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Activity of the Novel Aminomethylcycline KBP-7072 and Comparators against 1,057 Geographically Diverse Recent Clinical Isolates from the SENTRY Surveillance Program, 2019
KBP-7072 is a novel broad-spectrum tetracycline (aminomethylcycline) antibacterial in clinical development (oral and intravenous formulations) for the treatment of acute bacterial skin and skin structure infections, community-acquired bacterial pneumonia, and complicated intra-abdominal infections....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8765295/ https://www.ncbi.nlm.nih.gov/pubmed/34633850 http://dx.doi.org/10.1128/AAC.01397-21 |
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author | Huband, Michael D. Thompson, Jennifer D. Gurung, Nabina D. Liu, Qingmei Li, Li Zhang, Jay Streit, Jennifer M. Castanheira, Mariana |
author_facet | Huband, Michael D. Thompson, Jennifer D. Gurung, Nabina D. Liu, Qingmei Li, Li Zhang, Jay Streit, Jennifer M. Castanheira, Mariana |
author_sort | Huband, Michael D. |
collection | PubMed |
description | KBP-7072 is a novel broad-spectrum tetracycline (aminomethylcycline) antibacterial in clinical development (oral and intravenous formulations) for the treatment of acute bacterial skin and skin structure infections, community-acquired bacterial pneumonia, and complicated intra-abdominal infections. KBP-7072 is active against many of the World Health Organization priority pathogens. In this study, KBP-7072 and tetracycline class comparators were susceptibility tested against 1,057 geographically diverse surveillance isolates from 2019 according to Clinical and Laboratory Standards Institute (CLSI) guidelines. KBP-7072 demonstrated potent in vitro activity against Gram-positive and Gram-negative bacterial pathogens. KBP-7072 was active against Staphylococcus aureus (MIC(50/90), 0.06/0.12 mg/liter), methicillin-resistant S. aureus (MIC(50/90), 0.06/0.12 mg/liter), S. lugdunensis (MIC(50/90), 0.03/0.03 mg/liter), and other coagulase-negative staphylococci (MIC(50/90), 0.06/0.25 mg/liter). KBP-7072 was active against Enterococcus faecalis (MIC(50/90), 0.03/0.06 mg/liter) and vancomycin-susceptible and -nonsusceptible E. faecium (MIC(50/90), 0.03/0.03 mg/liter); Streptococcus pneumoniae (MIC(50/90), ≤0.015/0.03 mg/liter), including penicillin- and tetracycline-resistant strains; S. agalactiae (MIC(50/90), 0.03/0.06 mg/liter), including macrolide-resistant strains; S. pyogenes (MIC(50/90), 0.03/0.03 mg/liter); and viridans group streptococci, including S. anginosus group (MIC(50/90), ≤0.015/0.03 mg/liter) isolates. KBP-7072 inhibited 90.2% (MIC(50/90), 0.25/2 mg/liter) of all Enterobacterales isolates, including expanded-spectrum β-lactamase-phenotype strains at ≤2 mg/liter. KBP-7072 demonstrated potent activity against Acinetobacter baumannii-calcoaceticus species complex and Stenotrophomonas maltophilia isolates (MIC(50/90) values, 0.5/1 mg/liter), Haemophilus influenzae (MIC(50/90), 0.12/0.25 mg/liter; 100.0% inhibited at ≤0.25 mg/liter), and Moraxella catarrhalis (MIC(50/90), 0.06/0.06 mg/liter). Based on MIC(90) values, KBP-7072 in vitro activity was generally superior to that the other tetracycline class comparators tested. The potent activity of KBP-7072, including resistant organism groups, merits further clinical investigation in infections where these organisms are likely to occur. |
format | Online Article Text |
