Helong Chen

Sugarcane (Saccharum spp.) is a globally vital sugar crop, yet its productivity faces severe challenges from infestation by Chilo sacchariphagus. To decipher the plant’s molecular and metabolic defense mechanisms, this study applied an integrated transcriptomic and metabolomic analysis to three field-grown sugarcane cultivars (Zhongtang 4, 5, and 6) under natural borer stress. The transcriptomic analysis identified a total of 34,004 differentially expressed genes (DEGs), of which 18,674 were up-regulated, and 15,330 were down-regulated. The three cultivars exhibited distinct transcriptional regulatory patterns: Z4 and Z5 showed a global suppression-type response and a strong activation-type response, respectively, and Z6 presented a balanced-type response. A functional enrichment analysis revealed that the DEGs were significantly involved in metabolic processes, stress response, plant hormone signal transduction, phenylpropanoid biosynthesis, and plant-pathogen interaction pathways. Metabolomic analysis detected 963 differentially accumulated metabolites (DAMs), primarily including flavonoids, phenolic acids, amino acids and their derivatives, and lipids. These metabolites were significantly enriched in pathways such as amino acid metabolism, biosynthesis of secondary metabolites, and glutathione metabolism. Integrated multi-omics analysis further revealed strong synergistic regulatory relationships between gene expression and metabolite accumulation, particularly in defense-related secondary metabolic pathways, such as phenylpropanoid and flavonoid biosynthesis. Several key regulatory hubs were identified, including novel transcripts and D-xylulose-5-phosphate. Sugarcane employs a genetic background-dependent, multi-layered transcriptional reprogramming and metabolic restructuring to cope with borer stress. Cultivars Z4 and Z6 tend to activate and accumulate defensive compounds, while Z5 exhibits a different pattern of metabolic resource allocation. This research provides a systematic elucidation of the molecular mechanisms underlying insect resistance in sugarcane and offers important candidate genes and metabolites for breeding resistant varieties.

Root rot diseases caused by Ganoderma pseudoferreum and Pyrrhoderma noxium inflict substantial economic losses in rubber tree (Hevea brasiliensis) cultivation, while conventional control methods face environmental and resistance challenges. This study aimed to specifically investigate the molecular mechanisms by which ammonium sulfate enhances the biocontrol efficacy of Bacillus subtilis Czk1. Using label-free quantitative proteomics (LC-MS/MS), we characterized ammonium sulfate-induced alterations in the secretory proteome of Czk1. A total of 351 differentially expressed proteins (DEPs) were identified, with 329 significantly up-regulated and 22 down-regulated. GO functional enrichment analysis indicated that up-regulated DEPs were associated with metabolic pathways (glyoxylate/dicarboxylate, arginine/proline, cofactor biosynthesis) and extracellular localization (13 proteins), while down-regulated DEPs were linked to small molecule catabolism. KEGG pathway annotation identified DEP involvement in 124 pathways, including secondary metabolite biosynthesis and membrane transport. These findings demonstrate that ammonium sulfate remodels the Czk1 secretome to enhance the expression of key antagonistic proteins, thereby providing crucial molecular targets and a scientific foundation for developing effective biofungicides against rubber root rot, with clear practical implications for sustainable disease management.

Agave, with its unique appearance and ability to produce hard fibers, holds high economic value. However, low temperatures during winter can restrict its growth and even damage the leaves, causing a loss of ornamental appeal or affecting the fiber quality. Conversely, the plant cyclic nucleotide-gated channel (CNGC) family plays an important role in the growth and development of plants and the response to stress. Studying the CNGC family genes is of great importance for analyzing the mechanism by which agave responds to cold stress. This research conducted a transcriptomic analysis of the ornamental plant Agave macroacantha. Through assembly via Illumina sequencing, 119,911 transcripts were obtained, including 78,083 unigenes. In total, 6, 10, 11, and 13 CNGC genes were successfully identified from A. macroacantha, Agave. H11648, Agave. deserti, and Agave. tequilana, respectively. These CNGC genes could be divided into four groups (I, II, III, and IV), and group IV could be divided into two subgroups (IV-A and IV-B). The relative expression levels were quantified by qRT-PCR assays, which revealed that AhCNGC4.1 was significantly upregulated after cold treatment and Ca(NO₃)₂ treatment, suggesting its importance in cold stress and calcium signaling. Additionally, the Y2H assay has preliminarily identified interacting proteins of AhCNGC4.1, including AhCML19 and AhCBSX3. This study has established a completely new transcriptome dataset of A. macroacantha for the first time, enriching the bioinformatics of agave’s transcriptome. The identified CNGC genes are of great significance for understanding the evolution of agave species. The cloned CNGC genes, expression pattern analysis, and protein interaction results laid a foundation for future research related to the molecular functions of agave CNGC genes in cold tolerance.

