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Fluorocycline TP-271 Is Potent against Complicated Community-Acquired Bacterial Pneumonia Pathogens
TP-271 is a novel, fully synthetic fluorocycline antibiotic in clinical development for the treatment of respiratory infections caused by susceptible and multidrug-resistant pathogens. TP-271 was active in MIC assays against key community respiratory Gram-positive and Gram-negative pathogens, includ...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5322343/ https://www.ncbi.nlm.nih.gov/pubmed/28251179 http://dx.doi.org/10.1128/mSphere.00004-17 |
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author | Grossman, Trudy H. Fyfe, Corey O’Brien, William Hackel, Meredith Minyard, Mary Beth Waites, Ken B. Dubois, Jacques Murphy, Timothy M. Slee, Andrew M. Weiss, William J. Sutcliffe, Joyce A. |
author_facet | Grossman, Trudy H. Fyfe, Corey O’Brien, William Hackel, Meredith Minyard, Mary Beth Waites, Ken B. Dubois, Jacques Murphy, Timothy M. Slee, Andrew M. Weiss, William J. Sutcliffe, Joyce A. |
author_sort | Grossman, Trudy H. |
collection | PubMed |
description | TP-271 is a novel, fully synthetic fluorocycline antibiotic in clinical development for the treatment of respiratory infections caused by susceptible and multidrug-resistant pathogens. TP-271 was active in MIC assays against key community respiratory Gram-positive and Gram-negative pathogens, including Streptococcus pneumoniae (MIC(90) = 0.03 µg/ml), methicillin-sensitive Staphylococcus aureus (MSSA; MIC(90) = 0.25 µg/ml), methicillin-resistant S. aureus (MRSA; MIC(90) = 0.12 µg/ml), Streptococcus pyogenes (MIC(90) = 0.03 µg/ml), Haemophilus influenzae (MIC(90) = 0.12 µg/ml), and Moraxella catarrhalis (MIC(90) ≤0.016 µg/ml). TP-271 showed activity (MIC(90) = 0.12 µg/ml) against community-acquired MRSA expressing Panton-Valentine leukocidin (PVL). MIC(90) values against Mycoplasma pneumoniae, Legionella pneumophila, and Chlamydia pneumoniae were 0.004, 1, and 4 µg/ml, respectively. TP-271 was efficacious in neutropenic and immunocompetent animal pneumonia models, generally showing, compared to the burden at the start of dosing, ~2 to 5 log(10) CFU reductions against MRSA, S. pneumoniae, and H. influenzae infections when given intravenously (i.v.) and ~1 to 4 log(10) CFU reductions when given orally (p.o.). TP-271 was potent against key community-acquired bacterial pneumonia (CABP) pathogens and was minimally affected, or unaffected, by tetracycline-specific resistance mechanisms and fluoroquinolone or macrolide drug resistance phenotypes. IMPORTANCE Rising resistance rates for macrolides, fluoroquinolones, and β-lactams in the most common pathogens associated with community-acquired bacterial pneumonia (CABP) are of concern, especially for cases of moderate to severe infections in vulnerable populations such as the very young and the elderly. New antibiotics that are active against multidrug-resistant Streptococcus pneumoniae and Staphylococcus aureus are needed for use in the empirical treatment of the most severe forms of this disease. TP-271 is a promising new fluorocycline antibiotic demonstrating in vitro potency and nonclinical efficacy by intravenous and oral administration against the major pathogens associated with moderate to severe CABP. |
format | Online Article Text |
