Nanoscale Structure–Activity Relationships, Mode of Action, and Biocompatibility of Gold Nanoparticle Antibiotics
The emergence of resistance to multiple antimicrobial agents by pathogenic bacteria has become a significant global public health threat. Multi-drug-resistant (MDR) Gram-negative bacteria have become particularly problematic, as no new classes of small-molecule antibiotics for Gram-negative bacteria...
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Veröffentlicht in: | Journal of the American Chemical Society 2014-04, Vol.136 (14), p.5295-5300 |
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creator | Bresee, Jamee Bond, Constance M Worthington, Roberta J Smith, Candice A Gifford, Jennifer C Simpson, Carrie A Carter, Carly J Wang, Guankui Hartman, Jesse Osbaugh, Niki A Shoemaker, Richard K Melander, Christian Feldheim, Daniel L |
description | The emergence of resistance to multiple antimicrobial agents by pathogenic bacteria has become a significant global public health threat. Multi-drug-resistant (MDR) Gram-negative bacteria have become particularly problematic, as no new classes of small-molecule antibiotics for Gram-negative bacteria have emerged in over two decades. We have developed a combinatorial screening process for identifying mixed ligand monolayer/gold nanoparticle conjugates (2.4 nm diameter) with antibiotic activity. The method previously led to the discovery of several conjugates with potent activity against the Gram-negative bacterium Escherichia coli. Here we show that these conjugates are also active against MDR E. coli and MDR Klebsiella pneumoniae. Moreover, we have shown that resistance to these nanoparticles develops significantly more slowly than to a commercial small-molecule drug. These results, combined with their relatively low toxicity to mammalian cells and biocompatibility in vivo, suggest that gold nanoparticles may be viable new candidates for the treatment of MDR Gram-negative bacterial infections. |
doi_str_mv | 10.1021/ja408505n |
format | Article |
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Multi-drug-resistant (MDR) Gram-negative bacteria have become particularly problematic, as no new classes of small-molecule antibiotics for Gram-negative bacteria have emerged in over two decades. We have developed a combinatorial screening process for identifying mixed ligand monolayer/gold nanoparticle conjugates (2.4 nm diameter) with antibiotic activity. The method previously led to the discovery of several conjugates with potent activity against the Gram-negative bacterium Escherichia coli. Here we show that these conjugates are also active against MDR E. coli and MDR Klebsiella pneumoniae. Moreover, we have shown that resistance to these nanoparticles develops significantly more slowly than to a commercial small-molecule drug. 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Am. Chem. Soc</addtitle><description>The emergence of resistance to multiple antimicrobial agents by pathogenic bacteria has become a significant global public health threat. Multi-drug-resistant (MDR) Gram-negative bacteria have become particularly problematic, as no new classes of small-molecule antibiotics for Gram-negative bacteria have emerged in over two decades. We have developed a combinatorial screening process for identifying mixed ligand monolayer/gold nanoparticle conjugates (2.4 nm diameter) with antibiotic activity. The method previously led to the discovery of several conjugates with potent activity against the Gram-negative bacterium Escherichia coli. Here we show that these conjugates are also active against MDR E. coli and MDR Klebsiella pneumoniae. Moreover, we have shown that resistance to these nanoparticles develops significantly more slowly than to a commercial small-molecule drug. These results, combined with their relatively low toxicity to mammalian cells and biocompatibility in vivo, suggest that gold nanoparticles may be viable new candidates for the treatment of MDR Gram-negative bacterial infections.