Bactericidal activities of cathelicidin LL-37 and select cationic lipids against the hypervirulent Pseudomonas aeruginosa strain LESB58
Pseudomonas aeruginosa Liverpool epidemic strain (LES) infections in cystic fibrosis (CF) patients are associated with transmissibility and increased patient morbidity. This study was designed to assess the in vitro activities of cathelicidin LL-37 peptide (LL-37) and select cationic lipids against...
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description | Pseudomonas aeruginosa Liverpool epidemic strain (LES) infections in cystic fibrosis (CF) patients are associated with transmissibility and increased patient morbidity. This study was designed to assess the in vitro activities of cathelicidin LL-37 peptide (LL-37) and select cationic lipids against Pseudomonas aeruginosa LESB58 in CF sputum and in a setting mimicking the CF airway. We found that LL-37 naturally present in airway surface fluid and some nonpeptide cationic lipid molecules such as CSA-13, CSA-90, CSA-131, and D2S have significant, but broadly differing, bactericidal activities against P. aeruginosa LESB58. We observed strong inhibition of LL-37 bactericidal activity in the presence of purified bacteriophage Pf1, which is highly expressed by P. aeruginosa LES, but the activities of the cationic lipids CSA-13 and CSA-131 were not affected by this polyanionic virus. Additionally, CSA-13 and CSA-131 effectively prevent LESB58 biofilm formation, which is stimulated by Pf1 bacteriophage, DNA, or F-actin. CSA-13 and CSA-131 display strong antibacterial activities against different clinical strains of P. aeruginosa, and their activities against P. aeruginosa LESB58 and Xen5 strains were maintained in CF sputum. These data indicate that synthetic cationic lipids (mimics of natural antimicrobial peptides) are suitable for developing an effective treatment against CF lung P. aeruginosa infections, including those caused by LES strains. |
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This study was designed to assess the in vitro activities of cathelicidin LL-37 peptide (LL-37) and select cationic lipids against Pseudomonas aeruginosa LESB58 in CF sputum and in a setting mimicking the CF airway. We found that LL-37 naturally present in airway surface fluid and some nonpeptide cationic lipid molecules such as CSA-13, CSA-90, CSA-131, and D2S have significant, but broadly differing, bactericidal activities against P. aeruginosa LESB58. We observed strong inhibition of LL-37 bactericidal activity in the presence of purified bacteriophage Pf1, which is highly expressed by P. aeruginosa LES, but the activities of the cationic lipids CSA-13 and CSA-131 were not affected by this polyanionic virus. Additionally, CSA-13 and CSA-131 effectively prevent LESB58 biofilm formation, which is stimulated by Pf1 bacteriophage, DNA, or F-actin. CSA-13 and CSA-131 display strong antibacterial activities against different clinical strains of P. aeruginosa, and their activities against P. aeruginosa LESB58 and Xen5 strains were maintained in CF sputum. These data indicate that synthetic cationic lipids (mimics of natural antimicrobial peptides) are suitable for developing an effective treatment against CF lung P. aeruginosa infections, including those caused by LES strains.</description><identifier>ISSN: 0066-4804</identifier><identifier>EISSN: 1098-6596</identifier><identifier>DOI: 10.1128/AAC.00421-15</identifier><identifier>PMID: 25870055</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Anti-Bacterial Agents ; Anti-Bacterial Agents - pharmacology ; Antimicrobial Cationic Peptides ; Antimicrobial Cationic Peptides - pharmacology ; Bacteria ; Bacteriophage Pf1 - pathogenicity ; Biofilms - drug effects ; Cystic Fibrosis - microbiology ; Experimental Therapeutics ; Humans ; Lipids - pharmacology ; Microbial Sensitivity Tests ; Microscopy, Atomic Force ; Models, Biological ; Pregnanes - pharmacology ; Propylamines - pharmacology ; Pseudomonas aeruginosa ; Pseudomonas aeruginosa - drug effects ; Pseudomonas aeruginosa - pathogenicity ; Steroids ; Steroids - pharmacology</subject><ispartof>Antimicrobial agents and chemotherapy, 2015-07, Vol.59 (7), p.3808-3815</ispartof><rights>Copyright © 2015, American Society for Microbiology. All Rights Reserved.</rights><rights>Copyright © 2015, American Society for Microbiology. All Rights Reserved. 