The effects of bacteria-nanoparticles interface on the antibacterial activity of green synthesized silver nanoparticles.
Identifieur interne : 000603 ( Main/Curation ); précédent : 000602; suivant : 000604The effects of bacteria-nanoparticles interface on the antibacterial activity of green synthesized silver nanoparticles.
Auteurs : Aftab Ahmad [République populaire de Chine] ; Yun Wei [République populaire de Chine] ; Fatima Syed [Pakistan] ; Kamran Tahir [République populaire de Chine] ; Aziz Ur Rehman [République populaire de Chine] ; Arifullah Khan [République populaire de Chine] ; Sadeeq Ullah [République populaire de Chine] ; Qipeng Yuan [République populaire de Chine]Source :
- Microbial pathogenesis [ 1096-1208 ] ; 2017.
Descripteurs français
- KwdFr :
- Antibactériens (composition chimique), Antibactériens (pharmacologie), Argent (composition chimique), Bactéries (effets des médicaments et des substances chimiques), Bactéries (métabolisme), Bactéries (ultrastructure), Diffraction des rayons X (MeSH), Espèces réactives de l'oxygène (métabolisme), Extraits de plantes (composition chimique), Extraits de plantes (pharmacologie), Nanoparticules métalliques (administration et posologie), Nanoparticules métalliques (composition chimique), Potentiels de membrane (effets des médicaments et des substances chimiques), Spectroscopie infrarouge à transformée de Fourier (MeSH), Spectroscopie photoélectronique (MeSH), Taille de particule (MeSH), Technologie de la chimie verte (MeSH), Tests de sensibilité microbienne (MeSH).
- MESH :
- administration et posologie : Nanoparticules métalliques.
- composition chimique : Antibactériens, Argent, Extraits de plantes, Nanoparticules métalliques.
- effets des médicaments et des substances chimiques : Bactéries, Potentiels de membrane.
- métabolisme : Bactéries, Espèces réactives de l'oxygène.
- pharmacologie : Antibactériens, Extraits de plantes.
- ultrastructure : Bactéries, Diffraction des rayons X, Spectroscopie infrarouge à transformée de Fourier, Spectroscopie photoélectronique, Taille de particule, Technologie de la chimie verte, Tests de sensibilité microbienne.
English descriptors
- KwdEn :
- Anti-Bacterial Agents (chemistry), Anti-Bacterial Agents (pharmacology), Bacteria (drug effects), Bacteria (metabolism), Bacteria (ultrastructure), Green Chemistry Technology (MeSH), Membrane Potentials (drug effects), Metal Nanoparticles (administration & dosage), Metal Nanoparticles (chemistry), Microbial Sensitivity Tests (MeSH), Particle Size (MeSH), Photoelectron Spectroscopy (MeSH), Plant Extracts (chemistry), Plant Extracts (pharmacology), Reactive Oxygen Species (metabolism), Silver (chemistry), Spectroscopy, Fourier Transform Infrared (MeSH), X-Ray Diffraction (MeSH).
- MESH :
- chemical , chemistry : Anti-Bacterial Agents, Plant Extracts, Silver.
- chemical , metabolism : Reactive Oxygen Species.
- chemical , pharmacology : Anti-Bacterial Agents, Plant Extracts.
- administration & dosage : Metal Nanoparticles.
- chemistry : Metal Nanoparticles.
- drug effects : Bacteria, Membrane Potentials.
- metabolism : Bacteria.
- ultrastructure : Bacteria.
- Green Chemistry Technology, Microbial Sensitivity Tests, Particle Size, Photoelectron Spectroscopy, Spectroscopy, Fourier Transform Infrared, X-Ray Diffraction.
Abstract
Neutralization of bacterial cell surface potential using nanoscale materials is an effective strategy to alter membrane permeability, cytoplasmic leakage, and ultimate cell death. In the present study, an attempt was made to prepare biogenic silver nanoparticles using biomolecules from the aqueous rhizome extract of Coptis Chinensis. The biosynthesized silver nanoparticles were surface modified with chitosan biopolymer. The prepared silver nanoparticles and chitosan modified silver nanoparticles were cubic crystalline structures (XRD) with an average particle size of 15 and 20 nm respectively (TEM, DLS). The biosynthesized silver nanoparticles were surface stabilized by polyphenolic compounds (FTIR). Coptis Chinensis mediated silver nanoparticles displayed significant activity against E. coli and Bacillus subtilus with a zone of inhibition 12 ± 1.2 (MIC = 25 μg/mL) and 18 ± 1.6 mm (MIC = 12.50 μg/mL) respectively. The bactericidal efficacy of these nanoparticles was considerably increased upon surface modification with chitosan biopolymer. The chitosan modified biogenic silver nanoparticles exhibited promising activity against E. coli (MIC = 6.25 μg/mL) and Bacillus subtilus (MIC = 12.50 μg/mL). Our results indicated that the chitosan modified silver nanoparticles were promising agents in damaging bacterial membrane potential and induction of high level of intracellular reactive oxygen species (ROS). In addition, these nanoparticles were observed to induce the release of the high level of cytoplasmic materials especially protein and nucleic acids into the media. All these findings suggest that the chitosan functionalized silver nanoparticles are efficient agents in disrupting bacterial membrane and induction of ROS leading to cytoplasmic leakage and cell death. These findings further conclude that the bacterial-nanoparticles surface potential modulation is an effective strategy in enhancing the antibacterial potency of silver nanoparticles.
