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Series GSE235286 Query DataSets for GSE235286
Status Public on Jul 05, 2023
Title Hearing of malaria mosquitoes is modulated by a beta-adrenergic-like octopamine receptor and serves as insecticide target
Organism Anopheles gambiae
Experiment type Expression profiling by high throughput sequencing
Summary Malaria mosquitoes acoustically detect their mating partners within large swarms that form transiently at dusk. Indeed, male malaria mosquitoes preferably respond to female flight tones during swarm time. This phenomenon implies a sophisticated context- and time-dependent modulation of mosquito audition, the mechanisms of which are largely unknown. Using transcriptomics, we identify a complex network of candidate neuromodulators regulating mosquito hearing in the species Anopheles gambiae. Among them, octopamine stands out as auditory modulator during swarm time. In-depth analysis of octopamine auditory function shows that it affects the mosquito ear on multiple levels: it modulates the tuning and stiffness of the flagellar sound receiver and controls the erection of antennal fibrillae. We show that two α- and β-adrenergic-like octopamine receptors drive octopamine’s auditory roles and demonstrate that the octopaminergic auditory control system can be targeted by insecticides. Our findings highlight octopamine as key for mosquito hearing and mating partner detection, and as a potential novel target for mosquito control.
 
Overall design To investigate expression, and circadian pattern of expression of transcripts in Anopheles gambiae mosquito ears we conducted the following: First, we entrained mosquitoes, in environmental incubators, to 12H:12H light/dark cycle with 1-hour ramped light transition to simulated dawn and dusk (ZT0-ZT1 and ZT12-ZT13, respectively; ZTX is the formalised notation of an entrained circadian cycle's phase). Temperature and relative humidity were set constantinside the incubators throughout the circadian day, at 28 °C and 80% respectively. Mosquitoes were exposed to the circadian entrainment in the incubators for three days before performing any experiment. Then, on day four of circadian entrainment, 35 male and 35 female mosquitoes were removed from the incubators at six different circadian time points (ZT0, ZT4, ZT8, ZT12, ZT16, ZT20), and we collected their Johnston's organs (JO; the mosquito's "internal ear"). This procedure was repeated 3 times, resulting in three biological replicates of JO samples at each circadian time point. Finally, we performed RNA sequencing of the samples, and conducted transcript expression, differential expression (between males and females), and circadian expression analyses on the sequenced data.
 
Contributor(s) Georgiades M, Alampounti AC, Somers J, Su MP, Ellis DA, Bagi J, Tytheridge S, Ntabaliba W, Moore SJ, Albert JT, Andrés M
Citation(s) 37468470
Submission date Jun 20, 2023
Last update date Sep 12, 2023
Contact name Marta Andrés
E-mail(s) marta.andres@ucl.ac.uk
Organization name University College London
Department Ear Institute
Lab Andrés lab
Street address 332 Grays Inn Rd
City London
ZIP/Postal code WC1X 8EE
Country United Kingdom
 
Platforms (1)
GPL22033 Illumina NextSeq 500 (Anopheles gambiae)
Samples (36)
GSM7498337 JO, Female, ZT00, Rep1
GSM7498338 JO, Female, ZT00, Rep2
GSM7498339 JO, Female, ZT00, Rep3
Relations
BioProject PRJNA985656

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE235286_raw_counts.tsv.gz 1.2 Mb (ftp)(http) TSV
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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