Parasitol Res. 2014 Sep;113(9):3241-50. doi: 10.1007/s00436-014-3986-6. Epub 2014 Jun 20.
Efficacy of herbal shampoo base on native plant against head lice (Pediculus humanus capitis De Geer, Pediculidae: Phthiraptera) in vitro and in vivo in Thailand. Soonwera M1.
Head lice infestation (or pediculosis) is an important public health problem in Thailand, especially in children between the ages 5 and 11 years. Head lice resistance is increasing, chemical pediculicides have lost their efficacy, and, therefore, alternative pediculicides such as herbal shampoos have been proposed to treat head lice infestation. Thus, the present study investigated the efficacy of three herbal shampoos based on native plants in Thailand (Acorus calamus Linn., Phyllanthus emblica Linn., and Zanthoxylum limonella Alston) against head lice and compared them with carbaryl shampoo (Hafif shampoo, 0.6% w/v carbaryl), malathion shampoo (A-Lice shampoo, 1.0% w/v malathion), and commercial shampoos (Babi Mild Natural' N Mild and Johnson's baby shampoo) in order to assess their in vitro and in vivo efficacy. For in vitro study, doses of 0.12 and 0.25 ml/cm(2) of each herbal shampoo were applied to filter paper, then 10 head lice were place on the filter paper. The mortalities of head lice were recorded at 5, 15, 30, and 60 min. The results revealed that all herbal shampoo were more effective on pediculicidal activity than chemical and commercial shampoos with 100% mortality at 15 min; LT₅₀ values ranged from 0.25 to 1.90 min. Meanwhile, chemical shampoos caused 20-80% mortality, and LT₅₀ values ranged from 6.50 to 85.43 min. On the other side, commercial shampoos showed 4.0% mortality. The most effective pediculicide was Z. limonella shampoo, followed by A. calamus shampoo, P. emblica shampoo, carbaryl shampoo, malathion shampoo, and commercial shampoo, respectively. In vivo results showed that all herbal shampoos were also more effective for head lice treatment than chemical and commercial shampoos with 94.67-97.68% of cure rate after the first treatment; the second treatment, 7 days later, revealed that the cure rate was 100%. Meanwhile, chemical shampoo showed 71.67-93.0% of cure rate and, unfortunately, commercial shampoos were nontoxic to head lice and showed 0% of cure rate after the first and the second treatments. Our data showed that three herbal shampoos of native plants in Thailand in this study are suitable to be used as pediculicides for Thai children since it is safe for children and there is no side-effect after application.
J Egypt Public Health Assoc. 2004;79(5-6):383-97.
Pediculicidal activity of certain plant essential oils against head lice Pediculus humanus capitis.
Abou El Ela NE1, El-Sahn AA, Enan EE.
This paper reports the pediculicidal activity of certain monoterpenoids of plant essential oils compared to several anti-head lice formulations. It also reports the molecular features required for a chemical to kill head lice. Live adult Pediculus humanus capitus were collected from children living in the Qabary area, Alexandria, Egypt and used in in vitro bioassays. The data demonstrated that the commercial formulation, Quick (0.5% malathion) was the most potent formulation against head lice, while Para plus was the least potent. It was clear that the potency of the tested monoterpenoids was at least similar to Quick. The data also revealed that, monoterpenoid phenols and alcohols were more potent against head lice than monoterpenoid aldehydes, esters and acyclic monoterpenoids. One of the molecular features that is evidently important for monoterpenoid toxicity against head lice is the presence of electronegative group such as a hydroxyl group. In conclusion, this study reports an alternative chemical control that is safer, and more effective against head lice.
Parasitol Res. 2016 Aug;115(8):3209-18. doi: 10.1007/s00436-016-5083-5. Epub 2016 Apr 25.
Chemical composition and efficacy of some selected plant oils against Pediculus humanus capitis in vitro.
Yones DA1, Bakir HY2, Bayoumi SA3.
Natural compounds have been suggested as alternative sources for pediculosis capitis control. We aimed to investigate the chemical composition and evaluate the pediculicidal activity of spearmint, clove, cassia, thyme, eucalyptus, and anise essential oils in addition to sesame oil against human head lice in vitro. A filter paper contact bioassay method was used by applying 0.25 and 0.5 mg/cm(2) of each tested oil to filter paper in Petri dishes with 15 females head lice and another with ten nits. The lice mortalities were reported every 5 min for 180 min. The percentage of inhibition of hatch (PIH) was used to calculate ovicidal activity by daily microscopic inspections 5 days after the hatching of controls. Comparison with the widely used pediculicide (malathion) was performed. The most effective essential oil was spearmint followed by cassia and clove with KT50 values of 4.06, 7.62, and 12.12 at 0.5 mg/cm(2) and 8.84, 11.38, and 19.73 at 0.25 mg/cm(2), respectively. Thyme, eucalyptus, and anise were also effective adulticides with KT50 values of 18.61, 32.65, and 37.34 at 0.5 mg/cm(2) and 29.92, 43.16, and 45.37 at 0.25 mg/cm(2), respectively. Essential oils were also successful in inhibiting nymph emergence. Spearmint oil was the most effective, with a complete inhibition of emergence at 0.5 mg/cm(2). Sesame fixed oil did not show any adulticidal or ovicidal activity against head lice in vitro. The observed insecticidal activity was comparable to malathion. The results herein described the effectiveness of these essential oils as potential pediculicides for head lice control. Incorporation of essential oils in pediculicide formulations needs proper formulation and clinical trials.
