Assessment of Aedes albopictus reference genes for quantitative PCR at different stages of development.

Members of the Aedes genus of mosquitoes are widely recognized as vectors of viral diseases. Ae.albopictus is its most invasive species, and are known to carry viruses such as Dengue, Chikugunya and Zika. Its emerging importance puts Ae.albopictus on the forefront of genetic interaction and evolutio...

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Main Authors: Najat Dzaki, Ghows Azzam
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5858815?pdf=render
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spelling doaj-242438c3264841abad4478c56231ef622020-11-25T02:36:00ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01133e019466410.1371/journal.pone.0194664Assessment of Aedes albopictus reference genes for quantitative PCR at different stages of development.Najat DzakiGhows AzzamMembers of the Aedes genus of mosquitoes are widely recognized as vectors of viral diseases. Ae.albopictus is its most invasive species, and are known to carry viruses such as Dengue, Chikugunya and Zika. Its emerging importance puts Ae.albopictus on the forefront of genetic interaction and evolution studies. However, a panel of suitable reference genes specific for this insect is as of now undescribed. Nine reference genes, namely ACT, eEF1-γ, eIF2α, PP2A, RPL32, RPS17, PGK1, ILK and STK were evaluated. Expression patterns of the candidate reference genes were observed in a total of seventeen sample types, separated by stage of development and age. Gene stability was inferred from obtained quantification data through three widely cited evaluation algorithms i.e. BestKeeper, geNorm, and NormFinder. No single gene showed a satisfactory degree of stability throughout all developmental stages. Therefore, we propose combinations of PGK and ILK for early embryos; RPL32 and RPS17 for late embryos, all four larval instars, and pupae samples; eEF1-γ with STK for adult males; eEF1-γ with RPS17 for non-blood fed females; and eEF1-γ with eIF2α for both blood-fed females and cell culture. The results from this study should be able to provide a more informed selection of normalizing genes during qPCR in Ae.albopictus.http://europepmc.org/articles/PMC5858815?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Najat Dzaki
Ghows Azzam
spellingShingle Najat Dzaki
Ghows Azzam
Assessment of Aedes albopictus reference genes for quantitative PCR at different stages of development.
PLoS ONE
author_facet Najat Dzaki
Ghows Azzam
author_sort Najat Dzaki
title Assessment of Aedes albopictus reference genes for quantitative PCR at different stages of development.
title_short Assessment of Aedes albopictus reference genes for quantitative PCR at different stages of development.
title_full Assessment of Aedes albopictus reference genes for quantitative PCR at different stages of development.
title_fullStr Assessment of Aedes albopictus reference genes for quantitative PCR at different stages of development.
title_full_unstemmed Assessment of Aedes albopictus reference genes for quantitative PCR at different stages of development.
title_sort assessment of aedes albopictus reference genes for quantitative pcr at different stages of development.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2018-01-01
description Members of the Aedes genus of mosquitoes are widely recognized as vectors of viral diseases. Ae.albopictus is its most invasive species, and are known to carry viruses such as Dengue, Chikugunya and Zika. Its emerging importance puts Ae.albopictus on the forefront of genetic interaction and evolution studies. However, a panel of suitable reference genes specific for this insect is as of now undescribed. Nine reference genes, namely ACT, eEF1-γ, eIF2α, PP2A, RPL32, RPS17, PGK1, ILK and STK were evaluated. Expression patterns of the candidate reference genes were observed in a total of seventeen sample types, separated by stage of development and age. Gene stability was inferred from obtained quantification data through three widely cited evaluation algorithms i.e. BestKeeper, geNorm, and NormFinder. No single gene showed a satisfactory degree of stability throughout all developmental stages. Therefore, we propose combinations of PGK and ILK for early embryos; RPL32 and RPS17 for late embryos, all four larval instars, and pupae samples; eEF1-γ with STK for adult males; eEF1-γ with RPS17 for non-blood fed females; and eEF1-γ with eIF2α for both blood-fed females and cell culture. The results from this study should be able to provide a more informed selection of normalizing genes during qPCR in Ae.albopictus.
url http://europepmc.org/articles/PMC5858815?pdf=render
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