Transcription activator-like (TAL) effectors from Xanthomonas citri subsp. malvacearum (Xcm) are essential for bacterial blight of cotton (BBC). Here, by combining transcriptome profiling with TAL effector-binding element (EBE) prediction, we show that GhSWEET10, encoding a functional sucrose transporter, is induced by Avrb6, a TAL effector determining Xcm pathogenicity. Activation of GhSWEET10 by designer TAL effectors (dTALEs) restores virulence of Xcm avrb6 deletion strains, whereas silencing of GhSWEET10 compromises cotton susceptibility to infections. A BBC-resistant line carrying an unknown recessive b6 gene bears the same EBE as the susceptible line, but Avrb6-mediated induction of GhSWEET10 is reduced, suggesting a unique mechanism underlying b6-mediated resistance. We show via an extensive survey of GhSWEET transcriptional responsiveness to different Xcm field isolates that additional GhSWEETs may also be involved in BBC. These findings advance our understanding of the disease and resistance in cotton and may facilitate the development cotton with improved resistance to BBC.
Cotton (Gossypium spp.) is an economically important crop and provides a significant source of fibre, feed, foodstuff, oil and biofuel products worldwide. The cotton genus is composed of at least 45 diploid and 5 tetraploid species1. The tetraploid (AD genome) species, including G. hirsutum that produces 95% of the world’s cotton fibre, is likely derived from a hybridization between an A-genome-like ancestral species resembling G. arboreum and a D-genome-like ancestral species resembling G. raimondii2. The availability of the draft genome sequences for G. raimondii, G. arboreum, G. hirsutum and G. barbadense not only provides genetic resources to study the complex genome evolution and polyploidization process, but also lays the foundation for functional genomic approaches to dissect cotton gene functions with a goal to improve its agricultural performance in the face of biotic and abiotic stresses3,4,5,6,7,8.
Bacterial blight of cotton (BBC), caused by Xanthomonas citri subsp. malvacearum (Xcm), is among the destructive diseases of cotton9. Following epidemics in the 1970s, the disease has occurred sporadically in the United States, but in the past several years re-emerged as a significant yield constraint. There are pressing needs to address the underlying mechanisms of susceptibility and resistance to BBC in cotton. Xcm injects effector proteins into plant cells via the type III secretion system to promote pathogenicity in plants. In the presence of corresponding resistance (R) proteins, some of these effectors trigger resistance and function as avirulence proteins. Interestingly, all known pathogenicity and avirulence factors (encoded by so called ‘pth’ and ‘avr’ genes) of Xcm are transcription activator-like (TAL) effectors10. TAL effectors functionally resemble eukaryotic transcription factors and upregulate host genes by directly binding to their promoters11,12. TAL effectors are highly conserved among different Xanthomonas spp., with an N-terminal type III translocation signal, a central repeat region (CRR) and C-terminal nuclear localization signals followed by an acidic activation domain. The proteins differ mainly in the CRR, which consists of 1.5–33.5 copies of near-perfect repeats of 33–34 amino acids. These repeats are conserved with the exception of the 12th and 13th residues of each copy, defined as the repeat variable di-residue (RVD)13,14. Each RVD targets a specific nucleotide of the promoters of host genes, creating a code, such that the sequence of RVDs defines the effector-binding element (EBE); each EBE starts, however, with a nearly invariant thymine, which is specified in a yet unclear manner by structures immediately N terminus of the CRR13,14,15,16.
Among the identified TAL effector targets include a group of pepper genes upregulated by AvrBs3 from X. campestris pv. vesicatoria (Xcv)17,18. These include the R gene Bs3 and UPA20, which encodes a basic helix-loop-helix transcription factor regulating plant cell hypertrophy19. Os8N3/Xa13/OsSWEET11, essential for reproductive development, is a rice susceptibility (S) gene targeted by TAL effector PthXo1 from X. oryzae pv. oryzae (Xoo)20. The xa13 allele, which is unable to be induced by PthXo1, acts as a recessive r gene against Xoo infection21,22. Notably, four Os8N3/Xa13/OsSWEET11 homologues, rice Os11N3/OsSWEET14 and Xa25/OsSWEET13, pepper UPA16 and cassava MeSWEET10a are also targeted by TAL effectors from Xoo, Xcv and X. axonopodis pv. manihotis (Xam), respectively23,24,25. It was hypothesized that Xanthomonas spp. induces the expression of SWEET genes during infection to transport sucrose to the apoplast, thereby providing the bacteria with a carbon source20,23,25,26,27,28,29,30. TAL effectors from X. citri sp. citri (Xcc), the causal agent for citrus bacterial canker, induce the expression of CsSWEET1 in citrus, but the CsSWEET1 does not contribute demonstrably to susceptibility; another TAL effector target, however, CsLOB1, does function as an S gene, promoting the characteristic pustule formation and bacterial multiplication31. Other characterized TAL effector targets include the rice bacterial blight R genes Xa27 (ref. 32), Xa23 (ref. 33) and Xa10 (ref. 34), the bacterial leaf streak of rice S gene OsSULTR3;6 (ref. 35) and the pepper bacterial spot R gene Bs4C (ref. 36).
Previous work identified at least 10 TAL effectors from the cotton pathogen XcmH1005 and showed that a mutant with a deletion of seven tal genes was no longer able to cause observable water-soaking symptoms on Acala44 (Ac44), a BBC susceptible line of cotton. Avrb6 from XcmH1005 was among the first examples of an individual TAL effector important for Xcm virulence. An avrb6 mutant of XcmH1005, XcmH1407 (XcmH1005Δavrb6), showed reduced water-soaking, whereas when expressed in a relatively weak virulent strain XcmN1003, Avrb6 enhances water-soaking37. Although it does not affect in planta bacterial multiplication, Avrb6 plays a major role in release of bacteria from the leaf interior to the leaf surface during infections37.
To identify the TAL effectors responsible for virulence and their targets, we sequenced the whole genomes of Xcm strains XcmH1005 and XcmN1003 and assembled the full repertoire of TAL effectors. Further, we deployed genome-wide gene expression profiling in cotton coupled with TAL effector DNA-binding code-assisted EBE prediction and identified the clade III sucrose transporter gene GhSWEET10 as a target of Avrb6. We determined that GhSWEET10 is a major S gene for BBC by using dTALEs to induce it independently of any other possible Avrb6 targets and by silencing it with Agrobacterium-mediated virus-induced gene silencing (VIGS). Significantly, other members of the clade III GhSWEET genes are strongly induced by different Xcm field strains responsible for recent re-emergence of the disease in the southern United States. Our data indicate that cotton GhSWEET10 and likely other SWEET sugar transporters in the same clade play a major role in BBC and suggest that newly evolved or horizontally transferred TAL effectors targeting these genes attribute to the re-emergence of BBC in the field. In addition, a BBC-resistant cotton line carrying b6, a genetically complex resistance gene that has not yet been molecularly identified, showed markedly reduced Avrb6-mediated induction of GhSWEET10, ostensibly due to promoter polymorphisms outside the EBE. This suggests a novel mechanism for resistance that may represent a genetic determinant of b6.
