Full Text Available
Note: Clicking the button above will open the full text document at the original institutional repository in a new window.
Investigating the effect of Staphylococcus epidermidis on the growth dynamics of Staphylococcus aureus in atopic dermatitis
Background: In atopic dermatitis (AD), studies have demonstrated inconsistencies in the interactions between Staphylococcus epidermidis and Staphylococcus aureus concerning growth and biofilm formation outcomes. This suggests that there might be a strain-level role played by the bacteria that affect...
Saved in:
| Main Author: | |
|---|---|
| Other Authors: | |
| Format: | Thesis |
| Language: | English English |
| Published: |
Department of Molecular and Cell Biology
2025
|
| Subjects: | |
| Tags: |
No Tags, Be the first to tag this record!
|
| _version_ | 1867613182697144320 |
|---|---|
| access_status_str | Open Access |
| author | Moonsamy, Rasalika Tamika |
| author2 | Dr Dube, Felix |
| author_browse | Dr Dube, Felix Moonsamy, Rasalika Tamika |
| author_facet | Dr Dube, Felix Moonsamy, Rasalika Tamika |
| author_sort | Moonsamy, Rasalika Tamika |
| collection | Thesis |
| description | Background: In atopic dermatitis (AD), studies have demonstrated inconsistencies in the interactions between Staphylococcus epidermidis and Staphylococcus aureus concerning growth and biofilm formation outcomes. This suggests that there might be a strain-level role played by the bacteria that affect the outcomes of their interactions, and consequently, the pathophysiology of AD. Furthermore, the factors that mediate these effects by S. epidermidis, are currently poorly characterised. Objective: To evaluate the effect of skin and nasal S. epidermidis on the growth dynamics and biofilm formation of co-colonising S. aureus in toddlers with and without AD. Methods: Twenty-eight (28) previously identified co-colonising pairs of S. aureus and S. epidermidis isolates were selected based on different combinations of biofilm-forming strengths. Filtered S. epidermidis-derived supernatant was incubated with S. aureus cultures to determine its effect on biofilm formation and growth. Biofilm formation was evaluated using crystal violets assays and Alamar Blue assays were used to determine cell viability. S. aureus biofilms were treated with Proteinase K (PK) or sodium metaperiodate (SM) to determine their composition. The expression of extracellular serine protease (esp) was determined by Real Time Polymerise Chain Reaction (RT-PCR). S. epidermidis-derived supernatants subjected to heat, PK and SM to characterise other potential effector molecules. Lastly, sequence types (ST) and clonal complexes (CC) of S. epidermidis and S. aureus isolates were inferred from multi-locus sequence typing profiling. Results: Pairs of S. aureus and S. epidermidis from 75% (6/8) of controls and 65% (13/20) of cases demonstrated a decrease in biofilm formation compared with S. aureus alone. No significant differences in biofilm formation were noted between pairs isolated from cases and controls. From the viability assays, we observed that pairs of S. epidermidis and S. aureus from 25% of cases compared with 80% of pairs from controls had an increase in cell viability. The majority (70%) of established biofilms were composed of a proteinaceous matrix. Expression of esp was detected in 63% of S. epidermidis isolates. Heat-treated supernatant resulted in 50% of controls and 35% of case pairs displaying an increase in biofilm biomass. Incubation with SM-treated S. epidermidis supernatants resulted in 50% of isolates from control and case pairs showing decreases in biofilm iv biomass. Pairs from control (88%) and case (65%) participants treated with PK showed decreases in biofilm formation. Only five S. epidermidis isolates matched to exact STs, while several partially matched to several possible STs. The clonal lineages of the S. aureus control isolates were made up of CC1, CC5, and CC121, whereas the case isolates also included CC15 and CC8. Conclusions: The variation displayed in the biofilm formation results indicates S. epidermidis strain specificity plays a role in the outcome of interactions. Results from treated supernatant suggest the possibility of multiple effector molecules with different constituents. Lastly, S. aureus strains exhibit monoclonality whereas S. epidermidis strains present diverse strain compositions, which could be the basis for the differential outcomes observed. Future research should apply a holistic approach to microbiome studies to understand the different factors influencing the outcome of interactions leading to biofilm production |
| format | Thesis |
| id | oai:open.uct.ac.za:11427/41777 |
| institution | University of Cape Town (South Africa) |
| language | English eng |
| last_indexed | 2026-06-10T12:32:05.102Z |
| license_str | Not specified — see source repository |
| provenance_str_mv | Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository |
| publishDate | 2025 |
| publishDateRange | 2025 |
| publishDateSort | 2025 |
| publisher | Department of Molecular and Cell Biology |
| publisherStr | Department of Molecular and Cell Biology |
| record_format | dspace |
| source_str | UCTD — University of Cape Town Open Access Repository |
