Gene sequences of oomycete species used in this study were retrieved from the database of the DOE Joint Genome Institute (http://www.jgi.doe.gov/) and the EnsemblGenomes (http://www.ensemblgenomes.org/). Based on additional searches genes of diatoms (Thalassiosira pseudonana), protists (Tetrahymena thermophile, Paramecium tetraurelia), and plants (Arabidopsis thaliana, Sorhum bicolor, Zea mays, Oryza sativa) were retrieved from the NCBI and KEGG databases (Table S1). Multiple alignments of the amino acid sequences were performed using ClustalW2 (http://www.ebi.ac.uk/Tools/msa/clustalw2/; Larkin et al., 2007). Phylogenetic trees were constructed with the maximum likelihood evolution algorithm in MEGA 5.22 (Tamura et al., 2011). A Poisson correction was used for multiple substitution models and pairwise deletion was used for gap split data treatment. The statistical strengths were assessed by bootstraps with 1000 replicates.

The “MX5-1” (A1 mating type; Han et al., 2012) and “80787-94L” (A2 mating type; Guo et al., 2010) isolates of P. infestans were used in this study. The WT strain and silenced transformants were maintained on tomato rye agar (TRA) medium (Guo et al., 2010) at 18°C in the darkness. Oospores were obtained by pairing “MX5-1” (A1 mating type) and “80787-94L” (A2 mating type) on TRA plates kept in the darkness for 7, 11, and 17 days. To test the mycelial growth rate, culture blocks (5 mm in diameter) cut from the edge of an actively growing culture were inoculated on the TRA plate at 18°C in the darkness, and the colony diameters were measured after a 7-day incubation. Sporangia of each strain were collected by washing 12-day-old cultures with pea broth. Zoospores were generated by incubating the sporangia suspension first at 4°C for 2 h and then at room temperature for 1 h. To test the oxidative sensitivity of each strain, culture blocks (5 mm in diameter) were placed on fresh TRA plates supplemented with 0.5, 1.0, 1.5, and 2.0 mM H₂O₂. The colony diameters were then measured after incubating the culture at 18°C in the darkness for 7 days. All of the experiments were performed twice, and each treatment was repeated in triplicate.

To determine the transcript profiles of the PiLLP gene in various stages of sexual development, the “MX5-1” (A1 mating type) and “80787-94L” (A2 mating type) isolates were incubated 2-cm apart from each other on polycarbonate membranes with 0.4 μm pores (Merck Millipore Ltd., Tullagreen, Ireland) overlaid on the surface of TRA plates and incubated at 18°C in the darkness. Each of these isolates, paired similarly with itself and cultured under the same conditions, was used as control. After 4, 6, 8, 10, 12, and 14 days, mycelia, and mycelia with oospores, were harvested from the junction area between the inoculation sites in each plate and were then ground in liquid nitrogen. The total RNA of each sample was extracted using a NucleoSpin RNA Plant kit (MACHEREY-NAGEL, Düren, Germany), and was reversely transcribed with an oligo (dT)₁₈ primer using the Reverse Transcriptase M-MLV (TaKaRa Bio Inc. Shiga, Japan) following the manufacturer's instructions. SYBR Green real-time qPCRs were performed in an ABI 7500 detection system (Applied Biosystems, Foster City, CA, USA). The elongation factor 1 (ef1) gene of P. infestans was used as an internal control. Means and standard deviations were calculated using data from three replicates. The whole experiment was repeated with a different set of biological samples.

We used the plasmid vector pTORmRFP4 to construct transformation plasmids. The 5′UTR, 3′UTR, and ORF regions of PiLLP were amplified from the cDNA of P. infestans “MX5-1” with specific primers (Table S2). The amplified fragments of 5′UTR and 3′UTR were joined by fusion PCR, and then inserted in an anti-sense orientation into pTORmRFP4 for silencing. The ORF of PiLLP was inserted in the sense orientation for overexpression. The plasmid constructs were all verified by DNA sequencing. Transformation of the P. infestans strain “MX5-1” was performed as described previously (Mcleod et al., 2008). To validate the transformants, PiLLP transcript levels during the growth of mycelia were measured by qRT-PCR.

