Effects of Adjuvants on Entomopathogenic Nematode Persistence and Efficacy Against Plutella xylostella

The effects of spray additives on entomopathogenic nematode persistence and efficacy against Plutella xylostella (L . ) were studied . Several adjuvants were toxic to radish seedlings ( Raphanus sativus var . capitata L . ) but none was toxic to the nematodes or P. xylostella. In the laboratory , the adjuvants that provided the best antidesiccant activity based on a rank score were TX7719 , Rodspray oil and Nufilm P . Those providing less protection but better than the remaining adjuvants were 38 - F , dextrose and Pluronic F - 127 . In greenhouse trials , TX7719 and Rodspray oil were more effective than the other adjuvants tested . The stilbene brightener , Blankophor BBH , did not increase nematode efficacy consistently in greenhouse trials probably because the concentration used was too low . In field trials , the combination of TX7719 plus Blankophor BBH increased nematode persistence on watercress leaves ( Nasturium officinale R . Br . ) and efficacy against P. xylostella significantly . In vitro- pro duced nematodes benefited more from additives than in vivo- produced nematodes in the laboratory , but that difference was lost in the field . Overall , it was found that additives generally improved nematode persistence and efficacy , but the improvement was probably not sufficient to increase the feasibility of foliar applications of nematodes against P. xylostella. However , further evaluation of adjuvants is warranted for applications of nematodes to watercress for the control of P. xylostella.     

Steinernema biddulphi n. sp., a New Entomopathogenic Nematode (Nematoda: Steinernematidae) from South Africa

A new species of entomopathogenic nematode (EPN), Steinernema biddulphi n. sp., was isolated from a maize field in Senekal, Free State Province of South Africa. Morphological and molecular studies indicated the distinctness of S. biddulphi n. sp. from other Steinernema species. Steinernema biddulphi n. sp. is characterized IJs with average body length of 663 μm (606–778 μm), lateral fields with six ridges in mid-body region forming the formula 2,6,2. Excretory pore located anterior to mid-pharynx (D% = 46). Hyaline layer occupies approximately half of tail length. Male spicules slightly to moderately curved, with a sharp tip and golden brown in color. The first generation of males lacking a mucron on the tail tip while the second generation males with a short filamentous mucron. Genital papillae with 11 pairs and one unpaired preanal papilla. The new species is further characterized by sequences of the internal transcribed spacer (ITS) and partial 28S regions (D2-D3) of the ribosomal DNA (rDNA). Phylogenetic data show that S. biddulphi n. sp. belongs to the “bicornutum” clade within the Steinernematidae family.     

Escape of Steinernema feltiae from Alginate Capsules Containing Tomato Seeds

The entomogenous nematode Steinernema feltiae was encapsulated in an alginate matrix containing a tomato seed. When these capsules were placed on 0.8% agar for 7 days, the seed germinated and ca. 20% of the nematodes escaped from the capsules, whereas only 0.1% escaped from capsules without seeds. When capsules containing nematodes and a seed were planted into sterilized or nonsterilized soil, nematodes escaped to infect Galleria mellonella larvae. When seed in capsules containing ca. 274 nematodes per capsule were planted in nonsterilized soil, Galleria mortality was 90% 1 week later. Galleria mortality declined to 27%, 23%, and 0% in weeks 2, 4, and 8 postplant, respectively. In sterilized soil, Galleria mortality was 96% and did not differ significantly from the nonsterilized soil in week 1, but was significantly higher in sterilized soil over nonsterilized soil for week 2 (81%) and week 4 (51%). When capsules containing nematodes only were used, Galleria mortality was 71% in sterilized soil 1 week after planting and 58%, 33%, and 12% in weeks 2, 4, and 8 postplant, respectively. In nonsterilized soil, Galleria mortality was 8%, 30%, 21%, and 28% after 1, 2, 4, and 8 weeks, respectively, using only encapsulated nematodes. When the number of nematodes per capsule was increased to ca. 817, Galleria mortality was 92 % or higher in sterilized soil from week 1 to week 4.     

