Potato cultivar ‘Desiree’ was used for gene amplification and genetic transformation. Plants were grown in vitro on Murashige and Skoog (MS) medium, under a luminous flux intensity of 3,000–4,000 Lx, 80% relative humidity, and a photoperiod of 16 h/8 h light/dark, at 25°C. The P. infestans strain (14-3) was kindly provided by Prof. Francine Gover, Wageningen University and Research (WUR), Netherlands. Tubers of six potato varieties ‘Zihuabai’ (ZHB), ‘Desiree’ (DXR), ‘Longshu No.7’ (L7), ‘Zhongshu No.4’ (ZS4), ‘Atlantic’ (DXY) and ‘Shepody’ (XPD), were planted in a nutrient pot and cultivated in a chamber under a luminous flux density of 18,000 Lx, 75% relative humidity, and a photoperiod of 16 h/8 h light/dark, at 25°C. These plants were used for expression profile analysis. Desiree seedlings cultivated in pots for 20 d were selected for induced expression.

Primers were designed using Primer 5.0 software and synthesized by the Beijing Hooseen Biotechnology Company, China. The primer sequences used in this study are listed in Supplementary Table 1 .

Luria-Bertani liquid medium (10 g tryptone, 5 g yeast extract, and 5 g NaCl) was prepared, and H₂O was added to bring the volume to 1,000 mL. YEB liquid medium (5 g beef extracts, 5 g tryptone, 5 g sucrose, 1 g yeast extract, MgSO₄·H₂O 0.5 g) with pH 7.0 was prepared, and H₂O was added to bring the volume to 1,000 mL. Agar powder (15 g) was added to each mixture media to prepare the corresponding solid medium. P. infestans was induced to produce zoospores at 4°C for 4 h. Zoospore suspensions were adjusted to a concentration of 5 × 10⁵ mL^-1 sporangia using a hemocytometer (Neubauer-improved, Germany). Approximately 10−15 μL of spore suspension was inoculated on plant leaves.

Relative expression quantitation was performed using Quantity one software for semi-quantitative RT-PCR (St Rab5b and PDS), and GAPDH was used as a reference gene. Q-PCR was performed on a LightCycler (96, Roche, Basel, Switzerland) using the SYBR Premix Ex Taq II Kit (TaKaRa Bio, Shiga, Japan). We analyzed the expression levels of ACS, LOX, NPR1, SOD, APX1, POD, CAT2, and PIO and used Actin as a reference gene.

Total RNA was extracted from potato plantlets grown for 30 d using the RNAiso reagent (TaKaRa Bio), and genomic DNA was extracted using the DNAiso reagent (TaKaRa). The quality of RNA and DNA was determined by performing gel electrophoresis on 1% agarose gels. The first cDNA chain was synthesized according to manufacturer instructions of a HiScript II reverse transcription Kit (Nanjing Vazyme Biotechnology Co., Ltd).

The PCR-amplification mixture (50 μL) included 10 μL of 5X Prime Star Buffer (Mg²⁺ plus), 4 μL of dNTP Mix (2.5 mM), 1 μL of Primer Rab5bF/Rab5bR, 1 μL of cDNA template, 0.5 μL of Prime STAR HS DNA Polymerase, and 32.5 μL of ddH₂O. Target fragments were purified using the EasyPure Quick Gel Extraction Kit (Beijing TransGen Biotech Company, China) according to manufacturer’s instructions. Plasmid extraction was performed according to the manufacturer’s instructions of the TIANprep Mini Plasmid Kit II (Beijing TIANGEN Biotech Company). PLG-Rop and pBIA1300-221 were provided by Prof. Yan Zhao, from the Institute of Genetics and Development, Chinese Academy of Sciences, Beijing, China. WUR kindly provided the P. infestans strains, pTRV1 and pTRV2 vectors. Fastdigest endonucleases KpnI, BglII, XbaI, and SacI were purchased from Thermo Fisher Scientific, (Waltham, MA, USA).