Oospores from STs (PiLLP-silenced transformants), CK (the transformant carrying the empty vector pTORmRFP4) and WT (MX5-1) strains were obtained as described above. MTT staining was performed by mixing the oospore suspension with equivalent volumes of 0.1% MTT (Sigma-Aldrich, St. Louis, MO, USA) in 0.1 M PBS (pH 5.8), and incubated at 37°C for 24 h before observing under an Olympus BX41 microscope (Olympus, Tokyo, Japan). The oospores in red or purple were considered to be dormant viable, whereas the black and unstained oospores were non-viable (Ribeiro, 1978).

The distribution of lipid bodies in oospores was determined using Nile red staining. The Nile red stock solution (1 mM) was prepared by dissolving 100 mg of Nile red powder (Sigma-Aldrich, St. Louis, MO, USA) in 314 ml of methanol. Before staining, 10 μl of stock solutions were diluted 20 × with dimethylsulphoxide (DMSO). An aliquot of 20 μl oospore suspension was mixed with an equal volume of diluted Nile red solution on a microscope slide, and incubated at room temperature for 5 min, followed by two washes with PBS (pH 5.8). The samples were then viewed under an Olympus FluoView™ FV1000 confocal laser scanning microscope (Olympus, Tokyo, Japan) with an excitation wavelength of 530 nm and an emission wavelength of 568 nm.

Trypan blue staining was performed as described by Koch and Slusarenko (1990). Infected leaves were stained with lactophenol-trypan blue (10 ml of lactic acid, 10 ml of glycerol, 10 g of phenol, and 10 mg of trypan blue dissolved in 10 ml of distilled water). The leaves were boiled for ~2 min in the staining solution and then destained in 2.5 g/ml chloral hydrate for 30–40 min.

ROS were stained with the oxidant-sensitive probe DAB (Sigma-Aldrich, St. Louis, MO, USA) as described by Liu and Friesen (2012). Detached Nicotiana benthamiana leaves were inoculated with the sporangia of WT, CK, and transformants. After 12 h, the leaves were incubated in 1 mg/ml DAB solution (pH 3.8) at room temperature for 8 h, and were destained with ethanol, followed by viewing using an Olympus Bx41 microscope (Olympus, Tokyo, Japan).

For plant inoculations, WT (MX5-1), CK, STs, and OTs (PiLLP-overexpressed transformants) strains were incubated on TRA medium- plates in the darkness for 14 days. Sporangia of each strain were collected by washing 12-day-old cultures with pea broth. A 20-μl droplet of a sporangial suspension of 1 × 10⁴ sporangia/ml for WT, CK, and OTs and 2 × 10⁴ sporangia/ml for ST strains was inoculated on a detached potato (cv. Impala) leaf. Three detached leaves placed on a moist filter paper in a Petri dish were used as a replicate, and three plates were used for each treatment. Inoculated leaves were then incubated at 21°C with a 12-h/12-h light/ dark cycle for 5 days. The size of each lesion was measured and analyzed with Student's t-test. The experiments were performed twice.

DPI, a flavoenzyme inhibitor, inhibits the activities of the plant NADPH oxidases that are necessary for ROS generation (Cross and Jones, 1986). To scavenge the host-derived ROS, leaves of potato (cv. Impala) were infiltrated with 0.5 μM DPI (Sigma-Aldrich, St. Louis, MO, USA) in 0.05% DMSO using a disposable, plastic needleless syringe. The leaves that were infiltrated with 0.05% DMSO served as controls (Eloy et al., 2015).

We used scanning electron microscopy (SEM) to observe the surfaces of oogonial walls in WT, CK and ST strains. Oospores were harvested as described early from 11-day-old cultures grown on TRA medium, and samples were prepared as described by Ho (1979). Images were obtained using a HitachiS-3400N (Hitachi, Tokyo, Japan).

In order to investigate the catalase activity of WT, CK, and transformants, mycelia cultured in Pea Broth (200 g/L) for 4 days were collected through filtration. Each sample was ground in liquid nitrogen and then mixed with ice-cold extraction buffer containing 50 mM HEPES (pH7.4), 137 mM NaCl, 10% Glycerol and protease inhibitors, Pepstatin A (1 μg/mL), Leupeptin (1 μg/mL), PMSF (1 mM). Mixtures were centrifuged at 10,000 g for 10 min at 4°C. Supernatant was collected and used as crude extract (Wang et al., 2016). The protein concentration was calculated based on the absorbance at 595 nm with Bio-Rad protein assay dye.