</description><subject>Anti-Bacterial Agents - chemical synthesis</subject><subject>Anti-Bacterial Agents - chemistry</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Biocompatible Materials - chemical synthesis</subject><subject>Biocompatible Materials - chemistry</subject><subject>Biocompatible Materials - pharmacology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Resistance, Multiple, Bacterial - drug effects</subject><subject>Escherichia coli - drug effects</subject><subject>Gold - chemistry</subject><subject>Gold - pharmacology</subject><subject>Klebsiella pneumoniae - drug effects</subject><subject>Metal Nanoparticles - chemistry</subject><subject>Microbial Sensitivity Tests</subject><subject>Structure-Activity Relationship</subject><issn>0002-7863</issn><issn>1520-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkE1OwzAQRi0EoqWw4ALIGxZIDYwdO02XpYKCVEDiZx1NbEe4SuMoTpC64w7ckJPgqNAVq9Hoe_M0-gg5ZXDJgLOrFQpIJchqjwyZ5BBJxpN9MgQAHk3SJB6QI-9XYRU8ZYdkwEXCxVTCkPhHrJxXWBr60jadarvGfH9-zVRrP2y7oc-mxNa6yr_b2o_pg9OGuoL2uavGFCtNr61Tbl0HLLdlfxPyhSs17dU1Nq1VwT6r-tyFxR-TgwJLb05-54i83d68zu-i5dPifj5bRhgz2UaYK4GxkBMJXAsTT8QUp1DESR5rwxAUmxqWmxRNkQhMmZZaKsilVAKKQkI8Ihdbr2qc940psrqxa2w2GYOsLy7bFRfYsy1bd_na6B3511QAzrcAKp-tXNdU4fV_RD_yBXel</recordid><startdate>20140409</startdate><enddate>20140409</enddate><creator>Bresee, Jamee</creator><creator>Bond, Constance M</creator><creator>Worthington, Roberta J</creator><creator>Smith, Candice A</creator><creator>Gifford, Jennifer C</creator><creator>Simpson, Carrie A</creator><creator>Carter, Carly J</creator><creator>Wang, Guankui</creator><creator>Hartman, Jesse</creator><creator>Osbaugh, Niki A</creator><creator>Shoemaker, Richard K</creator><creator>Melander, Christian</creator><creator>Feldheim, Daniel L</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20140409</creationdate><title>Nanoscale Structure–Activity Relationships, Mode of Action, and Biocompatibility of Gold Nanoparticle Antibiotics</title><author>Bresee, Jamee ; Bond, Constance M ; Worthington, Roberta J ; Smith, Candice A ; Gifford, Jennifer C ; Simpson, Carrie A ; Carter, Carly J ; Wang, Guankui ; Hartman, Jesse ; Osbaugh, Niki A ; Shoemaker, Richard K ; Melander, Christian ; Feldheim, Daniel L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a315t-abc4a3457502d4e3749a90f36b3de1a0c19e1be8aef64a81d5d5c0b55c40ff503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Anti-Bacterial Agents - chemical synthesis</topic><topic>Anti-Bacterial Agents - chemistry</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Biocompatible Materials - chemical synthesis</topic><topic>Biocompatible Materials - chemistry</topic><topic>Biocompatible Materials - pharmacology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Resistance, Multiple, Bacterial - drug effects</topic><topic>Escherichia coli - drug effects</topic><topic>Gold - chemistry</topic><topic>Gold - pharmacology</topic><topic>Klebsiella pneumoniae - drug effects</topic><topic>Metal Nanoparticles - chemistry</topic><topic>Microbial Sensitivity Tests</topic><topic>Structure-Activity Relationship</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bresee, Jamee</creatorcontrib><creatorcontrib>Bond, Constance M</creatorcontrib><creatorcontrib>Worthington, Roberta J</creatorcontrib><creatorcontrib>Smith, Candice A</creatorcontrib><creatorcontrib>Gifford, Jennifer C</creatorcontrib><creatorcontrib>Simpson, Carrie A</creatorcontrib><creatorcontrib>Carter, Carly J</creatorcontrib><creatorcontrib>Wang, Guankui</creatorcontrib><creatorcontrib>Hartman, Jesse</creatorcontrib><creatorcontrib>Osbaugh, Niki A</creatorcontrib><creatorcontrib>Shoemaker, Richard K</creatorcontrib><creatorcontrib>Melander, Christian</creatorcontrib><creatorcontrib>Feldheim, Daniel L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of the American Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bresee, Jamee</au><au>Bond, Constance M</au><au>Worthington, Roberta J</au><au>Smith, Candice A</au><au>Gifford, Jennifer C</au><au>Simpson, Carrie A</au><au>Carter, Carly J</au><au>Wang, Guankui</au><au>Hartman, Jesse</au><au>Osbaugh, Niki A</au><au>Shoemaker, Richard K</au><au>Melander, Christian</au><au>Feldheim, Daniel L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nanoscale Structure–Activity Relationships, Mode of Action, and Biocompatibility of Gold Nanoparticle Antibiotics</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J. 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subjects | Anti-Bacterial Agents - chemical synthesis Anti-Bacterial Agents - chemistry Anti-Bacterial Agents - pharmacology Biocompatible Materials - chemical synthesis Biocompatible Materials - chemistry Biocompatible Materials - pharmacology Dose-Response Relationship, Drug Drug Resistance, Multiple, Bacterial - drug effects Escherichia coli - drug effects Gold - chemistry Gold - pharmacology Klebsiella pneumoniae - drug effects Metal Nanoparticles - chemistry Microbial Sensitivity Tests Structure-Activity Relationship |
title | Nanoscale Structure–Activity Relationships, Mode of Action, and Biocompatibility of Gold Nanoparticle Antibiotics |
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