Larvicidal Potential of Caribbean Plants

Layne-Yarde, Rhaheem N. A.; Sandiford, Simone L.

doi:https://doi.org/10.1155/2023/5518863

BioMed Research International

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Abstract Introduction Conclusion Conflicts of Interest References Copyright Related Articles

Review Article | Open Access

Volume 2023 | Article ID 5518863 | https://doi.org/10.1155/2023/5518863

Larvicidal Potential of Caribbean Plants

Rhaheem N. A. Layne-Yarde¹and Simone L. Sandiford^1,2

Academic Editor: Cassiano Felippe Gonçalves-de-Albuquerque

Received26 Feb 2023

Revised12 Jun 2023

Accepted01 Aug 2023

Published26 Aug 2023

Abstract

Mosquitoes are vectors for numerous arboviruses such as dengue, chikungunya, and Zika which continue to negatively impact the health of Caribbean populations. Within the region, synthetic insecticides are primarily used to control mosquito populations. In many countries however, these compounds are becoming less effective due to resistance, and they may also be harmful to the environment. Thus, there is a significant need for the development of alternative agents to combat the mosquito threat in the Caribbean. Worldwide, botanical-based products are being increasingly investigated for vector control because they are environmentally friendly and are often highly effective mosquitocidal agents. Although the botanical diversity within the Caribbean is remarkable, work on plant biopesticides in the region remains limited. The aim of this review, therefore, is to discuss the use of Caribbean botanical extracts as larvicidal agents. Additionally, we highlight the need for future work in this area which may subsequently lead to the implementation of transformative public health policies.

1. Introduction

The Caribbean is rich in botanical biodiversity with over 10,000 individual species having been discovered to date [1]. Located between North and South America, it consists of three island groups: The Bahamas, the Greater Antilles, and the Lesser Antilles. The Greater Antilles is comprised of the islands found in the western regions of the Caribbean Sea, whereas the Lesser Antilles is a group of smaller islands forming an archipelago in the eastern Caribbean Sea. The region has many endemic plants with a rich history of ethnomedical uses. Interestingly, many of these understudied species have phytochemical compositions which may be of great interest to researchers in the field of tropical medicine.

Although part of the same region, the islands of the Caribbean vary by geological evolution, and as such, their flora and fauna differ significantly. Not surprisingly, endemic plants are most abundant on the larger and more diverse continental islands of the Greater Antilles such as Cuba and Hispaniola [2, 3]. As the phytochemical profile of plants is influenced by factors such as location as well as environmental stress [4], variations may also be seen throughout the islands. The most abundant components of the leaf essential oils of Canella winterana (L.) Gaertn (Canellaceae) from the Dominican Republic, for instance, were myrcene, caryophyllene, and cis-ocimene [5], whereas those from the same plant in Guadeloupe were myrcene, (E)-β-farnesene and 2,3-methylenedioxy anisole safrole [6]. Likewise, analysis of the essential oils from Jamaican Hyptis verticillata Jacq. (Lamiaceae) revealed that the compound aromadendr-1(10)-en-9-one (30.7%) was the major constituent [7], while a similar study reported that cadin-4,10(15)-dien-3-one (14.8%) and isocaryophyllene epoxide (14.4%) were the most abundant compounds in the Cuban variety [8]. Selective ecological pressures over centuries have led plants to produce secondary metabolites to combat and defend against herbivorous insects [9]; therefore, it is not surprising that increased toxic activity is sometimes observed when local plant extracts are used as insecticides against some local insect species [10].

In the region, the productivity of many Caribbean territories has been severely impacted by epidemics of mosquito-borne diseases caused by arboviruses primarily transmitted by Aedes aegypti (Linnaeus) mosquitoes. These include cyclic outbreaks of dengue, and in more recent years, chikungunya and Zika. The unfortunate lack of effective vaccines or antiviral agents means that control of the mosquito vector is of paramount importance. To compound matters, the existing synthetic insecticides used for mosquito vector control are becoming less effective coupled with the fact that they may also cause harm to the environment. In Jamaica, Ae. aegypti mosquitoes have been found to be resistant to common insecticides such as permethrin and malathion [11], and mutations in voltage-gated sodium channels are thought to be a cause for pyrethroid resistance [12]. Additionally, resistance in Ae. aegypti mosquitoes to temephos was observed in Cuba [13] and in the Lesser Antilles where they were reported to be highly resistant to dichlorodiphenyltrichloroethane (DDT) [14]. Due to increasing worldwide use, there is now compelling evidence that botanical-based substances possess potent mosquitocidal properties [15]. Yet, work in this area in the region remains limited as these agents continue to be used primarily as mosquito repellents and not for their mosquitocidal activity. The aim of this review is therefore to discuss studies that have evaluated larvicidal activity of plants from the Caribbean as well as to identify research gaps that currently exist in the region.

