SRX1771617 IL-17RAfl/fl K13 Cre- Sham replicate 1 SRP075350 PRJNA322012 Total RNA from tngue was used as starting material for deep sequencing using the Illumina TrueSeq RNA Sample Preparation v2 library preparation kit. Cluster generation and 75 bp single-end dual-indexed sequencing was performed on Illumina NextSeq 500. Total RNA libraries were generated using Illumina TruSeq Stranded mRNA sample preparation kit. The first step in the workflow involves purifying the poly-A containing mRNA molecules using poly-T oligo attached magneticb eads.Following purification, the mRNA is fragmented into small pieces using divalent cations. The cleaved RNA fragments are copied into first strand cDNA using reverse transcriptase and random primers. Strands pecificity is achieved by using dUTP in the Second Strand Marking Mix, followed by second strand cDNA synthesis using DNA Polymerase I and RNase H. These cDNA fragments then have the addition of a single 'A' base and subsequent ligation of the adapter. The products are then purified and enriched with PCR to create the final cDNA library. The cDNA libraries are validated using KAPA Biosystems primer premix kit with Illumina-compatible DNA primers and Qubit 2.0 fluorometer. Quality is examined using Agilent Tapestation 2200.The cDNA libraries were pooled at a final concentration 1.8pM. Cluster generation and 75 bp single-read dual-indexed sequencing was performed on Illumina NextSeq 500’s. SRS1443714 SAMN05007379 IL-17RAfl/fl K13 Cre- Sham replicate 1 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX1771618 IL-17RAfl/fl K13 Cre- Sham replicate 2 SRP075350 PRJNA322012 Total RNA from tngue was used as starting material for deep sequencing using the Illumina TrueSeq RNA Sample Preparation v2 library preparation kit. Cluster generation and 75 bp single-end dual-indexed sequencing was performed on Illumina NextSeq 500. Total RNA libraries were generated using Illumina TruSeq Stranded mRNA sample preparation kit. The first step in the workflow involves purifying the poly-A containing mRNA molecules using poly-T oligo attached magneticb eads.Following purification, the mRNA is fragmented into small pieces using divalent cations. The cleaved RNA fragments are copied into first strand cDNA using reverse transcriptase and random primers. Strands pecificity is achieved by using dUTP in the Second Strand Marking Mix, followed by second strand cDNA synthesis using DNA Polymerase I and RNase H. These cDNA fragments then have the addition of a single 'A' base and subsequent ligation of the adapter. The products are then purified and enriched with PCR to create the final cDNA library. The cDNA libraries are validated using KAPA Biosystems primer premix kit with Illumina-compatible DNA primers and Qubit 2.0 fluorometer. Quality is examined using Agilent Tapestation 2200.The cDNA libraries were pooled at a final concentration 1.8pM. Cluster generation and 75 bp single-read dual-indexed sequencing was performed on Illumina NextSeq 500’s. SRS1443714 SAMN05007379 IL-17RAfl/fl K13 Cre- Sham replicate 2 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX1771619 IL-17RAfl/fl K13 Cre- Candida replicate 2 SRP075350 PRJNA322012 Total RNA from tngue was used as starting material for deep sequencing using the Illumina TrueSeq RNA Sample Preparation v2 library preparation kit. Cluster generation and 75 bp single-end dual-indexed sequencing was performed on Illumina NextSeq 500. Total RNA libraries were generated using Illumina TruSeq Stranded mRNA sample preparation kit. The first step in the workflow involves purifying the poly-A containing mRNA molecules using poly-T oligo attached magneticb eads.Following purification, the mRNA is fragmented into small pieces using divalent cations. The cleaved RNA fragments are copied into first strand cDNA using reverse transcriptase and random primers. Strands pecificity is achieved by using dUTP in the Second Strand Marking Mix, followed by second strand cDNA synthesis using DNA Polymerase I and RNase H. These cDNA fragments then have the addition of a single 'A' base and subsequent ligation of the adapter. The products are then purified and enriched with PCR to create the final cDNA library. The cDNA libraries are validated using KAPA Biosystems primer premix kit with Illumina-compatible DNA primers and Qubit 2.0 fluorometer. Quality is examined using Agilent Tapestation 2200.The cDNA libraries were pooled at a final concentration 1.8pM. Cluster generation and 75 bp single-read dual-indexed sequencing was performed on Illumina NextSeq 500’s. SRS1443715 SAMN05007382 IL-17RAfl/fl K13 Cre- Candida replicate 2 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX1771621 