已发表论文

对聚乙二醇化纳米-杆菌肽 A 抵抗肺炎链球菌抗菌机制的见解: 包括对青霉素敏感和具有青霉素抗性两种菌株

 

Authors Hong W, Liu L, Zhang Z, Zhao Y, Zhang D, Liu M

Received 28 June 2018

Accepted for publication 18 September 2018

Published 10 October 2018 Volume 2018:13 Pages 6297—6309

DOI https://doi.org/10.2147/IJN.S178596

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Colin Mak

Peer reviewer comments 2

Editor who approved publication: Dr Linlin Sun

Background: Multidrug-resistant (MDR) Streptococcus pneumonia  constitute a major worldwide public health concern.
Materials and methods: In our preliminary study, PEGylated nano-self-assemblies of bacitracin A (PEGylated Nano-BA12K) showed strong antibacterial potency against reference S. pneumonia  strain (ATCC 49619). In this study, the possibility of applying PEGylated Nano-BA12K against penicillin-resistant S. pneumonia  was further investigated. In addition, the underlying antibacterial mechanism of PEGylated Nano-BA12K against both sensitive and resistant S. pneumonia  was also clarified systematically, since S. pneumonia  was naturally resistant to its unassembled counterpart bacitracin A (BA).
Results: PEGylated Nano-BA12K showed strong antibacterial potency against 13 clinical isolates of S. pneumonia , including five penicillin-resistant strains. Structural changes, partial collapse, and even lysis of both penicillin-sensitive and penicillin-resistant bacteria were observed after incubation with PEGylated Nano-BA12K via transmission electron microscopy and atomic force microscopy. Thus, the cell wall or/and cell membrane might be the main target of PEGylated Nano-BA12K against S. pneumonia . PEGylated Nano-BA12K exhibited limited effect on the permeabilization and peptidoglycan content of cell wall. Surface pressure measurement suggested that PEGylated Nano-BA12K was much more tensioactive than BA, which was usually translated into a good membranolytic effect, and is helpful to permeabilize the cell membrane and damage membrane integrity, as evidenced by depolarization of the membrane potential, permeabilization of membrane and leakage of calcein from liposomes.
Conclusion: Collectively, great cell membrane permeability and formidable membrane disruption may work together for the strong antibacterial activity of PEGylated Nano-BA12K against S. pneumonia . Taken together, PEGylated Nano-BA12K has excellent potential against both penicillin-sensitive and penicillin-resistant S. pneumonia  and might be suitable for the treatment of S. pneumonia  infectious diseases.
Keywords: PEGylated Nano-BA12K, multidrug-resistant, Streptococcus pneumonia , penicillin-sensitive and penicillin-resistant




Figure 4 AFM micrographs of S. pneumonia ATCC 49619 treated with...