Antibiofilm and antivirulence potential of silver nanoparticles against multidrug-resistant Acinetobacter baumannii

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作者
Helal F. Hetta
Israa M. S. Al-Kadmy
Saba Saadoon Khazaal
Suhad Abbas
Ahmed Suhail
Mohamed A. El-Mokhtar
Noura H. Abd Ellah
Esraa A. Ahmed
Rasha B. Abd-ellatief
Eman A. El-Masry
Gaber El-Saber Batiha
Azza A. Elkady
Nahed A. Mohamed
Abdelazeem M. Algammal
机构
[1] Assiut University,Department of Medical Microbiology and Immunology, Faculty of Medicine
[2] University of Cincinnati College of Medicine,Department of Internal Medicine
[3] AL-Mustansiriyah University,Branch of Biotechnology, Department of Biology, College of Science
[4] University of Plymouth,Faculty of Science and Engineering, School of Engineering
[5] Plymouth University,Wolfson Nanomaterials and Devices Laboratory, School of Computing, Electronics and Mathematics, Faculty of Science and Engineering
[6] Assiut University,Department of Pharmaceutics, Faculty of Pharmacy
[7] Assiut University,Department of Pharmacology, Faculty of Medicine
[8] King Abdulaziz University,Centre of Excellence in Environmental Studies (CEES)
[9] Jouf University,Microbiology and Immunology Unit, Department of Pathology, College of Medicine
[10] Menoufia University,Department of Medical Microbiology and Immunology, College of Medicine
[11] Damanhour University,Department of Pharmacology and Therapeutics, Faculty of Veterinary Medicines
[12] Sohag University,Sohag University Medical Administration
[13] Assiut University,Department of Medical Biochemistry, Faculty of Medicine
[14] Suez Canal University,Department of Bacteriology, Immunology, and Mycology, Faculty of Veterinary Medicine
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We aimed to isolate Acinetobacter baumannii (A. baumannii) from wound infections, determine their resistance and virulence profile, and assess the impact of Silver nanoparticles (AgNPs) on the bacterial growth, virulence and biofilm-related gene expression. AgNPs were synthesized and characterized using TEM, XRD and FTIR spectroscopy. A. baumannii (n = 200) were isolated and identified. Resistance pattern was determined and virulence genes (afa/draBC, cnf1, cnf2, csgA, cvaC, fimH, fyuA, ibeA, iutA, kpsMT II, PAI, papC, PapG II, III, sfa/focDE and traT) were screened using PCR. Biofilm formation was evaluated using Microtiter plate method. Then, the antimicrobial activity of AgNPs was evaluated by the well-diffusion method, growth kinetics and MIC determination. Inhibition of biofilm formation and the ability to disperse biofilms in exposure to AgNPs were evaluated. The effect of AgNPs on the expression of virulence and biofilm-related genes (bap, OmpA, abaI, csuA/B, A1S_2091, A1S_1510, A1S_0690, A1S_0114) were estimated using QRT-PCR. In vitro infection model for analyzing the antibacterial activity of AgNPs was done using a co-culture infection model of A. baumannii with human fibroblast skin cell line HFF-1 or Vero cell lines. A. baumannii had high level of resistance to antibiotics. Most of the isolates harbored the fimH, afa/draBC, cnf1, csgA and cnf2, and the majority of A. baumannii produced strong biofilms. AgNPs inhibited the growth of A. baumannii efficiently with MIC ranging from 4 to 25 µg/ml. A. baumannii showed a reduced growth rate in the presence of AgNPs. The inhibitory activity and the anti-biofilm activity of AgNPs were more pronounced against the weak biofilm producers. Moreover, AgNPs decreased the expression of kpsMII , afa/draBC,bap, OmpA, and csuA/B genes. The in vitro infection model revealed a significant antibacterial activity of AgNPs against extracellular and intracellular A. baumannii. AgNPs highly interrupted bacterial multiplication and biofilm formation. AgNPs downregulated the transcription level of important virulence and biofilm-related genes. Our findings provide an additional step towards understanding the mechanisms by which sliver nanoparticles interfere with the microbial spread and persistence.
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