IL-17RAfl/fl K13 Cre- Candida replicate 3 SRP075350 PRJNA322012 Total RNA from tngue was used as starting material for deep sequencing using the Illumina TrueSeq RNA Sample Preparation v2 library preparation kit. Cluster generation and 75 bp single-end dual-indexed sequencing was performed on Illumina NextSeq 500. Total RNA libraries were generated using Illumina TruSeq Stranded mRNA sample preparation kit. The first step in the workflow involves purifying the poly-A containing mRNA molecules using poly-T oligo attached magneticb eads.Following purification, the mRNA is fragmented into small pieces using divalent cations. The cleaved RNA fragments are copied into first strand cDNA using reverse transcriptase and random primers. Strands pecificity is achieved by using dUTP in the Second Strand Marking Mix, followed by second strand cDNA synthesis using DNA Polymerase I and RNase H. These cDNA fragments then have the addition of a single 'A' base and subsequent ligation of the adapter. The products are then purified and enriched with PCR to create the final cDNA library. The cDNA libraries are validated using KAPA Biosystems primer premix kit with Illumina-compatible DNA primers and Qubit 2.0 fluorometer. Quality is examined using Agilent Tapestation 2200.The cDNA libraries were pooled at a final concentration 1.8pM. Cluster generation and 75 bp single-read dual-indexed sequencing was performed on Illumina NextSeq 500’s. SRS1443715 SAMN05007382 IL-17RAfl/fl K13 Cre- Candida replicate 3 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX1771622 IL-17RAfl/fl K13 Cre+ Candida replicate 1 SRP075350 PRJNA322012 Total RNA from tngue was used as starting material for deep sequencing using the Illumina TrueSeq RNA Sample Preparation v2 library preparation kit. Cluster generation and 75 bp single-end dual-indexed sequencing was performed on Illumina NextSeq 500. Total RNA libraries were generated using Illumina TruSeq Stranded mRNA sample preparation kit. The first step in the workflow involves purifying the poly-A containing mRNA molecules using poly-T oligo attached magneticb eads.Following purification, the mRNA is fragmented into small pieces using divalent cations. The cleaved RNA fragments are copied into first strand cDNA using reverse transcriptase and random primers. Strands pecificity is achieved by using dUTP in the Second Strand Marking Mix, followed by second strand cDNA synthesis using DNA Polymerase I and RNase H. These cDNA fragments then have the addition of a single 'A' base and subsequent ligation of the adapter. The products are then purified and enriched with PCR to create the final cDNA library. The cDNA libraries are validated using KAPA Biosystems primer premix kit with Illumina-compatible DNA primers and Qubit 2.0 fluorometer. Quality is examined using Agilent Tapestation 2200.The cDNA libraries were pooled at a final concentration 1.8pM. Cluster generation and 75 bp single-read dual-indexed sequencing was performed on Illumina NextSeq 500’s. SRS1443716 SAMN05007383 IL-17RAfl/fl K13 Cre+ Candida replicate 1 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX1771623 IL-17RAfl/fl K13 Cre+ Candida replicate 2 SRP075350 PRJNA322012 Total RNA from tngue was used as starting material for deep sequencing using the Illumina TrueSeq RNA Sample Preparation v2 library preparation kit. Cluster generation and 75 bp single-end dual-indexed sequencing was performed on Illumina NextSeq 500. Total RNA libraries were generated using Illumina TruSeq Stranded mRNA sample preparation kit. The first step in the workflow involves purifying the poly-A containing mRNA molecules using poly-T oligo attached magneticb eads.Following purification, the mRNA is fragmented into small pieces using divalent cations. The cleaved RNA fragments are copied into first strand cDNA using reverse transcriptase and random primers. Strands pecificity is achieved by using dUTP in the Second Strand Marking Mix, followed by second strand cDNA synthesis using DNA Polymerase I and RNase H. These cDNA fragments then have the addition of a single 'A' base and subsequent ligation of the adapter. The products are then purified and enriched with PCR to create the final cDNA library. The cDNA libraries are validated using KAPA Biosystems primer premix kit with Illumina-compatible DNA primers and Qubit 2.0 fluorometer. Quality is examined using Agilent Tapestation 2200.The cDNA libraries were pooled at a final concentration 1.8pM. Cluster generation and 75 bp single-read dual-indexed sequencing was performed on Illumina NextSeq 500’s. SRS1443716 SAMN05007383 IL-17RAfl/fl K13 Cre+ Candida replicate 2 