Genome Editing of eIF4E1 in Tomato Confers Resistance to Pepper Mottle Virus

Many of the recessive virus-resistance genes in plants encode eukaryotic translation initiation factors (eIFs), including eIF4E, eIF4G, and related proteins. Notably, eIF4E and its isoform eIF(iso)4E are pivotal for viral infection and act as recessive resistance genes against various potyviruses in a wide range of plants. In this study, we used Clustered Regularly Interspaced Palindromic Repeats/CRISPR-associated protein 9 (CRISPR/Cas9)-mediated targeted mutagenesis to test whether novel sequence-specific mutations at eIF4E1 in Solanum lycopersicum (tomato) cv. Micro-Tom could confer enhanced resistance to potyviruses. This approach produced heritable homozygous mutations in the transgene-free E1 generation. Sequence analysis of eIF4E1 from E0 transgenic plants expressing Cas9 and eIF4E-sgRNA transcripts identified chimeric deletions ranging from 11 to 43 bp. Genotype analysis of the eIF4E1-edited lines in E0, E1, and E2 transgenic tomato plants showed that the mutations were transmitted to subsequent generations. When homozygous mutant lines were tested for resistance to potyviruses, they exhibited no resistance to tobacco etch virus (TEV). Notably, however, several mutant lines showed no accumulation of viral particles upon infection with pepper mottle virus (PepMoV). These results indicate that site-specific mutation of tomato eIF4E1 successfully conferred enhanced resistance to PepMoV. Thus, this study demonstrates the feasibility of the use of CRISPR/Cas9 approach to accelerate breeding for trait improvement in tomato plants.

