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      Multitarget Approaches against Multiresistant Superbugs

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          Abstract

          Despite efforts to develop new antibiotics, antibacterial resistance still develops too fast for drug discovery to keep pace. Often, resistance against a new drug develops even before it reaches the market. This continued resistance crisis has demonstrated that resistance to antibiotics with single protein targets develops too rapidly to be sustainable. Most successful long-established antibiotics target more than one molecule or possess targets, which are encoded by multiple genes. This realization has motivated a change in antibiotic development toward drug candidates with multiple targets. Some mechanisms of action presuppose multiple targets or at least multiple effects, such as targeting the cytoplasmic membrane or the carrier molecule bactoprenol phosphate and are therefore particularly promising. Moreover, combination therapy approaches are being developed to break antibiotic resistance or to sensitize bacteria to antibiotic action. In this Review, we provide an overview of antibacterial multitarget approaches and the mechanisms behind them.

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          Mechanisms of drug combinations: interaction and network perspectives.

          Understanding the molecular mechanisms underlying synergistic, potentiative and antagonistic effects of drug combinations could facilitate the discovery of novel efficacious combinations and multi-targeted agents. In this article, we describe an extensive investigation of the published literature on drug combinations for which the combination effect has been evaluated by rigorous analysis methods and for which relevant molecular interaction profiles of the drugs involved are available. Analysis of the 117 drug combinations identified reveals general and specific modes of action, and highlights the potential value of molecular interaction profiles in the discovery of novel multicomponent therapies.
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            Combination therapy for treatment of infections with gram-negative bacteria.

            Combination antibiotic therapy for invasive infections with Gram-negative bacteria is employed in many health care facilities, especially for certain subgroups of patients, including those with neutropenia, those with infections caused by Pseudomonas aeruginosa, those with ventilator-associated pneumonia, and the severely ill. An argument can be made for empiric combination therapy, as we are witnessing a rise in infections caused by multidrug-resistant Gram-negative organisms. The wisdom of continued combination therapy after an organism is isolated and antimicrobial susceptibility data are known, however, is more controversial. The available evidence suggests that the greatest benefit of combination antibiotic therapy stems from the increased likelihood of choosing an effective agent during empiric therapy, rather than exploitation of in vitro synergy or the prevention of resistance during definitive treatment. In this review, we summarize the available data comparing monotherapy versus combination antimicrobial therapy for the treatment of infections with Gram-negative bacteria.
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              Drug combinations: a strategy to extend the life of antibiotics in the 21st century

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                Author and article information

                Journal
                ACS Infect Dis
                ACS Infect Dis
                id
                aidcbc
                ACS Infectious Diseases
                American Chemical Society
                2373-8227
                10 March 2020
                12 June 2020
                : 6
                : 6 , Antibiotics
                : 1346-1365
                Affiliations
                []Newcastle University Biosciences Institute, Newcastle University , NE2 4HH Newcastle upon Tyne, United Kingdom
                []Division of Chemical Biology, Department of Biology and Biological Engineering, Chalmers University of Technology , 412 96 Gothenburg, Sweden
                Author notes
                [* ]Email: wenzelm@ 123456chalmers.se . Tel: 0046-31-772-2074.
                Article
                10.1021/acsinfecdis.0c00001
                7307902
                32156116
                954bb4f8-7f2b-4d57-bc8d-e47943c6dc50
                Copyright © 2020 American Chemical Society

                This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.

                History
                : 01 January 2020
                Categories
                Review
                Custom metadata
                id0c00001
                id0c00001

                polypharmacology,multifunctional antibiotic,multiresistant bacteria,antibiotic combination therapy,synergy

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