- Open Access
Biocontrol potential of the entomopathogenic nematodes (Rhabditida: Steinernematidae and Heterorhabditidae) against the termite species, Microtermes obesi (Holmgren) (Blattodea: Termitidae)
Egyptian Journal of Biological Pest Control volume 31, Article number: 99 (2021)
Globally, termites cause a great problem for the farmers which eat the stalk of the wheat, maize, and the sugarcane and also affect the growth of vegetables. For ecological farming system, biocontrol agents represent a vital implement in pest management policies. Biological control can play a probable, even more considerable part to reduce the adverse possessions of synthetic chemical pesticides.
The present study aimed to evaluate the biocontrol potential of one heterorhabditid species and 4 steinernematid species against the termite species (Microtermes obesi (Holmgren) (Blattodea: Termitidae)) on filter paper bioassay and wooden logs. Among all tested species of the entomopathogenic nematodes, maximum mortality rates 100% were obtained by using Steinernema pakistanense N-KA.04 and S. bifurcatum N-KA.93 after 48 h of the application. S. siamkayai N-KA.12 mortality ranged (85–87%), followed by S. ceratophorum N-KA.57 (77–80%) and then Heterorhabditis indica N-KA.03 (70–77%) at the highest concentrations (350–650 IJs/ml).
The expansion of appropriate application products for the management of termite effectiveness, observing and timing of application, participation of farmers in checking, and judgment is essential to avert disasters of entomopathogenic nematodes (EPNs) in field conditions and to make farmers’ confident with the use of the most promising species of EPNs.
Biological control program establishes a more ecologically tolerable substitute to traditional chemical control procedures. When efficaciously executed, it can yield long lasting, economical controlling pest populations with negligible ecofriendly disruption. Entomopathogenic nematodes (EPNs) have been found parasitizing the species in the orders of Coleoptera, Diptera, Hemiptera, Hymenoptera, Orthoptera, Lepidoptera, Siphonaptera, Thysanoptera, and Isoptera. These nematodes deal with an ecologically innocuous substitute to chemical insecticides in the controlling of termites (Khan et al. 2016).
Microtermes obesi (Holmgren) (Blattodea: Termitidae) is one of the most communal termite species of Pakistan. It has been found aggressive forest plants as well as timbers which are used as building materials; doors and windows and ventilators are commonly devastated (Manzoor et al. 2014). Synthetic pesticides which are used for the control of agricultural pests are directly board the human vigor triggering serious syndromes such as cancer and they are more expensive than natural products (Bounias, 2003). Termites forage and live in environments that are humid, cool, and without direct sunrays such as wood materials or soil. These ecofriendly situations are perfect for the existence and association of steinernematid and heterorhabditid nematodes and afford the origin for the curiosity in their role in control of subterranean termites (Wang et al. 2002). The performance of EPNs for successful control of target insect pest is dependent on the motility and perseverance of the infective juveniles (IJs).
The aim of the present study was to evaluate the biocontrol potential of 5 species of EPNs against the termite species, M. obesi.
Collection of Microtermes obesi
M. obesi termite’s colonies were collected from infested trees of Gulshan-e-Maymar, Gadap Town (25° 7′ 55′′ North, 67° 13′ 57′′ East) Sindh, Karachi, Pakistan.
Surveys for entomopathogenic nematodes
Collected EPN species from soil samples (of 500 gm) of Pakistani localities as Karachi, Sindh of Pakistan were identified and confirmed on supervision of NNRC, Uok. All nematodes’ isolates were propagated in larvae of Galleria mellonella L. greater wax moth. Infective progenies were harvested by White traps (White, 1927), collected, and maintained in 50 ml beaker having distilled water at 12 °C for 15 days to performed experiment.
Filter paper bioassay
Filter paper bioassay was conducted in Petri dishes (90 cm) lined with filter paper Whatman No. 1, with 20 termites in each dish. Nematode species in 3 ml were inoculated with 3 different concentrations of infective juvenile at 150, 250, and 350 IJs/ml. Control treatments received 3ml water without nematodes. Petri dishes were wrapped with Parafilm and kept in chamber maintained at 30 °C and 80% RH.
Spray on infested logs
Ten inch pieces of wooden logs of trees infested with 50 termites were placed in a plastic container (28 × 16 × 8 cm), each EPN species was sprayed by 3 different concentrations; 250, 450, and 650 IJs/ml, separately in 20 ml water suspension. Containers were protected by aerated lids and incubated at 25 °C. Control trial with infested wooden logs was sprayed only with 20 ml water.