In-gel assay was performed as described previously (Lledıas et al., 1998). Equal amounts of total protein (20 μg) of different strains (WT, CK, STs, and OTs) were loaded into a 7.5% native polyacrylamide slab gel. The gel was immersed in 7 mM H₂O₂ for 10 min after electrophoresis, and then incubated in a 1/1 mixture of freshly prepared 1% potassium hexacyanoferrate (III) and 1% iron (III) chloride hexahydrate. Blue color was observed in the gel except at zones where H₂O₂ was decomposed by catalases (Harris and Hopkinson, 1987).

We identified a gene encoding LLP in P. infestans, and designated it as PiLLP (http://protists.ensembl.org/Phytophthora_infestans/Gene/Compara_Tree?anc=1452626;db=core;g=PITG_15862;g1=BN9_002120;r=supercont1.39:614858-615784;t=PITG_15862T0, gene ID: PITG_15862). The PiLLP gene is 927 bp in length and encodes a protein of 308 amino acids (aa) with a glycine content of 12.7%. Only one homolog of PiLLP was found in each oomycete genome, and a phylogenetic analysis showed that all of the oomycete LLPs were grouped into one clade, clustering with the Class V GRPs in plants (Figure 1A). A structural analysis showed that these LLPs contain mixed patterns of GGX/GXGX repeats, similar to the plant Class V GRPs (Figures 1B,C). However, the plant Class V GRPs are larger, around 600 aa, so almost double the size of the oomycete LPPs. These results suggest that the LLP genes are highly conserved in oomycetes and are phylogenetically related to the Class V GRPs of plants. No orthologs of oomycete or plant LLPs were found in fungi.

To examine the expression pattern of PiLLP, we analyzed the transcript levels in P. infestans during sexual development (mating), asexual development (mycelia, sporangia, zoospores, cysts, and germinated cysts) and in planta growth (infection stages) using real-time qPCR. During mating, the PiLLP transcript level was up-regulated from 4 to 14 day, with the highest expression value at 10 day (Figure 2A; Table S4), and the PiLLP transcript level in sporangia was 80-fold that in mycelia (Figure 2B; Table S4). During infection, the PiLLP expression was highest at 12-h post-inoculation, then dropped and maintained a low level from 1-day post-inoculation (Figure 2B; Table S4). Thus, PiLLP may play important roles in reproduction and plant infection of P. infestans.

To investigate the function of PiLLP, PiLLP-silenced transformants (STs) and PiLLP-overexpressed transformants (OTs) were generated by polyethylene glycol-mediated protoplast transformation. The STs were generated with pTORmRFP4 vectors containing 5′ and 3′ untranslated regions (UTR) of PiLLP, whereas the OTs were generated with pTORmRFP4 vectors containing the PiLLP open reading frame (ORF) region. A transformant harboring the empty vector pTORmRFP4 was used as the control (CK). In total, three STs (S3, S16, and S84), three OTs (O15, O36, and O38), and a CK strain were used in this study. The expression levels of PiLLP in STs were from 10 to 45% of that in the WT strain, whereas the values in the OTs were significantly higher than those of WT and CK strains (Figure 3; Table S4).

All of the transformants, WT and CK were mated with the A2 mating-type isolate (80787-94L) on TRA medium to produce oospores. Less oospores were formed in paired-cultures of STs in comparison with the WT, CK, and OTs, and ~45% (Table S3) of the oogonia in these ST strains did not form thick-walled oospores, whereas this was only ~4% in WT, CK and OT cultures (Figures 4A,B).

To investigate the effects of PiLLP-silencing on oospore development, sexual apparatuses (oogonia–antheridia) formed in 7-, 11-, and 17-day-old cultures were investigated. Because the same A2 mating-type isolate (80787-94L) was used in all the pairings, the oogonia were referred as 7-, 11-, and 17-days-old for convenience. No obvious difference was found among the 7-day-old oogonia of different strains (Figure 5A). However, about half of the 11-day-old oogonia of the STs showed a decline in the amount of cytoplasm in oogonia compared with those of the WT and CK strains at the same stage (Figure 5A). Moreover, the cytoplasm in ~45% of the 17-day-old oogonia of the STs was completely void, without oospores, whereas the majority of the oogonia of WT and CK strains at the same stage contained mature thick-walled oospores (Figure 5A).