2. Search Strategy

The scientific databases of PubMed (https://pubmed.ncbi.nlm.nih.gov/ (accessed on 25 February 2023)) and Google Scholar (https://scholar.google.com/ (accessed on 25 February 2023)) were searched for peer-reviewed literature relevant to this topic. A list of keywords and phrases used to initiate the searches included “larvicidal essential oils,” “Caribbean essential oils as larvicides,” and “larvicidal potential of essential oils”. Articles that involved larvicidal activity of Caribbean plants were included. The review focused on English-language papers but also included literature published in Spanish.

3. Larvicidal Activity of Plants from the Greater Antilles

Only one island of the Greater Antilles, Cuba, has reported larvicidal activity of botanical agents. Proactive public health policies have limited the mosquito threat in that country, and as such significant interest has been placed on the development of alternatives to traditional pesticides [16]. Being the largest island in the Caribbean, Cuba is also home to a vast array of unique endemic plant species, and studies have begun to assess their larvicidal potential. The essential oils from the leaves of Eugenia melanadenia Krug & Urb. var. melanadenia (Myrtaceae) and Psidium rotundatum Griseb (Myrtaceae) both Cuban endemic plants, were investigated against an Ae. aegypti reference laboratory strain from the Caribbean epidemiology centre for larvicidal activity [17]. The and values for E. melanadenia were 0.0085% and 0.0104%, while that of P. rotundatum were 0.0063% and 0.0071% [17] (Table 1). According to Komalamisra et al., essential oils with values between 50 and 100 ppm are considered effective, while those with values under 50 ppm are highly effective [18]. As such, both oils can be classified as effective larvicidal agents. Although phytochemical analysis was not done in this study, other researchers have demonstrated that the major chemical constituents of E. melanadenia were 1,8-cineole (45.3%), terpinen-4-ol (10.6%), p-cymene (8.2%), P-eudesmol (7.0%), and a-terpineol (6.7%) [19]. Interestingly, work performed in Egypt showed that 1,8-cineole was an ineffective larvicide against another mosquito species, Culex pipiens (Linnaeus) [20]. Other studies have also suggested that 1,8-cineole has low larvicidal activity against Aedes aegypti [21]. In contrast, terpinen-4-ol was shown to have significant larvicidal activity against both Anopheles and Culex species [22] in India. Similarly, chemical analysis of P. rotundatum revealed that α-pinene (18.3%) and 1,8-cineole (28.0%) were its major components [23]. In studies conducted in Lebanon, α-pinene was shown to possess potent larvicidal activity against the Cx. pipiens [24]. Therefore, the larvicidal activity demonstrated by both plants could be a result of synergistic effects of the chemical constituents.

Leyva et al. assessed the effect of the essential oils from Piper auritum H.B.K (Piperaceae), Pimenta racemosa (Mill.) J. Moore (Myrtaceae), Chenopodium ambrosioides L. (Amaranthaceae), and Piper aduncum L. (Piperaceae) against the established Ae. aegypti Rockefeller laboratory strain [25]. Piper auritum, P. racemosa, and C. ambrosioides were highly effective larvicides with values below 50 ppm, while P. aduncum can be classified as effective [25] (Table 1). In the same study, safrol (93.2%) was identified as the major component of the essential oils from P. auritum, the most effective oil assayed in the study. Intriguingly, safrol showed the greatest larvicidal activity against laboratory strains of both Ae. aegypti and Cx. pipiens in work conducted in the Republic of Korea [26]. Thus, these studies suggest that safrol is the active larvicidal agent from the essential oil of P. auritum.

The essential oil from Pinus tropicalis Morelet (Pinaceae) referred to as turpentine oil showed significant developmental inhibition and larvicidal death in Ae. aegypti mosquitoes [27]. The turpentine oil was reported to have a greater inhibitory effect on the Ae. aegypti Rockefeller strain when compared to the “San Miguel del Padrón 2011” Ae. aegypti field strain from Cuba. The and values of the modified turpentine oil tested against the Rockefeller strain were 0.0023 mg/mL and 0.0043 mg/mL, respectively, while the and values against the “San Miguel del Padrón 2011” field strain were 0.0058 mg/mL and 0.011 mg/mL [27] (Table 1). These results indicate that turpentine oil is a highly effective larvicidal agent based on the classification of Komalamisra et al. [18] and warrant further investigation of the constituents of the oil. Although chemical analysis was not performed in the study, reports from Greece suggest that essential oils from plants of the Pinus genus predominantly contain the monoterpene compounds α-pinene, β-pinene, and limonene as well as the sesquiterpenoid compounds germacrene D or β-caryophyllene [28].

