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1. Bio-inspired synthesis of amino acids modified sulfated cellulose nanofibrils into multivalent viral inhibitors via the Mannich reaction.

Author

Hu S, Li Y, Yue F, Chen Y, and Qi H

Subjects
Cellulose, Sulfates, Arginine, Antiviral Agents, Sulfur Oxides, Amino Acids, Bacteriophages
Abstract

Virus cross-infection via surfaces poses a serious threat to public health. Inspired by natural sulfated polysaccharides and antiviral peptides, we prepared multivalent virus blocking nanomaterials by introducing amino acids to sulfated cellulose nanofibrils (SCNFs) via the Mannich reaction. The antiviral activity of the resulting amino acid-modified sulfated nanocellulose was significantly improved. Specifically, 1 h treatment with arginine modified SCNFs at a concentration of 0.1 g/mL led to a complete inactivation of the phage-X174 (reduction by more than three orders of magnitude). Atomic force microscope showed that amino acid-modified sulfated nanofibrils can bind phage-X174 to form linear clusters, thus preventing the virus from infecting the host. When we coated wrapping paper and the inside of a face-mask with our amino acid-modified SCNFs, phage-X174 was completely deactivated on the coated surfaces, demonstrating the potential of our approach for use in the packaging and personal protective equipment industries. This work provides an environmentally friendly and cost-efficient approach to fabricating multivalent nanomaterials for antiviral applications., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022. Published by Elsevier Ltd.)

Published
2023
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2. Effect of unassembled phage protein complexes on the attachment to cellulose of genetically modified bacteriophages containing cellulose binding modules.

Author

Li Z, Tolba M, Griffiths M, and van de Ven TG

Subjects
Binding Sites, Escherichia coli chemistry, Bacteriophages chemistry, Cellulose chemistry, Escherichia coli Proteins chemistry
Abstract

One way to make bioactive paper is to incorporate in it bacteriophages, which can capture and deactivate bacteria. The release of newly assembled phages from lysed bacteria can also serve as a measure of the number of bacteria that were deactivated. We have studied the deposition of genetically modified phages, containing cellulose binding modules, on model cellulose surfaces by evanescent wave light scattering. It was shown that unassembled protein complexes, released with the phages during the lysis of bacteria, limit the deposition of phages to about one per 10-20 microm2, as there are far more unassembled protein complexes than phages. The implication is that a few thousand phages can attach to a cellulose fiber, with most of the surface area taken up by protein complexes. This is more than sufficient for the production of bioactive paper. The unassembled protein complexes may be beneficial, as they will prevent non-specific deposition of bacteria. Thus, it may not be necessary to separate the protein complexes from phages in an expensive purification operation., (Copyright (c) 2010 Elsevier B.V. All rights reserved.)

Published
2010
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3. Taxonomy of prokaryotic viruses: 2017 update from the ICTV Bacterial and Archaeal Viruses Subcommittee