Subsequently, we determined the viability of oospores through tetrazolium bromide (MTT) staining. The 7-, 11-, and 17-day-old oospores of WT and CK strains, and the 7-day-old oogonia of the STs were stained purple (Figure 5B), indicating that they are viable. However, nearly half of the 11- and 17-day-old oogonia in the STs were black or unstained, suggesting the loss of viability (Figure 5B). Thus, some STs could form viable immature oogonia, but others could not form oospores (Figure 5B). When the 11-day-old oogonia from STs, WT, and CK strains were observed by SEM, smooth oogonial walls appeared in the oogonia of WT and CK, whereas many sunken areas were observed on the surfaces of ~50% of the oogonia of the STs, indicating the loss of turgor in these oogonia (Figure 5C).

A previous study showed that oogonia of Phytophthora went through the following three distinct stages during the oogonial expansion phase: (1) the oogonial wall thickens from 200 nm to 800 nm; (2) the largely “functional” cytoplasm of the oogonium changes to vacuoles and lipid bodies by the time the oosphere is formed; (3) the oospore forms and the central ooplast is surrounded by a cortex of lipid bodies (Hemmes, 1983; Figure 5D). We stained the developing oogonia with Nile red to explore in which stage development is blocked. As shown in Figure 5E, the 7-day-old oogonia of STs exhibited the same phenotypes as those of the WT and the CK strains, emitting red fluorescence both in oogonia and in antheridia, indicating that lipid bodies were present in both. Almost all the 11-day-old oogonia of WT and CK showed red fluorescence only in oogonia, indicating that the lipid body in the antheridium is either degenerated or translocated into the oogonium, while the substance with red fluorescence was aggregated to form a “red ball.” This kind of “red ball” was then observed in almost all of the oospores formed in the 17-day-old oogonia of WT and CK strains, while a little red fluorescence remained in the area between the wall of the oospore and the oogonium. However, nearly half of the 11-day-old oogonia of STs showed red fluorescence both in oogonia and in antheridia, and the red fluorescence-emitting substance was scattered instead of aggregating into a red ball (Figure 5E). In the 17-day-old oogonia of STs, no mature oospores were formed and only a small amount of red fluorescence-emitting substance was left in oogonia and antheridia (Figure 5E). Thus, the sexual development in STs is blocked in the stage of oospore wall formation.

The colony diameters of STs (S3, S16, and S84) were significantly smaller than those of the WT and CK strains, whereas those of the OTs (O36 and O38) were not different from those of WT and CK, except that the mycelia of OTs colonies were denser (Figures 6A,B) (P < 0.01). In addition, the STs produced significantly less sporangia than the WT and CK strains (Figure 6C) (P < 0.01), and fewer zoospores were released from these sporangia in comparison with the WT and CK strains (Figure 6D). The OTs (O36 and O38) produced significantly more sporangia than WT and CK strains, and the number of zoospores released from these sporangia was almost equal to those of WT and CK strains (Figures 6C,D). In addition, the germination rates of the STs' sporangia were close to half the rates of WT and CK sporangia, whereas the germination rates of the OTs' sporangia were similar to those of the WT and CK strains (Figure 6E).

In order to investigate the subcellular localization of PiLLP in P. infestans, we labeled PiLLP by fusing PiLLP with the gene encoding monomeric red fluorescent protein (mRFP) to investigate the subcellular localization of the PiLLP protein in P. infestans. In asexual stages, the red fluorescence was observed in the cytoplasm of mycelia, sporangia, cysts, and germinated cysts. This fluorescence pattern was the same in the control strain CK and in three OT strains and therefore it is not possible to draw conclusions about the localization of PiLLP during asexual development. In the sexual stage, the fluorescence pattern in the three OT strains was different from the pattern seen in the CK strain. In the OT strains, the red fluorescence was specifically associated with the wall of the oogonia (Figure 7), indicating that PiLLP was localized in the oogonial walls.

To determine whether PiLLP is an oxidative-associated gene, the PiLLP expression levels in cultures treated with various concentration of H₂O₂ were investigated. The expression of PiLLP in the WT strain increased with increased H₂O₂ concentrations in the medium and was ~10-fold greater when the H₂O₂ concentration reached 2.0 mM (Figure 8A; Table S4). The growth rates of STs decreased greatly at 0.5, 1.0, 1.5, and 2.0 mM H₂O₂, and completely ceased at 2.0 mM H₂O₂. The inhibition rate of H₂O₂ on OTs growth was consistent with those of WT and CK strains (Figures 8B,C).

