Cargando…

Impact of the new membrane-targeting lipoglycopeptide antibiotic MCC5145 on the treatment of bacteremic pneumococcal pneumonia in mice

Bacteremic Streptococcus pneumoniae pneumonia is one of the most severe forms of invasive pneumococcal disease (IPD) and with particularly high case-fatality rates among the elderly and individuals with comorbidities, exacerbated by rising antibiotic resistance and time to initiation of therapy. Her...

Descripción completa

Detalles Bibliográficos
Autores principales: Ogunniyi, Abiodun D., Nguyen, Hang Thi, Hansford, Karl A., Cooper, Matthew A., Trott, Darren J., Blaskovich, Mark A. T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10580989/
https://www.ncbi.nlm.nih.gov/pubmed/37606382
http://dx.doi.org/10.1128/spectrum.04459-22
_version_ 1785122054767378432
author Ogunniyi, Abiodun D.
Nguyen, Hang Thi
Hansford, Karl A.
Cooper, Matthew A.
Trott, Darren J.
Blaskovich, Mark A. T.
author_facet Ogunniyi, Abiodun D.
Nguyen, Hang Thi
Hansford, Karl A.
Cooper, Matthew A.
Trott, Darren J.
Blaskovich, Mark A. T.
author_sort Ogunniyi, Abiodun D.
collection PubMed
description Bacteremic Streptococcus pneumoniae pneumonia is one of the most severe forms of invasive pneumococcal disease (IPD) and with particularly high case-fatality rates among the elderly and individuals with comorbidities, exacerbated by rising antibiotic resistance and time to initiation of therapy. Here, we examined the efficacy of the preclinical “vancapticin” glycopeptide MCC5145 against fulminant infection by S. pneumoniae serotype 2 strain D39 in a bioluminescent, neutropenic mouse model of bacteremic pneumonia. MCC5145 is a semisynthetic vancomycin derivative chemically modified at the C-terminus with a membrane-targeting motif designed to preferentially bind the anionic bacterial surface. We show that similar to vancomycin, subcutaneous administration of MCC5145 to mice 1 day after intranasal infection with a bioluminescent derivative of S. pneumoniae D39 elicited time and concentration-dependent reduction in total flux in the lungs and blood. Together, our finding supports the further development of MCC5145 as a potential new treatment option for pneumonia and/or bacteremic pneumonia in clinical settings, particularly for immunocompromised individuals. IMPORTANCE: S. pneumoniae (the pneumococcus) causes severe community acquired lung and blood infection, especially among the elderly and people with underlying medical conditions and/or weakened immune systems. The rising incidence of antibiotic resistance and delays between diagnosis of infection and commencement of effective therapy make treatment difficult and result in high mortality rates. In this work, we show that a new derivative (MCC5145) of an existing antibiotic (vancomycin) rapidly eradicated lethal pneumococcal challenge from the lungs and blood of mice with a suppressed immune system. Our findings support that MCC5145 is a promising option for the treatment of lung and blood infections caused by the pneumococcus at point-of-care settings, particularly for the elderly and individuals with a weakened immune system.
format Online
Article
Text
id pubmed-10580989
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-105809892023-10-18 Impact of the new membrane-targeting lipoglycopeptide antibiotic MCC5145 on the treatment of bacteremic pneumococcal pneumonia in mice Ogunniyi, Abiodun D. Nguyen, Hang Thi Hansford, Karl A. Cooper, Matthew A. Trott, Darren J. Blaskovich, Mark A. T. Microbiol Spectr Observation Bacteremic Streptococcus pneumoniae pneumonia is one of the most severe forms of invasive pneumococcal disease (IPD) and with particularly high case-fatality rates among the elderly and individuals with comorbidities, exacerbated by rising antibiotic resistance and time to initiation of therapy. Here, we examined the efficacy of the preclinical “vancapticin” glycopeptide MCC5145 against fulminant infection by