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      Nano-Strategies to Fight Multidrug Resistant Bacteria—“A Battle of the Titans”

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          Abstract

          Infectious diseases remain one of the leading causes of morbidity and mortality worldwide. The WHO and CDC have expressed serious concern regarding the continued increase in the development of multidrug resistance among bacteria. Therefore, the antibiotic resistance crisis is one of the most pressing issues in global public health. Associated with the rise in antibiotic resistance is the lack of new antimicrobials. This has triggered initiatives worldwide to develop novel and more effective antimicrobial compounds as well as to develop novel delivery and targeting strategies. Bacteria have developed many ways by which they become resistant to antimicrobials. Among those are enzyme inactivation, decreased cell permeability, target protection, target overproduction, altered target site/enzyme, increased efflux due to over-expression of efflux pumps, among others. Other more complex phenotypes, such as biofilm formation and quorum sensing do not appear as a result of the exposure of bacteria to antibiotics although, it is known that biofilm formation can be induced by antibiotics. These phenotypes are related to tolerance to antibiotics in bacteria. Different strategies, such as the use of nanostructured materials, are being developed to overcome these and other types of resistance. Nanostructured materials can be used to convey antimicrobials, to assist in the delivery of novel drugs or ultimately, possess antimicrobial activity by themselves. Additionally, nanoparticles (e.g., metallic, organic, carbon nanotubes, etc.) may circumvent drug resistance mechanisms in bacteria and, associated with their antimicrobial potential, inhibit biofilm formation or other important processes. Other strategies, including the combined use of plant-based antimicrobials and nanoparticles to overcome toxicity issues, are also being investigated. Coupling nanoparticles and natural-based antimicrobials (or other repurposed compounds) to inhibit the activity of bacterial efflux pumps; formation of biofilms; interference of quorum sensing; and possibly plasmid curing, are just some of the strategies to combat multidrug resistant bacteria. However, the use of nanoparticles still presents a challenge to therapy and much more research is needed in order to overcome this. In this review, we will summarize the current research on nanoparticles and other nanomaterials and how these are or can be applied in the future to fight multidrug resistant bacteria.

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          Most cited references300

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          Bacterial biofilms: from the natural environment to infectious diseases.

          Biofilms--matrix-enclosed microbial accretions that adhere to biological or non-biological surfaces--represent a significant and incompletely understood mode of growth for bacteria. Biofilm formation appears early in the fossil record (approximately 3.25 billion years ago) and is common throughout a diverse range of organisms in both the Archaea and Bacteria lineages, including the 'living fossils' in the most deeply dividing branches of the phylogenetic tree. It is evident that biofilm formation is an ancient and integral component of the prokaryotic life cycle, and is a key factor for survival in diverse environments. Recent advances show that biofilms are structurally complex, dynamic systems with attributes of both primordial multicellular organisms and multifaceted ecosystems. Biofilm formation represents a protected mode of growth that allows cells to survive in hostile environments and also disperse to colonize new niches. The implications of these survival and propagative mechanisms in the context of both the natural environment and infectious diseases are discussed in this review.
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            The antimicrobial activity of nanoparticles: present situation and prospects for the future

            Nanoparticles (NPs) are increasingly used to target bacteria as an alternative to antibiotics. Nanotechnology may be particularly advantageous in treating bacterial infections. Examples include the utilization of NPs in antibacterial coatings for implantable devices and medicinal materials to prevent infection and promote wound healing, in antibiotic delivery systems to treat disease, in bacterial detection systems to generate microbial diagnostics, and in antibacterial vaccines to control bacterial infections. The antibacterial mechanisms of NPs are poorly understood, but the currently accepted mechanisms include oxidative stress induction, metal ion release, and non-oxidative mechanisms. The multiple simultaneous mechanisms of action against microbes would require multiple simultaneous gene mutations in the same bacterial cell for antibacterial resistance to develop; therefore, it is difficult for bacterial cells to become resistant to NPs. In this review, we discuss the antibacterial mechanisms of NPs against bacteria and the factors that are involved. The limitations of current research are also discussed.
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              Nanoparticle size and surface properties determine the protein corona with possible implications for biological impacts.

              Nanoparticles in a biological fluid (plasma, or otherwise) associate with a range of biopolymers, especially proteins, organized into the "protein corona" that is associated with the nanoparticle and continuously exchanging with the proteins in the environment. Methodologies to determine the corona and to understand its dependence on nanomaterial properties are likely to become important in bionanoscience. Here, we study the long-lived ("hard") protein corona formed from human plasma for a range of nanoparticles that differ in surface properties and size. Six different polystyrene nanoparticles were studied: three different surface chemistries (plain PS, carboxyl-modified, and amine-modified) and two sizes of each (50 and 100 nm), enabling us to perform systematic studies of the effect of surface properties and size on the detailed protein coronas. Proteins in the corona that are conserved and unique across the nanoparticle types were identified and classified according to the protein functional properties. Remarkably, both size and surface properties were found to play a very significant role in determining the nanoparticle coronas on the different particles of identical materials. We comment on the future need for scientific understanding, characterization, and possibly some additional emphasis on standards for the surfaces of nanoparticles.
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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                02 July 2018
                2018
                : 9
                : 1441
                Affiliations
                [1] 1UCIBIO, Departamento de Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa , Caparica, Portugal
                [2] 2School of Food Science and Environmental Health, College of Sciences and Health, Dublin Institute of Technology , Dublin, Ireland
                [3] 3Department of Microbiology, Moyne Institute of Preventive Medicine, Schools of Genetics and Microbiology, Trinity College Dublin, University of Dublin , Dublin, Ireland
                [4] 4Nuritas Limited , Dublin, Ireland
                Author notes

                Edited by: Rebecca Thombre, Pune University, India

                Reviewed by: Shahper Nazeer Khan, Aligarh Muslim University, India; Rodolfo García-Contreras, Universidad Nacional Autónoma de México, Mexico

                *Correspondence: Pedro V. Baptista pmvb@ 123456fct.unl.pt
                Alexandra R. Fernandes ma.fernandes@ 123456fct.unl.pt

                This article was submitted to Antimicrobials, Resistance and Chemotherapy, a section of the journal Frontiers in Microbiology

                †Present Address: Matthew P. McCusker, Kerry Europe, Global Technology & Innovation Centre, Naas, Ireland

                Article
                10.3389/fmicb.2018.01441
                6036605
                30013539
                9e755824-6d73-4f32-96d6-95941e9c1bbc
                Copyright © 2018 Baptista, McCusker, Carvalho, Ferreira, Mohan, Martins and Fernandes.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 31 March 2018
                : 11 June 2018
                Page count
                Figures: 1, Tables: 2, Equations: 0, References: 297, Pages: 26, Words: 21580
                Funding
                Funded by: Ministério da Ciência, Tecnologia e Ensino Superior 10.13039/501100006111
                Award ID: UID/Multi/04378/2013
                Award ID: POCI-01-0145-FEDER-007728
                Award ID: PTDC_CVT-EPI_6685_2014
                Funded by: Trinity College Dublin 10.13039/501100001637
                Award ID: Trinity College Dublin Postgraduate Research 1252 Studentship
                Funded by: Irish Research Council 10.13039/501100002081
                Award ID: EBPPG/2015/233
                Categories
                Microbiology
                Review

                Microbiology & Virology
                antimicrobial resistance,multidrug resistance,nanomaterials,nanoparticles,plant-based compounds,novel antimicrobial agents,nanotheranostics

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