Review PDP Plant Derived Products
Pesticidal potential
Several pesticides based on PDPs are already available, and in some cases widely utilised, in modern pest management [2, 5, 6, 7]. Numerous proof of concept studies support that additional PDPs could be of further use, including targeting numerous veterinary and medical pests. Many more have a long and continuing history of use in poorer areas of the globe where access to synthetic pesticides is often limited. However, though such use may greatly assist researchers in identifying novel PDPs for further testing [8, 9], we do not consider traditional use to necessarily confirm efficacy. Hence, examples that only report on such use without further study have not been included.
Pyrethrum
Technical grade pyrethrum is extracted from dried and ground flowers of the daisy Tanacetum cinerariaefolium and typically contains 20-25% pyrethrins (I and II) as its main pesticidal components [2]. Use of pyrethrum to treat pests of veterinary and medical significance greatly pre-dates the advent of synthetic 'second generation’ pesticides [10], to which pyrethroids (synthetic modifications of pyrethrins that remain in widespread use to the present day) belong. Pyrethrum remains in widespread use to the present day, with its current contribution to veterinary and medical pest management being primarily in the treatment of premise pests, such as cockroaches and flies, which could serve as disease vectors.
The pesticidal potential of pyrethrum was apparently recognised in the 17th Century, though verification is reported to have occurred later in 1840 [11]. Following verification, pyrethrum was rapidly adopted as a household insecticide, also being incorporated into mosquito control as the primary active component of sticks/coils. Issues regarding photostability limit the use of pyrethrum outdoors (see Potential issues) and this drove the development of synthetic pyrethroids in the mid-1900s. Though the advent of pyrethroids led to dramatic declines in pyrethrum use, the latter remains popular where product safety is paramount (e.g. organic production, residential use and use in food handling premises) [11].
It has been reported that resistance is less likely to be developed to the natural vs. synthetic product [12], with resistance to pyrethroids now widely reported in numerous pest groups [11], (it should be noted, however, that this does not mean that resistance to natural compounds cannot develop; see Emerging and future potential). In work with D. gallinae, for example, permethrin tested at 100% only led to complete in vitro mortality of mites collected from 1 in 6 farms, with mortality as low as 30% for two of the farms tested [13]. Such resistance does not appear to effect pyrethrum toxicity, however, with work in mosquitoes supporting that pyrethrum may be effectively used to target pyrethroid-resistant Anopheles gambiae[14]. This latter finding, and the range of synthetic pyrethroids that have been developed/used in the past century, raises the possibility that the lack of resistance seen to the natural product may be as much a consequence of its low level of use in comparison to pyrethroids as its natural status [12]. This limited use may be attributable to the low photostability of pyrethrum, despite the fact that knock-down with pyrethrum is generally rapid [2].
Neem
The neem tree (Azadirachta indica) has a long history of traditional use in its country of origin (India). Subsequent research has revealed a vast and diverse chemistry to this species, including within this the triterpene azadirachtin to which much of the pesticidal activity of neem is attributed [15]. Most neem-based products are formed from seed extracts, where azadirachtin naturally occurring at relatively low levels (<1%) is concentrated to 10-50% to form technical grade material [2].
Neem seed extract is known to display activity to a vast range of pest invertebrates [16], including against a multitude of pests of veterinary and medical significance [17, 18]. Consequently, it is of no surprise that many neem-based products are commercially available for use in these sectors. Tre-san®, MiteStop®, Wash Away Louse® and Picksan LouseStop®, all based on neem seed extracts, are typical examples resulting from the work of one research group alone [18]. These products have been developed for use against a range of veterinary and medical pests including dust mites, ticks, ectoparasitic mites (including D. gallinae), scabies mites (Sarcoptes scabiei) and head lice (Pediculus humanus capitis). Such products may be highly efficacious, with MiteStop® reported to be more effective against D. gallinae than the synthetic organophosphate phoxim [19]. This same group has recently shown that a similar product (Licener®) can be highly efficacious against the human head louse [20], as are comparable products based on work elsewhere [21]. NeemAzal® is another example of a commercial neem-based product available in several countries, in this case to target ticks [22].
It deserves note that the above studies were performed under laboratory conditions and the effects observed were dependant on exposure methodologies. In the laboratory, for example, a 1:40 dilution of MiteStop® killed Ixodes ticks irrespective of the mode of contact, but only direct spraying on the backs of Rhipicephalus ticks had a significant effect [18]. Though such laboratory data do not necessarily translate to field effectiveness, studies in livestock have now confirmed in vivo tick potential [22], with topical application proving successful in cattle [23, 24] and oral administration in lambs suggesting future potential for administration in feed [25]. In the studies performed in cattle, it was confirmed that the seed extract had the highest acaricidal effect, where in addition a significant reduction in egg laying potential was observed in ticks that survived treatment. In comparison to the synthetic pyrethroid, cypremethrin, neem seed extract was found to be comparable in terms of reducing oviposition, despite having a longer period to knockdown (5 days as opposed to 3) [24]. Oral administration to lambs was found not to result in lethality to Dermacentor vairiabilis ticks, though based on a significant reduction in tick weight the authors concluded that the presence of azadirachtin in the host’s blood interfered with tick feeding. The authors speculated that oral administration may have a greater effect on one-host tick species, though this has yet to be tested [25].
