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Transcriptomic meta-signatures identified in Anopheles gambiae populations reveal previously undetected insecticide resistance mechanisms
Victoria A. Ingham, Simon C. Wagstaff, Hilary Ranson
Nature Communications · 2018 · ▲ 150 citations
Abstract
Increasing insecticide resistance in malaria-transmitting vectors represents a public health threat, but underlying mechanisms are poorly understood. Here, a data integration approach is used to analyse transcriptomic data from comparisons of insecticide resistant and susceptible Anopheles populations from disparate geographical regions across the African continent. An unbiased, integrated analysis of this data confirms previously described resistance candidates but also identifies multiple novel genes involving alternative resistance mechanisms, including sequestration, and transcription factors regulating multiple downstream effector genes, which are validated by gene silencing. The integrated datasets can be interrogated with a bespoke Shiny R script, deployed as an interactive web-based application, that maps the expression of resistance candidates and identifies co-regulated transcripts that may give clues to the function of novel resistance-associated genes.
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- 10.1038/s41467-018-07615-x
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- 2026-07-25 MST
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APA
Ingham, V.A., Wagstaff, S.C., & Ranson, H. (2018). Transcriptomic meta-signatures identified in Anopheles gambiae populations reveal previously undetected insecticide resistance mechanisms. <em>Nature Communications</em>. https://doi.org/10.1038/s41467-018-07615-x
Vancouver
Ingham VA, Wagstaff SC, Ranson H. Transcriptomic meta-signatures identified in Anopheles gambiae populations reveal previously undetected insecticide resistance mechanisms. Nature Communications. 2018. doi:10.1038/s41467-018-07615-x.
BibTeX
@article{victoria2018Transc,
title = {Transcriptomic meta-signatures identified in Anopheles gambiae populations reveal previously undetected insecticide resistance mechanisms},
author = {Victoria A. Ingham and Simon C. Wagstaff and Hilary Ranson},
journal = {Nature Communications},
year = {2018},
doi = {10.1038/s41467-018-07615-x},
}
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