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This work aimed to investigate candidate biological control agents against the cattle tick Rhipicephalus microplus by studying three entomopathogenic nematodes (EPN) isolates from two species, Heterorhabditis bacteriophora (isolates LPP30 and HP88) and Heterorhabditis baujardi (isolate LPP7). The study comprised the pharmacotechnical development of four test formulations, and their biological evaluation, in three stages: 1) selection of the fittest EPN isolate at 16 ± 1 °C after 120 h of incorporation in the formulations; 2) determination of the effects of temperature and incubation time on the survival of the selected isolate in formulations; 3) evaluation of the in vitro efficacy (infectivity) of the selected EPN formulations and their components against R. microplus females after 72 h exposure. H. baujardi LPP7 presented the highest survival rates in 0.1% carboxymethyl cellulose sodium (CMC) formulations (100% at 25 °C, up to 10 days after incorporation). At the highest tested temperature (34.2 °C), 54% of LPP7 survived for up to 72 h in CMC formulations. The infectivity of LPP7-containing formulation against R. microplus was 99%, reducing oviposition, egg production index and larval hatching. Considering the pressing need for safer acaricide products, incorporation of EPNs in pharmaceutical formulations is presented as a promising approach for the biological control of cattle tick infestations, potentially reducing environmental impact and resistance development associated with chemical acaricides.

The present study evaluated, in the laboratory, the virulence of Heterorhabditis bacteriophora LPP30 against engorged females of Rhipicephalus microplus; in addition, we evaluated, in semi-field tests, the effects of four isolates of Heterorhabditis spp. (i.e., H. bacteriophora HP88, Heterorhabditis baujardi LPP7, Heterorhabditis indica LPP1 and H. bacteriophora LPP30) in insect cadaver formulation against the non-parasitic phase of R. microplus. In the first experiment (in vitro), engorged females were exposed, in Petri dish, to H. bacteriophora LPP30 at 75, 150, 300, 600, 1200 and 2400 nematodes/tick (10 ticks per concentration tested). In the second experiment (semi-field), five engorged females and four cadavers of Galleria mellonella infected with nematodes were placed in pots with soil and grown Brachiaria decumbens; the pots were hold outdoor, exposed to natural environment conditions during the tests. In the third experiment (semi-field), 65 days after the cadavers had been placed in the pots for the second experiment, new engorged females (five per pot) were placed in the pots of the groups treated with H. bacteriophora HP88 or H. baujardi LPP7, to assess their persistence in the soil. In the first test, the percent control was higher than 95% in all treatment groups. In the second experiment, at day 22, the mean mortality rate was 78% in the groups treated with H. bacteriophora LPP30 or H. indica LPP1, and reached 100% and 98% when treated with H. bacteriophora HP88 and H. baujardi LPP7, respectively. In this experiment, the egg-laying inhibition index was higher than 90% in the groups treated with H. bacteriophora HP88 (97.2%) or H. baujardi LPP7 (91.9%). In the third experiment with H. bacteriophora HP88 and H. baujardi LPP7, the egg-laying inhibition index was 59.1% and 43.1%, respectively. We concluded that the isolate LPP30 was highly virulent under laboratory conditions, whereas in semi-field tests, HP88 and LPP7 were the most effective isolates. Moreover, HP88 and LPP7 remained active against engorged females of R. microplus in the soil for 65 days after application of EPN-infected cadavers of G. mellonella.

The aim of this study was to evaluate the effect of different concentrations of the entomopathogenic nematodes (EPNs) Heterorhabditis bacteriophora HP88 and Heterorhabditis indica LPP1 on the reproductive biology of partially engorged females of Dermacentor nitens. Four groups were formed, with each group containing 10 females and exposed to concentrations of 0, 75, 300, and 1200 nematodes for each female. This procedure was performed separately for each nematode. The following biological parameters were evaluated: egg mass weight, egg production index, hatching percentage, and percentage of control. H. bacteriophora HP88 at the two highest concentrations (300 and 1200 EPNs/female) caused a reduction (p < 0.05) on the egg mass and egg production index. Was noted a significant reduction (p < 0.05) in the percentage of hatched in all the treated groups. For H. indica LPP1, all treatments resulted in decreased (p < 0.05) values for all the parameters. The percentages of controls obtained at concentrations of 75, 300, and 1200 EPNs/female were 56.3, 89.3, and 98.8 and 77.5, 77.1, and 95.9 for H. bacteriophora HP88 and H. indica LPP1, respectively. Therefore, it is concluded that these nematodes showed pathogenicity toward partially engorged females of D. nitens, thereby negatively affecting the reproductive biology of this tick.