Bioactivity of neem-based products is not limited to seed extracts and other preparations may also be of use. In work with ixodid ticks, for example, 70% mortality was achieved following exposure to a methanolic bark extract [26]. Cold presses from neem seeds (syn: neem oils) are also reported to be effective against mites and soft-bodied insects [2], with use of cardboard traps impregnated with 20% neem oil reducing D. gallinae populations in vivo by more than 90% [27]. Various formulations based on neem, such as those in water and methyl-tert-butylether/water, may also be of use in mosquito control, particularly as larvicides or growth regulators/inhibitors [17, 28].
Neem has been reported to retain its pesticidal efficacy relatively well, even against pests renowned for development of resistance (including to other biological insecticides such as Bt and spinosad). Laboratory study has shown, for example, that even after 42 generations, diamondback moth (Plutella xylostella) larvae were still susceptible to neem oil [29]. Neem also has a history of safe use as an insecticide. Though negative impacts on mammals may result from sub-acute or chronic exposure to neem, a review of these balanced against likely ingestion of neem residues concluded that its use as a pesticide “should not be discouraged” [30].
Essential oils and other plant extracts
Essential oils are naturally produced by plants as secondary compounds, being obtained for commercial use by various forms of distillation. They are notably diverse in terms of chemistry, containing up to 60 separate components (per oil) primarily composed of terpenes, terpenoids and other aromatic compounds [31]. Plant extracts on the other hand are obtained through various forms of solvent extraction, as for many neem formulations and pyrethrum above, with or without subsequent purification and/or separation/concentration/drying as required. Distillation is based on separation via differences in volatility and requires heating the liquid to the boiling point which is specific for each substance. Distillation methods can include: water or steam distillation; rectification; cohobation; fractional distillation and percolation. Extraction methodologies, typically used for botanical material that has a low yield of essential oils, include: maceration; enfleurage; supercritical CO2; expression (cold press extraction) and solvent free microwave extraction.
Work tends to either focus on commercially available products from the flavour/perfume industry, for example against D. gallinae[32], or lab-prepared products often sourced from novel wild-growing plant material, for example against mosquitoes [8, 9, 33, 34, 35, 36] or head lice [37, 38]. Though the literature on the subject has been dominated with proof of concept 'screening’ studies, as the potential of oils of extracts has been recognised more work has been devoted to investigating product chemistries and active components (see Potential issues), as well as disentangling modes of action at both the mechanistic [39, 40] and bio-molecular (see Modes of action) level.
Due to their high chemical diversity and consequent potential for bioactivity, essential oils have received significant interest from scientists seeking novel and natural alternatives to synthetic pesticides in all sectors, including agriculture, veterinary/medical medicine and apiculture [2, 5, 7]. An extensive account of research into essential oils for pest control per se is given by Bakkali et al. [31], where the potential of these products to target viruses, fungi, bacteria and protozoa is also covered in depth. In addition to general works on essential oil pesticidal potential, authors have also presented reviews focusing on key target groups, particularly mosquitoes [28, 41, 42].
George et al.[5] reviewed the potential of both essential oils and extracts to a range of ectoparasites of veterinary significance, citing examples of their use against pests of livestock, poultry and domestic animals. Amongst the examples given, 100% mortality was achieved for Psoroptes cuniculi with a floral extract of chamomile [43], and for D. gallinae with numerous essential oils [44], as later supported in the authors’ own work [32]. In a study employing extracts from indigenous Indian plants, Zahir et al.[9] similarly showed that products could be of use in targeting multiple ectoparasites of veterinary and medical significance, in this case Rhipicephalus (Boophilus) microplus ticks and the larvae of Anopheles subpictus and Culex tritaeniorhynchus. Examples of the successful use of several commercial PDP-based products to target fleas, ticks and mange mites in cats and dogs were also cited, as were cases involving ectoparasitic mites infesting honeybees [5]. More recently, Kiss et al. [22] devoted multiple sections of their review on tick prevention to botanicals, noting research undertaken with both essential oils and extracts targeting larvae and adults alike. Importantly, the authors highlighted the potential influence of factors such as solvent selection and the life-stage of the target organism on efficacy. Younger stages were typically more susceptible than adults [22], as has also been reported for D. gallinae where higher toxicity of essential oils to juvenile (vs. adult) mites was recorded for cade, clove bud and garlic [45]. To highlight the importance of solvent selection, the authors cited work in which ethyl acetate root extracts of Senna italica were effective against Hyalomma marginatum rufipes, whilst extracts derived from numerous other solvents were not [46].
Essential oils and extracts have also been investigated to target pests of medical significance. Studies with mosquitoes and these products are particularly abundant and weighted towards development of repellents (see Repellent potential) and larvicides; potentially for combined use in an IMM (Integrated Mosquito Management) approach. Pitasawat et al. [47], for example, tested five essential oils for larvicidal activity against Anopheles dirus and Aedes aegypti. All products killed larvae in 24 hr toxicity tests, with the authors citing separate studies in which basil, cinnamon, citronella and thymus essential oils showed similar promise [47]. Ghosh et al. [42] produced a recent review of plant extracts as mosquito larvicides, presenting an extensive list of products, including octacosane, germacrene D and azadirachtin, shown to be toxic to multiple species. In all the authors tabulated 186 examples of PDP toxicity to mosquitoes (extract type x plant species x mosquito species), adding to previous reviews by Shaalan et al. [28] and Sukumar et al. [41] covering the same subject. These earlier reviews also suggest that many extracts can play a role in IMM as growth/reproduction inhibitors or oviposition deterrents [28, 41].