Another study from Cuba involved the investigation of the larvicidal potential of Melaleuca quinquenervia (Cav.) S.T. Blake (Myrtaceae) against field Ae. aegypti, Aedes albopictus (Skuse) and Culex quinquefasciatus (Say). Importantly, M. quinquenervia essential oil was shown to be a highly effective larvicidal agent against field mosquitoes and was most prominent against Cx. quinquefasciatus with relatively low values of 0.0021% and 0.0064% [29]. and values obtained against Ae. aegypti were 0.0047% and 0.014%, respectively, and Ae. albopictus 0.0049% and 0.0089% respectively [29] (Table 1). This highlights the fact that some essential oils may be more effective against some mosquito species when compared to others. The major chemical components of M. quinquenervia were shown to be 1,8-cineole, α-pinene, β-pinene, aterpineol, limonene, and the hydroxylated sesquiterpenoid viridiflorol.

Work conducted on the essential oils of Eucalyptus globulus Labill (Myrtaceae) and Bursera graveolens (Kunth) Triana & Planch (Burseraceae) demonstrated their larvicidal activity against the Ae. aegypti Rockefeller strain and field strains from multiple species. Interestingly, the larvicidal activity of E. globulus was greater against the Ae. aegypti Cuban field strain when compared to the Ae. aegypti Rockefeller laboratory strain [10] (Table 1), indicating that in some instances, local plants may have greater activity against local mosquitoes. When comparing the activity of the oils against the various field strains, E. globulus was more effective against Ae. aegypti and Cx. quinquefasciatus field strain and B. graveolens against Ae. albopictus [10] (Table 1). These results support the fact that the activity of the oils varies with mosquito species. The major constituents of the essential oils from E. globulus were p-cymene, γ-terpinene and 1,8-cineol, while limonene and β-elemene were the major components in the essential oils from B. graveolens [10].

In a similar study, the essential oils from Piper aduncum subsp. Ossanum (Piperaceae) and Ocimim basilicum L. (Lamiaceae) were tested for their larvicidal activity against the Ae. aegypti Rockefeller strain as well as field strains of Ae. aegypti, Ae. albopictus and Cx. quinquefasciatus [30]. The essential oils from P. aduncum subsp. Ossanum were most effective against the Rockefeller strain when compared to the other strains. It was previously reported from other studies in Cuba that camphor and camphene were the major components of the essential oils from this plant [31]. On the other hand, O. basilicum essential oils were most effective against the Ae. albopictus field strain (Table 1). Phytochemical analysis was not performed; however, reports from studies conducted in India found that methyl chavicol and methyl eugenol were the most abundant constituents in the essential oils of O. basilicum [32]. Further work needs to be done to determine if the Cuban variety of O. basilicum also contains similar constituents.

Phytochemical studies on the essential oils from Croton linearis Jacq. (Euphorbiaceae) revealed the presence of 1,8-cineole (26.66%), sabinene (9.37%), and 10-epi-γ-eudesmol (6.83%) as its major constituents [33]. The larvicidal activity of the whole essential oil from C. linearis was compared to a nanoemulsion preparation of the same oil. The and values for the whole essential oil were found to be μg/mL and μg/mL, respectively. The nanoemulsion preparation was more potent than the whole essential oil with a value of μg/mL and a value of μg/mL (Table 1) because of increased water solubility resulting in greater bioavailability [33].