S. pneumoniae serotype 2 strain D39 in a bioluminescent, neutropenic mouse model of bacteremic pneumonia. MCC5145 is a semisynthetic vancomycin derivative chemically modified at the C-terminus with a membrane-targeting motif designed to preferentially bind the anionic bacterial surface. We show that similar to vancomycin, subcutaneous administration of MCC5145 to mice 1 day after intranasal infection with a bioluminescent derivative of S. pneumoniae D39 elicited time and concentration-dependent reduction in total flux in the lungs and blood. Together, our finding supports the further development of MCC5145 as a potential new treatment option for pneumonia and/or bacteremic pneumonia in clinical settings, particularly for immunocompromised individuals. IMPORTANCE: S. pneumoniae (the pneumococcus) causes severe community acquired lung and blood infection, especially among the elderly and people with underlying medical conditions and/or weakened immune systems. The rising incidence of antibiotic resistance and delays between diagnosis of infection and commencement of effective therapy make treatment difficult and result in high mortality rates. In this work, we show that a new derivative (MCC5145) of an existing antibiotic (vancomycin) rapidly eradicated lethal pneumococcal challenge from the lungs and blood of mice with a suppressed immune system. Our findings support that MCC5145 is a promising option for the treatment of lung and blood infections caused by the pneumococcus at point-of-care settings, particularly for the elderly and individuals with a weakened immune system. American Society for Microbiology 2023-08-22 /pmc/articles/PMC10580989/ /pubmed/37606382 http://dx.doi.org/10.1128/spectrum.04459-22 Text en Copyright © 2023 Ogunniyi 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 Observation
Ogunniyi, Abiodun D.
Nguyen, Hang Thi
Hansford, Karl A.
Cooper, Matthew A.
Trott, Darren J.
Blaskovich, Mark A. T.
Impact of the new membrane-targeting lipoglycopeptide antibiotic MCC5145 on the treatment of bacteremic pneumococcal pneumonia in mice
title Impact of the new membrane-targeting lipoglycopeptide antibiotic MCC5145 on the treatment of bacteremic pneumococcal pneumonia in mice
title_full Impact of the new membrane-targeting lipoglycopeptide antibiotic MCC5145 on the treatment of bacteremic pneumococcal pneumonia in mice
title_fullStr Impact of the new membrane-targeting lipoglycopeptide antibiotic MCC5145 on the treatment of bacteremic pneumococcal pneumonia in mice
title_full_unstemmed Impact of the new membrane-targeting lipoglycopeptide antibiotic MCC5145 on the treatment of bacteremic pneumococcal pneumonia in mice
title_short Impact of the new membrane-targeting lipoglycopeptide antibiotic MCC5145 on the treatment of bacteremic pneumococcal pneumonia in mice
title_sort impact of the new membrane-targeting lipoglycopeptide antibiotic mcc5145 on the treatment of bacteremic pneumococcal pneumonia in mice
topic Observation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10580989/
https://www.ncbi.nlm.nih.gov/pubmed/37606382
http://dx.doi.org/10.1128/spectrum.04459-22
work_keys_str_mv AT ogunniyiabiodund impactofthenewmembranetargetinglipoglycopeptideantibioticmcc5145onthetreatmentofbacteremicpneumococcalpneumoniainmice
AT nguyenhangthi impactofthenewmembranetargetinglipoglycopeptideantibioticmcc5145onthetreatmentofbacteremicpneumococcalpneumoniainmice
AT hansfordkarla impactofthenewmembranetargetinglipoglycopeptideantibioticmcc5145onthetreatmentofbacteremicpneumococcalpneumoniainmice
AT coopermatthewa impactofthenewmembranetargetinglipoglycopeptideantibioticmcc5145onthetreatmentofbacteremicpneumococcalpneumoniainmice
AT trottdarrenj impactofthenewmembranetargetinglipoglycopeptideantibioticmcc5145onthetreatmentofbacteremicpneumococcalpneumoniainmice
AT blaskovichmarkat impactofthenewmembranetargetinglipoglycopeptideantibioticmcc5145onthetreatmentofbacteremicpneumococcalpneumoniainmice