Phylogenetic analyses were performed with DNAMAN software. The Rab or Rab5b sequences of Oryza sativa (AF323991), Nicotiana benthamiana (DQ335217), Solanum tuberosum (ABK96799 and AK323357), Hevea brasiliensis (KC577146), Physcomitrella patens (AB379973), Phoenix dactylifera (AK287492), Nicotiana sylvestris (X63875), Mangifera indica (KF768563), Athaliana (D89824), Selaginella moellendorffii (KF516567), Medicago sativa (X79278), Triticum aestivum (X59133), Lotus japonicus (Z73939), and Medicago truncatula (BT147767) were retrieved from Genbank separately.

The StRab5b gene was linked to the pEASY-Blunt Simple cloning vector and transferred into DH5α cells (TransGen Biotech Company, Beijing, China). Positive DH5α colonies were screened and sequenced. Target gene purification was performed using the EasyPure Quick Gel Extraction Kit (TransGen Biotech Company). Recombinant vectors PLG-Rop and pEASY-Blunt Simple-StRab5b were digested with BglII and KpnI to obtain the PLG-StRab5b vector. Recombinant plasmid PLG-StRab5b and vector pBIA1300-221 were digested with XbaI and SacI to obtain the recombinant plasmid pBIA1300-StRab5b. Plasmid pBIA1300-StRab5b was transferred into Agrobacterium tumefaciens GV3101 for preservation.

The length and width of the leaf lesions formed on the plant leaves were measured using an electronic caliper (DL91150, China). Each lesion was measured three times (Vleeshouwers et al., 1999). The lesion area (A1) was calculated using the formula: A1 = 1/4π × length × width.

Inoculation method of P. infestans for analysis of the expression profile of StRab5b was described as follows. The seedlings of different potato varieties were cultured in a pot (10 cm height * 10 diameter) for 50 d. The abaxial surface of potato leaves was scratched with sterile toothpicks and inoculated with 10 uL zoospore suspension (5 × 10⁵ mL^-1) of P. infestans on one side; the other side was inoculated with water as control. The inoculated leaves were placed in a plastic box with wet filter paper on the bottom and kept in an incubator (day and night 16 h/8 h, 25/18°C).

Induction of StRab5b after inoculation with P. infestans: Potato seedlings (‘Desiree’) were planted in a pot (10 cm height * 10 diameter) for 20 d, then inoculated with 10 μL of sporulation of P. infestans (5 × 10⁵ mL^-1). Then, inoculated leaves were collected at 0, 12, 24, 48, 72, 96, and 108 h post-inoculation (hpi). Using potato GAPDH as a reference gene, RT-PCR was performed to detect the relative expression levels of StRab5b, and the results were analyzed using Quantity one software.

A. tumefaciens containing pBIA1300-StRab5b and pBIA1300 were inoculated in 10 mL YEB liquid medium (100 μg/mL rifampicin and 50 μg/mL kanamycin). The oscillating culture was incubated overnight at 180 rpm, followed by centrifugation for 2 min at 7,104×g to collect the bacteria; then, the culture was resuspended in a liquid mixture containing 150 μM acetyleugenone, 10 mM MgCl₂, and 10 mM MES. The bacterial solution was suitable for use when the OD₆₀₀ value reached 0.5–0.6. The bacterial liquid (15–20 μL) was drawn using a needle-free syringe, injected into the right side of the abaxial surface of the N. benthamiana leaf, and incubated for 24 h (night and day alternate 16 h/8 h) at 21°C. The N. benthamiana leaves were inoculated with P. infestans spores and incubated for 4 h at 4°C before being transferred to a 21-23°C incubator with 80% humidity. The lesion area was measured at different inoculation time points.

