Parade Towards Green Revolution: Larvicidal Activity Of Catunaregam Spinosa Against Aedes Aegypti
DOI:
https://doi.org/10.47743/jemb-2026-244Keywords:
Catunaregam spinosa, seeds, Aedes aegypti,, larvicide, phytochemicalsAbstract
Dengue is a common vector-borne disease prominent in tropical and subtropical climates. It causes losing of millions of human lives per year around the world. Catunaregam spinosa is an underrated medicinal plant in Sri Lanka which rumored in possessing larvicidal activity against mosquitoes. Present study investigated the toxicity of seed extract of C. spinosa against fourth instar larvae of Aedes aegypti L to provide a scientific validation to the embedded property and to support the ethnobotanical vector control approaches. Mosquito larval cultures exposed to a series of concentrations (75.0, 125.0, 250.0, 500.0, 1000.0 mg L-1) showed concentration dependent mortalities and teratogenic effects after 24 hours. Statistical analysis computed 24 h, LC50 as 233.67 mg L-1 and LC90 as 659.93 mg L-1 reporting a moderate larvicidal activity. Preliminary phytochemical analysis revealed the presence of alkaloids, coumarins, saponins and flavonoids. Presence of butanoic acid, octadecanoic acid, n-hexadecenoic acid and palmitic acid along with 19 compounds were identified using Gas Chromatography Mass Spectrometry. In conclusion, the study unveils a lodged property in an abandoned plant in Sri Lanka whilst supporting the green-revolution and sustainable health system for future developments of bio-larvicides using natural compounds available in C. spinosa.
References
World Health Organization (WHO). Dengue: WHO Health Emergency Appeal 2024. 2024. URL: https://www.who.int/publications/m/item/dengue-who-health-emergency-appeal-2024
The International Federation of Red Cross (IFRC). Sri Lanka - Dengue Outbreak & Floods, DREF Final Report MDRLK017. 2024. 1-24. URL: https://reliefweb.int/report/sri-lanka/sri-lanka-dengue-outbreak-floods-dref-final-report-mdrlk017
Ranathunge T, Harishchandra J, Maiga H, Bouyer J, Gunawardena YINS, Hapugoda MD. Development of the Sterile Insect Technique to control the dengue vector Aedes aegypti (Linnaeus) in Sri Lanka. PLoS One. 2022; 17(4): e0265244. Doi: 10.1371/journal.pone.0265244. PMID: 35377897; PMCID: PMC8979456. DOI: https://doi.org/10.1371/journal.pone.0265244
Kandasamy C, Balasubramanian B, Prakash P, Baskaran R, Kamyab H, Chelliapan S, Arjunan N. Molecular docking analysis of mosquito ribosomal protein in selenium nanoparticle bio-synthesis: Implications for pest and pathogen mitigation. Journal of the Taiwan Institute of Chemical Engineers. 2025; 166 (2): 105602. Doi: https://doi.org/10.1016/j.jtice.2024.105602 DOI: https://doi.org/10.1016/j.jtice.2024.105602
Balaraman P, Balasubramanian B, Liu WC, et al. Sargassum myriocystum-mediated TiO2-nanoparticles and their antimicrobial, larvicidal activities and enhanced photocatalytic degradation of various dyes. Environmental Research. 2022; 204(c): 112278. Doi: https://doi.org/10.1016/j.envres.2021.112278 DOI: https://doi.org/10.1016/j.envres.2021.112278
Manojkumar U, Kaliannan D, Srinivasan V, et al. Green synthesis of zinc oxide nanoparticles using Brassica oleracea var. botrytis leaf extract: Photocatalytic, antimicrobial and larvicidal activity. Chemosphere. 2023; 323: 138263 Doi: https://doi.org/10.1016/j.chemosphere.2023.138263 DOI: https://doi.org/10.1016/j.chemosphere.2023.138263
Demirak MSS and Canpolat E. Plant-based bioinsecticides for mosquito control: impact on insecticide resistance and disease transmission. Insects. 2022; 13: 162. Doi: 10.3390/insects13020162 DOI: https://doi.org/10.3390/insects13020162