The eIF protein eIF4E is a component of a multiprotein complex that aids the initiation of protein translation by enabling recognition and interaction with the mRNA cap structure and recruitment of ribosomes. The viral genome-linked protein (VPg) of potyviruses is covalently connected to the 5′ end of viral RNA and acts as an analog of the eukaryotic mRNA cap structure during protein translation (Wang, 2015). The physical interaction between the host factor, eIF4E (or its homolog eIF (iso)4E), and VPg is crucial for potyvirus infectivity (Miyoshi et al., 2006;Robaglia and Caranta, 2006;Hwang et al., 2009;Kim et al., 2013;Kim et al., 2014;Tavert-Roudet et al., 2017;de Oliveira et al., 2019). Moreover, mutations in these host factors can inhibit the interaction between the host factor and the VPg, and consequently inhibit viral proliferation and host infection (Duprat et al., 2002;Lellis et al., 2002;Sato et al., 2005;Rodrıǵuez-Hernańdez et al., 2012).
The majority of naturally occurring plant recessive resistance genes have been mapped to mutations in genes encoding the isoforms of the translation initiation factors eIF4E and eIF4G that hinder their interactions with viral RNAs or proteins (Kang et al., 2005a;Ruffel et al., 2006;Le Gall et al., 2011;Wang and Krishnaswamy, 2012;Lee et al., 2013). Natural recessive resistance to potyviruses has been exploited in numerous breeding programs (Kang et al., 2005b;Ruffel et al., 2006;Lee et al., 2013). However, conventional breeding requires massive backcrossing to introgress the trait of interest into an elite background; furthermore, the availability of favorable alleles in natural populations is limited. New alleles can be created by random mutagenesis (Nicaise, 2014), but this requires laborintensive, time-consuming screening of large populations to select mutants with desirable properties.
Advances in genome-editing tools have accelerated site-directed mutagenesis in crops. Clustered regularly interspersed palindromic repeats (CRISPR)/CRISPR-associated protein 9 (CRISPR/Cas9) is a targeted genome-editing technique derived from the adaptive immune mechanism of Staphylococcus pyogenes against bacteriophages (Hsu et al., 2014). Since its first report in 2012, CRISPR/Cas9 has become the technology of choice for genome editing due to its ease, low cost, and significantly shorter timeframe for construct preparation compared to those of other genomeediting tools, such as zinc finger nucleases (ZFN) and transcription activator-like effector nucleases (TALENs) (Cong and Zhang, 2015). CRISPR/Cas9 has been utilized for site-directed mutagenesis in microbes, animals, human cells, and plants (Jiang et al., 2013;Wu et al., 2013;Zhang et al., 2017;Shapiro et al., 2018). Precise genome editing of host factors can be deployed for development of recessive genetic resistance against viral diseases in plants (Wang, 2015). However, the application of CRISPR/Cas9 tools to improve plant resistance to pathogens has not been widely explored, with only a few reports to date (Chandrasekaran et al., 2016;Pyott et al., 2016;Wang et al., 2016;Peng et al., 2017;Gomez et al., 2019). Recently, CRISPR/Cas9 genome editing of plants for potyvirus resistance has been reported. For instance, knockout of the gene eIF(iso)4E in the model crop plant Arabidopsis thaliana was shown to confer resistance to turnip mosaic virus (TuMV) (Pyott et al., 2016). In another study, CRISPR/Cas9-mediated knockout of eIF4E in cucumber resulted in broad-spectrum viral resistance to several plant viruses, including cucumber vein yellowing virus (CVYV), zucchini yellow mosaic virus (ZYMV), and papaya ringspot mosaic virus-w (PRSV-W) (Chandrasekaran et al., 2016). Similarly novel allelic variants of rice eIF4G generated through CRISPR/Cas9 mediated genome editing conferred resistance to rice tungro spherical virus (Macovei et al., 2018). Thus, targeted genome editing can be expected to accelerate plant breeding for diseaseresistant crop plants by facilitating the introduction of precise and predictable genetic changes directly into an elite strain background.
In this study, to introduce allelic variations in the eIF4E gene, we mutated eIF4E1 in the tomato cultivar Micro-Tom using CRISPR/Cas9 technology and Agrobacterium-mediated transformation, and bred the E 0 transgenic plants carrying eIF4E1 mutations to produce E 1 and E 2 progeny. We then tested the resistance of the homozygous mutant lines to the potyviruses TEV and PepMoV. The homozygous Micro-Tom mutant lines carrying genome-edited eIF4E1 were resistant to PepMoV, although not to TEV, and showed normal plant growth and development after PepMoV challenge. Furthermore, by segregation in the E 1 generation, we were able to select virusresistant plants that carried an edited eIF4E1 gene or genes but not the introduced transgene. Altogether, this study thus provides important information for understanding and analyzing tomato CRISPR/Cas9 mutants, and accelerating breeding for trait improvement.

Plant Materials and Growth Conditions
Seeds of Solanum lycopersicum cv. Micro-Tom were surface sterilized in 70% ethanol for 1 min and in 2% NaOCl with one drop of Tween 20 for 15 min, and then rinsed four or five times with sterilized water. Seeds were germinated on 1/2 MS medium (Murashige and Skoog, 1962) containing 20 g/L sucrose and 8 g/ L agar agar. All cultures were grown at 24°C with a 16 h light/8 h dark cycle under cool fluorescent light. Cotyledons of 7-8-dayold seedlings, before the appearance of the first true leaves, were used as explants for tissue culture.
Single Guide RNA (sgRNA) Design and Vector Construction eIF4E is a plant cellular translation initiation factor essential for potyvirus infection, and mutations in the eIF4E gene can confer resistance to potyviruses. In this study, we aimed to use CRISPR/ Cas9-mediated targeted genome editing of eIF4E1 (GenBank: AY723733) to develop potyvirus-resistant tomato plants. The gene phytoene desaturase (PDS) (GenBank: EF650011), encoding the key enzyme in carotenoid biosynthesis, was used as a control gene to test genome-editing efficiency due to the easily detectable photobleached phenotype of PDS mutants. To design sgRNAs, we identified appropriate target sgRNA sequences using the CCTop -CRISPR/Cas9 target online predictor (https://crispr. cos.uni-heidelberg.de/index.html). sgRNAs targeting the first exon with high prediction scores were used for genome editing (Figure 1), since mutations in the 5′ region or first exon would increase the chance of creating nonfunctional proteins by causing frameshifts or early stop codons. These sgRNAs were cloned under the control of the AtU6-26 promoter into a binary vector (pHSE401) carrying a maize codon-optimized Cas9 gene driven by the CaMV 35S promoter. The 23-bp sequences of the corresponding primers, PDSgRNA_F and PDSgRNA_R (or eIF4E1gRNA_F and eIF4E1gRNA_R), flanked by a BsaI recognition site, were annealed and cloned into a BsaI site in the vector pHSE401 by Golden Gate cloning according to a previously reported method (Xing et al., 2014). CRISPR/Cas9 vectors were transformed into Agrobacterium tumefaciens strain GV3101 by electroporation.

