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‘Artilysation’ of endolysin λSa2lys strongly improves its enzymatic and antibacterial activity against streptococci
Endolysins constitute a promising class of antibacterials against Gram-positive bacteria. Recently, endolysins have been engineered with selected peptides to obtain a new generation of lytic proteins, Artilysins, with specific activity against Gram-negative bacteria. Here, we demonstrate that artily...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075790/ https://www.ncbi.nlm.nih.gov/pubmed/27775093 http://dx.doi.org/10.1038/srep35382 |
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author | Rodríguez-Rubio, Lorena Chang, Wai-Ling Gutiérrez, Diana Lavigne, Rob Martínez, Beatriz Rodríguez, Ana Govers, Sander K. Aertsen, Abram Hirl, Christine Biebl, Manfred Briers, Yves García, Pilar |
author_facet | Rodríguez-Rubio, Lorena Chang, Wai-Ling Gutiérrez, Diana Lavigne, Rob Martínez, Beatriz Rodríguez, Ana Govers, Sander K. Aertsen, Abram Hirl, Christine Biebl, Manfred Briers, Yves García, Pilar |
author_sort | Rodríguez-Rubio, Lorena |
collection | PubMed |
description | Endolysins constitute a promising class of antibacterials against Gram-positive bacteria. Recently, endolysins have been engineered with selected peptides to obtain a new generation of lytic proteins, Artilysins, with specific activity against Gram-negative bacteria. Here, we demonstrate that artilysation can also be used to enhance the antibacterial activity of endolysins against Gram-positive bacteria and to reduce the dependence on external conditions. Art-240, a chimeric protein of the anti-streptococcal endolysin λSa2lys and the polycationic peptide PCNP, shows a similar species specificity as the parental endolysin, but the bactericidal activity against streptococci increases and is less affected by elevated NaCl concentrations and pH variations. Time-kill experiments and time-lapse microscopy demonstrate that the killing rate of Art-240 is approximately two-fold higher compared to wildtype endolysin λSa2lys, with a reduction in viable bacteria of 3 log units after 10 min. In addition, lower doses of Art-240 are required to achieve the same bactericidal effect. |
format | Online Article Text |
id | pubmed-5075790 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50757902016-10-28 ‘Artilysation’ of endolysin λSa2lys strongly improves its enzymatic and antibacterial activity against streptococci Rodríguez-Rubio, Lorena Chang, Wai-Ling Gutiérrez, Diana Lavigne, Rob Martínez, Beatriz Rodríguez, Ana Govers, Sander K. Aertsen, Abram Hirl, Christine Biebl, Manfred Briers, Yves García, Pilar Sci Rep Article Endolysins constitute a promising class of antibacterials against Gram-positive bacteria. Recently, endolysins have been engineered with selected peptides to obtain a new generation of lytic proteins, Artilysins, with specific activity against Gram-negative bacteria. Here, we demonstrate that artilysation can also be used to enhance the antibacterial activity of endolysins against Gram-positive bacteria and to reduce the dependence on external conditions. Art-240, a chimeric protein of the anti-streptococcal endolysin λSa2lys and the polycationic peptide PCNP, shows a similar species specificity as the parental endolysin, but the bactericidal activity against streptococci increases and is less affected by elevated NaCl concentrations and pH variations. Time-kill experiments and time-lapse microscopy demonstrate that the killing rate of Art-240 is approximately two-fold higher compared to wildtype endolysin λSa2lys, with a reduction in viable bacteria of 3 log units after 10 min. In addition, lower doses of Art-240 are required to achieve the same bactericidal effect. Nature Publishing Group 2016-10-24 /pmc/articles/PMC5075790/ /pubmed/27775093 http://dx.doi.org/10.1038/srep35382 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Rodríguez-Rubio, Lorena Chang, Wai-Ling Gutiérrez, Diana Lavigne, Rob Martínez, Beatriz Rodríguez, Ana Govers, Sander K. Aertsen, Abram Hirl, Christine Biebl, Manfred Briers, Yves García, Pilar ‘Artilysation’ of endolysin λSa2lys strongly improves its enzymatic and antibacterial activity against streptococci |
title | ‘Artilysation’ of endolysin λSa2lys strongly improves its enzymatic and antibacterial activity against streptococci |
title_full | ‘Artilysation’ of endolysin λSa2lys strongly improves its enzymatic and antibacterial activity against streptococci |
title_fullStr | ‘Artilysation’ of endolysin λSa2lys strongly improves its enzymatic and antibacterial activity against streptococci |
title_full_unstemmed | ‘Artilysation’ of endolysin λSa2lys strongly improves its enzymatic and antibacterial activity against streptococci |
title_short | ‘Artilysation’ of endolysin λSa2lys strongly improves its enzymatic and antibacterial activity against streptococci |
title_sort | ‘artilysation’ of endolysin λsa2lys strongly improves its enzymatic and antibacterial activity against streptococci |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075790/ https://www.ncbi.nlm.nih.gov/pubmed/27775093 http://dx.doi.org/10.1038/srep35382 |
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