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      Counteraction of Biofilm Formation and Antimicrobial Potential of Terminalia catappa Functionalized Silver Nanoparticles against Candida albicans and Multidrug-Resistant Gram-Negative and Gram-Positive Bacteria

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          Abstract

          Biofilms not only protect bacteria and Candida species from antibiotics, but they also promote the emergence of drug-resistant strains, making eradication more challenging. As a result, novel antimicrobial agents to counteract biofilm formation are desperately needed. In this study, Terminalia catappa leaf extract (TCE) was used to optimize the TCE-capped silver nanoparticles (TCE-AgNPs) via a one-pot single-step method. Varied concentrations of TCE have yielded different sized AgNPs. The physico-chemical characterization of TCE-AgNPs using UV-Vis, SEM, TEM, FTIR, and Raman spectroscopy have confirmed the formation of nanostructures, their shape and size and plausible role of TCE bio-active compounds, most likely involved in the synthesis as well as stabilization of NPs, respectively. TCE-AgNPs have been tested for antibiofilm and antimicrobial activity against multidrug-resistant Pseudomonas aeruginosa (MDR-PA), methicillin-resistant Staphylococcus aureus (MRSA), and Candida albicans using various microbiological protocols. TCE-Ag-NPs−3 significantly inhibits biofilm formation of MDR-PA, MRSA, and C. albicans by 73.7, 69.56, and 63.63%, respectively, at a concentration of 7.8 µg/mL, as determined by crystal violet microtiter assay. Furthermore, SEM micrograph shows that TCE-AgNPs significantly inhibit the colonization and adherence of biofilm forming cells; individual cells with loss of cell wall and membrane integrity were also observed, suggesting that the biofilm architecture and EPS matrix were severely damaged. Moreover, TEM and SEM images showed that TCE-AgNPs brutally damaged the cell wall and membranes of MDR-PA, MRSA, and C. albicans. Additionally, extreme ultrastructural changes such as deformation, disintegration, and separation of cell wall and membrane from the cells, have also been observed, indicating significant loss of membrane and cell wall integrity, which eventually led to cell death. Overall, the research revealed a simple, environmentally friendly, and low-cost method for producing colloidal TCE-AgNPs with promising applications in advanced clinical settings against broad-spectrum biofilm-forming antibiotic-resistant bacteria and candida strains.

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          Does the antibacterial activity of silver nanoparticles depend on the shape of the nanoparticle? A study of the Gram-negative bacterium Escherichia coli.

          In this work we investigated the antibacterial properties of differently shaped silver nanoparticles against the gram-negative bacterium Escherichia coli, both in liquid systems and on agar plates. Energy-filtering transmission electron microscopy images revealed considerable changes in the cell membranes upon treatment, resulting in cell death. Truncated triangular silver nanoplates with a {111} lattice plane as the basal plane displayed the strongest biocidal action, compared with spherical and rod-shaped nanoparticles and with Ag(+) (in the form of AgNO(3)). It is proposed that nanoscale size and the presence of a {111} plane combine to promote this biocidal property. To our knowledge, this is the first comparative study on the bactericidal properties of silver nanoparticles of different shapes, and our results demonstrate that silver nanoparticles undergo a shape-dependent interaction with the gram-negative organism E. coli.
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            A review of the antibacterial effects of silver nanomaterials and potential implications for human health and the environment

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              Bacterial Extracellular Polysaccharides in Biofilm Formation and Function.

