Research papers presented on entomopathogenic nematodes at 49th annual meeting of the Society of Nematologists

Recently, 49th annual meeting of the Society of Nematologists was held from July 11- 14, 2010 in Boise, Idaho.  This meeting was a great success and was attended by over 200 participants from all over the world. A total of 5 symposiums entitled "Potato Nematology (Convener: David Chitwood), Expanding Frontiers of Nematology (Conveners: Parwinder Grewal and Charles Opperman), Education (Convener: TJ Bliss), Nematode-Microbe Interactions (Conveners: Amy Treonis and Parwinder Grewal) and Frontiers in Insect Nematology (Conveners: David I Shapiro-Ilan and Ganpati Jagdale)" were organised in this meeting. Also, two workshops namely "Molecular Ecology (Conveners: Raquel Campos-Herrera and Byron J. Adams) and Industry (Conveners: Tom Hewlett) were organised to cover topics regarding molecular basis for the nematode- environment interactions and various technologies in nematode research, respectively. There were 7 contributed paper sessions covering various nematode research topics including host-parasite interactions (Convener: Russ Ingham), management 1 (Convener: Maurice Moens) & 2 (Convener: Shabeg Briar), registance and genetics (Convener: Richard Davis), biological control (Convener: Kris Lambert), ecology/evolution/behavior (Convener: George Bird) and variou topics (Convener: Robin Giblin-Davis). Following is the list of papers presented on entomopathogenic nematodes at the meeting

Following papers were presented in the symposium on entomopathogenic nematodes (Frontiers in Insect Nematology).

Abd-Elgawad, Mahfouz M. M., A.S. Abdel-Razek, and A.E. Abd El-Wahab. 2010. Protection of citrus fruits against the medfly using entomopathogenic nematodes and fungi.

Bal, Harit K., R. A. J. Taylor, and P.S. Grewal. 2010. Do ambusher and cruiser entomopathogenic nematodes disperse differently in soil in the absence of hosts?

Campos-Herrera, Raquel, E. Pathak, R.J., Stuart, F.E. El-Borai, C. Gutiérrez, J.H. Graham, and L.W. Duncan. 2010.  Entomopathogenic nematode ecology as a basis for their use in pest management.

Dolinski, Claudia 2010.  Recent advancements in applied entomopathogenic Nematology in South America.

Grewal, Parwinder S., and R. An. 2010.  Partnership between entomopathogenic nematodes and bacteria.

Holmes, Len D. and F.L. Inman III. 2010.  Learning to raise the entomopathogenic nematode Heterorhabditis bacteriophora in submerged culture.

Moens, Maurice and R.-U. Ehlers. 2010.   The latest developments in applied entomopathogenic nematology in Europe.

Pathak, Ekta, R. Campos-Herrera, R.J. Stuart, F.E. El-Borai, A.W. Schumann, J.H. Graham, and L.W. Duncan. 2010.  The impact of a new tactic to manage a citrus disease on biological control of a citrus pest by entomopathogenic nematodes.

Shapiro-Ilan, David I., and Lawrence A. Lacey. 2010.  Novel entomopathogenic nematode formulations and targets in north american orchards.

Entomopathogenic nematodes and insect parasitoids can work together to kill insect pests

In a laboratory study, recently it has been demonstrated that the combined application of an entomopathogenic nematode,  Heterorhabditis indica and an insect parasitoid, Habrobracon hebetor can enhance the mortality of Indianmeal moth, Plodia interpunctella.

Please read following literature for more information on compatibility of entomopathogenic nematodes and insect parasitoides

Mbata, G.N. and Shapiro-Ilan, D.I. 2010 Compatibility of Heterorhabditis indica (Rhabditida: Heterorhabditidae) and Habrobracon hebetor (Hymenoptera: Braconidae) for biological control of Plodia interpunctella (Lepidoptera: Pyralidae). Biological Control. 54: 75-82.

Management of small hive beetles with insect-parasitic nematodes

Entomopathogenic nematodes including Steinernema riobrave and Heterorhabditis indica were evalusted against a small hive beetle Aethina tumida Murray (Coleoptera: Nitidulidae) in the field. According to Ellis et al. (2010) both nematode species caused over 76% mortality of hive beetles. Shapiro-Ilan et al. (2010) tested efficacy of H. indica and Steinernema carpocapsae against hive beetles and demonstrated that both nematode species when applied through infected host cadavers can cause up to 78% control in hive beetles. This suggests that entomopathogenic nematodes have a potential to use as biological control agents against hive beetles.

