SRX18700328 Unfed Ornithodoros hermsi larvae biological replicate 1 R1 SRP413059 bp0 Total RNA was extracted from whole body Ornithodoros hermsi larvae. Ticks were grouped in three biological replicates (n 20 individual per replicate) and are composed of unfed larvae (Oh-UN) and larvae fed on neonate mice at 6h-post detachment (Oh-6h), 12h-post detachment (Oh-12h), 24h-post detachment (Oh-24h), 5-days-post detachment (Oh-5d). RNA extraction was performed with the PureLink RNA Mini Kit (Invitrogen) according to manufacturer`s specifications and analyzed with an Agilent High Sensitivity RNA ScreenTape System in an TapeStation 4150 (Agilent). The library was constructed using the NEBNextUltraTM II (Directional) RNA with polyA selection library prep kit and sequencing was performed in an Illumina Novaseq 6000 DNA sequencer. SRS16141428 Unfed Ornithodoros hermsi larvae biological replicate 1 Unfed Ornithodoros hermsi larvae biological replicate 1 R1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX18700329 Fed Ornithodoros hermsi larvae 6h post-detachment biological replicate 3 R1 SRP413059 bp0 Total RNA was extracted from whole body Ornithodoros hermsi larvae. Ticks were grouped in three biological replicates (n 20 individual per replicate) and are composed of unfed larvae (Oh-UN) and larvae fed on neonate mice at 6h-post detachment (Oh-6h), 12h-post detachment (Oh-12h), 24h-post detachment (Oh-24h), 5-days-post detachment (Oh-5d). RNA extraction was performed with the PureLink RNA Mini Kit (Invitrogen) according to manufacturer`s specifications and analyzed with an Agilent High Sensitivity RNA ScreenTape System in an TapeStation 4150 (Agilent). The library was constructed using the NEBNextUltraTM II (Directional) RNA with polyA selection library prep kit and sequencing was performed in an Illumina Novaseq 6000 DNA sequencer. SRS16141429 Fed Ornithodoros hermsi larvae 6h post-detachment biological replicate 3 Fed Ornithodoros hermsi larvae 6h post-detachment biological replicate 3 R1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX18700330 Fed Ornithodoros hermsi larvae 12h post-detachment biological replicate 1 R1 SRP413059 bp0 Total RNA was extracted from whole body Ornithodoros hermsi larvae. Ticks were grouped in three biological replicates (n 20 individual per replicate) and are composed of unfed larvae (Oh-UN) and larvae fed on neonate mice at 6h-post detachment (Oh-6h), 12h-post detachment (Oh-12h), 24h-post detachment (Oh-24h), 5-days-post detachment (Oh-5d). RNA extraction was performed with the PureLink RNA Mini Kit (Invitrogen) according to manufacturer`s specifications and analyzed with an Agilent High Sensitivity RNA ScreenTape System in an TapeStation 4150 (Agilent). The library was constructed using the NEBNextUltraTM II (Directional) RNA with polyA selection library prep kit and sequencing was performed in an Illumina Novaseq 6000 DNA sequencer. SRS16141430 Fed Ornithodoros hermsi larvae 12h post-detachment biological replicate 1 Fed Ornithodoros hermsi larvae 12h post-detachment biological replicate 1 R1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX18700331 Fed Ornithodoros hermsi larvae 12h post-detachment biological replicate 2 R1 SRP413059 bp0 Total RNA was extracted from whole body Ornithodoros hermsi larvae. Ticks were grouped in three biological replicates (n 20 individual per replicate) and are composed of unfed larvae (Oh-UN) and larvae fed on neonate mice at 6h-post detachment (Oh-6h), 12h-post detachment (Oh-12h), 24h-post detachment (Oh-24h), 5-days-post detachment (Oh-5d). RNA extraction was performed with the PureLink RNA Mini Kit (Invitrogen) according to manufacturer`s specifications and analyzed with an Agilent High Sensitivity RNA ScreenTape System in an TapeStation 4150 (Agilent). The library was constructed using the NEBNextUltraTM II (Directional) RNA with polyA selection library prep kit and sequencing was performed in an Illumina