Agrobacterium-Mediated Tomato Transformation
A single Agrobacterium colony was inoculated into 15 mL of liquid LB medium containing 50 mg/mL kanamycin and 50 mg/mL rifampicin and incubated in a shaking incubator at 28°C for 12-16 h until it reached an OD 600 of 0.6. The Agrobacterium suspension was then centrifuged at 8,000 rpm for 10 min at 20°C to collect the pellet. The pellet was completely resuspended in liquid 1/2 MS medium containing 3% sucrose and 200 mM acetosyringone. Cotyledons from 7-8-day-old seedlings were excised under sterile conditions, and then the tip of each cotyledon was removed, sectioned transversely into two fragments, and incubated adaxial side down in a preculture medium consisting of MS with 30 g/L sucrose, 1 mg/L 1-naphthaleneacetic acid (NAA), 1 mg/L benzylaminopurine (BAP) for 2 days, and 8 g/L agar agar. Explants were co-cultured in the Agrobacterium suspension for 20 min, transferred to sterile filter paper to briefly drain excess suspension, and then placed on the same medium used for preculture and incubated for 2 days. Then, explants were transferred to shoot induction medium consisting of MS with 30 g/L sucrose, 2 mg/L trans-zeatin riboside, 0.1 mg/L indole-3-acetic acid (IAA), 20 mg/L hygromycin, 250 mg/L carbenicillin, and 8 g/L agar agar for 4-6 weeks. Explants with shoot buds were moved to shoot elongation medium consisting of MS with 30 g/L sucrose, 1 mg/L trans-zeatin riboside, 0.1 mg/L IAA, 20 mg/L hygromycin, 250 mg/L carbenicillin, and 8 g/L agar agar. Tomato shoots of about 2 cm height were cut and transferred to rooting medium consisting of MS with 30 g/L sucrose, 1 mg/L IAA, 10 mg/L hygromycin, 250 mg/L carbenicillin, and 8 g/L agar agar. Rooted plants were transferred into plastic pots containing potting mixture (Hanarum, Minong Fertilizer, Korea) and kept in a growth room maintained at 24°C and a 16 h light/8 h dark cycle.

Nucleic Acid Extraction and Molecular Characterization
Genomic DNA (gDNA) was extracted from leaf samples of putative transgenic plants by the cetyltrimethylammonium bromide (CTAB) method (Porebski et al., 1997). gDNA was quantified by NanoDrop spectrophotometer (Nanodrop Technology, Inc., Wilmington, DE, USA) and diluted to 100 ng/mL. The status of putative transgenic plants was confirmed by PCR using Hpt (Hygromycin phosphotransferase) and Cas9 gene-specific primers (Table 1). PCR conditions were as follows: 94°C for 5 min, followed by 34 cycles of denaturing at 94°C for 30 s, annealing from 55°C for 30 s, 72°C extension for 30 s, and then final extension at 72°C 5 min. Total RNA was extracted from young leaf tissues using an MG RNAzol kit according to the manufacturer's instructions (MGmed, Seoul, Korea). The integrity and concentration of the total RNA were analyzed on a 1% agarose gel and a NanoDrop ND-1000 spectrophotometer (Thermo Scientific, Wilmington, USA), respectively. One microgram of total RNA was used to synthesize complementary DNA (cDNA) using an EasyScript Reverse Transcriptase kit (TransGen, Beijing, China) with oligo(dT) primers. The resulting cDNAs were used for further expression analysis. RT-PCR was performed as described for gene confirmation using 1 µL cDNA as a template.