Phytophthora-induced crop diseases, commonly known as “plant plagues”, pose a significant threat to global food security. In this study, strain ASG80 was isolated from sisal roots and demonstrated a broad-spectrum antagonistic activity against several Phytophthora species and fungal pathogens. Strain ASG80 was identified as Streptomyces luteireticuli via phylogenetic analysis, digital DNA–DNA hybridization (dDDH), and average nucleotide identity (ANI). Whole-genome sequencing identified 40 biosynthetic gene clusters (BGCs) related to secondary metabolite production, including antimicrobial compounds. Strain ASG80 extract exhibited broad-spectrum inhibitory activity against Phytophthora nicotianae, P. vignae, P. cinnamomi, and P. sojae. Pot experiments showed that strain ASG80 extract significantly reduced sisal zebra disease incidence, with an efficacy comparable to the fungicide metalaxyl. These findings suggest that strain ASG80 is a promising biocontrol agent with substantial potential for managing Phytophthora-related diseases in agriculture.

Phytophthora-induced crop diseases, commonly known as “plant plagues,” pose a significant threat to global food security. In this study, strain ASG80 was isolated from sisal roots and demonstrated broad-spectrum antagonistic activity against several Phytophthora species and fungal pathogens. Strain ASG80 was identified as Streptomyces luteireticuli via phylogenetic analysis, digital DNA-DNA hybridization (dDDH), and average nucleotide identity (ANI). Whole-genome sequencing identified 40 biosynthetic gene clusters (BGCs) related to secondary metabolite production, including antimicrobial compounds. Strain ASG80 extract exhibited broad-spectrum inhibitory activity against Phytophthora nicotianae, P. vignae, P. cinnamomi, and P. sojae. Pot experiments showed that strain ASG80 extract significantly reduced sisal zebra disease incidence, with efficacy comparable to the fungicide metalaxyl. These findings suggest that strain ASG80 is a promising biocontrol agent with substantial potential for managing Phytophthora-related diseases in agriculture.

Intercropping is widely utilised in agricultural production to enhance land use efficiency because of its benefits, such as heightened crop productivity and optimised resource utilisation. We investigated the effects of Pinto peanut/sisal (HST), Stylo/sisal (strT) and Grona styracifolia/sisal (JqT) intercropping systems on soil bacterial communities compared with sisal continuous cropping (CK) by using Illumina MiSeq high-throughput sequencing technology. The intercropping system significantly increased the total nitrogen (TN), soil pH and soil moisture levels and decreased the levels of available phosphorus (AP) and available potassium (AK). Minimal variations were observed in Shannon’s and Simpson’s diversity indices between the monoculture and intercropping systems as well as among different intercropping systems. The most abundant phyla observed within the four groups were Proteobacteria, Acidobacteria, Cyanobacteria and Bacteroidetes. At the phylum level, the relative abundances of Proteobacteria, Acidobacteria, Cyanobacteria and Bacteroidetes were 37.37–54.35%, 10.54–21.21%, 3.46–20.43% and 2.15–5.67%, respectively. Compared with ZCK, StrT, JqT and HST treatments led to higher abundance of Cyanobacteria (from 3.46% to 20.43%, 11.37% and 16.58%, respectively) and Bacteroidetes (from 2.15% to 5.67%, 5.21% and 5.10%, respectively). The results of the linear discriminant analysis of effect sizes demonstrated notable variations in the relative abundance of bacterial taxa among various intercropping systems. The dominant categories of the genus in strT and JqT groups were Blastocatellia and Blastocatellaceae-Subgroup4, while Firmicutes was the dominant category of the genus in the HST group. The structure of bacterial communities did not vary between intercropping and monoculture systems. The findings indicated that the impact of the intercropping system on the bacterial community structure was not contingent on the specific intercropping patterns employed.

Sisal is an important tropical cash crop in southern China. Unfortunately, it is threatened by various diseases. In 2022, a new disease tentatively named marginal leaf blight disease (MLBD) was first observed in sisal fields across Guangxi and Guangdong provinces, with an incidence rate ranging from 13% to 30%. In this work, to isolate and identify the pathogens causing MLBD, sisal leaves exhibiting the typical MLBD symptoms were collected, and nine strains were obtained. Pathogenicity tests, morphological observations, and phylogenetic analyses confirmed that two strains, namely 22GX1-3 and 22GD1-4, identified as Phaeosphaeriopsis obtusispora, were the causative pathogens of MLBD. Further investigations into the biological characteristics of P. obtusispora showed that its mycelia exhibited optimal growth on PDA medium, with the most favourable temperature and pH being 25 °C and 7.0, respectively. The mycelia could grow in temperatures ranging from 10 °C to 32 °C but ceased at 35 °C. Lactose and yeast extract powder were also identified as the optimal carbon and nitrogen sources, respectively. Additionally, the effectiveness of various control agents was assessed on a single strain, 22GX1-3. Among the twelve fungicides tested, difenoconazole was proven the most effective, with an EC₅₀ value of 0.5045 µg/mL. To our knowledge, this is the first report for sisal MLBD caused by P. obtusispora. Our results provide crucial pieces of information for the development of effective management strategies to control sisal MLBD caused by P. obtusispora.