4. Larvicidal Activity of Plants from the Lesser Antilles

Only two islands of the Lesser Antilles have reported studies on the larvicidal activity of plants. In Martinique, Alpinia zerumbet (Pers.) B.L. Burtt & R.M.Sm. (Zingiberaceae) was investigated for its toxic activity against the Ae. aegypti Société Béninoise d’Electricité strain [34]. Reports from India have indicated that plant species from the Zingiberaceae family are effective insecticides against moths [35]. Of all the plants of the Alpina genus, this plant is the most common in Martinique, and the phytochemical composition of its essential oils is known to vary depending on the geographical location. Some of the key constituents from the Martinique variety include terpinen-4-ol (14.7 to 22.6%), p-cymene (2.1 to 8.8%), γ-terpinene (6.9 to 14.7%), sabinene (7.0 to 16.5%), eucalyptol (17.4 to 25.2%), and α-terpinene (1.9 to 8.1%) [34]. For the Cuban variety, Mendiola et al. found that the major chemical components were the sesquiterpene compound viridiflorol (32.2%), terpinen-4-ol (14.1%), caryophyllene oxide (6.9%), and eucalyptol (5.0%) [36]. Essential oils from the flowers of the plant showed larvicidal activity at a concentration of 1% (Table 1) against the Ae. aegypti mosquito [34], indicating that it is not a very effective larvicidal agent. This lack of activity could be a result of several factors such as the strain that was tested and the fact that the chemical composition of the essential oil varies between different plant parts [37]. It should be noted, however, that in a Brazilian study in which the larvicidal activity of the leaf essential oils of A. zerumbet were tested against an Ae. aegypti laboratory strain from Ceará, Brazil, an value of 313 ppm was reported. Both studies, therefore, suggest that A. zerumbet essential oil is not very effective when compared to other leaf oil extracts [38].

In Trinidad, Chariandy et al. investigated the larvicidal activity of various plants using different solvents to obtain the plant extracts [39]. Using multiple solvents for extraction is beneficial as more compounds with varying polarities can be obtained from the plant. These differing polarities are due to key structural differences between compounds which may impact their biological effects. The petroleum ether and ethyl acetate plant extracts are from Justicia pectoralis Jacq. (Acanthaceae) were reported to be the most effective larvicidal agents when compared to Manihot utilissima Pohl (Euphorbiaceae) and Stachytarpheta jamaicensis Vahl (Verbenaceae). However, neither values nor chemical constituents were reported. The three plants were also reported to possess growth-retardant properties which would inhibit the mosquito larvae from progressing further in the mosquito life cycle. Other phytochemical studies on J. pectoralis conducted in Brazil revealed the presence of coumarins, alkaloids, and triterpenoids [40] which are secondary metabolites produced by the plant and may have been responsible for the mosquitocidal activity observed.

In another study, conducted in Trinidad, the larvicidal activity of methanol, acetone, and aqueous leaf extracts of Cordia curassavica (Jacq.) Roem & Schult (Boraginaceae), Azadirachta indica A. Juss (Meliaceae), Mangifera indica L. (Anacardiaceae), Rhizophora mangle L. (Rhizophoraceae), Avicennia germinans (L.) L. (Acanthaceae), and Languncularia racemosa (L.) C.F. Gaertn (Combretaceae) were evaluated [41]. Of the tested plants, the extracts of C. curassavica had the lowest of 758 mg/L for the methanol extract, and the highest was from M. indica with an value of greater than 20,000 mg/L against the Ae. aegypti larvae (Table 1). These values suggest that none of the tested extracts were effective larvicidal agents.

5. Significance of Studies

Although work from only three Caribbean countries has been reported in this review, it is evident that the use of botanicals as larvicidal agents is an area that is slowly gaining momentum. Cuba is at the forefront in the region, and multiple studies evaluating the larvicidal activity of essential oils have been conducted. Based on the values listed in Table 1, results obtained with essential oils are superior to that of other plant extracts similar to what has been reported elsewhere [42]. Additionally, as seen with studies targeting multiple species of field mosquitoes, the toxic effects of essential oils vary significantly with different mosquito species. Further emphasis should be placed on investigating combinations of different oils if targeting multiple species in one area is necessary.

6. Present Applications of Plant Extracts against Mosquitoes

Over the past hundred years, plant oils have been applied to the skin to repel insects. This practice is commonplace in the Caribbean especially during outbreaks of arboviral diseases. Applying botanical oils to the skin is a simple yet effective way to deter mosquitoes from biting and would therefore reduce the incidence of disease spread and contraction. Other ways people have been taking advantage of plant aromas are by placing botanical incense around the household. In the Caribbean, some incenses are made of powder from the pyrethrum plants and have proven to be very effective repellents [43]. Nevertheless, the importance of mosquito repellents as a measure of mosquito control is often underscored.

7. Future Work

There is great botanical biodiversity amongst the islands, and as such, there are many currently undiscovered species with great potential as mosquitocidal agents. It would be worthwhile for researchers in the region to delve deeper and seek to potentially characterize the many plant species that show prominent toxic effects against the Ae. aegypti mosquito or any other mosquito species that may pose a threat. Although this review is focused on larvicidal activity, even fewer studies have examined the use of botanicals as adulticides [10, 29]. There is therefore a pressing need for the evaluation of botanicals as mosquitocidal agents to continue. Comparative studies between the crude essential oil extracts and individual isolated compounds from the oils would give further insight into the specific phytochemicals responsible for the observed activity. Since there have been relatively few Caribbean countries involved in these studies, there are still likely many discoveries left to be uncovered.

