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Article

Efficacy of Two Monoterpenoids, Carvacrol and Thymol, and Their Combinations against Eggs and Larvae of the West Nile Vector Culex pipiens

by
Mohammad Reza Youssefi
1,
Mohaddeseh Abouhosseini Tabari
2,
Aryan Esfandiari
3,
Sohrab Kazemi
4,
Ali Akbar Moghadamnia
4,*,
Stefania Sut
5,
Stefano Dall’Acqua
6,*,
Giovanni Benelli
7,* and
Filippo Maggi
8
1
Department of Veterinary Parasitology, Babol-Branch, Islamic Azad University, Babol 484, Iran
2
Faculty of Veterinary Medicine, Amol University of Special Modern Technologies, Amol 46131-46391, Iran
3
Young Researchers and Elite Club, Babol Branch, Islamic Azad University, Babol 484, Iran
4
Cellular and Molecular Biology Research Center, Health Research Center, Babol University of Medical Sciences, Babol 47176-47745, Iran
5
Department of Agronomy, Food, Natural Resources, Animals and Environment (DAFNAE), University of Padova, 35020 Legnaro, Italy
6
Department of Pharmaceutical and Pharmacological Sciences, University of Padova, 35139 Padova, Italy
7
Department of Agriculture, Food and Environment, University of Pisa, via del Borghetto 80, 56124 Pisa, Italy
8
School of Pharmacy, University of Camerino, 62032 Camerino, Italy
*
Authors to whom correspondence should be addressed.
Molecules 2019, 24(10), 1867; https://doi.org/10.3390/molecules24101867
Submission received: 6 April 2019 / Revised: 30 April 2019 / Accepted: 11 May 2019 / Published: 15 May 2019
(This article belongs to the Special Issue Natural Products as Effective Biopesticides and Antiprotozoal Agents)

Abstract

:
Background: Insect vector control is facing the challenges of resistance development and environmental hazards caused by synthetic pesticides. This has led to a considerable market opportunity for botanical insecticides. In this scenario, our study investigated the potential of selected bioactive monoterpenoids, carvacrol and thymol, as safe and effective tools to control the West Nile vector Culex pipiens. Furthermore, the combined effect of thymol-carvacrol mixtures and their possible interactions were assessed. Methods: For determining larvicidal and ovicidal 50% lethal concentration (LC50), each monoterpenoid was tested at different concentrations (5–500 mg/L). Then, the fixed ratio method was used for evaluating their combinational efficacy. Results: Carvacrol was more toxic against larvae of Cx. pipiens, with a LC50 value of 14 mg/L, whereas thymol exhibited a LC50 value of 49 mg/L. Comparable trends of efficacy were observed when toxicity on Cx. pipiens eggs was investigated, with LC50 values of 7 and 13 mg/L for carvacrol and thymol, respectively. In combinational toxicity assays, the mixture thymol-carvacrol at 1:4 ratio achieved a synergistic effect against larvae of Cx. pipiens, whereas an additive effect was observed on eggs. Other ratios showed antagonistic effects. Conclusions: Overall, our findings pointed out that the 1:4 ratio of thymol-carvacrol blend can enhance the insecticidal efficacy on Cx. pipiens young instars and can be considered further as active ingredient for developing botanical insecticides to be used in mosquito control operations.

Graphical Abstract

1. Introduction

The effective and environmentally sustainable management of arthropod vectors is of great relevance and has attracted the attention of researchers for centuries [1,2,3,4]. Mosquitoes (Diptera: Culicidae) are currently recognized as the most important vectors in terms of public health importance, playing a crucial role in the spread of malaria, yellow fever, dengue, West Nile, Rift Valley fever, Japanese encephalitis, chikungunya and Zika virus, just to cite a few examples [5,6].
However, concerning mosquito control programs, several challenges still need to be faced [6,7], including the quick development of insecticide resistance in targeted vector populations [8,9], as well as severe non-target effects of synthetic pesticides on human health and the environment [10]. A possible route to tackle this challenge is the development of novel pesticides based on plant secondary metabolites, which are characterized by multiple modes of action [11,12,13,14]. Indeed, in recent years, researchers have attempted to find out new sources of safe and eco-friendly plant-based insecticides and acaricides [15,16,17]. In this framework, a significant number of studies provides interesting insights into the efficacy of plant extracts and essential oils as ovicides and larvicides against many mosquito vectors of medical and veterinary importance [18,19].
However, plant essential oil composition can vary consistently according to many factors, including botanical species, geographical area of origin, growing conditions, genetic variability, harvesting time and extraction technique, just to cite some of the main ones [20]. This can play a major impact on their insecticidal activity, making the development of products for real-world use challenging. Therefore, an approach to deal with this issue is the detection of the bioactive components from plant essential oils, and their encapsulation or micro- and nanoformulations for highly stable pesticide development [21,22,23,24,25].
Ten-carbon components of plant essential oils as monoterpenoids have been widely recognized as toxic, repellent, and antifeedant agents on insect pests and vectors. Thus, they are considered as potential molecules for the development of novel and eco-friendly pesticides [26,27]. Monoterpenoids are synthesized in the cytoplasm and plastids of the plant cell through two distinct pathways, namely mevalonate and methyl erythritol phosphate, respectively [28]. They are endowed with a multitude of different chemical structures (e.g., linear, monocyclic, bicyclic) and functional groups (e.g., double bonds, alcoholic, aldehydic, ketonic, phenolic). Among them, phenolic monoterpenes as thymol and carvacrol have been recognized as two of the most powerful bioactive constituents produced by higher plants [29]. Research on the toxicity of these phenolic monoterpenes on various insect pests have highlighted their potential as ovicides, fumigants and contact toxicants [30]. Carvacrol is a monoterpene phenol that occurs in many essential oils of the Lamiaceae family, including Origanum, Satureja, Thymbra, Thymus, and Coridothymus species [31,32]. Its isomer thymol can be found in high amounts in essential oils of Thymus species, Ocimum gratissimum L. and Trachyspermum ammi (L.) Sprague [33,34,35,36,37]. Carvacrol and thymol were reported to have broad insecticidal activity against arthropod species of agricultural, medical and veterinary importance [23,38,39,40,41], including Anopheles, Aedes and Culex mosquitoes [42,43,44,45]. Noteworthy, these compounds are recognized as Generally Recognized as Safe (GRAS) by the FDA and EPA and have LD50, values as determined in rats after oral administration, of around 1 g/kg, making their formulations likely devoid of toxic effects on humans and animals.
To our knowledge, no data are available on the efficacy of these two monoterpenes and their mixtures against the mosquito species Culex pipiens L. The latter is part of the Culex pipiens complex, whose species, found worldwide in urban and sub-urban areas of temperate and tropical regions, vector important pathogens including West Nile and St. Louis encephalitis virus, among others, as well as parasites like lymphatic filariasis and avian malaria [46]. In particular, since West Nile is expanding its geographical range in Europe causing an increasing number of epidemics/outbreaks [47], the effective management of Cx. pipiens mosquitoes under the Integrated Vector Management (IVM) is timely and important. Thus, to develop novel insecticides of botanical origin characterized by a multiple mechanism of action [11,48] and active at very low doses [14], the present study was conducted to assess the toxicity of carvacrol and thymol on eggs and larvae of Cx. pipiens. Furthermore, when formulating selected plant essential oil constituents in insecticidal blends, an important issue needing attention is the possible synergistic and antagonistic effects of the blend, as outlined by research conducted on various arthropod species of economic importance, including agricultural pests [49], houseflies [50], mites [51], mosquitoes [22] and ticks [41]. Therefore, in our study, the combined effect of thymol-carvacrol and their possible interaction were assessed on both eggs and larvae of Cx. pipiens mosquitoes, using the fixed ratio method.

