Polysaccharide‐Targeting Lipid Nanoparticles to Kill Gram‐Negative Bacteria
The rapid increase and spread of Gram‐negative bacteria resistant to many or all existing treatments threaten a return to the preantibiotic era. The presence of bacterial polysaccharides that impede the penetration of many antimicrobials and protect them from the innate immune system contributes to...
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creator | Lai, Xiangfeng Chow, Seong Hoong Le Brun, Anton P. Muir, Benjamin W. Bergen, Phillip J. White, Jacinta Yu, Heidi H. Wang, Jiping Danne, Jill Jiang, Jhih‐hang Short, Francesca L. Han, Mei‐Ling Strugnell, Richard A. Song, Jiangning Cameron, Neil R. Peleg, Anton Y. Li, Jian Shen, Hsin‐Hui |
description | The rapid increase and spread of Gram‐negative bacteria resistant to many or all existing treatments threaten a return to the preantibiotic era. The presence of bacterial polysaccharides that impede the penetration of many antimicrobials and protect them from the innate immune system contributes to resistance and pathogenicity. No currently approved antibiotics target the polysaccharide regions of microbes. Here, describe monolaurin‐based niosomes, the first lipid nanoparticles that can eliminate bacterial polysaccharides from hypervirulent Klebsiella pneumoniae, are described. Their combination with polymyxin B shows no cytotoxicity in vitro and is highly effective in combating K. pneumoniae infection in vivo. Comprehensive mechanistic studies have revealed that antimicrobial activity proceeds via a multimodal mechanism. Initially, lipid nanoparticles disrupt polysaccharides, then outer and inner membranes are destabilized and destroyed by polymyxin B, resulting in synergistic cell lysis. This novel lipidic nanoparticle system shows tremendous promise as a highly effective antimicrobial treatment targeting multidrug‐resistant Gram‐negative pathogens.
The first reported instance of a lipid nanoparticle that efficiently targets the polysaccharide regions of Gram‐negative bacteria is described. In conjunction with polymyxin B, the lipid nanoparticle synergistically eradicates polysaccharides via multimodal mechanisms. This promising innovation holds immense potential in countering the escalating challenge of antibiotic resistance in Gram‐negative bacteria. |
doi_str_mv | 10.1002/smll.202305052 |
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The first reported instance of a lipid nanoparticle that efficiently targets the polysaccharide regions of Gram‐negative bacteria is described. In conjunction with polymyxin B, the lipid nanoparticle synergistically eradicates polysaccharides via multimodal mechanisms. This promising innovation holds immense potential in countering the escalating challenge of antibiotic resistance in Gram‐negative bacteria.</description><identifier>ISSN: 1613-6810</identifier><identifier>EISSN: 1613-6829</identifier><identifier>DOI: 10.1002/smll.202305052</identifier><identifier>PMID: 37798622</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>antibiotic resistance ; Bacteria ; Biocompatibility ; Immune system ; In vivo methods and tests ; Klebsiella ; lipid nanoparticles ; Lipids ; model membranes ; Nanoparticles ; neutron reflectometry ; polysaccharide ; Polysaccharides</subject><ispartof>Small (Weinheim an der Bergstrasse, Germany), 2024-02, Vol.20 (6), p.e2305052-n/a</ispartof><rights>2023 The Authors. Small published by Wiley‐VCH GmbH</rights><rights>2023 The Authors. Small published by Wiley-VCH GmbH.</rights><rights>2023. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4132-7b045c9c827c0070b66b33b928b37f581c08afb375af5940a7e849ba9e5478d23</citedby><cites>FETCH-LOGICAL-c4132-7b045c9c827c0070b66b33b928b37f581c08afb375af5940a7e849ba9e5478d23</cites><orcidid>0000-0002-2558-4415 ; 0000-0002-8541-4370</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fsmll.202305052$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fsmll.202305052$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37798622$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lai, Xiangfeng</creatorcontrib><creatorcontrib>Chow, Seong Hoong</creatorcontrib><creatorcontrib>Le Brun, Anton P.</creatorcontrib><creatorcontrib>Muir, Benjamin W.</creatorcontrib><creatorcontrib>Bergen, Phillip J.</creatorcontrib><creatorcontrib>White, Jacinta</creatorcontrib><creatorcontrib>Yu, Heidi H.</creatorcontrib><creatorcontrib>Wang, Jiping</creatorcontrib><creatorcontrib>Danne, Jill</creatorcontrib><creatorcontrib>Jiang, Jhih‐hang</creatorcontrib><creatorcontrib>Short, Francesca L.</creatorcontrib><creatorcontrib>Han, Mei‐Ling</creatorcontrib><creatorcontrib>Strugnell, Richard A.</creatorcontrib><creatorcontrib>Song, Jiangning</creatorcontrib><creatorcontrib>Cameron, Neil R.</creatorcontrib><creatorcontrib>Peleg, Anton Y.</creatorcontrib><creatorcontrib>Li, Jian</creatorcontrib><creatorcontrib>Shen, Hsin‐Hui</creatorcontrib><title>Polysaccharide‐Targeting Lipid Nanoparticles to Kill Gram‐Negative Bacteria</title><title>Small (Weinheim an der Bergstrasse, Germany)</title><addtitle>Small</addtitle><description>The rapid increase and spread of Gram‐negative bacteria resistant to many or all existing treatments threaten a return to the preantibiotic era. The presence of bacterial polysaccharides that impede the penetration of many antimicrobials and protect them from the innate immune system contributes to resistance and pathogenicity. No currently approved antibiotics target the polysaccharide regions of microbes. Here, describe monolaurin‐based niosomes, the first lipid nanoparticles that can eliminate bacterial polysaccharides from hypervirulent Klebsiella pneumoniae, are described. Their combination with polymyxin B shows no cytotoxicity in vitro and is highly effective in combating K. pneumoniae infection in vivo. Comprehensive mechanistic studies have revealed that antimicrobial activity proceeds via a multimodal mechanism. Initially, lipid nanoparticles disrupt polysaccharides, then outer and inner membranes are destabilized and destroyed by polymyxin B, resulting in synergistic cell lysis. This novel lipidic nanoparticle system shows tremendous promise as a highly effective antimicrobial treatment targeting multidrug‐resistant Gram‐negative pathogens.