Read following papers for detail information on effect of entomopathogenic nematodes on the small hive beetles.

Ellis, J.D., Spiewok, S., Delaplane, K.S., Buchholz, S., Neumann, P. and Tedders, W.L. 2010.  Susceptibility of Aethina tumida (Coleoptera: Nitidulidae) larvae and pupae to entomopathogenic nematodes. Journal of Economic Entomology. 103: 1-9.

Shapiro-Ilan, D.I., Morales-Ramos, J.A., Rojas, M.G. and Tedders, W.L. 2010.  Effects of a novel entomopathogenic nematode-infected host formulation on cadaver integrity, nematode yield, and suppression of Diaprepes abbreviatus and Aethina tumida. Journal of Invertebrate Pathology. 103: 103-108.

Mode of action of entomopathogenic nematodes

When the infective juveniles of entomopathogenic nematodes are applied to the soil surface in the fields or thatch layer on golf courses, they start searching for their insect hosts. Once insect larva has been located, the nematode infective juveniles penetrate into the larval body cavity via natural openings such as mouth, anus and spiracles. Infective juveniles of Heterorhabditis nematodes can also enter through the intersegmental membranes of the grub cuticle. Once in the body cavity, infective juveniles release symbiotic bacteria (Xenorhabdus spp. for Steinernematidae and Photorhabdus spp. for Heterorhabditidae) from their gut in insect blood. In the blood, multiplying nematode-bacterium complex causes septicemia and kill their insect host usually within 48 h after infection. Nematodes feed on multiplying bacteria, mature into adults, reproduce and then emerge as infective juveniles from the host cadaver to seek new larvae in the soil.

Control of annual bluegrass weevil, Listronotus maculicollis with entomopathogenic nematodes

It has been reported that the entomopathogenic nematodes including Steinernema carpocapsae, S. feltiae and Heterorhabditis bacteriophora when applied at rate of 2.5 billion infective juveniles/ha can cause 69- 94% mortality of first generation late instars of annual bluegrass weevil, Listronotus maculicollis. Of the 3 species of entomopathogenic nematodes, S. feltiae showed higher virulence against annual bluegrass weevil than the other two nematode species (see McGraw et al., 2010).

Read following research papers for more information on interaction between entomopathogenic nematodes and annual bluegrass weevil, L. maculicollis.

McGraw, B.A., Vittumb, P.J. Cowlesc, R.S.and Koppenhoumlfera, A.M. 2010.  Field evaluation of entomopathogenic nematodes for the biological control of the annual bluegrass weevil, Listronotus maculicollis (Coleoptera: Curculionidae), in golf course turfgrass. Journal Biocontrol Science and Technology. 20: 149 - 163.

Entomopathogenic nematodes can be used for controlling pests of stored grains

It has been demonstrated that the efficacy of entomopathogenic nematodes (Heterorhabditis bacteriophora, Steinernema carpocapsae, and Steinernema feltiae against various stored grain pests (Mediterranean flour moth, Ephestia kuehniella, lesser grain borer, Rhyzopertha dominica, rice weevil, Sitophilus oryzae and confused flour beetle, Tribolium confusum) of wheat (Triticum aestivum L.) varied with nematode dosages and temperature in the storage structures. Please read following papers for detailed information on the interaction between entomopathogenic nematodes and stored grain pests.

Athanassiou, C.G., Kavallieratos, N.C., Menti, H. and Karanastasi, E. 2010.  Mortality of four stored product pests in stored wheat when exposed to doses of three entomopathogenic nematodes.  Journal of Economic Entomology. 103: 977-984.

Athanassiou, C.G., Palyvos, N.E. and Kakoull-Duarte, T. 2008.  Insecticidal effect of Steinernema feltiae (Filipjev) (Nematoda : Steinernematidae) against Tribolium confusum du Val (Coleoptera : Tenebrionidae) and Ephestia kuehniella (Zeller) (Lepidoptera: Pyralidae) in stored wheat  Journal of Stored Products Research. 44: 52-57.

Mbata, G.N., and Shapiro-Ilan, D.I. 2005.  Laboratory evaluation of virulence of heterorhabditid nematodes to Plodia interpunctella Hübner (Lepidoptera: Pyralidae). Environmental Entomology. 34: 676 – 682.

Ramos-Rodríguez, O., Campbell, J. F. and Ramaswamy, S. 2006.  Pathogenicity of three species of entomopathogenic nematodes to some major stored- product insect pest. Journal of Stored Product Research 42: 241 – 252.