Novaseq 6000 DNA sequencer. SRS16141431 Fed Ornithodoros hermsi larvae 12h post-detachment biological replicate 2 Fed Ornithodoros hermsi larvae 12h post-detachment biological replicate 2 R1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX18700332 Fed Ornithodoros hermsi larvae 12h post-detachment biological replicate 3 R1 SRP413059 bp0 Total RNA was extracted from whole body Ornithodoros hermsi larvae. Ticks were grouped in three biological replicates (n 20 individual per replicate) and are composed of unfed larvae (Oh-UN) and larvae fed on neonate mice at 6h-post detachment (Oh-6h), 12h-post detachment (Oh-12h), 24h-post detachment (Oh-24h), 5-days-post detachment (Oh-5d). RNA extraction was performed with the PureLink RNA Mini Kit (Invitrogen) according to manufacturer`s specifications and analyzed with an Agilent High Sensitivity RNA ScreenTape System in an TapeStation 4150 (Agilent). The library was constructed using the NEBNextUltraTM II (Directional) RNA with polyA selection library prep kit and sequencing was performed in an Illumina Novaseq 6000 DNA sequencer. SRS16141432 Fed Ornithodoros hermsi larvae 12h post-detachment biological replicate 3 Fed Ornithodoros hermsi larvae 12h post-detachment biological replicate 3 R1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX18700333 Fed Ornithodoros hermsi larvae 24h post-detachment biological replicate 1 R1 SRP413059 bp0 Total RNA was extracted from whole body Ornithodoros hermsi larvae. Ticks were grouped in three biological replicates (n 20 individual per replicate) and are composed of unfed larvae (Oh-UN) and larvae fed on neonate mice at 6h-post detachment (Oh-6h), 12h-post detachment (Oh-12h), 24h-post detachment (Oh-24h), 5-days-post detachment (Oh-5d). RNA extraction was performed with the PureLink RNA Mini Kit (Invitrogen) according to manufacturer`s specifications and analyzed with an Agilent High Sensitivity RNA ScreenTape System in an TapeStation 4150 (Agilent). The library was constructed using the NEBNextUltraTM II (Directional) RNA with polyA selection library prep kit and sequencing was performed in an Illumina Novaseq 6000 DNA sequencer. SRS16141433 Fed Ornithodoros hermsi larvae 24h post-detachment biological replicate 1 Fed Ornithodoros hermsi larvae 24h post-detachment biological replicate 1 R1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX18700334 Unfed Ornithodoros hermsi larvae biological replicate 2 R1 SRP413059 bp0 Total RNA was extracted from whole body Ornithodoros hermsi larvae. Ticks were grouped in three biological replicates (n 20 individual per replicate) and are composed of unfed larvae (Oh-UN) and larvae fed on neonate mice at 6h-post detachment (Oh-6h), 12h-post detachment (Oh-12h), 24h-post detachment (Oh-24h), 5-days-post detachment (Oh-5d). RNA extraction was performed with the PureLink RNA Mini Kit (Invitrogen) according to manufacturer`s specifications and analyzed with an Agilent High Sensitivity RNA ScreenTape System in an TapeStation 4150 (Agilent). The library was constructed using the NEBNextUltraTM II (Directional) RNA with polyA selection library prep kit and sequencing was performed in an Illumina Novaseq 6000 DNA sequencer. SRS16141434 Unfed Ornithodoros hermsi larvae biological replicate 2 Unfed Ornithodoros hermsi larvae biological replicate 2 R1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX18700335 Fed Ornithodoros hermsi larvae 24h post-detachment biological replicate 2 R1 SRP413059 bp0 Total RNA was extracted from whole body Ornithodoros hermsi larvae. Ticks were grouped in three biological replicates (n 20 individual per replicate) and are composed of unfed larvae (Oh-UN) and larvae fed on neonate mice at 6h-post detachment (Oh-6h), 12h-post detachment (Oh-12h), 24h-post detachment (Oh-24h), 5-days-post detachment (Oh-5d). RNA extraction was performed with the PureLink RNA Mini Kit (Invitrogen) according to manufacturer`s specifications and analyzed