2. Results

Culex pipiens egg mortality was recorded after 24 h exposure to different concentrations of carvacrol and thymol (Figure 1a). A significant effect of the tested compound (F1,32 = 96.121, p < 0.0001), the concentration (F3,32 = 708.862, p < 0.0001), and their interaction (F3,32 = 11.949, p < 0.0001) was observed. At the minimum tested concentration of 5 mg/L, both thymol and carvacrol resulted in 20.2 and 40.4% decrease in egg hatchability, respectively, while 50 mg/L led to 100% egg mortality (Figure 1a). Overall, carvacrol achieved LC50 and LC90 values of 7 and 20 mg/L, respectively, showing higher toxicity on mosquito eggs if compared with thymol, which had LC50 and LC90 values of 13 and 27 mg/L, respectively (Table 1).
Larvicidal assays also showed a significant effect of the tested compounds (F1,56 = 472.971, p < 0.0001), the concentration (F6,56 = 885.684, p < 0.0001), and their interaction (F6,56 = 34.418, p < 0.0001). As shown in Figure 1b, after 24 h of exposure to 50 mg/L of carvacrol, 92% mosquito mortality was achieved, while thymol tested at the same concentration led to 52% mortality of Cx. pipiens larvae. Concerning probit analysis conducted on larvicidal results, carvacrol showed LC50 and LC90 values of 14 and 44 mg/L, respectively, while thymol achieved LC50 and LC90 values of 49 and 112 mg/L, respectively (Table 1).
Results of the quantitative analysis of LC50 combinational toxicity of carvacrol and thymol and their FLC indices are provided in Table 2. The trend of interaction between thymol-carvacrol combinations against eggs and 3rd instar larvae of Cx. pipiens was analysed by the fixed ratio method and the obtained isobolograms were given in Figure 2. The 1:4 ratio of thymol-carvacrol caused the highest toxicity, showing a synergistic effect against larvae of Cx. pipiens with FLC index of 0.79, whereas an additive effect was observed (FLC = 1) against eggs (Figure 2). Other ratios led to antagonistic effects.

3. Discussion

3.1. Ovicidal and Larvicidal Efficacy

Monoterpenoids are among the most important bioactive compounds in essential oil research. Concerning the development of novel insecticides, they have been reported as effective against a wide variety of species of medical, veterinary and agricultural importance, highlight their efficacy as ovicides, larvicides and even adulticides [21,22,23,26,27]. The present study highlighted the promising potential of carvacrol and thymol as ovicidal and larvicidal agents against the West Nile vector Cx. pipiens. To the best of our knowledge, little has been reported on these two compounds as mosquito ovicides. On the other hand, our larvicidal results substantiated the earlier report by Traboulsi et al. [42], who highlighted the toxicity of eight components of plant essential oils against 4th instar larvae of Cx. pipiens molestus. Among the eight tested compounds, carvacrol and thymol were the most toxic ones. However, against this latter mosquito, they achieved LC50 values of 36 and 37.6 mg/L, respectively [42]; carvacrol LC50 value was substantially higher if compared to probit results achieved by the same compound in our study on Cx. pipiens 3rd instar larvae (LC50 of 14 mg/L).
Besides, the larvicidal activity of carvacrol, the major constituent of O. vulgare L. essential oil, has been evaluated against 3rd stage larvae of other mosquito species. Carvacrol has been reported effective against Anopheles stephensi Liston, with a LC50 value of 21.15 μg/mL, and exhibited LC50 values of 26.08 and 27.95 μg/mL on Cx. quinquefasciatus Say and Cx. tritaeniorhynchus Giles, respectively [44]. Knio et al. [52] reported LC50 of 35.5 and 33.7 ppm for carvacrol and thymol against larvae of the seaside mosquito, Aedes (Ochlerotatus) caspius (Pallas). Finally, Carvalho et al. [53] evaluated the larvicidal activity of the essential oil from Lippia sidoides Cham., and its two major components, carvacrol and thymol, against Aedes aegypti L. Thymol caused 100% mortality even at 0.017 % concentration. However, in contrast to our findings on Cx. pipiens and to the studies detailed above, these authors failed to observe any mosquito larvicidal activity for carvacrol tested at 0.04 % [53].

