Näytä suppeat kuvailutiedot

dc.contributor.advisorPenttinen, Reetta
dc.contributor.advisorJonsdottir, Ilmur
dc.contributor.authorVacker, Sanna
dc.date.accessioned2024-04-30T07:01:43Z
dc.date.available2024-04-30T07:01:43Z
dc.date.issued2024
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/94585
dc.description.abstractAntimicrobial resistance (AMR) is an escalating global health threat, attributable to the diminishing availability of efficient antibiotics against bacterial infections. Phage therapy is considered an alternative therapeutic solution to treat resistant infections. In phage therapy, the bacteria are treated with phages, which are natural viruses that infect bacteria. However, the development of phage resistance in bacterial communities can be affected by various host-associated factors. Mucin is a glycoprotein found in the mucosal layer of the human gut, which primarily protects the cellular surface. The interactions between bacteria and phages often occur in the mucous membrane. Also, recent studies have found the potential of mucin to alter phage-bacteria interactions. In this research, the evolution of phage resistance in Escherichia coli and Klebsiella pneumoniae strains was studied in the presence of mucin and antibiotics. First, bacterial growth was measured under various mucin and antibiotic concentrations in the absence of phage to select optimal conditions for the evolution experiment. In the evolution experiment, ESBL-producing E. coli and K. pneumoniae strains were sequentially exposed to phages, one at a time, in the presence of tetracycline and/or mucin. After the experiment, the development of phage resistance was tested in the exposed bacteria by a co-culture experiment. The results demonstrate that the phage-treated bacteria exhibited consistent development of phage resistance compared to the original strains. In an effort to develop efficient phage therapy, the findings of this research help comprehend the potential factors that may hamper the successful treatment of bacterial infections.fi
dc.format.extent61
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.rightsIn Copyright
dc.subject.othermucin
dc.subject.othertetracycline
dc.titleDevelopment of phage resistance in clinical Escherichia coli and Klebsiella pneumoniae isolates
dc.identifier.urnURN:NBN:fi:jyu-202404303213
dc.type.ontasotMaster’s thesisen
dc.type.ontasotPro gradu -tutkielmafi
dc.contributor.tiedekuntaFaculty of Sciencesen
dc.contributor.tiedekuntaMatemaattis-luonnontieteellinen tiedekuntafi
dc.contributor.laitosDepartment of Biological and Environmental Scienceen
dc.contributor.laitosBio- ja ympäristötieteiden laitosfi
dc.contributor.yliopistoUniversity of Jyväskyläen
dc.contributor.yliopistoJyväskylän yliopistofi
dc.contributor.oppiaineCell and molecular biologyen
dc.contributor.oppiaineSolu- ja molekyylibiologiafi
dc.rights.copyright© The Author(s)
dc.rights.accesslevelrestrictedAccess
dc.contributor.oppiainekoodi4013
dc.subject.ysobiofilmit
dc.subject.ysoevoluutio
dc.subject.ysobakteerit
dc.subject.ysoantibiootit
dc.subject.ysoinfektiot
dc.subject.ysobiofilms
dc.subject.ysoevolution
dc.subject.ysobacteria
dc.subject.ysoantibiotics
dc.subject.ysoinfections
dc.format.contentfulltext
dc.rights.urlhttps://rightsstatements.org/page/InC/1.0/
dc.rights.accessrightsThe author has not given permission to make the work publicly available electronically. Therefore the material can be read only at the archival workstation at Jyväskylä University Library (https://kirjasto.jyu.fi/en/workspaces/facilities/facilities#autotoc-item-autotoc-2).en
dc.rights.accessrightsTekijä ei ole antanut lupaa avoimeen julkaisuun, joten aineisto on luettavissa vain Jyväskylän yliopiston kirjaston arkistotyösemalta. Ks. https://kirjasto.jyu.fi/fi/tyoskentelytilat/laitteet-ja-tilat#autotoc-item-autotoc-2.fi


Aineistoon kuuluvat tiedostot

Thumbnail

Aineisto kuuluu seuraaviin kokoelmiin

Näytä suppeat kuvailutiedot

In Copyright
Ellei muuten mainita, aineiston lisenssi on In Copyright