Ramos-Rodríguez,O., Campbell, J. F. and Ramaswamy, S. 2007.  Efficacy of the   entomopathogenic nematodes Steinernema riborave against the stored-product pests Tribolium castaneum and Plodia interpunctella. Biological Control 40:15 -21.

Tradan, S., Vidric, M. and Valic, N. 2006.  Activity of four entomopathogenic nematodes against young adult of Sitophilus granarious (Coleptera: Curculionidae ) and Oryzophilus surinamensis ( Coleoptera: Silvanidae ) under laboratory condition. Plant Disease and Protection. 113: 168 – 173.

Control Rhipicephalus (Boophilus) microplus with an entomopathogenic nematode Steinernema glaseri

It has been demonstrated that the entomopathogenic nematode Steinernema glaseri CCA strain can infect engorged Rhipicephalus ( Boophilus) microplus female ticks within two hours of exposure.  However, nematodes can cause over 90% mortality of ticks when they are in contact with the ticks for 24 hours. Read following papers for more information on interaction between entomopathogenic nematodes and ticks.

de Carvalho, L.B., Furlong, J., Prata, M.C.D., dos Reis, E.S., Batista, E.S.D., Faza, A.P. and Leite R.C. 2010.  Evaluation in vitro of the infection times of engorged females of Rhipicephalus (Boophilus) microplus by the entomopathogenic nematode Steinernema glaseri CCA strain. Ciencia Rural. 40: 939-943.

Freitas-Ribeiro G.M., Furlong, J., Vasconcelos, V.O., Dolinski, C. and Loures-Ribeiro, A. 2005.  Analysis of biological parameters of Boophilus microplus Canestrini, 1887 exposed to entomopathogenic nematodes Steinernema carpocapsae Santa Rosa and all strains (Steinernema : Rhabditida). Brazilian Archives of Biology and Technology. 48: 911-919.

Kocan, K.M., Pidherney, M.S., Blouin, E.F., Claypool, P.L., Samish, M. and Glazer, I. 1998.  Interaction of entomopathogenic nematodes (Steinernematidae) with selected species of ixodid ticks (Acari : Ixodidae). Journal of Medical Entomology. 35: 514-520.

Monteiro, C.M.D., Prata, M.C.D., Furlong, J., Faza, A.P., Mendes, A.S., Andalo, V. and Moino, A.2010.  Heterorhabditis amazonensis (Rhabditidae: Heterorhabditidae), strain RSC-5, for biological control of the cattle tick Rhipicephalus (Boophilus) microplus (Acari: Ixodidae). Parasitology Research. 106: 821-826.

Reis-Menini, C.M.R., Prata, M.C.A., Furlong, J. and Silva, E.R. 2008.  Compatibility between the entomopathogenic nematode Steinernema glaseri (Rhabditida : Steinernematidae) and an acaricide in the control of Rhipicephalus (Boophilus) microplus (Acari : Ixodidae). Parasitology Research. 103: 1391-1396.

Do you know that the queens of red imported fire ants can be susceptible to entomopathogenic nematodes?

As we know that the red imported fire ants (Solenopsis invicta Buren) are most notorious and difficult to control.  These ants are considered as a major agricultural and urban pest and they can be medically and environmentally harmful.  Red imported fire ants generally invade home lawns, school yards, athletic fields, golf courses and parks.  Natural enemies including microsporidian protozoan (Thelohania solenopsae) the fungus (Beauveria bassiana),  South African parasitoid flies (Pseudacteon tricuspis and Pseudacteon curvatus) and entomopathogenic nematodes have a potential to use as a biological control agents to kill red imported fire ants. Recently, it has been reported that the infective juveniles of two entomopathogenic nematode species including Steinernema carpocapsae All and S. scapterisci can infect the queens of the red imported fire ant, Solenopsis invicta under laboratory conditions.  Both nematodes can cause up to  100% mortality of fire ant queens 9 days after their exposure. 

For correct dosages of nematodes and their efficacy, please read the paper listed below.

Zhang, L.K., Zhang, P.B., Cao, L. and Han, R.C. 2010.  Susceptibility of red imported fire ant queens to the entomopathogenic nematodes Steinernema carpocapsae All and S. scapterisci. Sociobiology. 55: 519-526.