Kumar LR, Ndao A, Valero J and Tyagi RD. Production of Bacillus thuringiensis based biopesticide formulation using starch industry wastewater (SIW) as a substrate: A techno-economic evaluation. Bioresource Technology. 2019; 294: 122144. Doi: 10.1016/j.biortech.2019.122144 DOI: https://doi.org/10.1016/j.biortech.2019.122144
Ranathunge T, Kusumawathie PHD, Abeyewickreme W, Udayanga L, Fernando T and Hapugoda MD. Biocontrol potential of six locally available fish species as predators of Aedes aegypti in Sri Lanka. Biological Control. 2021; 160: 104638. Doi: https://doi.org/10.1016/j.biocontrol.2021.104638 DOI: https://doi.org/10.1016/j.biocontrol.2021.104638
Estep AS, Becnel JJ and Lee ST. Toxicity of compounds isolated from White Snakeroot (Ageratina altissima) to adult and larval Yellow Fever Mosquitoes (Aedes aegypti). Nature Product Communication. 2016; 11(11): 1675-1677. Doi: https://doi.org/10.1177/1934578X1601101113 DOI: https://doi.org/10.1177/1934578X1601101113
Pavela R, Maggi F, Iannarelli R and Benelli G. Plant extracts for developing mosquito larvicides: From laboratory to the field, with insights on the modes of action. Acta Tropica. 2019; 193: 236-271. Doi: https://doi.org/10.1016/j.actatropica.2019.01.019 DOI: https://doi.org/10.1016/j.actatropica.2019.01.019
Ahbirami R, Zuharah W, Thiagaletchumi M, Subramaniam S and Sundarasekar J. Larvicidal efficacy of different plant parts of railway creeper, Ipomoea cairica extract against dengue vector mosquitoes, Aedes albopictus (Diptera: Culicidae) and Aedes aegypti (Diptera: Culicidae). Journal of Insect Science. 2014; 14(1): 180-186. Doi: 10.1093/jisesa/ieu042 DOI: https://doi.org/10.1093/jisesa/ieu042
Srinivasan PV, Nathan SS, Ponsankar A, et al. Comparative analysis of mosquito (Diptera: Culicidae: Aedes aegypti Liston) responses to the insecticide Temephos and plant derived essential oil derived from Piper betle L. Ecotoxicology and Environmental Safety. 2017; 139: 439-446. Doi: 10.1016/j.ecoenv.2017.01.026 DOI: https://doi.org/10.1016/j.ecoenv.2017.01.026
Kumar S, Wahab N, Mishra M and Warikoo R. Evaluation of 15 local plant species as larvicidal agents against an Indian strain of dengue fever mosquito, Aedes aegypti L. (Diptera: Culicidae). Frontier in Physiology. 2012; 3: 104-110. Doi: 10.3389/fphys.2012.00104 DOI: https://doi.org/10.3389/fphys.2012.00104
Silvério MRS, Espindola LS, Lopes NP and Vieira PC. Plant natural products for the control of Aedes aegypti: The Main Vector of Important Arboviruses. Molecules. 2020; 25(15): 3484. Doi: 10.3390/molecules25153484 DOI: https://doi.org/10.3390/molecules25153484
Maroyi A. Gardenia ternifolia Schum. & Thonn. (Rubiaceae): Review of medicinal uses, phytochemistry and biological activities. International Journal of Research in Pharmaceutical Sciences. 2020; 11(4): 5876-5885. Doi: 10.26452/ijrps.v11i4.3238 DOI: https://doi.org/10.26452/ijrps.v11i4.3238
Carvalho DO, Nimmo D, Naish N, et al. Mass production of genetically modified Aedes aegypti for field releases in Brazil. Journal of Visualized Experiments. 2014; (83): e3579. Doi: 10.3791/3579 DOI: https://doi.org/10.3791/3579
Ghante MH, Bhusari KP, Duragkar NJ, Jain NS and Warokar AS. Bronchorelaxant, mast cell stabilizing, anti-inflammatory and antioxidant activity of Randia Dumetorum (Retz.) Lamk. extracts. Acta Poloniae Pharmaceutica - Drug Research. 2012; 69(3): 465-474. PMID: 22594261
Sharon K and Damle S. Location specific phytochemical and antibacterial analysis of methanolic extracts of Catunaregam spinosa (Thunb.) Triveng. International Journal of Biology Research. 2018; 3(2): 75-80. URL: https://www.biologyjournal.in/archives/2018/vol3/issue2/3-2-19
Jangwan JS and Singh R (2014) In vitro cytotoxic activity of triterpene isolated from bark of Randia dumentorum Lamk. Journal of current chemical and pharmaceutical sciences 4(1): 1-9.