Various lice and scabies mites have also received interest as targets for essential oils and extracts, this being at least partially encouraged by consumer health concerns regarding topical synthetics and the resulting search for alternatives. In work by Oladimeji et al. [48], the authors tested the essential oil of Lippia multiflora against body lice, head lice and scabies mites, with knock-down and overall efficacy exceeding that of the standard synthetic treatments tested. Several products based on oils and/or extracts are already commercially available, especially for head lice. Scientific scrutiny of such products often suggests that 'field’ efficacy may be questionable [49, 50], with similar conclusions drawn for commercial repellents aimed at the same pest (see Repellent potential). Nevertheless, some products do appear effective, with Tea Tree Gel® outperforming 1% permethrin in an Australian study [50]. Commercial extracts have also found a place in poultry pest management with approval of Breck-a-Sol®, a garlic-based acaricide, for use against D. gallinae[5].
Repellent potential
Studies considering PDPs as repellents tend to focus upon essential oils and their bioactive constituents, for the probable reason that high volatility of these products lends itself well to such work. To date, research into the repellent potential of PDPs has been dominated by work targeting biting flies of medical significance, particularly mosquitoes, with the bulk of research and development in this field concentrated on topical repellents [51, 52]. The over-riding aim of this work is to generate alternatives to DEET, which though effective carries a health risk, particularly for infants [2]. In many cases PDPs have been found to compare well to synthetic repellents in terms of short-term repellence, though effects tend to be short-lived and comparable longer-term repellence is harder to achieve. 0.1 ml undiluted clove oil per 30 cm2 skin has, for example, been found to provide excellent repellence to Aedes aegypti, Culex quinquefasciatus and Anopheles dirus, being 100% effective if only for 2–4 hr [53]. Neem-based preparations have been found to offer protection from mosquito species for a similar period, but with reduced efficacy at a rate of 2 g/person [15] and variability between studies [51]. In contrast, 100% DEET may provide reliable protection for 10 hrs or more, depending upon the formulation used and environmental variables experienced post-application. DEET may not be readily accessible to inhabitants of poorer communities, however, and in these instances identifying locally available plants with repellent properties against a range of mosquito species has obvious advantages [54].
Several PDPs are already widely used as insect repellents, despite their current requirement for relatively frequent re-application. Indeed, the US Environmental Protection Agency has registered citronella, lemon and eucalyptus essential oils as insect repellent ingredients for topical use [52]. Many more examples of the use of essential oils and their chemical constituents as repellents against mosquitoes are provided in recent reviews by Maia and Moore [51] and Nerio et al. [52]. In the latter work examples are also provided for numerous other pest Orders of veterinary, medical and agricultural interest, particularly beetles.
After mosquitoes it seems that most work on PDPs as repellents for pests of veterinary and medical significance has centred on ticks, often with encouraging results [22, 55]. The livestock brown ear tick, Rhipicephalus appendiculatus, for example, was repelled just as effectively by Gynandropsis gyandra essential oil at high dose as by DEET when tested using the tick climbing assay [56]. Essential oils of citronella, clove and lily of the valley were similarly effective in comparison to DEET when tested against Ixodes ricinus[57], as was diluted rhododendron oil when tested against the same species in vitro and in vivo (via a blanket-dragging method) [58].
The repellent properties of PDPs to other pest groups have also been investigated, albeit not as extensively. George et al. [59], for example, tested the repellence of seven essential oils to D. gallinae. All showed at least short-term repellence and that of thyme lasted for the entire 13 day study duration [59]. Birkett et al. [60] tested the repellence of catmint essential oil and its main iridoid compounds to D. gallinae as well as ticks (R. appendiculatus) and multiple mosquito species. The results demonstrated general repellence to all groups, though the authors reported variable results across mosquito species and improved activity of whole essential oils over isolated or simple mixes of their compounds. Finally, work with permethrin-resistant head lice has shown certain essential oils from Argentinian plants, and their components, to be effective repellents [37, 38]. The most effective essential oils included those extracted from Myrcianthes cisplatensis and Mentha pulegium[37] and Cinnamomum porphyrium and Aloysia citriodora (Type 2) [38], with the most effective components within these oils being 1,8-cineole, anisole and benzyl alcohol. While these are encouraging and promising findings, in work that compared commercially-available PDP-based repellents to DEET for in vitro repellence to head lice, neither were found to be effective [61].
Potential issues
Development and deployment of PDPs to target medical and veterinary pests is not without issue, where variable efficacy is perhaps the most significant restraint. Variations in product chemistries, caused by any combination of a number of post- and pre-harvest biotic and abiotic factors, may result in dramatically altered bioactivity of the 'end product’ to target pests [2, 22, 28, 42]. Chemical variation has, for example, been reported between essential oils from different varieties [62, 63], parts [63, 64] and geographic locales [65, 66] of a single plant species, with seasonality [67, 68], method of oil extraction [69], year of harvest [70] and storage conditions [70] also influencing essential oil chemistry. In work with D. gallinae variable efficacy of essential oils has been reported within a single study [39], with comparison of results from this work to independent research [44], suggesting similar variability between studies concerning the toxicity of pennyroyal to this pest. However, analysis of essential oils suggests that some plants appear less likely to vary their chemical profiles in response to environmental changes than others, even within a single species, as illustrated in work carried out on Thymus pulegioides[71]. Careful strain selection may thus, at least partially, overcome this issue, even for highly chemically diverse products like essential oils.
