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Use of Recombinant Escherichia coli Strains in Immunofluorescence Assays for Melioidosis Diagnosis

Burkholderia pseudomallei is a Gram-negative bacterium and the causative agent of melioidosis in humans and animals in the tropics. The clinical manifestations of melioidosis are diverse, ranging from localized infections to whole-body sepsis. The effective serological method is crucial for the poin...

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Autores principales: Lantong, Kanoknart, Songsri, Jirarat, Wisessombat, Sueptrakool, Mala, Wanida, Prommachote, Warinda, Senghoi, Wilaiwan, Kotepui, Manas, Kaewrakmuk, Jedsada, Jiranantasak, Treenate, Tuanyok, Apichai, Klangbud, Wiyada Kwanhian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148196/
https://www.ncbi.nlm.nih.gov/pubmed/34066462
http://dx.doi.org/10.3390/pathogens10050559
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author Lantong, Kanoknart
Songsri, Jirarat
Wisessombat, Sueptrakool
Mala, Wanida
Prommachote, Warinda
Senghoi, Wilaiwan
Kotepui, Manas
Kaewrakmuk, Jedsada
Jiranantasak, Treenate
Tuanyok, Apichai
Klangbud, Wiyada Kwanhian
author_facet Lantong, Kanoknart
Songsri, Jirarat
Wisessombat, Sueptrakool
Mala, Wanida
Prommachote, Warinda
Senghoi, Wilaiwan
Kotepui, Manas
Kaewrakmuk, Jedsada
Jiranantasak, Treenate
Tuanyok, Apichai
Klangbud, Wiyada Kwanhian
author_sort Lantong, Kanoknart
collection PubMed
description Burkholderia pseudomallei is a Gram-negative bacterium and the causative agent of melioidosis in humans and animals in the tropics. The clinical manifestations of melioidosis are diverse, ranging from localized infections to whole-body sepsis. The effective serological method is crucial for the point-of-care diagnosis of melioidosis. The aim of this study was to develop indirect immunofluorescence assay (IFA)-based methods for detecting immunoglobulin G (IgG) antibodies in melioidosis patients. These methods use whole-cell antigens made from recombinant E. coli strains that express major B. pseudomallei antigens, including TssM, OmpH, AhpC, BimA, and Hcp1. A total of 271 serum samples from culture-confirmed melioidosis patients (n = 81), patients with other known infections (n = 70), and healthy donors (n = 120) were tested. Our study showed that the recombinant TssM strain had the highest performance, with 92.6% sensitivity, 100% specificity, 100% positive predictive value, 96.9% negative predictive value, 97.8% efficiency, 97.0% accuracy, and no cross-reactivity. The method agreement analysis based on k efficiency calculations showed that all five IFA methods perfectly agreed with the standard culturing method, while the traditional indirect hemagglutination (IHA) method moderately agreed with the culture. In summary, our investigations showed that the TssM-IFA method could be used for melioidosis diagnosis.
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spelling pubmed-81481962021-05-26 Use of Recombinant Escherichia coli Strains in Immunofluorescence Assays for Melioidosis Diagnosis Lantong, Kanoknart Songsri, Jirarat Wisessombat, Sueptrakool Mala, Wanida Prommachote, Warinda Senghoi, Wilaiwan Kotepui, Manas Kaewrakmuk, Jedsada Jiranantasak, Treenate Tuanyok, Apichai Klangbud, Wiyada Kwanhian Pathogens Article Burkholderia pseudomallei is a Gram-negative bacterium and the causative agent of melioidosis in humans and animals in the tropics. The clinical manifestations of melioidosis are diverse, ranging from localized infections to whole-body sepsis. The effective serological method is crucial for the point-of-care diagnosis of melioidosis. The aim of this study was to develop indirect immunofluorescence assay (IFA)-based methods for detecting immunoglobulin G (IgG) antibodies in melioidosis patients. These methods use whole-cell antigens made from recombinant E. coli strains that express major B. pseudomallei antigens, including TssM, OmpH, AhpC, BimA, and Hcp1. A total of 271 serum samples from culture-confirmed melioidosis patients (n = 81), patients with other known infections (n = 70), and healthy donors (n = 120) were tested. Our study showed that the recombinant TssM strain had the highest performance, with 92.6% sensitivity, 100% specificity, 100% positive predictive value, 96.9% negative predictive value, 97.8% efficiency, 97.0% accuracy, and no cross-reactivity. The method agreement analysis based on k efficiency calculations showed that all five IFA methods perfectly agreed with the standard culturing method, while the traditional indirect hemagglutination (IHA) method moderately agreed with the culture. In summary, our investigations showed that the TssM-IFA method could be used for melioidosis diagnosis. MDPI 2021-05-06 /pmc/articles/PMC8148196/ /pubmed/34066462 http://dx.doi.org/10.3390/pathogens10050559 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lantong, Kanoknart
Songsri, Jirarat
Wisessombat, Sueptrakool
Mala, Wanida
Prommachote, Warinda
Senghoi, Wilaiwan
Kotepui, Manas
Kaewrakmuk, Jedsada
Jiranantasak, Treenate
Tuanyok, Apichai
Klangbud, Wiyada Kwanhian
Use of Recombinant Escherichia coli Strains in Immunofluorescence Assays for Melioidosis Diagnosis
title Use of Recombinant Escherichia coli Strains in Immunofluorescence Assays for Melioidosis Diagnosis
title_full Use of Recombinant Escherichia coli Strains in Immunofluorescence Assays for Melioidosis Diagnosis
title_fullStr Use of Recombinant Escherichia coli Strains in Immunofluorescence Assays for Melioidosis Diagnosis
title_full_unstemmed Use of Recombinant Escherichia coli Strains in Immunofluorescence Assays for Melioidosis Diagnosis
title_short Use of Recombinant Escherichia coli Strains in Immunofluorescence Assays for Melioidosis Diagnosis
title_sort use of recombinant escherichia coli strains in immunofluorescence assays for melioidosis diagnosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148196/
https://www.ncbi.nlm.nih.gov/pubmed/34066462
http://dx.doi.org/10.3390/pathogens10050559
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