with an Agilent High Sensitivity RNA ScreenTape System in an TapeStation 4150 (Agilent). The library was constructed using the NEBNextUltraTM II (Directional) RNA with polyA selection library prep kit and sequencing was performed in an Illumina Novaseq 6000 DNA sequencer. SRS16141435 Fed Ornithodoros hermsi larvae 24h post-detachment biological replicate 2 Fed Ornithodoros hermsi larvae 24h post-detachment biological replicate 2 R1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX18700336 Fed Ornithodoros hermsi larvae 24h post-detachment biological replicate 3 R1 SRP413059 bp0 Total RNA was extracted from whole body Ornithodoros hermsi larvae. Ticks were grouped in three biological replicates (n 20 individual per replicate) and are composed of unfed larvae (Oh-UN) and larvae fed on neonate mice at 6h-post detachment (Oh-6h), 12h-post detachment (Oh-12h), 24h-post detachment (Oh-24h), 5-days-post detachment (Oh-5d). RNA extraction was performed with the PureLink RNA Mini Kit (Invitrogen) according to manufacturer`s specifications and analyzed with an Agilent High Sensitivity RNA ScreenTape System in an TapeStation 4150 (Agilent). The library was constructed using the NEBNextUltraTM II (Directional) RNA with polyA selection library prep kit and sequencing was performed in an Illumina Novaseq 6000 DNA sequencer. SRS16141436 Fed Ornithodoros hermsi larvae 24h post-detachment biological replicate 3 Fed Ornithodoros hermsi larvae 24h post-detachment biological replicate 3 R1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX18700337 Fed Ornithodoros hermsi larvae 5 days post-detachment biological replicate 1 R1 SRP413059 bp0 Total RNA was extracted from whole body Ornithodoros hermsi larvae. Ticks were grouped in three biological replicates (n 20 individual per replicate) and are composed of unfed larvae (Oh-UN) and larvae fed on neonate mice at 6h-post detachment (Oh-6h), 12h-post detachment (Oh-12h), 24h-post detachment (Oh-24h), 5-days-post detachment (Oh-5d). RNA extraction was performed with the PureLink RNA Mini Kit (Invitrogen) according to manufacturer`s specifications and analyzed with an Agilent High Sensitivity RNA ScreenTape System in an TapeStation 4150 (Agilent). The library was constructed using the NEBNextUltraTM II (Directional) RNA with polyA selection library prep kit and sequencing was performed in an Illumina Novaseq 6000 DNA sequencer. SRS16141437 Fed Ornithodoros hermsi larvae 5 days post-detachment biological replicate 1 Fed Ornithodoros hermsi larvae 5 days post-detachment biological replicate 1 R1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX18700338 Fed Ornithodoros hermsi larvae 5 days post-detachment biological replicate 3 R1 SRP413059 bp0 Total RNA was extracted from whole body Ornithodoros hermsi larvae. Ticks were grouped in three biological replicates (n 20 individual per replicate) and are composed of unfed larvae (Oh-UN) and larvae fed on neonate mice at 6h-post detachment (Oh-6h), 12h-post detachment (Oh-12h), 24h-post detachment (Oh-24h), 5-days-post detachment (Oh-5d). RNA extraction was performed with the PureLink RNA Mini Kit (Invitrogen) according to manufacturer`s specifications and analyzed with an Agilent High Sensitivity RNA ScreenTape System in an TapeStation 4150 (Agilent). The library was constructed using the NEBNextUltraTM II (Directional) RNA with polyA selection library prep kit and sequencing was performed in an Illumina Novaseq 6000 DNA sequencer. SRS16141438 Fed Ornithodoros hermsi larvae 5 days post-detachment biological replicate 3 Fed Ornithodoros hermsi larvae 5 days post-detachment biological replicate 3 R1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX18700339 Fed Ornithodoros hermsi larvae 5 days post-detachment biological replicate 2 R1 SRP413059 bp0 Total RNA was extracted from whole body Ornithodoros hermsi larvae. Ticks were grouped in three biological replicates (n 20 individual per replicate) and