Cargando…
Equipment-free recombinase polymerase amplification assay using body heat for visual and rapid point-of-need detection of canine parvovirus 2
A visible and equipment-free recombinase polymerase amplification assay combined with a lateral flow strip (LFS RPA) was developed to detect canine parvovirus type 2 (CPV-2), which is the etiological agent of canine parvovirus disease. The CPV-2 LFS RPA assay was developed based on the VP2 gene and...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127419/ https://www.ncbi.nlm.nih.gov/pubmed/29705183 http://dx.doi.org/10.1016/j.mcp.2018.04.004 |
_version_ | 1783516355875569664 |
---|---|
author | Liu, Libing Wang, Jianchang Geng, Yunyun Wang, Jinfeng Li, Ruiwen Shi, Ruihan Yuan, Wanzhe |
author_facet | Liu, Libing Wang, Jianchang Geng, Yunyun Wang, Jinfeng Li, Ruiwen Shi, Ruihan Yuan, Wanzhe |
author_sort | Liu, Libing |
collection | PubMed |
description | A visible and equipment-free recombinase polymerase amplification assay combined with a lateral flow strip (LFS RPA) was developed to detect canine parvovirus type 2 (CPV-2), which is the etiological agent of canine parvovirus disease. The CPV-2 LFS RPA assay was developed based on the VP2 gene and is performed in a closed fist using body heat for 15 min; the products are visible to the naked eye on the LFS within 5 min. The assay could detect CPV-2a, CPV-2b and CPV-2c, and there was no cross-reaction with the other viruses tested. Using the standard CPV-2 DNA as a template, the analytical sensitivity was 1.0 × 10(2) copies per reaction, which was the same result as that of a real-time PCR. The assay performance was further evaluated by testing 60 canine fecal samples, and CPV-2 DNA was detected in 46 samples (76.7%, 46/60) by LFS RPA, which was the same result as that of the real-time PCR assay and higher than that of the SNAP method (48.3%, 29/60). The novel CPV-2 LFS RPA assay is an attractive and promising tool for rapid and convenient diagnosis of CPV disease, especially cage side and in underequipped laboratories. |
format | Online Article Text |
id | pubmed-7127419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71274192020-04-08 Equipment-free recombinase polymerase amplification assay using body heat for visual and rapid point-of-need detection of canine parvovirus 2 Liu, Libing Wang, Jianchang Geng, Yunyun Wang, Jinfeng Li, Ruiwen Shi, Ruihan Yuan, Wanzhe Mol Cell Probes Article A visible and equipment-free recombinase polymerase amplification assay combined with a lateral flow strip (LFS RPA) was developed to detect canine parvovirus type 2 (CPV-2), which is the etiological agent of canine parvovirus disease. The CPV-2 LFS RPA assay was developed based on the VP2 gene and is performed in a closed fist using body heat for 15 min; the products are visible to the naked eye on the LFS within 5 min. The assay could detect CPV-2a, CPV-2b and CPV-2c, and there was no cross-reaction with the other viruses tested. Using the standard CPV-2 DNA as a template, the analytical sensitivity was 1.0 × 10(2) copies per reaction, which was the same result as that of a real-time PCR. The assay performance was further evaluated by testing 60 canine fecal samples, and CPV-2 DNA was detected in 46 samples (76.7%, 46/60) by LFS RPA, which was the same result as that of the real-time PCR assay and higher than that of the SNAP method (48.3%, 29/60). The novel CPV-2 LFS RPA assay is an attractive and promising tool for rapid and convenient diagnosis of CPV disease, especially cage side and in underequipped laboratories. Elsevier Ltd. 2018-06 2018-04-27 /pmc/articles/PMC7127419/ /pubmed/29705183 http://dx.doi.org/10.1016/j.mcp.2018.04.004 Text en © 2018 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Liu, Libing Wang, Jianchang Geng, Yunyun Wang, Jinfeng Li, Ruiwen Shi, Ruihan Yuan, Wanzhe Equipment-free recombinase polymerase amplification assay using body heat for visual and rapid point-of-need detection of canine parvovirus 2 |
title | Equipment-free recombinase polymerase amplification assay using body heat for visual and rapid point-of-need detection of canine parvovirus 2 |
title_full | Equipment-free recombinase polymerase amplification assay using body heat for visual and rapid point-of-need detection of canine parvovirus 2 |
title_fullStr | Equipment-free recombinase polymerase amplification assay using body heat for visual and rapid point-of-need detection of canine parvovirus 2 |
title_full_unstemmed | Equipment-free recombinase polymerase amplification assay using body heat for visual and rapid point-of-need detection of canine parvovirus 2 |
title_short | Equipment-free recombinase polymerase amplification assay using body heat for visual and rapid point-of-need detection of canine parvovirus 2 |
title_sort | equipment-free recombinase polymerase amplification assay using body heat for visual and rapid point-of-need detection of canine parvovirus 2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127419/ https://www.ncbi.nlm.nih.gov/pubmed/29705183 http://dx.doi.org/10.1016/j.mcp.2018.04.004 |
work_keys_str_mv | AT liulibing equipmentfreerecombinasepolymeraseamplificationassayusingbodyheatforvisualandrapidpointofneeddetectionofcanineparvovirus2 AT wangjianchang equipmentfreerecombinasepolymeraseamplificationassayusingbodyheatforvisualandrapidpointofneeddetectionofcanineparvovirus2 AT gengyunyun equipmentfreerecombinasepolymeraseamplificationassayusingbodyheatforvisualandrapidpointofneeddetectionofcanineparvovirus2 AT wangjinfeng equipmentfreerecombinasepolymeraseamplificationassayusingbodyheatforvisualandrapidpointofneeddetectionofcanineparvovirus2 AT liruiwen equipmentfreerecombinasepolymeraseamplificationassayusingbodyheatforvisualandrapidpointofneeddetectionofcanineparvovirus2 AT shiruihan equipmentfreerecombinasepolymeraseamplificationassayusingbodyheatforvisualandrapidpointofneeddetectionofcanineparvovirus2 AT yuanwanzhe equipmentfreerecombinasepolymeraseamplificationassayusingbodyheatforvisualandrapidpointofneeddetectionofcanineparvovirus2 |