Replication and mortality evaluation
Three replicates were used for each species and set of experiment. After 48 h of application, dead cadavers of each treatment were transferred separately to White traps for assessment of mortal source and confirmation by emergence of nematode progeny.
SPSS statistical software, 2002 was used to analyze ANOVA, analysis of variance; significant differences in treatments were elucidated through Duncan’s multiple range test (P ≤ 0.05) (Duncan, 1955).
Surveyed entomopathogenic nematodes
EPNs; H. indica N-KA.03, S. pakistanense N-KA.04, S. siamkayai N-KA.12, S. ceratophorum N-KA.57, and S. bifutcatum N-KA.93 were recovered from soil samples (500 gm) collected from different localities of Karachi, Sindh, Pakistan as mentioned in Table 1.
Filter paper bioassay
In filter paper bioassay with 20 termites per Petri dish, the corrected mortalities were significantly affected by using EPN species (F = 51.032, df = 3, 24, P < 0.001) and the tested concentrations (F = 7.247, df = 2, 24, P = 0.003), with a significant interaction between the 2 factors (F = 2.674, df = 6, 24, P = 0.039). Control treatment showed non-response against termite. S. pakistanense N-KA.04 and S. bifurcatum N-KA.93 showed the highest mortality rates up 100% at 250 and 350 IJs/ml, with non-significant difference. The second highest mortal rate of termite achieved by S. siamkayai N-KA.12, followed by S. ceratophorum N-KA.57and H. indica N-KA.03 at the 3 tested concentrations after 48 h (Fig. 1).
Spray on infested logs
In the spray method on infested wooden logs, 50 termites were treated by different EPN species at different concentrations. The corrected mortalities of the termite were significantly influenced by both the EPN species (F = 48.15, df = 3, 24, P < 0.001) and their concentrations (F = 10.20, df = 2, 24, P = 0.004), with a significant interaction between the 2 factors (F = 1.05, df = 6, 24, P = 0.029). All the 5 species of EPNs were found significantly effective against termites by spray on infested logs (Fig. 2). No mortality response was found in the control treatment. Maximum mortality 100% was observed by S. pakistanense (ANOVA: F = 64.7; df = 2, 9; P < 0.01) and S. bifutcatum (ANOVA: F = 14.5; df = 2, 9; P < 0.01) at 250 and 350 IJs/ml after 48 h of application (Fig. 2). H. indica (ANOVA: F = 76. 02; df = 2, 9; P < 0.01) showed the least mortality rate as than the other EPN species, when a maximum mortality rate (77%) was achieved at 350 IJs/ml. On both methods, increase of EPNs’ concentration significantly increased the mortality rates of the termites
Use of different species of EPNs for pest control that occur in cryptic habitats including termites is a rapid, defensible, ecologically nontoxic, and cost-effective method (Vashish et al. 2013). They are capable to reprocess in the atmosphere, are willing to genetic selection for desirable traits, and are exempt from registration in many countries (Shahina et al. 2017). The nematodes can be practical with customary spray equipment under field conditions (Hazir et al. 2004). Numerous trials revealed the efficiency of EPNs to control termites. Laboratory trials with termites and EPNs were generally tested out in Eppendorf tubes, packed cell volume (PCV) tubes, containers, Petri dishes bottom with sterile sand, or wet filter paper. For termites, under all circumstances, corrugated wood blocks and straw piece of filter paper are commonly used in to serve as nourishment (Baïmey et al. 2017). In the present investigation, 1 heterorhabditid and 4 steinernematid species showed the best biocontrol potential as compared to other species. Similar results were found by same species against Coptotermes heimi (Tabassum and Salma, 2020). In sand assay method, S. pakistanense showed also significant results, causing 100% mortality of Reticulitermes flavipes and Odontotermis hornei within 24 h as reported by Razia and Sivaramakrishnan (2016). Wang et al. (2002) reported that H. indica was more efficient against R. flavipes. Zadji et al. (2014) tested the pathogenicity against the workers of Macrotermes bellicosus with 1 H. indica and 29 Benin isolates of H. sonorensis in Eppendorf tubes. The outcomes of the trial presented that 73% of the nematode isolates killed more than 80% of the termite. In the present study experiment, mortality of H. indica N-KA.03 reached up to 77% at the highest concentration. Jawad et al. (2020) tested S. carpocapsae, H. bacteriophora, and H. bacteriophora (IRQ.1 strain) against Microcerotermes diversus using 6 concentrations conducted in filter paper and wood bioassays. The percent mortality caused by native H. bacteriophora against termites was higher showed 43.6 ± 2.7% than both commercial strains of S. carpocapsae and H. bacteriophora 36.9 ± 1.6% and 29.9 ± 1.4% respectively.