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX1771624 IL-17RAfl/fl K13 Cre+ Candida replicate 3 SRP075350 PRJNA322012 Total RNA from tngue was used as starting material for deep sequencing using the Illumina TrueSeq RNA Sample Preparation v2 library preparation kit. Cluster generation and 75 bp single-end dual-indexed sequencing was performed on Illumina NextSeq 500. Total RNA libraries were generated using Illumina TruSeq Stranded mRNA sample preparation kit. The first step in the workflow involves purifying the poly-A containing mRNA molecules using poly-T oligo attached magneticb eads.Following purification, the mRNA is fragmented into small pieces using divalent cations. The cleaved RNA fragments are copied into first strand cDNA using reverse transcriptase and random primers. Strands pecificity is achieved by using dUTP in the Second Strand Marking Mix, followed by second strand cDNA synthesis using DNA Polymerase I and RNase H. These cDNA fragments then have the addition of a single 'A' base and subsequent ligation of the adapter. The products are then purified and enriched with PCR to create the final cDNA library. The cDNA libraries are validated using KAPA Biosystems primer premix kit with Illumina-compatible DNA primers and Qubit 2.0 fluorometer. Quality is examined using Agilent Tapestation 2200.The cDNA libraries were pooled at a final concentration 1.8pM. Cluster generation and 75 bp single-read dual-indexed sequencing was performed on Illumina NextSeq 500’s. SRS1443716 SAMN05007383 IL-17RAfl/fl K13 Cre+ Candida replicate 3 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX1771625 IL-17RAfl/fl K13 Cre- Sham replicate 3 SRP075350 PRJNA322012 Total RNA from tngue was used as starting material for deep sequencing using the Illumina TrueSeq RNA Sample Preparation v2 library preparation kit. Cluster generation and 75 bp single-end dual-indexed sequencing was performed on Illumina NextSeq 500. Total RNA libraries were generated using Illumina TruSeq Stranded mRNA sample preparation kit. The first step in the workflow involves purifying the poly-A containing mRNA molecules using poly-T oligo attached magneticb eads.Following purification, the mRNA is fragmented into small pieces using divalent cations. The cleaved RNA fragments are copied into first strand cDNA using reverse transcriptase and random primers. Strands pecificity is achieved by using dUTP in the Second Strand Marking Mix, followed by second strand cDNA synthesis using DNA Polymerase I and RNase H. These cDNA fragments then have the addition of a single 'A' base and subsequent ligation of the adapter. The products are then purified and enriched with PCR to create the final cDNA library. The cDNA libraries are validated using KAPA Biosystems primer premix kit with Illumina-compatible DNA primers and Qubit 2.0 fluorometer. Quality is examined using Agilent Tapestation 2200.The cDNA libraries were pooled at a final concentration 1.8pM. Cluster generation and 75 bp single-read dual-indexed sequencing was performed on Illumina NextSeq 500’s. SRS1443714 SAMN05007379 IL-17RAfl/fl K13 Cre- Sham replicate 3 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX1771626 IL-17RAfl/fl K13 Cre+ Sham replicate 1 SRP075350 PRJNA322012 Total RNA from tngue was used as starting material for deep sequencing using the Illumina TrueSeq RNA Sample Preparation v2 library preparation kit. Cluster generation and 75 bp single-end dual-indexed sequencing was performed on Illumina NextSeq 500. Total RNA libraries were generated using Illumina TruSeq Stranded mRNA sample preparation kit. The first step in the workflow involves purifying the poly-A containing mRNA molecules using poly-T oligo attached magneticb eads.Following purification, the mRNA is fragmented into small pieces using divalent cations. The cleaved RNA fragments are copied into first strand cDNA using reverse transcriptase and random primers. Strands pecificity is achieved by using dUTP in the Second Strand Marking Mix, followed by second strand cDNA synthesis using DNA Polymerase I and RNase H. These cDNA fragments then have the addition of a single 'A' base and subsequent ligation of the adapter. The products are then purified and enriched with PCR to create the final cDNA library. The cDNA libraries are validated using KAPA Biosystems primer premix kit with Illumina-compatible DNA primers and Qubit 2.0 fluorometer. Quality is examined using Agilent Tapestation 2200.The cDNA libraries were pooled at a final concentration 1.8pM. Cluster generation and 75 bp single-read dual-indexed sequencing was performed on Illumina NextSeq 500’s. SRS1443718 SAMN05007380 IL-17RAfl/fl K13 Cre+ Sham replicate 1 