Biological control of filbertworm, Cydia latiferreana with entomopathogenic nematodes

Filbertworm, Cydia latiferreana is considered as an economically important insect pest of hazelnuts, Corylus avellana in North America.  Three entomopathogenic nematode species including Heterorhabditis marelatus Pt. Reyes strain, Steinernema carpocapsae All strain and Steinernema kraussei L137 strain have been tested as biological control agents against filbertworm under both laboratory and field condition (Chambers et al., 2010; Bruck and Walton, 2007). These studies showed that these nematodes can cause about 73–100% mortality of filbertworms (Bruck and Walton, 2007) and can be used to manage overwintering worms on the hazelnut orchard floor (Chambers et al., 2010).

Read following literature for information on the interaction between entomopathogenic nematodes and filbertworm.

Bruck, D.J. and Walton, V.M. 2007.  Susceptibility of the filbertworm (Cydia latiferreana, Lepidoptera:Tortricidae) and filbert weevil (Curculio occidentalis, Coleoptera: Curculionidae) to entomopathogenic nematodes. Journal of Invertebrate Pathology. 96: 93–96.

Chambers, U. Bruck, D.J., Olsen, J. and Walton, V.M. 2010.  Control of overwintering filbertworm (Lepidoptera: Tortricidae) larvae with Steinernema carpocapsae. Journal of Economic Entomology. 103: 416-422.

Biological control of the red palm weevil, Rhynchophorus ferrugineus with entomopathogenic nematodes

The red palm weevil, Rhynchophorus ferrugineus is considered as a major pest of palms in the Mediterranean Basin. Because of cryptic habitats of these weevils, their management with chemical insecticides is difficult.  It has been demonstrated that the entomopathogenic nematodes have a potential to use as biological control agents against red palm weevils.  For example, Steinernema carpocapsae can cause over 80% mortality of weevils under field conditions when applied in a chitosan formulation (Dembilio et al., 2010, Llacer et al., 2009).

Read following literature for more information

Abbas, M.S.T., Saleh, M.M.E. and Akil, A.M. 2001.  Laboratory and field evaluation of the pathogenicity of entomopathogenic nematodes to the red palm weevil, Rhynchophorus ferrugineus (Oliv.) (Col.: Curculionidae). Anzeiger Fur Schadlingskunde-Journal of Pest Science. 74: 167-168.

Dembilio, O., Llacer, E., de Altube, M.D.M. and Jacas, J.A. 2010.  Field efficacy of imidacloprid and Steinernema carpocapsae in a chitosan formulation against the red palm weevil Rhynchophorus ferrugineus (Coleoptera: Curculionidae) in Phoenix canariensis. Pest Management Science. 66: 365-370.

Llacer, E., de Altube, M.M.M. and Jacas, J.A. 2009.  Evaluation of the efficacy of Steinernema carpocapsae in a chitosan formulation against the red palm weevil, Rhynchophorus ferrugineus, in Phoenix canariensis. Biocontrol. 54: 559-565.

Monzer, A.E, and El-Rahman, R.A. 2003.  Effect on Heterorhabditis indica of substances occurring in decomposing palm tissues infested by Rhynchophorus ferrugineus. Nematology. 5: 647-652.

Salama, H.S., Abd-Elgawad, M. 2001.  Isolation of heterorhabditid nematodes from palm tree planted areas and their implications in the red palm weevil control. Anzeiger Fur Schadlingskunde-Journal of Pest Science. 74: 43-45.

Salama, H.S. and Abd-Elgawad, M. 2002.  Activity of heterorhabditid nematodes at high temperature and in combination with cytoplasmic polyhedrosis virus. Anzeiger Fur Schadlingskunde-Journal of Pest Science. 75: 78-80.

A first report of occurrence of entomopathogenic nematodes in Nepal

Recently a survey was conducted to study the occurrence and distribution of entomopathogenic nematodes in Nepal.  Although a total of 276 soil samples were collected from various habitats, entomopathogenic nematode were found only in 29 samples.  Nematodes were isolates using the Galleria-baiting technique (Bedding and Akhurst,1975). Both heterorhabditid and steinernematid nematodes were identified at their species level using both molecular and morphological techniques.  In this survey, the occurrence of only one species of heterorhabditids including Heterorhabditis indica and four described species of steinernematids such as Steinernema abbasi, S. cholashanense, S. feltiae and S. siamkayai were reported for the first time in Nepal (Khatri-Chhetri et al., 2010). Read following literature for more information

Bedding, R.A. and R.J. Akhurst. 1975. A simple technique for detection of insect parasitic rhabditid nematodes in soil. Nematologica. 21: 109-110.

Khatri-Chhetri, H.B., Waeyenberge, L., Manandhar, H.K. and Moens, M. 2010.  Natural occurrence and distribution of entomopathogenic nematodes (Steinernematidae and Heterorhabditidae) in Nepal. Journal of Invertebrate Pathology. 103: 74-78.