3.2. Ovicidal and Larvicidal Efficacy of the Blend Containing Carvacrol and Thymol

The increasing levels of insecticide resistance in targeted arthropod populations worldwide [8,9] require highly effective strategies to establish reliable vector control methods within the IVM framework, with proven epidemiological impact [1]. The employ of botanical-based insecticidal blends as well as combinations of synthetic or bacterial-borne (e.g., toxins from Bacillus thuringiensis Berliner serovar. israelensis) pesticides with plant secondary metabolites can be a promising strategy to reduce the development of resistance [19,54], relying on components with multiple mechanisms of action [54,55].
Overall, decreasing the risk of pesticide resistance development, reducing the employed concentrations, and exploiting the synergistic actions between selected molecules are some of the main advantages of combining phytochemicals [31,37,56,57]. Shaalan et al. [55] showed that binary mixtures of selected botanical extracts were more effective than non-mixed ones against 4th instar larvae of Ae. aegypti and Cx. annulirostris Skuse. Besides mosquitoes, Hummelbrunner and Isman [58] earlier evaluated the toxicity of some monoterpenoids commonly found in plant essential oils on the moth pest Spodoptera litura Fabr. (Lepidoptera: Noctuidae). They showed synergistic acute toxicity and feeding deterrence of (E)-anethole with thymol, citronellal, and (R)-terpineol, and suggested synergistic 1:1 mixtures for development of effective control agents since the use of smaller amounts in the mixture resulted in achieving satisfactory levels of efficacy [58]. In agreement with these authors, our results revealed enhanced activity of the thymol-carvacrol mixture on larvae of Cx. pipiens, when compared to the bioactivity of individual components tested alone.
The fixed ratio method and isobologram construction showed different interactions of the two monoterpene phenols when administered in combination. The most efficient ratio of thymol-carvacrol was 1:4, which resulted in synergistic effect against larvae and additive effect against eggs of Cx. pipiens. The various physiological interactions of plant-borne products with different insect targets is a complex issue to deal with. Concerning our findings, we may hypothesize that the 1:4 thymol-carvacrol combination is able to completely inhibit some receptors (e.g., octopamine and GABA ones) causing to insect neurotoxicity, or is the most effective in interacting with more than one target, leading to synergistic effects. Further research on this is warranted, since studies on the molecular effects of synergistic mixtures are extremely limited. More generally, when searching literature about the synergistic effects of natural products in mosquito ovicidal studies we faced a severe lack of literature. On the other hand, important research has been done on the essential oil toxicity to mosquito larvae [31,37,55] and pure compounds [19]. Concerning the latter category, Pavela tested binary mixtures of 30 selected essential oil constituents on Cx. quinquefasciatus larvae showing that thymol was the most effective, with a LC50 of 18 mg/L, while carvacrol was among the 9 substances showing synergy with >20 compounds [18]. It is noteworthy that carvacrol and thymol tested in a binary blend had a synergistic effect on Cx. quinquefasciatus, as also highlighted by our results on Cx. pipiens. However, in the study by Pavela [19], the highest larvicidal synergy on Cx. quinquefasciatus was observed testing carvacrol + carvone, carvacrol + 4-allylanisole, and carvacrol + terpineol, among others. Besides, the author outlined, as shown for carvacrol + thymol on Cx. pipiens data presented here, that some of the most effective mixtures varied in their efficacy according to the mixing ratio. In particular, 100% larvicidal efficacy was obtained formulating carvacrol + carvone at a ratio >2. Overall, Pavela et al. [24] selected two binary mixtures leading to mortality > 90% when tested at <20 mg/L: limonene + (E)-anethole (1:1) and carvacrol + carvone (1:2–3). In contrast to our findings, Karpouhtsis et al. [59] reported that mixing carvacrol and thymol, resulted in reduction of insecticidal activity on Drosophila melanogaster Meigen (Diptera: Drosophilidae), suggesting an antagonistic interaction between them. It was observed that the toxicity of carvacrol was reduced in presence of thymol. Interestingly, the obtained data and the trend of isobologram curve in the present study pointed out a loss of synergy when increasing the concentration of thymol and decreasing that of carvacrol. In other words, adding thymol to carvacrol, especially in the combinations containing higher amounts of thymol over carvacrol, can result in antagonistic interactions between these two molecules (FLC > 1).
Synergistic activity of carvacrol combined with thymol has also been reported recently for mite and tick species. Indeed, carvacrol + thymol particularly in a 4:1 ratio led to high acaricidal activity against the poultry red mite, Dermanyssus gallinae (De Geer) [27]. Furthermore, according to Novato et al. [41] thymol + carvacrol at a 1:1 ratio of LC50 achieved synergistic effect towards larvae of Dermacentor nitens Neumann and Amblyomma sculptum Berlese, while at 1/4 LC50 showed an additive effect against D. nitens [41]. Araujo et al. [60] also evaluated, among others, the synergistic effect of thymol and carvacrol in larvae of the cattle tick, Rhipicephalus (Boophilus) microplus (Canestrini), and brown dog tick, Rhipicephalus sanguineus (Latreille). They reported that combinations of carvacrol + thymol, carvacrol + eugenol and thymol + eugenol had synergistic effects against R. microplus and R. sanguineus s.l. larvae [60].
The toxicity of carvacrol and thymol to arthropod pests and vectors can be due to different mechanisms. Research has suggested that carvacrol and thymol potentiate ligand-gated chloride channels in insect nervous system and probably act as neurotoxic insecticides [48,61]. Furthermore, it was shown that thymol may work by blocking octopamine receptors, which are unique to insects and considered as an important target site for pest and vector control [10,14]. On the other hand, the actual role of thymol and carvacrol to interact with the cholinergic system of insects cannot be neglected [62]. Instead, their interaction with the detoxification system of insects can be excluded [63].
Based on these findings, only the thymol-carvacrol ratio 1:4 in the mixture was found effective in producing synergistic toxicity in young instars. The latter may be given by the concomitant multiple mode of actions of the two compounds that surely deserves further investigation.

