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      Factors mediating Acinetobacter baumannii biofilm formation: Opportunities for developing therapeutics

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          Highlights

          • A. baumannii rapidly acquires antimicrobial resistance and causes biofilm associated infections.

          • Strategies to target intrinsic factors mediating A. baumannii biofilm formation offer therapeutic prospects.

          • Antimicrobial polymers and coating medical devices with antibiofilm agents may prevent biofilm associated infections.

          • Biofilm matrix or regulatory mechanisms such as quorum sensing are potential targets for treating chronic infections.

          • Phage therapy, photodynamic therapy and nanoparticle therapy are novel promising approaches for treating biofilm associated infections.

          Abstract

          Acinetobacter baumannii has notably become a superbug due to its mounting risk of infection and escalating rates of antimicrobial resistance, including colistin, the last-resort antibiotic. Its propensity to form biofilm on biotic and abiotic surfaces has contributed to the majority of nosocomial infections. Bacterial cells in biofilms are resistant to antibiotics and host immune response, and pose challenges in treatment. Therefore current scenario urgently requires the development of novel therapeutic strategies for successful treatment outcomes. This article provides a holistic understanding of sequential events and regulatory mechanisms directing A. baumannii biofilm formation. Understanding the key factors functioning and regulating the biofilm machinery of A. baumannii will provide us insight to develop novel approaches to combat A. baumannii infections. Further, the review article deliberates promising strategies for the prevention of biofilm formation on medically relevant substances and potential therapeutic strategies for the eradication of preformed biofilms which can help tackle biofilm-associated A. baumannii infections. Advances in emerging therapeutic opportunities such as phage therapy, nanoparticle therapy and photodynamic therapy are also discussed to comprehend the current scenario and future outlook for the development of successful treatment against biofilm-associated A. baumannii infections.

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          Most cited references185

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          Bad bugs, no drugs: no ESKAPE! An update from the Infectious Diseases Society of America.

          The Infectious Diseases Society of America (IDSA) continues to view with concern the lean pipeline for novel therapeutics to treat drug-resistant infections, especially those caused by gram-negative pathogens. Infections now occur that are resistant to all current antibacterial options. Although the IDSA is encouraged by the prospect of success for some agents currently in preclinical development, there is an urgent, immediate need for new agents with activity against these panresistant organisms. There is no evidence that this need will be met in the foreseeable future. Furthermore, we remain concerned that the infrastructure for discovering and developing new antibacterials continues to stagnate, thereby risking the future pipeline of antibacterial drugs. The IDSA proposed solutions in its 2004 policy report, "Bad Bugs, No Drugs: As Antibiotic R&D Stagnates, a Public Health Crisis Brews," and recently issued a "Call to Action" to provide an update on the scope of the problem and the proposed solutions. A primary objective of these periodic reports is to encourage a community and legislative response to establish greater financial parity between the antimicrobial development and the development of other drugs. Although recent actions of the Food and Drug Administration and the 110th US Congress present a glimmer of hope, significant uncertainly remains. Now, more than ever, it is essential to create a robust and sustainable antibacterial research and development infrastructure--one that can respond to current antibacterial resistance now and anticipate evolving resistance. This challenge requires that industry, academia, the National Institutes of Health, the Food and Drug Administration, the Centers for Disease Control and Prevention, the US Department of Defense, and the new Biomedical Advanced Research and Development Authority at the Department of Health and Human Services work productively together. This report provides an update on potentially effective antibacterial drugs in the late-stage development pipeline, in the hope of encouraging such collaborative action.
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            Acinetobacter baumannii: emergence of a successful pathogen.

            Acinetobacter baumannii has emerged as a highly troublesome pathogen for many institutions globally. As a consequence of its immense ability to acquire or upregulate antibiotic drug resistance determinants, it has justifiably been propelled to the forefront of scientific attention. Apart from its predilection for the seriously ill within intensive care units, A. baumannii has more recently caused a range of infectious syndromes in military personnel injured in the Iraq and Afghanistan conflicts. This review details the significant advances that have been made in our understanding of this remarkable organism over the last 10 years, including current taxonomy and species identification, issues with susceptibility testing, mechanisms of antibiotic resistance, global epidemiology, clinical impact of infection, host-pathogen interactions, and infection control and therapeutic considerations.
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              • Record: found
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              Is Open Access

              List of Prokaryotic names with Standing in Nomenclature (LPSN) moves to the DSMZ

              The List of Prokaryotic names with Standing in Nomenclature (LPSN) was acquired in November 2019 by the DSMZ and was relaunched using an entirely new production system in February 2020. This article describes in detail the structure of the new site, navigation, page layout, search facilities and new features.
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                Author and article information

                Contributors
                Journal
                Curr Res Microb Sci
                Curr Res Microb Sci
                Current Research in Microbial Sciences
                Elsevier
                2666-5174
                28 March 2022
                2022
                28 March 2022
                : 3
                : 100131
                Affiliations
                [a ]ICMR-National Institute of Pathology, Safdarjung Hospital Campus, New Delhi, 110029, India
                [b ]Department of Biosciences, Jamia Millia Islamia, New Delhi, India
                Author notes
                [* ]Corresponding author.
                Article
                S2666-5174(22)00028-1 100131
                10.1016/j.crmicr.2022.100131
                9325880
                35909621
                43e6a2e7-f2d6-4d90-b07f-0a5f80697b5b
                © 2022 Published by Elsevier B.V.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                Categories
                Review Article

                biofilm formation,antibiotic resistance,therapeutic strategies,biofilm inhibition,biofilm eradication

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