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      Intestinal colonization with multidrug-resistant Enterobacterales: screening, epidemiology, clinical impact, and strategies to decolonize carriers

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          Abstract

          The clinical impact of infections due to extended-spectrum β-lactamase (ESBL)- and/or carbapenemase-producing Enterobacterales ( Ent) has reached dramatic levels worldwide. Infections due to these multidrug-resistant (MDR) pathogens—especially Escherichia coli and Klebsiella pneumoniae—may originate from a prior asymptomatic intestinal colonization that could also favor transmission to other subjects. It is therefore desirable that gut carriers are rapidly identified to try preventing both the occurrence of serious endogenous infections and potential transmission. Together with the infection prevention and control countermeasures, any strategy capable of effectively eradicating the MDR- Ent from the intestinal tract would be desirable. In this narrative review, we present a summary of the different aspects linked to the intestinal colonization due to MDR- Ent. In particular, culture- and molecular-based screening techniques to identify carriers, data on prevalence and risk factors in different populations, clinical impact, length of colonization, and contribution to transmission in various settings will be overviewed. We will also discuss the standard strategies (selective digestive decontamination, fecal microbiota transplant) and those still in development (bacteriophages, probiotics, microcins, and CRISPR-Cas-based) that might be used to decolonize MDR- Ent carriers.

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          Drug-Resistant E. coli Bacteremia Transmitted by Fecal Microbiota Transplant

          Fecal microbiota transplantation (FMT) is an emerging therapy for recurrent or refractory Clostridioides difficile infection and is being actively investigated for other conditions. We describe two patients in whom extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli bacteremia occurred after they had undergone FMT in two independent clinical trials; both cases were linked to the same stool donor by means of genomic sequencing. One of the patients died. Enhanced donor screening to limit the transmission of microorganisms that could lead to adverse infectious events and continued vigilance to define the benefits and risks of FMT across different patient populations are warranted.
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            Polymyxins: Antibacterial Activity, Susceptibility Testing, and Resistance Mechanisms Encoded by Plasmids or Chromosomes.

            SUMMARYPolymyxins are well-established antibiotics that have recently regained significant interest as a consequence of the increasing incidence of infections due to multidrug-resistant Gram-negative bacteria. Colistin and polymyxin B are being seriously reconsidered as last-resort antibiotics in many areas where multidrug resistance is observed in clinical medicine. In parallel, the heavy use of polymyxins in veterinary medicine is currently being reconsidered due to increased reports of polymyxin-resistant bacteria. Susceptibility testing is challenging with polymyxins, and currently available techniques are presented here. Genotypic and phenotypic methods that provide relevant information for diagnostic laboratories are presented. This review also presents recent works in relation to recently identified mechanisms of polymyxin resistance, including chromosomally encoded resistance traits as well as the recently identified plasmid-encoded polymyxin resistance determinant MCR-1. Epidemiological features summarizing the current knowledge in that field are presented.
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              A century of the phage: past, present and future.

              Viruses that infect bacteria (bacteriophages; also known as phages) were discovered 100 years ago. Since then, phage research has transformed fundamental and translational biosciences. For example, phages were crucial in establishing the central dogma of molecular biology - information is sequentially passed from DNA to RNA to proteins - and they have been shown to have major roles in ecosystems, and help drive bacterial evolution and virulence. Furthermore, phage research has provided many techniques and reagents that underpin modern biology - from sequencing and genome engineering to the recent discovery and exploitation of CRISPR-Cas phage resistance systems. In this Timeline, we discuss a century of phage research and its impact on basic and applied biology.
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                Author and article information

                Contributors
                andrea.endimiani@unibe.ch , aendimiani@gmail.com
                Journal
                Eur J Clin Microbiol Infect Dis
                Eur J Clin Microbiol Infect Dis
                European Journal of Clinical Microbiology & Infectious Diseases
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0934-9723
                1435-4373
                21 January 2023
                21 January 2023
                2023
                : 42
                : 3
                : 229-254
                Affiliations
                [1 ]GRID grid.5734.5, ISNI 0000 0001 0726 5157, Institute for Infectious Diseases, , University of Bern, ; Bern, Switzerland
                [2 ]GRID grid.5734.5, ISNI 0000 0001 0726 5157, Graduate School of Cellular and Biomedical Sciences, , University of Bern, ; Bern, Switzerland
                [3 ]GRID grid.411230.5, ISNI 0000 0000 9296 6873, Department of Microbiology, School of Medicine, , Ahvaz Jundishapur University of Medical Sciences, ; Ahvaz, Iran
                [4 ]GRID grid.411230.5, ISNI 0000 0000 9296 6873, Infectious and Tropical Diseases Research Center, , Health Research Institute, Ahvaz Jundishapur University of Medical Sciences, ; Ahvaz, Iran
                [5 ]GRID grid.411463.5, ISNI 0000 0001 0706 2472, Department of Computer Engineering and Information Technology, , Islamic Azad University Tehran Central Branch, ; Tehran, Iran
                [6 ]GRID grid.7400.3, ISNI 0000 0004 1937 0650, Institute of Medical Virology, , University of Zurich, ; Zurich, Switzerland
                Author information
                http://orcid.org/0000-0003-3186-5421
                Article
                4548
                10.1007/s10096-023-04548-2
                9899200
                36680641
                cd7dc0da-54f2-4a46-8982-e733ac1911ef
                © The Author(s) 2023

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 12 October 2022
                : 11 January 2023
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001711, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung;
                Award ID: 192514
                Award ID: 206400
                Award Recipient :
                Funded by: University of Bern
                Categories
                Review
                Custom metadata
                © Springer-Verlag GmbH Germany, part of Springer Nature 2023

                Infectious disease & Microbiology
                esbl,sdd,fmt,bacteriophages,probiotics,microcins
                Infectious disease & Microbiology
                esbl, sdd, fmt, bacteriophages, probiotics, microcins

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