The GATA proteins, functioning as transcription factors (TFs), are involved in multiple plant physiological and biochemical processes. In this study, 28 GATA TFs of Brachypodium distachyon (BdGATA) were systematically characterized via whole-genome analysis. BdGATA genes unevenly distribute on five chromosomes of B. distachyon and undergo purifying selection during the evolution process. The putative cis-acting regulatory elements and gene interaction network of BdGATA were found to be associated with hormones and defense responses. Noticeably, the expression profiles measured by quantitative real-time PCR indicated that BdGATA genes were sensitive to methyl jasmonate (MeJA) and salicylic acid (SA) treatment, and 10 of them responded to invasion of the fungal pathogen Magnaporthe oryzae, which causes rice blast disease. Genome-wide characterization, evolution, and expression profile analysis of BdGATA genes can open new avenues for uncovering the functions of the GATA genes family in plants and further improve the knowledge of cellular signaling in plant defense.

Rice (Oryza sativa) is an important food crop in China and root-knot nematode Meloidogyne graminicola has been one of the most important diseases on rice in recently five years (Ju et al. 2020). In August 2020, rice plants were found to be maldeveloped, yellow leaves and hooked root tips in an irrigated paddy field of Yuanyang County, Xinxiang City, Henan Province. Fifty rice plants were randomly collected and 84.0 percent plants were infected with root-knot nematodes, with root-gall index of 56.0. Then nematodes from rice roots were isolated with 100-μm and 25-μm sieves. A large number of females, some third-stage juveniles (J3s), and a small number of males of Meloidogyne spp. were found in root galls of all samples after dissected, and then were identified and measured under the microscope. In females (n = 20), the perineal pattern was dorsoventrally oval with low and round dorsal arch, and the lateral field was not obvious or absent, striae are usually smooth, with occasional short and irregular striatal fragmentation. The morphological data of females are as follows: body length (BL) = 516.9 ± 72.5 μm (424.2 to 611.6 μm), body width (BW)= 328.4 ± 80.7 μm (232.1 to 437.4 μm), stylet length = 11.2 ± 1.3 μm (7.7 to 13.9 μm), dorsal pharyngeal gland orifice to stylet base (DGO) = 3.9 ± 0.5 μm (3.2 to 4.5 μm), vulval slit length = 24.3 ± 4.6 μm (15.2 to 31.4 μm), vulval slit to anus distance = 16.2 ± 2.5 μm (10.1 to 20.2 μm). Males are long cylindrical, wormlike, with a short round tail. Morphological measurements of males (n = 20) were BL = 1,218.0 ± 150.7μm (1,085.7 to 1,692.2 μm), BW = 34.2 ± 4.6 μm (28.5 to 39.7 μm), stylet = 17.4 ± 0.7 μm (15.9 to 19.3 μm), DGO = 3.6 ± 0.7 μm (2.5 to 4.5 μm), tail = 10.8 ± 2.1 μm (8.0 to 14.8 μm), spicule = 30.3 ± 2.6 μm (24.7 to 36.3 μm). The egg masses from the females were incubated at 28℃ for 48 hours. Measurements of J2s (n = 20) were BL = 444.2 ± 37.8 μm (315.7 to 547.5 μm), BW = 21.2 ± 2.7 μm (16.7 to 26.4 μm), stylet = 14.2 ± 0.3 μm (13.6 to 14.8 μm), DGO = 3.5 ± 0.5 μm (2.7 to 4.5 μm), tail = 70.8 ± 5.1 μm (61.3 to 80.8 μm), hyaline tail length = 21.0 ± 2.5 μm (16.3 to 26.1 μm). These morphological features are consistent with the original description by Golden and Birchfield (1965). DNA of a single female from each sample was extracted for molecular identification. Primer pairs D2A/D3B (5´-ACAAGTACCGTGAGGGAAAGTTG-3´/ 5´-TCGGAAGGAACCAGCTACTA-3´) (De Ley et al. 1999) and the species-specific primers Mg-F3/Mg-R2 (5'-TTATCGCATCATTTTATTTG-3'/ 5'-CGCTTTGTTAGAAAATGACCCT-3') (Htay et al. 2016) were used to amplify D2/D3 region of 28S RNA and the internal transcribed spacer (ITS) region, respectively. The amplified sequences of D2/D3 region (GenBank MW490724, 766 bp) shared 99.9% and 99.7% homology with the sequences of M. graminicola (MN647592, MT576694) isolated from Guangxi and Anhui Province (Ju et al. 2020), respectively, while ITS region sequences (MW487239, 369 bp) shared 100% and 99.7% homology to M. graminicola isolate GXL3 (MN636702) and FQJJ01 (MT159690), respectively. In order to verify the pathogenicity of nematodes, about 300 J2s were inoculated on ten 14-week-old rice (Oryza sativa cv. Nipponbare) planted in pots with sterilized sandy soil, respcectively, and maintained in a greenhouse at 28°C/26°C with a 16h/8h light/dark photoperiod and 75% relative humidity. At 14 days post inoculation, obvious symptoms of hook galls were observed on roots in all inoculated rice plants, and females and males in the same shape as the collected samples were found in the root galls under the stereoscopic microscope. No symptoms were observed on non-inoculated rice plants. After 28 days, the growth of the inoculated rice plants was significantly worse than that of uninoculated ones, with yellow leaves and short plants. These results confirmed the pathogenicity of M. graminicola on rice and it indicated that M. graminicola was already spread from the main rice-producing areas to the wheat and rice rotation areas. To our knowledge, this is the first report of M. graminicola in the Henan Province of China.

