{"id":{"repo_id":"southwales","oai_identifier":"oai:pure.atira.dk:studenttheses/15338b5a-4ccd-462e-ba09-e8d730be85e1"},"canonical_url":"https://search.dev.ndltd.org/etd/southwales/oai:pure.atira.dk:studenttheses/15338b5a-4ccd-462e-ba09-e8d730be85e1","repository":{"repo_id":"southwales","name":"University of South Wales","base_url":"https://pure.southwales.ac.uk/ws/oai"},"display":{"title":"Development and Use of Loop-Mediated Isothermal Amplification (LAMP) Assays to Detect the Presence of Pathogens Which Cause Urinary Tract Infection and Genes Which Cause Resistance to 3rd Generation Cephalosporins","abstract":"Urinary tract infection (UTI) is an area of infectious disease which has long been neglected, despite <br/>the fact it affects ~50% of the female population worldwide and if left untreated/mis-diagnosed can <br/>cause life threatening illness, such as sepsis. <br/><br/>Current methods of diagnosis, although known to be imperfect, have not been changed or improved<br/>in many years. However, with the emergence of antimicrobial resistance (AMR) and the focus being <br/>firmly placed on improving diagnostic pathways, this is set to change. There is a fundamental need <br/>to reduce the misuse and overuse of antibiotics, which is driving AMR and causing an increasing <br/>number of deaths worldwide.<br/><br/>In June 2023, the World Health Organisation published their Global Research Agenda for AMR in <br/>Human Health. Listing 40 research topics which should be prioritised in the fight against AMR, some <br/>of which feed directly into the aim of this research.<br/><br/>Aim - To develop and test a rapid molecular diagnostic test designed for near patient/point-of-care, <br/>for the detection of bacterial uropathogens direct from urine, using loop-mediated isothermal <br/>amplification (LAMP) technology. Then, to assess whether the same technology could be adapted to <br/>detect bacterial AMR genes, with the potential to direct treatment decisions and improve current <br/>methods of UTI diagnosis.<br/><br/>Using the Llusern Scientific Lodestar DX analyser and LAMP bacterial ID tests, initial assessment was<br/>carried out for assays designed to detect 6 common uropathogens, selected using pathogen <br/>prevalence data from Cardiff, Wales in 2022. These were combined into a UTI test panel with ~87% <br/>coverage of all UTIs. Throughout testing, improvements were made to the sampling methodology<br/>and testing algorithm, prior to design freeze. A clinical performance evaluation was then carried out, <br/>comparing the Lodestar DX UTI test with standard laboratory methods (flow cytometry and culture)<br/>for a total of 199 urine samples from symptomatic adult females, suspected of experiencing acute, <br/>uncomplicated UTI.<br/><br/>An overall sensitivity and specificity of 88.1% (95% CI: 77.8%– 94.7%) and 83.9% (95% CI: 72.3%–<br/>92.0%) respectively was achieved. Along with a positive predictive value (PPV) of 85.5% (95% CI: <br/>76.9%–91.3%), a negative predictive value (NPV) of 86.7% (95% CI: 77.1%–92.6%) and an overall <br/>accuracy of 86.1% (95% CI: 78.9%–91.5%). This data allowed the test to achieve UK CA accreditation <br/>and it is now commercially available in the UK as a result.<br/><br/>Following this, Llusern Scientific provided LAMP assays designed to detect antibiotic resistance <br/>genes. The Lodestar DX platform was used to demonstrate proof-of-concept in successfully detecting <br/>these targets, with minor changes to the sampling methodology.<br/><br/>The Lodestar DX platform and UTI test performs well in comparison with culture, for acute <br/>uncomplicated UTI in symptomatic adult females. However, there is much scope for future <br/>improvements, further development, and assessment of its true point-of-care compatibility. There is<br/>a need to assess its effectiveness in improving current prescribing methods and the question <br/>remains whether knowing the bacterial ID will have any effect on clinical decision making and<br/>whether a positive impact on patient outcomes is possible.","abstract_html":"Urinary tract infection (UTI) is an area of infectious disease which has long been neglected, despite &lt;br/&gt;the fact it affects ~50% of the female population worldwide and if left untreated/mis-diagnosed can &lt;br/&gt;cause life threatening illness, such as sepsis. &lt;br/&gt;&lt;br/&gt;Current methods of diagnosis, although known to be imperfect, have not been changed or improved&lt;br/&gt;in many years. However, with the emergence of antimicrobial resistance (AMR) and the focus being &lt;br/&gt;firmly placed on improving diagnostic pathways, this is set to change. There is a fundamental need &lt;br/&gt;to reduce the misuse and overuse of antibiotics, which is driving AMR and causing an increasing &lt;br/&gt;number of deaths worldwide.