Background Plant natriuretic peptides (PNPs) are a class of peptide hormones that regulate plant responses to salt stress, water balance, and pathogen attacks. However, the precise underlying role of PNPs in plant defense mechanisms remains poorly understood.
Results In this study, we investigated the role of the cotton gene GhEG45 in plant response to Verticillium dahliae infection. GhEG45 overexpression in cotton (Gossypium hirsutum) enhanced resistance to V. dahliae by increasing the expression levels of salicylic acid (SA)-related defense genes and upregulating antioxidant activities. GhEG45 expression was significantly induced by both V. dahliae infection and exogenous treatments with SA, hydrogen peroxide (H₂O₂), and other stress signals, which indicates its potential involvement in modulating plant defense mechanisms via SA signaling, oxidative stress pathways, and cell wall-based defenses. Transcriptomic analysis showed that GhEG45 regulates SA signaling and reactive oxygen species (ROS) metabolism. GhEG45 silencing via virus-induced gene silencing (VIGS) increased susceptibility to V. dahliae, impaired SA signaling, and disrupted ROS regulation.
Conclusions This study provides evidences that GhEG45 plays a pivotal role in defense against V. dahliae infection in cotton, primarily by regulating SA signaling and ROS metabolism. Although GhEG45 shares some functional characteristics with PNPs, further structural and biochemical studies are needed to comprehensively categorize GhEG45 as a natriuretic peptide. Our findings suggest that GhEG45 enhances cotton resistance to V. dahliae by potentiating defense responses.

Background Achieving a synergistic enhancement in both the yield and insect resistance of Bt cotton holds substantial importance for boosting farmers' income and ecological advantages. This study investigated the impact of amino acid foliar fertilizer (AAF) on the yield and Cry1Ac protein (CP) content, providing valuable insights for enhancing its productivity and insect-resistance capabilities. In 2021, Sikang 1 and Sikang 3 were treated with AAF once (A1) and water (CK) during the peak flowering stage. In 2022, AAF was sprayed one (A1), two (A2), and three (A3) times, respectively, with CK serving as the control.
Results Compared with the control, the A3 treatment increased seed cotton yield (SCY) by 16.0% and CP by 40.98% at 30 days after flowering. AAF application enhanced soluble protein content (SP) and glutamate pyruvate transaminase (GPT) activity, while suppressing protease and peptidase activities. Concurrently, AAF improved sucrose metabolism through elevated sucrose content and increased activities of sucrose synthase (SS) and sucrose conversion enzyme (SCE), which were also positively correlated with yield. A lower ratio of carbon-to-nitrogen (C/N) was linked to higher yields and CP content. Path analysis confirmed that SP, GPT, SS, and SCE demonstrated positive effects on CP content and SCY, respectively. Peptidase activity had negative effects on CP and SCY. The C/N ratio had negative effects on SCY and CP, respectively.
Conclusions Triple foliar application of AAF maintained lower C/N ratios with enhanced carbon metabolism and protein synthesis capacity, thereby simultaneously increasing both Cry1Ac protein content and yield in Bt cotton. These findings provide critical insights for improving both pest resistance and agronomic performance in Bt cotton cultivation.

Background Cotton lodging has become increasingly prevalent due to extreme environmental conditions and agronomic practices, severely compromising yield, fiber quality, and mechanical harvesting efficiency. However, research on cotton lodging remains limited, with most studies focusing on individual or isolated indices rather than a comprehensive system. This study systematically compared four lodging-resistant varieties (LR-1, LR-2, LR-3, LR-4) and four lodging varieties (L-1, L-2, L-3, L-4) across multiple indices: morphological traits, boll distribution, internode filling degree, stem density, mechanical strength, anatomical structure, and chemical composition.
Results The results showed that at the boll-opening stage, lodging-resistant varieties exhibited higher density in the first (increased by 11.6%) and third (increased by 23.5%) basal internodes compared with lodging varieties and significantly greater filling degree in the first (increased by 22.6%), second (increased by 23.1%), and third (increased by 26.1%) basal internodes; significantly higher stem puncture strength (increased by 41.2%) and stem bending resistance (increased by 38.2%); and a significantly lower stem lodging coefficient (19.0% lower in lodging-resistant varieties). Additionally, lodging-resistant varieties showed significantly enhanced anatomical structures, including greater cortex thickness, more mechanical tissue layers, and larger pith cavity, xylem, and phloem areas. Conversely, no significant differences were observed in morphological traits, boll distribution, or chemical composition between the lodging-resistant and lodging types.
Conclusion Lodging-resistant varieties exhibited thicker cortical tissue and mechanical tissue layers, along with larger xylem area and phloem area in basal internodes. These structural characteristics provide superior support for the filling degree and density of basal internodes, thereby enhancing stem puncture strength and bending resistance, and ultimately improving lodging resistance in cotton. These findings provide a theoretical basis for reducing the occurrence of cotton lodging.