4. Materials and Methods

4.1. Chemicals

Carvacrol and thymol were purchased from Sigma-Aldrich (Steinheim, Germany) and stored in a sealed brown container until bioassays. All other chemicals were analytical grade and commercially available.

4.2. Ovicidal and Larvicidal Assays

A laboratory strain of Cx. pipiens was reared as described by Tabari et al. [22]. Ovicidal activity was evaluated according to the method of Tabari et al. [22]. Freshly laid egg rafts of Cx. pipiens (about 100 eggs per replicate) were submerged for 24 h with water plus different concentrations of carvacrol and thymol (i.e., 5, 10, 20, and 50 mg/L in 5 mL tap water containing 0.4% DMSO). Negative control was water + 0.4% DMSO. 5 replicates were done for each tested concentration and control as well. 24 h post-treatment, egg mortality (%) was estimated as follows:
Egg   mortality   ( % )   =   Total   no .   of   eggs     no .   of   hatched   larvae Total   no .   of   eggs   ×   100
Larvicidal activity of carvacrol and thymol was evaluated on 3rd instar larvae according to the WHO protocol [64] with slight modifications [22]. Both carvacrol and thymol were tested at 5, 10, 20, 50, 100, 200, and 500 mg/L in tap water. To formulate the concentrations detailed above, both compounds were dissolved in 1 mL of dimethyl sulfoxide DMSO then diluted in water [24]. Negative control was 1 mL DMSO + 249 mL of water. In each replicate, 20 larvae were tested, 5 replicates were done per each concentration. Larval mortality was noted after 24 h [1].

4.3. Combinational Bioassays

This second series of experiments was aimed to determine possible synergistic or antagonistic activity of combination of carvacrol and thymol. Based on the fixed ratio method, four different ratios of thymol-carvacrol, i.e., 4:1, 3:2, 2:3, and 1:4 v/v, were tested for their combinational toxicity on eggs and larvae of Cx. pipiens. The method by Pastor et al. [57] was followed; for each ratio, two-fold serial dilutions were performed to give final concentrations ranging from 1 to 100 mg/L. Three replicates were performed for each combination ratio.

4.4. Statistical Analysis

Egg and larval mortality data transformed by arcsine√ were analyzed by ANOVA and Tukey’s HSD test (p ≤ 0.05). To determine LC50 and LC90 values, mortality data, corrected with Abbott’s [65] formula where needed, were subjected to probit analysis [66]. When 95% confidence limits (95% CL) failed to overlap, LC50 and LC90 values were considered significantly different from one another. Concerning the combination assays, the obtained data were plotted for the construction of an isobologram for both larvicidal and ovicidal activity of thymol-carvacrol combinations. Then, 50% lethal concentration (LC50) and the fractional lethal concentration (FLC) index for each ratio were calculated. FLC index was calculated according to the following formula:
FLC index = LC50 A in combination/LC50 A alone + LC50 B in combination/LC50 B alone.
An FLC index equal to 1.0 indicates additivity, FLC < 1.0 indicates tendency to synergy, and FLC > 1.0 indicates a trend toward antagonism [67].

5. Conclusions and Outlooks for Future Research

Overall, the present investigation firstly shed light on the high toxicity of carvacrol and thymol against mosquito eggs. In addition, outstanding larvicidal activity was observed on Cx. pipiens larvae, with LC50 values lower < 50 mg/L for both molecules. Extremely low LC50 were detected both on eggs and larvae of Cx. pipiens, with values always lower than 20 mg/L. Combinational assays pointed out a synergistic effect testing 1:4 ratio of thymol plus carvacrol. Detecting a synergistic effect in bioactive phytochemical mixtures could be helpful in future operations aimed to manage West Nile and filariasis mosquito vectors exploiting low concentrations of the active ingredients, and their multiple mode of action, which can be helpful to reduce the risk of insecticide resistance development. Lastly, further ecotoxicology research to assess the impact of the binary mixtures proposed here on non-target species, with special reference to chronic toxicity on aquatic organisms, are still needed.

Author Contributions

Conceptualization, M.R.Y., A.A.M., F.M., G.B., S.D. and S.S.; methodology, A.E., M.A.T., S.K.; software, M.A.T., G.B.; validation, M.A.T.; data curation, G.B.; writing—original draft preparation, E.M.; writing—review and editing, M.R.Y., F.M., G.B., S.D. and S.S.; A.A.M., G.B. and F.M.

Funding

This research was funded by Babol University of Medical Sciences, grant number 944059.

