SRX6801779 PH1_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346394 PH1 PH1_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801780 PH2_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346395 PH2 PH2_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801781 PH11_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346396 PH11 PH11_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801782 PH12_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346397 PH12 PH12_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801783 PH13_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346398 PH13 PH13_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801784 PH14_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346399 PH14 PH14_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801785 PH15_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346400 PH15 PH15_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801786 PH17_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346401 PH17 PH17_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801787 PH19_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346402 PH19 PH19_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801788 PH20_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346403 PH20 PH20_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801789 PH21_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346404 PH21 PH21_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801790 PH22_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346405 PH22 PH22_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801791 PH3_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346406 PH3 PH3_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801792 PH23_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346407 PH23 PH23_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801793 PH24_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346408 PH24 PH24_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801794 PH25_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346409 PH25 PH25_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801795 PH26_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346410 PH26 PH26_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801796 PH27_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346411 PH27 PH27_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801797 PH28_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346412 PH28 PH28_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801798 PH29_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346413 PH29 PH29_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801799 PH30_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346414 PH30 PH30_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801800 PH31_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346415 PH31 PH31_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801801 PH32_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346416 PH32 PH32_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801802 PH4_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346417 PH4 PH4_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801803 PH33_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346418 PH33 PH33_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801804 PH34_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346419 PH34 PH34_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801805 PH35_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346420 PH35 PH35_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801806 PH36_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346421 PH36 PH36_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801807 PH37_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346422 PH37 PH37_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801808 PH38_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346423 PH38 PH38_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801809 PH39_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346424 PH39 PH39_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801810 PH40_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346425 PH40 PH40_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801811 32M2_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346426 32M2 32M2_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801812 72M1_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346427 72M1 72M1_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801813 PH5_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346428 PH5 PH5_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801814 72M2_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346429 72M2 72M2_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801815 87M1_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346430 87M1 87M1_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801816 87M2_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346431 87M2 87M2_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801817 32F1_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346432 32F1 32F1_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801818 32F2_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346433 32F2 32F2_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801819 72F1_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346434 72F1 72F1_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801820 87F1_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346435 87F1 87F1_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801821 87F2_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346436 87F2 87F2_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801822 PH6_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346437 PH6 PH6_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801823 PH7_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346438 PH7 PH7_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801824 PH8_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346439 PH8 PH8_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801825 PH9_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346440 PH9 PH9_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq SRX6801826 PH10_Bt_psyllid SRP220365 bp0 Genomic DNA was extracted from whole individual psyllids using QiaAmp Mini DNA Extraction kit (Qiagen) including RNase treatment. Amplification of the 16S rRNA gene was performed using primers 341F (5' CCTACGGGNGGCWGCAG 3') and 805R (5' GACTACHVGGGTATCTAATCC 3'), which encompass the V3-V4 region and produce a fragment of approximately 464bp, including primers. Library preparation, inputting 7ng of DNA extract, was utilised the Nextera XT kit, and 2 x 300bp paired end fragments sequenced on a 384-multiplexed Illumina MiSeq run. SRS5346441 PH10 PH10_Bt_psyllid AMPLICON METAGENOMIC PCR Illumina MiSeq