The importance of fungal infections in both human and animals has increased over the last decades. This article represents an overview of the different categories of fungal infections that can be encountered in animals originating from environmental sources without transmission to humans. In addition, the endemic infections with indirect transmission from the environment, the zoophilic fungal pathogens with near-direct transmission, the zoonotic fungi that can be directly transmitted from animals to humans, mycotoxicoses and antifungal resistance in animals will also be discussed. Opportunistic mycoses are responsible for a wide range of diseases from localized infections to fatal disseminated diseases, such as aspergillosis, mucormycosis, candidiasis, cryptococcosis and infections caused by melanized fungi. The amphibian fungal disease chytridiomycosis and the Bat White-nose syndrome are due to obligatory fungal pathogens. Zoonotic agents are naturally transmitted from vertebrate animals to humans and vice versa. The list of zoonotic fungal agents is limited but some species, like Microsporum canis and Sporothrix brasiliensis from cats, have a strong public health impact. Mycotoxins are defined as the chemicals of fungal origin being toxic for warm-blooded vertebrates. Intoxications by aflatoxins and ochratoxins represent a threat for both human and animal health. Resistance to antifungals can occur in different animal species that receive these drugs, although the true epidemiology of resistance in animals is unknown, and options to treat infections caused by resistant infections are limited.

Elevated zero maze is a modification of the elevated plus maze model of anxiety in rodents. The novel design comprises an elevated annular platform with two opposite, enclosed quadrants and two open quadrants, removing any ambiguity in the interpretation of the time spent in the central square of the traditional design and allowing uninterrupted exploration. In the present study, we validated elevated zero maze as a tool to study antianxiety activity, using various standard anxiolytics belonging to different pharmacological groups, such as benzodiazepines, barbiturates, alcohol etc., and compared the results with elevated plus maze. Bidirectional sensitivity of the model was also assessed using picrotoxin, pentylenetetrazol and flumazenil, the modulators of GABA(A) and benzodiazepine modulators. Animals were administered different standard antianxiety and anxiogenic drugs, and were allowed to explore the elevated zero maze (time spent in open arm, latency to enter in open arm, total number of entries in open arm and number of stretch attend postures [SAPs]) and elevated plus maze (time spent in open arm, latency to enter in open arm, total number of entries in open arm, first preference of the animal [open/closed] and number of stretchings). Selected drugs and doses were then assessed on the mirror chamber paradigm. Results of the present study indicated that elevated zero maze offered a better animal model to study antianxiety activity, when compared with elevated plus maze and mirror chamber.

Aims: To study the biocontrol potential of nematode-trapping fungus Arthrobotrys oligospora in protecting tomato (Lycopersicon esculentum Mill.) against Meloidogyne incognita and Rhizoctonia solani under greenhouse and field conditions. Methods and Results: Five isolates of the nematode-trapping fungus Arthrobotrys oligospora isolated from different parts of India were tested against Meloidogyne incognita and Rhizoctonia solani in tomato (Lycopersicon esculentum Mill.) plants grown under greenhouse and field conditions. Arthrobotrys oligospora-treated plants showed enhanced growth in terms of shoot and root length and biomass, chlorophyll and total phenolic content and high phenylalanine ammonia lyase activity in comparison with M. incognitaand R. solani-inoculated plants. Biochemical profiling when correlated with disease severity and intensity in A. oligospora-treated and untreated plants indicate that A. oligospora VNS-1 offered significant disease reduction in terms of number of root galls, seedling mortality, lesion length, disease index, better plant growth and fruit yield as compared to M. incognita-and R. solanichallenged plants. Conclusion: The result established that A. oligospora VNS-1 has the potential to provide bioprotection agents against M. incognita and R. solani. Significance and Impact of the Study: Arthrobotrys oligospora can be a better environment friendly option and can be incorporated in the integrated disease management module of crop protection. Application of A. oligospora not only helps in the control of nematodes but also increases plant growth and enhances nutritional value of tomato fruits. Thus, it proves to be an excellent biocontrol as well as plant growth promoting agent.

Five isolates of Arthrobotrys dactyloides were isolated from different locations of India and their in vitro predacity was tested against Meloidogyne incognita (J 2 ), Tylenchorhynchus brassicae and Hoplolaimus indicus. All isolates of A. dactyloides captured and killed M. incognita and T. brassicae but not H. indicus. The isolates also differed in their predacity of the first two nematode species. The application of mass culture of A. dactyloides in soil infested with 2000 juveniles of M. incognita per ÔkgÕ before planting of tomato seedlings reduced the number of root knots by 5.6-45.6%, of females by 44.7-72.9%, of egg masses by 44.5-51.3% and of juveniles by 37.9-81.8% and increased the plant growth in a pot experiment. The effect of this fungus as biocontrol agent was enhanced when its mass culture was applied with cow dung manure, which reduced the number of root knots by 61.7-66.6%, of females by 80.6-94.7%, of egg masses by 80.3-89.6% and of juveniles by 68.1-88.0%.www.blackwell-synergy.com

Emerging drug resistance varieties and hyper-virulent strains of microorganisms have compelled the scientific fraternity to develop more potent and less harmful therapeutics. Antimicrobial peptides could be one of such therapeutics. This review is an attempt to explore antifungal peptides naturally produced by prokaryotes as well as eukaryotes. They are components of innate immune system providing first line of defence against microbial attacks, especially in eukaryotes. The present article concentrates on types, structures, sources and mode of action of gene-encoded antifungal peptides such as mammalian defensins, protegrins, tritrpticins, histatins, lactoferricins, antifungal peptides derived from birds, amphibians, insects, fungi, bacteria and their synthetic analogues such as pexiganan, omiganan, echinocandins and Novexatin. In silico drug designing, a major revolution in the area of therapeutics, facilitates drug development by exploiting different bioinformatics tools. With this view, bioinformatics tools were used to visualize the structural details of antifungal peptides and to predict their level of similarity. Current practices and recent developments in this area have also been discussed briefly.