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.

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.