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      Heteroaggregation of an enveloped bacteriophage with colloidal sediments and effect on virus viability

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          Abstract

          Four sediments in the colloidal size range: goethite, montmorillonite, illite, and kaolinite, were suspended with the bacteriophage φ6, a model enveloped virus, to determine relative rates of heteroaggregation and the effect of aggregation on virus viability. Turbidity was measured on combinations of virus and each sediment type at low concentration to determine aggregation rates. Aggregation of sediment with virus occurred regardless of mineral type, and larger fraction of virus is expected to aggregate with increasing sediment concentration leading to higher deposition rates. The negatively charged sediments, aggregated with φ6 (also negatively charged at neutral pH) at a faster rate than the positively charged sediments, yielding turbidity slopes of 4.94 × 10 −3 s −1 and 7.50 × 10 −4 s −1 for φ6-montmorillonite and φ6-illite aggregates, respectively, and 2.98 × 10 −5 s −1 and 2.84 × 10 −5 s −1, for φ6-goethite and φ6-kaolinite, respectively. This indicates that the interaction between sediments and virus is hydrophobic, rather than electrostatic. Large numbers of virions remained viable post-aggregation, despite the fragility of the viral envelope, indicating that small-sized aggregates, which may travel more readily through porous media, may pose an infection risk. The fraction of φ6 that remained viable varied with sediment type, with montmorillonite-φ6 aggregates experiencing the greatest reduction in infectivity at 35%. TEM analyses reveal that in all sediment-φ6 combinations, infectivity loss was likely due to disassembly of the viral envelope as a result of aggregation.

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          Highlights

          • Sediments interact with enveloped viruses but effects on viability are unknown.

          • Light scattering measured aggregation rates of virus with four mineral types.

          • Heteroaggregation was hydrophobic and faster with negatively-charged sediments.

          • The greatest reduction in infectivity occurred in virus-montmorillonite aggregates.

          • Aggregation with sediment caused virus disassembly and infectivity loss.

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          Most cited references45

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          Acid—base interfacial interactions in aqueous media

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            Analysis of bacteriophage T7 early RNAs and proteins on slab gels.

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              Persistence of avian influenza viruses in water.

              Persistence of five avian influenza viruses (AIVs) derived from four waterfowl species in Louisiana and representing five hemagglutinin and neuraminidase subtypes was determined in distilled water at 17 C and 28 C. Infectivity was determined over 60 days by microtiter endpoint titration. One AIV was tested over 91 days at 4 C. Linear regression models for these viruses predicted that an initial concentration of 1 x 10(6) TCID50/ml water could remain infective for up to 207 days at 17 C and up to 102 days at 28 C. Significant differences in slopes for AIV persistence models were detected between treatment temperatures and among viruses. Results suggest that these viruses are adapted to transmission on waterfowl wintering habitats. Results also suggest a potential risk associated with waterfowl and domestic poultry sharing a common water source.
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                Author and article information

                Contributors
                Journal
                Sci Total Environ
                Sci. Total Environ
                The Science of the Total Environment
                Elsevier B.V.
                0048-9697
                1879-1026
                7 May 2018
                1 October 2018
                7 May 2018
                : 637
                : 104-111
                Affiliations
                [a ]Department of Physics Department of Earth and Atmospheric Science, The City College of New York, 160 Convent Ave., New York, NY 10031, United States
                [b ]Department of Earth and Atmospheric Science, The City College of New York, 160 Convent Ave., New York, NY 10031, United States
                [c ]Sophie Davis School of Biomedical Education, The City College of New York, 160 Convent Ave., New York, NY 10031, United States
                [d ]Department of Physics, Fairfield University, Fairfield, CT 06824, United States
                Author notes
                [* ]Corresponding author. kblock@ 123456ccny.cuny.edu
                Article
                S0048-9697(18)31624-3
                10.1016/j.scitotenv.2018.04.425
                7112063
                29747115
                c15714e5-afcf-4755-a15a-745838922535
                © 2018 Elsevier B.V. All rights reserved.

                Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

                History
                : 16 March 2018
                : 27 April 2018
                : 30 April 2018
                Categories
                Article

                General environmental science
                virus,bacteriophage,clay minerals,montmorillonite,aggregation
                General environmental science
                virus, bacteriophage, clay minerals, montmorillonite, aggregation

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