Kill cereal leaf beetles, Oulema melanopus with entomopathogenic nematodes

Recently, it has been demonstrated that the entomopathogenic nematodes including Steinernema feltiae strain B30, S. carpocapsae strain C101, and Heterorhabditis bacteriophora strain D54 have a potential to use as biological control agents against cereal leaf beetles (Oulema melanopus), which is a most common pest of many cereal crops including barley, corn, oats, wheat, rye, millet and rice.

For more information on interaction between entomopathogenic nematodes and cereal leaf beetles read following research paper.

Laznik, Z., Toth, I., Lakatos, T., Vidrih, M. and Trdan, S. 2010.  Oulema melanopus (L.) (Coleoptera: Chrysomelidae) adults are susceptible to entomopathogenic nematodes (Rhabditida) attack: results from a laboratory study. Journal of Plant Diseases and Protection. 117: 30-32.

Entomopathogenic nematodes can be applied through infected insect host cadavers

Entomopathogenic nematodes are generally applied as infective juveniles in aqueous suspensions using various techniques including irrigation systems, sprayers and water cans. These nematodes can also be applied through infected host cadavers. It has been demonstrated that the application of nematode infected insect cadavers can provide superior nematode dispersal (Shapiro and Glazer, 1996), infectivity (Shapiro and Lewis, 1999) and survival (Perez et al., 2003) when compared with the nematodes that applied in aqueous suspensions. Please read following literature to learn more about the advantages and disadvantages of applying nematodes through infected insect cadavers.

Creighton, C.S. and Fassuliotis, G. 1985.  Heterorhabditis sp. (Nematoda: Heterorhabditidae): a nematode parasite isolated from the banded cucumber beetle Diabrotica balteata. Journal of Nematology. 17: 150–153.

Del Valle, E.E., Dolinksi, C., Barreto, E.L.S. and Souza, R.M. 2009.  Effect of cadaver coatings on emergence and infectivity of the entomopathogenic nematode Heterorhabditis baujardi LPP7 (Rhabditida: Heterorhabditidae) and the removal of cadavers by ants. Biological Control 50: 21–24.

Del Valle, E.E., Dolinksi, C., Barreto, E.L.S., Souza, R.M. and Samuels, R.I. 2008.  Efficacy of Heterorhabditis baujardi LP77 (Nematoda: Rhabditida) applied in Galleria mellonella (Lepidoptera: Pyralidae) insect cadavers to Conotrachelus psidii (Coleoptera: Curculionidae) larvae. Biocontrol Science and Technology. 18: 33–41.

Perez, E.E., Lewis, E.E and Shapiro-Ilan, D.I. 2003.  Impact of host cadaver on survival and infectivity of entomopathogenic nematodes (Rhabditida: Steinernematidae and Heterorhabditidae) under desiccating conditions. Journal of Invertebrate Pathology. 82: 111–118.

Shapiro, D.I and Lewis, E.E. 1999.  Comparison of entomopathogenic nematode infectivity from infected hosts versus aqueous suspension. Environmental Entomology. 28: 907–911.

Shapiro, D.I. and Glazer, I. 1996.  Comparison of entomopathogenic nematode dispersal from infected hosts versus aqueous suspension. Environmental Entomology. 25: 1455–1461.

Shapiro-Ilan, D.I., Lewis, E.E., Behle, R.W and McGuire, M.R. 2001.  Formulation of entomopathogenic nematode-infected-cadavers. Journal of Invertebrate Pathology 78: 17–23.

Shapiro-Ilan, D.I., Lewis, E.E., Tedders, W.L. and Son, Y. 2003.  Superior efficacy observed in entomopathogenic nematodes applied in infected-host cadavers compared with application in aqueous suspension, Journal of Invertebrate Pathology 83: 270–272.

Shapiro-Ilan, D.I., Tedders, W.L. and Lewis, E.E., 2008. Application of entomopathogenic nematode-infected cadavers from hard-bodied arthropods for insect suppression. US Patent 7374,773.

