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Antisense Peptide Nucleic Acid–Diaminobutanoic Acid Dendron Conjugates with SbmA-Independent Antimicrobial Activity against Gram-Negative Bacteria
[Image: see text] Precision antisense antibacterial agents may be developed into novel antibiotics in the fight against multidrug-resistant Gram-negative bacteria. In this study, a series of diaminobutanoic acid (DAB) dendrons are presented as novel carriers for the delivery of antisense antibacteri...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9112330/ https://www.ncbi.nlm.nih.gov/pubmed/35436109 http://dx.doi.org/10.1021/acsinfecdis.2c00089 |
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author | Iubatti, Mirko Gabas, Isabel Maicas Cavaco, Lina M. Mood, Elnaz Harifi Lim, Ernest Bonanno, Federica Yavari, Niloofar Brolin, Camilla Nielsen, Peter E. |
author_facet | Iubatti, Mirko Gabas, Isabel Maicas Cavaco, Lina M. Mood, Elnaz Harifi Lim, Ernest Bonanno, Federica Yavari, Niloofar Brolin, Camilla Nielsen, Peter E. |
author_sort | Iubatti, Mirko |
collection | PubMed |
description | [Image: see text] Precision antisense antibacterial agents may be developed into novel antibiotics in the fight against multidrug-resistant Gram-negative bacteria. In this study, a series of diaminobutanoic acid (DAB) dendrons are presented as novel carriers for the delivery of antisense antibacterial peptide nucleic acids (PNAs). The dendron–PNA conjugates targeting the essential acpP gene exhibit specific antisense antimicrobial bactericidal activity against Escherichia coli and Klebsiella pneumoniae at one-digit micromolar concentrations, while showing low toxicity to human cells. One compound selected from a structure–activity relationship series showed high stability in mouse and human serum (t(1/2) ≫ 24 h) as well as in vivo activity against a multidrug-resistant, extended spectrum beta-lactamase-producing E. coli in a murine peritonitis model. The compound was also well tolerated in mice upon i.v. administration up to a dose of 20 mg/kg, and in vivo fluorescence imaging indicated clearance via renal excretion with slight accumulation in the kidneys and liver. Thus, DAB-based dendrons constitute a promising new chemistry platform for development of effective delivery agents for antibacterial drugs with possible in vivo use. |
format | Online Article Text |
id | pubmed-9112330 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-91123302022-05-18 Antisense Peptide Nucleic Acid–Diaminobutanoic Acid Dendron Conjugates with SbmA-Independent Antimicrobial Activity against Gram-Negative Bacteria Iubatti, Mirko Gabas, Isabel Maicas Cavaco, Lina M. Mood, Elnaz Harifi Lim, Ernest Bonanno, Federica Yavari, Niloofar Brolin, Camilla Nielsen, Peter E. ACS Infect Dis [Image: see text] Precision antisense antibacterial agents may be developed into novel antibiotics in the fight against multidrug-resistant Gram-negative bacteria. In this study, a series of diaminobutanoic acid (DAB) dendrons are presented as novel carriers for the delivery of antisense antibacterial peptide nucleic acids (PNAs). The dendron–PNA conjugates targeting the essential acpP gene exhibit specific antisense antimicrobial bactericidal activity against Escherichia coli and Klebsiella pneumoniae at one-digit micromolar concentrations, while showing low toxicity to human cells. One compound selected from a structure–activity relationship series showed high stability in mouse and human serum (t(1/2) ≫ 24 h) as well as in vivo activity against a multidrug-resistant, extended spectrum beta-lactamase-producing E. coli in a murine peritonitis model. The compound was also well tolerated in mice upon i.v. administration up to a dose of 20 mg/kg, and in vivo fluorescence imaging indicated clearance via renal excretion with slight accumulation in the kidneys and liver. Thus, DAB-based dendrons constitute a promising new chemistry platform for development of effective delivery agents for antibacterial drugs with possible in vivo use. American Chemical Society 2022-04-18 2022-05-13 /pmc/articles/PMC9112330/ /pubmed/35436109 http://dx.doi.org/10.1021/acsinfecdis.2c00089 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Iubatti, Mirko Gabas, Isabel Maicas Cavaco, Lina M. Mood, Elnaz Harifi Lim, Ernest Bonanno, Federica Yavari, Niloofar Brolin, Camilla Nielsen, Peter E. Antisense Peptide Nucleic Acid–Diaminobutanoic Acid Dendron Conjugates with SbmA-Independent Antimicrobial Activity against Gram-Negative Bacteria |
title | Antisense Peptide Nucleic Acid–Diaminobutanoic
Acid Dendron Conjugates with SbmA-Independent Antimicrobial Activity
against Gram-Negative Bacteria |
title_full | Antisense Peptide Nucleic Acid–Diaminobutanoic
Acid Dendron Conjugates with SbmA-Independent Antimicrobial Activity
against Gram-Negative Bacteria |
title_fullStr | Antisense Peptide Nucleic Acid–Diaminobutanoic
Acid Dendron Conjugates with SbmA-Independent Antimicrobial Activity
against Gram-Negative Bacteria |
title_full_unstemmed | Antisense Peptide Nucleic Acid–Diaminobutanoic
Acid Dendron Conjugates with SbmA-Independent Antimicrobial Activity
against Gram-Negative Bacteria |
title_short | Antisense Peptide Nucleic Acid–Diaminobutanoic
Acid Dendron Conjugates with SbmA-Independent Antimicrobial Activity
against Gram-Negative Bacteria |
title_sort | antisense peptide nucleic acid–diaminobutanoic
acid dendron conjugates with sbma-independent antimicrobial activity
against gram-negative bacteria |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9112330/ https://www.ncbi.nlm.nih.gov/pubmed/35436109 http://dx.doi.org/10.1021/acsinfecdis.2c00089 |
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