2015 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a451t-9b93d053eaf544c8888b0f1752554e85d60735314a106ce6382fc8e0baedce1b3</citedby><cites>FETCH-LOGICAL-a451t-9b93d053eaf544c8888b0f1752554e85d60735314a106ce6382fc8e0baedce1b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4468669/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4468669/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25870055$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wnorowska, Urszula</creatorcontrib><creatorcontrib>Niemirowicz, Katarzyna</creatorcontrib><creatorcontrib>Myint, Melissa</creatorcontrib><creatorcontrib>Diamond, Scott L</creatorcontrib><creatorcontrib>Wróblewska, Marta</creatorcontrib><creatorcontrib>Savage, Paul B</creatorcontrib><creatorcontrib>Janmey, Paul A</creatorcontrib><creatorcontrib>Bucki, Robert</creatorcontrib><title>Bactericidal activities of cathelicidin LL-37 and select cationic lipids against the hypervirulent Pseudomonas aeruginosa strain LESB58</title><title>Antimicrobial agents and chemotherapy</title><addtitle>Antimicrob Agents Chemother</addtitle><addtitle>Antimicrob Agents Chemother</addtitle><description>Pseudomonas aeruginosa Liverpool epidemic strain (LES) infections in cystic fibrosis (CF) patients are associated with transmissibility and increased patient morbidity. This study was designed to assess the in vitro activities of cathelicidin LL-37 peptide (LL-37) and select cationic lipids against Pseudomonas aeruginosa LESB58 in CF sputum and in a setting mimicking the CF airway. We found that LL-37 naturally present in airway surface fluid and some nonpeptide cationic lipid molecules such as CSA-13, CSA-90, CSA-131, and D2S have significant, but broadly differing, bactericidal activities against P. aeruginosa LESB58. We observed strong inhibition of LL-37 bactericidal activity in the presence of purified bacteriophage Pf1, which is highly expressed by P. aeruginosa LES, but the activities of the cationic lipids CSA-13 and CSA-131 were not affected by this polyanionic virus. Additionally, CSA-13 and CSA-131 effectively prevent LESB58 biofilm formation, which is stimulated by Pf1 bacteriophage, DNA, or F-actin. CSA-13 and CSA-131 display strong antibacterial activities against different clinical strains of P. aeruginosa, and their activities against P. aeruginosa LESB58 and Xen5 strains were maintained in CF sputum. These data indicate that synthetic cationic lipids (mimics of natural antimicrobial peptides) are suitable for developing an effective treatment against CF lung P. aeruginosa infections, including those caused by LES strains.</description><subject>Anti-Bacterial Agents</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antimicrobial Cationic Peptides</subject><subject>Antimicrobial Cationic Peptides - pharmacology</subject><subject>Bacteria</subject><subject>Bacteriophage Pf1 - pathogenicity</subject><subject>Biofilms - drug effects</subject><subject>Cystic Fibrosis - microbiology</subject><subject>Experimental Therapeutics</subject><subject>Humans</subject><subject>Lipids - pharmacology</subject><subject>Microbial Sensitivity Tests</subject><subject>Microscopy, Atomic Force</subject><subject>Models, Biological</subject><subject>Pregnanes - pharmacology</subject><subject>Propylamines - pharmacology</subject><subject>Pseudomonas aeruginosa</subject><subject>Pseudomonas aeruginosa - drug effects</subject><subject>Pseudomonas aeruginosa - pathogenicity</subject><subject>Steroids</subject><subject>Steroids - pharmacology</subject><issn>0066-4804</issn><issn>1098-6596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFks1u1DAUhS0EotPCjjXyEiRSrhPbcTZI01ELSCOBBKwtx7mZcZXYg52M1CfgtXGYUsEC4Y1_znePrn1MyAsGl4yV6u16vbkE4CUrmHhEVgwaVUjRyMdkBSBlwRXwM3Ke0i3kvWjgKTkrhaoBhFiRH1fGThiddZ0ZaF67o5scJhp6as20x2GRnKfbbVHV1PiOJhzQTovqgneWDu7gukTNzjifJppr6P7ugPHo4jygn-jnhHMXxuBNpjDOO-dDMjRN0SzG11-uhHpGnvRmSPj8fr4g326uv24-FNtP7z9u1tvCcMGmommbqgNRoekF51bl0ULPalEKwVGJTkJdiYpxw0BalJUqe6sQWoOdRdZWF-Tdyfcwt-Ny5nMXgz5EN5p4p4Nx-m_Fu73ehaPmXCopm2zw6t4ghu8zpkmPLlkcBuMxzEmzGpgAUDX_PyqVAmANg4y-OaE2hpQi9g8dMdBLzDrHrH_FrJnI-OsTbtJY6tswR58f7V_syz9v_GD8-w9UPwHJKLEn</recordid><startdate>20150701</startdate><enddate>20150701</enddate><creator>Wnorowska, Urszula</creator><creator>Niemirowicz, Katarzyna</creator><creator>Myint, Melissa</creator><creator>Diamond, Scott L</creator><creator>Wróblewska, Marta</creator><creator>Savage, Paul B</creator><creator>Janmey, Paul A</creator><creator>Bucki, Robert</creator><general>American Society for Microbiology</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><scope>7X8</scope><scope>7QL</scope><scope>7T7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>5PM</scope></search><sort><creationdate>20150701</creationdate><title>Bactericidal activities of cathelicidin LL-37 and select cationic lipids against the hypervirulent Pseudomonas aeruginosa strain LESB58</title><author>Wnorowska, Urszula ; Niemirowicz, Katarzyna ; Myint, Melissa ; Diamond, Scott