Background Aquaporins (AQPs) are integral membrane proteins belonging to the major intrinsic protein (MIP) family, playing a crucial role in water transport, cell elongation, and stress responses. However, their evolutionary dynamics and functional roles in Gossypium species remain poorly characterized.
Results In the present study, a total of 55, 54, 54, 103, 106, 108, and 104 AQP genes were found in G. herbaceum, G. arboreum, G. raimondii, G. barbadense, G. tomentosum, G. mustelinum, and G. darwinii, respectively. Phylogenetic analysis classified them into five conserved subfamilies (PIP, TIP, NIP, SIP, and XIP), with 95 genes showing synteny across species and 17 displaying divergence, suggesting subgenome differentiation. Transcriptome analysis revealed that specific GbAQP genes are involved in early salt stress responses and fiber development. Physiological assays demonstrated stronger salt tolerance in tetraploid cottons, particularly G. darwinii, compared with diploids. Co-expression network analysis linked AQPs to abiotic stress and fiber traits, and virus-induced gene silencing (VIGS) confirmed four AQP genes as critical for salt tolerance.
Conclusion This study provides comprehensive insights into the evolution, expression, and functional roles of AQPs in cotton, identifying key candidate genes for improving salt tolerance and fiber quality in Gossypium species.

Background Thidiazuron (TDZ) is a widely used chemical defoliant in commercial cotton production and is often combined with the herbicide Diuron to form the commercial defoliant mixture known as TDZ·Diuron (T·D, 540 g·L^-1 suspension). However, due to increasing concerns about the environmental and biological risks posed by Diuron, there is an urgent need to develop safer and more effective alternatives. Jasmonic acid (JA) and its derivatives are key phytohormones in organ senescence and abscission.
Results Greenhouse experiments at the seedling stage revealed that Me-JA (0.8 mmol·L^-1) alone did not induce defoliation. However, its co-application with TDZ (0.45 mmol·L^-1) at concentrations of 0.6, 0.8, and 1.0 mmol·L^-1 significantly enhanced defoliation efficacy. The most effective combination—TDZ with 0.8 mmol·L^-1 Me-JA—achieved a 100% defoliation rate at 5 days after treatment (DAT), 23.7 percentage points higher than TDZ alone, and comparable to the commercial TDZ·Diuron formulation with equivalent TDZ content. Field trials conducted in Beijing (Shangzhuang), Hebei (Hejian), and Xinjiang (Shihezi) confirmed that the combination of 0.6 mmol·L^-1 Me-JA with 1.70 mmol·L^-1 TDZ provided optimal defoliation performance. At 21 DAT, the defoliation rate increased by 13.5-16.3 percentage points compared with TDZ alone. Furthermore, boll opening rates improved by 5.7-12.7 percentage points relative to TDZ-only treatments. Phytohormonal analyses from the Shangzhuang site showed that the combined treatment significantly altered hormone levels in both leaves and petioles. Compared with TDZ alone, the mixture reduced concentrations of auxin (IAA), cytokinins (Z + ZR, iP + iPA, DHZ + DHZR), and gibberellic acid (GA₃), while increasing levels of JA, abscisic acid (ABA), and brassinosteroids (BR). These hormonal shifts may underlie the enhanced defoliation observed with the combined treatment. Importantly, the TDZ-Me-JA combination did not adversely affect cotton yield, yield components, or fiber quality.
Conclusion The combination of Me-JA and TDZ has a good defoliation effect without affecting crop yield or fiber quality. And it provides a promising foundation for the development of novel, environmentally friendly cotton defoliants.

Background Mepiquat chloride (MC) is a widely used plant growth regulator in cotton (Gossypium hirsutum L.). It regulates endogenous hormone content and crosstalk to control plant height and promote lateral root (LR) development. However, the roles of cytokinins (CTKs) in the MC-induced increase in LR number in cotton seedlings remain unclear. Therefore, in this study, whole-genome transcriptome analysis was performed to elucidate the molecular mechanisms, CTK transformation, and CTK signaling pathway response to MC in cotton roots.
Results In the present study, MC reduced the contents of the active CTK trans-zeatin (tZ) and N⁶-isopentenyladenine (iP) but increased the levels of the nucleoside CTK trans-zeatin riboside (tZR) and N⁶-isopentenyladenine riboside (iPR). RNA-seq data showed that the CTK biosynthesis genes GhIPTs and active CTK catabolism genes GhCKXs were obviously upregulated after MC treatment. The CTK-activating enzyme gene GhLOGs was repressed compared with the control. Furthermore, MC inhibited the expression of GhAHK4 and GhARR2/12, which are involved in the CTK signaling pathway, and activated the IAA-IAA14-ARF7/19 signaling module. Meanwhile, MC increased the expression levels of genes involved in sucrose synthesis, the cell cycle, cell division, and cell wall biosynthesis pathways. Silencing the GhCKX family separately decreased the LR number and active indole-3-acetic acid (IAA) level. The expression levels of GhPIN1, GhARF7, GhARF19, GhLBD16, GhLBD18, GhLBD29, and GhLBD33 were downregulated, but GhARR2/12 and GhIAA14 were upregulated. The total content of active CTKs was noticeably increased. The results of silencing the GhLOGs family were opposite to those of silencing GhCKXs. Silencing GhARR12 could upregulate GhPIN1 expression and increase LR number. In addition, the silenced GhCKXs, GhLOGs, and GhARR12 were less responsive to MC-induced LR growth than the control.
Conclusion These results suggested that MC treatment could upregulate CTK-nucleoside biosynthesis and CTK metabolism genes to decrease active CTK levels, promoting crosstalk between CTKs and auxin signaling pathways to enhance LR initiation.