María M Montero, Sandra Domene-Ochoa, Núria Prim, Eliana Ferola, Carla López-Causapé, Daniel Echeverria, Mario F Ampuero Morisaki, Victoria Vega-Toribio, Luisa Sorlí, Sonia Luque, Eduardo Padilla, Antonio Oliver, Juan P Horcajada
{"title":"头孢他啶/阿维菌素和阿兹曲南对产碳青霉烯酶铜绿假单胞菌的协同疗效:中空纤维感染模型的启示。","authors":"María M Montero, Sandra Domene-Ochoa, Núria Prim, Eliana Ferola, Carla López-Causapé, Daniel Echeverria, Mario F Ampuero Morisaki, Victoria Vega-Toribio, Luisa Sorlí, Sonia Luque, Eduardo Padilla, Antonio Oliver, Juan P Horcajada","doi":"10.1080/23744235.2024.2396882","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Combination therapy is an attractive therapeutic option for extensively drug-resistant (XDR) <i>Pseudomonas aeruginosa</i> infections. Existing data support the combination of aztreonam and ceftazidime/avibactam (CZA) against class serine-β-lactamase (SBL)- and metallo-β-lactamase (MBL) - producing <i>Enterobacterales.</i> However, data about that combination against SBL- and MBL-producing <i>P. aeruginosa</i> are scarce. The objective of the study was to assess the <i>in vitro</i> activity of CZA and aztreonam alone and in combination against SBL- and MBL-producing XDR <i>P. aeruginosa</i> isolates.</p><p><strong>Methods: </strong>The combination was analyzed by means of the hollow-fiber infection model in three selected carbapenemase-producing <i>P. aeruginosa</i> isolates that were representative of the three most common XDR<i>P. aeruginosa</i> high-risk clones (ST175, ST111, ST235) responsible for global nosocomial infection outbreaks.</p><p><strong>Results: </strong>The three isolates were nonsusceptible to CZA and nonsusceptible to aztreonam. In the dynamic hollow-fiber infection model, the combination of CZA plus aztreonam exerts a bactericidal effect on the isolates, regardless of their resistance mechanism and demonstrates synergistic interactions against three isolates, achieving a bacterial reduction of 5.07 log<sub>10</sub> CFU/ml, 5.2 log<sub>10</sub> CFU/ml and 4 log<sub>10</sub> CFU/ml, respectively.</p><p><strong>Conclusion: </strong>The combination of CZA and aztreonam significantly enhanced the <i>in vitro</i> efficacy against XDR <i>P. aeruginosa</i> isolates compared to each monotherapy. This improvement suggests that the combination could serve as a feasible treatment alternative for infections caused by carbapenemase-producing XDR <i>P. aeruginosa</i>, especially in scenarios where no other treatment options are available.</p>","PeriodicalId":73372,"journal":{"name":"Infectious diseases (London, England)","volume":" ","pages":"81-88"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synergistic efficacy of ceftazidime/avibactam and aztreonam against carbapenemase-producing <i>Pseudomonas aeruginosa</i>: insights from the hollow-fiber infection model.\",\"authors\":\"María M Montero, Sandra Domene-Ochoa, Núria Prim, Eliana Ferola, Carla López-Causapé, Daniel Echeverria, Mario F Ampuero Morisaki, Victoria Vega-Toribio, Luisa Sorlí, Sonia Luque, Eduardo Padilla, Antonio Oliver, Juan P Horcajada\",\"doi\":\"10.1080/23744235.2024.2396882\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Combination therapy is an attractive therapeutic option for extensively drug-resistant (XDR) <i>Pseudomonas aeruginosa</i> infections. Existing data support the combination of aztreonam and ceftazidime/avibactam (CZA) against class serine-β-lactamase (SBL)- and metallo-β-lactamase (MBL) - producing <i>Enterobacterales.</i> However, data about that combination against SBL- and MBL-producing <i>P. aeruginosa</i> are scarce. The objective of the study was to assess the <i>in vitro</i> activity of CZA and aztreonam alone and in combination against SBL- and MBL-producing XDR <i>P. aeruginosa</i> isolates.</p><p><strong>Methods: </strong>The combination was analyzed by means of the hollow-fiber infection model in three selected carbapenemase-producing <i>P. aeruginosa</i> isolates that were representative of the three most common XDR<i>P. aeruginosa</i> high-risk clones (ST175, ST111, ST235) responsible for global nosocomial infection outbreaks.</p><p><strong>Results: </strong>The three isolates were nonsusceptible to CZA and nonsusceptible to aztreonam. In the dynamic hollow-fiber infection model, the combination of CZA plus aztreonam exerts a bactericidal effect on the isolates, regardless of their resistance mechanism and demonstrates synergistic interactions against three isolates, achieving a bacterial reduction of 5.07 log<sub>10</sub> CFU/ml, 5.2 log<sub>10</sub> CFU/ml and 4 log<sub>10</sub> CFU/ml, respectively.</p><p><strong>Conclusion: </strong>The combination of CZA and aztreonam significantly enhanced the <i>in vitro</i> efficacy against XDR <i>P. aeruginosa</i> isolates compared to each monotherapy. This improvement suggests that the combination could serve as a feasible treatment alternative for infections caused by carbapenemase-producing XDR <i>P. aeruginosa</i>, especially in scenarios where no other treatment options are available.</p>\",\"PeriodicalId\":73372,\"journal\":{\"name\":\"Infectious diseases (London, England)\",\"volume\":\" \",\"pages\":\"81-88\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Infectious diseases (London, England)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/23744235.2024.2396882\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/8/30 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Infectious diseases (London, England)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/23744235.2024.2396882","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/30 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
Synergistic efficacy of ceftazidime/avibactam and aztreonam against carbapenemase-producing Pseudomonas aeruginosa: insights from the hollow-fiber infection model.
Background: Combination therapy is an attractive therapeutic option for extensively drug-resistant (XDR) Pseudomonas aeruginosa infections. Existing data support the combination of aztreonam and ceftazidime/avibactam (CZA) against class serine-β-lactamase (SBL)- and metallo-β-lactamase (MBL) - producing Enterobacterales. However, data about that combination against SBL- and MBL-producing P. aeruginosa are scarce. The objective of the study was to assess the in vitro activity of CZA and aztreonam alone and in combination against SBL- and MBL-producing XDR P. aeruginosa isolates.
Methods: The combination was analyzed by means of the hollow-fiber infection model in three selected carbapenemase-producing P. aeruginosa isolates that were representative of the three most common XDRP. aeruginosa high-risk clones (ST175, ST111, ST235) responsible for global nosocomial infection outbreaks.
Results: The three isolates were nonsusceptible to CZA and nonsusceptible to aztreonam. In the dynamic hollow-fiber infection model, the combination of CZA plus aztreonam exerts a bactericidal effect on the isolates, regardless of their resistance mechanism and demonstrates synergistic interactions against three isolates, achieving a bacterial reduction of 5.07 log10 CFU/ml, 5.2 log10 CFU/ml and 4 log10 CFU/ml, respectively.
Conclusion: The combination of CZA and aztreonam significantly enhanced the in vitro efficacy against XDR P. aeruginosa isolates compared to each monotherapy. This improvement suggests that the combination could serve as a feasible treatment alternative for infections caused by carbapenemase-producing XDR P. aeruginosa, especially in scenarios where no other treatment options are available.