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      In vitro passage alters virulence, immune activation and proteomic profiles of Burkholderia pseudomallei

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          Abstract

          Serial passage is a problem among many bacterial species, especially those where strains have been stored (banked) for several decades. Prior to banking with an organization such as ATCC, many bacterial strains were passaged for many years, so the characteristics of each strain may be extremely different. This is in addition to any differences in the original host environment. For Burkholderia pseudomallei, the number of serial passages should be carefully defined for each experiment because it undergoes adaptation during the course of serial passages. In the present study, we found that passaged B. pseudomallei fresh clinical isolates and reference strain in Luria-Bertani broth exhibited increased plaque formation, invasion, intracellular replication, Galleria mellonella killing abilities, and cytokine production of host cells. These bacteria also modulated proteomic profiles during in vitro passage. We presume that the modulation of protein expression during in vitro passage caused changes in virulence and immunogenicity phenotypes. Therefore, we emphasize the need for caution regarding the use of data from passaged B. pseudomallei. These findings of phenotypic adaptation during in vitro serial passage can help researchers working on B. pseudomallei and on other species to better understand disparate findings among strains that have been reported for many years.

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          Carbon metabolism of intracellular bacterial pathogens and possible links to virulence.

          New technologies such as high-throughput methods and 13C-isotopologue-profiling analysis are beginning to provide us with insight into the in vivo metabolism of microorganisms, especially in the host cell compartments that are colonized by intracellular bacterial pathogens. In this Review, we discuss the recent progress made in determining the major carbon sources and metabolic pathways used by model intracellular bacterial pathogens that replicate either in the cytosol or in vacuoles of infected host cells. Furthermore, we highlight the possible links between intracellular carbon metabolism and the expression of virulence genes.
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            Metabolic adaptation of human pathogenic and related nonpathogenic bacteria to extra- and intracellular habitats.

            Most bacteria pathogenic for humans have closely related nonpathogenic counterparts that live as saprophytes, commensals or even symbionts (mutualists) in similar or different habitats. The knowledge of how these bacteria adapt their metabolism to the preferred habitats is critical for our understanding of pathogenesis, commensalism and symbiosis, and - in the case of bacterial pathogens - could help to identify targets for new antimicrobial agents. The focus of this review is on the metabolic potentials and adaptations of three different groups of human extra- and intracellular bacterial pathogens and their nonpathogenic relatives. All bacteria selected have the potential to reach the interior of mammalian host cells. However, their ability to replicate intracellularly differs significantly. The question therefore arises whether there are specific metabolic requirements that support stable intracellular replication. Furthermore, we discuss - whenever relevant data for the pathogenic representatives are available - the possible effect of the metabolism on the expression of virulence genes. © 2011 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. All rights reserved.
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              Bacterial serine/threonine protein kinases in host-pathogen interactions.

              In bacterial pathogenesis, monitoring and adapting to the dynamically changing environment in the host and an ability to disrupt host immune responses are critical. The virulence determinants of pathogenic bacteria include the sensor/signaling proteins of the serine/threonine protein kinase (STPK) family that have a dual role of sensing the environment and subverting specific host defense processes. STPKs can sense a wide range of signals and coordinate multiple cellular processes to mount an appropriate response. Here, we review some of the well studied bacterial STPKs that are essential virulence factors and that modify global host responses during infection.
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                Author and article information

                Contributors
                pornpan.pum@mahidol.ac.th
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                20 May 2020
                20 May 2020
                2020
                : 10
                : 8320
                Affiliations
                [1 ]ISNI 0000 0004 1937 0490, GRID grid.10223.32, Department of Microbiology and Immunology, , Faculty of Tropical Medicine, Mahidol University, ; Bangkok, Thailand
                [2 ]ISNI 0000 0001 0944 049X, GRID grid.9723.f, Department of Companion Animal Clinical Sciences, , Faculty of Veterinary Medicine, Kasetsart University, ; Bangkok, Thailand
                [3 ]ISNI 0000 0004 1937 0490, GRID grid.10223.32, Department of Molecular Tropical Medicine and Genetics, , Faculty of Tropical Medicine, Mahidol University, ; Bangkok, Thailand
                [4 ]ISNI 0000 0004 1937 0490, GRID grid.10223.32, Faculty of Veterinary Science, Veterinary Diagnostic Center, Mahidol University, ; Nakhon Pathom, Thailand
                [5 ]ISNI 0000 0004 5936 4917, GRID grid.501272.3, Mahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, ; Bangkok, Thailand
                [6 ]ISNI 0000 0004 1937 0490, GRID grid.10223.32, Department of Tropical Hygiene, Faculty of Tropical Medicine, Mahidol University, ; Bangkok, Thailand
                Article
                64914
                10.1038/s41598-020-64914-4
                7239947
                32433516
                3dd5c900-62ee-4181-ab66-5d9cad49cc2a
                © The Author(s) 2020

                Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 21 November 2019
                : 27 February 2020
                Categories
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                Custom metadata
                © The Author(s) 2020

                Uncategorized
                bacteria,molecular biology
                Uncategorized
                bacteria, molecular biology

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