<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Xu Z</submitter><funding>Natural Science Foundation of Jiangsu Province (Jiangsu Provincial Natural Science Foundation)</funding><funding>NIDCR NIH HHS</funding><pagination>3713</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6137151</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(1)</volume><pubmed_abstract>The use of natural substance to ward off microbial infections has a long history. However, the large-scale production of natural extracts often reduces antibacterial potency, thus limiting practical applications. Here we present a strategy for converting natural organosulfur compounds into nano-iron sulfides that exhibit enhanced antibacterial activity. We show that compared to garlic-derived organosulfur compounds nano-iron sulfides exhibit an over 500-fold increase in antibacterial efficacy to kill several pathogenic and drug-resistant bacteria. Furthermore, our analysis reveals that hydrogen polysulfanes released from nano-iron sulfides possess potent bactericidal activity and the release of polysulfanes can be accelerated by the enzyme-like activity of nano-iron sulfides. Finally, we demonstrate that topical applications of nano-iron sulfides can effectively disrupt pathogenic biofilms on human teeth and accelerate infected-wound healing. Together, our approach to convert organosulfur compounds into inorganic polysulfides potentially provides an antibacterial alternative to combat bacterial infections.</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Converting organosulfur compounds to inorganic polysulfides against resistant bacterial infections.</pubmed_title><pmcid>PMC6137151</pmcid><funding_grant_id>R01 DE025848</funding_grant_id><funding_grant_id>20161333</funding_grant_id><pubmed_authors>Jiang J</pubmed_authors><pubmed_authors>Li D</pubmed_authors><pubmed_authors>Gu Y</pubmed_authors><pubmed_authors>He J</pubmed_authors><pubmed_authors>Koo H</pubmed_authors><pubmed_authors>Liu Q</pubmed_authors><pubmed_authors>Yan X</pubmed_authors><pubmed_authors>Xu J</pubmed_authors><pubmed_authors>Qiu Z</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Xi J</pubmed_authors><pubmed_authors>Huang Y</pubmed_authors><pubmed_authors>Fan K</pubmed_authors><pubmed_authors>Gao L</pubmed_authors><pubmed_authors>Gao X</pubmed_authors><pubmed_authors>Shen X</pubmed_authors><pubmed_authors>Xu Z</pubmed_authors><pubmed_authors>Tang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Converting organosulfur compounds to inorganic polysulfides against resistant bacterial infections.</name><description>The use of natural substance to ward off microbial infections has a long history. However, the large-scale production of natural extracts often reduces antibacterial potency, thus limiting practical applications. Here we present a strategy for converting natural organosulfur compounds into nano-iron sulfides that exhibit enhanced antibacterial activity. We show that compared to garlic-derived organosulfur compounds nano-iron sulfides exhibit an over 500-fold increase in antibacterial efficacy to kill several pathogenic and drug-resistant bacteria. Furthermore, our analysis reveals that hydrogen polysulfanes released from nano-iron sulfides possess potent bactericidal activity and the release of polysulfanes can be accelerated by the enzyme-like activity of nano-iron sulfides. Finally, we demonstrate that topical applications of nano-iron sulfides can effectively disrupt pathogenic biofilms on human teeth and accelerate infected-wound healing. Together, our approach to convert organosulfur compounds into inorganic polysulfides potentially provides an antibacterial alternative to combat bacterial infections.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Sep</publication><modification>2021-02-20T13:14:16Z</modification><creation>2019-03-26T23:56:14Z</creation></dates><accession>S-EPMC6137151</accession><cross_references><pubmed>30213949</pubmed><doi>10.1038/s41467-018-06164-7</doi></cross_references></HashMap>