              Microbes produce a biofilm matrix consisting of proteins, extracellular DNA, and polysaccharides that is integral in the formation of bacterial communities. Historical studies of polysaccharides revealed that their overproduction often alters the colony morphology and can be diagnostic in identifying certain species. The polysaccharide component of the matrix can provide many diverse benefits to the cells in the biofilm, including adhesion, protection, and structure. Aggregative polysaccharides act as molecular glue, allowing the bacterial cells to adhere to each other as well as surfaces. Adhesion facilitates the colonization of both biotic and abiotic surfaces by allowing the bacteria to resist physical stresses imposed by fluid movement that could separate the cells from a nutrient source. Polysaccharides can also provide protection from a wide range of stresses, such as desiccation, immune effectors, and predators such as phagocytic cells and amoebae. Finally, polysaccharides can provide structure to biofilms, allowing stratification of the bacterial community and establishing gradients of nutrients and waste products. This can be advantageous for the bacteria by establishing a heterogeneous population that is prepared to endure stresses created by the rapidly changing environments that many bacteria encounter. The diverse range of polysaccharide structures, properties, and roles highlight the importance of this matrix constituent to the successful adaptation of bacteria to nearly every niche. Here, we present an overview of the current knowledge regarding the diversity and benefits that polysaccharide production provides to bacterial communities within biofilms.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Antibiotics (Basel)
                Antibiotics (Basel)
                antibiotics
                Antibiotics
                MDPI
                2079-6382
                16 June 2021
                June 2021
                : 10
                : 6
                : 725
                Affiliations
                [1 ]Department of Epidemic Disease Research, Institute for Research & Medical Consultations (IRMC), Imam Abdulrahman Bin Faisal University, Dammam 31441, Saudi Arabia; maansari@ 123456iau.edu.sa
                [2 ]Department of Chemistry, Faculty of Science, King Khalid University, Abha 61413, Saudi Arabia; agsehemi@ 123456kku.edu.sa
                [3 ]Research Center for Advanced Materials Science (RCAMS), King Khalid University, Abha 61413, Saudi Arabia
                [4 ]National Centre for Biotechnology, King Abdulaziz City for Science and Technology (KACST), Riyadh 11442, Saudi Arabia; malomary@ 123456kacst.edu.sa (M.N.A.); salyahya@ 123456kacst.edu.sa (S.A.)
                [5 ]Department of Chemistry, Faculty of Science, University of Allahabad, Allahabad 211001, Uttar Pradesh, India; mohdkashifaziz@ 123456allduni.ac.in (M.K.A.); diriids@ 123456allduni.ac.in (S.S.)
                [6 ]Laboratory Medicine Department, Faculty of Applied Medical Sciences, Umm Al-Qura University, Makkah 24231, Saudi Arabia; ssalghamdi@ 123456uqu.edu.sa
                [7 ]Department of Biophysics, Institute for Research & Medical Consultation (IRMC), Imam Abdulrahman Bin Faisal University, Dammam 31441, Saudi Arabia; suakhtar@ 123456iau.edu.sa
                [8 ]Department of Chemistry, University College in Al-Qunfudah, Umm Al-Qura University, Makkah Al-Mukarramah 1109, Saudi Arabia; hdmalki@ 123456uqu.edu.sa
                [9 ]Department of Chemistry, College of Science, King Saud University, Riyadh 11451, Saudi Arabia; kmujeeb@ 123456ksu.edu.sa (M.K.); mhatshan@ 123456ksu.edu.sa (M.R.H.)
                Author notes
                [* ]Correspondence: abulkalam@ 123456kku.edu.sa (A.K.); sfadil@ 123456ksu.edu.sa (S.F.A.)
                Author information
                https://orcid.org/0000-0002-6122-5479
                https://orcid.org/0000-0002-6793-3038
                https://orcid.org/0000-0001-7909-4377
                https://orcid.org/0000-0003-4532-9128
                https://orcid.org/0000-0002-9473-4739
                https://orcid.org/0000-0002-2768-1235
                https://orcid.org/0000-0002-4088-6913
                https://orcid.org/0000-0003-3100-5747
                Article
                antibiotics-10-00725
                10.3390/antibiotics10060725
                8234839
                34208591
                0b8a2a5b-e31a-4c95-b2be-b461aaa0e0f7
                © 2021 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 28 April 2021
                : 11 June 2021
                Categories
                Article

                biofilm,antibiotics resistant,bio-actives capping,silver nanoparticles,tem,ultrastructural changes,candida albicans,mrsa

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