{"id":{"repo_id":"abertay","oai_identifier":"oai:rke.abertay.ac.uk:studenttheses/ee318b1c-d3f5-4357-8165-2bf1caed633d"},"canonical_url":"https://search.dev.ndltd.org/etd/abertay/oai:rke.abertay.ac.uk:studenttheses/ee318b1c-d3f5-4357-8165-2bf1caed633d","repository":{"repo_id":"abertay","name":"Abertay University","base_url":"https://rke.abertay.ac.uk/ws/oai"},"display":{"title":"Studies on the effects of sub-minimal inhibitory concentrations of antibiotics on the virulence factors of biofilm bacteria","abstract":"<i>Pseudomonas aeruginosa</i> is a notorious nosocomial opportunist. Planktonic forms of this pathogen have been traditionally studied for its pathogenicity. Such studies have shown that sub-minimal inhibitory concentrations (sub-MICs) of antibiotics are able to negatively modulate pathogenicity. However, more recent findings suggest a biofilm basis of infection. In this study, monospecies and binary biofilms of <i>Pseudomonas aeruginosa</i> ATCC 15692 (PAOl) and <i>Escherichia coli</i> ATCC 10000 were investigated for their pathogenic potential using resistance and virulence as key pathogenic determinants, in the presence of sub-MICs of selected antibiotics (Ampicillin, Nalidixic acid and Streptomycin).<br/><br/>MICs of biofilms were observed to be at least 7-fold greater than those of the corresponding planktonic form of the same species (as judged from results obtained from MIC experiments). SDS-PAGE and 2D-PAGE analysis indicate alteration of outer membrane proteins (OMPs) within the envelope of the pathogen in sub-MIC antibiotic treated samples. The observed rearrangement of lipopolysaccharide (LPS; as observed in LPS gel experiments) may also contribute to the pathogens increased tolerance to antibiotics within the biofilm state.<br/><br/>While LPS changes may possibly help the biofilm bacteria escape host immune system <i>in vivo</i>, more direct evidence of increases in virulence of the pathogen comes from investigation of its secreted proteases and cytotoxins (leucocidin). Virulence-specific azocasein and micro-culture tetrazolium (MTT) assays against both monospecies and binary biofilms of <i>Pseudomonas aeruginosa</i> indicate significant increases in virulence potential of proteases and cytotoxins, respectively. These results were further substantiated in phase contrast microscopy images showing advanced stages of oncosis in tissue cultured mouse spleen myeloma (Sp2) cells treated with leucocidin isolated from <i>Ps. aeruginosa</i> treated with sub-MIC of<br/>ampicillin (8 pg mL'1).<br/><br/>The results reported in this thesis provide evidence of observed increases in virulence and pathogenicity in biofilm cells of <i>Pseudomonas aeruginosa</i> in the presence of sub-MICs of selected antibiotics, <i>in vitro</i>. Although these findings are those of <i>in vitro</i> experiments, they may have significant implications regarding the usage and therapeutic control of antibiotics in clinical situations.","abstract_html":"&lt;i&gt;Pseudomonas aeruginosa&lt;/i&gt; is a notorious nosocomial opportunist. Planktonic forms of this pathogen have been traditionally studied for its pathogenicity. Such studies have shown that sub-minimal inhibitory concentrations (sub-MICs) of antibiotics are able to negatively modulate pathogenicity. However, more recent findings suggest a biofilm basis of infection. In this study, monospecies and binary biofilms of &lt;i&gt;Pseudomonas aeruginosa&lt;/i&gt; ATCC 15692 (PAOl) and &lt;i&gt;Escherichia coli&lt;/i&gt; ATCC 10000 were investigated for their pathogenic potential using resistance and virulence as key pathogenic determinants, in the presence of sub-MICs of selected antibiotics (Ampicillin, Nalidixic acid and Streptomycin).&lt;br/&gt;&lt;br/&gt;MICs of biofilms were observed to be at least 7-fold greater than those of the corresponding planktonic form of the same species (as judged from results obtained from MIC experiments). SDS-PAGE and 2D-PAGE analysis indicate alteration of outer membrane proteins (OMPs) within the envelope of the pathogen in sub-MIC antibiotic treated samples. The observed rearrangement of lipopolysaccharide (LPS; as observed in LPS gel experiments) may also contribute to the pathogens increased tolerance to antibiotics within the biofilm state.