Biological control potential of native entomopathogenic nematodes (Steinernematidae and Heterorhabditidae) against Spodoptera cilium (Lepidoptera: Noctuidae) in turfgrass

In laboratory studies, we demonstrated that five native entomopathogenic nematode species/isolates caused 100% mortality of Spodoptera cilium larvae, a soil surface-feeding pest of turfgrass. At 25 infective juveniles/cm² applied to sod, two selected Turkish species, Steinernema carpocapsae and Heterorhabditis bacteriophora (Sarigerme isolate), averaged 77% and 29% larval mortality, respectively.     

Control of the Oriental Fruit Moth, Grapholita molesta, Using Entomopathogenic Nematodes in Laboratory and Fruit Bin Assays

The oriental fruit moth (OFM), Grapholita molesta (Busck), which is among the most important insect pests of peaches and nectarines, has developed resistance to a wide range of insecticides. We investigated the ability of the entomopathogenic nematodes (EPN) Steinernema carpocapsae (Weiser), S. feltiae (Filipjev), S. riobrave (Cabanillas et al.), and Heterorhabditis marelatus (Liu and Berry) to control OFM under laboratory and fruit bin conditions. At a dosage of 10 infective juveniles (IJ)/cm² in the laboratory, S. carpocapsae caused 63%, S. feltiae 87.8%, S. riobrave 75.6%, and H. marelatus 67.1% OFM mortality. All four nematode species caused significant OFM larval mortality in comparison to the nontreated controls. Steinernema feltiae was used for the bin assays due to the higher OFM mortality it caused than the other tested EPN species and to its ability to find OFM under cryptic environments. Diapausing cocooned OFM larvae in miniature fruit bins were susceptible to IJ of S. feltiae in infested corner supports and cardboard strips. Treatment of bins with suspensions of 10 or 25 S. feltiae IJ/ml water with wetting agent (Silwet L77) resulted in 33.3 to 59% and 77.7 to 81.6% OFM mortality in corner supports and cardboard strips, respectively. This paper presents new information on the use of EPN, specifically S. feltiae, as nonchemical means of OFM control.     

Assessing the Potential of Entomopathogenic Nematodes to Control the Grape Root Borer Vitacea polistiformis (Lepidoptera: Sesiidae) Through Laboratory and Greenhouse Bioassays

Seventeen entomopathogenic nematode species and strains were evaluated for virulence to the grape root borer, Vitacea polistiformis (Harris) in laboratory and greenhouse bioassays. Heterohabditis bacteriophora strain GPS11 and H. zealandica strain X1 produced a larval mortality rate of over 85% of larvae embedded in the root cambium in laboratory bioassays. The nematode species H. marelata and H. bacteriophora strain Oswego produced mortality rates of over 75%. Of the Steinernema species tested, S. carpocapsae strain 'All' performed the best with a mortality rate of 69%. All other nematode species and strains tested, with the exception of S. bicornutum , produced some degree of larval mortality. In the greenhouse bioassays, 93% control was achieved with H. zealandica strain X1 applied at 4 ×109 infective juveniles (IJs) acre1 -1 (9.88 ×10 9 IJs ha -1 ). H. bacteriophora strain GPS11 successfully reproduced in grape root borer larvae. The numbers of IJs produced within infected larvae were related to larval size. The survival rate of neonate larvae on grape root sections was 61%, which thus provides a means to rear the neonate larvae for bioassays.     

Effect of Application Method on Fitness of Entomopathogenic Nematodes Emerging at Different Times

The entomopathogenic nematode species Steinernema feltiae and Heterorhabditis bacteriophora were compared for survival and infectivity of infective juveniles (IJ) collected with a standard White trap (i.e., emerging from hosts and accumulating in water) and later applied to sand (treatment A) to IJ allowed to emerge from hosts into sand (treatment C). Percentage IJ survival and infectivity was compared between treatments for S. feltiae IJ that emerged between days 1 to 3 and days 4 to 6. For H. bacteriophora, percentage IJ survival and infectivity was compared between treatments only for infective juveniles that emerged between days 4 to 6. For S. feltiae IJ percentage survival and infectivity decreased with time (P ≤ 0.05) and was greater (P ≤ 0.05) for IJ from treatment C than for IJ from treatment A. For H. bacteriophora IJ percentage survival decreased (P ≤ 0.05) and percentage infectivity increased (P ≤ 0.05) with time. While percent survival was higher (P ≤ 0.05) for treatment C than for A, percent infectivity was not different between treatments.     

