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Real-time quantitative PCR for analysis of candidate fungal biopesticides against malaria: Technique validation and first applications

Recent research has indicated that fungal biopesticides could augment existing malaria vector control tools. Here we present a set of methodologies to monitor the in vivo kinetics of entomopathogenic fungi in Anopheles in the presence or absence of malaria parasites using quantitative real-time PCR....

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Detalles Bibliográficos
Autores principales: Bell, Andrew S., Blanford, Simon, Jenkins, Nina, Thomas, Matthew B., Read, Andrew F.
Formato: Texto
Lenguaje:English
Publicado: Academic Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2666797/
https://www.ncbi.nlm.nih.gov/pubmed/19320043
http://dx.doi.org/10.1016/j.jip.2009.01.006
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author Bell, Andrew S.
Blanford, Simon
Jenkins, Nina
Thomas, Matthew B.
Read, Andrew F.
author_facet Bell, Andrew S.
Blanford, Simon
Jenkins, Nina
Thomas, Matthew B.
Read, Andrew F.
author_sort Bell, Andrew S.
collection PubMed
description Recent research has indicated that fungal biopesticides could augment existing malaria vector control tools. Here we present a set of methodologies to monitor the in vivo kinetics of entomopathogenic fungi in Anopheles in the presence or absence of malaria parasites using quantitative real-time PCR. Three qPCR assays were successfully developed for counting fungal genomes: “specific” assays capable of distinguishing two well characterized fungal entomopathogens Beauveria bassiana isolate IMI391510 and Metarhizium anisopliae var. acridum isolate IMI330189, both of which have previously been shown to be virulent to Anopheles mosquitoes, and a “generic” fungal assay for determining any fungal burden. A fourth assay to Plasmodium chabaudi enabled quantification of co-infecting malarial parasites. All qPCR assays provide sensitive, target-specific, and robust quantification over a linear range of greater than five orders of magnitude (seven orders of magnitude for the fungal assays). B. bassiana growth within mosquitoes exposed to three different conidial challenge doses was monitored using the B. bassiana-specific assay and represents the first description of entomopathogenic fungal replication within an insect host. This revealed that, irrespective of challenge dose, after several days of relatively little replication, a sudden on-set of substantial nuclear division occurs, accompanied by physical fungal growth (hyphae) within the mosquito haemocoel shortly before death. Exposure to higher densities of conidia resulted in significantly greater pick-up by mosquitoes and to elevated fungal burdens at each time point sampled. High fungal burdens, comparable to those identified in cadavers, were attained more rapidly and mortalities occurred earlier post-exposure with increasing challenge dose. The lines of research made possible by the qPCR assays described here will contribute to optimization of fungal biopesticides against malaria and other vector-borne diseases.
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spelling pubmed-26667972009-07-01 Real-time quantitative PCR for analysis of candidate fungal biopesticides against malaria: Technique validation and first applications Bell, Andrew S. Blanford, Simon Jenkins, Nina Thomas, Matthew B. Read, Andrew F. J Invertebr Pathol Article Recent research has indicated that fungal biopesticides could augment existing malaria vector control tools. Here we present a set of methodologies to monitor the in vivo kinetics of entomopathogenic fungi in Anopheles in the presence or absence of malaria parasites using quantitative real-time PCR. Three qPCR assays were successfully developed for counting fungal genomes: “specific” assays capable of distinguishing two well characterized fungal entomopathogens Beauveria bassiana isolate IMI391510 and Metarhizium anisopliae var. acridum isolate IMI330189, both of which have previously been shown to be virulent to Anopheles mosquitoes, and a “generic” fungal assay for determining any fungal burden. A fourth assay to Plasmodium chabaudi enabled quantification of co-infecting malarial parasites. All qPCR assays provide sensitive, target-specific, and robust quantification over a linear range of greater than five orders of magnitude (seven orders of magnitude for the fungal assays). B. bassiana growth within mosquitoes exposed to three different conidial challenge doses was monitored using the B. bassiana-specific assay and represents the first description of entomopathogenic fungal replication within an insect host. This revealed that, irrespective of challenge dose, after several days of relatively little replication, a sudden on-set of substantial nuclear division occurs, accompanied by physical fungal growth (hyphae) within the mosquito haemocoel shortly before death. Exposure to higher densities of conidia resulted in significantly greater pick-up by mosquitoes and to elevated fungal burdens at each time point sampled. High fungal burdens, comparable to those identified in cadavers, were attained more rapidly and mortalities occurred earlier post-exposure with increasing challenge dose. The lines of research made possible by the qPCR assays described here will contribute to optimization of fungal biopesticides against malaria and other vector-borne diseases. Academic Press 2009-03 /pmc/articles/PMC2666797/ /pubmed/19320043 http://dx.doi.org/10.1016/j.jip.2009.01.006 Text en © 2009 Elsevier Inc. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Article
Bell, Andrew S.
Blanford, Simon
Jenkins, Nina
Thomas, Matthew B.
Read, Andrew F.
Real-time quantitative PCR for analysis of candidate fungal biopesticides against malaria: Technique validation and first applications
title Real-time quantitative PCR for analysis of candidate fungal biopesticides against malaria: Technique validation and first applications
title_full Real-time quantitative PCR for analysis of candidate fungal biopesticides against malaria: Technique validation and first applications
title_fullStr Real-time quantitative PCR for analysis of candidate fungal biopesticides against malaria: Technique validation and first applications
title_full_unstemmed Real-time quantitative PCR for analysis of candidate fungal biopesticides against malaria: Technique validation and first applications
title_short Real-time quantitative PCR for analysis of candidate fungal biopesticides against malaria: Technique validation and first applications
title_sort real-time quantitative pcr for analysis of candidate fungal biopesticides against malaria: technique validation and first applications
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2666797/
https://www.ncbi.nlm.nih.gov/pubmed/19320043
http://dx.doi.org/10.1016/j.jip.2009.01.006
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