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      Cultivation-Free Typing of Bacteria Using Optical DNA Mapping

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          Abstract

          A variety of pathogenic bacteria can infect humans, and rapid species identification is crucial for the correct treatment. However, the identification process can often be time-consuming and depend on the cultivation of the bacterial pathogen(s). Here, we present a stand-alone, enzyme-free, optical DNA mapping assay capable of species identification by matching the intensity profiles of large DNA molecules to a database of fully assembled bacterial genomes (>10 000). The assay includes a new data analysis strategy as well as a general DNA extraction protocol for both Gram-negative and Gram-positive bacteria. We demonstrate that the assay is capable of identifying bacteria directly from uncultured clinical urine samples, as well as in mixtures, with the potential to be discriminative even at the subspecies level. We foresee that the assay has applications both within research laboratories and in clinical settings, where the time-consuming step of cultivation can be minimized or even completely avoided.

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          Most cited references36

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          Is Open Access

          Next-generation sequencing technologies and their application to the study and control of bacterial infections

          Background With the decreasing cost and efficiency of next generation sequencing, the technology is rapidly introduced into clinical and public health laboratory practice. Aims In this review, the historical background and principles of first, second and third generation sequencing are described as are the characteristics of the most commonly used sequencing instruments. Sources Peer reviewed literature, white papers and meeting reports. Content & implications Next generation sequencing is a technology that potentially could replace many traditional microbiological workflows, providing clinicians and public health specialists with more actionable information than hitherto achievable. Examples of the clinical and public health uses of the technology are provided. The challenge of comparability of different sequencing platforms is discussed. Finally, the future directions of the technology integrating it with laboratory management and public health surveillance systems, and moving it towards performing sequencing directly from the clinical specimen (metagenomics) could lead to yet another fundamental transformation of clinical diagnostics and public health surveillance.
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            Is Open Access

            Phylogenetically Novel Uncultured Microbial Cells Dominate Earth Microbiomes

            In the past few decades, it has become apparent that most of the microbial diversity on Earth has never been characterized in laboratory cultures. We show that these unknown microbes, sometimes called “microbial dark matter,” are numerically dominant in all major environments on Earth, with the exception of the human body, where most of the microbes have been cultured. We also estimate that about one-quarter of the population of microbial cells on Earth belong to phyla with no cultured relatives, suggesting that these never-before-studied organisms may be important for ecosystem functions.
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              Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time.

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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
                15 April 2020
                08 May 2020
                : 6
                : 5
                : 1076-1084
                Affiliations
                []Department of Biology and Biological Engineering, Chalmers University of Technology , Kemivägen 10, 412 96 Gothenburg, Sweden
                []Department of Mathematical Sciences, Chalmers University of Technology and the University of Gothenburg , 412 96 Gothenburg, Sweden
                [§ ]Systems and Data Analysis, Fraunhofer-Chalmers Centre , Chalmers Science Park, 412 88 Gothenburg, Sweden
                []Centre for Antibiotic Resistance Research, CARe, University of Gothenburg , Box 440, 405 30 Gothenburg, Sweden
                []Department of Medical Biochemistry and Microbiology, Uppsala University , Husargatan 3, Box 582, 751 23 Uppsala, Sweden
                [# ]Department of Astronomy and Theoretical Physics, Lund University , Sölvegatan 14A, 223 62 Lund, Sweden
                []Department of Laboratory Medicine, Karolinska Institutet , Alfred Nobels Allé 8, 141 86 Stockholm, Sweden
                []Department of Clinical Microbiology, Karolinska University Hospital , 171 76 Stockholm, Sweden
                Author notes
                Article
                10.1021/acsinfecdis.9b00464
                7304876
                32294378
                0cd33a44-f6ab-43f4-80b3-762e7e7bb6fc
                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
                : 27 November 2019
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                Custom metadata
                id9b00464
                id9b00464

                nanofluidics,optical dna mapping,diagnostics,bacteria,uti
                nanofluidics, optical dna mapping, diagnostics, bacteria, uti

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