&lt;br/&gt;&lt;br/&gt;While LPS changes may possibly help the biofilm bacteria escape host immune system &lt;i&gt;in vivo&lt;/i&gt;, more direct evidence of increases in virulence of the pathogen comes from investigation of its secreted proteases and cytotoxins (leucocidin). Virulence-specific azocasein and micro-culture tetrazolium (MTT) assays against both monospecies and binary biofilms of &lt;i&gt;Pseudomonas aeruginosa&lt;/i&gt; indicate significant increases in virulence potential of proteases and cytotoxins, respectively. These results were further substantiated in phase contrast microscopy images showing advanced stages of oncosis in tissue cultured mouse spleen myeloma (Sp2) cells treated with leucocidin isolated from &lt;i&gt;Ps. aeruginosa&lt;/i&gt; treated with sub-MIC of&lt;br/&gt;ampicillin (8 pg mL&#x27;1).&lt;br/&gt;&lt;br/&gt;The results reported in this thesis provide evidence of observed increases in virulence and pathogenicity in biofilm cells of &lt;i&gt;Pseudomonas aeruginosa&lt;/i&gt; in the presence of sub-MICs of selected antibiotics, &lt;i&gt;in vitro&lt;/i&gt;. Although these findings are those of &lt;i&gt;in vitro&lt;/i&gt; experiments, they may have significant implications regarding the usage and therapeutic control of antibiotics in clinical situations.","abstract_has_math":false,"creators":["Masadeh, Majed"],"institution":"University of Abertay Dundee","degree_name":"PhD","degree_level":"Doctoral Thesis","degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":["Collier, Phillip"],"committee_chairs":[],"committee_members":[],"year":2005,"date_issued":"2005-5","date_published":"2005-5","updated_at":"2026-07-24T00:50:10Z","subjects":[],"languages":["eng"],"rights":[],"rights_urls":[],"identifier_entries":[{"key":"dc:identifier","label":"Identifier","values":["oai:rke.abertay.ac.uk:studenttheses/ee318b1c-d3f5-4357-8165-2bf1caed633d"],"render_values":[{"text":"oai:rke.abertay.ac.uk:studenttheses/ee318b1c-d3f5-4357-8165-2bf1caed633d","href":null,"code":true}]}]},"links":{"outbound_url":"https://rke.abertay.ac.uk/en/studentTheses/ee318b1c-d3f5-4357-8165-2bf1caed633d","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Collier, Phillip"]},{"key":"dc:creator","label":"Author","values":["Masadeh, Majed"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2005-5"]},{"key":"dc:date.issued","label":"Date","values":["2005-5"]},{"key":"dc:publisher.department","label":"Dc Publisher Department","values":["Abertay University"]},{"key":"dc:publisher.institution","label":"Dc Publisher Institution","values":["University of Abertay Dundee"]},{"key":"dc:relation.isreferencedby","label":"Dc Relation Isreferencedby","values":["https://rke.abertay.ac.uk/en/studentTheses/ee318b1c-d3f5-4357-8165-2bf1caed633d"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]},{"key":"dc:type.qualificationlevel","label":"Dc Type Qualificationlevel","values":["Doctoral Thesis"]},{"key":"dc:type.qualificationname","label":"Dc Type Qualificationname","values":["PhD"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["eng"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["oai:rke.abertay.ac.uk:studenttheses/ee318b1c-d3f5-4357-8165-2bf1caed633d","https://rke.abertay.ac.uk/en/studentTheses/ee318b1c-d3f5-4357-8165-2bf1caed633d"]},{"key":"dc:identifier.uri","label":"Identifier URI","values":["https://rke.abertay.ac.uk/files/15231316/Masadeh_2005_Studies_on_the_effects_of_PhD.pdf"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["<i>Pseudomonas aeruginosa</i> is a notorious nosocomial opportunist. Planktonic forms of this pathogen have been traditionally studied for its pathogenicity. Such studies have shown that sub-minimal inhibitory concentrations (sub-MICs) of antibiotics are able to negatively modulate pathogenicity. However, more recent findings suggest a biofilm basis of infection. In this study, monospecies and binary biofilms of <i>Pseudomonas aeruginosa</i> ATCC 15692 (PAOl) and <i>Escherichia coli</i> ATCC 10000 were investigated for their pathogenic potential using resistance and virulence as key pathogenic determinants, in the presence of sub-MICs of selected antibiotics (Ampicillin, Nalidixic acid and Streptomycin).<br/><br/>MICs of biofilms were observed to be at least 7-fold greater than those of the corresponding planktonic form of the same species (as judged from results obtained from MIC experiments). SDS-PAGE and 2D-PAGE analysis indicate alteration of outer membrane proteins (OMPs) within the envelope of the pathogen in sub-MIC antibiotic treated samples. The observed rearrangement of lipopolysaccharide (LPS; as observed in LPS gel experiments) may also contribute to the pathogens increased tolerance to antibiotics within the biofilm state.