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Isolation and Characterization of Bacteriophage SSU5 Specific for Salmonella enterica serovar Typhimurium Rough Strain

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dc.contributor.advisor유상렬-
dc.contributor.author김수진-
dc.date.accessioned2017-07-14T06:50:08Z-
dc.date.available2017-07-14T06:50:08Z-
dc.date.issued2013-02-
dc.identifier.other000000008701-
dc.identifier.urihttps://hdl.handle.net/10371/126020-
dc.description학위논문 (석사)-- 서울대학교 대학원 : 농생명공학부, 2013. 2. 유상렬.-
dc.description.abstractSalmonella sp. is a major food-borne pathogen causing a variety of diseases. Use of bacteriophage for control of foodborne pathogen is a newly promising way as an alternative antibiotic therapy. Previously, our group has isolated several phages specific for S. Typhimurium to develop phage cocktail for Salmonella biocontrol. However, most of them bind only one of 3 types of the cell surface structure: BtuB, O-antigen (O-Ag) and flagella. Using the ΔbtuB and the ΔbtuB ΔrfbP double mutant strains of Salmonella as a host, I isolated SSU5 phage that does not use BtuB, O-antigen, or flagella as a receptor. TEM analysis showed that SSU5 belongs to the family Siphoviridae and genomic analysis revealed that SSU5 contains a linear dsDNA consisting of 103, 229 bp with a G+C content of 51.11%. The genome of SSU5 showed high homology to that of cryptic plasmid pHCM2 harbored by Salmonella Typhi strain CT18, and 72 out of 130 predicted ORFs were annotated as hypothetical proteins, supporting the novelty of this phage. The inhibition of SSU5 adsorption to the periodate treated-bacteria allowed me to hypothesize that the rough lipopolysaccharide (LPS) may be the host receptor for SSU5, and it was verified by a spotting assay on the mutants that have various truncations in their core LPS. Analysis of the receptor of SSU5 revealed that this phage would be a promising tool as a phage cocktail component to control rough strains of S. Typhimurium generated by mutation or phase variation.-
dc.description.tableofcontentsABSTRACT
CONTENTS
I. INTRODUCTION
Ⅱ. MATERIALS AND METHODS
1. Bacterial strains and growth condition
2. Bacteriophage Isolation and purification
3. Bacteriophage host range
4. Transmission electron microscopy
5. Construction of gene deletion mutant
6. Bacteriophage adsorption assay
7. Bacteriophage bacterial challenge test
8. Periodate or Proteinase K treatment
9. Isolation of P22H5-resistant S. Typhimurium mutant
10. LPS extraction and analysis from P22H5-resistant S. Typhimurium mutant
11. Bacteriophage DNA purification
12. Full-genome sequencing of bacteriophage SSU5 and bioinformatic analysis
13. Nucleotide sequence accession number
Ⅲ. RESULTS
1. Isolation and the receptor determination of Salmonella phages
2. Bacteriophage SSU5 morphology and classification
3. Host range of phage SSU5
4. Bacteriophage SSU5 genomic analysis
5. Identification of phage SSU5 receptor
6. Effect of various LPS core truncation on SSU5 adsorption
7. SSU5 infection to P22H5 resistant mutants
8. Bacterial challenge tests with SSU5 and phage cocktail
Ⅳ. DISCUSSION
Ⅴ. REFFERENCES
국문초록
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dc.formatapplication/pdf-
dc.format.extent1198637 bytes-
dc.format.mediumapplication/pdf-
dc.language.isoen-
dc.publisher서울대학교 대학원-
dc.subjectBacteriophage-
dc.subjectSalmonella Typhimurium-
dc.subjectphage receptor-
dc.subjectcore-oligosaccharide-
dc.subject.ddc664-
dc.titleIsolation and Characterization of Bacteriophage SSU5 Specific for Salmonella enterica serovar Typhimurium Rough Strain-
dc.typeThesis-
dc.description.degreeMaster-
dc.citation.pages52-
dc.contributor.affiliation농업생명과학대학 식품공학과-
dc.date.awarded2013-02-
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