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Therapeutic Options for Metallo-β-Lactamase-Producing Enterobacterales
The spread of metallo-β-lactamase (MBL)-producing Enterobacterales worldwide without the simultaneous increase in active antibiotics makes these organisms an urgent public health threat. This review summarizes recent advancements in diagnostic and treatment strategies for infections caused by MBL-pr...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822077/ https://www.ncbi.nlm.nih.gov/pubmed/33500635 http://dx.doi.org/10.2147/IDR.S246174 |
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author | Tan, Xing Kim, Hwan Seung Baugh, Kimberly Huang, Yanqin Kadiyala, Neeraja Wences, Marisol Singh, Nidhi Wenzler, Eric Bulman, Zackery P |
author_facet | Tan, Xing Kim, Hwan Seung Baugh, Kimberly Huang, Yanqin Kadiyala, Neeraja Wences, Marisol Singh, Nidhi Wenzler, Eric Bulman, Zackery P |
author_sort | Tan, Xing |
collection | PubMed |
description | The spread of metallo-β-lactamase (MBL)-producing Enterobacterales worldwide without the simultaneous increase in active antibiotics makes these organisms an urgent public health threat. This review summarizes recent advancements in diagnostic and treatment strategies for infections caused by MBL-producing Enterobacterales. Adequate treatment of patients infected with MBL-producing Enterobacterales relies on detection of the β-lactamase in the clinic. There are several molecular platforms that are currently available to identify clinically relevant MBLs as well as other important serine-β-lactamases. Once detected, there are several antibiotics that have historically been used for the treatment of MBL-producing Enterobacterales. Antimicrobials such as aminoglycosides, tetracyclines, fosfomycin, and polymyxins often show promising in vitro activity though clinical data are currently lacking to support their widespread use. Ceftazidime-avibactam combined with aztreonam is promising for treatment of infections caused by MBL-producing Enterobacterales and currently has the most clinical data of any available antibiotic to support its use. While cefiderocol has displayed promising activity against MBL-producing Enterobacterales in vitro and in preliminary clinical studies, further clinical studies will better shed light on its place in treatment. Lastly, there are several promising MBL inhibitors in the pipeline, which may further improve the treatment of MBL-producing Enterobacterales. |
format | Online Article Text |
id | pubmed-7822077 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-78220772021-01-25 Therapeutic Options for Metallo-β-Lactamase-Producing Enterobacterales Tan, Xing Kim, Hwan Seung Baugh, Kimberly Huang, Yanqin Kadiyala, Neeraja Wences, Marisol Singh, Nidhi Wenzler, Eric Bulman, Zackery P Infect Drug Resist Review The spread of metallo-β-lactamase (MBL)-producing Enterobacterales worldwide without the simultaneous increase in active antibiotics makes these organisms an urgent public health threat. This review summarizes recent advancements in diagnostic and treatment strategies for infections caused by MBL-producing Enterobacterales. Adequate treatment of patients infected with MBL-producing Enterobacterales relies on detection of the β-lactamase in the clinic. There are several molecular platforms that are currently available to identify clinically relevant MBLs as well as other important serine-β-lactamases. Once detected, there are several antibiotics that have historically been used for the treatment of MBL-producing Enterobacterales. Antimicrobials such as aminoglycosides, tetracyclines, fosfomycin, and polymyxins often show promising in vitro activity though clinical data are currently lacking to support their widespread use. Ceftazidime-avibactam combined with aztreonam is promising for treatment of infections caused by MBL-producing Enterobacterales and currently has the most clinical data of any available antibiotic to support its use. While cefiderocol has displayed promising activity against MBL-producing Enterobacterales in vitro and in preliminary clinical studies, further clinical studies will better shed light on its place in treatment. Lastly, there are several promising MBL inhibitors in the pipeline, which may further improve the treatment of MBL-producing Enterobacterales. Dove 2021-01-18 /pmc/articles/PMC7822077/ /pubmed/33500635 http://dx.doi.org/10.2147/IDR.S246174 Text en © 2021 Tan et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Review Tan, Xing Kim, Hwan Seung Baugh, Kimberly Huang, Yanqin Kadiyala, Neeraja Wences, Marisol Singh, Nidhi Wenzler, Eric Bulman, Zackery P Therapeutic Options for Metallo-β-Lactamase-Producing Enterobacterales |
title | Therapeutic Options for Metallo-β-Lactamase-Producing Enterobacterales |
title_full | Therapeutic Options for Metallo-β-Lactamase-Producing Enterobacterales |
title_fullStr | Therapeutic Options for Metallo-β-Lactamase-Producing Enterobacterales |
title_full_unstemmed | Therapeutic Options for Metallo-β-Lactamase-Producing Enterobacterales |
title_short | Therapeutic Options for Metallo-β-Lactamase-Producing Enterobacterales |
title_sort | therapeutic options for metallo-β-lactamase-producing enterobacterales |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822077/ https://www.ncbi.nlm.nih.gov/pubmed/33500635 http://dx.doi.org/10.2147/IDR.S246174 |
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