Bats are indispensable members of the natural world, supporting its delicate balance. Bats have vital roles in controlling insect populations and enhancing soil fertility. They also help in the harvesting and dispersal of seeds, pollination in plants, and nutrient recycling and distribution. However, through evolution over millions of years, they have also adapted their immune system so that they may carry numerous types of pathogens, the majority of which are viruses, without these pathogens having any serious ill effects on bats themselves. Their anatomical adaptation to flight and the reduced immune response to DNA damage during flight have also contributed to bats becoming reservoirs of deadly pathogenic diseases. This review discusses the different adaptations of bats with a special focus on the immune system that have helped them evolve as a reservoir for various viruses. The study also enumerates how the increase in global warming, the consequent changes in climatic conditions, habitat destruction, and bushmeat consumption increase the chances of an outbreak of novel zoonotic disease when humans come in contact with bats.

Magnaporthe oryzae causes a fungal disease that poses a serious risk to global food security. Nanoagrochemicals are perceived as sustainable, economical, and environmentally friendly alternatives to traditional pesticides. Plant immune activators can be applied as the active ingredients of nanopesticides to control diseases in agriculture, but their use is limited and corresponding research is lacking. In this study, a nanodelivery system (PBZ@CaCO3@SG) for the on-demand release of a plant immune activator (probenazole; PBZ) was prepared using nano-CaCO3 after coating with sodium alginate-gelatin (SG). In vitro, at 48 h, the release rate reached 97.9% and 88.4% at pH 4.5 and 6.0, respectively, which greatly exceeded that under neutral conditions (pH 7.4), with acid-responsive release characteristics. Moreover, it responded quickly to the acidic microenvironment generated during M. oryzae infestation and rationally released PBZ, effectively improving plant resistance to M. oryzae and minimizing disease. Notably, M. oryzae infection was markedly reduced, by 60.6%, after PBZ@CaCO3@SG treatment. Mechanistically, PBZ@CaCO3@SG enhanced both physical barrier formation and systemic acquired resistance in rice, enhancing resistance to M. oryzae. It also showed good biosafety for both microbial communities and earthworms in the soil. This comprehensive study revealed multiple mechanisms by which PBZ@CaCO3@SG interacts with plants and pathogens, inhibits damage, and maintains nontarget biosafety, emphasizing its great potential for plant disease management.

The current study aimed to isolate Beauveria brongniartii conidia from forest soils, identify the fungus, and evaluate its effectiveness on the eggs, larvae, pupae, and adults of Spodoptera litura. Insect mortality rates were recorded every 3, 6, 9, and 12 days. The identification of entomopathogenic fungi was carried out using molecular techniques, including PCR, DNA sequencing, and molecular markers, to detect species-specific 18 S rDNA genetic sequences, all performed under aseptic conditions. The results indicated that higher conidia concentrations (2.7 x 109 conidia/mL) exhibited greater virulence, with eggs showing a mortality rate of 98.66%, followed by larvae 96%, adults 90.66%, and pupae 77.33% after 12 days. Probit analysis revealed minimal LC50 and LC90 values: eggs (5.5 x 102; 1.0 x 106 spores/mL), larvae (8.2 x 102; 1.2 x 107 spores/mL), pupae (9.6 x 104; 7.3 x 1010 spores/mL), and adults (1.0 x 103; 2.0 x 108 spores/mL). The total hemocyte counts and detailed observational results revealed that B. brongniartii induces cellular breakdown and cell lysis in S. litura larvae by producing enzymes that degrade the cuticle and cell membranes. Earthworm bioindicator studies showed minimal effects from B. brongniartii conidia compared to controls, while chemical treatments resulted in 96% mortality at 100 ppm. Histopathological examinations revealed no significant differences in gut tissue between earthworms treated with fungal conidia and those in the control group, unlike the substantial damage caused by chemical treatments. Biochemical analysis revealed significant alterations in enzyme activity, including reduced levels of phosphatase and catalase, as well as increased levels of lipid peroxides and superoxide dismutase. This study highlights the effectiveness of B. brongniartii in controlling S. litura, demonstrating its potential as a viable biocontrol agent and promoting eco-friendly alternatives to chemical pesticides, with no risk to non-target species or the environment.