Recombinant vectors pTRV2 and pEASY-Blunt Simple-StRab5b were digested with XbaI and SacI to construct the silence-expression vector pTRV2-Rab5b (98% amino acid identity with Rab5b of N. benthamiana). The Agrobacterium tumefaciens vector pTRV1 was provided by WUR. Plasmid pTRV2-Rab5b was then transferred to A. tumefaciens GV3101. A. tumefaciens plasmids were resuspended with VIGS mixture containing 20 mM MgCl₂, 100 mM MES, and 20 mM acetosyringone. The photobleaching phenotype was obtained by inhibiting the expression of endogenous phytoene desaturase gene (PDS). A 536 bp fragment of StPDS (95% amino acid identity with PDS of N. benthamiana) was linked with pTRV2 and transformed into A. tumefaciens GV3101 (pTRV2-PDS). Thereafter, A. tumefaciens containing pTRV1 was mixed with pTRV2-PDS or pTRV2-StRab5b at a 1:1 ratio after the OD₆₀₀ value reached 0.5−0.6. A needle-free syringe was used to draw 20 μL of the bacterial suspension to inject into N. benthamiana and potato leaves. Three to four leaves of each plant were inoculated. After photobleaching, leaf samples were collected to identify the relative expression levels of PDS, StRab5b and StRab5b homologous gene using RT-PCR, after 25 d (N. benthamiana) and 60 d (potato). GAPDH was used as a reference.

Potato stems (2 cm long) were placed in the suspended Agrobacterium solution, soaked for 10 min, and dried with sterile filter paper. Stems were then transferred to the co-culture medium (MS + 1.0 mg/L IAA + 0.2 mg/L GA3 + 2.0 mg/L ZT + 0.5 mg/L 6-BA, pH 5.8) and cultured in darkness for 2–3 d. Thereafter, they were transferred to the bud inductive-differentiation medium (MS + 1.0 mg/L IAA + 0.2 mg/L GA3 + 2.0 mg/L ZT + 0.5 mg/L 6-BA + 50 mg/L Kan + 300 mg/L TMT, pH 5.8), and incubated at 25°C under a light intensity of 4,000 μmol/m²·s, and a photoperiod of 16 h/8 h. The medium was replaced at 2-week intervals. When adventitious buds grew to 2.0 cm, they were transferred to the rooting medium (MS + 50 mg/L Kan, pH 5.8). When plantlets were formed, total leaf RNA was extracted, and positive transgenic plants were identified using PCR and q-PCR separately.

Leaves infected with P. infestans were decolorized in anhydrous ethanol by boiling for 2 to 2.5 h. Decolorized leaves were placed in 0.5% trypan blue solution (0.5 g trypan blue dissolved in 100 mL distilled H₂O), stained for 10–15 min, washed twice with distilled water, and then treated with lactophenol water (lactic acid, phenol, and dd H₂O mixed in a ratio of 1:1:1).

Leaves infected with P. infestans were soaked overnight in 1 mg/mL 3,3′-Diaminobenzidine (DAB) dyeing solution (0.1 g DAB dissolved in 100 mL distilled water, pH 3.8). The leaves were decolorized by boiling for 2 h in absolute ethanol, then treated with lactophenol water (lactic acid, phenol, and water were mixed in a ratio of 1:1:1), and photographed. The H₂O₂ content of P. infestans-inoculated transgenic plants was determined as described by Zhang et al. (2014).

Activities of APX CAT, POD, and SOD enzymes were determined according to manufacturer’s instructions using the corresponding kits (APX-1-W, CAT-1-W, POD-1-Y and SOD-1-W), purchased from Suzhou Keming Biotechnology Co., Ltd., (Suzhou, China). The infected leaf samples were collected from all treated plants. The data were analyzed using SPSS 16.0.

0.1 g smples collected from potato leaves were cut into pieces, and grinded into powders in liquid nitrogen. The content of JA in potato was determined by plant JA ELISA Kit (Jiangsu Jingmei Biological Technology Co., Ltd) (Yi et al., 2020).