In addition, determining the mechanism by which the oils result in toxicity would be a crucial and necessary step to fully weaponize the effects of the oils against mosquitoes. Essential oils are thought to work via multiple mechanisms including modification of GABA receptors and binding to octopamine receptors [44]. Current synthetic insecticidal agents work via many different mechanisms including acetylcholinesterase inhibition (organophosphates) [45] and activity at sodium-gated channels (pyrethroids) [46]. There is still much left to learn about how mosquitoes acquire resistance to these mechanisms and how to combat this issue. Hence, knowing the mechanisms of action of the oils could further increase the potency of combined formulations of multiple oils or oils blended with synthetic insecticides where the toxic activities would compound to produce synergistic effects. Chansang et al. elaborated on the significant adulticidal activity observed against Ae. aegypti mosquitoes when essential oils were combined with the insecticide pyrethrin [47]. These methods may become necessary in the future as insecticide resistance continues to increase in the Caribbean.

As essential oils are known to target mosquitoes in many different ways [48], future plans for mosquito biocontrol could encompass the spraying of plant extract formulations into and around open sources of water. Based on previously described behaviour of mosquitoes regarding where they are expected to lay eggs [49], this act could simultaneously accomplish up to three measures of mosquito biocontrol, namely, oviposition deterrence, direct ovicidal activity, and larvicidal activity. Due to the well-described toxic activities of these plant extracts against mosquitoes, people would be able to utilize low-concentrated formulations to great effect with little to no harm to themselves or the environment [15]. Researchers in the region would therefore need to investigate chemical formulations that would make this most feasible.

Lastly, companies in the United States have begun to market effective household insecticides whose active ingredients are phytochemicals extracted from plants. One such instance is the case with the house product Orange Guard^® which contains limonene. To fully benefit from the larvicidal potential of plant extracts, it is evident that more translational science needs to be done within the Caribbean. One way to achieve this is through multidisciplinary collaborations between researchers within the region. Additionally, the support of national, regional, and international stakeholders is of paramount importance as financial resources and manufacturing expertise are needed to bring these discoveries to market. Once achieved, the next stages in the region should focus on the development of effective botanical-based household agents that can be made available to the wider populations in the Caribbean.

8. Conclusion

Though limited in number, various studies have been carried out in many territories within the region. There is now much evidence to suggest that botanical-based agents can be used as alternatives to synthetic larvicidal products in the Caribbean. However, more impetus is still required before the use of these novel products can begin to be fully actualized and integrated into vector control programmes in Caribbean societies.

Conflicts of Interest

The authors declare that there is no conflict of interest regarding the publication of this paper.