id | pubmed-8765295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-87652952022-01-24 Activity of the Novel Aminomethylcycline KBP-7072 and Comparators against 1,057 Geographically Diverse Recent Clinical Isolates from the SENTRY Surveillance Program, 2019 Huband, Michael D. Thompson, Jennifer D. Gurung, Nabina D. Liu, Qingmei Li, Li Zhang, Jay Streit, Jennifer M. Castanheira, Mariana Antimicrob Agents Chemother Susceptibility KBP-7072 is a novel broad-spectrum tetracycline (aminomethylcycline) antibacterial in clinical development (oral and intravenous formulations) for the treatment of acute bacterial skin and skin structure infections, community-acquired bacterial pneumonia, and complicated intra-abdominal infections. KBP-7072 is active against many of the World Health Organization priority pathogens. In this study, KBP-7072 and tetracycline class comparators were susceptibility tested against 1,057 geographically diverse surveillance isolates from 2019 according to Clinical and Laboratory Standards Institute (CLSI) guidelines. KBP-7072 demonstrated potent in vitro activity against Gram-positive and Gram-negative bacterial pathogens. KBP-7072 was active against Staphylococcus aureus (MIC(50/90), 0.06/0.12 mg/liter), methicillin-resistant S. aureus (MIC(50/90), 0.06/0.12 mg/liter), S. lugdunensis (MIC(50/90), 0.03/0.03 mg/liter), and other coagulase-negative staphylococci (MIC(50/90), 0.06/0.25 mg/liter). KBP-7072 was active against Enterococcus faecalis (MIC(50/90), 0.03/0.06 mg/liter) and vancomycin-susceptible and -nonsusceptible E. faecium (MIC(50/90), 0.03/0.03 mg/liter); Streptococcus pneumoniae (MIC(50/90), ≤0.015/0.03 mg/liter), including penicillin- and tetracycline-resistant strains; S. agalactiae (MIC(50/90), 0.03/0.06 mg/liter), including macrolide-resistant strains; S. pyogenes (MIC(50/90), 0.03/0.03 mg/liter); and viridans group streptococci, including S. anginosus group (MIC(50/90), ≤0.015/0.03 mg/liter) isolates. KBP-7072 inhibited 90.2% (MIC(50/90), 0.25/2 mg/liter) of all Enterobacterales isolates, including expanded-spectrum β-lactamase-phenotype strains at ≤2 mg/liter. KBP-7072 demonstrated potent activity against Acinetobacter baumannii-calcoaceticus species complex and Stenotrophomonas maltophilia isolates (MIC(50/90) values, 0.5/1 mg/liter), Haemophilus influenzae (MIC(50/90), 0.12/0.25 mg/liter; 100.0% inhibited at ≤0.25 mg/liter), and Moraxella catarrhalis (MIC(50/90), 0.06/0.06 mg/liter). Based on MIC(90) values, KBP-7072 in vitro activity was generally superior to that the other tetracycline class comparators tested. The potent activity of KBP-7072, including resistant organism groups, merits further clinical investigation in infections where these organisms are likely to occur. American Society for Microbiology 2022-01-18 /pmc/articles/PMC8765295/ /pubmed/34633850 http://dx.doi.org/10.1128/AAC.01397-21 Text en Copyright © 2022 Huband et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Susceptibility Huband, Michael D. Thompson, Jennifer D. Gurung, Nabina D. Liu, Qingmei Li, Li Zhang, Jay Streit, Jennifer M. Castanheira, Mariana Activity of the Novel Aminomethylcycline KBP-7072 and Comparators against 1,057 Geographically Diverse Recent Clinical Isolates from the SENTRY Surveillance Program, 2019 |
title | Activity of the Novel Aminomethylcycline KBP-7072 and Comparators against 1,057 Geographically Diverse Recent Clinical Isolates from the SENTRY Surveillance Program, 2019 |
title_full | Activity of the Novel Aminomethylcycline KBP-7072 and Comparators against 1,057 Geographically Diverse Recent Clinical Isolates from the SENTRY Surveillance Program, 2019 |
title_fullStr | Activity of the Novel Aminomethylcycline KBP-7072 and Comparators against 1,057 Geographically Diverse Recent Clinical Isolates from the SENTRY Surveillance Program, 2019 |
title_full_unstemmed | Activity of the Novel Aminomethylcycline KBP-7072 and Comparators against 1,057 Geographically Diverse Recent Clinical Isolates from the SENTRY Surveillance Program, 2019 |
title_short | Activity of the Novel Aminomethylcycline KBP-7072 and Comparators against 1,057 Geographically Diverse Recent Clinical Isolates from the SENTRY Surveillance Program, 2019 |
title_sort | activity of the novel aminomethylcycline kbp-7072 and comparators against 1,057 geographically diverse recent clinical isolates from the sentry surveillance program, 2019 |
topic | Susceptibility |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8765295/ https://www.ncbi.nlm.nih.gov/pubmed/34633850 http://dx.doi.org/10.1128/AAC.01397-21 |
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