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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
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.
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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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