Identification of individual bioactive PDP components for use in place of chemically less-stable 'raw’ or 'whole’ products may also be a solution to variable efficacy [72]. Neem, for example, is manufactured based on azadirachtin content providing some stability in technical grade products. Terpenes such as thymol (found in high concentrations in thyme essential oil amongst others) may offer a similar solution for essential oils. Thymol has shown significant potential against multiple ectoparasitic mites of veterinary significance (along with other terpenes); with several thymol-based commercial formulations widely used in apiculture to target bee mites [5]. Eugenol has shown similar promise against scabies mites, providing comparable toxicity to benzyl benzoate and killing mites within 1 hour under laboratory conditions [73]. Terpenes have also been considered for their repellent potential. Both terpineol and 1,8-cineole (3% in olive oil), for example, offered complete protection from Culex pipiens molestus[74]. Nevertheless, some studies report improved toxicity [1] or repellence [60] of whole essential oils vs. simple mixtures of their component chemicals, supporting use of the former for optimal efficacy. Diverse blends of individual components to effectively create artificial 'essential oils’ may offer a best-of-both-worlds solution, potentially allowing products to be tailored to pests. Whether or not such a product could still be considered 'natural’ may, however, be questionable. A recent study has also illustrated the importance of other components used in product formulation, with a simple change in the type of alcohol used (isopropanol for ethanol) having a significant effect on the repellency of geraniol based products to Amblyomma americanum in both laboratory and field-based tests [75], just as solvent selection may effect PDP toxicity (see Essential oils and other plant extracts). Stability of essential oils post-processing whilst in storage may also present an issue, though one beyond the scope of the current review and recently considered elsewhere [76].
Short residual activities are a further drawback for many PDPs. Pyrethrum and neem, for example, are both relatively highly UV-degradable [2]. The high volatility of essential oils has a similar effect on their residual activity as both pesticides and repellents. George et al. [77], for example, demonstrated mortality in D. gallinae of up to 90% after exposure to arenas treated with lavender essential oil minutes before adding mites. Where mites were not added to arenas for 24 hrs post-treatment, however, mortality fell to nearer 10%. The residual activity of terpenes is often similarly limited. In the aforementioned work by Traboulsi et al. [74], for example, terpenes only offered protection from mosquito bites for a maximum of 2 hrs, comparing poorly with synthetics as a result (see Repellent potential). Nevertheless, slow-release technologies are being increasingly developed to prolong the bioactivity of PDPs, suggesting that limited residual efficacy should pose an ever-decreasing problem in the future. In their recent review of PDPs as mosquito repellents, Maia and Moore [51] cite examples of both encapsulation and microencapsulation as a means to prolong essential oil repellence, with the latter being used to increase efficacy of citronella-treated fabric for up to 30 days [78]. Saha et al. [79] have similarly reported on the potential benefits of microencapsulation, inclusion complexes, microemulsions and granular formulations to enhance efficacy and shelf life of neem-based products.
Where pesticides are concerned, in some instances short persistence times may even be considered advantageous [22]. As long as rapid knock-down can be achieved, which seems the case for at least some PDPs such as pyrethrum [2], essential oils [80] and terpenes [73], low residual activity should infer minimal impact on non-target organisms and the environment, also supporting optimally short product withdrawal periods where relevant. Rapid knock-down cannot be assumed universal for PDPs, however, with extracts (including neem) noted as being comparatively slow in exerting their full effect [22]. Prolonging the persistence times of PDPs may raise new issues regarding their environmental toxicity. Half-lives of most essential oil based products, for example, are currently <24 hrs on treated surfaces and in soil/water [81], allowing rapid breakdown of active ingredients and consequent minimal effects on non-target organisms, at least in comparison to longer lasting synthetics. PDPs may exert broad spectrum effects on groups such as insects, however, and prolonged persistence times may lead to increased exposure to non-target species, including beneficials (e.g. pollinators and pest natural enemies). Ensuring that developments in extending PDP persistence progress without compromising their generally favourable environmental profile is an important challenge for future work in this field.
Though generally considered safe for mammals, some PDPs have been shown to exert negative health and welfare effects in humans and other animals. As noted in Background, for example, the PDP rotenone is no-longer widely available as a pesticide, having been withdrawn from markets due to health and environmental concerns associated with its use. Multiple studies have, for example, linked rotenone to Parkinson’s Disease [82, 83]. Even seemingly innocuous products, such as essential oils, may invoke negative responses at sufficient concentrations or in certain vertebrates. In work with laying hens, for example, birds were found to tolerate high exposure to thyme essential oil without incident, but became lethargic, depressed and unproductive when exposed to pennyroyal [84]. Indeed, certain botanicals that exert their effect on insect nervous systems (see Modes of action), may be relatively toxic to birds, fish, reptiles and amphibians [28]. It is also reported that commercial flea products containing essential oils may have negative effects on companion animals, with cats in particular being unable to metabolise these products due to an inability to glucoronidate [85]. In extreme cases death of companion animals has been recorded following exposure, though responses are typically less severe (e.g. agitation, tremors, lethargy) [85]. Further examples of deleterious effects of various PDPs in domestic animals are given by Russo et al. [3], where increased emphasis is given to orally administered products. Evidence such as this dispels the common misconception that all PDPs can be considered “safe” to vertebrates, though this may hold true in many cases [7], albeit with some 'purified’ products such as terpenes being more generally toxic than their parent material [86].