Potassium is an essential element for plant growth and development, and also plays a pivotal role in plant immunity against nematodes. However, it is not clear how plant nematodes manipulate host K ⁺ signalling pathways to disrupt host immunity and promote their parasitism. Here, we demonstrate the rice K ⁺ transporter OsHAK17 was targeted by the effector protein MgCOL from Meloidogyne graminicola nematodes. Genetic and phenotypic analyses revealed that knockout of OsHAK17 in rice resulted in decreased resistance to M. graminicola , while overexpression of OsHAK17 in rice enhanced resistance to M. graminicola . The yeast two‐hybrid assay showed OsHAK17 interacted with MgCOL. In situ hybridisation assay showed MgCOL mRNA accumulating in the subventral oesophageal gland of J2 nematodes, while immunolocalisation analysis revealed MgCOL localises to the giant cells during M. graminicola parasitism. Host‐induced gene silencing of MgCOL reduced the infection ability of M. graminicola , and over‐expressing MgCOL enhanced rice susceptibility to M. graminicola . More importantly, MgCOL ‐overexpression rice showed decreased K ⁺ accumulation in roots, which was consistent with it in nematode‐infected rice. In conclusion, when M. graminicola nematodes infect rice and secrete MgCOL into rice, MgCOL interacts with OsHAK17, resulting in the change of K ⁺ uptake and transportation in rice to enhance susceptibility.

Background Potassium (K), an important nutrient element, can improve the stress resistance/tolerance of crops. The application of K in resisting plant parasitic nematodes shows that the K treatment can effectively reduce the occurrence of nematode diseases and increase crop yield. However, data on K₂SO₄ induced rice resistance to Meloidogyne graminicola are still lacking. To evaluate rice resistance against M. graminicola induced by K2SO4 and to further clarify its mechanism is essential for the rational use of K fertilizer to ensure the safety of rice production.Results In this work, K₂SO₄ treatment effectively reduced the numbers of both galls and nematodes in rice roots, and delayed the development of nematodes to the adult stage. Rather than by affecting the attractiveness of roots to nematodes and the morphological phenotype of giant cells at feeding sites, such effect was achieved by rapidly stimulating hydrogen peroxide (H₂O₂) accumulation, increasing callose deposition. Meanwhile, such induced resistance required the active participation of the potassium channel OsAKT1 and the potassium transporter OsHAK5. The numbers of both galls and nematodes were higher in both gene deficient plants than that in the wild-type plants, and the K₂SO₄-induced resistance showed weaker in the defective plants than in the wild-type plants.Conclusions K₂SO₄ treatment effectively induces rice resistance to root-knot nematode M. graminicola. The mechanism of inducing resistance is to prime the basic defense of rice, up-regulating the expression of resistance-related genes and with the involvement of K⁺ channel and transporter. These laid a foundation for further study on the mechanism of rice to defense against root-knot nematodes and the effective use of potassium fertilizer to improve rice resistance against nematodes in the field.