Biological control of the cattle tick Rhipicephalus microplus with entomopathogenic nematodes

Recently, it has been demonstrated that the entomopathogenic nematode, Heterorhabditis amazonensis strain RSC-5 have a potential to use as a biological control agent against cattle tick,  Rhipicephalus (Boophilus) microplus (Monteiro et al., 2010), which is considered to be the most important tick parasite of livestock in the world.  This hardy tick can be found on many hosts including cattle, buffalo, horses, donkeys, goats, sheep, deer, pigs, dogs and some wild animals. This tick can also transmit babesiosis (cattle fever), which is caused by the protozoal parasites,  Babesia bigemina and Babesia bovis.  Also, transmit  anaplasmosis caused by Anaplasma marginale. Read following literature for more information on interaction between entomopathogenic nematodes and animal parasitic ticks

Freitas-Ribeiro G.M., Furlong, J., Vasconcelos, V.O., Dolinski, C. and Loures-Ribeiro, A. 2005.  Analysis of biological parameters of Boophilus microplus Canestrini, 1887 exposed to entomopathogenic nematodes Steinernema carpocapsae Santa Rosa and all strains (Steinernema : Rhabditida). Brazilian Archives of Biology and Technology. 48: 911-919.

Kocan, K.M., Pidherney, M.S., Blouin, E.F., Claypool, P.L., Samish, M. and Glazer, I. 1998.  Interaction of entomopathogenic nematodes (Steinernematidae) with selected species of ixodid ticks (Acari : Ixodidae). Journal of Medical Entomology. 35: 514-520.

Monteiro, C.M.D., Prata, M.C.D., Furlong, J., Faza, A.P., Mendes, A.S., Andalo, V. and Moino, A.2010.  Heterorhabditis amazonensis (Rhabditidae: Heterorhabditidae), strain RSC-5, for biological control of the cattle tick Rhipicephalus (Boophilus) microplus (Acari: Ixodidae). Parasitology Research. 106: 821-826.

Reis-Menini, C.M.R., Prata, M.C.A., Furlong, J. and Silva, E.R. 2008.  Compatibility between the entomopathogenic nematode Steinernema glaseri (Rhabditida : Steinernematidae) and an acaricide in the control of Rhipicephalus (Boophilus) microplus (Acari : Ixodidae). Parasitology Research. 103: 1391-1396.

How do entomopathogenic nematodes kill their insect hosts?

When the infective juveniles of entomopathogenic nematodes are applied to the soil surface in the fields or thatch layer on glf courses, they start searching for their insect hosts. Once insect larva has been located, the nematode infective juveniles penetrate into the larval body cavity via natural openings such as mouth, anus and spiracles. Infective juveniles of Heterorhabditis nematodes can also enter through the intersegmental membranes of the grub cuticle. Once in the body cavity, infective juveniles release symbiotic bacteria (Xenorhabdus spp. for Steinernematidae and Photorhabdus spp. for Heterorhabditidae) from their gut in insect blood. In the blood, multiplying nematode-bacterium complex causes septicemia and kill their insect host usually within 48 h after infection. Nematodes feed on multiplying bacteria, mature into adults, reproduce and then emerge as infective juveniles from the host cadaver to seek new larvae in the soil.

Biological control of grape root borer Vitacea polistiformis using entomopathogenic nematodes.

Efficacy of two entomopathogenic nematodes including Heterorhabditis zealandica strain X1 and H. bacteriophora Strain GPS11 was studied in the field against grape root borer Vitacea polistiformis (Williams et al., 2010).  This borer can damage roots of both wild and cultivated Vitis and Muscadinia grapes and is considered as a major pest of grapes grown in the eastern United States.  According to Williams et al. (2010), both H. zealandica and H. bacteriophora can cause up to 92% control of grape root borer and they can also persist in the soil for a extended period after their application.

Read following literature for more information on interaction between entomopathogenic nematodes and the grape root borers.

Williams, R.N., Fickle, D.S., Grewal, P.S. and Dutcher, J. 2010.  Field efficacy against the grape root borer, Vitacea polistiformis (Lepidoptera: Sesiidae) and persistence of Heterorhabditis zealandica and H. bacteriophora (Nematoda: Heterorhabditidae) in vineyards. Biological Control. 53: 86-91.

Williams, D.S. Fickle, P.S. Grewal and J.R. Meyer. 2002.  Assessing the potential of entomopathogenic nematodes to control the grape root borer, Vitacea polistiformis (Lepidopetera: Sesiidae) through laboratory and greenhouse bioassays. Biocontrol Science and Technology 12: 35-42.

Can you kill small hive beetles (Aethina tumida) with entomopathogenic nematodes?

Entomopathogenic nematodes including Steinernema riobrave and Heterorhabditis indica were evalusted against a small hive beetle Aethina tumida Murray (Coleoptera: Nitidulidae) in the field. According to Ellis et al. (2010) both nematode species caused over 76% mortality of hive beetles. Shapiro-Ilan et al. (2010) tested efficacy of H. indica and Steinernema carpocapsae against hive beetles and demonstrated that both nematode species when applied through infected host cadavers can cause up to 78% control in hive beetles. This suggests that entomopathogenic nematodes have a potential to use as biological control agents against hive beetles.