Mutation Detection
The transgenic plants were genotyped for mutation detection using primers flanking sgRNA target regions. PCR products were purified using a LaboPass PCR clean-up kit (Cosmo Genetech, Seoul, Korea). The purified amplicons were also cloned into the TA cloning vector, pMD20-T (Mighty TA-cloning kit, TAKARA, Shiga, Japan), according to the manufacturer's instructions, and positive colonies were selected by blue/white colony selection. Plasmids were extracted from least five positive clones and sequenced using M13F and M13R primers at Bionics (Seoul, Korea). To identify CRISPR/Cas9 induced mutations, DNA sequence alignments were performed using Lasergene's SeqMan program (DNASTAR, Madison, WI, USA). Mutations in E 1 progeny was detected by directly sequencing the PCR amplicons of the target region as well as by sequencing positive TA clones.

Virus Inoculations
For virus inoculum preparation, frozen stocks of TEV-HAT and PepMoV-Vb1, which were stored at -80°C, were used to inoculate 3-week-old Nicotiana benthamiana plants. Frozen inocula were ground in 0.1 M potassium phosphate buffer (pH 7.0), mixed with 400-grit carborundum, and rubbed on the lower leaves of N. benthamiana. After 10-20 min of inoculation, leaves were washed with distilled water (Hull, 2009). To inoculate the tomato plants, infected N. benthamiana leaves were collected and inocula were prepared as mentioned above. Tomato plants with two fully expanded leaves were used for viral inoculation. Two pairs of cotyledons were inoculated; inoculated and non-inoculated control plants (mock) were grown in a growth chamber (16 h light and 8 h night under white fluorescent light). To ensure viral infection, plants were reinoculated 7 days after the first inoculation.

Evaluation of Resistance to Potyviruses
After viral inoculation, plants were monitored regularly for the appearance of symptoms. Leaf tissue was tested for the presence of virus using double-antibody sandwich enzymelinked immunosorbent assay (DAS-ELISA), according to the manufacturer's instructions (Agdia, Inc. Elkhart, IN, USA). Virus accumulation was tested at 7/20 days post inoculation (DPI). DAS-ELISA was performed to detect the accumulation of the coat protein (CP) of TEV or PepMoV. Three replicates of inoculated and upper non-inoculated leaves of E 1 lines were used for ELISA analysis. Absorbance of samples at 405 nm was measured using a microplate reader (Biotek, VT, USA). The statistical significance of the data was performed with Student's t-test using Microsoft Excel 2016 (Microsoft, Redmond, WA, USA).

Generation and Characterization of Genome-Edited Tomato Plants
To develop tomato plants with edited PDS and eIF4E1 genes, we delivered the pHSE401-PDS and pHSE401-eIF4E1 CRISPR/Cas9 constructs harboring the respective sgRNAs into S. lycopersicum cv. Micro-Tom via Agrobacterium transformation. We transferred putatively genome-edited shoots regenerated from the callus to shoot elongation medium and allowed them to elongate, and then cut elongated shoots and transferred them to rooting medium to encourage root formation. We observed the photobleached phenotype in four out of 113 PDS-edited explants transformed with the pHSE401-PDS construct (Figure 2A), demonstrating about 3.5% gene-editing efficiency of the PDS gene with both copies expected to be edited. However, the PDS-edited, photobleached shoots failed to develop into rooted shoots (Figure 2A). After sampling the photobleached shoots of the PDS-edited explants and putative eIF4E1-edited plants, we confirmed the integration of the transfer DNA (T-DNA) by genomic DNA PCR of the samples using Cas9-and Hpt-specific primers (Supplementary Figure  S1A). We obtained PCR products with the expected amplicon sizes from the photobleached shoots, demonstrating the successful integration of Cas9 and Hpt (Supplementary Figure S1A). We also regenerated 22 putative eIF4E1-edited transgenic plants, which we tested for the presence of the transgenes, the Cas9 and Hpt genes by PCR using transgene-specific primers (Supplementary Figure S1B). Sixteen of the 22 plants contained both Cas9 and Hpt, with a transformation efficiency of 72%. Furthermore, RT-PCR results confirmed the expression of the Cas9 gene in all the PCR positive plants (Supplementary Figure  S1C). No morphological changes were observed in eIF4E1edited plants.