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX1771627 IL-17RAfl/fl K13 Cre+ Sham replicate 2 SRP075350 PRJNA322012 Total RNA from tngue was used as starting material for deep sequencing using the Illumina TrueSeq RNA Sample Preparation v2 library preparation kit. Cluster generation and 75 bp single-end dual-indexed sequencing was performed on Illumina NextSeq 500. Total RNA libraries were generated using Illumina TruSeq Stranded mRNA sample preparation kit. The first step in the workflow involves purifying the poly-A containing mRNA molecules using poly-T oligo attached magneticb eads.Following purification, the mRNA is fragmented into small pieces using divalent cations. The cleaved RNA fragments are copied into first strand cDNA using reverse transcriptase and random primers. Strands pecificity is achieved by using dUTP in the Second Strand Marking Mix, followed by second strand cDNA synthesis using DNA Polymerase I and RNase H. These cDNA fragments then have the addition of a single 'A' base and subsequent ligation of the adapter. The products are then purified and enriched with PCR to create the final cDNA library. The cDNA libraries are validated using KAPA Biosystems primer premix kit with Illumina-compatible DNA primers and Qubit 2.0 fluorometer. Quality is examined using Agilent Tapestation 2200.The cDNA libraries were pooled at a final concentration 1.8pM. Cluster generation and 75 bp single-read dual-indexed sequencing was performed on Illumina NextSeq 500’s. SRS1443718 SAMN05007380 IL-17RAfl/fl K13 Cre+ Sham replicate 2 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX1771628 IL-17RAfl/fl K13 Cre+ Sham replicate 3 SRP075350 PRJNA322012 Total RNA from tngue was used as starting material for deep sequencing using the Illumina TrueSeq RNA Sample Preparation v2 library preparation kit. Cluster generation and 75 bp single-end dual-indexed sequencing was performed on Illumina NextSeq 500. Total RNA libraries were generated using Illumina TruSeq Stranded mRNA sample preparation kit. The first step in the workflow involves purifying the poly-A containing mRNA molecules using poly-T oligo attached magneticb eads.Following purification, the mRNA is fragmented into small pieces using divalent cations. The cleaved RNA fragments are copied into first strand cDNA using reverse transcriptase and random primers. Strands pecificity is achieved by using dUTP in the Second Strand Marking Mix, followed by second strand cDNA synthesis using DNA Polymerase I and RNase H. These cDNA fragments then have the addition of a single 'A' base and subsequent ligation of the adapter. The products are then purified and enriched with PCR to create the final cDNA library. The cDNA libraries are validated using KAPA Biosystems primer premix kit with Illumina-compatible DNA primers and Qubit 2.0 fluorometer. Quality is examined using Agilent Tapestation 2200.The cDNA libraries were pooled at a final concentration 1.8pM. Cluster generation and 75 bp single-read dual-indexed sequencing was performed on Illumina NextSeq 500’s. SRS1443718 SAMN05007380 IL-17RAfl/fl K13 Cre+ Sham replicate 3 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX1771629 IL-17RA-/- Candida replicate 1 SRP075350 PRJNA322012 Total RNA from tngue was used as starting material for deep sequencing using the Illumina TrueSeq RNA Sample Preparation v2 library preparation kit. Cluster generation and 75 bp single-end dual-indexed sequencing was performed on Illumina NextSeq 500. Total RNA libraries were generated using Illumina TruSeq Stranded mRNA sample preparation kit. The first step in the workflow involves purifying the poly-A containing mRNA molecules using poly-T oligo attached magneticb eads.Following purification, the mRNA is fragmented into small pieces using divalent cations. The cleaved RNA fragments are copied into first strand cDNA using reverse transcriptase and random primers. Strands pecificity is achieved by using dUTP in the Second Strand Marking Mix, followed by second strand cDNA synthesis using DNA Polymerase I and RNase H. These cDNA fragments then have the addition of a single 'A' base and subsequent ligation of the adapter. The products are then purified and enriched with PCR to create the final cDNA library. The cDNA libraries are validated using KAPA Biosystems primer premix kit with Illumina-compatible DNA primers and Qubit 2.0 fluorometer. Quality is examined using Agilent Tapestation 2200.The cDNA libraries were pooled at a final concentration 1.8pM. Cluster generation and 75 bp single-read dual-indexed sequencing was performed on Illumina NextSeq 500’s. SRS1443719 SAMN05007381 IL-17RA-/- Candida replicate 1 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX1771630 