Genome and TAL effector sequences of XcmH1005 and N1003
The strains XcmH1005, a rifamycin-resistant derivative of XcmH, and XcmN1003, a spectinomycin- and rifamycin-resistant derivative of XcmN, are two Xcm strains that cause water-soaking on Ac44 cotton38. To set the stage for identifying the role that TAL effectors in these strains play in BBC, we generated complete genome sequences using single molecule real-time sequencing (Pacific Biosciences; hereafter ‘PacBio sequencing’). The H1005 genome consists of a circular chromosome of 5,212,564 bp and a plasmid, pXcmH39 of 88,283 bp. The N1003 genome consists of a circular chromosome of 5,218,607 bp and a plasmid, herein designated as pXcmN, of 59,644 bp. The general features of each genome are presented in Table 1. The overall architectures of the two chromosomes are highly similar, with a single, large inversion (Fig. 1a). The plasmids are dissimilar, with only a few, relatively small regions of homology (Fig. 1a). The tal genes of the two strains are largely distinct (Fig. 1b and Supplementary Table 2). H1005 encodes 12 TAL effectors with six in the chromosome and six in pXcmH. Ten of these are Avr proteins named previously based on reactions of differential cotton lines to transformants of an otherwise-compatible Xcm strain carrying corresponding cosmid subclones: AvrB4, AvrB5, Avrb6, Avrb7, AvrB101, AvrB102, AvrB103, AvrB104, AvrBIn and AvrBn38,39,40. Another is PthN2, originally characterized in XcmN1003 (ref. 10). The twelfth is uncharacterized, and we designated it as Tal6XcmH1005, following a previously described naming scheme41. XcmN1003 harbours nine tal genes, five on the chromosome and four on pXcmN. Four on the chromosome and one on the plasmid however are disrupted by a frameshift mutation or a large insertion in the repeat region or the 3′ end of the gene. One of the disrupted genes, tal1’, on the chromosome, carries only a last repeat and is otherwise complete until an integrase insertion further downstream. Another of the disrupted genes, pthN’ on pXcmN, is otherwise identical to pthN, an XcmN1003 tal gene shown previously to contribute to water-soaking without triggering resistance on commercial US cotton varieties10. The intact pthN gene is also located on pXcmN, along with pthN2, which also contributes to water-soaking, but less strongly10. Another intact tal gene, tal7XcmN1003, also resides on the plasmid. The fourth intact gene is avrBn located on the chromosome. Apart from pthN’, pthN, pthN2 and avrBn, no other XcmN1003 tal genes show obvious similarity in their RVD sequences to any other tal genes in either strain. The divergence in tal gene content between the two strains, both with respect to RVD composition and genomic location of orthologs, is striking, which is in line with the fact that they were isolated from geographically distant regions38.
Candidate targets of Avrb6
Avrb6 is a TAL effector in XcmH1005 that causes strong water-soaking in the cotton line Ac44 (ref. 37). In this study, we used the Ac44E-tetraploid genotype, which is a single plant selection from Brinkerhoff’s original Ac44 parent42. Ac44E has similar morphology to Ac44 except it has more abundant flowers and is slightly more susceptible to BBC than Ac44 (ref. 42). To identify the cotton genes that are specifically activated by Avrb6, we used an integrative approach involving a whole-genome RNA-sequencing (RNA-Seq) analysis of protoplasts of Ac44E expressing Avrb6 and computational prediction of Avrb6 EBEs in cotton (Fig. 2a). Compared to the whole plant-pathogen infection assay, the homogenous protoplast mesophyll cell system expressing the individual bacterial effector circumvents the complication of multiple pathogen effectors and elicitors that could spontaneously activate or suppress a large number of host genes. We cloned the full-length coding sequence of Avrb6 from XcmH1005 into a plant expression vector with an HA-epitope tag at the C terminus under the control of the 35S CaMV promoter. The sequence was confirmed via Sanger sequencing (Supplementary Fig. 1). An immunoblot analysis with an α-HA antibody detected a major polypeptide slightly above the 100 kDa marker, which matches the predicted molecular mass of 108 kDa for Avrb6 (Fig. 2b). We further subcloned the 35S::avrb6-HA expression cassette into a binary vector and performed Agrobacterium-mediated transient expression assays in Ac44E cotton and Nicotiana benthamiana. As shown in Fig. 2c, we observed a similar result as in cotton protoplasts with a major polypeptide being detected at ∼108 kDa. Next, we performed RNA-Seq analysis with cotton protoplasts 12 h after transfection with the avrb6 construct or a vector control. Approximately 39–50 million raw read pairs and 36–46 million cleaned read pairs were obtained for each sample, which corresponds to ∼450 × coverage of 77,267 annotated protein-coding transcripts1. Using a twofold expression change and an adjusted P value <0.05 as cutoffs, and using the G. raimondii genome sequence as a reference (the tetraploid genome sequence was not available at the time), we identified 2,026 genes that were induced by Avrb6 (Fig. 2d and Supplementary Data 2). To identify genes with potential EBEs for Avrb6, we used the TALE-NT 2.0 Target Finder tool to examine all gene promoter sequences in the G. raimondii genome, using the standard score ratio cutoff of 3.0 (Fig. 2e). The list of genes displaying one or more putative EBEs was then intersected with the list of genes upregulated by Avrb6 to produce a list of candidate of Avrb6 targets (Table 2 and Supplementary Data 2). These candidates were ranked by the probability that the predicted EBE is functional by using a machine-learning algorithm based on the output of TALE-NT 2.0 and the genomic context of the predicted EBEs35. Interestingly, among the top candidates, Gorai.008G209000.1, a homologue of the SWEET sucrose transporter genes that serve as S genes in rice and cassava, was induced ∼6,000-fold by Avrb6 and has an EBE with a probability of 1 (Table 2). Other top candidates include Gorai.007G067700.1, Gorai.010G056300.1, Gorai.009G327300.1 and Gorai.008G047400.1. We then used the gene IDs from G. raimondii to identify their homologues in G. hirsutum. The gene IDs of the homologues identified in G. hirsutum are Gh_D12G1898 for Gorai.008G209000.1, Gh_D11G0631 for Gorai.007G067700.1, Gh_D06G0459 for Gorai.010G056300.1, Gh_D05G2954 for Gorai.009G327300.1 and Gh_D12G0420 for Gorai.008G047400.1. These genes were named GhSWEET10D (see below for explanation), Gh067700, GhKBS1, GhHLH1 and GhMDR1, respectively, based on their predicted gene annotation.