After EPNs’ application, termite shell can be remodeled being ruined subsequently, so nematode persistence in the nest zone can obligatory evading regular disruptions. For fruitful management, repeated applications of the EPNs must acquire (Baïmey et al. 2017).
Practical application of effective species of EPNs is obligatory for environmentally sound and sustainable termite control alternative to synthetic chemicals.
Availability of data and materials
Analysis of variance
- M. obesi :
Baïmey H, Lionel Z, Léonard A, André F, Régina KWD (2017) Searching for better methodologies for successful control of termites using Entomopathogenic Nematodes, nematology - concepts, diagnosis and control, Mohammad Manjur Shah and Mohammad Mahamood. IntechOpen. https://doi.org/10.5772/intechopen.69861
Bounias M (2003) Etiological factors and mechanism involved in relationships between pesticide exposure and cancer. J Environ Biol 24(1):1–8
Duncan DB (1955) Multiple range and multiple F-test. Biometrics. 11(1):1–41. https://doi.org/10.2307/3001478
Hazir S, Kaya HK, Stock SP, Keskin N (2004) Entomopathogenic nematodes (Steinernematidae and Heterorhabditidae) for biological control of soil pests. Turk J Biol 27:181–202
Jawad BZ, Javad K, Esmat MM (2020) Entomopathogenic nematodes as potential biological control agents of Subterranean termite, Microcerotermes diversus (Blattodea: Termitidae) in Iraq. Environ Entomol 49(2):412–421
Khan MA, Ahmad W, Paul B, Paul S, Khan Z, Aggarwal C (2016) Entomopathogenic nematodes for the management of subterranean termites. In: Hakeem KR, Akhtar MS, Abdullah SNA (eds) Plant, Soil and Microbes, vol 1. Implications in Crop Science. Springer International Publishing, Switzerland. https://doi.org/10.1007/978-3-319-27455-3_16
Manzoor F, Sumaira S, Moneeza A (2014) Laboratory evaluation of Imidacloprid against Microtermes obesi (Holmgren) (Isoptera: Macrotermitinae). Proc Pakistan Acad Sci 51(1):43–48
Razia M, Sivaramakrishnan S (2016) Evaluation of entomopathogenic nematodes against termites. J Entomol and Zool Stud 4(4):324–327
Shahina F, Salma J, Christos IR, Christos GA (2017) Control of stored grain pests by entomopathogenic nematodes. In: biocontrol agents, entomopathogenic and slug parasitic nematodes. Elagawad, Tariq and James, p 629pp. https://doi.org/10.1079/9781786390004.0000
Tabassum AK, Salma J (2020) Virulence of four Steinernema species as a biological control agent in controlling the termite, Coptotermes heimi (Wasmann) (Isoptera: Rhinotermitidae). Egypt J Biol Pest Cont 30:26
Vashisth S, Chandel YS, Sharma PK (2013) Entomopathogenic nematodes – a review. Agricultural Reviews 34(3):163–175. https://doi.org/10.5958/j.0976-0741.34.3.001
Wang C, Janine EP, Nguyen K (2002) Laboratory evaluations of four entomopathogenic nematodes for control of Subterranean termites (Isoptera: Rhinotermitidae). Environ Entomol 31(2):381–387
White GF (1927) A method for obtaining infective nematode larvae from cultures. Science 66(1709):302–303. https://doi.org/10.1126/science.66.1709.302-a
Zadji L, Baimey H, Afouda L, Moens M, Decraemer W (2014) Characterization of biocontrol traits of heterorhabditid entomopathogenic nematode isolates from South Benin targeting the termite pest Macrotermes bellicosus. Bio Control 59(3):333–344
This research was not funded by any funding agency.
This research was not funded by any funding agency.
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Javed, S., Ali, A. & Khanum, T.A. Biocontrol potential of the entomopathogenic nematodes (Rhabditida: Steinernematidae and Heterorhabditidae) against the termite species, Microtermes obesi (Holmgren) (Blattodea: Termitidae). Egypt J Biol Pest Control 31, 99 (2021). https://doi.org/10.1186/s41938-021-00448-9
- Microtermes obesi