Aflatoxin (AF) is a toxic metabolite produced by the fungus Aspergillus. The various subtypes of AFs include B1, B2, G1, G2, M1, and M2, with Aflatoxin B1 (AFB1) being the most toxic. These AFs are widespread in the environment, particularly in soil and food crops. The World Health Organization (WHO) has classified AFB1 as a highly potent natural Class 1A carcinogen. Excessive exposure to AFB1 can lead to poisoning in both humans and animals, posing substantial risks to food safety and livestock breeding industries. This review provides an overview of the metabolic processes, detection methods, and the detrimental impacts of AFB1 on animal reproduction, immunity, nerves, intestines, and metabolism. Furthermore, it explores the preventive and control capacities of natural active substances, trace elements, and microorganisms against AFB1. Ultimately, this paper serves as a reference for further research on the pathogenic mechanism of AFB1, the development of preventive drugs, and the selection of effective detoxification measures for AFB1 in animal feed.

Per- and polyfluoroalkyl substances (PFAS) are a class of persistent organic pollutants that pose a growing threat to environmental and human health. Soil acts as a long-term reservoir for PFAS, potentially impacting soil biodiversity and ecosystem function. Earthworms, as keystone species in soil ecosystems, are particularly vulnerable to PFAS exposure. In this study, we investigated the sublethal effects of three short-chain (C4-C6) next-generation perfluoropropylene oxide acids (PFPOAs) on the earthworm Eisenia fetida, using a legacy perfluoroalkyl carboxylic acid (PFCA), perfluorooctanoic acid (PFOA), as a reference. We assessed a suite of biochemical endpoints, including markers for oxidative stress (catalase and superoxide dismutase activity), immunity (phenol oxidase activity), neurotoxicity (acetylcholinesterase activity), and behavioural endpoints (escape test). Results indicate that all tested PFAS, even at sub-micromolar concentrations, elicited significant effects across multiple physiological domains. Interestingly, HFPO-DA demonstrated the most substantial impact across all endpoints tested, indicating broad and significant biochemical and neurotoxic effects. Our findings underscore the potential risks of both legacy and emerging PFAS to soil ecosystems, emphasising the need for further research to understand the long-term consequences of PFAS contamination.

BACKGROUND Chemotherapy-associated ovarian damage (CAOD) is one of the most feared short- and long-term side effects of anticancer treatment in premenopausal women. Accumulating detailed data show that different chemotherapy regimens can lead to disturbance of ovarian hormone levels, reduced or lost fertility, and an increased risk of early menopause. Previous studies have often focused on the direct effects of chemotherapeutic drugs on ovarian follicles, such as direct DNA damage-mediated apoptotic death and primordial follicle burnout. Emerging evidence has revealed an imbalance in the ovarian microenvironment during chemotherapy. The ovarian microenvironment provides nutritional support and transportation of signals that stimulate the growth and development of follicles, ovulation, and corpus luteum formation. The close interaction between the ovarian microenvironment and follicles can determine ovarian function. Therefore, designing novel and precise strategies to manipulate the ovarian microenvironment may be a new strategy to protect ovarian function during chemotherapy.OBJECTIVE AND RATIONALE This review details the changes that occur in the ovarian microenvironment during chemotherapy and emphasizes the importance of developing new therapeutics that protect ovarian function by targeting the ovarian microenvironment during chemotherapy.SEARCH METHODS A comprehensive review of the literature was performed by searching PubMed up to April 2024. Search terms included 'ovarian microenvironment' (ovarian extracellular matrix, ovarian stromal cells, ovarian interstitial, ovarian blood vessels, ovarian lymphatic vessels, ovarian macrophages, ovarian lymphocytes, ovarian immune cytokines, ovarian oxidative stress, ovarian reactive oxygen species, ovarian senescence cells, ovarian senescence-associated secretory phenotypes, ovarian oogonial stem cells, ovarian stem cells), terms related to ovarian function (reproductive health, fertility, infertility, fecundity, ovarian reserve, ovarian function, menopause, decreased ovarian reserve, premature ovarian insufficiency/failure), and terms related to chemotherapy (cyclophosphamide, lfosfamide, chlormethine, chlorambucil, busulfan, melphalan, procarbazine, cisplatin, doxorubicin, carboplatin, taxane, paclitaxel, docetaxel, 5-fluorouraci, vincristine, methotrexate, dactinomycin, bleomycin, mercaptopurine).OUTCOMES The ovarian microenvironment shows great changes during chemotherapy, inducing extracellular matrix deposition and stromal fibrosis, angiogenesis disorders, immune microenvironment disturbance, oxidative stress imbalances, ovarian stem cell exhaustion, and cell senescence, thereby lowering the quantity and quality of ovarian follicles. Several methods targeting the ovarian microenvironment have been adopted to prevent and treat CAOD, such as stem cell therapy and the use of free radical scavengers, senolytherapies, immunomodulators, and proangiogenic factors.WIDER IMPLICATIONS Ovarian function is determined by its 'seeds' (follicles) and 'soil' (ovarian microenvironment). The ovarian microenvironment has been reported to play a vital role in CAOD and targeting the ovarian microenvironment may present potential therapeutic approaches for CAOD. However, the relation between the ovarian microenvironment, its regulatory networks, and CAOD needs to be further studied. A better understanding of these issues could be helpful in explaining the pathogenesis of CAOD and creating innovative strategies for counteracting the effects exerted on ovarian function. Our aim is that this narrative review of CAOD will stimulate more research in this important field.REGISTRATION NUMBER Not applicable. Graphical Abstract Chemotherapy causes an imbalance of the ovarian microenvironment leading to chemotherapy-associated ovarian damage and dysfunction, and further research is needed to explore the possible protective treatments. Created with BioRender.com, with permission.