Direct induction of targets by Avrb6
To independently determine the induction of the candidate genes, we performed reverse transcription (RT)–PCR assays using Ac44E cotton protoplasts transfected with Avrb6 or with an empty vector as control. The top five candidates, GhSWEET10, Gh067700, GhKBS1, GhHLH1 and GhMDR1, were strongly induced by Avrb6 compared to the vector control (Fig. 3a). We further confirmed induction in cotton leaves by inoculating Xcm strains with or without avrb6. HM2.2S is derived from H1005 with a deletion of at least seven tal genes including avrb6, while HM2.2S (avrb6) is HM2.2S carrying avrb6 in plasmid vector pUFR127 (ref. 10). H1005Δavrb6 is an avrb6 mutant derivative of XcmH1005 (ref. 37). As previously reported, avrb6 in different Xcm strains induced strong water-soaking on Ac44E cotton37 (Fig. 3b). We observed that water-soaking was only induced by the Xcm strains carrying avrb6 (HM2.2S (avrb6), HM2.2S (placZ::avrb6)—a strain that contains the plasmid pUFR135 which expresses avrb6 driven by the lacZ promoter, H1005 (placZ::avrb6) and H1005). As shown in Fig. 3c, the induction of GhSWEET10, Gh067700, GhKBS1 and GhMDR1 by the strains carrying avrb6, HM2.2S (avrb6) and H1005, was stronger than that by strains lacking avrb6, HM2.2S and H1005Δavrb6, at 12- and 24-h post inoculation (hpi). We could not amplify the GhHLH1 gene in cotton likely due to low transcript level. To explore whether GhSWEET10, Gh067700, GhKBS1 and GhMDR1 are directly induced by Avrb6, we added the eukaryotic protein synthesis inhibitor cycloheximide (CHX; 50 μM final concentration) to the Xcm suspensions and inoculated into Ac44E cotton leaves. Each gene was still induced by strains carrying avrb6, H1005 and HM2.2S (avrb6), in the presence of CHX at 24 hpi (Fig. 3d), suggesting that new protein biosynthesis is not required for induction of these genes and that they are direct targets of Avrb6. The effectiveness of CHX in suppressing protein synthesis in this context was confirmed by its suppression of Avrb6 protein expression in a separate Agrobacterium-mediated transient expression assay in Ac44E cotton (Supplementary Fig. 2). To examine potential polymorphisms in these gene promoters between the sequenced cotton and Ac44E cotton used in this study, we amplified each promoter from Ac44E for sequencing. This revealed that each of the promoters possesses an Avrb6 EBE except Gh067700, which has a 1 bp deletion in the EBE in Ac44E (Supplementary Fig. 3). To confirm whether Avrb6 activates the genes by targeting the EBEs, we amplified ∼800 bp upstream of the translational start site of each gene, cloned each of these fragments upstream of a luciferase reporter gene (LUC) and performed a cotton protoplast-based transactivation assay (Fig. 3e). Compared to an empty vector control, co-transfection of Avrb6 strongly activated pGhSWEET10D::LUC with about 110-fold induction, and also activated pGhKBS1::LUC and pGhMDR1::LUC with about 15–20-fold induction (Fig. 3f). Significantly, these promoters were not activated by PthN, another Xcm TAL effector with an RVD sequence distinct from Avrb6, indicating specificity of activation by Avrb6 (Fig. 3f). Consistent with the observation that Gh067700 in cotton Ac44E carries a nucleotide deletion in Avrb6 EBE, pGh067700::LUC was not activated by Avrb6. In addition, pGhHLH1::LUC was not significantly activated by Avrb6, though its promoter possesses a predicted Avrb6 EBE. Since the promoter of GhSWEET10D was strongly induced by Avrb6, we tested the role of the EBE by mutating two nucleotides to create a version of pGhSWEET10D::LUC with a ‘CA’ to ‘GG’ substitution in the EBE (mEBE; Fig. 3g). Avrb6 strongly activated pGhSWEET10D::LUC carrying the wild-type EBE, but not the mEBE (Fig. 3h). Taken together, these data indicate that Avrb6 directly and specifically activates GhSWEET10D, and likely GhKBS1 and GhMDR1, and that the EBE is required for Avrb6-induced expression of GhSWEET10D.
GhSWEET10 activation using a dTALE induces water-soaking
We generated dTALEs to specifically activate GhSWEET10D, GhKBS1 or GhMDR1 via EBEs distinct from the corresponding Avrb6 EBEs, introduced these into the Xcm HM2.2S strain, which lacks avrb6, and performed disease assays in cotton. The dTALEs were expressed from the low-copy, broad-host range vector, pKEB1, a derivative we constructed from pUFR047 (ref. 38) that carries a gateway cloning cassette (Fig. 4a). Significantly, HM2.2S transformants carrying the dTALE targeting GhSWEET10D (dTALE1), but not those targeting GhMDR1 (dTALE3) or GhKBS1 (dTALE4), or the vector control, induced water-soaking in Ac44E cotton, similarly to XcmH1005 (Fig. 4b). To determine if the dTALEs used indeed activate the transcripts of their respective target genes, we performed RT–PCR analysis. As shown in Fig. 4c, GhSWEET10D and GhMDR1 were induced by the cognate dTALEs. These data indicate that activation of GhSWEET10D on Xcm infection contributes to water-soaking development, thus identifying GhSWEET10D as a relevant target of Avrb6 in cotton and an S gene. We did not detect the induction of GhKBS1 by its dTALE, and cannot conclude whether GhKBS1 plays a role in BBC.
Avrb6 targets GhSWEET10 in both A and D genomes of cotton
The tetraploid G. hirsutum has two subgenomes, A and D. The above studies of GhSWEET10D were mainly based on the D genome of G. raimondii and the corresponding D subgenome of G. hirsutum. We examined if Avrb6 also targets SWEET10 in the A-genome of G. arboreum, which is closest to the progenitor species of the A subgenome of G. hirsutum. We identified a homologue of GhSWEET10D, named GaSWEET10, which bears 98% similarity to GhSWEET10D at the amino-acid level. We expressed Avrb6 in G. arboreum cotton protoplasts and determined whether GaSWEET10 was induced by Avrb6. RT–PCR analysis showed that GaSWEET10 was induced by Avrb6 (Fig. 4d). To determine whether Avrb6 could specifically activate the promoter of GaSWEET10, we cloned the promoter, pGaSWEET10, upstream of the luciferase gene for a transactivation assay. As shown in Fig. 4e, Avrb6 activated pGaSWEET10::LUC to a similar level as Avrb6 activation of pGhSWEET10D::LUC. Notably, an alignment of the Avrb6 EBE from pGhSWEET10D with the one from pGaSWEET10 revealed them to be identical except for a single nucleotide polymorphism near the 3′ end of the EBE (position 14, counting the initial thymine), where mismatches are known to be generally tolerated43. Additionally, an alignment of protein-coding sequences revealed that GrSWEET10 from G. raimondii is identical to D subgenome GhSWEET10D, whereas GaSWEET10 from G. arboreum is identical to A subgenome GhSWEET10A (Supplementary Fig. 4). Similarly, the promoter sequence, including the EBE, of pGhSWEET10A from tetraploid Ac44E was more closely related to pGaSWEET10 from G. arboreum versus pGrSWEET10 from G. raimondii (Supplementary Fig. 4b). We used the dTALE approach to determine if GaSWEET10 is also a direct target of Avrb6 that causes water-soaking. As shown in Fig. 4f, the dTALE2 construct, but not the dTALE1 construct specific to pGhSWEET10D or an empty vector introduced in H1005Δavrb6-induced water-soaking in G. arboreum. Notably, H1005 induced relatively weak water-soaking on G. arboreum compared to G. hirsutum, likely due to G. arboreum carrying some strain-specific resistance as noted previously44. Taken together, these results indicate that Avrb6 can directly target SWEET10 in both the A and D genomes to contribute to the development of BBC.