Author

Adriaenssens, Evelien M, Wittmann, Johannes, Kuhn, Jens H, Turner, Dann, Sullivan, Matthew B., Dutilh, Bas E, Jang, Ho Bin, van Zyl, Leonardo J, Klumpp, Jochen, Lobocka, Malgorzata, Moreno Switt, Andrea I, Rumnieks, Janis, Edwards, Robert A, Uchiyama, Jumpei, Alfenas-Zerbini, Poliane, Petty, Nicola K, Kropinski, Andrew M, Barylski, Jakub, Gillis, Annika, Clokie, Martha R C, Prangishvili, David, Lavigne, Rob, Aziz, Ramy Karam, Duffy, Siobain, Krupovic, Mart, Poranen, Minna M., Knezevic, Petar, Enault, Francois, Tong, Yigang, Oksanen, Hanna M., Rodney Brister, J, Sub Bioinformatics, Theoretical Biology and Bioinformatics, University of Liverpool, Leibniz-Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH / Leibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures (DSMZ), National Institute of Allergy and Infectious Diseases [Bethesda] (NIAID-NIH), National Institutes of Health [Bethesda] (NIH), University of the West of England [Bristol] (UWE Bristol), Ohio State University [Columbus] (OSU), Utrecht University [Utrecht], Radboud University Medical Center [Nijmegen], University of the Western Cape, Eidgenössische Technische Hochschule - Swiss Federal Institute of Technology [Zürich] (ETH Zürich), Polish Academy of Sciences (PAN), Universidad Andrés Bello - UNAB (CHILE), Latvian Biomedical Research and Study Centre [Rīga], San Diego State University (SDSU), Azabu University, Universidade Federal de Vicosa (UFV), iThree Institute, University of Technology Sydney (UTS), University of Guelph, Adam Mickiewicz University in Poznań (UAM), Université Catholique de Louvain = Catholic University of Louvain (UCL), University of Leicester, Biologie Moléculaire du Gène chez les Extrêmophiles (BMGE), Institut Pasteur [Paris], Catholic University of Leuven - Katholieke Universiteit Leuven (KU Leuven), Cairo University, University of Warwick [Coventry], University of Helsinki, University of Novi Sad, Laboratoire Microorganismes : Génome et Environnement (LMGE), Centre National de la Recherche Scientifique (CNRS)-Université Clermont Auvergne [2017-2020] (UCA [2017-2020]), Beijing Institute of Microbiology and Epidemiology, This work was funded in part through Battelle Memorial Institute’s prime contract with the US National Institute of Allergy and Infectious Diseases (NIAID) under Contract No. HHSN272200700016I (J.H.K.). B.E.D. was supported by the Netherlands Organization for Scientific Research (NWO), Vidi Grant 864.14.004. R.A.E was supported by grant MCB-1330800 from the National Science Foundation. J.R.B. was supported by the Intramural Research Program of the National Institutes of Health, National Library of Medicine. R.L. is a member of the phagebiotics research community, supported by FWO Vlaanderen. M.M.P. was supported by the Academy of Finland (272507). A.G. was supported by the National Fund for Scientific Research (FNRS). H.M.O. was supported by University of Helsinki funding for Instruct-F1 research infrastructure., The committee would like to thank Dr. Graham Hatfull (University of Pittsburgh) for permitting us to use Actinobacteriophage Database electron micrographs in 2017’s taxonomy proposals. The authors thank Laura Bollinger (National Institutes of Health/National Institute of Allergy and Infectious Diseases, Integrated Research Facility at Fort Detrick, Frederick, MD, USA) for editing this paper., University of the Western Cape (UWC), Universidad Andrés Bello [Santiago] (UNAB), Universidade Federal de Viçosa = Federal University of Viçosa (UFV), Institut Pasteur [Paris] (IP), Helsingin yliopisto = Helsingfors universitet = University of Helsinki, Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Centre National de la Recherche Scientifique (CNRS), UCL - SST/ELI/ELIM - Applied Microbiology, Sub Bioinformatics, and Theoretical Biology and Bioinformatics

Subjects
0301 basic medicine, Archaeal Viruses, viruses, [SDV]Life Sciences [q-bio], 030106 microbiology, education, Coronacrisis-Taverne, Zoology, Computational biology, Biology, [SDV.BID.SPT]Life Sciences [q-bio]/Biodiversity/Systematics, Phylogenetics and taxonomy, 03 medical and health sciences, Phylogenetics, Virology, MESH: Archaeal Viruses, Tumours of the digestive tract Radboud Institute for Molecular Life Sciences [Radboudumc 14], Bacteriophages, MESH: Bacteriophages, Virus classification, Taxonomy, General Medicine, 030104 developmental biology, [SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology, ICTV bacterial, Classification methods, Taxonomy (biology), Bacterial virus
Abstract

International audience; The prokaryotic virus community is represented at the International Committee on Taxonomy of Viruses (ICTV) by the Bacterial and Archaeal Viruses Subcommittee. Since our last report [5], the committee composition has changed, and a large number of taxonomic proposals (TaxoProps) were submitted to the ICTV Executive Committee (EC) for approval.

Published
2018
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