DOI: 10.1016/j.micpath.2016.11.030
PubMed: 27916692
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<series><title level="j">Microbial pathogenesis</title>
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<term>Bacteria (metabolism)</term>
<term>Bacteria (ultrastructure)</term>
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<term>Metal Nanoparticles (administration & dosage)</term>
<term>Metal Nanoparticles (chemistry)</term>
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<term>Plant Extracts (pharmacology)</term>
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<term>Bactéries (métabolisme)</term>
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<front><div type="abstract" xml:lang="en">Neutralization of bacterial cell surface potential using nanoscale materials is an effective strategy to alter membrane permeability, cytoplasmic leakage, and ultimate cell death. In the present study, an attempt was made to prepare biogenic silver nanoparticles using biomolecules from the aqueous rhizome extract of Coptis Chinensis. The biosynthesized silver nanoparticles were surface modified with chitosan biopolymer. The prepared silver nanoparticles and chitosan modified silver nanoparticles were cubic crystalline structures (XRD) with an average particle size of 15 and 20 nm respectively (TEM, DLS). The biosynthesized silver nanoparticles were surface stabilized by polyphenolic compounds (FTIR). Coptis Chinensis mediated silver nanoparticles displayed significant activity against E. coli and Bacillus subtilus with a zone of inhibition 12 ± 1.2 (MIC = 25 μg/mL) and 18 ± 1.6 mm (MIC = 12.50 μg/mL) respectively. The bactericidal efficacy of these nanoparticles was considerably increased upon surface modification with chitosan biopolymer. The chitosan modified biogenic silver nanoparticles exhibited promising activity against E. coli (MIC = 6.25 μg/mL) and Bacillus subtilus (MIC = 12.50 μg/mL). Our results indicated that the chitosan modified silver nanoparticles were promising agents in damaging bacterial membrane potential and induction of high level of intracellular reactive oxygen species (ROS). In addition, these nanoparticles were observed to induce the release of the high level of cytoplasmic materials especially protein and nucleic acids into the media. All these findings suggest that the chitosan functionalized silver nanoparticles are efficient agents in disrupting bacterial membrane and induction of ROS leading to cytoplasmic leakage and cell death. These findings further conclude that the bacterial-nanoparticles surface potential modulation is an effective strategy in enhancing the antibacterial potency of silver nanoparticles.</div>
</front>
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<Day>06</Day>
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<Month>12</Month>
<Day>25</Day>
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<PubDate><Year>2017</Year>
<Month>Jan</Month>
</PubDate>
</JournalIssue>
<Title>Microbial pathogenesis</Title>
<ISOAbbreviation>Microb Pathog</ISOAbbreviation>
</Journal>
<ArticleTitle>The effects of bacteria-nanoparticles interface on the antibacterial activity of green synthesized silver nanoparticles.</ArticleTitle>
<Pagination><MedlinePgn>133-142</MedlinePgn>
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<Abstract><AbstractText>Neutralization of bacterial cell surface potential using nanoscale materials is an effective strategy to alter membrane permeability, cytoplasmic leakage, and ultimate cell death. In the present study, an attempt was made to prepare biogenic silver nanoparticles using biomolecules from the aqueous rhizome extract of Coptis Chinensis. The biosynthesized silver nanoparticles were surface modified with chitosan biopolymer. The prepared silver nanoparticles and chitosan modified silver nanoparticles were cubic crystalline structures (XRD) with an average particle size of 15 and 20 nm respectively (TEM, DLS). The biosynthesized silver nanoparticles were surface stabilized by polyphenolic compounds (FTIR). Coptis Chinensis mediated silver nanoparticles displayed significant activity against E. coli and Bacillus subtilus with a zone of inhibition 12 ± 1.2 (MIC = 25 μg/mL) and 18 ± 1.6 mm (MIC = 12.50 μg/mL) respectively. The bactericidal efficacy of these nanoparticles was considerably increased upon surface modification with chitosan biopolymer. The chitosan modified biogenic silver nanoparticles exhibited promising activity against E. coli (MIC = 6.25 μg/mL) and Bacillus subtilus (MIC = 12.50 μg/mL). Our results indicated that the chitosan modified silver nanoparticles were promising agents in damaging bacterial membrane potential and induction of high level of intracellular reactive oxygen species (ROS). In addition, these nanoparticles were observed to induce the release of the high level of cytoplasmic materials especially protein and nucleic acids into the media. All these findings suggest that the chitosan functionalized silver nanoparticles are efficient agents in disrupting bacterial membrane and induction of ROS leading to cytoplasmic leakage and cell death. These findings further conclude that the bacterial-nanoparticles surface potential modulation is an effective strategy in enhancing the antibacterial potency of silver nanoparticles.</AbstractText>
<CopyrightInformation>Copyright © 2016 Elsevier Ltd. All rights reserved.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Ahmad</LastName>
