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      Eggshell spheres protect brown widow spider ( Latrodectus geometricus ) eggs from bacterial infection

      1 , 1 , 2 , 3
      Journal of The Royal Society Interface
      The Royal Society

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          Abstract

          Eggs provide a rich source of nutrients for the developing embryo, making them a favoured food source for other organisms as well. Several defence mechanisms have evolved to protect the developing embryos against microbial threats. In this article, we elucidate the defence strategy of brown widow spider ( Latrodectus geometricus ) eggs against bacteria. Antibacterial activity was shown by inhibition of bacterial growth on agar plate, liquid culture and retarded biofilm formation. The defence strategy against bacterial invasion was demonstrated in the whole egg, whole egg extract, egg surface extract, eggshell and eggshell extract. The source and characteristics of this antibacterial activity are distinctive and stem in part from a dense layer of spheres covering the egg surface, likely originated from the oviposition fluid. The spheres are rich in low-molecular-weight proteins, yet their exact composition remains unknown. In this study, we demonstrate that the egg surface is hydrophobic, while the spheres are superhydrophilic. Egg surface roughness and hydrophobicity combined with its antibacterial chemical properties reduce the ability of bacteria to grow on the egg surface. Understanding the properties of these unique structures may contribute significantly to our knowledge of how nature deals with bacterial infections.

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          Microtiter plate assay for assessment of Listeria monocytogenes biofilm formation.

          Listeria monocytogenes has the ability to form biofilms on food-processing surfaces, potentially leading to food product contamination. The objective of this research was to standardize a polyvinyl chloride (PVC) microtiter plate assay to compare the ability of L. monocytogenes strains to form biofilms. A total of 31 coded L. monocytogenes strains were grown in defined medium (modified Welshimer's broth) at 32 degrees C for 20 and 40 h in PVC microtiter plate wells. Biofilm formation was indirectly assessed by staining with 1% crystal violet and measuring crystal violet absorbance, using destaining solution. Cellular growth rates and final cell densities did not correlate with biofilm formation, indicating that differences in biofilm formation under the same environmental conditions were not due to growth rate differences. The mean biofilm production of lineage I strains was significantly greater than that observed for lineage II and lineage III strains. The results from the standardized microtiter plate biofilm assay were also compared to biofilm formation on PVC and stainless steel as assayed by quantitative epifluorescence microscopy. Results showed similar trends for the microscopic and microtiter plate assays, indicating that the PVC microtiter plate assay can be used as a rapid, simple method to screen for differences in biofilm production between strains or growth conditions prior to performing labor-intensive microscopic analyses.
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            Bioinspired self-cleaning surfaces with superhydrophobicity, superoleophobicity, and superhydrophilicity

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              Surface characteristics influencing bacterial adhesion to polymeric substrates

              Effective surface area on rough substrates for bacterial adhesion is examined by analyzing the solid area fraction of surfaces, where the bacterial medium is in contact with the solid surface. Superhydrophobic surfaces have been reported to reduce bacterial adhesion, but interactions between bacterial media and solid surfaces at the interface have rarely been associated with the solid area fraction ( f ) from the Cassie–Baxter wetting state. This study aimed to investigate the effective surface area for bacterial adhesion by analyzing the solid area fraction of surfaces where the bacterial medium is in contact with a solid surface. Also, the self-cleaning ability of the superhydrophobic surface against adhered bacteria was examined. The influences of roughness, surface energy, entrapped air, and surface charge of substrate materials on bacterial adhesion were examined, and the critical surface characteristics that are conducive to reducing Escherichia coli adherence to polymeric surfaces were determined. Moderate hydrophobicity with water contact angle of about 90° produced the highest level of bacterial adhesion. Entrapped air at the interface of superhydrophobic surfaces interfered with the direct contact of bacteria to solid surfaces, leading to less bacterial adhesion. The superhydrophobic surface with a reduced solid area fraction displayed self-cleaning ability, where initially-adhered bacteria were removed by washing. The superhydrophilic substrate with negative zeta potential exhibited limited bacterial binding, due to the reduced hydrophobic interaction and possible repulsive interaction between bacteria and surface. The findings of this study can be utilized for an effective surface design to circumvent bacterial adhesion as an alternative solution to using antibiotics.
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                Author and article information

                Journal
                Journal of The Royal Society Interface
                J. R. Soc. Interface
                The Royal Society
                1742-5689
                1742-5662
                January 02 2019
                January 31 2019
                January 09 2019
                January 31 2019
                : 16
                : 150
                : 20180581
                Affiliations
                [1 ]Department of Environmental Hydrology and Microbiology, Zuckerberg Institute for Water Research, Blaustein Institutes for Desert Research, Ben-Gurion University, Midreshet Ben-Gurion, Israel
                [2 ]Marco and Louise Mitrani Department of Desert Ecology, Blaustein Institutes for Desert Research, Ben-Gurion University, Midreshet Ben-Gurion, Israel
                [3 ]Avram and Stella Goldstein–Goren Department of Biotechnology Engineering, Ben-Gurion University, Beer Sheva, Israel
                Article
                10.1098/rsif.2018.0581
                6364662
                30958158
                4aabee42-f093-4ba1-8066-da778a9ab5dd
                © 2019

                https://royalsociety.org/-/media/journals/author/Licence-to-Publish-20062019-final.pdf

                https://royalsociety.org/journals/ethics-policies/data-sharing-mining/

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