id | pubmed-5322343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-53223432017-03-01 Fluorocycline TP-271 Is Potent against Complicated Community-Acquired Bacterial Pneumonia Pathogens Grossman, Trudy H. Fyfe, Corey O’Brien, William Hackel, Meredith Minyard, Mary Beth Waites, Ken B. Dubois, Jacques Murphy, Timothy M. Slee, Andrew M. Weiss, William J. Sutcliffe, Joyce A. mSphere Research Article TP-271 is a novel, fully synthetic fluorocycline antibiotic in clinical development for the treatment of respiratory infections caused by susceptible and multidrug-resistant pathogens. TP-271 was active in MIC assays against key community respiratory Gram-positive and Gram-negative pathogens, including Streptococcus pneumoniae (MIC(90) = 0.03 µg/ml), methicillin-sensitive Staphylococcus aureus (MSSA; MIC(90) = 0.25 µg/ml), methicillin-resistant S. aureus (MRSA; MIC(90) = 0.12 µg/ml), Streptococcus pyogenes (MIC(90) = 0.03 µg/ml), Haemophilus influenzae (MIC(90) = 0.12 µg/ml), and Moraxella catarrhalis (MIC(90) ≤0.016 µg/ml). TP-271 showed activity (MIC(90) = 0.12 µg/ml) against community-acquired MRSA expressing Panton-Valentine leukocidin (PVL). MIC(90) values against Mycoplasma pneumoniae, Legionella pneumophila, and Chlamydia pneumoniae were 0.004, 1, and 4 µg/ml, respectively. TP-271 was efficacious in neutropenic and immunocompetent animal pneumonia models, generally showing, compared to the burden at the start of dosing, ~2 to 5 log(10) CFU reductions against MRSA, S. pneumoniae, and H. influenzae infections when given intravenously (i.v.) and ~1 to 4 log(10) CFU reductions when given orally (p.o.). TP-271 was potent against key community-acquired bacterial pneumonia (CABP) pathogens and was minimally affected, or unaffected, by tetracycline-specific resistance mechanisms and fluoroquinolone or macrolide drug resistance phenotypes. IMPORTANCE Rising resistance rates for macrolides, fluoroquinolones, and β-lactams in the most common pathogens associated with community-acquired bacterial pneumonia (CABP) are of concern, especially for cases of moderate to severe infections in vulnerable populations such as the very young and the elderly. New antibiotics that are active against multidrug-resistant Streptococcus pneumoniae and Staphylococcus aureus are needed for use in the empirical treatment of the most severe forms of this disease. TP-271 is a promising new fluorocycline antibiotic demonstrating in vitro potency and nonclinical efficacy by intravenous and oral administration against the major pathogens associated with moderate to severe CABP. American Society for Microbiology 2017-02-22 /pmc/articles/PMC5322343/ /pubmed/28251179 http://dx.doi.org/10.1128/mSphere.00004-17 Text en Copyright © 2017 Grossman et al. http://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 (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Grossman, Trudy H. Fyfe, Corey O’Brien, William Hackel, Meredith Minyard, Mary Beth Waites, Ken B. Dubois, Jacques Murphy, Timothy M. Slee, Andrew M. Weiss, William J. Sutcliffe, Joyce A. Fluorocycline TP-271 Is Potent against Complicated Community-Acquired Bacterial Pneumonia Pathogens |
title | Fluorocycline TP-271 Is Potent against Complicated Community-Acquired Bacterial Pneumonia Pathogens |
title_full | Fluorocycline TP-271 Is Potent against Complicated Community-Acquired Bacterial Pneumonia Pathogens |
title_fullStr | Fluorocycline TP-271 Is Potent against Complicated Community-Acquired Bacterial Pneumonia Pathogens |
title_full_unstemmed | Fluorocycline TP-271 Is Potent against Complicated Community-Acquired Bacterial Pneumonia Pathogens |
title_short | Fluorocycline TP-271 Is Potent against Complicated Community-Acquired Bacterial Pneumonia Pathogens |
title_sort | fluorocycline tp-271 is potent against complicated community-acquired bacterial pneumonia pathogens |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5322343/ https://www.ncbi.nlm.nih.gov/pubmed/28251179 http://dx.doi.org/10.1128/mSphere.00004-17 |
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