L ; Wróblewska, Marta ; Savage, Paul B ; Janmey, Paul A ; Bucki, Robert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a451t-9b93d053eaf544c8888b0f1752554e85d60735314a106ce6382fc8e0baedce1b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Anti-Bacterial Agents</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Antimicrobial Cationic Peptides</topic><topic>Antimicrobial Cationic Peptides - pharmacology</topic><topic>Bacteria</topic><topic>Bacteriophage Pf1 - pathogenicity</topic><topic>Biofilms - drug effects</topic><topic>Cystic Fibrosis - microbiology</topic><topic>Experimental Therapeutics</topic><topic>Humans</topic><topic>Lipids - pharmacology</topic><topic>Microbial Sensitivity Tests</topic><topic>Microscopy, Atomic Force</topic><topic>Models, Biological</topic><topic>Pregnanes - pharmacology</topic><topic>Propylamines - pharmacology</topic><topic>Pseudomonas aeruginosa</topic><topic>Pseudomonas aeruginosa - drug effects</topic><topic>Pseudomonas aeruginosa - pathogenicity</topic><topic>Steroids</topic><topic>Steroids - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wnorowska, Urszula</creatorcontrib><creatorcontrib>Niemirowicz, Katarzyna</creatorcontrib><creatorcontrib>Myint, Melissa</creatorcontrib><creatorcontrib>Diamond, Scott L</creatorcontrib><creatorcontrib>Wróblewska, Marta</creatorcontrib><creatorcontrib>Savage, Paul B</creatorcontrib><creatorcontrib>Janmey, Paul A</creatorcontrib><creatorcontrib>Bucki, Robert</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Antimicrobial agents and chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wnorowska, Urszula</au><au>Niemirowicz, Katarzyna</au><au>Myint, Melissa</au><au>Diamond, Scott L</au><au>Wróblewska, Marta</au><au>Savage, Paul B</au><au>Janmey, Paul A</au><au>Bucki, Robert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bactericidal activities of cathelicidin LL-37 and select cationic lipids against the hypervirulent Pseudomonas aeruginosa strain LESB58</atitle><jtitle>Antimicrobial agents and chemotherapy</jtitle><stitle>Antimicrob Agents Chemother</stitle><addtitle>Antimicrob Agents Chemother</addtitle><date>2015-07-01</date><risdate>2015</risdate><volume>59</volume><issue>7</issue><spage>3808</spage><epage>3815</epage><pages>3808-3815</pages><issn>0066-4804</issn><eissn>1098-6596</eissn><abstract>Pseudomonas aeruginosa Liverpool epidemic strain (LES) infections in cystic fibrosis (CF) patients are associated with transmissibility and increased patient morbidity. This study was designed to assess the in vitro activities of cathelicidin LL-37 peptide (LL-37) and select cationic lipids against Pseudomonas aeruginosa LESB58 in CF sputum and in a setting mimicking the CF airway. We found that LL-37 naturally present in airway surface fluid and some nonpeptide cationic lipid molecules such as CSA-13, CSA-90, CSA-131, and D2S have significant, but broadly differing, bactericidal activities against P. aeruginosa LESB58. We observed strong inhibition of LL-37 bactericidal activity in the presence of purified bacteriophage Pf1, which is highly expressed by P. aeruginosa LES, but the activities of the cationic lipids CSA-13 and CSA-131 were not affected by this polyanionic virus. Additionally, CSA-13 and CSA-131 effectively prevent LESB58 biofilm formation, which is stimulated by Pf1 bacteriophage, DNA, or F-actin. CSA-13 and CSA-131 display strong antibacterial activities against different clinical strains of P. aeruginosa, and their activities against P. aeruginosa LESB58 and Xen5 strains were maintained in CF sputum. These data indicate that synthetic cationic lipids (mimics of natural antimicrobial peptides) are suitable for developing an effective treatment against CF lung P. aeruginosa infections, including those caused by LES strains.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>25870055</pmid><doi>10.1128/AAC.00421-15</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anti-Bacterial Agents Anti-Bacterial Agents - pharmacology Antimicrobial Cationic Peptides Antimicrobial Cationic Peptides - pharmacology Bacteria Bacteriophage Pf1 - pathogenicity Biofilms - drug effects Cystic Fibrosis - microbiology Experimental Therapeutics Humans Lipids - pharmacology Microbial Sensitivity Tests Microscopy, Atomic Force Models, Biological Pregnanes - pharmacology Propylamines - pharmacology Pseudomonas aeruginosa Pseudomonas aeruginosa - drug effects Pseudomonas aeruginosa - pathogenicity Steroids Steroids - pharmacology |
title | Bactericidal activities of cathelicidin LL-37 and select cationic lipids against the hypervirulent Pseudomonas aeruginosa strain LESB58 |
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