This study investigated the possible biological, biochemical and histological changes in Bradybaena similaris (Gastropoda: Pulmonata) infected by Heterorhabditis indica (Rhabditida: Heterorhabditidae), strain LPP1. Two groups of 16 snails were formed: the control group (unexposed) and the treated group, which was exposed for three weeks to infective juveniles (J3) of H. indica LPP1. The experiment was conducted in duplicate, using a total of 64 snails. After the exposure period, the snails were dissected to collect the hemolymph and tissues, for evaluation of the physiological changes caused by the infection. The number of eggs laid/snail and the viability of these eggs were also assessed as indicators of the reproductive activity of B. similaris. Intense glycogenolysis was accompanied by a significant reduction (p

The aim of this study was to assess the influence of different exposure times of engorged female the Rhipicephalus microplus to infective juveniles of Heterorhabditis bacteriophora isolate HP88. The engorged females were divided into seven groups (six treatments and one control) of 20 ticks each with statistically similar average weights (p>0.05) and exposed to concentrations of 300 nematodes/tick for periods of 3, 6, 12, 24, 48 and 72h. The following biological parameters were monitored: pre-oviposition period; egg mass weight; hatching percentage; and efficacy of treatment. There was no influence of the exposure time on the pre-oviposition period (p>0.05), while there were significant differences (p

In orchards, in cases where the insect pests are concentrated under the canopy, entomopathogenic nematodes can be applied as infected host cadavers. This study evaluated the distribution of Heterorhabditis baujardi Phan, Subbotin, Nguyen & Moens strain LPP7 applied as one or 15 host cadavers per plot in a guava orchard. The plots were located between guava trees, with the host cadavers being placed in the centre. Soil samples were taken at 1, 3, 5, 8 and 10 weeks after cadaver application. On each date, the plots were sampled at 30, 60, 90 and 120 cm from the cadaver application point and at three different depths (0 – 10, 10 – 20 and 20 – 30 cm). The highest average number of recovered infective juveniles was found at 90 cm from the cadaver application point, and at 10 cm depth and on the fifth week after application. There was no significant effect on the number of recovered infective juvenile nematodes, when they were applied as one or 15 cadavers, although the most uniform dispersal was found when 15 ...

Entomopathogenic nematodes (EPNs) are currently being used as successful biological control agents of soil-dwelling insect pests. Previous field and greenhouse studies demonstrated that application techniques and non-biotic factors (temperature and pressure) have a significant effect on EPNs efficacy. The objective of this study was to evaluate the influence of an irrigation spray application system on the viability, infectivity and host search capability of Heterorhabditis baujardi LPP7 (Nematoda: Heterorhabditidae) infective juveniles (IJ). Two assays were proposed. Their viability was evaluated under the microscope after the IJ passed through the irrigation system. Infectivity on Galleria mellonella larvae, and host search capability, as evidenced by larval mortality, were evaluated in containers (Experiment 1). In the field (Experiment 2), mortality of G. mellonella larvae was evaluated under different nematode concentrations (0, 100,000, 300,000 and 500,000 IJ per tree). No differences were recorded on the viability, infectivity and host search capability of the IJ in Experiment 1. In Experiment 2, differences were recorded among the different concentrations used (p < 0.05), and a higher mortality was observed at the highest nematode concentration (28.3% and 37% in each one of the two experiment repetitions). This irrigation system did not affected adversely the viability, infectivity and host search capability of H. baujardi LPP7. Nematóides entomopatogênicos (NEPs) vêm sendo usados com sucesso como agentes do controle biológico de pragas de solo. Estudos anteriores mostraram que técnicas de aplicação e fatores abióticos (temperatura e pressão) afetam a eficiência dos NEPs em testes de campo e casa-de-vegetação. O objetivo deste trabalho foi avaliar a influência de condições geradas por um sistema de irrigação por microaspersão, na viabilidade, infectividade e na capacidade de busca de hospedeiros nos juvenis infectantes (JI) de Heterorhabditis baujardi LPP7 (Nematoda: Heterorhabditidae). Dois experimentos foram propostos. A viabilidade dos juvenis infectantes (JI) foi avaliada no microscópio imediatamente após sua passagem pelo sistema de irrigação. A infectividade e a capacidade de busca pelo hospedeiro em larvas de Galleria mellonella foram avaliadas em vasos (Experimento 1). A campo (Experimento 2), foi avaliada a mortalidade de larvas de G. mellonella sob diferentes concentrações do nematóide (0, 100.000, 300.000 e 500.000 JI por árvore). A viabilidade, infectividade e a capacidade de busca dos nematóides após a passagem pelo sistema não foi diferente da testemunha. No Experimento 2, houve diferença entre os tratamentos (p < 0.05) e se observou maior mortalidade na maior concentração de nematóides, com mortalidade de 28,3% e 37% em cada uma das duas repetições do experimento. Este sistema de micro-aspersão não afeta a viabilidade, infectividade e capacidade de busca dos JIs de H. baujardi LPP7 até o inseto-alvo.