GhSWEET10 silencing reduces water-soaking caused by Xcm
Having determined that GhSWEET10 mediates Avrb6-induced water-soaking, we subsequently investigated whether GhSWEET10 is genetically required for water-soaking during Xcm infection in cotton. We employed the Agrobacterium-mediated VIGS system to silence GhSWEET10 and examined BBC development after subsequent inoculation of Xcm. The VIGS construct was designed to silence both GhSWEET10A and GhSWEET10D because of sequence conservation. There was no apparent difference in plant growth between the VIGS-GhSWEET10 plants and plants inoculated with the GFP control (VIGS-Ctrl) up to 3 weeks after VIGS (Supplementary Fig. 5). Three weeks after Agrobacterium infiltration, the silenced plants were vacuum infiltrated with XcmH1005. Compared to the control, the VIGS-GhSWEET10 plants consistently showed fewer water-soaked lesions after XcmH1005 infection (Fig. 5a,b). RT–PCR analysis confirmed reduced induction of GhSWEET10 in VIGS-GhSWEET10 plants compared to VIGS-Ctrl plants (Fig. 5c). Taken together, the data indicate that silencing of GhSWEET10 in cotton reduces the development of water-soaking following Xcm inoculation, providing genetic evidence that GhSWEET10 is functionally required for normal BBC symptom development upon infection by Xcm strains carrying avrb6.
GhSWEET10D encodes a functional sucrose transporter
Since GhSWEET10 belongs to the SWEET gene family, we examined whether GhSWEET10 functions as a sugar transporter. To measure activity, we transiently expressed the coding sequence of GhSWEET10D along with a Förster resonance energy transfer (FRET) sucrose sensor in human embryonic kidney T293 (HEK293T) cells45. Compared to the vector control, expression of GhSWEET10D enabled HEK293T cells to accumulate sucrose, which was detected as a negative ratio change, to a level comparable to the well-characterized Arabidopsis transporter AtSWEET11 (Fig. 6a). In addition, when we transiently expressed GhSWEET10D under the control of the 35S CaMV promoter in N. benthamiana, the sucrose concentration of the apoplastic fluids from the 35S::GhSWEET10D-inoculated leaves was higher than that from the vector control-inoculated leaves (Supplementary Fig. 6a), indicating that GhSWEET10D is able to transport sucrose in planta. Interestingly, GhSWEET10D did not restore the growth defect of yeast EBY4000, a hexose transport-deficient yeast strain, on the medium supplemented with 2% glucose or 2% fructose as the sole carbon source, indicating that GhSWEET10D does not mediate efficient fructose or glucose transport (Supplementary Fig. 6b). Taken together, the data suggested that GhSWEET10D encodes a functional sucrose transporter.
GhSWEET10D is a member of a large gene family in cotton
In bacterial blight of rice, several closely related SWEET genes can each serve as an S gene28. To better understand the relationship within the SWEET family in cotton, especially which SWEETs are most closely related to GhSWEET10, the full-length protein sequence of GhSWEET10D was used as the query for a BLASTp analysis against the G. hirsutum NBI protein database (www.cottongen.org/tools/blast). The search identified 50 additional GhSWEETs, for a total of 51 SWEETs in G. hirsutum, with each possessing the conserved domains found in the AtSWEET superfamily in Arabidopsis (Supplementary Figs 7 and 8). Based on the well-characterized phylogenetic analysis of AtSWEETs, we generated a phylogenetic tree and classified the GhSWEET family into four clades with nine in clade I, 14 in clade II, 18 in clade III and 10 in clade IV. The individual members of GhSWEETs are named using the tree described by Eom et al.46, as a reference where GhSWEET1-3 are in clade I, GhSWEET4-8 are in clade II, GhSWEET9-15 are in clade III and GhSWEET16-18 are in clade IV. Considering the gene duplication and polyploidy in tetraploid cotton, lowercase and uppercase letters are used, respectively, to distinguish closely related members. If multiple members are co-orthologous to the closest AtSWEET, lowercase letters (a–c) are added after the numbers to differentiate genes in the same subclade. An uppercase ‘A’ is further added to indicate the gene is from the A subgenome, or an uppercase ‘D’ for the D subgenome. For example, there appear to be two pairs of GhSWEETs that are closely related to AtSWEET1 as shown in the phylogenetic tree. Therefore, we distinguish these by naming one pair as GhSWEET1a and another pair as GhSWEET1b. Each of these pairs is further named according to their subgenome locations as GhSWEET1aA and GhSWEET1aD, and GhSWEET1bA and GhSWEET1bD, respectively (Fig. 6b and Supplementary Fig. 7). Like the SWEET genes in rice and cassava that serve as S genes, GhSWEET10 is a member of the clade III family (Fig. 6c).