The potato StRab5b gene was amplified using Prime STAR HS DNA Polymerase (Takara). The fragment identified via agarose gel electrophoresis and the amplicon size was approximately 607 bp. To analyze the conserved domains of StRab5b, Rab 5b proteins isolated from rice, N. benthamiana, lotus, and Physcomitrella patens were retrieved from Genbank and used for multi-sequence analysis. The results suggested that StRab5b contained the basic general characteristics of Rab proteins, including RabF2 (83−87), RabF4 (YYRGA, 102−106) and RabF5 (131−135) domains, which are the conserved domains of the Rab proteins. Additionally, it also contained the GTP/GDP binding domain, phosphate binding loop G1 (39−46), G2 (79−80), and the coordination of GTP β and γ phosphate motifs G3 (88−91) and G5 (176−178), binding motifs NKAD (146−149) and ETSA (174−177) ( Figure 1A ). Therefore, the potato StRab5b protein belongs to Rab protein family.

Furthermore, the phylogenetic tree was constructed with StRab5b and the other 15 Rab proteins, derived from Oryza sativa, Nicotiana benthamiana, Solanum tuberosum, Hevea brasiliensis, Physcomitrella patens, Phoenix dactylifera, Nicotiana sylvestris, Mangifera indica, Arabidopsis thaliana, Selaginella moellendorffii, Medicago sativa, Triticum aestivum, Lotus japonicus, and Medicago truncatula, showed that StRab5b exhibited the highest similarity (95%) with NbRab5b, whereas, it showed the lowest similarity (44%) with TaRab ( Figure 1B ).

The relative expression levels of StRab5b in ‘ZHB’, ‘XPD’, ‘L7’, ‘DXR’, ‘ZS4’, and ‘DXY’ showed a decreasing tendency ( Figure 2A ). The expression profiles indicated that the expression levels of StRab5b differed substantially among different organs; the highest expression was in young leaves, followed by expression in stems, old leaves, and roots ( Figure 2B ). The tendency of symptoms in ‘Desiree’ leaves at different time points increased firstly at 12 hpi, followed by reaching the highest point 72 hpi, then dropping to basal level at 108 hpi, indicating the induction of StRab5b by P. infestans ( Figures 2C, D ).

Transient expression of StRab5b in N. benthamiana leaves was performed via infiltration, followed by inoculation with P. infestans. The lesions on the control leaves gradually increased after inoculation, and reached the largest size (102.1 mm²) at 108 hpi; it is much bigger than the lesion size on leave which transiently expressed StRab5b, indicating that transiently ectopic expression of StRab5b could enhance N. benthamiana resistance to P. infestans ( Figure 3A ).

To verify the function of StRab5b on regulating the resistance to P. infestans, VIGS was used to silence StRab5b and NbRab5b in potato and N. benthamiana respectively. PDS gene was taken alone as an indicator. When photobleaching was observed on N. benthamiana and potato leaves at 25 and 60 dpi, respectively, the expression of StRab5b, NbRab5b and PDS genes was quantified using qRT-PCR and the average silencing efficiencies of StRab5b, NbRab5b and PDS were 59%, 65%, and 100%, respectively ( Figures 3B, D ). The leaf lesion was recorded upon inoculation with P. infestans. The lesion area on the infiltrated leaves was 259.9, 253.4, 284, and 152.8 mm² at different time points, which were significantly larger than that on control leaves at the same time point. The average increase in the rate of the lesion area was 3.1 mm²/h ( Figure 3C ). However, the leaf lesion areas of potato were 67.4, 83.7, 63.6, and 40.1 mm² at 96 hpi, respectively ( Figure 3E ).

Positive transgenic lines were obtained via Agrobacteria-mediated transformation of StRab5b in potato cultivar ‘Desiree’ ( Figure 4A ). The relative expression levels of StRab5b among the nine transgenic lines were variable, but significantly higher than its expression levels in control plants. After 96 hpi, the leaf lesions among three transgenic lines (2, 3, and 8) did not differ extensively (5.1, 5.4, and 5.6 mm², respectively) ( Figure 4C ). Meanwhile, the lesions on control leaves increased gradually and reached 96.9 mm² at the same inoculation point ( Figure 4B ). The dead cells on potato leaves were monitored with trypan blue staining; much less blue color was observed on transgenic leaves, indicating a lower number of dead cells on transgenic leaves compared with those in control leaves ( Figure 4D ). However, Quantitative analyze the amount of colonization of P. infestans showed that there were significant differences among the three transgenic lines and EV. In addition, the phenotypic characteristics of transgenic plants showed that the stems, leaves and tubers of transgenic plants presented as red, while the control remained green ( Supplementary Figures 1A, B ). The anthocyanin accumulation in leaves and tubers of transgenic lines were greatly higher than that in the EV control ( Supplementary Figure 1C ).