The guava weevil, Conotrachelus psidii, is a major pest of guava in Brazil causing severe reduction in fruit quality. We assessed its susceptibility to Heterhorhabditis baujardi LPP7 infective juveniles (IJs) in the greenhouse and under field conditions applying the nematodes in cadavers of seventh instar Galleria mellonella larvae. Field persistence of these nematodes in the soil was evaluated through G. mellonella-baiting. Insect cadaver concentrations of 2, 4 and 6 applied in pots in the greenhouse experiment caused significant mortality compared to the control. Significance differences were observed in the field between control and treatments only when six cadavers per 0.25 m2 were applied. Infective juveniles from the cadavers persisted 6 weeks after application in the field, but decreased greatly thereafter. Our work demonstrates that H. baujardi LPP7 IJs emerging from G. mellonella cadavers can be efficacious against guava weevil fourth instar larvae. Also, we demonstrated the long-term pe...

Engorged and partially engorged females of Boophilus microplus were exposed to 600; 3,000; 6,000 and 30,000 infective juveniles of Steinernema carpocapsae Weiser, 1955 Santa Rosa and All strains per dish, under lab conditions. Eggs weight, pre-laying period, laying period, survival period, reproductive efficiency rate, percentage of larval eclosion and lethal concentrations of 50% and 90% (CL50 and CL90) were calculated for engorged females. In the case of partially engorged females, only egg weight, survival period and CL50 and CL90 were calculated. All biological parameters of engorged or partially engorged females were altered by exposition of S. carpocapsae infective juveniles (IJs), Santa Rosa and All strains (pFêmeas ingurgitadas e parcialmente ingurgitadas de B. microplus foram expostas a 600, 3000, 6000 e 30000 juvenis infectivos de Steinernema carpocapsae Weiser, 1955 linhagens Santa Rosa e ALL por placa, sob condições de laboratório. Foram investigados para fêmeas ingurgitadas: peso da massa de ovos, período pré-postura, período de postura, tempo de sobrevivência, índice de eficiência reprodutiva, percentual de aclosão de larvas e concentrações letais 50% e 90% (CL50 e CL90). Para fêmeas parcialmente ingurgitadas somente foram observados peso da massa de ovos, tempo de sobrevivência, CL50 e CL90. Todos os parâmetros biológicos de fêmeas ingurgitadas foram e parcialmente ingurgitadas foram alterados pela exposição a juvenis infectivos de S. carpocapsae linhagens Santa Rosa e ALL (P

This study evaluated the efficacy of four entomopathogenic nematode (EPN) strains in insect cadaver formulations against Rhipicephalus microplus and compared the efficacy of the most virulent EPNs applied in cadavers of Galleria mellonella and Tenebrio molitor. In the first experiment, infected G. mellonela larvae were used as the source of EPNs. Engorged females of R. microplus were placed in pots filled with soil and different numbers of G. mellonella larvae infected with one of four species of nematodes. All treatments with EPNs of the genus Heterorhabditis caused significant reduction (p

Heterorhabditis is a nematode found in the soil that is used as an important biological control agent against various organisms. However, few studies have been performed of its use against snails and the present study is the first to investigate the effect of experimental exposure of Bradybaena similaris to Heterorhabditis indica LPP1. Two groups of 16 snails were formed: the control group (not exposed) and the treatment, which was exposed for three weeks to infective juveniles (J3) of H. indica LPP1. The entire experiment was conducted in duplicate, using a total of 64 snails. After this period, the snails were dissected to collect the hemolymph to evaluate the possible physiological alterations, namely total proteins, uric acid and hemolymph urea, as well as the activities of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) as a result of the infection. The terrariums were analyzed on alternate days throughout the experiment to count the dead snails. Intense proteolysis was observed in the infected snails. An increase in the level of uric acid and reduction of the hemolymph urea content indicated that the infection by H. indica results in the inversion of the excretion pattern of the host snail. Variations in the aminotransferase activities were also observed, with the infected group presenting significantly higher values (p

Two assays were conducted to assess the influence of infective juveniles (IJs) of Heterorhabditis baujardi LPP7 on the embryogenesis and hatching of Meloidogyne mayaguensis. In the first assay, eggs were incubated in water alone or in the presence of infective juveniles, and completion of embryogenesis was evaluated 14 days later. In the second assay, unhatched second-stage juveniles were incubated in distilled water alone or in the presence of infective juveniles. Cumulative hatching was compared at various time intervals. Embryogenesis was not affected, whereas second-stage juveniles hatching was delayed probably because of the eggs permeability to noxious metabolites released by Photorhabdus luminescens, which is the bacterial symbiont of H. baujardi.

