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Development of a Real-Time qPCR Assay for Quantification of Covert Baculovirus Infections in a Major African Crop Pest

Many pathogens and parasites are present in host individuals and populations without any obvious signs of disease. This is particularly true for baculoviruses infecting lepidopteran hosts, where studies have shown that covert persistent viral infections are almost ubiquitous in many species. To date...

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Autores principales: Graham, Robert I., Tummala, Yamini, Rhodes, Glenn, Cory, Jenny S., Shirras, Alan, Grzywacz, David, Wilson, Kenneth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598664/
https://www.ncbi.nlm.nih.gov/pubmed/26463414
http://dx.doi.org/10.3390/insects6030746
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author Graham, Robert I.
Tummala, Yamini
Rhodes, Glenn
Cory, Jenny S.
Shirras, Alan
Grzywacz, David
Wilson, Kenneth
author_facet Graham, Robert I.
Tummala, Yamini
Rhodes, Glenn
Cory, Jenny S.
Shirras, Alan
Grzywacz, David
Wilson, Kenneth
author_sort Graham, Robert I.
collection PubMed
description Many pathogens and parasites are present in host individuals and populations without any obvious signs of disease. This is particularly true for baculoviruses infecting lepidopteran hosts, where studies have shown that covert persistent viral infections are almost ubiquitous in many species. To date, the infection intensity of covert viruses has rarely been quantified. In this study, we investigated the dynamics of a covert baculovirus infection within the lepidopteran crop pest Spodoptera exempta. A real-time quantitative polymerase chain reaction (qPCR) procedure using a 5' nuclease hydrolysis (TaqMan) probe was developed for specific detection and quantification of Spodoptera exempta nucleopolyhedrovirus (SpexNPV). The qPCR assay indicated that covert baculovirus dynamics varied considerably over the course of the host life-cycle, with infection load peaking in early larval instars and being lowest in adults and final-instar larvae. Adult dissections indicated that, contrary to expectation, viral load aggregation was highest in the head, wings and legs, and lowest in the thorax and abdomen. The data presented here have broad implications relating to our understanding of transmission patterns of baculoviruses and the role of covert infections in host-pathogen dynamics.
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spelling pubmed-45986642015-10-15 Development of a Real-Time qPCR Assay for Quantification of Covert Baculovirus Infections in a Major African Crop Pest Graham, Robert I. Tummala, Yamini Rhodes, Glenn Cory, Jenny S. Shirras, Alan Grzywacz, David Wilson, Kenneth Insects Article Many pathogens and parasites are present in host individuals and populations without any obvious signs of disease. This is particularly true for baculoviruses infecting lepidopteran hosts, where studies have shown that covert persistent viral infections are almost ubiquitous in many species. To date, the infection intensity of covert viruses has rarely been quantified. In this study, we investigated the dynamics of a covert baculovirus infection within the lepidopteran crop pest Spodoptera exempta. A real-time quantitative polymerase chain reaction (qPCR) procedure using a 5' nuclease hydrolysis (TaqMan) probe was developed for specific detection and quantification of Spodoptera exempta nucleopolyhedrovirus (SpexNPV). The qPCR assay indicated that covert baculovirus dynamics varied considerably over the course of the host life-cycle, with infection load peaking in early larval instars and being lowest in adults and final-instar larvae. Adult dissections indicated that, contrary to expectation, viral load aggregation was highest in the head, wings and legs, and lowest in the thorax and abdomen. The data presented here have broad implications relating to our understanding of transmission patterns of baculoviruses and the role of covert infections in host-pathogen dynamics. MDPI 2015-08-25 /pmc/articles/PMC4598664/ /pubmed/26463414 http://dx.doi.org/10.3390/insects6030746 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Graham, Robert I.
Tummala, Yamini
Rhodes, Glenn
Cory, Jenny S.
Shirras, Alan
Grzywacz, David
Wilson, Kenneth
Development of a Real-Time qPCR Assay for Quantification of Covert Baculovirus Infections in a Major African Crop Pest
title Development of a Real-Time qPCR Assay for Quantification of Covert Baculovirus Infections in a Major African Crop Pest
title_full Development of a Real-Time qPCR Assay for Quantification of Covert Baculovirus Infections in a Major African Crop Pest
title_fullStr Development of a Real-Time qPCR Assay for Quantification of Covert Baculovirus Infections in a Major African Crop Pest
title_full_unstemmed Development of a Real-Time qPCR Assay for Quantification of Covert Baculovirus Infections in a Major African Crop Pest
title_short Development of a Real-Time qPCR Assay for Quantification of Covert Baculovirus Infections in a Major African Crop Pest
title_sort development of a real-time qpcr assay for quantification of covert baculovirus infections in a major african crop pest
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598664/
https://www.ncbi.nlm.nih.gov/pubmed/26463414
http://dx.doi.org/10.3390/insects6030746
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