GhSWEET10 induction by Avrb6 is reduced in b6 cotton
Avrb6 causes severe water-soaking in the susceptible Ac44E cotton line. However, in the near-isogenic resistant line Acb6, which harbours the apparently genetically complex BBC recessive resistance locus b6, Avrb6 causes the resistance-associated hypersensitive response (HR) instead (ref. 38 and Supplementary Fig. 9a,b). We examined whether b6-mediated resistance is in part due to the inability of Avrb6 to activate GhSWEET10 in Acb6. When we expressed Avrb6 in Ac44E and Acb6 protoplasts, respectively, the induction of GhSWEET10 by Avrb6 was significantly lower in Acb6 than that in Ac44E (Fig. 7a). We further compared GhSWEET10 induction in Ac44E and Acb6 cotton plants inoculated with different Xcm strains with or without avrb6. Both Ac44E and Acb6 plants showed increased induction of GhSWEET10 on inoculation with HM2.2S carrying avrb6 compared to the plants inoculated with HM2.2S (Fig. 7b). However, the induction was significantly reduced in Acb6 plants relative to Ac44E plants. A similar trend was observed when H1005 was used to inoculate both lines (Fig. 7b). To examine whether the reduced induction by Avrb6 in Acb6 could be due to polymorphisms at the GhSWEET10D EBE, we sequenced the GhSWEET10D promoter region from Acb6. The EBE is perfectly conserved, but in Acb6, there is a SNP immediately adjacent to the 5′ of the EBE and a 2 bp insertion surrounded by six additional SNPs ∼20 bp downstream of the EBE (Supplementary Fig. 9c). We cloned the promoter of GhSWEET10D from Acb6 in front of the luciferase reporter for a transactivation assay in cotton protoplasts. Similar to what we observed for the endogenous GhSWEET10D gene, the induction of the pGhSWEET10DAcb6::LUC reporter by Avrb6 was nearly three folds lower than that of the reporter carrying the promoter from Ac44E (pGhSWEET10DAc44E::LUC) (Fig. 7c). The promoter of GhSWEET10A is almost identical in Ac44E and Acb6 (Supplementary Fig. 4b). Thus, the polymorphisms outside the GhSWEET10D EBE may impair full induction by Avrb6. In addition, when we inoculated H1005Δavrb6 carrying dTALE2, which activates pGhSWEET10D (Fig. 4a,f), into cotyledons of Acb6, the bacterium triggered water-soaking, but not HR in Acb6 (Supplementary Fig. 9d). The data suggest that GhSWEET10D may not mediate Avrb6-induced HR and Avrb6 targets another gene for HR in Acb6.
Clade III GhSWEET responsiveness to different Xcm isolates
Clade III SWEET genes have been implicated in disease susceptibility in rice and cassava. We here identified a clade III SWEET gene in cotton, GhSWEET10, that encodes a sucrose transporter and that also plays a role in disease susceptibility. To examine how general the involvement of clade III GhSWEET genes in BBC is, we investigated the transcriptional changes of these genes in response to nine Xcm isolates collected from infected cotton fields from different locations in Texas. Notably, these isolates are suspected to be the causal agents of the recent rampant re-emergence of BBC in the United States. However, it has not been determined yet whether these isolates represent a new race. We found that the field isolates were unable to induce GhSWEET10. However, all of the field isolates highly induced GhSWEET14a (200–4,000-fold) (Fig. 7d). In addition, all of the isolates, except for Xcm9, also significantly induced GhSWEET14b (20–300-fold). As expected, H1005, but not H1005Δavrb6, induced GhSWEET10 by 15-fold. Notably, GhSWEET14a and GhSWEET14b are clade III SWEET genes (Fig. 6c). Taken together, these data suggest that in addition to GhSWEET10, GhSWEET14a and GhSWEET14b are potential S genes, and that activating clade III GhSWEET genes might be broadly important to the ability of different Xcm strains to cause BBC.
BBC caused by Xcm is among devastating diseases that limit cotton yields. Despite several TAL effectors being cloned from Xcm, no R or S genes have yet been molecularly identified, mainly because of the large and polyploidy nature of the cotton genome and limited molecular and genomic tools. The approach taken in this study successfully overcame these challenges to establish a role for SWEET-mediated susceptibility in BBC. GhSWEET10 was strongly induced by Avrb6 during Xcm infection and was identified as an S gene for BBC. Characterization of BBC-resistant line Acb6 revealed sequence differences in the GhSWEET10D promoter, but not in the EBE, that impair activation by Avrb6, possibly relating to resistance mediated by the b6 gene. Finally, surveys of different Xcm field isolates showed that two additional clade III GhSWEETs were highly induced during infection. It appears that the evolution of novel TAL effectors that induce these additional clade III GhSWEET members may have contributed to the recent re-emergence of BBC in the United States.
The SWEET family members are key S genes common to several diseases caused by different Xanthomonas species47. So far, only clade III SWEET genes are targeted by pathogens that use TAL effectors to facilitate disease46,48. Members of clade III SWEET genes are known to transport sucrose, which likely serves as a carbon source for the pathogen. Interestingly, it was recently shown that two clade III SWEET genes in Arabidopsis, AtSWEET13 and AtSWEET14, can also transport plant hormone gibberellin to modulate growth and development49. In rice, Xoo can target three clade III SWEET genes to cause susceptibility. Xoo TAL effector PthXo1 targets OsSWEET11 (ref. 20); PthXo2 targets OsSWEET13 (ref. 27); and AvrXa7 targets OsSWEET14 (ref. 23). In cassava, Xam can use TAL20Xam668 to target MeSWEET10a, another clade III SWEET gene25. In at least one case, a host SWEET gene is targeted by multiple TAL effectors from different strains of the pathogen: in addition to AvrXa7, OsSWEET14 is targeted by PthXo3, TalC and Tal5, each from a different Xoo strain23,28,50. The central role of SWEETs in susceptibility is further supported by our data, as we have identified GhSWEET10 as a clade III SWEET gene in cotton targeted by Avrb6. In addition, we observed that several different Xcm field isolates strongly induce two additional clade III GhSWEETs, GhSWEET14a and GhSWEET14b, but not GhSWEET10, during infections. Since XcmH1005 is a strain derived from an older race, and since these field isolates were collected within the past year, this strongly suggests that new TAL effectors have evolved in these field isolates to target new SWEETs and break resistance. The striking differences of the tal gene content and the localization of the pthN2 gene on chromosome or plasmid in XcmH1005 and XcmN1003 are consistent with the notion that TAL effectors in Xcm may evolve rapidly. However, it is also possible that TAL effectors from these recent strains can activate another target, either another SWEET gene or a gene in different family, to cause susceptibility. It was revealed that TalC from Xoo can still cause disease on rice, despite having its corresponding EBE from OsSWEET14 artificially mutated, suggesting that preventing TalC-mediated SWEET14 activation alone is not sufficient to prevent susceptibility51. Additionally, even though GhSWEET10, GhSWEET14a and GhSWEET14b reside in clade III, it is still unclear if they function similarly. Additional biochemical analyses are needed to further understand the function of these genes in BBC. Characterizing the spectrum of SWEET-targeting TAL effectors and the relative contributions of their targets to susceptibility, both in the older strains and the recent isolates, is an important future objective.
The CRR of TAL effectors determines their DNA-binding specificity for targeted gene activation in disease or resistance. Inventory of the repeat sequences is essential to predict important TAL effector targets. However, the repeats are generally impossible to assemble from Illumina-sequencing reads and challenge remains even with Sanger sequencing. PacBio sequencing has proven to be an effective approach however52,53,54. We used PacBio sequencing to reveal the whole repertoire of TAL effectors in XcmH1005 and XcmN1003. We identified 12 TAL effectors encoded by H1005 (six in the chromosome and six in the plasmid) and 9 encoded by N1003 (five in the chromosome and four in the plasmid). In addition to GhSWEET genes, another shared class of targets across TAL effectors of different Xanthomonas species is transcription factor genes19,31,55. In at least one case, the CsLOB1 transcription factor of citrus, and other members of CsLOB1 family also function as S genes31,56. It will be interesting to determine whether targets of other TAL effectors in H1005 and N1003 similarly include transcription factor genes, or yet novel types of targets.
