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Scorpionfish BPI is highly active against multiple drug-resistant Pseudomonas aeruginosa isolates from people with cystic fibrosis
Chronic pulmonary infection is a hallmark of cystic fibrosis (CF) and requires continuous antibiotic treatment. In this context, Pseudomonas aeruginosa (Pa) is of special concern since colonizing strains frequently acquire multiple drug resistance (MDR). Bactericidal/permeability-increasing protein...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10353861/ https://www.ncbi.nlm.nih.gov/pubmed/37461324 http://dx.doi.org/10.7554/eLife.86369 |
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author | Holzinger, Jonas Maurice Toelge, Martina Werner, Maren Ederer, Katharina Ursula Siegmund, Heiko Ingo Peterhoff, David Blaas, Stefan Helmut Gisch, Nicolas Brochhausen, Christoph Gessner, André Bülow, Sigrid |
author_facet | Holzinger, Jonas Maurice Toelge, Martina Werner, Maren Ederer, Katharina Ursula Siegmund, Heiko Ingo Peterhoff, David Blaas, Stefan Helmut Gisch, Nicolas Brochhausen, Christoph Gessner, André Bülow, Sigrid |
author_sort | Holzinger, Jonas Maurice |
collection | PubMed |
description | Chronic pulmonary infection is a hallmark of cystic fibrosis (CF) and requires continuous antibiotic treatment. In this context, Pseudomonas aeruginosa (Pa) is of special concern since colonizing strains frequently acquire multiple drug resistance (MDR). Bactericidal/permeability-increasing protein (BPI) is a neutrophil-derived, endogenous protein with high bactericidal potency against Gram-negative bacteria. However, a significant range of people with CF (PwCF) produce anti-neutrophil cytoplasmic antibodies against BPI (BPI-ANCA), thereby neutralizing its bactericidal function. In accordance with literature, we describe that 51.0% of a total of 39 PwCF expressed BPI-ANCA. Importantly, an orthologous protein to human BPI (huBPI) derived from the scorpionfish Sebastes schlegelii (scoBPI) completely escaped recognition by these autoantibodies. Moreover, scoBPI exhibited high anti-inflammatory potency towards Pa LPS and was bactericidal against MDR Pa derived from PwCF at nanomolar concentrations. In conclusion, our results highlight the potential of highly active orthologous proteins of huBPI in treatment of MDR Pa infections, especially in the presence of BPI-ANCA. |
format | Online Article Text |
id | pubmed-10353861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-103538612023-07-19 Scorpionfish BPI is highly active against multiple drug-resistant Pseudomonas aeruginosa isolates from people with cystic fibrosis Holzinger, Jonas Maurice Toelge, Martina Werner, Maren Ederer, Katharina Ursula Siegmund, Heiko Ingo Peterhoff, David Blaas, Stefan Helmut Gisch, Nicolas Brochhausen, Christoph Gessner, André Bülow, Sigrid eLife Immunology and Inflammation Chronic pulmonary infection is a hallmark of cystic fibrosis (CF) and requires continuous antibiotic treatment. In this context, Pseudomonas aeruginosa (Pa) is of special concern since colonizing strains frequently acquire multiple drug resistance (MDR). Bactericidal/permeability-increasing protein (BPI) is a neutrophil-derived, endogenous protein with high bactericidal potency against Gram-negative bacteria. However, a significant range of people with CF (PwCF) produce anti-neutrophil cytoplasmic antibodies against BPI (BPI-ANCA), thereby neutralizing its bactericidal function. In accordance with literature, we describe that 51.0% of a total of 39 PwCF expressed BPI-ANCA. Importantly, an orthologous protein to human BPI (huBPI) derived from the scorpionfish Sebastes schlegelii (scoBPI) completely escaped recognition by these autoantibodies. Moreover, scoBPI exhibited high anti-inflammatory potency towards Pa LPS and was bactericidal against MDR Pa derived from PwCF at nanomolar concentrations. In conclusion, our results highlight the potential of highly active orthologous proteins of huBPI in treatment of MDR Pa infections, especially in the presence of BPI-ANCA. eLife Sciences Publications, Ltd 2023-07-18 /pmc/articles/PMC10353861/ /pubmed/37461324 http://dx.doi.org/10.7554/eLife.86369 Text en © 2023, Holzinger et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Immunology and Inflammation Holzinger, Jonas Maurice Toelge, Martina Werner, Maren Ederer, Katharina Ursula Siegmund, Heiko Ingo Peterhoff, David Blaas, Stefan Helmut Gisch, Nicolas Brochhausen, Christoph Gessner, André Bülow, Sigrid Scorpionfish BPI is highly active against multiple drug-resistant Pseudomonas aeruginosa isolates from people with cystic fibrosis |
title | Scorpionfish BPI is highly active against multiple drug-resistant Pseudomonas aeruginosa isolates from people with cystic fibrosis |
title_full | Scorpionfish BPI is highly active against multiple drug-resistant Pseudomonas aeruginosa isolates from people with cystic fibrosis |
title_fullStr | Scorpionfish BPI is highly active against multiple drug-resistant Pseudomonas aeruginosa isolates from people with cystic fibrosis |
title_full_unstemmed | Scorpionfish BPI is highly active against multiple drug-resistant Pseudomonas aeruginosa isolates from people with cystic fibrosis |
title_short | Scorpionfish BPI is highly active against multiple drug-resistant Pseudomonas aeruginosa isolates from people with cystic fibrosis |
title_sort | scorpionfish bpi is highly active against multiple drug-resistant pseudomonas aeruginosa isolates from people with cystic fibrosis |
topic | Immunology and Inflammation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10353861/ https://www.ncbi.nlm.nih.gov/pubmed/37461324 http://dx.doi.org/10.7554/eLife.86369 |
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