Acknowledgments

The authors are grateful to Prof. Mario Giorgi, University of Pisa, for his kind help in the construction of isobologram.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Benelli, G.; Beier, J. Current vector control challenges in the fight against malaria. Acta Trop. 2017, 174, 91–96. [Google Scholar] [CrossRef]
  2. Badawy, M.E.; Taktak, N.E.; Awad, O.M.; Elfiki, S.A.; Abou El-Ela, N.E. Preparation of ecofriendly formulations containing biologically active monoterpenes with their fumigant and residual toxicities against adults of Culex pipiens. J. Trop. Med. 2016, 2016, 8540830. [Google Scholar] [CrossRef] [PubMed]
  3. Dantas-Torres, F.; Otranto, D. Best practices for preventing vector-borne diseases in dogs and humans. Trends Parasitol. 2016, 32, 43–55. [Google Scholar] [CrossRef]
  4. Fernandes, J.N.; Moise, I.K.; Maranto, G.L.; Beier, J.C. Revamping mosquito-borne disease control to tackle future threats. Trends Parasitol. 2018, 34, 359–368. [Google Scholar] [CrossRef] [PubMed]
  5. Benelli, G.; Romano, D. Mosquito vectors of Zika virus. Entomol. Gen. 2017, 36, 309–318. [Google Scholar] [CrossRef]
  6. Mayer, S.V.; Tesh, R.B.; Vasilakis, N. The emergence of arthropod-borne viral diseases: A global prospective on dengue, chikungunya and Zika fevers. Acta Trop. 2017, 166, 155–163. [Google Scholar] [CrossRef]
  7. Wilke, A.B.; Beier, J.C.; Benelli, G. Transgenic mosquitoes–fact or fiction? Trends Parasitol. 2018, 34, 456–465. [Google Scholar] [CrossRef]
  8. Liu, N. Insecticide resistance in mosquitoes: Impact, mechanisms, and research directions. Annu. Rev. Entomol. 2015, 60, 537–559. [Google Scholar] [CrossRef] [PubMed]
  9. Ranson, H.; Lissenden, N. Insecticide resistance in African Anopheles mosquitoes: A worsening situation that needs urgent action to maintain malaria control. Trends Parasitol. 2016, 32, 187–196. [Google Scholar] [CrossRef]
  10. Desneux, N.; Decourtye, A.; Delpuech, J.M. The sublethal effects of pesticides on beneficial arthropods. Annu. Rev. Entomol. 2007, 52, 81–106. [Google Scholar] [CrossRef]
  11. Enan, E.E. Molecular and pharmacological analysis of an octopamine receptor from American cockroach and fruit fly in response to plant essential oils. Arch. Insect Biochem. Physiol. 2005, 59, 161–171. [Google Scholar] [CrossRef] [PubMed]
  12. Isman, M.B. Botanical insecticides, deterrents, and repellents in modern agriculture and an increasingly regulated world. Annu. Rev. Entomol. 2006, 51, 45–66. [Google Scholar] [CrossRef] [PubMed]
  13. Isman, M.B. A renaissance for botanical insecticides? Pest. Manag. Sci. 2015, 71, 1587–1590. [Google Scholar] [CrossRef] [PubMed]
  14. Pavela, R.; Benelli, G. Essential oils as ecofriendly biopesticides? Challenges and constraints. Trends Plant. Sci. 2016, 21, 1000–1007. [Google Scholar] [CrossRef] [PubMed]
  15. Rattan, R.S. Mechanism of action of insecticidal secondary metabolites of plant origin. Crop. Prot. 2010, 29, 913–920. [Google Scholar] [CrossRef]
  16. Isman, M.B.; Grieneisen, M.L. Botanical insecticide research: Many publications, limited useful data. Trends Plant. Sci. 2014, 19, 140–145. [Google Scholar] [CrossRef]
  17. Benelli, G.; Pavela, R. Beyond mosquitoes – Essential oil toxicity and repellency against bloodsucking insects. Ind. Crops Prod. 2018, 117, 382–392. [Google Scholar] [CrossRef]
  18. Benelli, G. Plant-borne ovicides in the fight against mosquito vectors of medical and veterinary importance: A systematic review. Parasitol. Res. 2015, 114, 3201–3212. [Google Scholar] [CrossRef]
  19. Pavela, R.; Maggi, F.; Iannarelli, R.; Benelli, G. Plant extracts for developing mosquito larvicides: From laboratory to the field, with insights on the modes of action. Acta Trop. 2019, 193, 236–271. [Google Scholar] [CrossRef]
  20. Stevenson, P.C.; Isman, M.B.; Belmain, S.R. Pesticidal plants in Africa: A global vision of new biological control products from local uses. Ind. Crops Prod. 2017, 110, 2–9. [Google Scholar] [CrossRef]
  21. Tabari, M.A.; Youssefi, M.R.; Barimani, A.; Araghi, A. Carvacrol as a potent natural acaricide against Dermanyssus gallinae. Parasitol. Res. 2015, 114, 3801–3806. [Google Scholar] [CrossRef] [PubMed]
  22. Tabari, M.A.; Youssefi, M.R.; Esfandiari, A.; Benelli, G. Toxicity of β-citronellol, geraniol and linalool from Pelargonium roseum essential oil against the West Nile and filariasis vector Culex pipiens (Diptera: Culicidae). Res. Vet. Sci. 2017, 114, 36–40. [Google Scholar] [CrossRef] [PubMed]
  23. Tabari, M.A.; Youssefi, M.R.; Maggi, F.; Benelli, G. Toxic and repellent activity of selected monoterpenoids (thymol, carvacrol and linalool) against the castor bean tick, Ixodes ricinus (Acari: Ixodidae). Vet. Parasitol. 2017, 245, 86–91. [Google Scholar] [CrossRef] [PubMed]
  24. Pavela, R. Acute toxicity and synergistic and antagonistic effects of the aromatic compounds of some essential oils against Culex quinquefasciatus Say larvae. Parasitol. Res. 2015, 114, 3835–3853. [Google Scholar] [CrossRef] [PubMed]
  25. Pavela, R.; Pavoni, L.; Bonacucina, G.; Cespi, M.; Kavallieratos, N.G.; Cappellacci, L.; Petrelli, R.; Maggi, F.; Benelli, G. Rationale for developing novel mosquito larvicides based on isofuranodiene microemulsions. J. Pest. Sci. 2019, 92, 909–921. [Google Scholar] [CrossRef]
  26. Koliopoulos, G.; Pitarokili, D.; Kioulos, E.; Michaelakis, A.; Tzakou, O. Chemical composition and larvicidal evaluation of Mentha, Salvia, and Melissa essential oils against the West Nile virus mosquito Culex pipiens. Parasitol. Res. 2010, 107, 327–335. [Google Scholar] [CrossRef] [PubMed]
  27. Masoumi, F.; Youssefi, M.R.; Tabari, M.A. Combination of carvacrol and thymol against the poultry red mite (Dermanyssus gallinae). Parasitol. Res. 2016, 115, 4239–4243. [Google Scholar] [CrossRef]
  28. Dewick, P.M. Medicinal Natural Products: A Biosynthetic Approach, 2nd ed.; Chichester: John Wiley & Sons Ltd.: Chichester, UK, 2002. [Google Scholar]
  29. Burt, S. Essential oils: Their antibacterial properties and potential applications in foods—A review. Int. J. Food Microbiol. 2004, 94, 223–253. [Google Scholar] [CrossRef]
  30. Pavela, R. Acute, synergistic and antagonistic effects of some aromatic compounds on the Spodoptera littoralis Boisd. (Lep., Noctuidae) larvae. Ind. Crops Prod. 2014, 60, 247–258. [Google Scholar] [CrossRef]
