - Ncibi, Saida Sadek
AU - Almuraikhi, Nihal
AU - Almaarik, Basmah
AU - Alaaullah, Malek Hassan Ibrahim
AU - Ali, Rizwan
AU - Abdalaziz, Halah Salah Mohammed
AU - Alaaullah, Mohammed Hassan Ibrahim
AU - Elsayim, Rasha
N1 - Publisher Copyright:
© 2024 the author(s), published by De Gruyter.
PY - 2024/1/1
Y1 - 2024/1/1
N2 - Background and objective ‒ As a last option, multidrug-resistant Gram-negative infections (caused by Enterobacteriaceae) are treated with the antibiotic colistin, also known as polymyxin E. Colistin-resistant superbugs predispose people to untreatable infections, possibly leading to a high mortality rate. This project aims to study the effect of Acacia nilotica aqueous extract and zinc oxide nanoparticles (ZnO-NPs) on colistin-resistant Klebsiella pneumonia (CRKP). Materials and methods ‒ ZnO-NPs were synthesized using the green method and characterized by UV-vis, Fourier transform infrared spectroscopy, and X-ray diffraction. The zone of inhibition (ZI) was measured using the agar-well diffusion method, and the minimum inhibitory concentration (MIC) and minimum bactericidal concentration were estimated to determine the antimicrobial activity of the tested compound. Scanning electron microscopy (SEM) and transmission electronic microscopy (TEM) were used to investigate the alterations in bacterial cells that were treated with the tested drugs. Results ‒ The synthesized ZnO-NPs presented good chemical and physical properties, and the plant extract and ZnO-NPs displayed a large ZI. ZnO-NPs had the lowest MIC (0.2 mg·mL−1). SEM and TEM observations revealed various morphological modifications in CRKP cells, including cell shrinkage, cell damage, cytoplasm loss, cell wall thinning, and cell death. Conclusion ‒ A. nilotica aqueous extract and ZnO-NPs could be used as alternative natural products to produce antibacterial drugs and to prevent CRKP infection.
AB - Background and objective ‒ As a last option, multidrug-resistant Gram-negative infections (caused by Enterobacteriaceae) are treated with the antibiotic colistin, also known as polymyxin E. Colistin-resistant superbugs predispose people to untreatable infections, possibly leading to a high mortality rate. This project aims to study the effect of Acacia nilotica aqueous extract and zinc oxide nanoparticles (ZnO-NPs) on colistin-resistant Klebsiella pneumonia (CRKP). Materials and methods ‒ ZnO-NPs were synthesized using the green method and characterized by UV-vis, Fourier transform infrared spectroscopy, and X-ray diffraction. The zone of inhibition (ZI) was measured using the agar-well diffusion method, and the minimum inhibitory concentration (MIC) and minimum bactericidal concentration were estimated to determine the antimicrobial activity of the tested compound. Scanning electron microscopy (SEM) and transmission electronic microscopy (TEM) were used to investigate the alterations in bacterial cells that were treated with the tested drugs. Results ‒ The synthesized ZnO-NPs presented good chemical and physical properties, and the plant extract and ZnO-NPs displayed a large ZI. ZnO-NPs had the lowest MIC (0.2 mg·mL−1). SEM and TEM observations revealed various morphological modifications in CRKP cells, including cell shrinkage, cell damage, cytoplasm loss, cell wall thinning, and cell death. Conclusion ‒ A. nilotica aqueous extract and ZnO-NPs could be used as alternative natural products to produce antibacterial drugs and to prevent CRKP infection.
KW - carpabenem resistant
KW - colistin resistant
KW - Klebsiella pneumonia
KW - scanning electron microscope
KW - transmission electron microscope
KW - zinc oxide nanoparticles
UR - http://www.scopus.com/inward/record.url?scp=85206827673&partnerID=8YFLogxK
U2 - 10.1515/gps-2024-0097
DO - 10.1515/gps-2024-0097
M3 - Article
AN - SCOPUS:85206827673
SN - 2191-9542
VL - 13
JO - Green Processing and Synthesis
JF - Green Processing and Synthesis
IS - 1
M1 - 20240097
ER -