Sweet potato virus disease (SPVD) is one of the main virus diseases in sweet potato [Ipomoea batatas (L.) Lam] that seriously affects the yield of sweet potato. Therefore, the establishment of a simple, rapid and effective method to detect SPVD is of great significance for the early warning and prevention of this disease. In this study, the experiment was carried out in two years to compare the grafting method and side grafting method for three sweet potato varieties, and the optimal grafting method was selected. After grafting with seedlings infected with SPVD, the symptomatic diagnosis and serological detection were performed in 86 host varieties, and the differences in SPVD resistance were determined by fluorescence quantitative PCR (qRT-PCR) and nitrocellulose membrane enzyme-linked immunosorbent assay (NCM-ELISA). The results showed that the survival rate of grafting by insertion method was significantly higher than that by side grafting method, and the disease resistance of different varieties to sweet potato virus disease was tested. The detection method established in this study can provide theoretical basis for identification and screening of resistant sweet potato varieties.

Potato (Solanum tuberosum L.) growth and production is highly dependent on potassium (K) levels in the soil. Southwest China is the largest potato production region but it has low availability of soil potassium. To assess the genetic variation in K use efficiency, 20 potato genotypes were collected to compare the yield and K content in a pot experiment. Moreover, ‘Huayu-5’ and ‘Zhongshu-19’ were cultivated in five K applications to investigate the K distribution and sucrose in different organs. The results indicated that there were highly significant effects of K, genotype and K×G interactions on tuber yield, plant and tuber K content, plant K uptake efficiency and K harvest index. Cluster analysis classified 20 potato genotypes into four types: DH (high efficiency at low and high K application), LKH (high efficiency at low K application), HKH (high efficiency at high K application) and DL (low efficiency at low and high K application). The potassium distribution percentage in the tubers of the potassium-efficient genotype was higher than that of the potassium-inefficient genotype under low potassium application. The sucrose content in the tuber gently declined as the application of K rose in both cultivars, and that in the tuber of ‘Huayu-5’ was higher than that in ‘Zhongshu-19’. ‘Huayu-5’ reached the highest yield when the potassium application was 159.45 kg ha-1, and ‘Zhongshu-19’ reached the highest yield when the potassium application was 281.4 kg ha-1. This study indicated that genetic variation for K utilization efficiency existed among 20 genotypes, and yield in low K application and relative yield were suitable criteria for screening K utilization efficiency genotypes.

Sweet potato [Ipomoea batatas (L.) Lam.] is an important food and industrial crop. Its storage root is rich in starch, which is present in the form of granules and represents the principal storage carbohydrate in plants. Starch content is an important trait of sweet potato controlling the quality and yield of industrial products. Vacuolar invertase encoding gene Ibβfruct2 was supposed to be a key regulator of starch content in sweet potato, but its function and regulation were unclear. In this study, three Ibβfruct2 gene members were detected. Their promoters displayed differences in sequence, activity, and cis-regulatory elements and might interact with different transcription factors, indicating that the three Ibβfruct2 family members are governed by different regulatory mechanisms at the transcription level. Among them, we found that only Ibβfruct2-1 show a high expression level and promoter activity, and encodes a protein with invertase activity, and the conserved domains and three conserved motifs NDPNG, RDP, and WEC are critical to this activity. Only two and six amino acid residue variations were detected in sequences of proteins encoded by Ibβfruct2-2 and Ibβfruct2-3, respectively, compared with Ibβfruct2-1; although not within key motifs, these variations affected protein structure and affinities for the catalytic substrate, resulting in functional deficiency and low activity. Heterologous expression of Ibβfruct2-1 in Arabidopsis decreased starch content but increased glucose content in leaves, indicating Ibβfruct2-1 was a negative regulator of starch content. These findings represent an important advance in understanding the regulatory and functional divergence among duplicated genes in sweet potato, and provide critical information for functional studies and utilization of these genes in genetic improvement.