To determine whether PiLLP is required for P. infestans pathogenicity, the detached leaves of potato (cv. Impala) were inoculated with equivalent amounts of germinated WT, CK, ST (S3, S16, and S84), and OT (O36 and O38) sporangia, independently. At 5 days post-inoculation, the typical disease symptoms of water-soaked lesions were observed on the leaves inoculated with WT, CK, and OTs (O36 and O38) strains, except that more aerial mycelia were observed on lesions induced by OTs. In contrast, only small brown spots were induced by the ST strains (Figures 9A–C). As the plant-derived ROS is an important defense mechanism of protecting plant from microorganism invasion, we pretreated the detached leaves with diphenyleneiodium (DPI), a flavoenzyme inhibitor that prevents the activation of NADPH oxidases, before inoculating with the STs. The lesion sizes on these treated leaves increased to half size of that induced by WT and were twice as large as those on the DPI-untreated leaves (Figures 10A,D). More mycelia were observed in cells at the inoculation site than in those of DPI-untreated leaves inoculated with STs (Figure 10B), and less reddish-brown precipitate was observed in the infection site of STs in DPI-treated leaves (Figure 10C). For leaves inoculated with OTs, no significant increase in lesions size was observed on DPI-treated leaves (Figure 10D). We observed the less dense of mycelia on lesions and in tissues at inoculation site treated with DPI or DMSO, and a lighter brown color in the infection site in DPI-treated leaves (Figures 10A–C). This finding indicates that the pathogenicity of STs could be partially restored by DPI treatment.

As the transcriptome analysis of P. infestans showed the up-regulation of two catalase genes, (PITG_15248 and PITG_07143) during the early infection stages (Haas et al., 2009), we then analyzed the expression level of these genes in WT, CK, and transformants. The expression levels of these two genes were significantly decreased in STs, whereas the expression level of PITG_15248 was significantly increased in OTs, compared with those in WT and CK (Figure 11A; Table S4). We then further investigated the activity of catalases of WT, CK, and transformants by analyzing the total catalase activities of the crude proteins extracts from these isolates with PAGE under non-denatured conditions (Figure 11B). As shown in Figure 11B, the bands of WT and CK strains were thicker and brighter than those of STs, but significantly lighter and thinner than those of OTs, indicating the decrease of catalase activity in STs and the increase of catalase activity in OTs.

In this study, we identified a P. infestans ortholog of the plant LLP gene. Bioinformatics analysis showed that LLP is highly conserved in oomycetes and contains mixed GGX and GX repeats. The protein is phylogenetically related to the LLP, Class V GRPs in plants, which function is not clear. The similarity between PiLLP and the rest of LLPs ranged from 32.1 to 90.9%. In animals and humans, loricrin is a highly insoluble structural protein and is the main component of the cornified cell envelope, which functions as structural reinforcement (Kalinin et al., 2001). Together with the indication of its localization in oogonial walls, this suggests that LLP is a structural component in the ooginial wall. The increase in PiLLP expression in asexual and sexual development stages also indicates that PiLLP is required for reproduction of P. infestans. Thus, the decrease in the colony expansion rate, the formation rates of sporangia and oospores, and the zoospore-releasing rate in PiLLP-silenced transformants is not surprising. However, further investigation is needed to confirm its localization on oogonia wall.

Previous studies showed that various types of proteins constitute 12.5% of the oospore–oogonium wall, and the most abundant amino acid residue in these proteins is glycine followed by alanine, arginine, aspartic acid, and glutamic acid (Lippman et al., 1974), which is consistent with the amino acid composition of PiLLP. The presence of layered patches of electron-dense deposits at the inner layer of oogonial wall likely belong to osmiophilic proteins or lipids, but these layered patches of electron-dense deposits are absent in the walls of hyphae, sporangia, zoospores, and cysts (Hegnauer and Hohl, 1978).

Here, some STs could form many normal immature oogonia but ~45% of these oogonia could not form oospores. The simultaneous loss of lipid bodies and turgor in the oogonia indicates that the loss of cytoplasm content and/or turgor is related to defective oospore formation in the STs. Previous studies on the gametangial development in Phytophthora spp. showed that fertilization occurs before oosphere formation, and the antheridial nucleus enters oogonia through the fertilization tube, rupturing the oogonial wall (Figure 5D; Hemmes and Bartnicki-Garcia, 1975; Hemmes and Ribeiro, 1977). As a consequence, the ruptured area on the oogonial wall requires patching to avoid leaking cytoplasm and nuclei from oogonium. However, the shortage of structural proteins in the oogonial wall may result in an unpatched oogonial wall break, ultimately leading to the failure of oospore formation. The Nile red staining of developing sexual apparatus provided evidence supporting this speculation. As shown, the red fluorescence-emitting substance indicated that the lipid bodies were present only in antheridia attached to the 17-day-old (late stage) partially emptied oogonia from STs, not in those attached to the oogonia with mature oospores, indicating the translocation of lipid bodies from the later stage oogonium to the antheridium (Figure 5E).