Despite their general non-toxicity to vertebrates, PDPs may exert broad-spectrum effects on invertebrates, including some non-target beneficial species. Reduced pupal emergence has been reported in predatory lacewings fed upon prey that had consumed neem oil [87], for example, with direct toxicity to Macrolophus caliginosus (a predatory mirid bug) also reported for neem formulations at lower than field rates [88]. Invertebrate selectivity is perhaps of greater concern when deploying PDPs over vast open areas in an agricultural setting, though should still be considered important in deployment against veterinary and medical pests, especially where release into the wider environment (e.g. mosquito repellents) or co-deployment with invertebrate-based biological control (e.g. for D. gallinae control) are factors. Fortuitously, research supports that specificity may be dependent upon the type of PDP and target pest under consideration, suggesting that some PDPs can display (at least relative) pest selectivity. Neem seed extract, for example, has been reported as generally safe for pollinators [89] and many pest natural enemies [90], despite being effective against 413 insect species per se[16]. Essential oils may also exert a stronger effect on some invertebrate groups than others [45], or on different members of the same pest group [42, 91], suggesting similar potential for selectivity.
Other potential drawbacks of PDPs include sustainability of the botanical resource, regulatory approval and industry confidence in the product [2]. However, we consider these to be of secondary importance to reliability, residuality and non-target toxicity, where resolving these 'primary concerns’ must necessarily take priority to support regulatory approvals and end-user confidence in commercial products. This must additionally be achieved in a cost-effective manner if PDP-based products are to be more widely adopted commercially.
Modes of action
For those PDPs with a long history of use, modes of action are relatively well established. Pyrethrum, for example, is known to act in much the same way as DDT; attacking sodium channels and serving as a neurotoxin. Knock-down is subsequently relatively fast for pyrethrum, particularly so in flying insects [2, 10]. The effects exerted by neem are also well known and primarily attributed to feeding deterrence and disruption to growth, though oviposition deterrence, repellence, reduced fitness and sterility may also result where neem is used [4, 79, 92]. In terms of its mode of action, neem has been shown to target the cholinergic system in insects through inhibition of acetylcholinestrase (AChE), and is also reported to disrupt hormonal balance [93]. Work with insect cell lines has further shown that azadirachtin (the main chemical component of neem) may exert an anti-mitotic effect by disrupting tubulin polymerisation [94]. More recent work in mammalian cell lines has revealed that azadirachtin may also cause cell-cycle arrest via down-regulation of cyclin B and cyclin D1, but also an induction of pro-apoptotic signals; a mode of action that relates to its insecticidal properties [95].
In contrast, relatively less has been done to establish modes of action in more novel PDPs with pesticidal potential, despite the wealth of research on the potential of essential oils and extracts in pest control [85]. The modes of action for many of these PDPs have been described in a general manner with toxic, antifeedant, antioviposition and developmental effects recorded per se[86]. This may, at least in part, result from many PDPs being classed as 'minimum risk pesticides’ according to the United States EPA. Products meeting the criteria of 'minimum risk’ (i.e. being 'demonstrably safe’) do not require EPA registration, negating the need for extensive data on modes of action to be collated prior to their commercialisation, at least in the US marketplace (though stricter legislation regarding the use of the same PDPs exists elsewhere where such 'exemption lists’ are not implemented). Nevertheless, those studies that have been conducted on the mode of action of essential oils suggest that these products can attack pests in a variety of ways [93]. Not all essential oils and/or terpenes are effective, however, and subtle structural differences in products may have large effects on their toxicity. In work with eugenol and iosoeugenol, for example, toxicity to the aphid Aphis craccavora varied according to product [96], despite the only difference being an alteration to the position of the double bond in the C6–C3 system. The authors speculated that the position of the double bond could be important in tempering mitochondrial respiration (or some other target) efficiently [96].
For those products that are effective, recent reviews covering various veterinary, medical and agricultural pests report essential oils and their constituents to primarily act upon on GABA, tyramine and octopamine receptors/synapses, and the inhibition of AChE [7, 93, 97]. In work with mosquitoes, the essential oil of Psoralea corylifolia has been reported to display genotoxic effects, through either direct interaction with DNA or by generation of DNA-damaging reactive oxygen species [98]. Disruption to transient receptor potential channels may be a further mode of action for numerous terpenoids, where, depending upon the product, exposure may result in activation or inhibition [97]. Whereas some terpenes may have opposing effects on a single system, others may act on several systems. Thymol, for example, has been reported to both block octopamine receptors and act upon the GABA-gated chloride channel [93]. Whatever the specific mode of action, lipophilicity of essential oils and their constituents may play an important role in efficacy, optimising penetration of products into the arthropod body [99]. The volatile nature of essential oils and their constituents may also optimise pest exposure to product. In independent studies with D. gallinae, for example, numerous essential oils including thyme, coriander and clove bud have been shown to exert fumigant toxicity [39, 44]. For a reclusive pest like D. gallinae the ability of a product to penetrate refugia in which mites spend the majority of their time could be highly advantageous [100]. It can be surmised that other pests with comparable life-history traits (e.g. bedbugs) may be similarly suited to treatment with highly fumigant PDPs. When considering modes of action it is pertinent to also consider potential detoxification pathways as it may not be the parent compound but a metabolite that is elucidating the toxicity.
Emerging and future potential
A long list of potentially pesticidal PDPs exists and this list will continue to grow in the future. However, in order to harness these products to their full potential there are several avenues that have to be explored further, primarily concerning the modes of action of these products (or the active components they contain) and their metabolic pathways. These are important research questions as it must be remembered that while of natural origin, PDPs are still viewed by arthropods as xenobiotics, thus having similar targets and metabolic pathways to synthetics. They are consequently not immune from the development of resistance given enough time and over use.