DAB staining was performed to detect whether H₂O₂ was involved in the resistance of StRab5b to late blight. A brownish color was observed in the StRab5b transgenic leaves at 24 hpi and the color deepened at 48 and 96 hpi. However, no signal was observed in control leaves at 24 hpi, and brownish color on control leaves was lighter than that on the transgenic leaves ( Figure 5A ). The quantification of H₂O₂ accumulation is shown in Figure 5B . The accumulation of H₂O₂ increased after inoculation, peaked at 72 hpi, then decreased in three transgenic and control plants. Compared with the H₂O₂ accumulation level in control (0.097 μmol/g), the highest H₂O₂ level of 0.156 μmol/g was detected in transgenic line 2 at 72 hpi, followed by other two transgenic lines 3 and 8 with values of 0.136 and 0.132 μmol/g, respectively. The value of H₂O₂ was significantly higher than that in control plants after inoculation. These results suggested that StRab5b positively regulates potato resistance through H₂O₂ accumulation.

Four antioxidant enzyme activities (APX, CAT, POD, and SOD) were monitored after inoculation. The results suggested that APX, CAT, POD, and SOD activities in StRab5b-transgenic leaves were substantially higher than those in control plants at different inoculation time points ( Figure 6 ). Particularly, SOD, POD, and APX showed a decreasing to- increasing pattern after inoculation, whereas, CAT showed an increasing to- decreasing pattern. Maximum activities of APX and SOD appeared at 72 hpi (54408.5 nmol/min·g and 2180.2 U/g), maximum activities of POD were 566.8 U/g at 96 hpi, except CAT, which had 2 peaks at 48 hpi and 96 hpi (353.1 and 376.8 nmol/min·g), respectively. The expression levels of these four genes (APX1, CAT2, POD, and SOD) that encode ROS scavenge enzymes were examined using qPCR after inoculation. The relative expression levels of four genes are consistent with the trend of enzyme activities. The maximum relative expression levels of APX1, CAT2, POD, and SOD genes were 5.3, 4.2, 6.2, and 7.5-fold, respectively.

Signaling pathways associated with SA, JA, and ET are directly involved in plant resistance to pathogens. To determine whether JA, SA, or ET are involved in StRab5b-mediated resistance to P. infestans, several marker genes related to different signaling pathways were analyzed at different time points. The results suggested that the expression levels of LOX and JA content in three transgenic lines (2, 3, and 8) were induced at 24 hpi and subsequently dropped at 48 hpi, followed by reaching the highest level at 72 hpi (158.2, 140.2, and 124.5-fold expression levels in the LOX gene, and 33.2, 24.4, and 20.7 ng/g JA content, respectively); moreover, JA content in transgenic plants was significantly higher than that in EV. Whereas, both NPR1 and ACS showed a different induction pattern compared with the LOX gene. They reached the peak at 24 hpi, then decreasing gradually. However, if we compared to the expression of the three marker genes, the induction of LOX was much more dramatic than ACS or NPR1. The induction rate was 67.5-fold at 24 hpi and 141.0-fold at 72 hpi separately, indicating that JA was the dominant molecular signal, which was involved in StRab5b-mediated resistance against P. infestans ( Figure 7 ).

