Table S1. Primers and PCR conditions used in this paper Primers Sequence (5 3 ) Thermal conditions Reference Rhizobacteria 27F 1492R

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Table S1. Primers and PCR conditions used in this paper Primers Sequence (5 3 ) Thermal conditions Reference Rhizobacteria 27F 1492R AAC MGG ATT AGA TAC CCK G GGY TAC CTT GTT ACG ACT T Detection of Candidatus Liberibacter asiaticus Conventional PCR A2 TAT AAA GGT TGA CCT TTC GAG TTT J5 ACA AAA GCA GAA ATA GCA CGA ACA A qpcr CQULA04F CQULAP10P CQULA04R Taxon/Group specific qpcr Total bacteria Eub338 Eub518 Acidobacteria Acid31 Eub518 Actinobacteria Actino235 Eub518 Alphaproteobacteria Eub338 Alfa685 TGG AGG TGT AAA AGT TGC CAA A ATC GTC TCG TCA AGA TTG CTA TCC GTG ATA CTA G CCA ACG AAA AGA TCA GAT ATT CCT CTA ACT CCT ACG GGA GGC AGC AG ATT ACC GCG GCT GCT GG GAT CCT GGC TCA GAA TC ATT ACC GCG GCT GCT GG CGC GGC CTA TCA GCT TGT TG ATT ACC GCG GCT GCT GG ACT CCT ACG GGA GGC AGC AG TCT ACG RAT TTC ACC YC TAC 94 C, 5 min, 1 cycle 94 C for 1 min, 48-58 C (gradient = 48.0, 48.3, 48.9, 49.7, 113 50.8, 52.3, 54.0, 55.4, 56.5, 57.3, 57.8, 58.0 C) for 45 s, 72 C for 1 min, 30 cycles 72 C for 8 min, 1 cycle 94 C for 2 min, 1 cycle, 94 C for 10 s, 65 C for 10s, 72 C for 1 min, 35 cycles 72 C for 4 min, 1 cycle 50 C for 2 min, 1 cycle 95 C for 15 min, 1 cycle 94 C for 15 s and 60 C for 1 min, 45 cycles 95 C for 1 min, 53 C for 30 s, 72 C for 1 95 C for 1 min, 50 C for 30 s, 72 C for 1 95 C for 1 min, 60 C for 30 s, 72 C for 1 95 C for 1 min, 60 C for 30 s, 72 C for 1 Lane, 1990 Hocquellet et al, 1999 Wang et al., 2006

Bacteroidetes Cfb319 Eub518 Betaproteobacteria Eub338 Bet680 Firmicutes Lgc353 Eub518 Pseudomonas spp. PsF PsR Burkholderia spp. Burk3 BurkR GTA CTG AGA CAC GGA CCA ATT ACC GCG GCT GCT GG ACT CCT ACG GGA GGC AGC AG TCA CTG CTA CAC GYG GCA GTA GGG AAT CTT CCG ATT ACC GCG GCT GCT GG TTA GCT CCA CCT CGC GGC GGT CTG AGA GGA TGA TCA GT CTG CGA AAG CCG GAT TGC CAT ACT CTA GCY YGC 95 C for 1 min, 65 C for 30 s, 72 C for 1 95 C for 1 min, 60 C for 30 s, 72 C for 1 95 C for 1 min, 60 C for 30 s, 72 C for 1 95 C for 1 min, 64 C for 30 s, 72 C for 1 95 C for 1 min, 64 C for 30 s, 72 C for 1 Drigo et Drigo et Bacillus spp. BacF 1378 qpcr of genes involved in nitrogen cycling narg narg1960m2f narg2050m2r nirk nirk876 nirk1040 GGG AAA CCG GGG CTA ATA CCG GAT CGG TGT GTA CAA GGC CCG GGA ACG TAY GTS GGG CAG GAR AAA CTG CGT AGA AGA AGC TGG TGC TGT T ATY GGC GGV CAY GGC GA GCC TCG ATC AGR TTR TGG TT 95 C for 1 min, 63 C for 30 s, 72 C for 1 95 C for 15 s, 65 to 60 C for 30 s (-1 C by cycle), 72 C for 30 s, 80 C for 15 s, 6 cycles 95 C for 15 s, 60 C for 30 s, 72 C for 30 s, 80 C for 15 s, 40 cycles 95 C for 15 s, 60 to 95 C, 1 cycle 95 C for 15 s, 63 to 58 C for 30 s (-1 C by cycle), 72 C for 30 s, 80 C for 15 s, 6 cycles Drigo et