Read following papers for detail information on effect of entomopathogenic nematodes on the small hive beetles.

Ellis, J.D., Spiewok, S., Delaplane, K.S., Buchholz, S., Neumann, P. and Tedders, W.L. 2010.  Susceptibility of Aethina tumida (Coleoptera: Nitidulidae) larvae and pupae to entomopathogenic nematodes. Journal of Economic Entomology. 103: 1-9.

Shapiro-Ilan, D.I., Morales-Ramos, J.A., Rojas, M.G. and Tedders, W.L. 2010.  Effects of a novel entomopathogenic nematode-infected host formulation on cadaver integrity, nematode yield, and suppression of Diaprepes abbreviatus and Aethina tumida. Journal of Invertebrate Pathology. 103: 103-108.

A record of new entomopathogenic nematode species from Brazil

An entomopathogenic nematode in a soil sample collected from a natural forest in Mato Grosso do Sul state, Brazil was described using both morphological and molecular characteristics as a new species "Steinernema brazilense (Rhabditida: Steinernematidae)" (Nguyen et al., 2010). Reference:

Nguyen, K.B., Ginarte, C.M.A., Leite, L.G., dos Santos, J.M. and Harakava, R. 2010. Steinernema brazilense n. sp (Rhabditida: Steinernematidae), a new entomopathogenic nematode from Mato Grosso, Brazil. Journal of Invertebrate Pathology. 103: 8-20.

How and when to apply insect-parasitic nematodes

How to apply nematodes Insect-parasitic nematodes can be easily applied using conventional pesticide and fertilizer sprayers that have up to 300 PSI pressures.  However, nematodes will be easily damaged, if they are agitated through excessive recirculation of spray mix or if the temperature in the tank increases beyond 86 degrees F. Nematodes can also be applied through different types of irrigation systems but pumps should have proper pressure to avoid damage to nematodes and screen sizes should be larger than 50 mesh so that nematodes will pass through them live. Watering cans are used to apply nematodes in small areas including vegetable and ornamental gardens.

How many nematodes should be applied

For the suscessful control most of the soil dweling insect pests, the optimal rate of 1 billion infective juvenile nematodes in 100 to 260 gallons of water per acre is generally recommended.

Optimal soil and environmental condtions to apply nematodes

All nematodes require proper soil moisture for their optimal movement and infectivity. The activity and infectivity of nematodes can be enhanced by maintaining optimum moisture levels in the soil before and after their application.  In case of nematode application in turf, turf should be irrigated immediately after applicationwith at least 1/2 inch of water to rinse off nematodes from the folliage and move them into the soil and thatch. As nematodes are very sensitiv to heat and cold, their infectivity will be reduced if soil temperature is below 4 degrees C and above 35 degrees C. Soil temperatures between 20 to 30 degrees C are considered favourable for application of majority of nematode species and their virulence.  Nematode survival and activity also influenced by soil type.  Both survival and activity of nematodes is higher in sandy-loam soils than in heavy clay soils.

When to apply nematodes

Since nematodes are very sensitive to UV light, they will die within a minute or two when exposed to full sun. Therefore, nematodes should be applied early in the morning or late in the evening to avoid exposure to UV light.

Can we control plant-parasitic nematodes with entomopathogenic nematodes?