IL-17RA-/- Candida replicate 2 SRP075350 PRJNA322012 Total RNA from tngue was used as starting material for deep sequencing using the Illumina TrueSeq RNA Sample Preparation v2 library preparation kit. Cluster generation and 75 bp single-end dual-indexed sequencing was performed on Illumina NextSeq 500. Total RNA libraries were generated using Illumina TruSeq Stranded mRNA sample preparation kit. The first step in the workflow involves purifying the poly-A containing mRNA molecules using poly-T oligo attached magneticb eads.Following purification, the mRNA is fragmented into small pieces using divalent cations. The cleaved RNA fragments are copied into first strand cDNA using reverse transcriptase and random primers. Strands pecificity is achieved by using dUTP in the Second Strand Marking Mix, followed by second strand cDNA synthesis using DNA Polymerase I and RNase H. These cDNA fragments then have the addition of a single 'A' base and subsequent ligation of the adapter. The products are then purified and enriched with PCR to create the final cDNA library. The cDNA libraries are validated using KAPA Biosystems primer premix kit with Illumina-compatible DNA primers and Qubit 2.0 fluorometer. Quality is examined using Agilent Tapestation 2200.The cDNA libraries were pooled at a final concentration 1.8pM. Cluster generation and 75 bp single-read dual-indexed sequencing was performed on Illumina NextSeq 500’s. SRS1443719 SAMN05007381 IL-17RA-/- Candida replicate 2 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX1771631 IL-17RA-/- Candida replicate 3 SRP075350 PRJNA322012 Total RNA from tngue was used as starting material for deep sequencing using the Illumina TrueSeq RNA Sample Preparation v2 library preparation kit. Cluster generation and 75 bp single-end dual-indexed sequencing was performed on Illumina NextSeq 500. Total RNA libraries were generated using Illumina TruSeq Stranded mRNA sample preparation kit. The first step in the workflow involves purifying the poly-A containing mRNA molecules using poly-T oligo attached magneticb eads.Following purification, the mRNA is fragmented into small pieces using divalent cations. The cleaved RNA fragments are copied into first strand cDNA using reverse transcriptase and random primers. Strands pecificity is achieved by using dUTP in the Second Strand Marking Mix, followed by second strand cDNA synthesis using DNA Polymerase I and RNase H. These cDNA fragments then have the addition of a single 'A' base and subsequent ligation of the adapter. The products are then purified and enriched with PCR to create the final cDNA library. The cDNA libraries are validated using KAPA Biosystems primer premix kit with Illumina-compatible DNA primers and Qubit 2.0 fluorometer. Quality is examined using Agilent Tapestation 2200.The cDNA libraries were pooled at a final concentration 1.8pM. Cluster generation and 75 bp single-read dual-indexed sequencing was performed on Illumina NextSeq 500’s. SRS1443719 SAMN05007381 IL-17RA-/- Candida replicate 3 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX1771632 IL-17RAfl/fl K13 Cre- Candida replicate 1 SRP075350 PRJNA322012 Total RNA from tngue was used as starting material for deep sequencing using the Illumina TrueSeq RNA Sample Preparation v2 library preparation kit. Cluster generation and 75 bp single-end dual-indexed sequencing was performed on Illumina NextSeq 500. Total RNA libraries were generated using Illumina TruSeq Stranded mRNA sample preparation kit. The first step in the workflow involves purifying the poly-A containing mRNA molecules using poly-T oligo attached magneticb eads.Following purification, the mRNA is fragmented into small pieces using divalent cations. The cleaved RNA fragments are copied into first strand cDNA using reverse transcriptase and random primers. Strands pecificity is achieved by using dUTP in the Second Strand Marking Mix, followed by second strand cDNA synthesis using DNA Polymerase I and RNase H. These cDNA fragments then have the addition of a single 'A' base and subsequent ligation of the adapter. The products are then purified and enriched with PCR to create the final cDNA library. The cDNA libraries are validated using KAPA Biosystems primer premix kit with Illumina-compatible DNA primers and Qubit 2.0 fluorometer. Quality is examined using Agilent Tapestation 2200.The cDNA libraries were pooled at a final concentration 1.8pM. Cluster generation and 75 bp single-read dual-indexed sequencing was performed on Illumina NextSeq 500’s. SRS1443715 SAMN05007382 IL-17RAfl/fl K13 Cre- Candida replicate 1 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500