Diversity and distribution of entomopathogenic nematodes (Rhabditida: Steinernematidae and Heterorhabditidae) in Turkey

The diversity and distribution of entomopathogenic nematodes in thefamilies Steinernematidae and Heterorhabditidae were assessed throughout anextensive soil survey in Turkey during 1999 and 2000. Entomopathogenic nematodeswere recovered from six out of seven regions sampled, with 22 positive sites(2%) out of 1080 sites sampled. A single nematode isolate was recovered at eachof the positive sites, of which 15 were steinernematid isolates and seven wereheterorhabditid isolates representing a total of four species. Based onmorphometric and molecular data, the nematode species were identified asHeterorhabditis bacteriophora, Steinernemafeltiae, S. affine, andSteinernema n. sp. The most common species was S.feltiae, which was isolated from 10 sites in six regions, followed byH. bacteriophora from seven sites in five regions,S. affine from four sites in two regions, andSteinernema n. sp. from one site. Heterorhabditisbacteriophora and S. feltiae have been found inmany parts of the world, whereas S. affine, so far, hasonly been recovered in Europe until our survey. Steinernemaaffine was isolated from the European (Marmara) as well as theAsiatic region (Middle Anatolia) of Turkey. A new undescribedSteinernema sp. was isolated from the most eastern region(East Anatolia) of Turkey. Soils of the positive sites were classified as sandy,sandy loam, or loam (68.2%) and sandy–clay–loam or clay loam (31.8%) and the pHranged from 5.6 to 7.9. The habitats from which the entomopathogenic nematodeswere isolated were broadly classified as disturbed (59.1%), which includedagricultural fields and poplar planted for lumber and wind breaks, andundisturbed (40.9%), which included pine forest, grassland, marsh and reed sites.Steinernema feltiae, S. affine, andH. bacteriophora were recovered from both disturbed andundisturbed habitats. The new Steinernema sp. was recoveredfrom grassland. Our survey showed that these nematodes occur widely throughoutTurkey, but at a frequency below that reported for other parts of the world.     

昆虫病原线虫对草地贪夜蛾幼虫的致死率及田间防治效果

【目的】为生产中应用昆虫病原线虫防治草地贪夜蛾提供参考。【方法】采用室内实验和田间试验相结合的方法,室内培养皿中测定4种不同品系线虫对3和6龄草地贪夜蛾幼虫的毒力、致死时间和剂量,田间玉米6～8叶期、日落后叶面喷施线虫至喇叭口内,测试防治草地贪夜蛾的施用剂量和持效天数。【结果】Steinernema feltiae SN、Heterorhabditis bacteriophora H06、Heterorhabditis beicherriana Cherry和Oscheius chongmingensis Tumian侵染草地贪夜蛾3龄幼虫72 h后的致死中浓度LC₅₀分别为22.13、36.54、60.01和1369.4 IJs·larva^-1;侵染6龄幼虫72 h后的致死中浓度LC₅₀分别为18.67、31.25、45.52和897.28 IJs·larva^-1。SN、H06、Cherry和Tumian品系的最佳致死时间72 h;最佳致死剂量100 IJs·larva^-1(...     

Pathogenicity of three entomopathogenic nematodes against the onion thrips,Thrips tabaci Lind. (Thys.; Thripidae)

Pathogenicity of a native isolate of Steinernema feltiae (H1) and two exotic strains, Heterorhabditis bacteriophora and Steinernema carpocapsae was assessed under laboratory conditions using different concentrations i.e. 4000, 6000, 8000 and 10,000 infective juveniles/ml against second instar larvae, prepupa and pupa of Thrips tabaci Lindeman. The mortality data were recorded 24 and 48?h post-inoculation. The highest mortality rate was recorded for prepupa (62%) than second instar (12.5%) by H. bacteriophora and S. carpocapsae, respectively, 24?h after treatment. No significant differences were found in mortality between prepupa and pupa with increasing the nematodes concentrations (from 4000 to 10,000 nematode/ml) but increasing nematode concentrations increased the mortality of second instar. At the end of the experiment (48?h.), S. feltiae H1 caused the highest mortality on second instar larvae (74%), whereas all other species caused 80–83% mortalities on pupa. This study suggests that native isolate of S. feltiae (H1) had high potential to infect soil-dwelling stages of T. tabaci.     

