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      Cross-kingdom signalling regulates spore germination in the moss Physcomitrella patens

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          Abstract

          Plants live in close association with microorganisms that can have beneficial or detrimental effects. The activity of bacteria in association with flowering plants has been extensively analysed. Bacteria use quorum-sensing as a way of monitoring their population density and interacting with their environment. A key group of quorum sensing molecules in Gram-negative bacteria are the N-acylhomoserine lactones (AHLs), which are known to affect the growth and development of both flowering plants, including crops, and marine algae. Thus, AHLs have potentially important roles in agriculture and aquaculture. Nothing is known about the effects of AHLs on the earliest-diverging land plants, thus the evolution of AHL-mediated bacterial-plant/algal interactions is unknown. In this paper, we show that AHLs can affect spore germination in a representative of the earliest plants on land, the Bryophyte moss Physcomitrella patens. Furthermore, we demonstrate that sporophytes of some wild isolates of Physcomitrella patens are associated with AHL-producing bacteria.

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          Speak, friend, and enter: signalling systems that promote beneficial symbiotic associations in plants.

          Plants associate with a wide range of microorganisms, with both detrimental and beneficial outcomes. Central to plant survival is the ability to recognize invading microorganisms and either limit their intrusion, in the case of pathogens, or promote the association, in the case of symbionts. To aid in this recognition process, elaborate communication and counter-communication systems have been established that determine the degree of ingress of the microorganism into the host plant. In this Review, I describe the common signalling processes used by plants during mutualistic interactions with microorganisms as diverse as arbuscular mycorrhizal fungi and rhizobial bacteria.
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            Progress in and promise of bacterial quorum sensing research

            This Review highlights how we can build upon the relatively new and rapidly developing field of research into bacterial quorum sensing (QS). We now have a depth of knowledge about how bacteria use QS signals to communicate with each other and to coordinate their activities.
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              Quorum sensing and environmental adaptation in Pseudomonas aeruginosa: a tale of regulatory networks and multifunctional signal molecules.

              Bacteria employ sophisticated cell-to-cell communication or 'quorum sensing' (QS) systems for promoting collective behaviours that depend on the actions of one or more chemically distinct diffusible signal molecules. As determinants of cell population density, multiple QS systems are often integrated with each other and within global regulatory networks and subject to the prevailing environmental conditions as well as the presence and activities of other organisms. QS signal molecules, although largely considered as effectors of QS-dependent gene expression are also emerging as multifunctional molecules that influence life, development and death in single and mixed microbial populations and impact significantly the outcome of host-pathogen interactions.
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                Author and article information

                Contributors
                Miguel.camara@nottingham.ac.uk
                j.c.coates@bham.ac.uk
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                13 February 2020
                13 February 2020
                2020
                : 10
                : 2614
                Affiliations
                [1 ]ISNI 0000 0004 1936 7486, GRID grid.6572.6, School of Biosciences, , University of Birmingham, ; Edgbaston, Birmingham UK
                [2 ]University Centre Shrewsbury, Guildhall, Frankwell Quay, Shrewsbury, Shropshire UK
                [3 ]ISNI 0000 0001 0075 5874, GRID grid.7892.4, Karlsruhe Institute of Technology, ; Karlsruhe, Baden-Württemberg Germany
                [4 ]ISNI 0000000096069301, GRID grid.10837.3d, School of Life, Health and Chemical Sciences, , Open University, Walton Hall, Kents Hill, ; Milton Keynes, UK
                [5 ]ISNI 0000 0004 1936 8868, GRID grid.4563.4, National Biofilm Innovations Centre, University of Nottingham Biodiscovery Institute, School of Life Sciences, University of Nottingham, University Park, ; Nottingham, UK
                [6 ]ISNI 0000 0001 0743 511X, GRID grid.440785.a, Institute of Life Sciences, , Jiangsu University, ; Zhenjiang, China
                Article
                59467
                10.1038/s41598-020-59467-5
                7018845
                32054953
                00c8e456-1427-4217-9c91-13c8f5783df7
                © 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
                : 11 November 2019
                : 17 January 2020
                Categories
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                © The Author(s) 2020

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                plant development,plant evolution,plant reproduction,plant sciences,environmental microbiology

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