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Anti‐biofilm and anti‐virulence effects of silica oxide nanoparticle–conjugation of lectin purified from Pseudomonas aeruginosa
Pseudomonas aeruginosa lectin is purified and nanoparticle‐conjugated in an attempt to inhibit biofilm formation. Thirteen (23.6%) P. aeruginosa isolates are obtained from chicken meat samples, of which 30.8% are biofilm producers and 69.2% are lectin producers. Lectin is purified 36.8‐fold to final...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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John Wiley and Sons Inc.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8675845/ https://www.ncbi.nlm.nih.gov/pubmed/34694672 http://dx.doi.org/10.1049/nbt2.12022 |
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author | Nsayef Muslim, Sahira Mohammed Ali, Alaa Naseer Auda, Ibtesam Ghadban |
author_facet | Nsayef Muslim, Sahira Mohammed Ali, Alaa Naseer Auda, Ibtesam Ghadban |
author_sort | Nsayef Muslim, Sahira |
collection | PubMed |
description | Pseudomonas aeruginosa lectin is purified and nanoparticle‐conjugated in an attempt to inhibit biofilm formation. Thirteen (23.6%) P. aeruginosa isolates are obtained from chicken meat samples, of which 30.8% are biofilm producers and 69.2% are lectin producers. Lectin is purified 36.8‐fold to final specific activity of 506.9 U/mg. Four nanoparticle types are prepared via laser ablation: platinum (Pt), gold (Au), silica oxide (SiO(2)), and tin oxide (SnO(2)). The four types are characterised, and pulse feeding is used to conjugate the lectin and nanoparticles. Pt, Au, SiO(2,) and SnO(2) nanoparticles inhibit biofilm formation, especially SiO(2) nanoparticles, which have higher effectiveness when conjugated with purified lectin. SiO(2)‐conjugated lectin significantly (p < 0.05) inhibits biofilm formation more effectively than control and other nanoparticle‐conjugated lectins. Au‐, Pt nanoparticle‐, and SnO(2)‐conjugated lectins inhibit biofilm significantly compared with control (p < 0.05), and rhlR gene expression is decreased in the presence of SiO(2)‐conjugated lectin. Furthermore, lectin and Pt, Au, SiO(2) and SnO(2) nanoparticles separately, and their conjugated lectins, are effective biofilm inhibitors. Of these, SiO(2)‐conjugated lectin was most significant as an anti‐biofilm. Moreover, virulence factors regulon and RhlR were reduced by SiO(2)‐conjugated lectin, indicating that this conjugation may also decrease the virulence of P. aeruginosa. |
format | Online Article Text |
id | pubmed-8675845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86758452022-02-03 Anti‐biofilm and anti‐virulence effects of silica oxide nanoparticle–conjugation of lectin purified from Pseudomonas aeruginosa Nsayef Muslim, Sahira Mohammed Ali, Alaa Naseer Auda, Ibtesam Ghadban IET Nanobiotechnol Original Research Papers Pseudomonas aeruginosa lectin is purified and nanoparticle‐conjugated in an attempt to inhibit biofilm formation. Thirteen (23.6%) P. aeruginosa isolates are obtained from chicken meat samples, of which 30.8% are biofilm producers and 69.2% are lectin producers. Lectin is purified 36.8‐fold to final specific activity of 506.9 U/mg. Four nanoparticle types are prepared via laser ablation: platinum (Pt), gold (Au), silica oxide (SiO(2)), and tin oxide (SnO(2)). The four types are characterised, and pulse feeding is used to conjugate the lectin and nanoparticles. Pt, Au, SiO(2,) and SnO(2) nanoparticles inhibit biofilm formation, especially SiO(2) nanoparticles, which have higher effectiveness when conjugated with purified lectin. SiO(2)‐conjugated lectin significantly (p < 0.05) inhibits biofilm formation more effectively than control and other nanoparticle‐conjugated lectins. Au‐, Pt nanoparticle‐, and SnO(2)‐conjugated lectins inhibit biofilm significantly compared with control (p < 0.05), and rhlR gene expression is decreased in the presence of SiO(2)‐conjugated lectin. Furthermore, lectin and Pt, Au, SiO(2) and SnO(2) nanoparticles separately, and their conjugated lectins, are effective biofilm inhibitors. Of these, SiO(2)‐conjugated lectin was most significant as an anti‐biofilm. Moreover, virulence factors regulon and RhlR were reduced by SiO(2)‐conjugated lectin, indicating that this conjugation may also decrease the virulence of P. aeruginosa. John Wiley and Sons Inc. 2021-03-03 /pmc/articles/PMC8675845/ /pubmed/34694672 http://dx.doi.org/10.1049/nbt2.12022 Text en © 2021 The Authors. IET Nanobiotechnology published by John Wiley & Sons Ltd on behalf of The Institution of Engineering and Technology. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Papers Nsayef Muslim, Sahira Mohammed Ali, Alaa Naseer Auda, Ibtesam Ghadban Anti‐biofilm and anti‐virulence effects of silica oxide nanoparticle–conjugation of lectin purified from Pseudomonas aeruginosa |
title | Anti‐biofilm and anti‐virulence effects of silica oxide nanoparticle–conjugation of lectin purified from Pseudomonas aeruginosa
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title_full | Anti‐biofilm and anti‐virulence effects of silica oxide nanoparticle–conjugation of lectin purified from Pseudomonas aeruginosa
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title_fullStr | Anti‐biofilm and anti‐virulence effects of silica oxide nanoparticle–conjugation of lectin purified from Pseudomonas aeruginosa
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title_full_unstemmed | Anti‐biofilm and anti‐virulence effects of silica oxide nanoparticle–conjugation of lectin purified from Pseudomonas aeruginosa
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title_short | Anti‐biofilm and anti‐virulence effects of silica oxide nanoparticle–conjugation of lectin purified from Pseudomonas aeruginosa
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title_sort | anti‐biofilm and anti‐virulence effects of silica oxide nanoparticle–conjugation of lectin purified from pseudomonas aeruginosa |
topic | Original Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8675845/ https://www.ncbi.nlm.nih.gov/pubmed/34694672 http://dx.doi.org/10.1049/nbt2.12022 |
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