Determination of specific oxygen uptake rate of Photorhabdus luminescens during submerged culture in lab scale bioreactor

Photorhabdus luminescens, a bacterial symbiont of entomoparasitic nematodes, was cultured in a 10 L bioreactor. Cellular density and bioluminescence were recorded and volumetric oxygen transfer coefficient (k_La) and specific oxygen transfer rates were determined during the batch process. Exponential phase of the bacterium lasted for 20 h, showing a maximum specific growth rate of 0.339 h^?1 in a defined medium. Bioluminescence peaked within 21h, and was maintained until the end of the batch process (48 h). The specific oxygen uptake rate (SOUR) was high during both lag and early exponential phase, and eventually reached a stable value of 0.33 mmol g^?1 h^?1 during stationary phase. Maintenance of 200 rpm agitation and 1.4 volume of air per volume of medium per minute (vvm) aeration, gave rise to a k_La value of 39.5 h^?1. This k_La value was sufficient to meet the oxygen demand of 14.4 g L^?1 (DCW) biomass. This research is particularly relevant since there are no reports available on SOURs of symbiotic bacteria or their nematode partners. The insight gained through this study will be useful during the development of a submerged monoxenic culture of Heterorhabditis bacteriophora and its symbiotic bacterium P. luminescens in bioreactors.     

Cryopreservation of Steinernema carpocapsae and Heterorhabditis bacteriophora

A method for the cryopreservation of third-stage infective juveniles (IJ) of Steinernema carpocapsae and Heterorhabiditis bacteriophora was developed. Cryoprotection was achieved by incubating the nematodes in 22% glycerol (S. carpocapsae) or 14% glycerol (H. bacteriophora) for 24 hours, followed by 70% methanol at 0 C for 10 minutes. The viability of S. carpocapsae frozen in liquid nitrogen as 20 μl volumes spread over cover slip glass was > 80%. Survival of H. bacteriophora frozen on glass varied from 10 to 60% but was improved to > 80% by replacing the glass with filter paper. Cryopreservation and storage of 1-ml aliqots of S. carpocapsae IJ resulted in > 50% survival after 8 months; pathogenicity was retained and normal in vitro development took place. Trehalose and glycerol levels increased and glycogen levels decreased during incubation of S. carpocapsae IJ in glycerol. Normal levels of trehalose, glycerol and glycogen were restored during post freezing rehydration.     

Colorado potato beetle control by application of the entomopathogenic nematode Heterorhabditis marelata and potato plant alkaloid manipulation

Control of the Colorado potato beetle (CPB), Leptinotarsa decemlineata (Say) (Coleoptera: Chrysomelidae), with the entomopathogenic nematode Heterorhabditis marelata Liu and Berry (Nematoda: Heterorhabditidae) was examined in the laboratory and in potato fields in north central Oregon. This research tested the hypothesis that varying nitrogen fertilizer levels would affect foliar alkaloid levels, which would stress the host, and allow increased nematode reproduction and long‐term control of the CPB. Laboratory results indicated that nematodes tended to reproduce more readily in CPB fed on potato plants with high levels of fertilizer. Field trials tested CPB population responses to four treatments: application of nematodes vs. no nematodes, with application of low vs. high rates of nitrogen fertilizer. The higher nitrogen application rate increased field foliar levels of the alkaloids solanine by 35%, and chaconine by 41% over the season. Nematodes were applied twice during the season, causing a 50% reduction in adult CPB populations, and producing six times as many dead prepupae in nematode‐treated soil samples as in the untreated samples. However, no reproducing nematodes were found in the 303 dead prepupae and pupae collected from nematode‐treated plots. Nitrogen fertilizer levels, and their related alkaloid levels, did not affect nematode infection rates or reproduction in the field. Foliar alkaloid levels of plants from the growth chamber were 3–6‐fold as high as those in the field, which may explain the variation in nematode response to nitrogen applications to host plants of the CPB. Heterorhabditis marelata is effective for controlling CPB in the field, and does not have negative non‐target effects on one of the most common endemic CPB control agents, Myiopharus doryphorae (Riley) (Diptera: Tachinidae), but the low rate of nematode reproduction cannot be manipulated through alkaloid stress to the beetle. Until H. marelata can be mass‐produced in an inexpensive manner, it will not be a commercially viable control for CPB.