Deciphering the modes of action of PDPs allows the grouping of these products based on their metabolic targets in a similar manner to synthetic compounds, facilitating educated decisions regarding which will be most effective based on knowledge of the resistance/susceptibility status of the target pest. McAllister and Adams carried out a study to this effect testing the efficacy of thymoquinone, nootkatone, and carvacrol on colony strains of Anopheles gambiae harbouring known mutations at three different target sites: the sodium channel para-locus mutation (L1014F KDR), the acetylcholinesterase (AChE-1) gene and a γ-aminobutyric acid receptor mutation of the Rdl locus, that confer pyrethrin, organophosphate/carbamate and dieldrin resistance, respectively [101]. A significant difference in the lethal doses between strains was not observed indicating their target sites to be different to those assessed and thus supporting that these products could be effectively employed as control measures to strains harbouring these resistance associated mutations. The inability of nootkatone and carvacrol to cause significant inhibition of acetylcholinesterase has also been confirmed by the work of Anderson and Coates in several important arthropod pests [102]. The same laboratory has provided evidence to suggest that the mode of action of carvacrol may, however, be via the non-competitive inhibition of agonist binding to the nicotine-acetylcholine receptor [103]. In contrast, several components of cashew nut shell liquid, namely anacardic acid, cardol and cardinal, have been shown to possess larvicidal activity against the yellow fever mosquito Aedes aegypti with a mode of action involving inhibition of acetylcholinesterase [104]. Inhibition of acetylcholinesterease has also been suggested as a possible mode of action for the anti-feeding effect of ethanolic senescent leaf extracts of Jatropha gossypifolia and Melia azedarach in larvae of Spodoptera frugiperda[105].
The studies described above illustrate the importance of identifying the target site proteins of PDPs in ascertaining their effectiveness, but a clear understanding of PDP detoxification pathways is also important. In this regard synergistic studies with compounds such as piperonyl butoxide, triphenyl phosphate and diethylmaleate, which are known to inhibit the activities cytochrome P450s, carboxylesterases, and glutathione S-transferases, respectively, can provide clues to the detoxification mechanism of PDPs. Several studies have shown that co-administration of piperonyl butoxide with various PDPs, including thymol, eugenol and pyrethum increases the toxicity of these compounds to a range of arthropods [106, 107, 108, 109]. In a study by Yadav and colleagues, co-administration with pacholli essential oil decreased the LD50 from >250 ppm to 50 ppm, making it almost as effective as basil oil (the most toxic oil tested) without the presence of a synergist [106]. These studies provide evidence that cytochrome P450s can play an active role in the detoxification of PDPs, also demonstrating the potential of previously labelled “non-effective” PDPs if co-administered with a synergist. As changes in the activity of cytochrome P450s, and indeed Glutathione S-transferases, have been identified as a mechanism underlying pesticide resistance, PDPs detoxified by this route may be relatively ineffective in targeting pests that have already developed resistance to synthetics through changes in these enzymes [110, 111].
A greater understanding of detoxification pathways and the enzymes involved will allow a more targeted approach to be adopted for the use of PDPs, also providing further avenues to be exploited. In a recent study investigating the effect of Mintostachy verticillate essential oil on the house fly Musca domestica, researchers discovered that co-administration with piperonyl butoxide resulted in decreased toxicity, indicating that metabolism by a cytochrome P450 was essential for the effectiveness of this essential oil [112]. It was found that menthofuran, a metabolite of the parental compounds (4R)(+)-pulegone and menthone was the active, toxic agent. Thus it may be possible to use detoxification pathways in an advantageous way to identify a range of PDPs that can be used on pesticide resistant arthropod strains, similar to the strategy used in chemotherapy where pro-drugs are used to target specific cancers that overexpress drug metabolising enzymes. Additionally, it may be possible to increase the toxicity of essential oils, such as that of Mintostachy verticillate, further by inducing the expression of detoxification enzymes. The ability of compounds to induce the expression of Phase I and II detoxification enzymes in mammals is well understood, but unfortunately this is not the case for arthropods. There is evidence that PDPs may modulate the expression levels of these enzymes as revealed by studies investigating the chemo-preventive effects of neem leaves/flowers and other PDPs in various animal models [113, 114]. In these studies neem extracts were found to decrease cytochrome P450 expression, but increase glutathione S-transferases and other Phase II detoxification enzymes, whereas feeding rats sweet basil induced both Phase I and II enzymes.
A final future potential for PDPs lies not in their potential as toxic compounds directly, but in their possible use as synergists or co-administered compounds. In this situation the activity of most interest is their inhibition of detoxification enzymes. In a study by Joffe and colleagues, parsley seed oil and dillapiole oil where found to inhibit cytochrome P450 activity, but not esterase activity, providing a synergistic effect for pyrethrum on Musca domestica[108]. In mosquitos, several groups have reported on PDPs and inhibition: plant flavanoids are potent inhibitors of CYP6Z2; thymol and eugenol appear to inhibit both cytochrome P450 and Glutatione S-transferase activities; and essential oils of several native Columbian plants that possess repellent activity are inhibitors of cytochrome P450 activity [115, 116, 117].
Conclusions
The potential of PDPs to target pests of veterinary and medical significance appears strong. Several PDPs are already widely used to this end, with the effectiveness of products such as pyrethrum and neem particularly well supported through a history of successful use against a range of pests in all sectors. Supported by this, the market for PDPs appears to be expanding, particularly for established products. The market for neem-based pesticides, for example, is reportedly growing by nearly 10% per year, with supply able to comfortably meet demand for the foreseeable future [118]. Even for established PDPs, however, the current share of the market occupied in comparison to synthetics remains relatively small [81].