<br/><br/>While LPS changes may possibly help the biofilm bacteria escape host immune system <i>in vivo</i>, more direct evidence of increases in virulence of the pathogen comes from investigation of its secreted proteases and cytotoxins (leucocidin). Virulence-specific azocasein and micro-culture tetrazolium (MTT) assays against both monospecies and binary biofilms of <i>Pseudomonas aeruginosa</i> indicate significant increases in virulence potential of proteases and cytotoxins, respectively. These results were further substantiated in phase contrast microscopy images showing advanced stages of oncosis in tissue cultured mouse spleen myeloma (Sp2) cells treated with leucocidin isolated from <i>Ps. aeruginosa</i> treated with sub-MIC of<br/>ampicillin (8 pg mL'1).<br/><br/>The results reported in this thesis provide evidence of observed increases in virulence and pathogenicity in biofilm cells of <i>Pseudomonas aeruginosa</i> in the presence of sub-MICs of selected antibiotics, <i>in vitro</i>. Although these findings are those of <i>in vitro</i> experiments, they may have significant implications regarding the usage and therapeutic control of antibiotics in clinical situations."]},{"key":"dc:title","label":"Title","values":["Studies on the effects of sub-minimal inhibitory concentrations of antibiotics on the virulence factors of biofilm bacteria"]}]}],"canonical_facts":{"dc:contributor.advisor":["Collier, Phillip"],"dc:creator":["Masadeh, Majed"],"dc:date":["2005-5"],"dc:date.issued":["2005-5"],"dc:description.abstract":["<i>Pseudomonas aeruginosa</i> is a notorious nosocomial opportunist. Planktonic forms of this pathogen have been traditionally studied for its pathogenicity. Such studies have shown that sub-minimal inhibitory concentrations (sub-MICs) of antibiotics are able to negatively modulate pathogenicity. However, more recent findings suggest a biofilm basis of infection. In this study, monospecies and binary biofilms of <i>Pseudomonas aeruginosa</i> ATCC 15692 (PAOl) and <i>Escherichia coli</i> ATCC 10000 were investigated for their pathogenic potential using resistance and virulence as key pathogenic determinants, in the presence of sub-MICs of selected antibiotics (Ampicillin, Nalidixic acid and Streptomycin).<br/><br/>MICs of biofilms were observed to be at least 7-fold greater than those of the corresponding planktonic form of the same species (as judged from results obtained from MIC experiments). SDS-PAGE and 2D-PAGE analysis indicate alteration of outer membrane proteins (OMPs) within the envelope of the pathogen in sub-MIC antibiotic treated samples. The observed rearrangement of lipopolysaccharide (LPS; as observed in LPS gel experiments) may also contribute to the pathogens increased tolerance to antibiotics within the biofilm state.<br/><br/>While LPS changes may possibly help the biofilm bacteria escape host immune system <i>in vivo</i>, more direct evidence of increases in virulence of the pathogen comes from investigation of its secreted proteases and cytotoxins (leucocidin). Virulence-specific azocasein and micro-culture tetrazolium (MTT) assays against both monospecies and binary biofilms of <i>Pseudomonas aeruginosa</i> indicate significant increases in virulence potential of proteases and cytotoxins, respectively. These results were further substantiated in phase contrast microscopy images showing advanced stages of oncosis in tissue cultured mouse spleen myeloma (Sp2) cells treated with leucocidin isolated from <i>Ps. aeruginosa</i> treated with sub-MIC of<br/>ampicillin (8 pg mL'1).<br/><br/>The results reported in this thesis provide evidence of observed increases in virulence and pathogenicity in biofilm cells of <i>Pseudomonas aeruginosa</i> in the presence of sub-MICs of selected antibiotics, <i>in vitro</i>. Although these findings are those of <i>in vitro</i> experiments, they may have significant implications regarding the usage and therapeutic control of antibiotics in clinical situations."],"dc:identifier":["oai:rke.abertay.ac.uk:studenttheses/ee318b1c-d3f5-4357-8165-2bf1caed633d","https://rke.abertay.ac.uk/en/studentTheses/ee318b1c-d3f5-4357-8165-2bf1caed633d"],"dc:identifier.uri":["https://rke.abertay.ac.uk/files/15231316/Masadeh_2005_Studies_on_the_effects_of_PhD.pdf"],"dc:language":["eng"],"dc:publisher.department":["Abertay University"],"dc:publisher.institution":["University of Abertay Dundee"],"dc:relation.isreferencedby":["https://rke.abertay.ac.uk/en/studentTheses/ee318b1c-d3f5-4357-8165-2bf1caed633d"],"dc:title":["Studies on the effects of sub-minimal inhibitory concentrations of antibiotics on the virulence factors of biofilm bacteria"],"dc:type":["Thesis"],"dc:type.qualificationlevel":["Doctoral Thesis"],"dc:type.qualificationname":["PhD"]},"updated_at":"2026-07-24T00:50:10Z"}