Cargando…
Development of rapid nucleic acid assays based on the recombinant polymerase amplification for monkeypox virus
• Two RPA methods (F-RPA and VF- RPA) have been developed for monkeypox virus rapid detection. • The limit of detection was 15.32 copies/μL for F-RPA and 8.53 copies/μL for VF-RPA. • No cross-reaction was found in 14 rash and fever-associated viruses. • The two RPA methods are simple and rapid, maki...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wuhan Institute of Virology, Chinese Academy of Sciences
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9724568/ https://www.ncbi.nlm.nih.gov/pubmed/36494078 http://dx.doi.org/10.1016/j.virs.2022.12.001 |
_version_ | 1784844448000114688 |
---|---|
author | Li, Yuchang Gao, Yanhong Tang, Ying Li, Jing Zhang, Sen Jiang, Tao Kang, Xiaoping |
author_facet | Li, Yuchang Gao, Yanhong Tang, Ying Li, Jing Zhang, Sen Jiang, Tao Kang, Xiaoping |
author_sort | Li, Yuchang |
collection | PubMed |
description | • Two RPA methods (F-RPA and VF- RPA) have been developed for monkeypox virus rapid detection. • The limit of detection was 15.32 copies/μL for F-RPA and 8.53 copies/μL for VF-RPA. • No cross-reaction was found in 14 rash and fever-associated viruses. • The two RPA methods are simple and rapid, making them potentially useful for detection of MPXV in the field/clinic. |
format | Online Article Text |
id | pubmed-9724568 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Wuhan Institute of Virology, Chinese Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-97245682022-12-07 Development of rapid nucleic acid assays based on the recombinant polymerase amplification for monkeypox virus Li, Yuchang Gao, Yanhong Tang, Ying Li, Jing Zhang, Sen Jiang, Tao Kang, Xiaoping Virol Sin Letter • Two RPA methods (F-RPA and VF- RPA) have been developed for monkeypox virus rapid detection. • The limit of detection was 15.32 copies/μL for F-RPA and 8.53 copies/μL for VF-RPA. • No cross-reaction was found in 14 rash and fever-associated viruses. • The two RPA methods are simple and rapid, making them potentially useful for detection of MPXV in the field/clinic. Wuhan Institute of Virology, Chinese Academy of Sciences 2022-12-06 /pmc/articles/PMC9724568/ /pubmed/36494078 http://dx.doi.org/10.1016/j.virs.2022.12.001 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Letter Li, Yuchang Gao, Yanhong Tang, Ying Li, Jing Zhang, Sen Jiang, Tao Kang, Xiaoping Development of rapid nucleic acid assays based on the recombinant polymerase amplification for monkeypox virus |
title | Development of rapid nucleic acid assays based on the recombinant polymerase amplification for monkeypox virus |
title_full | Development of rapid nucleic acid assays based on the recombinant polymerase amplification for monkeypox virus |
title_fullStr | Development of rapid nucleic acid assays based on the recombinant polymerase amplification for monkeypox virus |
title_full_unstemmed | Development of rapid nucleic acid assays based on the recombinant polymerase amplification for monkeypox virus |
title_short | Development of rapid nucleic acid assays based on the recombinant polymerase amplification for monkeypox virus |
title_sort | development of rapid nucleic acid assays based on the recombinant polymerase amplification for monkeypox virus |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9724568/ https://www.ncbi.nlm.nih.gov/pubmed/36494078 http://dx.doi.org/10.1016/j.virs.2022.12.001 |
work_keys_str_mv | AT liyuchang developmentofrapidnucleicacidassaysbasedontherecombinantpolymeraseamplificationformonkeypoxvirus AT gaoyanhong developmentofrapidnucleicacidassaysbasedontherecombinantpolymeraseamplificationformonkeypoxvirus AT tangying developmentofrapidnucleicacidassaysbasedontherecombinantpolymeraseamplificationformonkeypoxvirus AT lijing developmentofrapidnucleicacidassaysbasedontherecombinantpolymeraseamplificationformonkeypoxvirus AT zhangsen developmentofrapidnucleicacidassaysbasedontherecombinantpolymeraseamplificationformonkeypoxvirus AT jiangtao developmentofrapidnucleicacidassaysbasedontherecombinantpolymeraseamplificationformonkeypoxvirus AT kangxiaoping developmentofrapidnucleicacidassaysbasedontherecombinantpolymeraseamplificationformonkeypoxvirus |