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LysGH15 kills Staphylococcus aureus without being affected by the humoral immune response or inducing inflammation
The lysin LysGH15, derived from the staphylococcal phage GH15, exhibits a wide lytic spectrum and highly efficient lytic activity against methicillin-resistant Staphylococcus aureus (MRSA). Here, we found that LysGH15 did not induce resistance in MRSA or methicillin-sensitive S. aureus (MSSA) strain...
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/PMC4935890/ https://www.ncbi.nlm.nih.gov/pubmed/27385518 http://dx.doi.org/10.1038/srep29344 |
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author | Zhang, Lei Li, Dong Li, Xinwei Hu, Liyuan Cheng, Mengjun Xia, Feifei Gong, Pengjuan Wang, Bin Ge, Jinli Zhang, Hao Cai, Ruopeng Wang, Yanmei Sun, Changjiang Feng, Xin Lei, Liancheng Han, Wenyu Gu, Jingmin |
author_facet | Zhang, Lei Li, Dong Li, Xinwei Hu, Liyuan Cheng, Mengjun Xia, Feifei Gong, Pengjuan Wang, Bin Ge, Jinli Zhang, Hao Cai, Ruopeng Wang, Yanmei Sun, Changjiang Feng, Xin Lei, Liancheng Han, Wenyu Gu, Jingmin |
author_sort | Zhang, Lei |
collection | PubMed |
description | The lysin LysGH15, derived from the staphylococcal phage GH15, exhibits a wide lytic spectrum and highly efficient lytic activity against methicillin-resistant Staphylococcus aureus (MRSA). Here, we found that LysGH15 did not induce resistance in MRSA or methicillin-sensitive S. aureus (MSSA) strains after repeated treatment. Although LysGH15 triggered the generation of LysGH15-specific antibodies in mice, these antibodies did not block lytic activity in vitro (nor the binding capacity of LysGH15). More importantly, when the antibody titre was highest in mice immunized with LysGH15, a single intravenous injection of LysGH15 was sufficient to protect mice against lethal infection with MRSA. These results indicated that LysGH15-specific antibodies did not affect the killing efficiency of LysGH15 against MRSA in vitro or in vivo. LysGH15 also reduced pro-inflammatory cytokines in mice with lethal infections. Furthermore, a high-dose LysGH15 injection did not cause significant adverse effects or pathological changes in the main organs of treated animals. These results provide further evidence for the administration of LysGH15 as an alternative strategy for the treatment of infections caused by MRSA. |
format | Online Article Text |
id | pubmed-4935890 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49358902016-07-08 LysGH15 kills Staphylococcus aureus without being affected by the humoral immune response or inducing inflammation Zhang, Lei Li, Dong Li, Xinwei Hu, Liyuan Cheng, Mengjun Xia, Feifei Gong, Pengjuan Wang, Bin Ge, Jinli Zhang, Hao Cai, Ruopeng Wang, Yanmei Sun, Changjiang Feng, Xin Lei, Liancheng Han, Wenyu Gu, Jingmin Sci Rep Article The lysin LysGH15, derived from the staphylococcal phage GH15, exhibits a wide lytic spectrum and highly efficient lytic activity against methicillin-resistant Staphylococcus aureus (MRSA). Here, we found that LysGH15 did not induce resistance in MRSA or methicillin-sensitive S. aureus (MSSA) strains after repeated treatment. Although LysGH15 triggered the generation of LysGH15-specific antibodies in mice, these antibodies did not block lytic activity in vitro (nor the binding capacity of LysGH15). More importantly, when the antibody titre was highest in mice immunized with LysGH15, a single intravenous injection of LysGH15 was sufficient to protect mice against lethal infection with MRSA. These results indicated that LysGH15-specific antibodies did not affect the killing efficiency of LysGH15 against MRSA in vitro or in vivo. LysGH15 also reduced pro-inflammatory cytokines in mice with lethal infections. Furthermore, a high-dose LysGH15 injection did not cause significant adverse effects or pathological changes in the main organs of treated animals. These results provide further evidence for the administration of LysGH15 as an alternative strategy for the treatment of infections caused by MRSA. Nature Publishing Group 2016-07-07 /pmc/articles/PMC4935890/ /pubmed/27385518 http://dx.doi.org/10.1038/srep29344 Text en Copyright © 2016, Macmillan Publishers Limited 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 Zhang, Lei Li, Dong Li, Xinwei Hu, Liyuan Cheng, Mengjun Xia, Feifei Gong, Pengjuan Wang, Bin Ge, Jinli Zhang, Hao Cai, Ruopeng Wang, Yanmei Sun, Changjiang Feng, Xin Lei, Liancheng Han, Wenyu Gu, Jingmin LysGH15 kills Staphylococcus aureus without being affected by the humoral immune response or inducing inflammation |
title | LysGH15 kills Staphylococcus aureus without being affected by the humoral immune response or inducing inflammation |
title_full | LysGH15 kills Staphylococcus aureus without being affected by the humoral immune response or inducing inflammation |
title_fullStr | LysGH15 kills Staphylococcus aureus without being affected by the humoral immune response or inducing inflammation |
title_full_unstemmed | LysGH15 kills Staphylococcus aureus without being affected by the humoral immune response or inducing inflammation |
title_short | LysGH15 kills Staphylococcus aureus without being affected by the humoral immune response or inducing inflammation |
title_sort | lysgh15 kills staphylococcus aureus without being affected by the humoral immune response or inducing inflammation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4935890/ https://www.ncbi.nlm.nih.gov/pubmed/27385518 http://dx.doi.org/10.1038/srep29344 |
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