&lt;br/&gt;&lt;br/&gt;In June 2023, the World Health Organisation published their Global Research Agenda for AMR in &lt;br/&gt;Human Health. Listing 40 research topics which should be prioritised in the fight against AMR, some &lt;br/&gt;of which feed directly into the aim of this research.&lt;br/&gt;&lt;br/&gt;Aim - To develop and test a rapid molecular diagnostic test designed for near patient/point-of-care, &lt;br/&gt;for the detection of bacterial uropathogens direct from urine, using loop-mediated isothermal &lt;br/&gt;amplification (LAMP) technology. Then, to assess whether the same technology could be adapted to &lt;br/&gt;detect bacterial AMR genes, with the potential to direct treatment decisions and improve current &lt;br/&gt;methods of UTI diagnosis.&lt;br/&gt;&lt;br/&gt;Using the Llusern Scientific Lodestar DX analyser and LAMP bacterial ID tests, initial assessment was&lt;br/&gt;carried out for assays designed to detect 6 common uropathogens, selected using pathogen &lt;br/&gt;prevalence data from Cardiff, Wales in 2022. These were combined into a UTI test panel with ~87% &lt;br/&gt;coverage of all UTIs. Throughout testing, improvements were made to the sampling methodology&lt;br/&gt;and testing algorithm, prior to design freeze. A clinical performance evaluation was then carried out, &lt;br/&gt;comparing the Lodestar DX UTI test with standard laboratory methods (flow cytometry and culture)&lt;br/&gt;for a total of 199 urine samples from symptomatic adult females, suspected of experiencing acute, &lt;br/&gt;uncomplicated UTI.&lt;br/&gt;&lt;br/&gt;An overall sensitivity and specificity of 88.1% (95% CI: 77.8%– 94.7%) and 83.9% (95% CI: 72.3%–&lt;br/&gt;92.0%) respectively was achieved. Along with a positive predictive value (PPV) of 85.5% (95% CI: &lt;br/&gt;76.9%–91.3%), a negative predictive value (NPV) of 86.7% (95% CI: 77.1%–92.6%) and an overall &lt;br/&gt;accuracy of 86.1% (95% CI: 78.9%–91.5%). This data allowed the test to achieve UK CA accreditation &lt;br/&gt;and it is now commercially available in the UK as a result.&lt;br/&gt;&lt;br/&gt;Following this, Llusern Scientific provided LAMP assays designed to detect antibiotic resistance &lt;br/&gt;genes. The Lodestar DX platform was used to demonstrate proof-of-concept in successfully detecting &lt;br/&gt;these targets, with minor changes to the sampling methodology.&lt;br/&gt;&lt;br/&gt;The Lodestar DX platform and UTI test performs well in comparison with culture, for acute &lt;br/&gt;uncomplicated UTI in symptomatic adult females. However, there is much scope for future &lt;br/&gt;improvements, further development, and assessment of its true point-of-care compatibility. There is&lt;br/&gt;a need to assess its effectiveness in improving current prescribing methods and the question &lt;br/&gt;remains whether knowing the bacterial ID will have any effect on clinical decision making and&lt;br/&gt;whether a positive impact on patient outcomes is possible.","abstract_has_math":false,"creators":["Diggle, Joanna Morfydd"],"institution":null,"degree_name":"Master's Thesis","degree_level":"Student thesis","degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":["Nieuwland, Jeroen"],"committee_chairs":[],"committee_members":[],"year":2025,"date_issued":"2025","date_published":"2025","updated_at":"2026-07-24T04:39:57Z","subjects":[],"languages":["eng"],"rights":[],"rights_urls":[],"identifier_entries":[{"key":"dc:identifier","label":"Identifier","values":["oai:pure.atira.dk:studenttheses/15338b5a-4ccd-462e-ba09-e8d730be85e1"],"render_values":[{"text":"oai:pure.atira.dk:studenttheses/15338b5a-4ccd-462e-ba09-e8d730be85e1","href":null,"code":true}]}]},"links":{"outbound_url":"https://pure.southwales.ac.uk/en/studentTheses/15338b5a-4ccd-462e-ba09-e8d730be85e1","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Nieuwland, Jeroen"]},{"key":"dc:contributor.sponsor","label":"Sponsor","values":["Public Health Wales","Llusern Scientific"]},{"key":"dc:creator","label":"Author","values":["Diggle, Joanna Morfydd"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2025"]},{"key":"dc:date.issued","label":"Date","values":["2025"]},{"key":"dc:relation.isreferencedby","label":"Dc