Confirmation of CRISPR/Cas9-Induced Mutations
To confirm that the CRISPR/Cas9 editing had introduced mutations in the PDS gene, we performed PCR amplification of the target region from the albino tomato mutants using primers ( Table 1) that flanked the sgRNA target, and then sequenced the PCR products by Sanger sequencing. Sequence analysis showed two types of sequence variations: one-and twonucleotide deletions with breakpoints 3 bp upstream of the protospacer-adjacent motif (PAM) sequence ( Figure 2B). stop codons, preventing the expression of functional PDS protein ( Figure 2C). Similarly, we identified CRISPR/Cas9-induced mutations in eIF4E1 by sequencing the PCR amplicons of the sgRNA target-flanking region from the genomic DNA of 16 Cas9-positive tomato lines. Sequencing of the sgRNA target region revealed no mutant homozygous lines among the E 0 plants; 15 of the 16 putative transgenic plants showed mixed sequence peaks at the sgRNA target site compared to the wildtype target sequence ( Figure 2D), indicating that a mixture of mutant (reflective of CRISPR-Cas9-induced mutation) and wildtype alleles of eIF4E1 were present. A single plant, E0-10 ( Figure  2D) showed sequence peaks similar to that of wild-type target sequence, indicating no editing the in target region despite showing expression of the Cas9 gene. To further characterize the mutations in the E 0 plants, we randomly selected the E0-3 and E0-8 transgenic lines for further investigation by TA cloning and sequencing of the target region. The sequencing results for the TA clones from E0-3 and E0-8 revealed four different alleles of eIF4E1 ( Figure 2E), with indels and/or substitutions at various positions both in proximity to the sgRNA target and outside the immediate sgRNA target region. The presence of a mixture of different mutant alleles in each E 0 line suggested that active somatic mutation was occurring in the edited plants. Therefore, we advanced selected E 0 plants to the E 1 and E 2 generations to create homozygous mutant lines.
To reveal sequence variations of E 1 plants, we performed TA cloning and sequencing of amplicons of the target region in E 1 plants derived from lines E0-3 and E0-8. New mutation patterns were evident in the E 1 lines as compared to the E 0 plant, and two lines (E1 3-8 and E1 3-17) derived from E0-3 were homozygous for the expected 43-bp deletion ( Figure 4A). The E1 3-11 line was biallelic, carrying two deletions of 43 and 11 bp; two other lines (E1 3-9 and 3-15) showed a 29-bp deletion and a tandem insertion of 38 bp of adjacent repeat sequence, respectively ( Figure 4C); and the E1 3-19 line carried mixed mutations, with deletions of the unexpected sizes of 12, 13, and 15 bp ( Figure 4A). The three lines (E1 8-3, 8-5, 8-7) derived from the E0-8 plant were homozygous for the expected 11-bp, 43-bp, and 29-bp deletions and 38-bp insertion of a repeat sequence ( Figures 4A, C). The E1 8-1 line was biallelic, with a 43-bp deletion and a 29-bp deletion and 38-bp repeat-sequence insertion, whereas the E1 8-4 line had mixed mutations along with a wild-type allele ( Figure 4B). The presence of new mutation patterns in E 1 lines that differed from those in the E 0 plants suggested that active somatic mutation was occurring in the E 0 plants (Figures 2E and 4). Notably, one line, E1 3-8, had a homozygous edited eIF4E1 gene but no T-DNA. Overall, several homozygous and biallelic lines were recovered in the E 1 generation ( Table 2), along with a smaller proportion of mosaic mutants carrying different allelic variants ( Table 2).