For the last several decades, entomopathogenic nematodes have been successfully used for the management of insect pests of many economically important crops (Grewal et al., 2005).  As an additional benefit, several researchers including Fallon et al. (2002), Gouge et al. (1997), Grewal et al. (1997; 1999), Jagdale et al. (2002), Jagdale and Grewal (2008), LaMondia and Cowles (2002), Lewis et al. (2001), Lewis and Grewal (2005), Molina et al. (2007), Nyczepir et al. (2004), Perez and Lewis (2002), Perry et al. (1998) and Shapiro et al. (2006) have demonstrated that entomopathogenic nematodes can also be used as biological control agents to control plant-parasitic nematodes infesting different crops in the fields and greenhouses . To control plant- parasitic nematodes, entomopathogenic nematodes can be applied using standard spraying equipments used for application of chemical pesticides. Entomopathogenic nematodes are generally applied against plant-parasitic nematodes at the rate of 1 billion infective juveniles per acre but this rate can vary with both entomopathogenic nematode and plant- parasitic nematode species.  Following are the examples of different species of entomopathogenic nematode that found to be successful in suppressing the population of different species of plant- parasitic nematodes.  Steinernema carpocapsae can reduce the population of ring nematodes (Mesocriconema spp., Criconemoides spp.) by 65%.  S. carpocapsae can reduce the population of stubby root nematodes (Paratrichodorus spp.) by 60%.  S. carpocapsae can reduce the population of potato cyst nematodes (Globodera rostochiensis).  S. carpocapsae can reduce the populations of foliar nematode Aphelenchoides fragariae.  Steinernema riobrave can reduce the population of stunt nematodes (Tylenchorynchu spp.) by 85%.  S. riobrave can reduce the population of lance nematodes (Hoplolaimus spp.).  S. riobrave can reduce the population of root-knot nematodes (Meloidogyne spp.) by 83%.  S. riobrave reduced egg masses of root-knot nematodes (Meloidogyne spp.).  S. riobrave can reduce the population of sting nematodes (Belonolaimus longocaudatus).  Steinernema feltiae can inhibit hatching root-knot nematode eggs and infection by hatched infective juveniles of root-knot nematodes (Meloidogyne spp.).  S. feltiae reduced egg masses of root-knot nematodes (Meloidogyne spp.) .  S. feltiae can reduce the population of root-knot nematodes (Meloidogyne spp.).  Steinernema glaseri reduced egg masses of root-knot nematodes (Meloidogyne spp.).  Heterorhabditis bacteriophora can reduce the population of ring nematodes (Mesocriconema spp., Criconemoides spp.) by 80%.  H. bacteriophora can reduce the population of stunt nematodes (Tylenchorynchus spp.) by 60%.  H. bacteriophora can reduce the population of lesion nematodes (Pratylenchus pratensis).   H. baujardi can inhibit hatching root-knot nematode eggs and infection by hatched infective juveniles of root-knot nematodes (Meloidogyne mayaguensis). Read following literature for more information on interaction between entomopathogenic nematodes and plant- parasitic nematodes:

1. Fallon, D.J., Kaya, H.K., Gaugler, R., Sipes, B.S., 2002. Effects of entomopathogenic nematodes on Meloidogyne javanica on tomatoes and soybeans. Journal of Nematology 34, 239-245.

2. Fallon, D.J., Kaya, H.K., Sipes, B.S., 2006. Enhancing Steinernema spp. suppression of Meloidogyne javanica. Journal of Nematology 38, 270-271.

3. Grewal, P.S., Ehlers, R.-U., Shapiro-Ilan, D.I. (Eds.), 2005. Nematodes As Biocontrol Agents. CABI Publishing, CAB International, Oxon, U.K.,

4. Grewal, P.S., Lewis, E.E., Venkatachari, S., 1999. Allelopathy: a possible mechanism of suppression of plant-parasitic nematodes by entomopathogenic nematodes. Nematology. 1, 735-743.

5. Grewal, P.S., Martin, W.R., Miller, R.W., Lewis E.E., 1997. Suppression of plant-parasitic nematode populations in turfgrass by application of entomopathogenic nematodes. Biocontrol Science and Technology 7, 393-399.

6. Jagdale, G.B., Grewal, P.S., 2008. Influence of the entomopathogenic nematode Steinernema carpocapsae in host cadavers or extracts from cadavers on the foliar nematode Aphelenchoides fragariae on Hosta. Biological Control 44, 13-23.

7. Jagdale, G.B., Somasekhar, N., Grewal, P.S., Klein, M.G., 2002. Suppression of plant parasitic nematodes by application of live and dead entomopathogenic nematodes on Boxwood (Buxus spp). Biological Control. 24, 42-49.

8. Lewis, E.E., Grewal, P.S., 2005. Interactions with plant-parasitic nematodes. In: Grewal, P.S., Ehlers, R.-U., Shapiro-Ilan, D.I. (Eds.), Nematodes As Biocontrol Agents. CABI Publishing, CAB International, Oxon, U.K., pp. 349-362.

9. Perry, R.N., Homonick, W.M., Beane, J., Briscose, B., 1998. Effects of the entomopathogenic nematodes, Steinernema feltiae and S. carpocapsae, on the potato cyst nematode, Globodera rostochiensis, in pot trials. Biocontrol Science and Technology 8:175 – 180.

10. Shapiro, D.I., Nyczepir, A.P., Lewis, E.E., 2006. Entomopathogenic nematodes and bacteria applications for control of the pecan root-knot nematode, Meloidogyne partityla in the greenhouse. Journal of Nematology 38, 449-454.