References

M. Maunder, A. Leiva, E. Santiago-Valentin et al., “Plant conservation in the Caribbean Island biodiversity hotspot,” The Botanical Review, vol. 74, no. 1, pp. 197–207, 2008.
View at: Publisher Site | Google Scholar
Caribbean Islands - Species, “CEPF,” 2019, Retrieved January 31, 2023, from https://www.cepf.net/our-work/biodiversity-hotspots/caribbean-islands/species.
View at: Google Scholar
S. Heileman, “Thematic Report for the Insular Caribbean Sub-Region,” in In Proceedings of the CLME Synthesis Workshop, Barbados, 2007, Retrieved August 8, 2023, from https://www.clmeproject.org/phaseone/dcenter/CLME%20Insular%20Caribbean%20Thematic%20Report%20draft%2016%20Feb%2007%5B1%5D.pdf.
View at: Google Scholar
G. Prinsloo and N. Nogemane, “The effects of season and water availability on chemical composition, secondary metabolites and biological activity in plants,” Phytochemistry Reviews, vol. 17, no. 4, pp. 889–902, 2018.
View at: Publisher Site | Google Scholar
R. P. Adams and T. A. Zanoni, “Essential oils of plants from Hispaniola: 3. The leaf oil of Canella winterana(Canellaceae),” Journal of Essential Oil Research, vol. 2, no. 4, pp. 163–165, 1990.
View at: Publisher Site | Google Scholar
J. Abaul, L. Udino, P. Bourgeois, and J.-M. Bessière, “Composition of the essential oils of Canella winterana(L.) Gaertn,” Journal of Essential Oil Research, vol. 7, no. 6, pp. 681–683, 1995.
View at: Publisher Site | Google Scholar
P. Facey, R. Porter, P. Reese, and A. D. Williams, “Biological Activity and Chemical Composition of the Essential Oil from Jamaican Hyptis verticillata Jacq,” Journal of Agricultural and Food Chemistry, vol. 53, no. 12, pp. 4774–4777, 2005.
View at: Publisher Site | Google Scholar
J. Pino, A. Bello, A. Urquiola, and R. Marbot, “Essential oil of Hyptis verticillata Jacq. from Cuba,” Revista CENIC. Ciencias Químicas, vol. 33, pp. 55-56, 2002.
View at: Google Scholar
A. Trowbridge, “Evolutionary ecology of chemically mediated plant-insect interactions,” Ecology and the Environment, vol. 8, pp. 143–176, 2014.
View at: Google Scholar
M. Leyva, M. Marquetti, D. Montada, J. Payroll, and R. Scull, “ACEITES ESENCIALES DE Eucalyptus globulus (labill) Y Bursera graveolens (kunth) Triana & planch PARA EL control DE MOSQUITOS DE IMPORTANCIA MÉDICA,” The Biologist, vol. 18, no. 2, 2020.
View at: Publisher Site | Google Scholar
S. Francis, K. Saavedra-Rodriguez, R. Perera, M. Paine, W. C. Black, and R. Delgoda, “Insecticide resistance to permethrin and malathion and associated mechanisms in Aedes aegypti mosquitoes from St. Andrew Jamaica,” PLoS One, vol. 12, no. 6, article e0179673, 2017.
View at: Publisher Site | Google Scholar
S. Francis, T. Campbell, S. McKenzie et al., “Screening of insecticide resistance in Aedes aegypti populations collected from parishes in eastern Jamaica,” PLoS Neglected Tropical Diseases, vol. 14, no. 7, article e0008490, 2020.
View at: Publisher Site | Google Scholar
M. M. Rodríguez, A. Ruiz, L. Piedra et al., “Multiple insecticide resistance in Aedes aegypti (Diptera: Culicidae) from Boyeros municipality, Cuba and associated mechanisms,” Acta Tropica, vol. 212, article 105680, 2020.
View at: Publisher Site | Google Scholar
K. A. Polson, S. C. Rawlins, W. G. Brogdon, and D. D. Chadee, “Characterisation of DDT and pyrethroid resistance in Trinidad and Tobago populations of Aedes aegypti,” Bulletin of Entomological Research, vol. 101, no. 4, pp. 435–441, 2011.
View at: Publisher Site | Google Scholar
A. Ghosh, N. Chowdhury, and G. Chandra, “Plant extracts as potential mosquito larvicides,” Indian Journal of Medical Research., vol. 135, no. 5, pp. 581–598, 2012.
View at: Google Scholar
R. Alexander and P. K. Anderson, “Pesticide use, alternatives and workers' health in Cuba,” International Journal of Health Services, vol. 14, no. 1, pp. 31–41, 1984.
View at: Publisher Site | Google Scholar
L. Aguilera, A. Navarro, J. E. Tacoronte Morales, M. Leyva, and M. Marquetti, “Lethal effect of Cuban Myrtaceae on Aedes aegypti (Diptera Cuilicidae),” Revista Cubana de Medicina Tropical, vol. 55, pp. 100–104, 2003.
View at: Google Scholar
N. Komalamisra, Y. Trongtokit, Y. Rongsriyam, and C. Apiwathnasorn, “Screening for larvicidal activity in some Thai plants against four mosquito vector species,” The Southeast Asian Journal of Tropical Medicine and Public Health, vol. 36, no. 6, pp. 1412–1422, 2005.
