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Real-time RT-PCR assay to detect Granada virus and the related Massilia and Arrabida phleboviruses
BACKGROUND: Granada virus belongs to the genus Phlebovirus within the Naples serocomplex and was detected for the first time in sand flies from Spain in 2003. Seroprevalence studies have revealed that Granada virus may infect humans with most cases being asymptomatic. Moreover, recent studies in vec...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7257231/ https://www.ncbi.nlm.nih.gov/pubmed/32471505 http://dx.doi.org/10.1186/s13071-020-04110-5 |
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author | Davó, Laura Herrero, Laura Sánchez-Seco, Maria Paz Labiod, Nuria Roiz, David Gómez-Díaz, Elena Hernandez, Lourdes Figuerola, Jordi Vázquez, Ana |
author_facet | Davó, Laura Herrero, Laura Sánchez-Seco, Maria Paz Labiod, Nuria Roiz, David Gómez-Díaz, Elena Hernandez, Lourdes Figuerola, Jordi Vázquez, Ana |
author_sort | Davó, Laura |
collection | PubMed |
description | BACKGROUND: Granada virus belongs to the genus Phlebovirus within the Naples serocomplex and was detected for the first time in sand flies from Spain in 2003. Seroprevalence studies have revealed that Granada virus may infect humans with most cases being asymptomatic. Moreover, recent studies in vector samples revealed that the related Massilia and Arrabida phleboviruses could be also circulating in Spain. The objective of this study was to develop and assess a new sensitive real-time RT-PCR assay for Granada virus diagnosis able to detect the related phleboviruses Massilia and Arrabida. METHODS: Two specific primers and one unique probe to detect Granada, Massilia and Arrabida viruses, without differentiating between them, were designed targeting the conserved L-segment of their genome. Sensitivity was assessed using 10-fold serial dilutions of quantified in vitro DNA samples. Specificity was evaluated by testing different genomic RNA extracted from other representative phleboviruses. The new assay was used for virus detection in sand flies collected in 2012 from the Balearic Archipelago, a touristic hotspot in the Mediterranean. RESULTS: The real-time RT-PCR assay exhibited a sensitivity per reaction of 19 copies for Granada and Arrabida, and 16 copies for Massilia. No other related phleboviruses were detected. From the 37 pools of sand fly samples studied from four different Balearic Islands, we detected one positive in the island of Cabrera. CONCLUSIONS: To our knowledge, the method described here is the first real-time RT-PCR designed to detect Granada virus and the related Massilia and Arrabida phleboviruses. The study demonstrated that this is a rapid, robust and reliable assay for the accurate diagnosis of human infections as well as for virus surveillance in vectors. [Image: see text] |
format | Online Article Text |
id | pubmed-7257231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72572312020-06-07 Real-time RT-PCR assay to detect Granada virus and the related Massilia and Arrabida phleboviruses Davó, Laura Herrero, Laura Sánchez-Seco, Maria Paz Labiod, Nuria Roiz, David Gómez-Díaz, Elena Hernandez, Lourdes Figuerola, Jordi Vázquez, Ana Parasit Vectors Methodology BACKGROUND: Granada virus belongs to the genus Phlebovirus within the Naples serocomplex and was detected for the first time in sand flies from Spain in 2003. Seroprevalence studies have revealed that Granada virus may infect humans with most cases being asymptomatic. Moreover, recent studies in vector samples revealed that the related Massilia and Arrabida phleboviruses could be also circulating in Spain. The objective of this study was to develop and assess a new sensitive real-time RT-PCR assay for Granada virus diagnosis able to detect the related phleboviruses Massilia and Arrabida. METHODS: Two specific primers and one unique probe to detect Granada, Massilia and Arrabida viruses, without differentiating between them, were designed targeting the conserved L-segment of their genome. Sensitivity was assessed using 10-fold serial dilutions of quantified in vitro DNA samples. Specificity was evaluated by testing different genomic RNA extracted from other representative phleboviruses. The new assay was used for virus detection in sand flies collected in 2012 from the Balearic Archipelago, a touristic hotspot in the Mediterranean. RESULTS: The real-time RT-PCR assay exhibited a sensitivity per reaction of 19 copies for Granada and Arrabida, and 16 copies for Massilia. No other related phleboviruses were detected. From the 37 pools of sand fly samples studied from four different Balearic Islands, we detected one positive in the island of Cabrera. CONCLUSIONS: To our knowledge, the method described here is the first real-time RT-PCR designed to detect Granada virus and the related Massilia and Arrabida phleboviruses. The study demonstrated that this is a rapid, robust and reliable assay for the accurate diagnosis of human infections as well as for virus surveillance in vectors. [Image: see text] BioMed Central 2020-05-29 /pmc/articles/PMC7257231/ /pubmed/32471505 http://dx.doi.org/10.1186/s13071-020-04110-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Methodology Davó, Laura Herrero, Laura Sánchez-Seco, Maria Paz Labiod, Nuria Roiz, David Gómez-Díaz, Elena Hernandez, Lourdes Figuerola, Jordi Vázquez, Ana Real-time RT-PCR assay to detect Granada virus and the related Massilia and Arrabida phleboviruses |
title | Real-time RT-PCR assay to detect Granada virus and the related Massilia and Arrabida phleboviruses |
title_full | Real-time RT-PCR assay to detect Granada virus and the related Massilia and Arrabida phleboviruses |
title_fullStr | Real-time RT-PCR assay to detect Granada virus and the related Massilia and Arrabida phleboviruses |
title_full_unstemmed | Real-time RT-PCR assay to detect Granada virus and the related Massilia and Arrabida phleboviruses |
title_short | Real-time RT-PCR assay to detect Granada virus and the related Massilia and Arrabida phleboviruses |
title_sort | real-time rt-pcr assay to detect granada virus and the related massilia and arrabida phleboviruses |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7257231/ https://www.ncbi.nlm.nih.gov/pubmed/32471505 http://dx.doi.org/10.1186/s13071-020-04110-5 |
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