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Evaluation of Reference Genes at Different Developmental Stages for Quantitative Real-time PCR in Aedes Aegypti

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Journal Sci Rep
Specialty Science
Date 2017 Mar 17
PMID 28300076
Citations 53
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Abstract

The mosquito Aedes aegypti (Ae. aegypti) is the most notorious vector of illness-causing viruses such as Dengue, Chikugunya, and Zika. Although numerous genetic expression studies utilizing quantitative real-time PCR (qPCR) have been conducted with regards to Ae. aegypti, a panel of genes to be used suitably as references for the purpose of expression-level normalization within this epidemiologically important insect is presently lacking. Here, the usability of seven widely-utilized reference genes i.e. actin (ACT), eukaryotic elongation factor 1 alpha (eEF1α), alpha tubulin (α-tubulin), ribosomal proteins L8, L32 and S17 (RPL8, RPL32 and RPS17), and glyceraldeyde 3-phosphate dehydrogenase (GAPDH) were investigated. Expression patterns of the reference genes were observed in sixteen pre-determined developmental stages and in cell culture. Gene stability was inferred from qPCR data through three freely available algorithms i.e. BestKeeper, geNorm, and NormFinder. The consensus rankings generated from stability values provided by these programs suggest a combination of at least two genes for normalization. ACT and RPS17 are the most dependably expressed reference genes and therefore, we propose an ACT/RPS17 combination for normalization in all Ae. aegypti derived samples. GAPDH performed least desirably, and is thus not a recommended reference gene. This study emphasizes the importance of validating reference genes in Ae. aegypti for qPCR based research.

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References
1.
Morlais I, Severson D . Identification of a polymorphic mucin-like gene expressed in the midgut of the mosquito, Aedes aegypti, using an integrated bulked segregant and differential display analysis. Genetics. 2001; 158(3):1125-36. PMC: 1461701. DOI: 10.1093/genetics/158.3.1125. View

2.
Long C, Levitzki A, Koshland Jr D . The subunit structure and subunit interactions of cytidine triphosphate synthetase. J Biol Chem. 1970; 245(1):80-7. View

3.
Anderson J, Rico-Hesse R . Aedes aegypti vectorial capacity is determined by the infecting genotype of dengue virus. Am J Trop Med Hyg. 2006; 75(5):886-92. PMC: 1993907. View

4.
Sun M, Lu M, Tang X, Du Y . Exploring valid reference genes for quantitative real-time PCR analysis in Sesamia inferens (Lepidoptera: Noctuidae). PLoS One. 2015; 10(1):e0115979. PMC: 4293147. DOI: 10.1371/journal.pone.0115979. View

5.
Cook P, Hugo L, Iturbe-Ormaetxe I, Williams C, Chenoweth S, Ritchie S . The use of transcriptional profiles to predict adult mosquito age under field conditions. Proc Natl Acad Sci U S A. 2006; 103(48):18060-5. PMC: 1838706. DOI: 10.1073/pnas.0604875103. View