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Bacteriophages Against Colistin-Resistant Klebsiella Pneumoniae- [electronic resource]
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Bacteriophages Against Colistin-Resistant Klebsiella Pneumoniae- [electronic resource]
자료유형  
 학위논문
Control Number  
0016933762
International Standard Book Number  
9798380262132
Dewey Decimal Classification Number  
616
Main Entry-Personal Name  
Fowler, Erin.
Publication, Distribution, etc. (Imprint  
[S.l.] : University of Pittsburgh., 2023
Publication, Distribution, etc. (Imprint  
Ann Arbor : ProQuest Dissertations & Theses, 2023
Physical Description  
1 online resource(34 p.)
General Note  
Source: Dissertations Abstracts International, Volume: 85-03, Section: B.
General Note  
Advisor: Mailliard, Robbie;Mattila, Joshua;Doi, Yohei.
Dissertation Note  
Thesis (M.Sc.)--University of Pittsburgh, 2023.
Restrictions on Access Note  
This item must not be sold to any third party vendors.
Summary, Etc.  
요약Klebsiella pneumoniae is one of the most common causes of hospital-acquired infections, and is becoming increasingly resistant to various agents including colistin, a last resort antibiotic. As there are limited treatment options for these types of infections, bacteriophages active against them are drawing attention as a potential treatment option. To identify such bacteriophages, environmental water samples were screened against five different colistin-resistant clinical strains. As a result, two individual bacteriophages, MC8 and MC9, with activity against a colistin-resistant Klebsiella pneumoniae strain were isolated. Both bacteriophages were exclusively active againstK. pneumoniae Sequence Type (ST) 258 clade I strains, except for MC9, which was also active against an additional K. pneumoniae ST433 strain. Sequence analysis of the two bacteriophages showed identical sequences except for a 52 base pair nucleotide deletion in the tail spike gene in MC9. Generation of phage-resistant mutants to each bacteriophage was performed to identify their targets. Upon analysis of the phage-resistant mutant sequences, an insertion sequence was found in the wcaJgene encoding undecaprenyl-phosphate glucose-1-phosphage transferase. This gene helps catalyze the synthesis of colanic acid, a polysaccharide in the extracellular membrane, and a known attachment point used for phage entry.
Subject Added Entry-Topical Term  
Genetic testing.
Subject Added Entry-Topical Term  
Infections.
Subject Added Entry-Topical Term  
Infectious diseases.
Subject Added Entry-Topical Term  
Pathogens.
Subject Added Entry-Topical Term  
Antibiotics.
Subject Added Entry-Topical Term  
Mutation.
Subject Added Entry-Topical Term  
Bacterial infections.
Subject Added Entry-Topical Term  
Bacteria.
Subject Added Entry-Topical Term  
Lawns.
Subject Added Entry-Topical Term  
Fatty acids.
Subject Added Entry-Topical Term  
Glucose.
Subject Added Entry-Topical Term  
Public health.
Subject Added Entry-Topical Term  
Genomes.
Subject Added Entry-Topical Term  
Biology.
Subject Added Entry-Topical Term  
Protozoa.
Subject Added Entry-Topical Term  
Gram-negative bacteria.
Subject Added Entry-Topical Term  
Research & development--R&D.
Subject Added Entry-Topical Term  
Enzymes.
Subject Added Entry-Topical Term  
Drug resistance.
Subject Added Entry-Topical Term  
Genetics.
Subject Added Entry-Topical Term  
Microbiology.
Subject Added Entry-Topical Term  
Pathology.
Subject Added Entry-Topical Term  
Pharmaceutical sciences.
Subject Added Entry-Topical Term  
Pharmacology.
Added Entry-Corporate Name  
University of Pittsburgh.
Host Item Entry  
Dissertations Abstracts International. 85-03B.
Host Item Entry  
Dissertation Abstract International
Electronic Location and Access  
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Control Number  
joongbu:641456
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