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Background <p>Resistance to organophosphate compounds is a serious concern in dealing with the control of mosquito vectors. Understanding the genetic and molecular basis of resistance is important not only to create strategies aimed at detecting and monitoring resistance in the field but also to implement efficient control measures and support the development of new insecticides. Despite the extensive literature on insecticide resistance, the molecular basis of metabolic resistance is still poorly understood.</p> Methods <p>To better understand the mechanisms of <i>Aedes aegypti</i> resistance to temephos, we performed high-throughput sequencing of RNA from the midgut tissue of <i>Aedes aegypti</i> larvae from a temephos-resistant laboratory colony, with long-term and continuous exposure to this insecticide (RecR), as well as from a reference, temephos-susceptible, colony (RecL). Bioinformatic analyses were then performed to assess the biological functions of differentially expressed genes, and the sequencing data were validated by quantitative reverse transcription-polymerase chain reaction (RT-qPCR).</p> Results <p>The transcriptome analysis mapped 6.084 genes, of which 202 were considered upregulated in RecR, including known and new genes representing many detoxification enzyme families, such as cytochrome-P450 oxidative enzymes, glutathione-S-transferases and glucosyl transferases. Other upregulated genes were mainly involved in the cuticle, carbohydrates and lipid biosynthesis. For the downregulated profiles, we found 106 downregulated genes in the RecR colony, with molecules involved in protein synthesis, immunity and apoptosis process. Furthermore, we observed an enrichment of KEGG metabolic pathways related to resistance mechanisms. The results found in RT-qPCR confirm the findings of the transcriptome data.</p> Conclusions <p>In this study, we investigated transcriptome-level changes maintained in a temephos-resistant <i>Ae. aegypti</i> colony under continuous and prolonged selection pressure. Our results indicate that metabolic resistance might involve a larger and more significant number of detoxification enzymes, with different functional roles, than previously shown with other mechanisms, also contributing to the resistance phenotype in the <i>Ae. aegypti</i> RecR colony.</p> Graphical Abstract <p></p>

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Characterization of the transcriptional cellular response in midgut tissue of temephos-resistant Aedes aegypti larvae

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年5月14日

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  • Elisama Helvecio,
  • Antonio Mauro Rezende,
  • Maria J. R. Bezerra,
  • Osvaldo Pompílio de-Melo-Neto,
  • Maria Alice Varjal de Melo Santos,
  • Tatiany Patrícia Romão,
  • Constância Flávia Junqueira Ayres

摘要

Background

Resistance to organophosphate compounds is a serious concern in dealing with the control of mosquito vectors. Understanding the genetic and molecular basis of resistance is important not only to create strategies aimed at detecting and monitoring resistance in the field but also to implement efficient control measures and support the development of new insecticides. Despite the extensive literature on insecticide resistance, the molecular basis of metabolic resistance is still poorly understood.

Methods

To better understand the mechanisms of Aedes aegypti resistance to temephos, we performed high-throughput sequencing of RNA from the midgut tissue of Aedes aegypti larvae from a temephos-resistant laboratory colony, with long-term and continuous exposure to this insecticide (RecR), as well as from a reference, temephos-susceptible, colony (RecL). Bioinformatic analyses were then performed to assess the biological functions of differentially expressed genes, and the sequencing data were validated by quantitative reverse transcription-polymerase chain reaction (RT-qPCR).

Results

The transcriptome analysis mapped 6.084 genes, of which 202 were considered upregulated in RecR, including known and new genes representing many detoxification enzyme families, such as cytochrome-P450 oxidative enzymes, glutathione-S-transferases and glucosyl transferases. Other upregulated genes were mainly involved in the cuticle, carbohydrates and lipid biosynthesis. For the downregulated profiles, we found 106 downregulated genes in the RecR colony, with molecules involved in protein synthesis, immunity and apoptosis process. Furthermore, we observed an enrichment of KEGG metabolic pathways related to resistance mechanisms. The results found in RT-qPCR confirm the findings of the transcriptome data.

Conclusions

In this study, we investigated transcriptome-level changes maintained in a temephos-resistant Ae. aegypti colony under continuous and prolonged selection pressure. Our results indicate that metabolic resistance might involve a larger and more significant number of detoxification enzymes, with different functional roles, than previously shown with other mechanisms, also contributing to the resistance phenotype in the Ae. aegypti RecR colony.

Graphical Abstract