nirs nirscd3afm nirsr3cdm nosz nosz2f nosz2r amoa(aob) amoa-1f amoa-2r amoa(aoa) 19F CrenamoA616r48x AAC GYS AAG GAR ACS GG GAS TTC GGR TGS GTC TTS AYG AA CGC RAC GGC AAS AAG GTS MSS GT CAK RTG CAK SGC RTG GCA GAA GGG GTT TCT ACT GGT GGT CCC CTC KGS AAA GCC TTC TTC ATG GTC TGG CTW AGA CG GCC ATC CAB CKR TAN GTC CA 95 C for 15 s, 60 C for 30 s, 72 C for 30 s, 80 C for 15 s, 40 cycles 95 C for 15 s, 60 to 95 C, 1 cycle 95 C for 15 s, 65 to 60 C for 30 s (-1 C by cycle), 72 C for 30 s, 80 C for 15 s, 6 cycles 95 C for 15 s, 60 C for 30 s, 72 C for 30 s, 80 C for 15 s, 40 cycles 95 C for 15 s, 60 to 95 C, 1 cycle 95 C for 15 s, 65 to 60 C for 30 s (-1 C by cycle), 72 C for 30 s, 80 C for 15 s, 6 cycles 95 C for 15 s, 60 C for 30 s, 72 C for 30 s, 80 C for 15 s, 40 cycles 95 C for 15 s, 60 to 95 C, 1 cycle 95 C, 10 min, 1 cycle 94 C for 45 s, 58 C for 45 s, 72 C for 45 s, 39 cycles 95 C for 15 s, 60 C for 30 s, to 95 C for 15 s, 1 cycle 95 C, 10 min, 1 cycle 94 C for 45 s, 55 C for 45 s, 72 C for 45 s, 39 cycles 95 C for 15 s, 60 C for 30 s, to 95 C for 15 s, 1 cycle

References: Drigo B, van Veen JA, Kowalchuk GA. (2009). Specific rhizosphere bacterial and fungal groups respond to elevated atmospheric CO 2. ISME J 3: 1204 1217. Fierer N, Jackson JA, Vilgalys R, Jackson RB. (2005). The assessment of soil microbial community structure by use of taxon-specific quantitative PCR assays. Appl Environ Microbiol 71: 4117-4120. Hallin S, Jones CJ, Schloter M, Philippot L. (2009). Relationship between N-cycling communities and ecosystem functioning in a 50-year-old fertilization experiment. ISME J. 3: 597 605 Hocquellet A, Bové JM, Garnier M. (1999). Isolation of DNA from the uncultured "Candidatus Liberobacter" species associated with citrus huanglongbing by RAPD. Curr Microbiol 38: 176-182. Lane DJ. (1990). 16S/23S rrna sequencing In: Stackebrandt E, Goodfellow M (eds.) Nucleic acid techniques in bacterial systematics. John Wiley & Sons-New York, 115-147pp. Wang Z, Yin Y, Hu H, Yuan Q, Peng G, Xia Y. (2006). Development and application of molecular-based diagnosis for Candidatus Liberibacter asiaticus,the causal pathogen of citrus huanglongbing. Plant Pathol 55: 630 638.

Figure S1. Rarefaction curves of 16S rrna gene clone libraries from the rhizosphere of healthy citrus (HT1, HT2, and HT3); Ca. Liberibacter asiaticus infected citrus (IT1, IT2, and IT3); and bulk soil samples. Figure S2. Relative abundances of the different bacterial phyla/genus in the rhizosphere of healthy (HT1, HT2, HT3); Ca. Liberibacter asiaticus infected citrus (IT1, IT2, and IT3); and bulk soil samples, as estimated using the qpcr assays. Error bars represent the standard errors of the means for three replicates. Statistical significance is represented by letters above each bar, with different letters signifying differences at P 0.01 for each bacterial phyla/genus. Figure S3. Hierarchical cluster analysis of (A) ribulose-l, 5-bisphosphate carboxylase oxygenase (Rubisco); (B) carbon monoxide dehydrogenase (CODH); and (C) propionyl-coa acetyl-coa carboxylase (PCC ACC) genes in rhizosphere of Ca. L. asiaticus infected (IT1- IT3) or healthy (HT1-HT3) citrus. Genes that were present in at least three samples were used for cluster analysis. Results were generated in CLUSTER and visualized using TREEVIEW. Red indicates signal intensities above background while black indicates signal intensities below background. Brighter red colouring indicates higher signal intensities.