Protein StRab5b is an important member of the small G protein Rab family that differs from previously characterized StRab proteins in amino acid structure and domains. The conserved domain motif RabF2 (YYRGA) of the StRab5b was analyzed using multiple sequence alignment. The guanine-binding motif NKAD and the guanine-binding and dissociation motif ETSA were consistent with the expression of TaRab5b protein (Chen et al., 2005). The specific motifs of G1, G3, G5, RabF4, and RabF5 were consistent with those of Dunaliella salina and potato StRab proteins. Although the homology of potato StRab and StRab5b was only 46% at amino acid level, StRab5b showed a structural and functional similarity to the Rab protein (Gao et al., 2012; Yu et al., 2013). Therefore, we replicated the StRab5b gene, analyzed its expression profile, and induced expression.

In this study, the relative expression levels of StRab5b were variable among different tissues. The highest expression level was detected in young leaves, followed by stems, old leaves and roots. This is in line with the order of the relative expression levels of another small G protein, StRac (Zhang et al., 2020). Additionally, the relative expression levels of StRab5b among different varieties is also variable, the order from higher to lower is ZHB, DXR, L7, ZS4, DXY, and XPD. It is also partially confirmed by the results that the relative expression of StBAG3 was also highest in ‘Zihuabai’ (Lu et al., 2017). Such different expression profiles are likely genotype-dependent. The clear induction pattern of StRab5b was also confirmed in ‘Desiree’, indicating the response of StRab5b to P. infestans infection.

Virus-induced gene silencing (VIGS) is an important method for studying gene function and has been used routinely in N. benthamiana, Lycopersicum esculentum, and A. thaliana (Ratcliff et al., 2001; Brigneti et al., 2004; Lacomme and Chapman, 2008; Senthil-Kumar and Mysore, 2014). In the present study, the StRab5b silenced leaves were more susceptible to P. infestans than control leaves ( Figure 3 ). Similar studies have been reported in N. benthamiana and potato. Specifically, small GTPase NbRanBP1-1-silencing reduced resistance to P. infestans in plants of N. benthamiana (Mizuno et al., 2019). Consistently, when silencing EIN2, which was involved in pre-invasion phase, facilitated the penetration rate of P. infestans (Rin et al., 2017). However, the silencing of Matrix metalloprotease 1 made N. benthamiana more susceptible to P. infestans, but enhanced Nep1-like protein induced cell death (Ha et al., 2017). Silencing five candidate genes TRV:12 (sodium dicarboxylate cotransporter), TRV:17 (UDP-arabinose 4-epimerase), TRV:21 (2-oxoglutarate dehydrogenase), TRV:22 (Lipoxygenase), and TRV:48 (suberization-associated anionic peroxidase) from N. benthamiana facilitated the infection of P. infestans (Du et al., 2013). Conversely, silencing StERF3 in potatoes not only enhanced foliage resistance to P. infestans, but also promoted plant tolerance to salt stress (Tian et al., 2015).

Currently, small G proteins reportedly respond to abiotic stress factors and regulate plant defense or stress-related gene expression (Miao et al., 2018). The H₂O₂ was previously recognized as a toxic metabolite in plant cells. However, it has been known that H₂O₂ also mediates stimulus responses to plant cells as a signaling factor (Bailey-Serres and Mittler, 2006). According to previous research, small G proteins of the RAB family play important roles in the establishment of plant defense responses (Lamb and Dixon, 1997). In this study, the results confirmed that H₂O₂ accumulation in the transgenic lines might be caused by StRab5b expression on the membrane. Previous studies on rice disease resistance have shown that small GTPase OsRac1 induces hydrogen peroxide products, and enhances resistance to rice blast disease in transgenic plants (Ono et al., 2001). Overexpression of NtRop activated H₂O₂ products in Arabidopsis transgenic lines (Cao et al., 2008). In potato, stable expression DN-AtRop1 led to H₂O₂ accumulation associated smaller lesions on leaves after inoculation with P. infestans (Zhang et al., 2014). Among Rab proteins, overexpression of StRab in potato reduced the leaf lesion area and increased H₂O₂ production after inoculation with P. infestans (Gao et al., 2012). However, less H₂O₂ was observed in miR172a transgenic tomato plants after inoculation with P. infestans than in the wild type (Luan et al., 2018). These findings indicate that the involvement of H₂O₂ in disease resistance is a complex phenomenon, and that H₂O₂ accumulation in plant tissues experiences early and late stages. Furthermore, when plants lose the ability for regulation in the late stage, H₂O₂ may be induced in the early or late stages after inoculation, and may thus increase in concentration, leading to the cell death.