  31. Benelli, G.; Pavela, R.; Canale, A.; Cianfaglione, K.; Ciaschetti, G.; Conti, F.; Nicoletti, M.; Senthil-Nathan, S.; Mehlhorn, H.; Maggi, F. Acute larvicidal toxicity of five essential oils (Pinus nigra, Hyssopus officinalis, Satureja montana, Aloysia citrodora and Pelargonium graveolens) against the filariasis vector Culex quinquefasciatus: Synergistic and antagonistic effects. Parasitol. Int. 2017, 66, 166–171. [Google Scholar] [CrossRef] [PubMed]
  32. Caprioli, G.; Lupidi, G.; Maggi, F. Comparison of chemical composition and antioxidant activities of two winter savory subspecies (Satureja montana subsp. variegata and Satureja montana subsp. montana) cultivated in Northern Italy. Nat. Prod. Res. 2018, 1–5. [Google Scholar] [CrossRef] [PubMed]
  33. Stahl-Biskup, E. The chemical composition of Thymus oils: A review of the literature 1960–1989. J. Essent. Oil Res. 1991, 3, 61–82. [Google Scholar] [CrossRef]
  34. Benelli, G.; Pavela, R.; Maggi, F.; Nkuimi Wandjou, J.G.; N’ Guessan Bra, Y.F.; Koné-Bamba, D.; Sagratini, G.; Vittori, S.; Caprioli, G. Insecticidal activity of the essential oil and polar extracts from Ocimum gratissimum grown in Ivory Coast: Efficacy on insect pests and vectors and impact on non-target species. Ind. Crops Prod. 2019, 132, 377–385. [Google Scholar] [CrossRef]
  35. Vitali, L.A.; Beghelli, D.; Nya, P.C.B.; Bistoni, O.; Cappellacci, L.; Damiano, S.; Lupidi, G.; Maggi, F.; Orsomando, G.; Papa, F.; et al. Diverse biological effects of the essential oil from Iranian Trachyspermum ammi. Arab. J. Chem. 2016, 9, 775–786. [Google Scholar] [CrossRef]
  36. Pavela, R.; Maggi, F.; Cianfaglione, K.; Bruno, M.; Benelli, G. Larvicidal activity of essential oils of five Apiaceae taxa and some of their main constituents against Culex quinquefasciatus. Chem. Biodivers. 2018, 15, e1700382. [Google Scholar] [CrossRef] [PubMed]
  37. Benelli, G.; Pavela, R.; Iannarelli, R.; Petrelli, R.; Cappellacci, L.; Cianfaglione, K.; Afshar, F.H.; Nicoletti, M.; Canale, A.; Maggi, F. Synergized mixtures of Apiaceae essential oils and related plant-borne compounds: Larvicidal effectiveness on the filariasis vector Culex quinquefasciatus Say. Ind. Crops Prod. 2017, 96, 186–195. [Google Scholar] [CrossRef]
  38. Ahn, Y.-J.; Lee, S.-B.; Lee, H.-S.; Kim, G.-H. Insecticidal and acaricidal activity of carvacrol and β-thujaplicine derived from Thujopsis dolabrata var. hondai sawdust. J. Chem. Ecol. 1998, 24, 81–90. [Google Scholar] [CrossRef]
  39. Kordali, S.; Cakir, A.; Ozer, H.; Cakmakci, R.; Kesdek, M.; Mete, E. Antifungal, phytotoxic and insecticidal properties of essential oil isolated from Turkish Origanum acutidens and its three components, carvacrol, thymol and p-cymene. Bioresour. Technol. 2008, 99, 8788–8795. [Google Scholar] [CrossRef] [PubMed]
  40. Senra, T.O.S.; Calmon, F.; Zeringóta, V.; Monteiro, C.M.O.; Maturano, R.; da Silva Matos, R.; Daemon, E. Investigation of activity of monoterpenes and phenylpropanoids against immature stages of Amblyomma cajennense and Rhipicephalus sanguineus (Acari: Ixodidae). Parasit Res. 2013, 112, 3471–3476. [Google Scholar] [CrossRef] [PubMed]
  41. Novato, T.P.L.; Araújo, L.X.; de Monteiro, C.M.O.; Maturano, R.; Senra, T.d.O.S.; da Silva Matos, R.; Gomes, G.A.; de Carvalho, M.G.; Daemon, E. Evaluation of the combined effect of thymol, carvacrol and (E)-cinnamaldehyde on Amblyomma sculptum (Acari: Ixodidae) and Dermacentor nitens (Acari: Ixodidae) larvae. Vet. Parasitol. 2015, 212, 331–335. [Google Scholar] [CrossRef] [PubMed]
  42. Traboulsi, A.F.; Taoubi, K.; El-Haj, S.; Bessiere, J.M.; Rammal, S. Insecticidal properties of essential plant oils against the mosquito Culex pipiens molestus (Diptera: Culicidae). Pest. Manag. Sci. 2002, 58, 491–495. [Google Scholar] [CrossRef] [PubMed]
  43. Pandey, S.K.; Upadhyay, S.; Tripathi, A.K. Insecticidal and repellent activities of thymol from the essential oil of Trachyspermum ammi (Linn) Sprague seeds against Anopheles stephensi. Parasitol. Res. 2009, 105, 507–512. [Google Scholar] [CrossRef] [PubMed]
  44. Govindarajan, M.; Rajeswary, M.; Hoti, S.; Benelli, G. 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). Res. Vet. Sci. 2016, 104, 77–82. [Google Scholar] [CrossRef] [PubMed]
  45. Andrade-Ochoa, S.; Sánchez-Aldana, D.; Chacón-Vargas, K.F.; Rivera-Chavira, B.E.; Sánchez-Torres, L.E.; Camacho, A.D.; Nogueda-Torres, B.; Nevárez-Moorillón, G.V. Oviposition deterrent and larvicidal and pupaecidal activity of seven essential oils and their major components against Culex quinquefasciatus Say (Diptera: Culicidae): Synergism–antagonism effects. Insects 2018, 9, 25. [Google Scholar] [CrossRef] [PubMed]
  46. Farajollahi, A.; Fonseca, D.M.; Kramer, L.D.; Kilpatrick, A.M. “Bird biting” mosquitoes and human disease: A review of the role of Culex pipiens complex mosquitoes in epidemiology. Infect. Genet. Evol. 2011, 11, 1577–1585. [Google Scholar] [CrossRef] [PubMed]
  47. Sambri, V.; Capobianchi, M.; Charrel, R.; Fyodorova, M.; Gaibani, P.; Gould, E.; Niedrig, M.; Papa, A.; Pierro, A.; Rossini, G.; et al. West Nile virus in Europe: Emergence, epidemiology, diagnosis, treatment, and prevention. Clin. Microbiol. Infect. 2013, 19, 699–704. [Google Scholar] [CrossRef]
  48. Priestley, C.M.; Williamson, E.M.; Wafford, K.A.; Sattelle, D.B. Thymol, a constituent of thyme essential oil, is a positive allosteric modulator of human GABAA receptors and a homo-oligomeric GABA receptor from Drosophila melanogaster. Br. J. Pharmacol. 2003, 140, 1363–1372. [Google Scholar] [CrossRef]
  49. Abbassy, M.A.; Abdelgaleil, S.A.; Rabie, R.Y. Insecticidal and synergistic effects of Majorana hortensis essential oil and some of its major constituents. Entomol. Exp. Appl. 2009, 131, 225–232. [Google Scholar] [CrossRef]
  50. Pavela, R. Acute and synergistic effects of some monoterpenoid essential oil compounds on the house fly (Musca domestica L.). J. Essent. Oil Bear. Plants 2008, 11, 451–459. [Google Scholar] [CrossRef]
  51. Wu, L.; Huo, X.; Zhou, X.; Zhao, D.; He, W.; Liu, S.; Feng, T.; Wang, C. Acaricidal activity and synergistic effect of thyme oil constituents against carmine spider mite (Tetranychus cinnabarinus (Boisduval)). Molecules 2017, 22, 1873. [Google Scholar] [CrossRef]