Relation Isreferencedby","values":["https://pure.southwales.ac.uk/en/studentTheses/15338b5a-4ccd-462e-ba09-e8d730be85e1"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]},{"key":"dc:type.qualificationlevel","label":"Dc Type Qualificationlevel","values":["Student thesis"]},{"key":"dc:type.qualificationname","label":"Dc Type Qualificationname","values":["Master's Thesis"]}]},{"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:pure.atira.dk:studenttheses/15338b5a-4ccd-462e-ba09-e8d730be85e1","https://pure.southwales.ac.uk/en/studentTheses/15338b5a-4ccd-462e-ba09-e8d730be85e1"]},{"key":"dc:identifier.uri","label":"Identifier URI","values":["https://pure.southwales.ac.uk/files/31637523/Joanna_Diggle_FULL_THESIS_-_POST_VIVA_-_FINAL.pdf"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Urinary tract infection (UTI) is an area of infectious disease which has long been neglected, despite <br/>the fact it affects ~50% of the female population worldwide and if left untreated/mis-diagnosed can <br/>cause life threatening illness, such as sepsis. <br/><br/>Current methods of diagnosis, although known to be imperfect, have not been changed or improved<br/>in many years. However, with the emergence of antimicrobial resistance (AMR) and the focus being <br/>firmly placed on improving diagnostic pathways, this is set to change. There is a fundamental need <br/>to reduce the misuse and overuse of antibiotics, which is driving AMR and causing an increasing <br/>number of deaths worldwide.<br/><br/>In June 2023, the World Health Organisation published their Global Research Agenda for AMR in <br/>Human Health. Listing 40 research topics which should be prioritised in the fight against AMR, some <br/>of which feed directly into the aim of this research.<br/><br/>Aim - To develop and test a rapid molecular diagnostic test designed for near patient/point-of-care, <br/>for the detection of bacterial uropathogens direct from urine, using loop-mediated isothermal <br/>amplification (LAMP) technology. Then, to assess whether the same technology could be adapted to <br/>detect bacterial AMR genes, with the potential to direct treatment decisions and improve current <br/>methods of UTI diagnosis.<br/><br/>Using the Llusern Scientific Lodestar DX analyser and LAMP bacterial ID tests, initial assessment was<br/>carried out for assays designed to detect 6 common uropathogens, selected using pathogen <br/>prevalence data from Cardiff, Wales in 2022. These were combined into a UTI test panel with ~87% <br/>coverage of all UTIs. Throughout testing, improvements were made to the sampling methodology<br/>and testing algorithm, prior to design freeze. A clinical performance evaluation was then carried out, <br/>comparing the Lodestar DX UTI test with standard laboratory methods (flow cytometry and culture)<br/>for a total of 199 urine samples from symptomatic adult females, suspected of experiencing acute, <br/>uncomplicated UTI.<br/><br/>An overall sensitivity and specificity of 88.1% (95% CI: 77.8%– 94.7%) and 83.9% (95% CI: 72.3%–<br/>92.0%) respectively was achieved. Along with a positive predictive value (PPV) of 85.5% (95% CI: <br/>76.9%–91.3%), a negative predictive value (NPV) of 86.7% (95% CI: 77.1%–92.6%) and an overall <br/>accuracy of 86.1% (95% CI: 78.9%–91.5%). This data allowed the test to achieve UK CA accreditation <br/>and it is now commercially available in the UK as a result.<br/><br/>Following this, Llusern Scientific provided LAMP assays designed to detect antibiotic resistance <br/>genes. The Lodestar DX platform was used to demonstrate proof-of-concept in successfully detecting <br/>these targets, with minor changes to the sampling methodology.<br/><br/>The Lodestar DX platform and UTI test performs well in comparison with culture, for acute <br/>uncomplicated UTI in symptomatic adult females. However, there is much scope for future <br/>improvements, further development, and assessment of its true point-of-care compatibility. There is<br/>a need to assess its effectiveness in improving current prescribing methods and the question <br/>remains whether knowing the bacterial ID will have any effect on clinical decision making and<br/>whether a positive impact on patient outcomes is possible."]