View at: Google Scholar
J. Pino, R. Marbot, A. Bello, and A. Urquiola, “Essential oil of Eugenia melanadenia Krug et Urb. From Cuba,” Journal of Essential Oil Research, vol. 15, no. 4, pp. 256–258, 2003.
View at: Publisher Site | Google Scholar
H. E.-D. M. Zahran and S. A. M. Abdelgaleil, “Insecticidal and developmental inhibitory properties of monoterpenes on Culex pipiens L. (Diptera: Culicidae),” Journal of Asia-Pacific Entomology, vol. 14, no. 1, pp. 46–51, 2011.
View at: Publisher Site | Google Scholar
W. J. Silva, G. A. Dória, R. T. Maia et al., “Effects of essential oils on Aedes aegypti larvae: alternatives to environmentally safe insecticides,” Bioresource Technology, vol. 99, no. 8, pp. 3251–3255, 2008.
View at: Publisher Site | Google Scholar
M. Govindarajan, M. Rajeswary, S. L. Hoti, and G. Benelli, “Larvicidal potential of carvacrol and terpinen-4-ol from the essential oil of Origanum vulgare (Lamiaceae) against Anopheles stephensi, Anopheles subpictus, Culex quinquefasciatus and Culex tritaeniorhynchus (Diptera: Culicidae),” Research in Veterinary Science, vol. 104, pp. 77–82, 2016.
View at: Publisher Site | Google Scholar
J. A. Pino, A. Rosado, A. Bello, A. Urquiobi, and S. Garcia, “Essential oil of Psidium rotundatum Griseb. from Cuba,” Journal of Essential Oil Research, vol. 11, no. 6, pp. 783-784, 1999.
View at: Publisher Site | Google Scholar
A. F. Traboulsi, K. Taoubi, S. El‐Haj, J. M. Bessiere, and S. Rammal, “Insecticidal properties of essential plant oils against the mosquito Culex pipiens molestus (Diptera: Culicidae),” Pest Management Science, vol. 58, no. 5, pp. 491–495, 2002.
View at: Publisher Site | Google Scholar
M. Leyva, M. del Carmen Marquetti, J. E. Tacoronte et al., “Actividad larvicida de aceites esenciales de plantas contra Aedes aegypti (L.)(Diptera: Culicidae),” Revista Biomédica, vol. 20, pp. 5–13, 2009.
View at: Google Scholar
H. Perumalsamy, N.-J. Kim, and Y.-J. Ahn, “Larvicidal activity of compounds isolated from Asarum heterotropoides against Culex pipiens pallens, Aedes aegypti, and Ochlerotatus togoi (Diptera: Culicidae),” Journal of Medical Entomology, vol. 46, no. 6, pp. 1420–1423, 2009.
View at: Publisher Site | Google Scholar
M. Leyva, M. del Carmen Marquetti, L. French, D. Montada, O. Tiomno, and J. E. Tacoronte, “Efecto de un aceite de trementina obtenido de Pinus tropicalis Morelet sobre la biología de una cepa de Aedes (Stegomyia) aegypti Linnaeus, 1762 resistente a insecticidas,” in Anales de Biologia, Servicio de Publicaciones de la Universidad de Murcia, 2013.
View at: Publisher Site | Google Scholar
E. Loannou, A. Koutsaviti, O. Tzakou, and V. Roussis, “The genus Pinus: a comparative study on the needle essential oil composition of 46 pine species,” Phytochemistry Reviews, vol. 13, no. 4, pp. 741–768, 2014.
View at: Publisher Site | Google Scholar
M. Leyva, L. French-Pacheco, F. Quintana et al., “Melaleuca quinquenervia (Cav.) S.T. Blake (Myrtales: Myrtaceae): natural alternative for mosquito control,” Journal of Tropical Medicine, vol. 9, no. 10, 984 pages, 2016.
View at: Publisher Site | Google Scholar
M. Leyva, M. Marquetti, D. Montada et al., “Actividad insecticida de los aceites esenciales de Piper aduncum subsp. ossanum y Ocimun basilicum sobre Aedes aegypti, Aedes albopictus y Culex quinquefasciatus,” Novitates Caribaea, vol. 16, pp. 122–132, 2020.
View at: Publisher Site | Google Scholar
O. Abreu and J. Pino, “Leaf oil composition of Piper aduncum subsp. ossanum(C. CD.) Saralegui from Cuba,” Natural Product Communications, vol. 3, no. 2, article 1934578X0800300, 2008.
View at: Publisher Site | Google Scholar
R. K. Joshi, “Chemical composition and antimicrobial activity of the essential oil of Ocimum basilicum L. (sweet basil) from Western Ghats of North West Karnataka, India,” Ancient Science of Life, vol. 33, no. 3, pp. 151–156, 2014.
View at: Publisher Site | Google Scholar
J. R. R. Amado, A. L. Prada, J. G. Diaz, R. N. P. Souto, J. C. E. Arranz, and T. P. de Souza, “Development, larvicide activity, and toxicity in nontarget species of the Croton linearis Jacq essential oil nanoemulsion,” Environmental Science and Pollution Research International, vol. 27, no. 9, pp. 9410–9423, 2020.
