Cargando…

Rapid detection of Burkholderia pseudomallei with a lateral flow recombinase polymerase amplification assay

Melioidosis is a severe infectious disease caused by gram-negative, facultative intracellular pathogen Burkholderia pseudomallei (B. pseudomallei). Although cases are increasing reported from other parts of the world, it is an illness of tropical and subtropical climates primarily found in southeast...

Descripción completa

Detalles Bibliográficos
Autores principales: Peng, Yao, Zheng, Xiao, Kan, Biao, Li, Wei, Zhang, Wen, Jiang, Taozhen, Lu, Jinxing, Qin, Aiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6613700/
https://www.ncbi.nlm.nih.gov/pubmed/31283772
http://dx.doi.org/10.1371/journal.pone.0213416
_version_ 1783433078476111872
author Peng, Yao
Zheng, Xiao
Kan, Biao
Li, Wei
Zhang, Wen
Jiang, Taozhen
Lu, Jinxing
Qin, Aiping
author_facet Peng, Yao
Zheng, Xiao
Kan, Biao
Li, Wei
Zhang, Wen
Jiang, Taozhen
Lu, Jinxing
Qin, Aiping
author_sort Peng, Yao
collection PubMed
description Melioidosis is a severe infectious disease caused by gram-negative, facultative intracellular pathogen Burkholderia pseudomallei (B. pseudomallei). Although cases are increasing reported from other parts of the world, it is an illness of tropical and subtropical climates primarily found in southeast Asia and northern Australia. Because of a 40% mortality rate, this life-threatening disease poses a public health risk in endemic area. Early detection of B. pseudomallei infection is vital for prognosis of a melioidosis patient. In this study, a novel isothermal recombinase polymerase amplification combined with lateral flow dipstick (LF-RPA) assay was established for rapid detection of B. pseudomallei. A set of primer-probe targeting orf2 gene within the putative type III secretion system (T3SS) cluster genes was generated and parameters for the LF-RPA assay were optimized. Result can be easy visualized in 30 minutes with the limit of detection (LOD) as low as 20 femtogram (fg) (ca. 25.6 copies) of B. pseudomallei genomic DNA without a specific equipment. The assay is highly specific as no cross amplification was observed with Burkholderia mallei, members of the Burkholderia cepacia-complex and 35 non-B. pseudomallei bacteria species. Moreover, isolates from patients in Hainan (N = 19), Guangdong (N = 1), Guangxi (N = 3) province of China as well as in Australia (N = 3) and Thailand (N = 1) were retrospectively confirmed by the newly developed method. LODs for B. pseudomallei-spiked soil and blood samples were 2.1×10(3) CFU/g and 4.2×10(3) CFU/ml respectively. The sensitivity of the LF-RPA assay was comparable to TaqMan Real-Time PCR (TaqMan PCR). In addition, the LF-RPA assay exhibited a better tolerance to inhibitors in blood than TaqMan PCR. Our results showed that the LF-RPA assay is an alternative to existing PCR-based methods for detection of B. pseudomallei with a potentiality of early accurate diagnosis of melioidosis at point of care or in-field use.
format Online
Article
Text
id pubmed-6613700
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-66137002019-07-23 Rapid detection of Burkholderia pseudomallei with a lateral flow recombinase polymerase amplification assay Peng, Yao Zheng, Xiao Kan, Biao Li, Wei Zhang, Wen Jiang, Taozhen Lu, Jinxing Qin, Aiping PLoS One Research Article Melioidosis is a severe infectious disease caused by gram-negative, facultative intracellular pathogen Burkholderia pseudomallei (B. pseudomallei). Although cases are increasing reported from other parts of the world, it is an illness of tropical and subtropical climates primarily found in southeast Asia and northern Australia. Because of a 40% mortality rate, this life-threatening disease poses a public health risk in endemic area. Early detection of B. pseudomallei infection is vital for prognosis of a melioidosis patient. In this study, a novel isothermal recombinase polymerase amplification combined with lateral flow dipstick (LF-RPA) assay was established for rapid detection of B. pseudomallei. A set of primer-probe targeting orf2 gene within the putative type III secretion system (T3SS) cluster genes was generated and parameters for the LF-RPA assay were optimized. Result can be easy visualized in 30 minutes with the limit of detection (LOD) as low as 20 femtogram (fg) (ca. 25.6 copies) of B. pseudomallei genomic DNA without a specific equipment. The assay is highly specific as no cross amplification was observed with Burkholderia mallei, members of the Burkholderia cepacia-complex and 35 non-B. pseudomallei bacteria species. Moreover, isolates from patients in Hainan (N = 19), Guangdong (N = 1), Guangxi (N = 3) province of China as well as in Australia (N = 3) and Thailand (N = 1) were retrospectively confirmed by the newly developed method. LODs for B. pseudomallei-spiked soil and blood samples were 2.1×10(3) CFU/g and 4.2×10(3) CFU/ml respectively. The sensitivity of the LF-RPA assay was comparable to TaqMan Real-Time PCR (TaqMan PCR). In addition, the LF-RPA assay exhibited a better tolerance to inhibitors in blood than TaqMan PCR. Our results showed that the LF-RPA assay is an alternative to existing PCR-based methods for detection of B. pseudomallei with a potentiality of early accurate diagnosis of melioidosis at point of care or in-field use. Public Library of Science 2019-07-08 /pmc/articles/PMC6613700/ /pubmed/31283772 http://dx.doi.org/10.1371/journal.pone.0213416 Text en © 2019 Peng et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Peng, Yao
Zheng, Xiao
Kan, Biao
Li, Wei
Zhang, Wen
Jiang, Taozhen
Lu, Jinxing
Qin, Aiping
Rapid detection of Burkholderia pseudomallei with a lateral flow recombinase polymerase amplification assay
title Rapid detection of Burkholderia pseudomallei with a lateral flow recombinase polymerase amplification assay
title_full Rapid detection of Burkholderia pseudomallei with a lateral flow recombinase polymerase amplification assay
title_fullStr Rapid detection of Burkholderia pseudomallei with a lateral flow recombinase polymerase amplification assay
title_full_unstemmed Rapid detection of Burkholderia pseudomallei with a lateral flow recombinase polymerase amplification assay
title_short Rapid detection of Burkholderia pseudomallei with a lateral flow recombinase polymerase amplification assay
title_sort rapid detection of burkholderia pseudomallei with a lateral flow recombinase polymerase amplification assay
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6613700/
https://www.ncbi.nlm.nih.gov/pubmed/31283772
http://dx.doi.org/10.1371/journal.pone.0213416
work_keys_str_mv AT pengyao rapiddetectionofburkholderiapseudomalleiwithalateralflowrecombinasepolymeraseamplificationassay
AT zhengxiao rapiddetectionofburkholderiapseudomalleiwithalateralflowrecombinasepolymeraseamplificationassay
AT kanbiao rapiddetectionofburkholderiapseudomalleiwithalateralflowrecombinasepolymeraseamplificationassay
AT liwei rapiddetectionofburkholderiapseudomalleiwithalateralflowrecombinasepolymeraseamplificationassay
AT zhangwen rapiddetectionofburkholderiapseudomalleiwithalateralflowrecombinasepolymeraseamplificationassay
AT jiangtaozhen rapiddetectionofburkholderiapseudomalleiwithalateralflowrecombinasepolymeraseamplificationassay
AT lujinxing rapiddetectionofburkholderiapseudomalleiwithalateralflowrecombinasepolymeraseamplificationassay
AT qinaiping rapiddetectionofburkholderiapseudomalleiwithalateralflowrecombinasepolymeraseamplificationassay