Involvement of larvicidal toxins in pathogenesis of insect parasitism with the rhabditoid nematodes,Steinernema feltiae andHeterorhabditis bacteriophora

The insect-parasitic rhabditoid nematodes,Steinernema feltiae andHeterorhabditis bacteriophora, released a compound/s/ toxic to larvae of the greater wax moth,Galleria mellonella, that caused paralysis and death of the insect. Larvicidal substances appeared in wax moth larvae during parasitism and after inoculation with the primary form of the bacterial associates of the nematodes. The nematodeS. feltiae and its associate,Xenorhabdus nematophilus, excreted much less toxic activity within larval body thanH. bacteriophora. The secondary form ofXenohabdus did not produce toxin in parasitized larvae, butX. luminescens, the bacterium associated withH. bacteriophora, released detectable titer of toxin activity in broth cultures. Both nematode toxins were sensitive to heat and produced a specific type of proteolytic activity. Preliminary identification of the compounds responsible for larval toxicity revealed similarities to immune inhibitors produced by some bacterial pathogens of insects.      

Genetic Variability among Strains of the Entomopathogenic Nematode Steinernema feltiae

A systematic program of genetic improvement was initiated by assessing the phenotypic variation of Steinernema feltiae strains for two traits assumed to limit efficacy: ultraviolet tolerance and host-finding ability. All of the strains assayed showed both low ultraviolet tolerance and poor host-finding ability, indicating that the likelihood of improving these traits through more extensive population sampling is remote. Limited genetic variation was detected among the strains for tolerance to ultraviolet, suggesting that selective breeding for increased tolerance would be inefficient. By contrast, highly significant phenotypic differences were found with regard to host-finding ability, suggesting that this trait would be responsive to selection. A genetically heterogeneous population was constructed by round-robin mating of 10 strains; it will serve as the foundation population for selective breeding.     

Control of diapausing codling moth,Cydia pomonella (Lepidoptera: Tortricidae) in wooden fruit bins,using entomopathogenic nematodes (Heterorhabditidae and Steinernematidae)

Stacked wooden fruit bins are frequent overwintering sites for overwintering diapausing codling moth larvae. Control strategies against the codling moth (Cydia pomonella) (Lepidoptera: Tortricidae) in South Africa have been hampered by the reinfestation of orchards from nearby stacked infested fruit bins and by the movement of infested bins between orchards. Worldwide, wooden fruit bins are systematically being replaced with plastic bins, however in South Africa this will not be accomplished in the near future. The objective of this study was to evaluate the potential of two recycled commercially available entomopathogenic nematode (EPN) species, Heterorhabditis bacteriophora and Steinernema feltiae, as well as of a local species, Steinernema yirgalemense, to disinfest miniature wooden fruit bins under controlled conditions in the laboratory. After dipping miniature bins loaded with codling moth larvae in a suspension of 25?IJs/mL of each of the three EPN species, under optimum conditions of temperature and humidity, the highest percentage of control was obtained using S. feltiae (75%). The addition of adjuvants significantly increased S. feltiae infectivity to >95%, whereas it did not result in a significant increase in H. bacteriophora or S. yirgalemense infectivity.     

Mortality of Immature Houseflies (Musca domestica L.) in Artificial Diet and Chicken Manure after Exposure to Encapsulated Entomopathogenic Nematodes (Rhabditida: Steinernematidae, Heterorhabditidae)