Potyvirus Resistance in eIF4E1 Edited Plants
To investigate whether these CRISPR/Cas9-derived eIF4E1 mutants conferred resistance to TEV, we inoculated E1 3-8 (homozygous line) and E1 3-11 (biallelic line) plants with TEV ( Figure 5). TEV symptoms appeared as early as 7 DPI; the wild-type plant showed typical TEV symptoms, including vein clearing and several small chlorotic spots in the leaves. Both eIF4E1 mutant lines showed similar symptoms ( Figure 5A). To confirm virus infection, we performed DAS-ELISA analysis using inoculated lower and uninoculated upper leaves. We detected similar high amounts of virus coat protein accumulation in the E1 3-8 and E1 3-11 lines, indicating that the eIF4E1-edited lines were susceptible to TEV-HAT ( Figure 5B). We next assessed whether CRISPR/Cas9 eIF4E1 mutants could confer resistance to another potyvirus, PepMoV, by challenging three E 1 mutant lines (E1 3-8, E1 3-11, and E1 3-15) with PepMoV. PepMoV coat protein accumulated to a high level in both the inoculated and uninoculated upper leaves of the susceptible wild-type control ( Figure 5), whereas no coat protein accumulated in any of the three mutant lines in either the inoculated lower or uninoculated systemic leaves, confirming that the eIF4E1-edited lines were resistant to PepMoV ( Figure 5C).