The first reported instance of a lipid nanoparticle that efficiently targets the polysaccharide regions of Gram‐negative bacteria is described. In conjunction with polymyxin B, the lipid nanoparticle synergistically eradicates polysaccharides via multimodal mechanisms. This promising innovation holds immense potential in countering the escalating challenge of antibiotic resistance in Gram‐negative bacteria.</description><subject>antibiotic resistance</subject><subject>Bacteria</subject><subject>Biocompatibility</subject><subject>Immune system</subject><subject>In vivo methods and tests</subject><subject>Klebsiella</subject><subject>lipid nanoparticles</subject><subject>Lipids</subject><subject>model membranes</subject><subject>Nanoparticles</subject><subject>neutron reflectometry</subject><subject>polysaccharide</subject><subject>Polysaccharides</subject><issn>1613-6810</issn><issn>1613-6829</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNqFkL1OwzAURi0EovytjCgSC0vLtZ3E9ggVFESgSJTZclynGDlNsVNQNx6BZ-RJMGopEgvT_YZzP917EDrE0MMA5DTUzvUIEAoZZGQD7eAc027OidhcZwwdtBvCMwDFJGXbqEMZEzwnZAcN7xu3CErrJ-Xt2Hy-f4yUn5jWTidJYWd2nNypaTNTvrXamZC0TXJjnUsGXtURvjMT1dpXk5wr3Rpv1T7aqpQL5mA199Dj5cWof9UthoPr_lnR1SmmpMtKSDMtNCdMAzAo87yktBSEl5RVGccauKpizlSViRQUMzwVpRImSxkfE7qHTpa9M9-8zE1oZW2DNs6pqWnmQRLOUpJDfDeix3_Q52bup_E6SQShOIoTPFK9JaV9E4I3lZx5Wyu_kBjkt2r5rVquVceFo1XtvKzNeI3_uI2AWAJv1pnFP3Xy4bYofsu_AFO-i3I</recordid><startdate>20240201</startdate><enddate>20240201</enddate><creator>Lai, Xiangfeng</creator><creator>Chow, Seong Hoong</creator><creator>Le Brun, Anton P.</creator><creator>Muir, Benjamin W.</creator><creator>Bergen, Phillip J.</creator><creator>White, Jacinta</creator><creator>Yu, Heidi H.</creator><creator>Wang, Jiping</creator><creator>Danne, Jill</creator><creator>Jiang, Jhih‐hang</creator><creator>Short, Francesca L.</creator><creator>Han, Mei‐Ling</creator><creator>Strugnell, Richard A.</creator><creator>Song, Jiangning</creator><creator>Cameron, Neil R.</creator><creator>Peleg, Anton Y.</creator><creator>Li, Jian</creator><creator>Shen, Hsin‐Hui</creator><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2558-4415</orcidid><orcidid>https://orcid.org/0000-0002-8541-4370</orcidid></search><sort><creationdate>20240201</creationdate><title>Polysaccharide‐Targeting Lipid Nanoparticles to Kill Gram‐Negative Bacteria</title><author>Lai, Xiangfeng ; Chow, Seong Hoong ; Le Brun, Anton P. ; Muir, Benjamin W. ; Bergen, Phillip J. ; White, Jacinta ; Yu, Heidi H. ; Wang, Jiping ; Danne, Jill ; Jiang, Jhih‐hang ; Short, Francesca L. ; Han, Mei‐Ling ; Strugnell, Richard A. ; Song, Jiangning ; Cameron, Neil R. ; Peleg, Anton Y. ; Li, Jian ; Shen, Hsin‐Hui</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4132-7b045c9c827c0070b66b33b928b37f581c08afb375af5940a7e849ba9e5478d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>antibiotic resistance</topic><topic>Bacteria</topic><topic>Biocompatibility</topic><topic>Immune system</topic><topic>In vivo methods and tests</topic><topic>Klebsiella</topic><topic>lipid nanoparticles</topic><topic>Lipids</topic><topic>model membranes</topic><topic>Nanoparticles</topic><topic>neutron reflectometry</topic><topic>polysaccharide</topic><topic>Polysaccharides</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lai, Xiangfeng</creatorcontrib><creatorcontrib>Chow, Seong Hoong</creatorcontrib><creatorcontrib>Le Brun, Anton P.</creatorcontrib><creatorcontrib>Muir, Benjamin W.</creatorcontrib><creatorcontrib>Bergen, Phillip J.</creatorcontrib><creatorcontrib>White, Jacinta</creatorcontrib><creatorcontrib>Yu, Heidi H.