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Genome editing of a dominant resistance gene for broad-spectrum resistance to bacterial diseases in rice without growth penalty
Wednesday, 2023/12/06 | 08:39:03

Meixia WangShaofang LiHuayang LiCongfeng SongWenya XieShimin ZuoXueping ZhouChangyong ZhouZhiyuan JiHuanbin Zhou

Plant Biotechnology Journal; First published: 23 November 2023 

https://doi.org/10.1111/pbi.14233

 

Bacterial blight (BB) and bacterial leaf streak (BLS), caused by Xanthomonas oryzae pv. oryzae (Xoo) and Xanthomonas oryzae pv. oryzicola (Xoc), respectively, are the two most devastating bacterial diseases of rice worldwide. Both bacterial pathogens infect rice plants relying on type III secreted transcriptional activation-like effectors (TALEs) that bind to specific effector binding elements (EBEs) in the promoter of susceptibility (S) genes, and activate its expressions for disease development (Chen et al., 2010). To counteract BB, rice has evolved a unique type of executor resistance (R) genes (Xa7Xa10Xa23etc.), which can specifically trap certain Xoo TALEs via EBEs within their promoters and trigger strong hypersensitive response (HR). Previously, we verified that gene correction of xa23 with EBEAvrXa23 restored its function in triggering defence responses against Xoo invasion (Wei et al., 2021). Considering Xa23-mediated resistance to BB has been overcome by new Xoo isolates in the field in recent years, and no natural R genes against Xoc have been identified in rice; here, we investigated whether an EBE-stacking-in-the-promoter strategy could be employed in the molecular rice breeding for durable and broad-spectrum resistance to both BB and BLS by genome-editing technology.

 

Sequencing analysis of the xa23 locus in the commercial rice cultivar Nangeng 46 (N46) revealed that it shared an identical coding region with Xa23 in CBB23, whereas it lacked the complete EBEAvrXa23 sequence in the promoter (Figure 1a). We presumed that introducing multiple EBEs, which were responsive to TALEs from various Xoo and Xoc strains, into the xa23N46 locus by genome editing would render host broad-spectrum and durable resistance to both pathogens. Thus, 10 EBEs (Table S1) responding to PthXo1, PthXo3, AvrXa23, Tal9aBLS256etc. were selected and constructed into a 220-bp EBEXoc/Xoo array (Figure 1a; Figure S1). It was synthesized, PCR amplified using a pair of chemically modified primers and used as the DNA donor (Figure S1) for targeted DNA insertion in the xa23N46 promoter through CRISPR/Cas9-induced non-homologous end joining (NHEJ) repair pathway as described previously (Lu et al., 2020).

 

Fig.1: Engineering broad-spectrum resistance to both BB and BLS by CRISPR/Cas9-mediated insertion of EBEXoc/Xoo array in N46. (a) Schematic map of Xa23 alleles in different rice varieties and the promoter-editing strategy of xa23 in N46. The polymorphisms between the Xa23 and xa23 promoters are shown in shadows. The nucleotide sequences of functional EBEAvrXa23 in rice variety CBB23 are underlined. The PAM sequence, target sequence, and TATA box are highlighted in green, bold, and red, respectively. (b) Sequencing chromatograms of the xa23N46 promoter region carrying an intact EBEXoc/Xoo array in T0 line #3. (c) Morphology of N46(Xa23R) and N46 plants at the heading stage. (d) Comparison of panicles, grain lengths, and widths between N46(Xa23R) and N46 plants. (e) HR analysis of N46(Xa23R) and N46 in response to Xoo PH strains harbouring single TALEs. (f) Transcription assays of Xa23 in N46(Xa23R) challenged by each Xoo PH derivative. (g) Defence reactions of N46(Xa23R) to standard Xoo strains from China, Philippines, and Japan. (h–j) Statistical analysis of the lesion length of N46(Xa23R) and N46 challenged by standard Xoo strains from China (h), those from Philippines (i), and those from Japan (j). (k, l), Defence reactions of N46(Xa23R) and N46 to standard strains (k) and field isolate (l) of Xoc. (m, n), Statistical analysis of the lesion length of N46 and N46(Xa23R) challenged by standard strains (m) and field isolates (n) of XocP values were calculated by t-test. **, P < 0.01; ***, P < 0.001; ****, P < 0.0001. In (g, k, l), R: N46(Xa23R).

 

After a screen of 79 hygromycin-resistant independent lines by PCR amplification (Figure S2) and Sanger sequencing, we identified three homozygous lines (#3, #12, and #60) which carried intact EBEXoc/Xoo array in the forward orientation (Figure 1b, Table S2). Transgene-free edited plants were identified in T1 populations (Figure S3; Table S4). Among them, the identity of homozygous plant #3–7 [named N46(Xa23R)] was verified by whole-genome sequencing. T2 and T3 progenies of N46(Xa23R) were planted in the paddy field, and no significant differences in major economic traits were observed compared with N46 (Figure 1c,d; Figure S4; Table S3), suggesting that the promoter-editing of xa23 does not cause growth penalty in N46.

 

Semi-quantitative RT-PCR analysis and HR assay revealed that the edited xa23 gene with the EBEXoc/Xoo array insertion is responsive to the different TALEs derived from the corresponding bacterial pathogens and regains the HR-eliciting activity in N46(Xa23R) (Figure 1e,f). Thus, 20 standard Xoo strains (seven from China, 10 from Philippines and three from Japan), which were known for their virulence or weakly virulence in N46, were selected and inoculated to N46(Xa23R) plants. Two weeks after inoculation, N46(Xa23R) exhibited robust resistance (reduced lesion lengths) against all strains compared with N46 (Figure 1g–j). Also, we challenged N46(Xa23R) plants with another 30 virulent Xoo isolates, which were collected from the paddy fields in China during the BB epidemic in recent years and known for virulence in N46. As a result, N46(Xa23R) plants were highly resistant to these field isolates (Figure S5). To examine the BLS resistance of N46(Xa23R) plants, two representative Xoc strains (RS105 and BLS256) were first tested. We observed typical HR in N46(Xa23R), whereas leaf streak lesions in N46 for both strains (Figure 1k,m). Next, another 28 virulent field isolates of Xoc were included. We observed that bacterial leaf streak lesions in N46(Xa23R) plants were significantly reduced compared with the control (Figure 1l,n). Combined, these data suggest that the EBEXoc/Xoo array renders N46(Xa23R) plants broad-spectrum resistance to a wide range of virulent Xoo and Xoc strains tested here (Figures S6 and S7). In other words, engineering the endogenous xa23 gene by EBE stacking in its promoter broadens Xa23's function in defence responses against different bacterial pathogens.

 

In the co-evolutionary arms race between hosts and pathogens, resistance conferred by a single R gene is often short-lived and is rapidly overcome by new pathogen strains bearing mutation events in relevant effector genes (Xu et al., 2022). In this regard, we assume that N46(Xa23R) line and its derived resistant rice lines by cross-breeding would be virtually impregnable to pathogen evolution and exhibit rice durable resistance given that the engineered Xa23 is responsive to multiple core virulence TALEs of both Xoo and Xoc. Overall, here we present a feasible promoter-editing strategy of executor gene for generating novel rice germplasms and upgrading current commercial japonica rice cultivar with robust, durable and broad-spectrum resistance to BB, especially to BLS, without defence-growth trade-off.

 

See https://onlinelibrary.wiley.com/doi/10.1111/pbi.14233

 

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