},{"key":"dc:title","label":"Title","values":["Development and Use of Loop-Mediated Isothermal Amplification (LAMP) Assays to Detect the Presence of Pathogens Which Cause Urinary Tract Infection and Genes Which Cause Resistance to 3rd Generation Cephalosporins"]}]}],"canonical_facts":{"dc:contributor.advisor":["Nieuwland, Jeroen"],"dc:contributor.sponsor":["Public Health Wales","Llusern Scientific"],"dc:creator":["Diggle, Joanna Morfydd"],"dc:date":["2025"],"dc:date.issued":["2025"],"dc:description.abstract":["Urinary tract infection (UTI) is an area of infectious disease which has long been neglected, despite <br/>the fact it affects ~50% of the female population worldwide and if left untreated/mis-diagnosed can <br/>cause life threatening illness, such as sepsis. <br/><br/>Current methods of diagnosis, although known to be imperfect, have not been changed or improved<br/>in many years. However, with the emergence of antimicrobial resistance (AMR) and the focus being <br/>firmly placed on improving diagnostic pathways, this is set to change. There is a fundamental need <br/>to reduce the misuse and overuse of antibiotics, which is driving AMR and causing an increasing <br/>number of deaths worldwide.<br/><br/>In June 2023, the World Health Organisation published their Global Research Agenda for AMR in <br/>Human Health. Listing 40 research topics which should be prioritised in the fight against AMR, some <br/>of which feed directly into the aim of this research.<br/><br/>Aim - To develop and test a rapid molecular diagnostic test designed for near patient/point-of-care, <br/>for the detection of bacterial uropathogens direct from urine, using loop-mediated isothermal <br/>amplification (LAMP) technology. Then, to assess whether the same technology could be adapted to <br/>detect bacterial AMR genes, with the potential to direct treatment decisions and improve current <br/>methods of UTI diagnosis.<br/><br/>Using the Llusern Scientific Lodestar DX analyser and LAMP bacterial ID tests, initial assessment was<br/>carried out for assays designed to detect 6 common uropathogens, selected using pathogen <br/>prevalence data from Cardiff, Wales in 2022. These were combined into a UTI test panel with ~87% <br/>coverage of all UTIs. Throughout testing, improvements were made to the sampling methodology<br/>and testing algorithm, prior to design freeze. A clinical performance evaluation was then carried out, <br/>comparing the Lodestar DX UTI test with standard laboratory methods (flow cytometry and culture)<br/>for a total of 199 urine samples from symptomatic adult females, suspected of experiencing acute, <br/>uncomplicated UTI.<br/><br/>An overall sensitivity and specificity of 88.1% (95% CI: 77.8%– 94.7%) and 83.9% (95% CI: 72.3%–<br/>92.0%) respectively was achieved. Along with a positive predictive value (PPV) of 85.5% (95% CI: <br/>76.9%–91.3%), a negative predictive value (NPV) of 86.7% (95% CI: 77.1%–92.6%) and an overall <br/>accuracy of 86.1% (95% CI: 78.9%–91.5%). This data allowed the test to achieve UK CA accreditation <br/>and it is now commercially available in the UK as a result.<br/><br/>Following this, Llusern Scientific provided LAMP assays designed to detect antibiotic resistance <br/>genes. The Lodestar DX platform was used to demonstrate proof-of-concept in successfully detecting <br/>these targets, with minor changes to the sampling methodology.<br/><br/>The Lodestar DX platform and UTI test performs well in comparison with culture, for acute <br/>uncomplicated UTI in symptomatic adult females. However, there is much scope for future <br/>improvements, further development, and assessment of its true point-of-care compatibility. There is<br/>a need to assess its effectiveness in improving current prescribing methods and the question <br/>remains whether knowing the bacterial ID will have any effect on clinical decision making and<br/>whether a positive impact on patient outcomes is possible."],"dc:identifier":["oai:pure.atira.dk:studenttheses/15338b5a-4ccd-462e-ba09-e8d730be85e1","https://pure.southwales.ac.uk/en/studentTheses/15338b5a-4ccd-462e-ba09-e8d730be85e1"],"dc:identifier.uri":["https://pure.southwales.ac.uk/files/31637523/Joanna_Diggle_FULL_THESIS_-_POST_VIVA_-_FINAL.pdf"],"dc:language":["eng"],"dc:relation.isreferencedby":["https://pure.southwales.ac.uk/en/studentTheses/15338b5a-4ccd-462e-ba09-e8d730be85e1"],"dc:title":["Development and Use of Loop-Mediated Isothermal Amplification (LAMP) Assays to Detect the Presence of Pathogens Which Cause Urinary Tract Infection and Genes Which Cause Resistance to 3rd Generation Cephalosporins"],"dc:type":["Thesis"],"dc:type.qualificationlevel":["Student thesis"],"dc:type.qualificationname":["Master's Thesis"]},"updated_at":"2026-07-24T04:39:57Z"}