Thus, this study suggested that PiLLP is a structural component of the oogonial wall and is likely related to the electron-dense deposits specific to the oogonial wall. However, further investigations are needed to illustrate the components of the electron-dense deposits on the inner oogonial wall. Previously, a small tyrosine rich protein, PoStr, was shown to be involved in the oogonial and oospore wall formation in Phythium sp. (Grenville-Briggs et al., 2013).

The accumulation of plant-derived ROS at the infection site is an early immunity response in plants (Mellersh et al., 2002; Torres and Dangl, 2005). To successfully invade plant cells, plant pathogens must avoid damage from ROS through self-protection or scavenging ROS, or both. In plant fungal pathogens, several genes, such as Yap1 in Ustilago maydis (Molina and Kahmann, 2007) and DES1 in Magnaporthe oryzae (Chi et al., 2009) are responsible for ROS detoxification at the infection site and are required for virulence.

STs being more sensitive to H₂O₂ than the WT and OTs strains, and the induced expression of PiLLP in the WT strain being highly increased as the H₂O₂ concentration increased in the medium, indicated that PiLLP is involved in resistance to H₂O_2. Additionally, a greater amount of H₂O₂ accumulation and a decline in mycelial expansion occurred in infection site tissues inoculated with STs than in those inoculated with WT, CK, and OTs. We also showed that the reduced pathogenicity of the STs could be partially restored with DPI treatments. These results indicate that the expansion of STs in infection site tissues is limited partially because of the attack of host-derived ROS. Therefore, we speculate that PiLLP is involved in scavenging plant ROS during infection. A transcriptome analysis of P. infestans revealed that two catalase genes (PITG_15248 and PITG_07143) were up-regulated during early infection stages (Haas et al., 2009). Here, we found that the expression levels of these two genes were decreased in STs compared with those in WT, CK, and OTs. We further investigated the activity of catalase in different isolates and found the decrease of catalase activity in STs and the increase of catalase activity in OTs compared with WT and CK. These results suggested that PiLLP affected the pathogenicity of isolates through affecting the catalase activity, which is important for scavenging plant ROS.

In the pathogenicity test, we placed a double amount of STs sporangia on the leaves to compensate for the lower germination rate of STs sporangia, which was around 50% of the WT and OTs. The growth rates of the two STs used in the pathogenicity test were about 50% lower than those of WT and OTs. Thus the defect in growth rate of STs may explain why pathogenicity of STs was not fully restored by DPI treatment. In P. infestans, two homologous genes of PiLLP were detected, and the expression of two genes with high sequence identities to PiLLP (PITG_10076, 51.1%; PITG_00234, 46.8%) in WT and STs did not show significant difference (Table S5).

Sequence analysis revealed that PiLLP does not contain a signal peptide or any structural domain with known functions but does contain a number of mixed GGX/GXGX repeats. Therefore, it is less likely that PiLLP could function as a secreted effector inducing plant cell death or as a cell wall-degrading enzyme. So, it is reasonable that the overexpression of this gene didn't increase the virulence of the OTs. DPI is a flavoenzyme inhibitor that can scavenge the host-derived ROS. As the pathogenicity test showed that WT, CK, and OTs can scavenge the host-derived ROS by itself, but not STs, it is expected that DPI treatment experiments have an obvious effect only on STs, but not on OTs.

Previous work suggested that the heat shock transcription factor PsHSF1 and histone acetyltransferase PsGcn5 were involved in oxidative stress responses and detoxifying oxidative bursts (Sheng et al., 2015; Zhao et al., 2015). Our study showed that PiLLP is involved in the H₂O₂ resistance and ROS scavenging, which are likely caused by affecting the transcription level of catalase genes. Previous research has shown the diverse functions of the GRPs in plants, but the function of the glycine-rich repeats in these proteins is not known (Mangeon et al., 2010). One speculation is that the glycine-rich repeats are necessary for interaction with other proteins in a multicomponent complex (Mangeon et al., 2010). However, further studies are expected to resolve the detailed mechanisms involved.

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.