  52. Knio, K.; Usta, J.; Dagher, S.; Zournajian, H.; Kreydiyyeh, S. Larvicidal activity of essential oils extracted from commonly used herbs in Lebanon against the seaside mosquito, Ochlerotatus caspius. Bioresour. Technol. 2008, 99, 763–768. [Google Scholar] [CrossRef] [PubMed]
  53. Carvalho, A.F.U.; Melo, V.M.M.; Craveiro, A.A.; Machado, M.I.L.; Bantim, M.B.; Rabelo, E.F. Larvicidal activity of the essential oil from Lippia sidoides Cham. against Aedes aegypti Linn. Memórias do Instituto Oswaldo Cruz 2003, 98, 569–571. [Google Scholar] [CrossRef]
  54. Benelli, G.; Maggi, F.; Canale, A.; Mehlhorn, H. Lyme disease is on the rise—How about tick repellents? A global view. Entomologia Generalis 2019. [Google Scholar] [CrossRef]
  55. Shaalan, E.A.-S.; Canyon, D.V.; Younes, M.W.F.; Abdel-Wahab, H.; Mansour, A.-H. Synergistic efficacy of botanical blends with and without synthetic insecticides against Aedes aegypti and Culex annulirostris mosquitoes. J. Vector Ecol. 2005, 30, 284–288. [Google Scholar] [PubMed]
  56. Tong, F.; Bloomquist, J.R. Plant essential oils affect the toxicities of carbaryl and permethrin against Aedes aegypti (Diptera: Culicidae). J. Med. Entomol. 2013, 50, 826–832. [Google Scholar] [CrossRef] [PubMed]
  57. Pastor, J.; García, M.; Steinbauer, S.; Setzer, W.N.; Scull, R.; Gille, L.; Monzote, L. Combinations of ascaridole, carvacrol, and caryophyllene oxide against Leishmania. Acta Trop. 2015, 145, 31–38. [Google Scholar] [CrossRef] [PubMed]
  58. Hummelbrunner, L.A.; Isman, M.B. Acute, sublethal, antifeedant, and synergistic effects of monoterpenoid essential oil compounds on the tobacco cutworm, Spodoptera litura (Lep., Noctuidae). J. Agric. Food Chem. 2001, 49, 715–720. [Google Scholar] [CrossRef] [PubMed]
  59. Karpouhtsis, I.; Pardali, E.; Feggou, E.; Kokkini, S.; Scouras, Z.G.; Mavragani-Tsipidou, P. Insecticidal and genotoxic activities of oregano essential oils. J. Agric. Food Chem. 1998, 46, 1111–1115. [Google Scholar] [CrossRef]
  60. Araújo, L.X.; Novato, T.P.L.; Zeringota, V.; Maturano, R.; Melo, D.; Da Silva, B.C.; Monteiro, C.M.O. Synergism of thymol, carvacrol and eugenol in larvae of the cattle tick, Rhipicephalus microplus, and brown dog tick, Rhipicephalus sanguineus. Med. Vet. Entomol. 2016, 30, 377–382. [Google Scholar] [CrossRef] [PubMed]
  61. Tong, F.; Coats, J.R. Effects of monoterpenoid insecticides on [3H]-TBOB binding in house fly GABA receptor and 36Cl− uptake in American cockroach ventral nerve cord. Pestic. Biochem. Physiol. 2010, 98, 317–324. [Google Scholar] [CrossRef]
  62. López, V.; Cascella, M.; Benelli, G.; Maggi, F.; Gómez-Rincón, C. Green drugs in the fight against Anisakis simplex—larvicidal activity and acetylcholinesterase inhibition of Origanum compactum essential oil. Parasitol. Res. 2018, 117, 861–867. [Google Scholar] [CrossRef] [PubMed]
  63. Azeez, S.; Babu, R.O.; Aykkal, R.; Narayanan, R. Virtual screening and in vitro assay of potential drug like inhibitors from spices against glutathione-S-transferase of filarial nematodes. J. Mol. Model. 2012, 18, 151–163. [Google Scholar] [CrossRef] [PubMed]
  64. World Health Organization. Guidelines for laboratory and field testing of mosquito larvicides. 2015. Available online: http://www.who.int/iris/handle/10665/69101 (accessed on 25 March 2019).
  65. Abbott, W.S. A method of computing the effectiveness of an insecticide. J. Econ. Entomol. 1925, 18, 265–267. [Google Scholar] [CrossRef]
  66. Finney, D.J. Probit Analysis; Cambridge University: London, UK, 1971; pp. 68–78. [Google Scholar]
  67. Ohrt, C.; Willingmyre, G.D.; Lee, P.; Knirsch, C.; Milhous, W. Assessment of azithromycin in combination with other antimalarial drugs against Plasmodium falciparum in vitro. Antimicrob. Agents Chemother. 2002, 46, 2518–2524. [Google Scholar] [CrossRef] [PubMed]
Sample Availability: Samples of thymol and carvacrol are available from the authors.
Figure 1. Insecticidal activity of the selected monoterpenoids carvacrol and thymol at different concentrations against eggs (a) and 3rd instar larvae (b) of Culex pipiens mosquitoes after 24 h. T-bars indicate standard errors; above each column, different letters indicate significant differences among means (ANOVA, Tukey’s HSD test, p < 0.05).
Figure 1. Insecticidal activity of the selected monoterpenoids carvacrol and thymol at different concentrations against eggs (a) and 3rd instar larvae (b) of Culex pipiens mosquitoes after 24 h. T-bars indicate standard errors; above each column, different letters indicate significant differences among means (ANOVA, Tukey’s HSD test, p < 0.05).
Molecules 24 01867 g001
Figure 2. Isobologram of the interaction between carvacrol and thymol in binary combinations using the fixed ratio method: activity on eggs (a) and 3rd instar larvae (b) of Culex pipiens.
Figure 2. Isobologram of the interaction between carvacrol and thymol in binary combinations using the fixed ratio method: activity on eggs (a) and 3rd instar larvae (b) of Culex pipiens.
Molecules 24 01867 g002
Table 1. Probit analysis showing the toxicity of carvacrol and thymol against eggs and 3rd instar larvae of the West Nile vector Culex pipiens.
Table 1. Probit analysis showing the toxicity of carvacrol and thymol against eggs and 3rd instar larvae of the West Nile vector Culex pipiens.
Tested CompoundTargeted InstarLC50 (mg/L)95% LCL-UCLLC90 (mg/L)95% LCL-UCLχ2(df)
CarvacrolEgg76-82019-222.08 (5) n.s.
3rd instar larva1411-174438-524.23 (5) n.s.
ThymolEgg1312-142725-311.56 (5) n.s.
3rd instar larva4942-5211299-1302.98 (5) n.s.
n.s. = not significant (p > 0.05).
Table 2. Ovicidal and larvicidal results achieved on Culex pipiens testing carvacrol-thymol combinations with the fixed ratio method.
Table 2. Ovicidal and larvicidal results achieved on Culex pipiens testing carvacrol-thymol combinations with the fixed ratio method.
Thymol:Carvacrol RatioLC50 Thymol:Carvacrol in Combination (mg/L) on EggsFLC index a on EggsLC50 Thymol:Carvacrol in Combination (mg/L) on 3rd Instar LarvaeFLC Index a on 3rd Instar Larvae
4:110:61.5648:101.65
3:27.2:6.51.4143:122.10
2:36:6.21.2825:101.19
1:43.5:5.51.0012:80.79
a FLC index = LC50 carvacrol in combination/LC50 carvacrol alone + LC50 thymol in combination/LC50 thymol alone.