Lawrence PK, Munasinghe MLAMS, Senarath WTPSK and Suresh S. Toxicity of methanolic extract of fruits of Catunaregam spinosa (Rubiaceae) on Danio rerio embryos. Journal of Pharmaceutical Research International. 2022; 34(50B): 33–41. Doi: 10.9734/jpri/2022/v34i50B36440 DOI: https://doi.org/10.9734/jpri/2022/v34i50B36440
Jyothirmayi B, Tejaswini L, Latha GA, Swathi C, Nishitha G and Unissa R. Anthelmintic evaluation of Randia dumetorum fruit extracts. Journal of Pharmacy Research. 2018; 12 (6): 880-883.
Ragib A, Hossain T, Hossain J and Jakaria J. Antioxidant potential and cytotoxicity of Randia dumetorum Lam. leaf extract. Journal of Pharmacognosy and Phytotherapy. 2017; 9(9): 138-145. Doi: 10.5897/JPP2016.0435 DOI: https://doi.org/10.5897/JPP2016.0435
Dharmishtha AM, Srihari HM and Falguni PG. Preliminary pharmacognostic and physicochemical evaluation of leaf of Randia dumetorum (Lamk.). Journal of Pharmacy Research. 2009; (2): 1212-1213.
Lawrence PK and Senarath WTPSK. Direct organogenesis of Catunaregam spinosa through nodal and internodal explants. Proceedings of XIII International Scientific Agriculture Symposium "AGROSYM 2022", Bosnia and Herzegovina: 2022; 338-344. URL: http://agrosym.ues.rs.ba/archive
Jayasinghe S, Bandara BR, Wickramasinghe A, Karunaratne DN, Wijesundara DSA, and Karunaratne V. The importance of harnessing the rich diversity of Sri Lankan flora for their medicinal value. Ceylon Journal of Science. 2017; 46(4), 3–13. Doi: 10.4038/cjs.v46i4.7473 DOI: https://doi.org/10.4038/cjs.v46i4.7473
Prozesky EA, Meyer JJM and Louw AI. In vitro antiplasmodial activity and cytotoxicity of ethnobotanically selected South African plants. Journal of Ethnopharmacology. 2001; 76(3): 239–245. Doi: https://doi.org/10.1016/S0378-8741(01)00245-8 DOI: https://doi.org/10.1016/S0378-8741(01)00245-8
Taware SP, Badnikar A, and Upadhye AS. Bio-efficacy evaluation of leaf extracts of some plant species against Tobacco caterpillar (Spodoptera litura Fab.) Soybean Research. 2014; 12(2): 208 - 212. Doi: https://doi.org/10.1016/j.sjbs.2010.09.004 DOI: https://doi.org/10.1016/j.sjbs.2010.09.004
Alapati PKP and Sulthana SK. Traditional medicinal practices for mosquito repellency by tribes of west central India: An overview. Journal of Pharmacognosy and Phytochemistry. 2018; 7(2): 2755-2759. URL: http://krishi.icar.gov.in/jspui/handle/123456789/24556
Pawar S, Patil DA. Ethnobotany of Jalgaon District, Maharastra. Daya Publishing House. New Delhi. 171- 286.
Navinkumar M, Nivetha G, Radha P, Ahamed Mohideen M. Therapeutic application of a siddha formulation Pataic Cankãran - A Review. International Journal of Ayurveda and Pharma Research. 2019;7(2):46-50. Available online: http://ijapr.in
Wuillda ACJ, Martins RC, Costa FN. Larvicidal activity of secondary plant metabolites in aedes aegypti control: An overview of the previous 6 years. Natural Product Communications. 2019;14(7). Doi:10.1177/1934578X19862893 DOI: https://doi.org/10.1177/1934578X19862893
Anoopkumar AN, Rebello S, Sudhikumar AV, Puthurand S and Aneesh EM. A novel intervention on the inhibiting effects of Catunaregam spinosa induced free radical formation and DNA damage in Aedes aegypti (Diptera: Culicidae): a verdict for new perspectives on microorganism targeted vector control approach. International Journal of Tropical Insect Science. 2020; 40: 989–1002. Doi: https://doi.org/10.1007/s42690-020-00157-0 DOI: https://doi.org/10.1007/s42690-020-00157-0
Gunathilaka N, Ranathunge T, Udayanga L and Abeyewickreme W. Efficacy of blood sources and artificial blood feeding methods in rearing of Aedes aegypti (Diptera: Culicidae) for sterile insect technique and incompatible insect technique approaches in Sri Lanka. BioMed Research International. 2017; 3196924. Doi: 10.1155/2017/3196924 DOI: https://doi.org/10.1155/2017/3196924