View at: Publisher Site | Google Scholar
A. Kerdudo, E. N. Ellong, P. Burger et al., “Chemical composition, antimicrobial and insecticidal activities of flowers essential oils of Alpinia zerumbet (Pers.) B.L.Burtt & R.M.Sm. from Martinique Island,” Chemistry & Biodiversity, vol. 14, no. 4, 2017.
View at: Publisher Site | Google Scholar
K. Singh, M. Singh, A. Sureja, and R. Bhardwaj, “Insecticidal activity of certain plants of zingiberaceae and araceae against Spodoptera litura F. and Plutella xylostella saunders in cabbage,” Indian Journal of Entomology, vol. 74, pp. 62–68, 2012.
View at: Google Scholar
J. Mendiola, J. Pino, A. Fernández-Calienes, D. Mendoza, and P. Herrera, “Chemical composition and in vitro antiplasmodial activity of essential oils of leaves and flowers of alpinia zerumbet grown in Cuba,” Pharmacology, vol. 2, pp. 1–5, 2015.
View at: Google Scholar
A. Barra, “Factors affecting chemical variability of essential oils: a review of recent developments,” Natural Product Communications, vol. 4, no. 8, article 1934578X0900400, 2009.
View at: Publisher Site | Google Scholar
E. S. Cavalcanti, S. M. Morais, M. A. Lima, and E. W. Santana, “Larvicidal activity of essential oils from Brazilian plants against Aedes aegypti L,” Memórias do Instituto Oswaldo Cruz, vol. 99, no. 5, pp. 541–544, 2004.
View at: Publisher Site | Google Scholar
C. M. Chariandy, C. E. Seaforth, R. H. Phelps, G. V. Pollard, and B. P. Khambay, “Screening of medicinal plants from Trinidad and Tobago for antimicrobial and insecticidal properties,” Journal of Ethnopharmacology, vol. 64, no. 3, pp. 265–270, 1999.
View at: Publisher Site | Google Scholar
L. Leal, A. Silva, and G. Viana, “Justicia pectoralis , a coumarin medicinal plant have potential for the development of antiasthmatic drugs?” Revista Brasileira de Farmacognosia, vol. 27, no. 6, pp. 794–802, 2017.
View at: Publisher Site | Google Scholar
A. Mohammed and D. D. Chadee, “An evaluation of some Trinidadian plant extracts against larvae of Aedes aegypti mosquitoes,” Journal of the American Mosquito Control Association, vol. 23, no. 2, pp. 172–176, 2007.
View at: Publisher Site | Google Scholar
H. D. Manh, D. T. Hue, N. T. T. Hieu, D. T. T. Tuyen, and O. T. Tuyet, “The mosquito Larvicidal activity of essential oils from Cymbopogon and eucalyptus species in Vietnam,” Insects, vol. 11, no. 2, p. 128, 2020.
View at: Publisher Site | Google Scholar
S. R. S. Simaremare, C. C. Hung, C. J. Hsieh, and L. M. Yiin, “Relationship between organophosphate and pyrethroid insecticides in blood and their metabolites in urine: a pilot study,” International Journal of Environmental Research and Public Health, vol. 17, no. 1, 2020.
View at: Publisher Site | Google Scholar
M. Jankowska, J. Rogalska, J. Wyszkowska, and M. Stankiewicz, “Molecular targets for components of essential oils in the insect nervous system-a review,” Molecules, vol. 23, no. 1, 2018.
View at: Publisher Site | Google Scholar
T. R. Fukuto, “Mechanism of action of organophosphorus and carbamate insecticides,” Environmental Health Perspectives, vol. 87, pp. 245–254, 1990.
View at: Publisher Site | Google Scholar
T. Narahashi, “Mode of action of DDT and allethrin on nerve: cellular and molecular mechanisms,” Residue Reviews, vol. 25, pp. 275–288, 1969.
View at: Google Scholar
A. Chansang, D. Champakaew, A. Junkum et al., “Synergy in the adulticidal efficacy of essential oils for the improvement of permethrin toxicity against Aedes aegypti L. (Diptera: Culicidae),” Parasites & Vectors, vol. 11, 2018.
View at: Publisher Site | Google Scholar
T. Pushpanathan, A. Jebanesan, and M. Govindarajan, “Larvicidal, ovicidal and repellent activities of Cymbopogan citratus Stapf (Graminae) essential oil against the filarial mosquito Culex quinquefasciatus (say) (Diptera: Culicidae),” Tropical Biomedicine, vol. 23, no. 2, pp. 208–212, 2006.
View at: Google Scholar
J. F. Day, “Mosquito oviposition behavior and vector control,” Insects, vol. 7, no. 4, p. 65, 2016.
View at: Publisher Site | Google Scholar

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Copyright © 2023 Rhaheem N. A. Layne-Yarde and Simone L. Sandiford. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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