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Youssefi, M.R.; Tabari, M.A.; Esfandiari, A.; Kazemi, S.; Moghadamnia, A.A.; Sut, S.; Dall’Acqua, S.; Benelli, G.; Maggi, F. Efficacy of Two Monoterpenoids, Carvacrol and Thymol, and Their Combinations against Eggs and Larvae of the West Nile Vector Culex pipiens. Molecules 2019, 24, 1867. https://doi.org/10.3390/molecules24101867

AMA Style

Youssefi MR, Tabari MA, Esfandiari A, Kazemi S, Moghadamnia AA, Sut S, Dall’Acqua S, Benelli G, Maggi F. Efficacy of Two Monoterpenoids, Carvacrol and Thymol, and Their Combinations against Eggs and Larvae of the West Nile Vector Culex pipiens. Molecules. 2019; 24(10):1867. https://doi.org/10.3390/molecules24101867

Chicago/Turabian Style

Youssefi, Mohammad Reza, Mohaddeseh Abouhosseini Tabari, Aryan Esfandiari, Sohrab Kazemi, Ali Akbar Moghadamnia, Stefania Sut, Stefano Dall’Acqua, Giovanni Benelli, and Filippo Maggi. 2019. "Efficacy of Two Monoterpenoids, Carvacrol and Thymol, and Their Combinations against Eggs and Larvae of the West Nile Vector Culex pipiens" Molecules 24, no. 10: 1867. https://doi.org/10.3390/molecules24101867

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