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Evaluation of E. coli inhibition by plain and polymer-coated silver nanoparticles

Escherichia coli causes various ailments such as septicemia, enteritis, foodborne illnesses, and urinary tract infections which are of concern in the public health field due to antibiotic resistance. Silver nanoparticles (AgNP) are known for their biocompatibility and antibacterial activity, and may...

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Autores principales: Ashmore, D'Andrea, Chaudhari, Atul, Barlow, Brandi, Barlow, Brett, Harper, Talia, Vig, Komal, Miller, Michael, Singh, Shree, Nelson, Edward, Pillai, Shreekumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Instituto de Medicina Tropical 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5956551/
https://www.ncbi.nlm.nih.gov/pubmed/29694600
http://dx.doi.org/10.1590/S1678-9946201860018
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author Ashmore, D'Andrea
Chaudhari, Atul
Barlow, Brandi
Barlow, Brett
Harper, Talia
Vig, Komal
Miller, Michael
Singh, Shree
Nelson, Edward
Pillai, Shreekumar
author_facet Ashmore, D'Andrea
Chaudhari, Atul
Barlow, Brandi
Barlow, Brett
Harper, Talia
Vig, Komal
Miller, Michael
Singh, Shree
Nelson, Edward
Pillai, Shreekumar
author_sort Ashmore, D'Andrea
collection PubMed
description Escherichia coli causes various ailments such as septicemia, enteritis, foodborne illnesses, and urinary tract infections which are of concern in the public health field due to antibiotic resistance. Silver nanoparticles (AgNP) are known for their biocompatibility and antibacterial activity, and may prove to be an alternative method of treatment, especially as wound dressings. In this study, we compared the antibacterial efficacy of two polymer-coated silver nanoparticles either containing 10% Ag (Ag 10% + Polymer), or 99% Ag (AgPVP) in relation to plain uncoated silver nanoparticles (AgNP). Atomic force microscopy was used to characterize the nanoparticles, and their antibacterial efficacy was compared by the minimum inhibitory concentration (MIC) and bacterial growth curve assays, followed by molecular studies using scanning electron microscopy (SEM) and (qRT- PCR). AgNP inhibited the growth of E. coli only at 0.621 mg/mL, which was double the concentration required for both coated nanoparticles (0.312 mg/mL). Similarly, bacterial growth was impeded as early as 8 h at 0.156 mg/mL of both coated nanoparticles as compared to 0.312 mg/mL for plain AgNP. SEM data showed that nanoparticles damaged the cell membrane, resulting in bacterial cell lysis, expulsion of cellular contents, and complete disintegration of some cells. The expression of genes associated with the TCA cycle (aceF and frdB) and amino acid metabolism (gadB, metL, argC) were substantially downregulated in E. coli treated with nanoparticles. The reduction in the silver ion (Ag(+)) concentration of polymer-coated AgNP did not affect their antibacterial efficacy against E. coli.
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spelling pubmed-59565512018-05-21 Evaluation of E. coli inhibition by plain and polymer-coated silver nanoparticles Ashmore, D'Andrea Chaudhari, Atul Barlow, Brandi Barlow, Brett Harper, Talia Vig, Komal Miller, Michael Singh, Shree Nelson, Edward Pillai, Shreekumar Rev Inst Med Trop Sao Paulo Original Article Escherichia coli causes various ailments such as septicemia, enteritis, foodborne illnesses, and urinary tract infections which are of concern in the public health field due to antibiotic resistance. Silver nanoparticles (AgNP) are known for their biocompatibility and antibacterial activity, and may prove to be an alternative method of treatment, especially as wound dressings. In this study, we compared the antibacterial efficacy of two polymer-coated silver nanoparticles either containing 10% Ag (Ag 10% + Polymer), or 99% Ag (AgPVP) in relation to plain uncoated silver nanoparticles (AgNP). Atomic force microscopy was used to characterize the nanoparticles, and their antibacterial efficacy was compared by the minimum inhibitory concentration (MIC) and bacterial growth curve assays, followed by molecular studies using scanning electron microscopy (SEM) and (qRT- PCR). AgNP inhibited the growth of E. coli only at 0.621 mg/mL, which was double the concentration required for both coated nanoparticles (0.312 mg/mL). Similarly, bacterial growth was impeded as early as 8 h at 0.156 mg/mL of both coated nanoparticles as compared to 0.312 mg/mL for plain AgNP. SEM data showed that nanoparticles damaged the cell membrane, resulting in bacterial cell lysis, expulsion of cellular contents, and complete disintegration of some cells. The expression of genes associated with the TCA cycle (aceF and frdB) and amino acid metabolism (gadB, metL, argC) were substantially downregulated in E. coli treated with nanoparticles. The reduction in the silver ion (Ag(+)) concentration of polymer-coated AgNP did not affect their antibacterial efficacy against E. coli. Instituto de Medicina Tropical 2018-04-23 /pmc/articles/PMC5956551/ /pubmed/29694600 http://dx.doi.org/10.1590/S1678-9946201860018 Text en https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ashmore, D'Andrea
Chaudhari, Atul
Barlow, Brandi
Barlow, Brett
Harper, Talia
Vig, Komal
Miller, Michael
Singh, Shree
Nelson, Edward
Pillai, Shreekumar
Evaluation of E. coli inhibition by plain and polymer-coated silver nanoparticles
title Evaluation of E. coli inhibition by plain and polymer-coated silver nanoparticles
title_full Evaluation of E. coli inhibition by plain and polymer-coated silver nanoparticles
title_fullStr Evaluation of E. coli inhibition by plain and polymer-coated silver nanoparticles
title_full_unstemmed Evaluation of E. coli inhibition by plain and polymer-coated silver nanoparticles
title_short Evaluation of E. coli inhibition by plain and polymer-coated silver nanoparticles
title_sort evaluation of e. coli inhibition by plain and polymer-coated silver nanoparticles
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5956551/
https://www.ncbi.nlm.nih.gov/pubmed/29694600
http://dx.doi.org/10.1590/S1678-9946201860018
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