In addition to revealing a host factor essential for disease symptom development, our study yields insight into the nature of BBC resistance mediated by b6. Initially characterized as recessive57, genetic linkage mapping analysis suggests that the genetic basis of b6-resistance is rather complex and exhibits a quantitative inheritance. In rice, a mechanism of recessive resistance is disruption of TAL effector-dependent activation of an OsSWEET S gene due to polymorphism at the EBE58. Our data revealed that the induction of GhSWEET10 by Avrb6 in Acb6 is compromised likely not due to the sequence polymorphism at the EBE, suggesting a novel mechanism underlying b6-mediated resistance. To our knowledge, this is the first report of polymorphisms outside the EBE itself that impair activation by a TAL effector. The b6-mediated resistance is accompanied by the HR at the site of infection, and this is triggered specifically in the presence of Avrb6 (refs 10, 38). However, a dTALE-activating GhSWEET10 only results in water-soaking, but not HR in Acb6, suggesting that GhSWEET10 does not mediate Avb6-induced HR. This is likely that HR is due to the activation of another target by Avrb6 in Acb6, but not in Ac44E. Thus, it seems possible that b6 comprises at least two genetic determinants, one manifesting in reduced susceptibility (lower expression of the GhSWEET10 S gene) and the other mediating the defence-associated HR. Perhaps both need to be present to support the full level of resistance.
Nevertheless, our findings suggest a strategy to improve BBC resistance in cotton through genome editing of TAL effector EBEs in SWEET genes. Genome editing has been successfully used in rice to mutate the OsSWEET13 S gene and generate plants resistant to Xoo strains that depend on TAL effector PthXo2 as a major virulence factor27. An advantage of this strategy is that relatively minor sequence changes could be made that will destroy the EBE while being unlikely to impinge on native promoter activity and without affecting the coding region, keeping endogenous function of the SWEET gene intact51,59. The successful knockout of all homeologs of the Mlo gene in hexaploid wheat in a single genome editing experiment indicates that disrupting EBEs in SWEET genes in cotton is likely feasible60. As new TAL effectors important for virulence of this pathogen are characterized in the future, this system could be used to edit the EBEs in the corresponding targets, whether GhSWEET genes or other BBC S genes yet to be discovered, and to generate plants with broad-spectrum BBC resistance via pyramiding. Not least, duplicating the Acb6 genotype of GhSWEET10 in the Ac44E background and in other susceptible genotypes would be a powerful approach to dissect the genetic determinants of b6-mediated resistance, potentially by uncoupling loss of susceptibility from the HR. Such characterizations would also likely lead to new strategies for improved control of BBC.
Plants and bacterial strains and growth conditions
The Gossypium hirsutum lines Acala44E (Ac44E), Acalab6 (Acb6) and FM706V, and G. arboreum line SA-1415 were grown in 3.5-inch square pots containing Metro Mix 900 soils (Sun Gro Horticulture, Agawam, MA) and tobacco Nicotiana benthamiana were grown in 3.5-inch square pots containing Metro Mix 366 soils in a growth chamber at 23 °C, 30% humidity and 100 μE m−2s−1 light with a 12-h light/12-h dark photoperiod. Two-week-old cotton plants were used for Agrobacterium-mediated VIGS assay, Agrobacterium-mediated transient protein expression assay or protoplast isolation. Plants after inoculation with Xanthomonas citri subsp. malvacearum (Xcm) were transferred into a growth chamber at 28 °C, 50% humidity and 100 μE m−2s−1 light with a 12-h light/12-h dark photoperiod. Bacterial strains used in this study are listed in Supplementary Table 3. E. coli and A. tumefaciens strains were grown in Luria–Bertani (LB) medium with appropriate antibiotics at 37 °C or 28 °C, respectively. Xcm strains were grown in nutrient broth medium with appropriate antibiotics at 28 °C. The Xcm field strains were isolated from infected cotton fields in Texas through Koch’s postulates with modifications. Water-soaked lesions were excised from infected cotton leaves using a sterile scalpel. The cut lesions were soaked and macerated in 100 μl of sterile water. The bacterial suspension was plated on nutrient agar from serial dilutions. Colonies were re-streaked and inoculated into cotton to confirm pathogenicity.
The Xcm strains were inoculated into 4 ml of nutrient broth medium with appropriate antibiotics for overnight. For syringe infiltration, bacterial suspensions adjusted to OD600=0.1 were inoculated into expanded cotyledons of 2-week-old plants or true leaves using a needleless syringe. Small holes were created with a 25G needle on the underside of the cotyledons to facilitate infiltration. For vacuum infiltration, a final bacterial suspension was made by adjusting the bacterial cultures to OD600=0.01 mixed with 0.04% of Silwet L-77 surfactant solution. Plants that were silenced via VIGS 3 weeks earlier were submerged into the bacterial suspension inside a desiccator connected to a vacuum pump. The plants were vacuum infiltrated for 5 min at 76 mmHg.
DNA isolation for Xcm whole-genome sequencing
The XcmH1005 and XcmN1003 DNA used for PacBio sequencing was prepared using a protocol for total genomic DNA isolation with modifications54. Bacteria were cultured overnight in 30 ml glucose yeast extract media (2% glucose, 1% yeast extract) in a 250 ml flask at 28 °C on a rotary shaker at 250 rpm, collected by centrifugation at 2,580g for 10 min at 4 °C, then gently resuspended and washed in 20 ml NE buffer (0.15 M NaCl, 50 mM EDTA) twice to remove the extracellular polysaccharide. Cells were then gently resuspended in 2.5 ml solution containing 50 mM Tris, pH 8.0 and 50 mM EDTA, and then 0.5 ml solution containing 25 mM Tris, pH 8.0, 10 μl ReadyLyse (Epicentre) and 50 μl RNase (10 mg ml−1). Suspensions were mixed gently by inversion and then incubated on ice for 45 min. Following incubation on ice, 1.0 ml STEP buffer (0.5% SDS, 50 mM Tris, pH 7.5, 40 mM EDTA, protease K at 2 mg ml−1) was added, and the lysate was mixed well by inversion and incubated at 37 °C for 1 h, mixing every 10–15 min. Next, 1.8 ml of 7.5 M ammonium acetate was added and the lysates were mixed gently before being subjected to two extractions with phenol/chloroform (10 ml) and one extraction with chloroform/isoamyl alcohol (24:1, pH 8.0, 10 ml), shaking vigorously by hand to mix and separating the aqueous and organic phases by centrifugation each time at 10,300g for 10 min at 4 °C. Following this, the aqueous phase was transferred to a 14 ml tube and DNA was precipitated by addition of two volumes of cold 95% ethanol and gentle, repeated inversion. Once solidified, the DNA was transferred to a 2 ml micro-centrifuge tube using a Pasteur pipette with the tip previously sealed and bent into a hook over a flame. Remaining liquid was then removed by centrifugation at 825g for 5 min and the pellet was washed once with 70% ethanol. The remaining liquid was removed as before and the tube left open to dry in a laminar flow hood until the edges of the pellet became glossy in appearance (10–15 min). Finally, the pellet was dissolved in 100 ml TE buffer (10 mM Tris/HCl, 1 mM EDTA, pH 8.0) overnight at 4 °C and then adjusted to a concentration of 1 μg ml−1.
