<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Koyasseril-Yehiya TM</submitter><funding>Universidad Autónoma de Nuevo León</funding><funding>NIAID NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIGMS NIH HHS</funding><pagination>20693-20698</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7581559</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(40)</volume><pubmed_abstract>The propensity of broad-spectrum antibiotics to indiscriminately kill both pathogenic and beneficial bacteria has a profound impact on the spread of resistance across multiple bacterial species. Alternative approaches that narrow antibacterial specificity towards desired pathogenic bacterial population are of great interest. Here, we report an enzyme-responsive antibiotic-loaded nanoassembly strategy for narrow delivery of otherwise broad-spectrum antibiotics. We specifically target Staphylococcus aureus (S. aureus), an important blood pathogen that secretes PC1 β-lactamases. Our nanoassemblies selectively eradicate S. aureus grown in vitro with other bacteria, highlighting its potential capability in targeting the desired pathogenic bacterial population.</pubmed_abstract><journal>Nanoscale</journal><pubmed_title>Supramolecular antibiotics: a strategy for conversion of broad-spectrum to narrow-spectrum antibiotics for &lt;i>Staphylococcus aureus&lt;/i>.</pubmed_title><pmcid>PMC7581559</pmcid><funding_grant_id>GM-136395</funding_grant_id><funding_grant_id>DP2 AI138238</funding_grant_id><funding_grant_id>R21 AI144748</funding_grant_id><funding_grant_id>R35 GM136395</funding_grant_id><funding_grant_id>T32 GM108556</funding_grant_id><pubmed_authors>Rangadurai P</pubmed_authors><pubmed_authors>Anson F</pubmed_authors><pubmed_authors>Thayumanavan S</pubmed_authors><pubmed_authors>Koyasseril-Yehiya TM</pubmed_authors><pubmed_authors>Siegrist MS</pubmed_authors><pubmed_authors>Garcia-Heredia A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Supramolecular antibiotics: a strategy for conversion of broad-spectrum to narrow-spectrum antibiotics for &lt;i>Staphylococcus aureus&lt;/i>.</name><description>The propensity of broad-spectrum antibiotics to indiscriminately kill both pathogenic and beneficial bacteria has a profound impact on the spread of resistance across multiple bacterial species. Alternative approaches that narrow antibacterial specificity towards desired pathogenic bacterial population are of great interest. Here, we report an enzyme-responsive antibiotic-loaded nanoassembly strategy for narrow delivery of otherwise broad-spectrum antibiotics. We specifically target Staphylococcus aureus (S. aureus), an important blood pathogen that secretes PC1 β-lactamases. Our nanoassemblies selectively eradicate S. aureus grown in vitro with other bacteria, highlighting its potential capability in targeting the desired pathogenic bacterial population.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Oct</publication><modification>2025-04-03T23:32:20.132Z</modification><creation>2025-04-03T23:32:20.132Z</creation></dates><accession>S-EPMC7581559</accession><cross_references><pubmed>33029599</pubmed><doi>10.1039/d0nr04886k</doi></cross_references></HashMap>