In plants, H₂O₂ is mainly produced through NADPH oxidase and polyamine oxidase (PAO) pathways. The production of H₂O₂ in plants generally suffer abiotic stress through the POD pathway. The extracellular PH value temporarily increases, which can activate the peroxidase of cell wall, and reduces O₂ to H₂O₂ (Khokon et al., 2010). The activities of SOD and POD were higher in miR172 transgenic tomato plants after inoculation with P. infestans, accompanied by less H₂O₂ (Luan et al., 2018). As shown in Figure 6 , the inoculated StRab5b-transgenic plants had higher APX, SOD, POD, CAT activities and expression levels of ROS related-genes, and increased H₂O₂ accumulation. These results suggested that StRab5b in potato may modulate antioxidants to eliminate redundant H₂O₂ and prevent cellular membrane injury after P. infestans infection. Similar results have been found in tomato, and the amounts of H₂O₂ and O₂ ⁻ were increased with the continuous salt stress in both roots and leaves. Compared to control, the plants had increased activities of SOD, CAT, POD, and APX after 6 or 12 days of salt stress (Raziq et al., 2022). In tomato, the melatonin-induced H₂O₂ generation through RBOH was attributed to activate some genes expression (CDPK1, MAPK1 and ERD15). Conversely, the inhibition of RBOH reduced stress defense response and antioxidant enzyme activity (SOD, CAT and APX) (Gong et al., 2017). In addition, a previous study reported that APX1 and SOD genes showed higher levels in SA- or CdCl₂-treated potato plants, when compared to CK plants (Li et al., 2019). Brassinosteroid (BR) activated the expression of the StPOD gene, and the expression level was partially increased in potato tubers at the end of wound healing (Han et al., 2022). Some researchers believe that the highly active antioxidant enzymes are used to eliminate active oxygen, and the concentration of H₂O₂ is reduced.

Plant defense responses refer to the resistance of plants to external infection, including the synthesis of pathogenesis-related (PR) proteins. Plant hormones SA, JA, and ET play major roles in the plant immune system (Verma et al., 2016). There are many studies regarding plant resistance and JA signaling pathway. For example, JA may be involved in resistance regulated by AtRop1 (Zhang et al., 2014). Overexpression of OsRab11 in Arabidopsis enhances plant resistance to Pseudomonas syringae by inducing the expression of JA-responsive genes, rather than SA-responsive genes (Hong et al., 2013). These results are consistent with those obtained in the present study. Thus, the key enzyme-encoding gene in the JA signaling pathway, i.e., LOX and JA content were dramatically induced in StRab5b transgenic lines at different inoculation time points, indicating the involvement of JA signaling pathway on potato resistance manipulated by StRab5b. This is in contrast with the enhanced late blight resistance observed by the overexpression of LecRK-I.9 in Arabidopsis by reducing SA-responsive gene expression (Bouwmeester et al., 2014). SA and ROS were confirmed as the primary signaling molecules that mediated potato resistance to P. infestans (Lamb and Dixon, 1997; Na et al., 2012), and the present study clearly highlights the involvement of the JA pathway in potato resistance to P. infestans. However, the cross talk of JA and SA signaling pathways were confirmed via hormone-responsive transcription factors WRKY70 and PDF1.2, which regulate plant defense responses (Petersen et al., 2000; Li et al., 2004). In other words, the mechanism underlying the involvement of small G proteins on manipulating potato resistance against late blight resistance is rather complex, and different signaling pathways interact with each other through key transcription factors to improve durable resistance in solanaceous crops. Whether the same mechanism occurs in small G protein-mediated establishment of potato resistance remains to be explored. Further experiments are needed to delineate the signaling transduction pathway mediated by small G proteins in potato.