PacBio sequencing and genome assembly
DNA library preparation and sequencing was performed according to the manufacturer’s instructions by the Genomics Core Facility of the Icahn School of Medicine at Mt. Sinai (New York, NY, USA)54. Separately, DNA preparation and electrophoresis to check for small plasmids in either strain that would be lost during library preparation was using standard methods50. Sequencing was conducted to >120 × coverage, which due to improvements in sequencing technology required only two SMRT cells per strain. In all data sets, read-length distribution showed a fat tail, with 20% of coverage after adaptor removal contained in subreads greater than or equal to 15,000 bp. The whole genomes of H1005 and N1003 were assembled using HGAP3 (ref. 61) and verified by carrying out local assemblies of reads containing tal genes and then comparing those assemblies to the whole-genome assembly as described in Booher et al.54. The assemblies conclusively match published Southern blot results using a tal gene probe, as well as restriction enzyme mapping and sequencing or partial sequencing of cosmid clones and subclones10,38,39,40.
The initial assembly of XcmH1005 showed frameshifts in avrB104, avr103 and avrb6 resulting from an extra cytosine (C) in a stretch of six Cs commonly found in the 3′ region of tal genes. Since avrb6 is functional, the previously published sequence of avrb6 shows an intact reading frame38, and residual errors in homopolymer runs sometimes persist after consensus calling by Quiver and are a known weak point of the error-correction software (https://github.com/PacificBiosciences/GenomicConsensus/blob/master/doc/FAQ.rst), we concluded that the frameshift in avrb6 was such an error, and we corrected it in the final assembly. Likewise, since clones containing avrB104 and avrB103 were functional, conferring avirulence on AcB5 and AcBIn3-containing cotton40, we concluded that the assembly contained the same error for each of these genes, and corrected them both. No other tal genes in the assembly harboured this or another frameshift within a homopolymer stretch. Note that the frameshift in pthN’, retained in the final assembly, is due to a deletion of a single thymine, not within a homopolymer, and pthN’ was shown to be non-functional10.
Construction of avrb6 in the expression vectors
Avrb6 was amplified from XcmH1005 plasmid DNA with primers containing restriction enzymes SpeI at the amino (N) terminus and SmaI at the carboxy (C) terminus (Supplementary Table 4) and ligated into a plant protoplast expression vector pHBT with a CaMV 35S promoter at the N terminus and a HA-epitope tag at the C terminus. To construct the pCB302 binary vector containing avrb6 for Agrobacterium-mediated transient expression assay in N. benthamiana, avrb6 was released from the pHBT vector through digestion with SpeI and SmaI and ligated into the pCB302 binary vector. All the clones were confirmed by sequencing.
Transient expression assays
Cotton protoplasts were isolated from 2-week-old cotyledons. Detached cotyledons were cut with a razor blade and digested in an enzyme solution (1.5% cellulose R10, 0.4% macerozyme R10, 0.4 M mannitol, 20 mM KCl, 20 mM MES pH 5.7) supplemented with 2% sucrose for 0.5 h under vacuum. Subsequently, the enzyme solution was incubated without vacuum at room temperature for 12 h. Protoplasts were released by filtering through a 30 μm-nylon mesh, washed with W5 solution (154 mM NaCl, 125 mM CaCl2, 5 mM KCl, 2 mM MES pH 5.7) and diluted in MMG solution (0.4 M mannitol, 15 mM MgCl2, 4 mM MES pH 5.7) to a density of 2 × 105 cells ml−1 (ref. 62). A measure of 100 μl of protoplasts for each sample were collected for western blotting after expressing avrb6-HA for 12 h. Avrb6-HA protein was detected by immunoblotting using the α-HA antibody. Agrobacterium tumefaciens strain GV3101 containing pCB302-avrb6-HA vector or an empty vector was cultured overnight in LB medium containing appropriate antibiotics at 28 °C. Bacteria were collected by centrifugation and resuspended with infiltration buffer (10 mM MES, pH 5.7, 10 mM MgCl2, 200 μM acetosyringone) at OD600=0.6. Leaves of 4-week-old soil-grown N. benthamiana or cotyledons of 2-week-old Ac44E cotton were hand infiltrated using a needleless syringe with Agrobacterium cultures. Leaf samples were collected 48 h after infiltration for protein sample and immunoblot analysis. Full blots are provided in Supplementary Fig. 10.
Cotton RNA isolation for RT–PCR and qRT–PCR analysis
Cotton total RNA was extracted from protoplasts (500 μl protoplasts with a cell density of 2 × 105 per ml for each sample) using TRIzol reagent (Invitrogen, USA) or leaves (one cotyledon or one true leaf for each sample) using a Spectrum plant total RNA kit (Sigma-Aldrich, USA) according to the manufacturer’s protocol. RNA was then treated with DNase (Invitrogen, USA) to remove genomic DNA. Purified RNA (1 μg) was subsequently reverse transcribed using a first-strand cDNA synthesis kit (Promega, USA) with oligo(dT) as a primer. PCR amplification was performed for 30 cycles of 15 s at 98 °C, 30 s at 55 °C and 45 s at 72 °C with primers listed in Supplementary Table 4. GhACTIN was used as an internal control for RT–PCR. qRT–PCR analysis was performed using iTaq SYBR green Supermix (Bio-Rad, USA) with a Bio-Rad CFX384 Real-Time PCR System. Expression of each gene was normalized to the expression of GhUBQ1.
RNA sequencing and data analysis
A measure of 500 μl of cotton protoplasts (2 × 105 per ml) were transfected with 35S::avrb6-HA or an empty vector control. Protoplasts were collected 12 h after transfection and RNA was extracted by the TRIzol reagent. Three independent biological repeats were performed for the RNA-Seq analysis. For each repeat, equal amount of RNA from two biological replicates was pooled for RNA-Seq library construction. RNA-Seq libraries were prepared using Illumina TruSeqTM RNA Sample Preparation Kit following the manufacturer’s instruction, and sequenced on an Illumina HiSeq 2000 platform with 125-nucleotide pair-end reads at Texas AgriLife Genomics and Bioinformatics Service (College Station, TX). RNA-Seq read processing, alignment to the G. raimondii genome and differential gene expression analysis were performed as described in Li et al.63. Genes with expression fold change ≥2 and P value <0.05 were considered as significantly different between samples with and without Avrb6.
