Evaluation of antigen-detecting and antibody-detecting diagnostic test combinations for diagnosing melioidosis
Background Melioidosis, an infectious disease caused by Burkholderia pseudomallei, is endemic in many tropical developing countries and has a high mortality. Here we evaluated combinations of a lateral flow immunoassay (LFI) detecting B. pseudomallei capsular polysaccharide (CPS) and enzyme-linked i...
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th-mahidol.776922022-08-04T16:07:28Z Evaluation of antigen-detecting and antibody-detecting diagnostic test combinations for diagnosing melioidosis Premjit Amornchai Viriya Hantrakun Gumphol Wongsuvan Vanaporn Wuthiekanun Surasakdi Wongratanacheewin Prapit Teparrakkul T. Eoin West David P. Aucoin Nicholas P.J. Day Paul J. Brett Mary N. Burtnick Narisara Chantratitra Direk Limmathurotsakul Faculty of Tropical Medicine, Mahidol University Faculty of Medicine, Khon Kaen University Nuffield Department of Medicine University of Nevada School of Medicine Harborview Medical Center Sunpasitthiprasong Hospital Medicine Background Melioidosis, an infectious disease caused by Burkholderia pseudomallei, is endemic in many tropical developing countries and has a high mortality. Here we evaluated combinations of a lateral flow immunoassay (LFI) detecting B. pseudomallei capsular polysaccharide (CPS) and enzyme-linked immunosorbent assays (ELISA) detecting antibodies against hemolysin co-regulated protein (Hcp1) or O-polysaccharide (OPS) for diagnosing melioidosis. Methodology/Principal findings We conducted a cohort-based case-control study. Both cases and controls were derived from a prospective observational study of patients presenting with community-acquired infections and sepsis in northeast Thailand (Ubon-sepsis). Cases included 192 patients with a clinical specimen culture positive for B. pseudomallei. Controls included 502 patients who were blood culture positive for Staphylococcus aureus, Escherichia coli or Klebsiella pneu-moniae or were polymerase chain reaction assay positive for malaria or dengue. Serum samples collected within 24 hours of admission were stored and tested using a CPS-LFI, Hcp1-ELISA and OPS-ELISA. When assessing diagnostic tests in combination, results were considered positive if either test was positive. We selected ELISA cut-offs correspond-ing to a specificity of 95%. Using a positive cut-off OD of 2.912 for Hcp1-ELISA, the combination of the CPS-LFI and Hcp1-ELISA had a sensitivity of 67.7% (130/192 case patients) and a specificity of 95.0% (477/502 control patients). The sensitivity of the combination (67.7%) was higher than that of the CPS-LFI alone (31.3%, p<0.001) and that of Hcp1-ELISA alone (53.6%, p<0.001). A similar phenomenon was also observed for the combination of CPS-LFI and OPS-ELISA. In case patients, positivity of the CPS-LFI was associated with a short duration of symptoms, high modified Sequential (sepsis-related) Organ Failure Assessment (SOFA) score, bacteraemia and mortality outcome, while positivity of Hcp1-ELISA was associated with a longer duration of symptoms, low modified SOFA score, non-bacteraemia and survival outcome. Conclusions/Significance A combination of antigen-antibody diagnostic tests increased the sensitivity of melioidosis diagnosis over individual tests while preserving high specificity. Point-of-care tests for melioidosis based on the use of combination assays should be further developed and evaluated. 2022-08-04T09:07:28Z 2022-08-04T09:07:28Z 2021-11-01 Article PLoS Neglected Tropical Diseases. Vol.15, No.11 (2021) 10.1371/journal.pntd.0009840 19352735 19352727 2-s2.0-85120675522 https://repository.li.mahidol.ac.th/handle/123456789/77692 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85120675522&origin=inward |
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Medicine Premjit Amornchai Viriya Hantrakun Gumphol Wongsuvan Vanaporn Wuthiekanun Surasakdi Wongratanacheewin Prapit Teparrakkul T. Eoin West David P. Aucoin Nicholas P.J. Day Paul J. Brett Mary N. Burtnick Narisara Chantratitra Direk Limmathurotsakul Evaluation of antigen-detecting and antibody-detecting diagnostic test combinations for diagnosing melioidosis |
