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DOI 10.1038/srep29344

Медицинская библиотека · Scientific reports · 2016

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

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

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.

Для цитирования: 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.. Scientific reports. 2016. DOI: 10.1038/srep29344.

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