Nanoplastics (NPs) are currently everywhere and environmental pollution by NPs is a pressing global problem. Nevertheless, until now, few studies have concentrated on the mechanisms and pathways of cytotoxic effects and immune dysfunction of NPs on soil organisms employing a multidimensional strategy. Hence, earthworm immune cells and immunity protein lysozyme (LZM) were selected as specific receptors to uncover the underlying mechanisms of cytotoxicity, genotoxicity, and immunotoxicity resulting from exposure to polystyrene nanoplastics (PS-NPs), and the binding mechanisms of PS-NPs-LZM interaction. Results on cells indicated that when earthworm immune cells were exposed to high-dose PS-NPs, it caused a notable rise in the release of reactive oxygen species (ROS), resulting in oxidative stress. PS-NPs exposure significantly decreased the cell viability of earthworm immune cells, inducing cytotoxicity through ROS-mediated oxidative stress pathway, and oxidative injury effects, including reduced antioxidant defenses, lipid peroxidation, DNA damage, and protein oxidation. Moreover, PS-NPs stress inhibited the intracellular LZM activity in immune cells, resulting in impaired immune function and immunotoxicity by activating the oxidative stress pathway mediated by ROS. The results from molecular studies revealed that PS-NPs binding destroyed the LZM structure and conformation, including

Bisphenol A (BPA) is one of the environmental endocrine disruptors, due to its chemical stability it exists in abundant concentrations in water and soil consequently accumulating in the food chain and causing many endocrine-related health problems. So far, studies on the effects of BPA on marine invertebrates have focused on acute toxicity, endocrine regulation, reproduction, and development. However, fewer studies have been conducted on marine benthos. The current study aimed to detect the accumulation of BPA and its impact on tissue structure, antioxidant capacity, and immune indexes in marine worm, Urechis unicinctus. U. unicinctus, as a common marine benthic animal, were exposed to different concentrations of BPA. Blood cells and intestinal tract were taken for tissue structure inspection, and supernatant of the coelomic fluid was collected for oxidative and antioxidant biomarkers. Results showed that the accumulation of BPA in muscles of U. unicinctus tended to increase with exposure time. BPA induced a rise in H2O2 and MDA content, and altered the activities of CAT, TSOD, GST, LSZ and ACP, weaken the immune system functions. Moreover, pathological observation showed that BPA caused severe histopathology in the respiratory intestine, stomach, and midgut. These results will be helpful to understand the response mechanism of U. unicinctus under BPA exposure and provide a reference for controlling the aquaculture conditions and marine water quality of U. unicinctus.