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Background Melioidosis, an infectious disease caused by Burkholderia pseudomallei, is endemic in many tropical developing countries and has a high mortality. Here we evaluated combinations of a lateral flow immunoassay (LFI) detecting B. pseudomallei capsular polysaccharide (CPS) and enzyme-linked immunosorbent assays (ELISA) detecting antibodies against hemolysin co-regulated protein (Hcp1) or O-polysaccharide (OPS) for diagnosing melioidosis. Methodology/Principal findings We conducted a cohort-based case-control study. Both cases and controls were derived from a prospective observational study of patients presenting with community-acquired infections and sepsis in northeast Thailand (Ubon-sepsis). Cases included 192 patients with a clinical specimen culture positive for B. pseudomallei. Controls included 502 patients who were blood culture positive for Staphylococcus aureus, Escherichia coli or Klebsiella pneu-moniae or were polymerase chain reaction assay positive for malaria or dengue. Serum samples collected within 24 hours of admission were stored and tested using a CPS-LFI, Hcp1-ELISA and OPS-ELISA. When assessing diagnostic tests in combination, results were considered positive if either test was positive. We selected ELISA cut-offs correspond-ing to a specificity of 95%. Using a positive cut-off OD of 2.912 for Hcp1-ELISA, the combination of the CPS-LFI and Hcp1-ELISA had a sensitivity of 67.7% (130/192 case patients) and a specificity of 95.0% (477/502 control patients). The sensitivity of the combination (67.7%) was higher than that of the CPS-LFI alone (31.3%, p<0.001) and that of Hcp1-ELISA alone (53.6%, p<0.001). A similar phenomenon was also observed for the combination of CPS-LFI and OPS-ELISA. In case patients, positivity of the CPS-LFI was associated with a short duration of symptoms, high modified Sequential (sepsis-related) Organ Failure Assessment (SOFA) score, bacteraemia and mortality outcome, while positivity of Hcp1-ELISA was associated with a longer duration of symptoms, low modified SOFA score, non-bacteraemia and survival outcome. Conclusions/Significance A combination of antigen-antibody diagnostic tests increased the sensitivity of melioidosis diagnosis over individual tests while preserving high specificity. Point-of-care tests for melioidosis based on the use of combination assays should be further developed and evaluated. |
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Faculty of Tropical Medicine, Mahidol University |
author_facet |
Faculty of Tropical Medicine, Mahidol University Premjit Amornchai Viriya Hantrakun Gumphol Wongsuvan Vanaporn Wuthiekanun Surasakdi Wongratanacheewin Prapit Teparrakkul T. Eoin West David P. Aucoin Nicholas P.J. Day Paul J. Brett Mary N. Burtnick Narisara Chantratitra Direk Limmathurotsakul |
format |
Article |
author |
Premjit Amornchai Viriya Hantrakun Gumphol Wongsuvan Vanaporn Wuthiekanun Surasakdi Wongratanacheewin Prapit Teparrakkul T. Eoin West David P. Aucoin Nicholas P.J. Day Paul J. Brett Mary N. Burtnick Narisara Chantratitra Direk Limmathurotsakul |
author_sort |
Premjit Amornchai |
title |
Evaluation of antigen-detecting and antibody-detecting diagnostic test combinations for diagnosing melioidosis |
title_short |
Evaluation of antigen-detecting and antibody-detecting diagnostic test combinations for diagnosing melioidosis |
title_full |
Evaluation of antigen-detecting and antibody-detecting diagnostic test combinations for diagnosing melioidosis |
title_fullStr |
Evaluation of antigen-detecting and antibody-detecting diagnostic test combinations for diagnosing melioidosis |
title_full_unstemmed |
Evaluation of antigen-detecting and antibody-detecting diagnostic test combinations for diagnosing melioidosis |
title_sort |
evaluation of antigen-detecting and antibody-detecting diagnostic test combinations for diagnosing melioidosis |
publishDate |
2022 |
url |
https://repository.li.mahidol.ac.th/handle/123456789/77692 |
_version_ |
1763492376606670848 |