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      Structural adaptation of fungal cell wall in hypersaline environment

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          Abstract

          Halophilic fungi thrive in hypersaline habitats and face a range of extreme conditions. These fungal species have gained considerable attention due to their potential applications in harsh industrial processes, such as bioremediation and fermentation under unfavorable conditions of hypersalinity, low water activity, and extreme pH. However, the role of the cell wall in surviving these environmental conditions remains unclear. Here we employ solid-state NMR spectroscopy to compare the cell wall architecture of Aspergillus sydowii across salinity gradients. Analyses of intact cells reveal that A. sydowii cell walls contain a rigid core comprising chitin, β-glucan, and chitosan, shielded by a surface shell composed of galactomannan and galactosaminogalactan. When exposed to hypersaline conditions, A. sydowii enhances chitin biosynthesis and incorporates α-glucan to create thick, stiff, and hydrophobic cell walls. Such structural rearrangements enable the fungus to adapt to both hypersaline and salt-deprived conditions, providing a robust mechanism for withstanding external stress. These molecular principles can aid in the optimization of halophilic strains for biotechnology applications.

          Abstract

          Solid-state NMR snapshots of Aspergillus sydowii and other halophilic fungal species reveal the structural rearrangement of polysaccharides and proteins, which create a thick, stiff and hydrophobic cell wall to withstand external stress and thrive in hypersaline environment

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          Life in extreme environments.

          Each recent report of liquid water existing elsewhere in the Solar System has reverberated through the international press and excited the imagination of humankind. Why? Because in the past few decades we have come to realize that where there is liquid water on Earth, virtually no matter what the physical conditions, there is life. What we previously thought of as insurmountable physical and chemical barriers to life, we now see as yet another niche harbouring 'extremophiles'. This realization, coupled with new data on the survival of microbes in the space environment and modelling of the potential for transfer of life between celestial bodies, suggests that life could be more common than previously thought. Here we examine critically what it means to be an extremophile, and the implications of this for evolution, biotechnology and especially the search for life in the Universe.
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            Aspergillus fumigatus and Aspergillosis in 2019

            Aspergillus fumigatus is a saprotrophic fungus; its primary habitat is the soil. In its ecological niche, the fungus has learned how to adapt and proliferate in hostile environments. This capacity has helped the fungus to resist and survive against human host defenses and, further, to be responsible for one of the most devastating lung infections in terms of morbidity and mortality. In this review, we will provide (i) a description of the biological cycle of A. fumigatus ; (ii) a historical perspective of the spectrum of aspergillus disease and the current epidemiological status of these infections; (iii) an analysis of the modes of immune response against Aspergillus in immunocompetent and immunocompromised patients; (iv) an understanding of the pathways responsible for fungal virulence and their host molecular targets, with a specific focus on the cell wall; (v) the current status of the diagnosis of different clinical syndromes; and (vi) an overview of the available antifungal armamentarium and the therapeutic strategies in the clinical context. In addition, the emergence of new concepts, such as nutritional immunity and the integration and rewiring of multiple fungal metabolic activities occurring during lung invasion, has helped us to redefine the opportunistic pathogenesis of A. fumigatus .
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              The cell wall: a carbohydrate armour for the fungal cell.

              The cell wall is composed of a polysaccharide-based three-dimensional network. Considered for a long time as an inert exoskeleton, the cell wall is now seen as a dynamic structure that is continuously changing as a result of the modification of culture conditions and environmental stresses. Although the cell wall composition varies among fungal species, chemogenomic comparative analysis have led to a better understanding of the genes and mechanisms involved in the construction of the common central core composed of branched beta1,3 glucan-chitin. Because of its essential biological role, unique biochemistry and structural organization and the absence in mammalian cells of most of its constitutive components, the cell wall is an attractive target for the development of new antifungal agents. Genomic as well as drug studies have shown that the death of the fungus can result from inhibition of cell wall polysaccharide synthases. To date, only beta1,3 glucan synthase inhibitors have been launched clinically and many more targets remain to be explored.
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                Author and article information

                Contributors
                rabg@uaem.mx
                wangtuo1@msu.edu
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                4 November 2023
                4 November 2023
                2023
                : 14
                : 7082
                Affiliations
                [1 ]Department of Chemistry, Michigan State University, ( https://ror.org/05hs6h993) East Lansing, MI USA
                [2 ]Centro de Investigación en Dinámica Celular, Universidad Autónoma del Estado de Morelos, ( https://ror.org/03rzb4f20) Cuernavaca, Mexico
                [3 ]GRID grid.436923.9, ISNI 0000 0004 0373 6523, Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, ; Richland, WA USA
                [4 ]Department of Biology, University of Ljubljana, ( https://ror.org/05njb9z20) Ljubljana, Slovenia
                [5 ]GRID grid.8127.c, ISNI 0000 0004 0576 3437, Institute of Molecular Biology and Biotechnology, , University of Crete, ; Heraklion, Greece
                [6 ]Fungal Respiratory Infections Research Unit, University of Angers, ( https://ror.org/04yrqp957) Angers, France
                [7 ]GRID grid.213876.9, ISNI 0000 0004 1936 738X, Present Address: Complex Carbohydrate Research Center, , University of Georgia, ; Athens, GA 30602 USA
                [8 ]Present Address: Department of Chemistry, University of Michigan, ( https://ror.org/00jmfr291) Ann Arbor, MI 48109 USA
                Author information
                http://orcid.org/0000-0002-0254-2239
                http://orcid.org/0000-0002-0170-3221
                http://orcid.org/0000-0003-4937-4145
                http://orcid.org/0000-0002-9464-3263
                http://orcid.org/0000-0002-1032-0767
                http://orcid.org/0000-0002-1801-924X
                Article
                42693
                10.1038/s41467-023-42693-6
                10625518
                37925437
                5e3df442-ca02-41d9-8072-71d183a42e79
                © The Author(s) 2023

                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 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
                : 25 April 2023
                : 18 October 2023
                Funding
                Funded by: FundRef https://doi.org/10.13039/100000002, U.S. Department of Health & Human Services | National Institutes of Health (NIH);
                Award ID: AI173270
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/100000015, U.S. Department of Energy (DOE);
                Award ID: DE-AC05-76RL01830
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/501100004329, Javna Agencija za Raziskovalno Dejavnost RS (Slovenian Research Agency);
                Award ID: P4-0432
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/501100007350, Consejo Nacional de Ciencia y Tecnología (CONCYT);
                Award ID: CB-285816
                Award Recipient :
                Categories
                Article
                Custom metadata
                © Springer Nature Limited 2023

                Uncategorized
                fungal biology,solid-state nmr,polysaccharides,fungi
                Uncategorized
                fungal biology, solid-state nmr, polysaccharides, fungi

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