Evidence map›Paper›PMID 40369600›Full record

ArticleParasites & vectors2025

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

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

Abstract read
In one paragraph

Article in Parasites & vectors, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Elisama HelvecioInstituto Aggeu Magalhães-FIOCRUZ, Av. Moraes Rego S/N Cidade Universitária, Recife, PE, 50740-465, Brazil.
Antonio Mauro RezendeInstituto René Rachou-FIOCRUZ, Av. Augusto de Lima, 1715, Barro Preto, Belo Horizonte, MG, 30190-002, Brazil.
Maria J R BezerraInstituto Aggeu Magalhães-FIOCRUZ, Av. Moraes Rego S/N Cidade Universitária, Recife, PE, 50740-465, Brazil.
Osvaldo Pompílio de-Melo-NetoInstituto Aggeu Magalhães-FIOCRUZ, Av. Moraes Rego S/N Cidade Universitária, Recife, PE, 50740-465, Brazil.
Maria Alice Varjal de Melo SantosInstituto Aggeu Magalhães-FIOCRUZ, Av. Moraes Rego S/N Cidade Universitária, Recife, PE, 50740-465, Brazil.
Tatiany Patrícia RomãoInstituto Aggeu Magalhães-FIOCRUZ, Av. Moraes Rego S/N Cidade Universitária, Recife, PE, 50740-465, Brazil. tatiany.romao@fiocruz.br.
Constância Flávia Junqueira AyresInstituto Aggeu Magalhães-FIOCRUZ, Av. Moraes Rego S/N Cidade Universitária, Recife, PE, 50740-465, Brazil. constancia.ayres@fiocruz.br.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 458492/2014-0Conselho Nacional de Desenvolvimento Científico e Tecnológico INCT Entomologia Molecular/CNPq/FAPERJ
6 · The paper itself

Abstract

backgroundResistance 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.

methodsTo 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).

resultsThe 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.

conclusionsIn 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.

Indexed as

AedesInsecticide ResistanceInsecticidesTemefosAnimalsGastrointestinal TractGene Expression ProfilingHigh-Throughput Nucleotide SequencingLarvaMosquito VectorsTranscriptomeInsecticidesTemefosAedes aegyptiMetabolic resistanceTemephosTranscriptome

Identifiers

PMID40369600
PMCPMC12076995

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.