Sisal is a leaf fiber crop with a high integrated value and a wide range of uses in the application of soil remediation of heavy metal contamination. This study provides a preliminary understanding of how sisal responds to Cd stress and presents a theoretical basis for exploring the potential of sisal in the remediation of Cd-contaminated soils. In this work, the activities of the antioxidant enzymes (SOD, POD, and CAT) of sisal were measured by hydroponics with the addition of CdCl₂·2.5H₂O and different concentrations of Cd stress. Whole transcriptome sequencing (RNA-Seq) analysis was performed with lllumina sequencing technology, and qRT-PCR was conducted to verify the differential genes. The results obtained were as follows: (1) Short-term low concentration of Cd stress (20 mg/kg) had a transient promotion effect on the growth of sisal roots, but Cd showed a significant inhibitory effect on the growth of sisal roots over time. (2) Under different concentrations of Cd stress, the Cd content in sisal root was greater than that in sisal leaf, and Cd accumulated mainly in sisal roots. (3) With the increase of Cd stress concentration, the antioxidant enzyme catalase activity increased, peroxidase activity showed a decreasing trend, and superoxide dismutase showed a trend of increasing and then decreasing. (4) Transcriptome sequencing analysis detected 123 differentially expressed genes (DEGs), among which 85 genes were up-regulated and 38 genes were down-regulated. The DEGs were mainly concentrated in flavonoid biosynthesis and glutathione metabolism, and both processes had some regulatory effects on the Cd tolerance characteristics of sisal. This study elucidated the physiological, biochemical and transcriptomic responses of sisal under cadmium stress, and provided a theoretical basis for the ecological restoration function of sisal.

Brown rot disease caused by Pyrrhoderma noxium is a widespread disease that severely affects the roots of rubber trees (Hevea brasiliensis Muell. Arg.). The economic losses, along with environmental and health problems arising from the use of disease control chemicals, have raised the interest of scholars to explore the use of biological control agents for the effective control of fungal pathogen P. noxium. Here, the inhibition effect of the culture filtrate of B. subtilis Czk1 on P. noxium was demonstrated. The findings indicate that the antifungal activity of this strain is mediated wholly or partly by compounds produced in the culture filtrate. The combined use of liquid chromatography–tandem mass spectrometry and antifungal activity assays rapidly identified compounds produced by B. subtilis Czk1. Metabolic profiles were assessed and used to identify major metabolites based on the scores of variable importance in the projection and the plot scores of principal component analysis. A total of 296 differential metabolites were screened, including 208 in positive ion mode and 88 in negative ion mode. Two key metabolites, diacetyl and trans-2-octenoic acid, were screened from 29 metabolites by antifungal activity assays. The median effective concentration (EC₅₀) of trans-2-octenoic acid and diacetyl were 0.9075 mg/mL and 4.8213 mg/mL, respectively. The antifungal metabolites can disrupt the internal structure of the pathogenic fungal mycelium, thereby impeding its growth. This study is expected to contribute to the existing knowledge of Czk1-produced metabolites and their future antifungal applications. This study is also expected to provide a new biopreservative perspective on unexplored antifungal metabolites produced by Czk1 as a biocontrol agent.

Agave species are widely planted for fiber production. However, the molecular basis of agave fiber development has not been well understood. In this study, we performed a transcriptomic analysis in A. amaniensi, a well-known variety with high-quality fiber production. Approximately 43.87 million clean reads were obtained using Illumina sequencing. The de novo assembly produced 66,746 unigrams, 54% of which were annotated in a public database. In the Nr database, 21,490 unigenes of A. amaniensis were shown to be most closely related to Asparagus officinalis. Nine expansin A orthologs with full coding regions were obtained, which were named EXP1a, EXP1b, EXP2, EXP3, EXP4a, EXP4b, EXP11, EXP12, and EXP13. The maximum likelihood phylogenetic tree revealed the species-specific expansion of expansin genes in Arabidopsis, rice and agave. The expression analysis suggested the negative correlation between the expression of expansin genes and the leaf growth rate, except AhEXP11. Moreover, expansin genes were differentially affected by abiotic and biotic stresses. Notably, AhEXP2 expression level was highly upgraded after the infection of Phytophthora nicotiana. Nutrient deficiency also influent expansin genes expression. Together, our research will benefit future studies related to fiber development, disease resistance and nutrient usage in agave.