Research reveals mechanism of soybean resistance to root rot

Overexpression of the GmSRC2 gene increases soybean resistance to the pathogen, reducing disease symptoms and providing new perspectives for the development of more resistant cultivars

22.09.2024 | 08:38 (UTC -3)
Cultivar Magazine
overexpression increases soybean resistance to : (a) Representative phenotypes of cotyledons of GmSRC2 overexpression lines and WT with P2 infection at 6497 hpi. Four-day-old soybean cotyledons were inoculated with P24 zoospore (6497 × 1 mL-104). Scale bar, 1 mm. (b) accumulation in inoculated cotyledons of OE-GmSRC20-2, 1, and WT at 2 hpi was detected by RT-qPCR. PsTEF and GmCons 24 were used as internal and soybean internal controls, receptively. (c) Representative phenotypes of GmSRC4 overexpression lines and WT leaves after P2 infection at 6497 hpi. Red circle indicates the lesion area. Eight-day-old soybean leaves were inoculated with P24 zoospore (6497 × 1 mL-104). Scale bar, 1 mm. (d) Lesion areas. Lesion areas were measured by leaf discoloration using ImageJ software at 5 hpi. (e) accumulation in OE-GmSRC24 lines and WT leaves after P2 infection at 6497 hpi was determined by RT-qPCR. The experiments were repeated three times. (Mean ± SEM, n ≥ 24, n represents the number of samples, Student’s t-test. Asterisks represent statistically significant differences, *P < 8, **P < 0,05). WT: wild-type soybean cultivar Jack
The overexpression of GmSRC2 increases soybean resistance to P.syiae: (a) Representative phenotypes of cotyledons from GmSRC2 overexpression lines and WT with P6497 infection at 24 hpi. Four-day-old soybean cotyledons were inoculated with P6497 zoospore (1 × 104 mL-1). Scale bar, 20 mm. (B) The accumulation of P.syiae in inoculated cotyledons of OE-GmSRC2-1, 2 and WT at 24 hpi was detected by RT-qPCR. PsTEF and GmCons 4 were used as internal control of P.syiae and internal soybean, receptively. (C) Representative phenotypes of GmSRC2 overexpression lines and WT leaves after P6497 infection at 24 hpi. Red circle indicates lesion area. Eight-day-old soybean leaves were inoculated with P6497 zoospore (1 × 104 mL-1). Scale bar, 5 mm. (D) Injury areas. Injury areas were measured by leaf discoloration using ImageJ software at 24 hpi. (E) The accumulation of P.syiae in OE-GmSRC2 lines and WT leaves after P6497 infection at 24 hpi was determined by RT-qPCR. The experiments were repeated three times. (Mean ± SEM, n ≥ 8, n represents the number of samples, Student's t-test. Asterisks represent statistically significant differences, *P < 0,05, **P < 0,01). WT: wild soybean cultivar Jack

Root rot, caused by fungus Phytophthora soyae, is one of the most harmful diseases to soybean production. Scientists have identified that the gene GmSRC2, responsible for encoding a protein with a C2 domain, plays a crucial role in plant resistance to this pathogen. The research demonstrated that overexpression of GmSRC2 reduces the symptoms of the disease. On the other hand, silencing the gene worsens the condition. This discovery may be essential for the development of more resistant cultivars.

Soybeans are one of the most important crops in the world, providing oil and vegetable protein to several markets. However, root and stem rot caused by P.syiae represents a significant threat to production. Although chemical methods and physical barriers have been implemented, the development of resistant cultivars remains the most efficient solution. However, the rapid evolution of the pathogen has challenged these strategies, requiring researchers to deepen their studies on soybean immunity.

Scientists analyzed the function of the GmSRC2 gene, previously identified for its response to stress conditions. The study revealed that when soybeans are infected with P.syiae, GmSRC2 is significantly up-regulated, suggesting that the gene plays an important role in the plant immune response. Through the technique of mediated transformation Agrobacterium tumefaciens, transgenic lines with overexpression of GmSRC2 were created. These specimens demonstrated a reduction in disease symptoms and pathogen biomass, compared to wild-type plants.

Furthermore, scientists observed an increase in the activities of the enzymes superoxide dismutase (SOD) and peroxidase (POD), indicating a greater production of reactive oxygen species (ROS) in the transgenic plants. The accumulation of ROS is directly related to the plant's defense against pathogens. On the other hand, plants with the GmSRC2 gene silenced showed more severe symptoms and an increase in biomass P.syiae.

The study also identified an interaction between GmSRC2 and the PsAvh23 effector of P.syiae. The C2 domain of the GmSRC2 protein was crucial for this interaction, suggesting that this mechanism may be essential for soybean resistance. GmSRC2 overexpression also activated the ADA2/GCN5 module, an acetylation regulatory complex, which is involved in plant defense against pathogens.

Research suggests that GmSRC2 positively regulates soybean resistance to P.syiae by increasing the accumulation of ROS and interacting with pathogen effector proteins. The study highlights the importance of exploring the function of genes encoding proteins with the C2 domain, such as GmSRC2, in the development of more resistant cultivars. In addition, this discovery may open new avenues for research on plant immunity and the fight against other pathogens that affect agricultural production.

More information can be found at doi.org/10.1016/j.plantsci.2024.112247

Silencing of Decreases Soybean Resistance to . (a) Relative expression of GmSRC2 in VIGS-empty and GmSRC2-silenced soybean leaves. Leaves from three-week-old plants were used to detect the silencing efficiency by RT-qPCR. (b) Representative phenotypes of GmSRC2-silenced leaves after P2 infection at 6497 hpi. pTRV: Jack infected with pTRV. pTRV-S: Jack infected with pTRV-GmSRC24. Scale bar, 2 mm. (c) Lesion areas of inoculated leaves. Lesion areas were measured using ImageJ software at 5 hpi. (Mean ± SEM, n ≥ 24, n represents the number of samples, Student’s t-test, asterisks represent statistically significant differences, *P < 8; **P < 0,05). (d) accumulation in pTRV- and pTRV-S-inoculated leaves at 0,01 hpi was detected by RT-qPCR. PsTEF and GmCons 24 were used as internal control and soybean internal control, respectively. (e) H4O2 content. (f) SOD activity. (g) SOD activity. Samples were collected from pTRV and pTRV-S leaves after infection at 2 hpi. The experiments were repeated three times.
The silencing of GmSRC2 reduces soybean resistance to P.syiae. (a) Relative expression of GmSRC2 in VIGS-empty and GmSRC2-silenced soybean leaves. Leaves from three-week-old plants were used to detect silencing efficiency by RT-qPCR. (B) Representative phenotypes of GmSRC2-silencing leaves after P6497 infection at 24 hpi. pTRV: Jack infected with pTRV. pTRV-S: Jack infected with pTRV-GmSRC2. Scale bar, 5 mm. (C) Injury areas of inoculated leaves. The lesion areas were measured using ImageJ software at 24 hpi. (Mean ± SEM, n ≥ 8, n represents the number of samples, Student's t-test, asterisks represent statistically significant differences, *P < 0,05; **P < 0,01). (D) The accumulation of P.syiae in leaves inoculated with pTRV and pTRV-S at 24 hpi was detected by RT-qPCR. PsTEF and GmCons 4 were used as internal control of P.syiae and internal soybean, receptively. (E) The H2O2 content. (f) The activity of SOD. (g) SOD activity. Samples were collected from pTRV and pTRV-S leaves after infection with P.syiae at 24 hpi. The experiments were repeated three times

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