The entomopathogenic nematodes, Steinernema felitae (=bibionis) and Heterorhabditis megidis, were encapsulated in calcium alginate and their efficacy was tested against immature houseflies. Aliquots of capsules (15 ml) containing either 1 000 000, 500 000, 250 000 or 125 000 nematodes were added to 70-ml portions of grassmeal diet containing either eggs of first, second or third instar larvae. After 2 days, the treatment with 1 000 000 encapsulated S. feltiae (=bibionis) had killed 94% of housefly eggs and 90% of first instar larvae. By day 6, both of these mortalities had increased significantly (P 0.005) to 100%. By day 2, in the same medium, 1 000 000 encapsulated H. megidis had killed 71.4% of eggs and 90% of first instar larvae. This increased significantly (P 0.01) by day 6, to 99.2% and 100% respectively. Another experiment was carried out where immature houseflies were placed in chicken manure. The emergence of houseflies as adults was used to measure the effect of the encapsulated nematodes. Depending on the numbers of nematodes and the original stage of the housefly, the treatment with encapsulated S. feltiae resulted in 55-96% reduction in adult housefly emergence, whereas treatment with encapsulated H. megidis resulted in 35-98% reduction in emergence. Finally, when encapsulated nematodes were presented as a bait to adult houseflies, little infectivity was observed.     

Modulation of immune responses of Rhynchophorus ferrugineus (Insecta: Coleoptera) induced by the entomopathogenic nematode Steinernema carpocapsae (Nematoda: Rhabditida)

Aim of this study was to investigate relationships between the red palm weevil (RPW) Rhynchophorus ferrugineus (Olivier) and the entomopathogenic nematode Steinernema carpocapsae (EPN); particularly, the work was focused on the immune response of the insect host in naive larvae and after infection with the EPN. Two main immunological processes have been addressed: the activity and modulation of host prophenoloxidase‐phenoloxidase (proPO) system, involved in melanization of not‐self and hemocytes recognition processes responsible for not‐self encapsulation. Moreover, immune depressive and immune evasive strategies of the parasite have been investigated. Our results suggest that RPW possess an efficient immune system, however in the early phase of infection, S. carpocapsae induces a strong inhibition of the host proPO system. In addition, host cell‐mediated mechanisms of encapsulation, are completely avoided by the parasite, the elusive strategies of S. carpocapsae seem to be related to the structure of its body‐surface, since induced alterations of the parasite cuticle resulted in the loss of its mimetic properties. S. carpocapsae before the release of its symbiotic bacteria, depress and elude RPW immune defenses, with the aim to arrange a favorable environment for its bacteria responsible of the septicemic death of the insect target.     

Influence of cell density and phase variants of bacterial symbionts (Xenorhabdus spp.) on dauer juvenile recovery and development of biocontrol nematodes Steinernema carpocapsae and S. feltiae (Nematoda: Rhabditida)

The rhabditid nematodes Steinernema carpocapsae and Steinernema feltiae are used in biological control of insect pests. Mass production is done in liquid culture media pre-incubated with their bacterial symbionts Xenorhabdus nematophila and Xenorhabdus bovienii, respectively, before nematode dauer juveniles (DJs) are inoculated. As a response to food signals produced by the bacterial symbionts, the DJs exit from the developmentally arrested dauer stage (they recover development) and grow to adults, which produce DJ offspring. Variable DJ recovery after inoculation often causes process failure due to non-synchronous population development and low numbers of adult nematodes. This contribution investigated the influence of the bacterial cell density on DJ recovery and development to adults. At higher density of 10¹⁰ bacterial cells ml⁻¹, a higher percentage of DJ recovery was induced, and adults occurred earlier in both Steinernema spp. than at lower density of 10⁹ and 10⁸ cells ml⁻¹. Xenorhabdus symbionts produce phase variants. Recovery in bacteria-free supernatants was lower than in supernatants containing bacterial cells for both primary and secondary phase Xenorhabdus spp. and lower in secondary than in primary phase supernatants or cell suspensions. In general, recovery was lower for Steinernema feltiae and the time at which 50% of the population had recovered after exposure to the food signal was longer (RT₅₀ = 17.1 h) than for Steinernema carpocapsae (RT₅₀ = 6.6 h). Whereas >90% S. carpocapsae DJs recovered in hemolymph serum of the lepidopteran insect Galleria mellonella, recovery of S. feltiae only reached 31%. Penetration into a host insect prior to exposure to the insect’s food signal did not enhance DJ recovery. Consequences for liquid culture mass production of the nematodes and differences between species of the genera Steinernema and Heterorhabditis are discussed.