World Health Organization (WHO). Guidelines for laboratory and field testing of mosquito larvicides Geneva: World Health Organization. 2005; 1–41. URL: https://iris.who.int/handle/10665/69101
Mdoe FP, Cheng S-S, Lyaruu L, Nkwengulila G, Chang S-T, Kweka EJ (2014) Larvicidal efficacy of Cryptomeria japonica leaf essential oils against Anopheles gambiae. Parasit Vectors 7:426. Doi: 10.1186/1756-3305-7-426 DOI: https://doi.org/10.1186/1756-3305-7-426
Gao G, Lu Z, Tao S, Zhang S and Wang F. Triterpenoid saponins with antifeedant activities from stem bark of Catunaregam spinosa (Rubiaceae) against Plutella xylostella (Plutellidae). Carbohydrate Research. 2011; 346 (14): 2200-2205. Doi: 10.1016/j.carres.2011.07.022 DOI: https://doi.org/10.1016/j.carres.2011.07.022
Liu ZL, Liu QZ, Du SS, Deng ZW. Mosquito larvicidal activity of alkaloids and limonoids derived from Evodia rutaecarpa unripe fruits against Aedes albopictus (Diptera: Culicidae). Parasitology. 2012; 111(3): 991-6. Doi: 10.1007/s00436-012-2923-9 PMID: 22526296. DOI: https://doi.org/10.1007/s00436-012-2923-9
Santiago VS, Alvero RG, Villaseñor IM. Aedes aegypti larvicide from the ethanolic extract of Piper nigrum black peppercorns. Natural Product Research. 2015; 29(5): 441-443. Doi: 10.1080/14786419.2014.947490 DOI: https://doi.org/10.1080/14786419.2014.947490
You CX, Guo SS, Geng ZF, et al. Repellent activity of compounds from Murraya alata Drake against Tribolium castaneum. Industrial Crops and Products. 2017; 95:460–466. Doi: https://doi.org/10.1016/j.indcrop.2016.10.056 DOI: https://doi.org/10.1016/j.indcrop.2016.10.056
Spochacz M, Chowanski S, Walkowiak-Nowicka K, Szymczak M and Adamski Z. Plant-derived substances used against beetles–pests of stored crops and food–and their mode of action: A Review. Comprehensive Reviews in Food Science and Food Safety. 2018; 17(5): 1-28. Doi: 10.1111/1541-4337.12377 DOI: https://doi.org/10.1111/1541-4337.12377
Cui C, Yang Y, Zhao T, et al. Insecticidal activity and insecticidal mechanism of total saponins from Camellia oleifera. Molecules. 2019; 24(24): 4518. Doi: 10.3390/molecules24244518 DOI: https://doi.org/10.3390/molecules24244518
Price D, Pirbay S, Weiland L, Zhu J and Thomson EF. Tannins as a Pesticide: The impact of tannic acid on the growth rates of Myzus persicae and Arabidopsis thaliana. Iscientist. 2019; 4(1): 26-35. URL: https://api.semanticscholar.org/CorpusID:208173476
Bosire CM, Deyou T, Kabaru JM, Kimata DM, Yenesew A. Larvicidal activities of the stem bark extract and rotenoids of Millettia usaramensis subspecies usaramensis on Aedes aegypti L. (Diptera: Culicidae). Journal of Asia Pacific Entomology. 2014; 17(3): 531-535. Doi: https://doi.org/10.1016/j.aspen.2014.05.003 DOI: https://doi.org/10.1016/j.aspen.2014.05.003
Pluempanupat S, Kumrungsee N, Pluempanupat W, et al. Laboratory evaluation of Dalbergia oliveri (Fabaceae: Fabales) extracts and isolated iso flavonoids on Aedes aegypti (Diptera: Culicidae) mosquitoes. Industrial Crops and Products. 2013; 44: 653-658. Doi: https://doi.org/10.1016/j.indcrop.2012.09.006 DOI: https://doi.org/10.1016/j.indcrop.2012.09.006
Rahuman AA, Gopalakrishnan G, Venkatesan P, Geetha K. Larvicidal activity of some Euphorbiaceae plant extracts against Aedes aegypti and Culex quinquefasciatus (Diptera: Culicidae). Parasitology Research. 2008; 102(5): 867-73. Doi: https://doi.org/10.1007/s00436-007-0839-6 PMID: 18163189. DOI: https://doi.org/10.1007/s00436-007-0839-6
Costa MS, Santana AE, Oliveira LL, Zanuncio JC and Serrão JE. Toxicity of squamocin on Aedes aegypti larvae, its predators and human cells. Pest Management Science. 2017;73(3):636-640. Doi: https://doi.org/10.1002/ps.4350 DOI: https://doi.org/10.1002/ps.4350
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