Entomopathogenic fungi and entomopathogenic nematodes are globally distributed soil organisms capable of infecting and killing a vast variety of insects. Therefore, these organisms are frequently used as biocontrol agents in insect pest management. Both entomopathogenic fungi and nematodes share the soil environment and thus can infest and compete for the same insect host; however, natural co-infections are rarely found due to the cryptic soil environment. Our current knowledge on their interactions within hosts mainly comes from laboratory experiments. Because of the recent trend of combining biocontrol agents to increase their efficacy, many studies have focused on the co-application of different species of EPF and EPNs against various insect pests with variable outcomes ranging from synergistic effects and additive effects to antagonism. In addition, the effect on the development and reproduction of each pathogen varies from normal reproduction to exclusion, and generally the outcomes of the interactions are dependent on pathogen and host species, pathogen doses, and the timing of infection. The present review aims to summarize the current knowledge on the interactions of entomopathogenic fungi and nematodes within an insect host and to estimate the possible effects of the interactions on natural pathogen populations and on their use in biocontrol.
Entomopathogenic nematodes of the genera Steinernema and Heterorhabditis, along with their bacterial symbionts from the genera Xenorhabdus and Photorhabdus, respectively, are important biological control agents against agricultural pests. Rapid progress in the development of genomic tools has catalyzed a transformation of the systematics of these organisms, reshaping our understanding of their phylogenetic and cophlylogenetic relationships. In this review, we discuss the major historical events in the taxonomy and systematics of this group of organisms, highlighting the latest advancements in these fields. Additionally, we synthesize information on nematode–bacteria associations and assess the existing evidence regarding their cophylogenetic relationships.
Phasmarhabditis bonaquaense n. sp. is described and illustrated from the body of Malacolimax tenellus, from the locality of České Švýcary near the village of Dobrá Voda, the Czech Republic. Females are characterized by a body length of 2349 (1878–2626) µm and a cupola shaped tail with a long hyaline hair-like tail tip. Extremely prominent papilla-like phasmids present. Males 1829 (1414–2121) µm long. Peloderan bursa with nine pairs of rays (papillae), 1/1/1/2/1/3. One non-paired apparent papilla-like structure located near the ventral appendage anterior to the cloaca. Prominent papilla-like phasmids located close to the tail tip. Small subunit (18S), ITS, and D2-D3 expansion segments of the large subunit of ribosomal DNA were used to analyze the phylogenetic relationships of sequenced species in the genus Phasmarhabditis and other closely related species. Phasmarhabditis bonaquaense n. sp. varied from other related nematodes both in morphological characterizations and phylogenetic analysis. The life cycle of the newly described species is not well known but it is probably a facultative, mollusc-parasitic nematode able to survive permanently in the saprobic phase on decaying organic matter.
A new species of entomopathogenic nematode,Steinernema pwaniensisn. sp., belonging to theglaserigroup, is described from Tanzania. The infective juveniles ofS. pwaniensisn. sp. are characterized by a body length of 978 μm (808–1131), distance from anterior end to excretory pore of 86 μm (80–95) and a tail length of 87 μm (75–95). The ratiosa,candE% ofS. pwaniensisn. sp. are substantially lower than those of all other African ‘glaseri’group members. The first-generation males ofS. pwaniensisn. sp. can be distinguished by a large spicule length of 92 μm (80–97) and by the absence of the caudal mucron, while second-generation males possess a short spine-like mucron. First-generation females have a peg-like tail tip bearing three spine-like projections. Second-generation females can be recognized by a slightly protruding vulva and well-developed post-anal swelling. The new species is further characterized by sequences of the internal transcribed spacer (ITS) and partial 28S regions of the ribosomal DNA. Phylogenetic analyses show thatS. pwaniensisn. sp. forms a strongly supported monophyletic clade with two other East African species,S. ethiopienseandS. karii.
Entomopathogenic nematodes and fungi are globally distributed soil organisms that are frequently used as bioagents in biological control and integrated pest management. Many studies have demonstrated that the combination of biocontrol agents can increase their efficacy against target hosts. In our study, we focused on another potential benefit of the synergy of two species of nematodes, Steinernema feltiae and Heterorhabditis bacteriophora, and the fungus Isaria fumosorosea. According to our hypothesis, these nematodes may be able to disseminate this fungus into the environment. To test this hypothesis, we studied fungal dispersal by the nematodes in different arenas, including potato dextrose agar (PDA) plates, sand heaps, sand barriers, and glass tubes filled with soil. The results of our study showed, for the first time, that the spreading of both conidia and blastospores of I. fumosorosea is significantly enhanced by the presence of entomopathogenic nematodes, but the efficacy of dissemination is negatively influenced by the heterogeneity of the testing arena. We also found that H. bacteriophora spread fungi more effectively than S. feltiae. This phenomenon could be explained by the differences in the presence and persistence of second-stage cuticles or by different foraging behavior. Finally, we observed that blastospores are disseminated more effectively than conidia, which might be due to the different adherence of these spores (conidia are hydrophobic, while blastospores are hydrophilic). The obtained results showed that entomopathogenic nematodes (EPNs) can enhance the efficiency of fungal dispersal.