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Microbial biofilm monitoring by Electrochemical methods / Mikrobiell biofilmövervakning med elektrokemiska metoder

Hospital Acquired Infections and equipment contamination are some of the biggest issues faced by the healthcare industry worldwide. These infections generally range from mild to life threatening human infections which lead to increased costs and prolonged hospitalization time. The primary factor which caused these issues were biofilm forming bacteria which are able to withstand medications and defend themselves from various cleaning procedures. Another aspect which make these bacteria troublesome is that they are able to hide inside the biofilm, thus evading a lot of diagnostic tests. The methods used to detect these biofilms are unfortunately toxic to cells and cannot be used in vivo. Though there is enough data on the formation of biofilm on abiotic surfaces, the data present on the biophysical properties, structural organizations within the biofilm or their viscoelastic properties is very limited. In this master’s degree project, a dynamic monitoring platform is made for 2 different strains of the Salmonella Enteritidis bacteria where their structural and biophysical properties was investigated. Each strain lacks either curli or cellulose which are major components responsible for proper biofilm formation so performing these experiments on them gave us important information on how their properties get affected over time. Bacterial growth monitoring for all the strains were performed by measuring the absorbance every hour over a period of 5h and it was observed that all the strains had a very similar growth pattern until the end of the 4th hour after which they showed very mild differences. The next set of experiments involved using an eQCM to monitor the formation of biofilm on the surface of a quartz chip over 48h. There were differences observed in the biofilm formation pattern and mass deposition which provided clues as to how the biofilm formation and their viscoelastic properties are affected due to the mutations. This led to finding further clues regarding which aspect of biofilm formation is targeted by a specific mutant.

Identiferoai:union.ndltd.org:UPSALLA1/oai:DiVA.org:kth-302540
Date January 2021
CreatorsSrikumar, Vivek
PublisherKTH, Skolan för kemi, bioteknologi och hälsa (CBH)
Source SetsDiVA Archive at Upsalla University
LanguageEnglish
Detected LanguageEnglish
TypeStudent thesis, info:eu-repo/semantics/bachelorThesis, text
Formatapplication/pdf
Rightsinfo:eu-repo/semantics/openAccess
RelationTRITA-CBH-GRU ; 2021:081

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