DISCUSSION
Here we subjected the eIF4E1 gene to CRISPR/Cas9 gene editing with the aim of creating potyvirus resistance in S. lycopersicum Micro-Tom, as recessive resistance genes are considered to be confer more durable resistance than dominant resistance (R) genes (Kang et al., 2005a;Borrelli et al., 2018). In this study, we developed CRISPR/Cas9-edited tomato PDS and eIF4E1 mutants through Agrobacterium-mediated delivery of CRISPR/Cas9 and  sgRNA reagents. Sequencing of the PDS gene target region revealed that DNA double-strand edits occurred 3 bp upstream of the PAM site, resulting in indels of one or two nucleotides in PDS, as reported previously (Garneau et al., 2010;Jinek et al., 2012). All the indel mutations led to early stop codons, causing loss of PDS gene function. In the eIF4E-edited lines, indels occurred at various positions near the sgRNA target and in some cases extending beyond the sgRNA target and PAM region, creating premature stop codons and truncated eIF4E1 proteins (Supplementary Data File 1). Notably, we observed a 38-bp insertion of a repeat sequence as well as a 29-bp deletion in several of the gene-edited lines, E1 3-9, E1 3-15, E1 8-1, and E1 8-3; the mechanism leading to the insertion of this adjacent repeat sequence will require further investigation. Unlike PDS-targeted photobleached plants, the eIF4E1targeted mutant plants in the E 0 generation were chimeric, with mixtures of different allelic variations, and the E 1 generation comprised a mixture of homozygous, biallelic, and mosaic mutants. Increasing evidence suggests that transgenic plants can be chimeric in the E 0 generation. For example, chimeric lines have also been reported in T 0 (E 0 ) genomeedited Arabidopsis, tomato, rice, and soybean (Brooks et al., 2014;Feng et al., 2014;Ma et al., 2015;Pan et al., 2016;Pyott et al., 2016;Liu et al., 2020). One study identified only three nonmosaic mutants among nearly 300 lines of Arabidopsis created by editing of the gene RRP42 (Yan et al., 2017). The mosaicism of the E 1 mutants could then be due to the fact that in some edited lines, one or more wild-type alleles might escape detection in the E 0 generation but then be detected in later generations (Brooks et al., 2014;Zhang et al., 2014;Zhang et al., 2019;Liu et al., 2020). Furthermore, other new alleles created from late-arising chimeric tissues might also be overlooked in E 0 plants, resulting in different flowers carrying different alleles (Brooks et al., 2014). In agreement with this contention, in the present study, some of the E 1 plants produced by gene editing of eIF4E1 were chimeric, and furthermore mutations different from those identified in E 0 plants were observed in E 1 plants.
Notwithstanding these complications, we advanced the E 0 plants carrying diverse alleles of the target gene to the next generation, and selected E 1 lines carrying homozygous alleles from segregating populations, as reported in previous studies (Xu et al., 2015;Chandrasekaran et al., 2016;Pyott et al., 2016). Accordingly, sequence analysis of the E 1 lines identified both homozygous and biallelic eIF4E1 mutants, both of which would be expected to stably pass on their mutant status to their descendants (Chandrasekaran et al., 2016), consistent with this, homozygous mutant alleles were stably inherited in the E 2 progeny.
Previous studies in pepper suggest that eIF4E is a key factor in the interaction between viruses and their hosts. Mutations in eIF4E cause conformational shifts in the encoded proteins, interrupting the interaction between VPg and eIF4E and conferring plant resistance to the virus at the cellular level (Kang et al., 2005a). This implied that site-directed mutagenesis could be used to create dominant negative mutations or targeted silencing of host genes (Azevedo et al., 2002;Kang et al., 2005b;Kang et al., 2007). We therefore assessed our eIF4E-edited E 1 lines, with or without the Cas9 transgene, for resistance to potyviruses. Edited plants carrying mutations in eIF4E1 showed resistant to PepMoV. Asterisks indicate significant differences (*P < 0.01; **P < 0.05) between 'mock′ and 'treatments′ according to Student's t-test.
Consistent with this, we did not detect accumulation of coat protein in either inoculated or uninoculated leaves. However, E 1 plants carrying mutations in eIF4E1 showed typical TEV symptoms, and ELISA analysis confirmed the presence of systemic infection. Viral coat protein accumulated to high levels in both inoculated and uninoculated upper leaves of the homozygous E1 3-8 and biallelic E1 3-11 lines. These results contrast with the findings of an earlier study indicating that transgenic tomato plants overexpressing a recessive resistance allele of eIF4E (pvr1) from Capsicum chinense showed dominant resistance to TEV (Kang et al., 2007). The transgenic expression of the Capsicum eIF4E mutant allele was suggested to perturb the interactions required for viral susceptibility in a heterologous host system (Kang et al., 2007). However, the susceptibility of the edited plants to TEV in tomato that we observed here could be due to the redundant activities of eIF4E homologs (eIF4E1 and eIF4E2) coupled with the absence of a dominant negative allele whose protein product could interfere with the endogenous wild-type proteins and inhibit viral infection (Kang et al., 2007). Furthermore, an eIF4E1-knockout tomato plant selected from a TILLING population was reported to be susceptible to potyviruses because TEV could utilize either eIF4E1 or eIF4E2 for its replication in tomato . Thus, development of a TEV virus-resistant tomato line is hindered by the gene redundancy of eIF4E homologs. eIF4E1 and eIF4E2 doubleknockout plants would be expected to show a broad-spectrum resistance to a wide range of potyviruses ; however, care should be taken to ensure that mutations in both candidate genes do not impair the plant growth and development, as often occurs with double mutants (Mazier et al., 2011;Gauffier et al., 2016).

CONCLUSION
We used CRISPR/Cas9 gene editing to induce mutations in the tomato eIF4E1 gene by A. tumefaciens-mediated transformation. Evaluation of the mutation and inheritance patterns of this gene in the E 0 and later generations by sequencing revealed high proportions of chimeric mutant lines in the E 0 generation and of homozygous and biallelic mutants of eIF4E1 in the E 1 generation. The CRISPR/Cas9-mediated gene mutations were stably transmitted to the E 1 and E 2 descendants irrespective of the presence or absence of T-DNA. Although the presence of redundant eIF4E homologs apparently precluded TEV resistance in the eIF4E1 genome-edited Micro-Tom plants, an edited eIF4E1 with an early stop codon conferred resistance to PepMoV. Thus, our system enabled successful CRISPR/Cas9 editing of tomato eIF4E1, resulting in resistance to a common viral pathogen of Solanaceae; further research is planned to obtain homozygous E 0 plants and to extend this work to pepper (Capsicum species) to produce strains with broad-spectrum virus resistance.

DATA AVAILABILITY STATEMENT
The original contributions presented in the study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding author.