<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Schneider EK</submitter><funding>National Institute of Allergy and Infectious Diseases</funding><funding>NIAID NIH HHS</funding><funding>Cystic Fibrosis Foundation</funding><funding>National Health and Medical Research Council</funding><pagination>478-88</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5300747</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>2(7)</volume><pubmed_abstract>Novel combination therapies are desperately needed for combating lung infections caused by bacterial "superbugs". This study aimed to investigate the synergistic antibacterial activity of polymyxin B in combination with the cystic fibrosis (CF) drugs KALYDECO (ivacaftor) and ORKAMBI (ivacaftor + lumacaftor) against Gram-negative pathogens that commonly colonize the CF lung, in particular, the problematic Pseudomonas aeruginosa. The in vitro synergistic activity of polymyxin B combined with ivacaftor or lumacaftor was assessed using checkerboard and static time-kill assays against a panel of polymyxin-susceptible and polymyxin-resistant P. aeruginosa isolates from the lungs of CF patients. Polymyxin B, ivacaftor, and lumacaftor were ineffective when used individually against polymyxin-resis</pubmed_abstract><journal>ACS infectious diseases</journal><pubmed_title>An "Unlikely" Pair: The Antimicrobial Synergy of Polymyxin B in Combination with the Cystic Fibrosis Transmembrane Conductance Regulator Drugs KALYDECO and ORKAMBI.</pubmed_title><pmcid>PMC5300747</pmcid><funding_grant_id>R01 AI111965</funding_grant_id><funding_grant_id>R01 AI104895</funding_grant_id><funding_grant_id>R01AI104895</funding_grant_id><funding_grant_id>R01AI111965</funding_grant_id><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Doi Y</pubmed_authors><pubmed_authors>Han ML</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Huang JX</pubmed_authors><pubmed_authors>Azad MA</pubmed_authors><pubmed_authors>Velkov T</pubmed_authors><pubmed_authors>Schneider EK</pubmed_authors><pubmed_authors>Cooper MA</pubmed_authors><pubmed_authors>Muller MT</pubmed_authors><pubmed_authors>Tony Zhou Q</pubmed_authors><pubmed_authors>Baker MA</pubmed_authors><pubmed_authors>Bergen PJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>An "Unlikely" Pair: The Antimicrobial Synergy of Polymyxin B in Combination with the Cystic Fibrosis Transmembrane Conductance Regulator Drugs KALYDECO and ORKAMBI.</name><description>Novel combination therapies are desperately needed for combating lung infections caused by bacterial "superbugs". This study aimed to investigate the synergistic antibacterial activity of polymyxin B in combination with the cystic fibrosis (CF) drugs KALYDECO (ivacaftor) and ORKAMBI (ivacaftor + lumacaftor) against Gram-negative pathogens that commonly colonize the CF lung, in particular, the problematic Pseudomonas aeruginosa. The in vitro synergistic activity of polymyxin B combined with ivacaftor or lumacaftor was assessed using checkerboard and static time-kill assays against a panel of polymyxin-susceptible and polymyxin-resistant P. aeruginosa isolates from the lungs of CF patients. Polymyxin B, ivacaftor, and lumacaftor were ineffective when used individually against polymyxin-resis</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Jul</publication><modification>2025-04-19T22:41:46.925Z</modification><creation>2019-03-27T02:36:11Z</creation></dates><accession>S-EPMC5300747</accession><cross_references><pubmed>27626100</pubmed><doi>10.1021/acsinfecdis.6b00035</doi></cross_references></HashMap>