| spelling | oai:open.uct.ac.za:11427/41777 Investigating the effect of Staphylococcus epidermidis on the growth dynamics of Staphylococcus aureus in atopic dermatitis Moonsamy, Rasalika Tamika Dr Dube, Felix Dr Ndhlovu, Gillian Dr Brigg, Siobhan Molecular and Cell Biology Background: In atopic dermatitis (AD), studies have demonstrated inconsistencies in the interactions between Staphylococcus epidermidis and Staphylococcus aureus concerning growth and biofilm formation outcomes. This suggests that there might be a strain-level role played by the bacteria that affect the outcomes of their interactions, and consequently, the pathophysiology of AD. Furthermore, the factors that mediate these effects by S. epidermidis, are currently poorly characterised. Objective: To evaluate the effect of skin and nasal S. epidermidis on the growth dynamics and biofilm formation of co-colonising S. aureus in toddlers with and without AD. Methods: Twenty-eight (28) previously identified co-colonising pairs of S. aureus and S. epidermidis isolates were selected based on different combinations of biofilm-forming strengths. Filtered S. epidermidis-derived supernatant was incubated with S. aureus cultures to determine its effect on biofilm formation and growth. Biofilm formation was evaluated using crystal violets assays and Alamar Blue assays were used to determine cell viability. S. aureus biofilms were treated with Proteinase K (PK) or sodium metaperiodate (SM) to determine their composition. The expression of extracellular serine protease (esp) was determined by Real Time Polymerise Chain Reaction (RT-PCR). S. epidermidis-derived supernatants subjected to heat, PK and SM to characterise other potential effector molecules. Lastly, sequence types (ST) and clonal complexes (CC) of S. epidermidis and S. aureus isolates were inferred from multi-locus sequence typing profiling. Results: Pairs of S. aureus and S. epidermidis from 75% (6/8) of controls and 65% (13/20) of cases demonstrated a decrease in biofilm formation compared with S. aureus alone. No significant differences in biofilm formation were noted between pairs isolated from cases and controls. From the viability assays, we observed that pairs of S. epidermidis and S. aureus from 25% of cases compared with 80% of pairs from controls had an increase in cell viability. The majority (70%) of established biofilms were composed of a proteinaceous matrix. Expression of esp was detected in 63% of S. epidermidis isolates. Heat-treated supernatant resulted in 50% of controls and 35% of case pairs displaying an increase in biofilm biomass. Incubation with SM-treated S. epidermidis supernatants resulted in 50% of isolates from control and case pairs showing decreases in biofilm iv biomass. Pairs from control (88%) and case (65%) participants treated with PK showed decreases in biofilm formation. Only five S. epidermidis isolates matched to exact STs, while several partially matched to several possible STs. The clonal lineages of the S. aureus control isolates were made up of CC1, CC5, and CC121, whereas the case isolates also included CC15 and CC8. Conclusions: The variation displayed in the biofilm formation results indicates S. epidermidis strain specificity plays a role in the outcome of interactions. Results from treated supernatant suggest the possibility of multiple effector molecules with different constituents. Lastly, S. aureus strains exhibit monoclonality whereas S. epidermidis strains present diverse strain compositions, which could be the basis for the differential outcomes observed. Future research should apply a holistic approach to microbiome studies to understand the different factors influencing the outcome of interactions leading to biofilm production 2025-09-12T07:01:04Z 2025-09-12T07:01:04Z 2025 2025-09-12T06:56:58Z Thesis / Dissertation Masters MSc http://hdl.handle.net/11427/41777 en eng application/pdf Department of Molecular and Cell Biology Faculty of Science University of Cape Town |
| spellingShingle | Molecular and Cell Biology Moonsamy, Rasalika Tamika Investigating the effect of Staphylococcus epidermidis on the growth dynamics of Staphylococcus aureus in atopic dermatitis |
| thesis_degree_str | Master's |
| title | Investigating the effect of Staphylococcus epidermidis on the growth dynamics of Staphylococcus aureus in atopic dermatitis |
| title_full | Investigating the effect of Staphylococcus epidermidis on the growth dynamics of Staphylococcus aureus in atopic dermatitis |
| title_fullStr | Investigating the effect of Staphylococcus epidermidis on the growth dynamics of Staphylococcus aureus in atopic dermatitis |
| title_full_unstemmed | Investigating the effect of Staphylococcus epidermidis on the growth dynamics of Staphylococcus aureus in atopic dermatitis |
| title_short | Investigating the effect of Staphylococcus epidermidis on the growth dynamics of Staphylococcus aureus in atopic dermatitis |
| title_sort | investigating the effect of staphylococcus epidermidis on the growth dynamics of staphylococcus aureus in atopic dermatitis |
| topic | Molecular and Cell Biology |
| url | http://hdl.handle.net/11427/41777 |
| work_keys_str_mv | AT moonsamyrasalikatamika investigatingtheeffectofstaphylococcusepidermidisonthegrowthdynamicsofstaphylococcusaureusinatopicdermatitis |