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Methodology for the Study of Horizontal Gene Transfer in Staphylococcus aureus
Published on: March 10, 2017
Identification and characterization of HolGH15: the holin of Staphylococcus aureus bacteriophage GH15
Jun Song1, Feifei Xia1, Haiyan Jiang2
1College of Veterinary Medicine,Jilin University, Changchun 130062, PRChina.
Abstract:
Holins are phage-encoded hydrophobic membrane proteins that spontaneously and non-specifically accumulate and form lesions in the cytoplasmic membrane. The ORF72 gene (also designated HolGH15) derived from the genome of the Staphylococcus aureus phage GH15 was predicted to encode a membrane protein. An analysis indicated that the protein encoded by HolGH15 potentially consisted of two hydrophobic transmembrane helices. This protein exhibited the structural characteristics of class II holins and belonged to the phage_holin_1 superfamily. Expression of HolGH15 in Escherichia coli BL21 cells resulted in growth retardation of the host cells, which was triggered prematurely by the addition of 2,4-dinitrophenol. The expression of HolGH15 caused morphological alterations in engineered E. coli cells, including loss of the cell wall and cytoplasmic membrane integrity and release of intracellular components, which were visualized by transmission electron microscopy. HolGH15 exerted efficient antibacterial activity at 37 °C and pH 5.2. Mutation analysis indicated that the two transmembrane domains of HolGH15 were indispensable for the activity of the full-length protein. HolGH15 showed a broad antibacterial range: it not only inhibited Staphylococcus aureus, but also demonstrated antibacterial activity against other species, including Listeria monocytogenes, Bacillus subtilis, Pseudomonas aeruginosa, Klebsiella pneumoniae and E. coli. At the minimal inhibitory concentration, HolGH15 evoked the release of cellular contents and resulted in the shrinkage and death of Staphylococcus aureus and Listeria monocytogenes cells. To the best of our knowledge, this study is the first report of a Staphylococcus aureus phage holin that exerts antibacterial activity against heterogeneous pathogens.
Insights
This study identifies a novel Staphylococcus aureus phage holin, HolGH15, which disrupts bacterial membranes. HolGH15 demonstrates broad-spectrum antibacterial activity against various pathogens, offering potential therapeutic applications.
Area of Science:
- Microbiology
- Molecular Biology
- Biochemistry
Background:
- Holins are essential phage proteins forming membrane lesions for progeny release.
- Staphylococcus aureus phage GH15 harbors the ORF72 gene encoding a potential holin, HolGH15.
- HolGH15 exhibits structural characteristics of class II holins.
Purpose of the Study:
- To characterize the HolGH15 protein from Staphylococcus aureus phage GH15.
- To investigate the antibacterial activity and mechanism of HolGH15.
- To assess the potential of HolGH15 as a therapeutic agent against bacterial pathogens.
Main Methods:
- Bioinformatic analysis of the HolGH15 gene and protein sequence.
- Expression of HolGH15 in Escherichia coli and assessment of host cell effects.
- Transmission electron microscopy to visualize cellular damage.
- Antibacterial activity assays at varying temperatures and pH.
- Mutation analysis of transmembrane domains.
- Determination of minimal inhibitory concentrations against multiple bacterial species.
Main Results:
- HolGH15, a hydrophobic membrane protein with two transmembrane helices, was identified.
- Expression of HolGH15 in E. coli caused growth retardation and cell lysis.
- HolGH15 demonstrated potent antibacterial activity against Staphylococcus aureus and a broad range of other pathogens.
- The two transmembrane domains were crucial for HolGH15's activity.
- HolGH15 induced cell membrane damage, leading to intracellular content release and cell death.
Conclusions:
- HolGH15 is a functional holin with significant antibacterial properties.
- This study presents the first report of a Staphylococcus aureus phage holin with broad-spectrum antibacterial activity.
- HolGH15 represents a promising candidate for novel antibacterial therapies against diverse pathogens.
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