<ForeName>Aftab</ForeName>
<Initials>A</Initials>
<AffiliationInfo><Affiliation>State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, No. 15 East Road of North Third Ring, Chao Yang District, Beijing 100029, China. Electronic address: aftabbiochem@yahoo.com.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Wei</LastName>
<ForeName>Yun</ForeName>
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<AffiliationInfo><Affiliation>State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, No. 15 East Road of North Third Ring, Chao Yang District, Beijing 100029, China.</Affiliation>
</AffiliationInfo>
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<ForeName>Fatima</ForeName>
<Initials>F</Initials>
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</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Tahir</LastName>
<ForeName>Kamran</ForeName>
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<ForeName>Aziz Ur</ForeName>
<Initials>AU</Initials>
<AffiliationInfo><Affiliation>State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, No. 15 East Road of North Third Ring, Chao Yang District, Beijing 100029, China.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Khan</LastName>
<ForeName>Arifullah</ForeName>
<Initials>A</Initials>
<AffiliationInfo><Affiliation>State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, No. 15 East Road of North Third Ring, Chao Yang District, Beijing 100029, China.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Ullah</LastName>
<ForeName>Sadeeq</ForeName>
<Initials>S</Initials>
<AffiliationInfo><Affiliation>State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, No. 15 East Road of North Third Ring, Chao Yang District, Beijing 100029, China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Yuan</LastName>
<ForeName>Qipeng</ForeName>
<Initials>Q</Initials>
<AffiliationInfo><Affiliation>State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, No. 15 East Road of North Third Ring, Chao Yang District, Beijing 100029, China. Electronic address: yuanqp@mail.buct.edu.cn.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic"><Year>2016</Year>
<Month>12</Month>
<Day>01</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo><Country>England</Country>
<MedlineTA>Microb Pathog</MedlineTA>
<NlmUniqueID>8606191</NlmUniqueID>
<ISSNLinking>0882-4010</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D000900">Anti-Bacterial Agents</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D010936">Plant Extracts</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D017382">Reactive Oxygen Species</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>3M4G523W1G</RegistryNumber>
<NameOfSubstance UI="D012834">Silver</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D000900" MajorTopicYN="N">Anti-Bacterial Agents</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D001419" MajorTopicYN="N">Bacteria</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="Y">drug effects</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
<QualifierName UI="Q000648" MajorTopicYN="N">ultrastructure</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D055772" MajorTopicYN="Y">Green Chemistry Technology</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008564" MajorTopicYN="N">Membrane Potentials</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D053768" MajorTopicYN="N">Metal Nanoparticles</DescriptorName>
<QualifierName UI="Q000008" MajorTopicYN="Y">administration & dosage</QualifierName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008826" MajorTopicYN="N">Microbial Sensitivity Tests</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010316" MajorTopicYN="N">Particle Size</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D056951" MajorTopicYN="N">Photoelectron Spectroscopy</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010936" MajorTopicYN="N">Plant Extracts</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D017382" MajorTopicYN="N">Reactive Oxygen Species</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D012834" MajorTopicYN="Y">Silver</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D017550" MajorTopicYN="N">Spectroscopy, Fourier Transform Infrared</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D014961" MajorTopicYN="N">X-Ray Diffraction</DescriptorName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="Y">Bacteria</Keyword>
<Keyword MajorTopicYN="Y">Coptis Chinensis</Keyword>
<Keyword MajorTopicYN="Y">Membrane potential</Keyword>
<Keyword MajorTopicYN="Y">Silver nanoparticles</Keyword>
</KeywordList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="received"><Year>2016</Year>
<Month>11</Month>
<Day>06</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="revised"><Year>2016</Year>
<Month>11</Month>
<Day>27</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted"><Year>2016</Year>
<Month>11</Month>
<Day>29</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed"><Year>2016</Year>
<Month>12</Month>
<Day>6</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>2017</Year>
<Month>4</Month>
<Day>7</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez"><Year>2016</Year>
<Month>12</Month>
<Day>6</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">27916692</ArticleId>
<ArticleId IdType="pii">S0882-4010(16)30746-X</ArticleId>
<ArticleId IdType="doi">10.1016/j.micpath.2016.11.030</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
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