</creatorcontrib><creatorcontrib>Wang, Jiping</creatorcontrib><creatorcontrib>Danne, Jill</creatorcontrib><creatorcontrib>Jiang, Jhih‐hang</creatorcontrib><creatorcontrib>Short, Francesca L.</creatorcontrib><creatorcontrib>Han, Mei‐Ling</creatorcontrib><creatorcontrib>Strugnell, Richard A.</creatorcontrib><creatorcontrib>Song, Jiangning</creatorcontrib><creatorcontrib>Cameron, Neil R.</creatorcontrib><creatorcontrib>Peleg, Anton Y.</creatorcontrib><creatorcontrib>Li, Jian</creatorcontrib><creatorcontrib>Shen, Hsin‐Hui</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Small (Weinheim an der Bergstrasse, Germany)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lai, Xiangfeng</au><au>Chow, Seong Hoong</au><au>Le Brun, Anton P.</au><au>Muir, Benjamin W.</au><au>Bergen, Phillip J.</au><au>White, Jacinta</au><au>Yu, Heidi H.</au><au>Wang, Jiping</au><au>Danne, Jill</au><au>Jiang, Jhih‐hang</au><au>Short, Francesca L.</au><au>Han, Mei‐Ling</au><au>Strugnell, Richard A.</au><au>Song, Jiangning</au><au>Cameron, Neil R.</au><au>Peleg, Anton Y.</au><au>Li, Jian</au><au>Shen, Hsin‐Hui</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polysaccharide‐Targeting Lipid Nanoparticles to Kill Gram‐Negative Bacteria</atitle><jtitle>Small (Weinheim an der Bergstrasse, Germany)</jtitle><addtitle>Small</addtitle><date>2024-02-01</date><risdate>2024</risdate><volume>20</volume><issue>6</issue><spage>e2305052</spage><epage>n/a</epage><pages>e2305052-n/a</pages><issn>1613-6810</issn><eissn>1613-6829</eissn><abstract>The rapid increase and spread of Gram‐negative bacteria resistant to many or all existing treatments threaten a return to the preantibiotic era. The presence of bacterial polysaccharides that impede the penetration of many antimicrobials and protect them from the innate immune system contributes to resistance and pathogenicity. No currently approved antibiotics target the polysaccharide regions of microbes. Here, describe monolaurin‐based niosomes, the first lipid nanoparticles that can eliminate bacterial polysaccharides from hypervirulent Klebsiella pneumoniae, are described. Their combination with polymyxin B shows no cytotoxicity in vitro and is highly effective in combating K. pneumoniae infection in vivo. Comprehensive mechanistic studies have revealed that antimicrobial activity proceeds via a multimodal mechanism. Initially, lipid nanoparticles disrupt polysaccharides, then outer and inner membranes are destabilized and destroyed by polymyxin B, resulting in synergistic cell lysis. This novel lipidic nanoparticle system shows tremendous promise as a highly effective antimicrobial treatment targeting multidrug‐resistant Gram‐negative pathogens.
The first reported instance of a lipid nanoparticle that efficiently targets the polysaccharide regions of Gram‐negative bacteria is described. In conjunction with polymyxin B, the lipid nanoparticle synergistically eradicates polysaccharides via multimodal mechanisms. This promising innovation holds immense potential in countering the escalating challenge of antibiotic resistance in Gram‐negative bacteria.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>37798622</pmid><doi>10.1002/smll.202305052</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-2558-4415</orcidid><orcidid>https://orcid.org/0000-0002-8541-4370</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | antibiotic resistance Bacteria Biocompatibility Immune system In vivo methods and tests Klebsiella lipid nanoparticles Lipids model membranes Nanoparticles neutron reflectometry polysaccharide Polysaccharides |
title | Polysaccharide‐Targeting Lipid Nanoparticles to Kill Gram‐Negative Bacteria |
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