All TAL effector EBE predictions were conducted using the TALE-NT 2.0 Target Finder tool64 to search the promoter regions defined in the G. raimondii genome as the 1,000 bp upstream of the transcriptional start site plus the 5′ UTR, if annotated. We identified promoter sequences for G. raimondii using genome assembly v2.0 and annotation v2.1 (ref. 3). Binding sites passing the standard target finder score ratio cutoff of 3.0 were ranked based on both target finder output and genomic context using the machine-learning classifier presented by Cernadas et al.35 and updated by Wilkins et al.65.
Construction of VIGS vector and Agrobacterium-mediated VIGS
GhSWEET10 was amplified by PCR from cDNA of G. hirsutum with primers described in Supplementary Table 4, and inserted into the pYL156 (pTRV-RNA2) vector with restriction enzymes EcoRI and KpnI, resulting in pYL156-GhSWEET10. The Agrobacterium tumefaciens strain GV3101 carrying the plasmids pTRV-RNA1 and pYL156 (pTRV-RNA2) or pYL156-GhSWEET10 was collected and resuspended with infiltration buffer (10 mM MES, pH 5.7, 10 mM MgCl2, 200 μM acetosyringone) at OD600=0.75. The culture suspension of pTRV-RNA1 was mixed with pYL156 or pYL156-GhSWEET10 at a 1:1 ratio and hand infiltrated using needleless syringes into two fully expanded cotyledons of 2-week-old plants66.
GhSWEET10D transporter analysis in HEK293T cells
HEK293T cells were co-transfected with FRET sucrose sensor FLIPsuc90μδ3A and GhSWEET10D in six-well plates and perfusion experiments were performed48. After 3.5 min buffer perfusion, cells were perfused with 25 mM sucrose for 4 min followed by 2.5 min buffer perfusion. Images were captured at the following settings: exposure time 800 ms, gain 3, binning 2, time interval 10 s. Fluorescence intensity of selected individual cells was recorded. The quantitative ratio of eCFP and Aphrodite emission at excitation of eCFP was calculated after the background was subtracted. All of ratios were normalized to the initial ratio.
Yeast mutant EBY4000 complementation growth assay
The yeast strain EBY4000 was transformed with the different plasmids following the standard protocol. Spotting assay with 10-fold serial dilutions was performed. Yeast cells were diluted to OD600=0.22 in water after cells grew to OD600=0.6, followed by a twofold dilution. Then, 10-fold serial dilutions were plated on synthetic medium containing either 2% maltose (as a control), 2% fructose or 2% glucose. Growth was documented by Gel-doc system after 2–4 days at 30 °C.
The reporter constructs, pGhSWEET10D::LUC, pGh067700::LUC, pGhKBS1::LUC, pGhMDR1::LUC, pGhHLH1::LUC and pGaSWEET10::LUC, were constructed by amplifying the promoters of candidate genes (∼800 bp upstream of translational start site) from genomic DNA of Ac44E, Acb6 or G. arboreum and were fused to a luciferase gene at the C terminus. Protoplasts were transfected with the effector and reporter construct and expressed at room temperature for 12 h. Protoplasts were then collected and lysed and the luciferase activity was detected by Glomax Multi-Detection System (Promega, USA) with the luciferase assay substrate (Promega, USA). UBQ10-GUS was included in all samples as the internal transfection control and the GUS activity was analysed with a Multilabel Plate Reader (Perkin-Elmer, USA). The pGhSWEET10D-mEBE::LUC construct was generated by the site-directed mutagenesis PCR using plasmid DNA of pGhSWEET10D::LUC as the template and primers are listed in Supplementary Table 4.
Construction of dTALEs
The dTALEs were constructed using golden gate cloning using a complete plasmid kit available through AddGene67. Four types of repeats encoding the RVDs NI, NN, NG and HD that correspond to the respective nucleotide A, G, T and C were used to assemble the repeat domains of the artificial dTALEs. The dTALEs were transformed into Xcm stains via bacterial tri-parental mating by using a helper plasmid, pRK2073 (ref. 38). In addition, the modifier plasmid pUFR054 was used to increase the efficiency of transferring the plasmids from E. coli DH5α to Xcm strains. The bacterial mating was carried out by mixing the donor, recipient, modifier and helper strains in a 1:1:1:1 ratio. The mixed culture was plated onto nutrient agar medium with appropriate antibiotics. Colonies were confirmed via Sanger sequencing of extracted plasmid DNA.
Measurement of sucrose concentration
Leaves from 4-week-old N. benthamiana plants were infiltrated with Agrobacterium carrying 35S::GhSWEET10D-HA or an empty vector control at OD600=1.0. Leaves were detached 3 dpi and fully vacuum infiltrated with sterile Millipore water. The leaves were blot dried, cut into small pieces with a razor blade and placed in a nylon mesh strainer at the top of a 50 ml centrifuge tube. The apoplastic solution was collected through centrifugation at 3,220g for 20 min at 4 °C. The concentration of sucrose was determined by using a sucrose assay kit (Sigma-Aldrich).
The XcmH1005 genome assembly has been deposited in GenBank under accessions CP013004 (chromosome) and CP013005 (pXcmH) and the XcmN1003 assembly under accessions CP013006 (chromosome) and CP013007 (pXcmN). Raw data as bas.h5 and bax.h5 files and associated metadata are available in the NCBI sequence read archive (SRA) under SRP065335 for XcmH and SRP065336 for XcmN. The RNA-Seq data were deposited in the NCBI SRA under accession number SRP100553. The authors declare that all other data supporting the findings of this study are included within the manuscript and its supplementary files or are available from the corresponding authors on request.
How to cite this article: Cox, K. L. et al. TAL effector driven induction of a SWEET gene confers susceptibility to bacterial blight of cotton. Nat. Commun. 8, 15588 doi: 10.1038/ncomms15588 (2017).
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We thank Dr Dean Gabriel for various Xcm strains, Dr Margaret Essenberg and Jared Harris for the seeds, Stephanie Yamashita and Tri Tran for excellent technical assistance and Karla Vogel for constructing pKEB1. This work was supported by the USDA NIFA (2012-67013-19433) to P.H. and L.S., the Cotton Inc (15-174) to L.S., Texas AgriLife Research Cotton Improvement Program to L.S., P.H. and T.W., the US National Science Foundation (Plant Genome Research Program Award IOS 1238189) to A.J.B., the Texas A&M University Graduate Diversity Fellowship and USDA NIFA AFRI Pre-doctoral Fellowship (Award No. 2017-67011-26060) to K.L.C., Graduate Research Fellowship Award (Grant No. DGE-1144153) to K.E.W.
Progressive MAUVE analysis on XcmH and XcmN genomes. The exact coordinates of the locally collinear blocks (LCB) are shown.
List of the genes that are significantly up-/down-regulated by Avrb6, the genes in G. raimondii with a predicted Avrb6 EBE, and all of the Avrb6 candidate targets in Ac44E cotton.
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