are composed of unfed larvae (Oh-UN) and larvae fed on neonate mice at 6h-post detachment (Oh-6h), 12h-post detachment (Oh-12h), 24h-post detachment (Oh-24h), 5-days-post detachment (Oh-5d). RNA extraction was performed with the PureLink RNA Mini Kit (Invitrogen) according to manufacturer`s specifications and analyzed with an Agilent High Sensitivity RNA ScreenTape System in an TapeStation 4150 (Agilent). The library was constructed using the NEBNextUltraTM II (Directional) RNA with polyA selection library prep kit and sequencing was performed in an Illumina Novaseq 6000 DNA sequencer. SRS16141439 Fed Ornithodoros hermsi larvae 5 days post-detachment biological replicate 2 Fed Ornithodoros hermsi larvae 5 days post-detachment biological replicate 2 R1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX18700340 Unfed Ornithodoros hermsi larvae biological replicate 3 R1 SRP413059 bp0 Total RNA was extracted from whole body Ornithodoros hermsi larvae. Ticks were grouped in three biological replicates (n 20 individual per replicate) and are composed of unfed larvae (Oh-UN) and larvae fed on neonate mice at 6h-post detachment (Oh-6h), 12h-post detachment (Oh-12h), 24h-post detachment (Oh-24h), 5-days-post detachment (Oh-5d). RNA extraction was performed with the PureLink RNA Mini Kit (Invitrogen) according to manufacturer`s specifications and analyzed with an Agilent High Sensitivity RNA ScreenTape System in an TapeStation 4150 (Agilent). The library was constructed using the NEBNextUltraTM II (Directional) RNA with polyA selection library prep kit and sequencing was performed in an Illumina Novaseq 6000 DNA sequencer. SRS16141440 Unfed Ornithodoros hermsi larvae biological replicate 3 Unfed Ornithodoros hermsi larvae biological replicate 3 R1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX18700341 Fed Ornithodoros hermsi larvae 6h post-detachment biological replicate 1 R1 SRP413059 bp0 Total RNA was extracted from whole body Ornithodoros hermsi larvae. Ticks were grouped in three biological replicates (n 20 individual per replicate) and are composed of unfed larvae (Oh-UN) and larvae fed on neonate mice at 6h-post detachment (Oh-6h), 12h-post detachment (Oh-12h), 24h-post detachment (Oh-24h), 5-days-post detachment (Oh-5d). RNA extraction was performed with the PureLink RNA Mini Kit (Invitrogen) according to manufacturer`s specifications and analyzed with an Agilent High Sensitivity RNA ScreenTape System in an TapeStation 4150 (Agilent). The library was constructed using the NEBNextUltraTM II (Directional) RNA with polyA selection library prep kit and sequencing was performed in an Illumina Novaseq 6000 DNA sequencer. SRS16141441 Fed Ornithodoros hermsi larvae 6h post-detachment biological replicate 1 Fed Ornithodoros hermsi larvae 6h post-detachment biological replicate 1 R1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000 SRX18700342 Fed Ornithodoros hermsi larvae 6h post-detachment biological replicate 2 R1 SRP413059 bp0 Total RNA was extracted from whole body Ornithodoros hermsi larvae. Ticks were grouped in three biological replicates (n 20 individual per replicate) and are composed of unfed larvae (Oh-UN) and larvae fed on neonate mice at 6h-post detachment (Oh-6h), 12h-post detachment (Oh-12h), 24h-post detachment (Oh-24h), 5-days-post detachment (Oh-5d). RNA extraction was performed with the PureLink RNA Mini Kit (Invitrogen) according to manufacturer`s specifications and analyzed with an Agilent High Sensitivity RNA ScreenTape System in an TapeStation 4150 (Agilent). The library was constructed using the NEBNextUltraTM II (Directional) RNA with polyA selection library prep kit and sequencing was performed in an Illumina Novaseq 6000 DNA sequencer. SRS16141442 Fed Ornithodoros hermsi larvae 6h post-detachment biological replicate 2 Fed Ornithodoros hermsi larvae 6h post-detachment biological replicate 2 R1 RNA-Seq TRANSCRIPTOMIC cDNA Illumina NovaSeq 6000