Entomopathogenic nematodes (EPNs) are used for the biological control of soil insect pests worldwide and are generally applied to the soil in aqueous suspension. An alternative application method that could be especially practical and effective under certain conditions is to apply the nematode-killed insect (referred to herein as infected insect cadavers) that are placed on or in the soil and from which the nematodes emerge to seek new hosts. However, physical damage to the insect cadavers during handling and application as well as the potential detrimental impact of various soil biotic and abiotic factors could reduce the efficacy of cadaver applications. Our objective was to test the effectiveness of various protective coverings applied to Galleria mellonella insect cadavers in terms of their potential impact on the emergence and virulence of infective juveniles of the EPN Heterorhabditis baujardi LPP7, and to evaluate whether these coverings influenced cadaver removal by ants (Ectatomma spp.). The protective coveringtreatments included a commercial calcareous powder, a commercial talc powder, and gelatin capsules. The number of emerging infective juveniles (IJs) from insect cadavers formulated with talc powder (9.722 ± 1.382) and gelatin capsules (7.892 ± 1.072) was similar to the control (6.346 ± 1.311), and indicated that these coverings do not interfere with IJ emergence. However, the powdered calcareous covering significantly reduced IJ emergence. High infectivity was observed for IJs that emerged from cadavers in all treatments. Ectatomma spp. ants removed all insect cadavers from the nest entrance to a distance of 20 cm, with the exception of insect cadavers formulated in gelatin capsules, which were not removed. 2009 Elsevier Inc. All rights reserved. Fil: del Valle, Eleodoro Eduardo. Universidad Nacional del Litoral; Argentina Fil: Dolinski, Claudia. Universidade Estadual Do Norte Fluminense Darcy Ribeiro; Brasil Fil: Barreto, Eduardo L.S.. Universidade Estadual Do Norte Fluminense Darcy Ribeiro; Brasil Fil: Souza, R.M.. Universidade Estadual Do Norte Fluminense Darcy Ribeiro; Brasil

In view of the need to combat the generalized spread of resistance in ticks to commercial acaricides, the objective of this study was to evaluate the action of entomopathogenic nematodes (Steinernema carpocapsae, strains Santa Rosa and ALL) on engorged female Anocentor nitens. Five ticks per Petri dish were exposed to concentrations of 500, 5,000, or 25,000 infective juveniles of S. carpocapsae for 72 h. After transferring the ticks to clean plates, biological parameters were analyzed. Related to strains Santa Rosa, the period of pre-oviposition (p = 0.0001), oviposition (p = 0.041), and the mass weight of eggs (p = 0.005) showed significant differences between the control group and treated group. When the strain ALL was tested, the control and treated groups differed between the periods of pre-oviposition (p = 0.001), oviposition (p = 0.001), and egg mass weight (p = 0.01). The egg mass conversion was less significant in the groups when exposed to strains Santa Rosa (p = 0.002) and ALL (p = 0.001) relative to the control. The efficacy of both entomopathogenic nematode strains used in this study was comparable to other biological control agents, showing their potential against A. nitens in the laboratory.

Interactions between the nematode Heterorhabditis bacteriophora isolate JPM4 and the fungus Metarhizium anisopliae , isolates LPP45 and LPP39, were studied during dual infections of Diatraea saccharalis . Mortality, production of infective juveniles (IJs) and production of conidia were evaluated. A positive effect was demonstrated for host mortality in duel infections of JPM4 and LPP39, causing 100% mortality with LT 50 and LT 95 values of 1.8 and 2.8 days, respectively. Higher values were seen when using the nematode or fungi individually. However, a combination of JPM4 + LPP39 caused a significant reduction in IJ production. The results show that faster time to death, a moderately virulent fungal isolate could be combined with the nematode, however at the expense of IJ production.

The present study was carried out to evaluate the action of Steinernema glaseri Santa Rosa strain and Heterorhabditis bacteriophora CCA strain as biological control agents of Boophilus microplus. Engorged females ticks were distributed on Petri dishes containing different concentrations of infective juvenile (IJ) nematodes (0, 375, 500, 750, 1,500, 2,500, 5,000 and 25,000). The data showed a reduction of approximately 90% in the eggs laid at a concentration of 5,000 S. glaseri IJs and approximately 80% at a concentration of 1,500 H. bacteriophora IJs. The female mortality increased linearly with the increase in S. glaseri concentrations. However, in the tests with H. bacteriophora this linearity was not observed. The effectiveness of the treatment with both species of entomopathogenic nematodes was compatible with other control methods. The results show the potential of S. glaseri and H. bacteriophora as biological control agents for the control of B. microplus under laboratory conditions.