Issue 24, 2015

Antimicrobial peptide-conjugated graphene oxide membrane for efficient removal and effective killing of multiple drug resistant bacteria

Abstract

According to the World Health Organization (WHO), multiple drug-resistant (MDR) bacterial infection is a top threat to human health. Since bacteria evolve to resist antibiotics faster than scientists can develop new classes of drugs, the development of new materials which can be used, not only for separation, but also for effective disinfection of drug resistant pathogens is urgent. Driven by this need, we report for the first time the development of a nisin antimicrobial peptide conjugated, three dimensional (3D) porous graphene oxide membrane for identification, effective separation, and complete disinfection of MDR methicillin-resistant Staphylococcus aureus (MRSA) pathogens from water. Experimental data show that due to the size differences, MRSA is captured by the porous membrane, allowing only water to pass through. SEM, TEM, and fluorescence images confirm that pathogens are captured by the membrane. RT-PCR data with colony counting indicate that almost 100% of MRSA can be removed and destroyed from the water sample using the developed membrane. Comparison of MDR killing data between nisin alone, the graphene oxide membrane and the nisin attached graphene oxide membrane demonstrate that the nisin antimicrobial peptide attached graphene oxide membrane can dramatically enhance the possibility of destroying MRSA via a synergistic effect due to the multimodal mechanism.

Graphical abstract: Antimicrobial peptide-conjugated graphene oxide membrane for efficient removal and effective killing of multiple drug resistant bacteria

Article information

Article type
Paper
Submitted
22 Jan 2015
Accepted
09 Feb 2015
First published
09 Feb 2015

RSC Adv., 2015,5, 18881-18887

Author version available

Antimicrobial peptide-conjugated graphene oxide membrane for efficient removal and effective killing of multiple drug resistant bacteria

R. Kanchanapally, B. P. Viraka Nellore, S. S. Sinha, F. Pedraza, S. J. Jones, A. Pramanik, S. R. Chavva, C. Tchounwou, Y. Shi, A. Vangara, D. Sardar and P. C. Ray, RSC Adv., 2015, 5, 18881 DOI: 10.1039/C5RA01321F

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