In the on-going search for alternatives to synthetic active ingredients, more 'novel’ PDPs, such as essential oils and their varied chemical components, may hold similar promise to more established products and have been shown to target pests in a number of ways. For many of these products more work is still needed to confirm efficacy, safety and modes of action, addressing limitations such as minimal residual activity with advances in fields such as slow-release technology. A selection of these 'novel’ PDPs has already advanced to commercialisation, perhaps prematurely in some cases as supported by their evidenced risk as veterinary products. Molecular based research, centred around the identification of targets and detoxification pathways/enzymes, could help greatly in ensuring product safety and efficacy, allowing those PDPs with novel arthropod-specific modes of action to be promoted over those with more general activity that target similar pathways to existing synthetics. Such research could also greatly advance combined use of PDPs, with either each other or synthetic compounds.
References
Miresmailli S, Bradbury R, Isman MB: Comparative toxicity of Rosmarinus officinalis L. essential oil and blends of its major constituents against Tetranychus urticae Koch (Acari: Tetranychidae) on two different host plants. Pest Manag Sci. 2006, 62: 366-371. 10.1002/ps.1157.PubMedView ArticleGoogle Scholar
Isman MB: Botanical insecticides, deterrents, and repellents in modern agriculture and an increasingly regulated world. Annu Rev Entomol. 2006, 51: 45-66. 10.1146/annurev.ento.51.110104.151146.PubMedView ArticleGoogle Scholar
Russo R, Autore G, Severino L: Pharmaco-toxicological aspects of herbal drugs used in domestic animals. Nat Prod Commun. 2009, 4: 1777-1784.PubMedGoogle Scholar
Ogbuewu IP, Odoemenam VU, Obikaonu HO, Opara MN, Emenalom OO, Uchegbu MC, Okoli IC, Esonu BO, Iloeje MU: The growing importance of neem (Azadirachta indica A. Juss) in agriculture, industry, medicine and environment: a review. Res J Med Plants. 2011, 5: 230-245.View ArticleGoogle Scholar
George DR, Guy JH, Arkle S, Harrington D, De Luna C, Okello EJ, Shiel RS, Port G, Sparagano OAE: Use of plant-derived products to control arthropods of veterinary importance: a review. Ann NY Acad Sci. 2008, 1149: 23-26. 10.1196/annals.1428.021.PubMedView ArticleGoogle Scholar
Isman MB: Plant essential oils for pest and disease management. Crop Prot. 2000, 19: 603-608. 10.1016/S0261-2194(00)00079-X.View ArticleGoogle Scholar
Regnault-Roger C, Vincent C, Arnason JT: Essential oils in insect control: low-risk products in a high-stakes world. Annu Rev Entomol. 2012, 57: 405-424. 10.1146/annurev-ento-120710-100554.PubMedView ArticleGoogle Scholar
Moore SJ, Hill N, Ruiz C, Cameron MM: Field evaluation of traditionally used plant-based insect repellents and fumigants against the malaria vector Anopheles darlingi in Riberalta, Bolivian Amazon. J Med Entomol. 2007, 44: 624-630. 10.1603/0022-2585(2007)44[624:FEOTUP]2.0.CO;2.PubMedView ArticleGoogle Scholar
Zahir AA, Rahuman AA, Kamaraj C, Bagavan A, Elango G, Sangaran A, Kumar BS: Laboratory determination of efficacy of indigenous plant extracts for parasites control. Parasitol Res. 2009, 105: 453-461. 10.1007/s00436-009-1405-1.PubMedView ArticleGoogle Scholar
Casida JE: Pyrethrum flowers and pyrethroid insecticides. Environ Health Persp. 1980, 34: 189-202.View ArticleGoogle Scholar
Katsuda Y: Progress and future of pyrethroids. Topic Curr Chem. 2012, 314: 1-30.View ArticleGoogle Scholar
Katsuda Y: Development of and future prospects for pyrethroid chemistry. Pestic Sci. 1999, 55: 775-782. 10.1002/(SICI)1096-9063(199908)55:8<775::AID-PS27>3.0.CO;2-N.View ArticleGoogle Scholar
Marangi M, Cafiero MA, Capelli G, Camarda A, Sparagano OAE, Giangaspero A: Evaluation of the poultry red mite,Dermanyssus gallinae (Acari: Dermanyssidae) susceptability to some acaricides in field populations from Italy. Exp Appl Acarol. 2009, 48: 11-18. 10.1007/s10493-008-9224-0.PubMedView ArticleGoogle Scholar
Duchon S, Bonnet J, Marcombe S, Zaim M, Corbel V: Pyrethrum: a mixture of natural pyrethrins has potential for malaria vector control. J Med Entomol. 2009, 46: 516-522. 10.1603/033.046.0316.PubMedView ArticleGoogle Scholar
Bracmachari G: Neem - an omnipotent plant: a retrospection. Chem Bio Chem. 2004, 5: 408-421. 10.1002/cbic.200300749.View ArticleGoogle Scholar
Singh RP, Saxena RC: Azadirachta indica A. Juss. 1999, Oxford: IBH Publishing Co. Pvt. LtdGoogle Scholar
Mulla MS, Su T: Activity and biological effects of neem products against arthropods of medical and veterinary importance. J Am Mosquito Contr. 1999, 15: 133-152.Google Scholar
Schmahl G, Al-Rasheid KAS, Abdel-Ghaffar F, Klimpel S, Mehlhorn H: The efficacy of neem seed extracts (Tre-san®, MiteStop®) on a broad spectrum of pests and parasites. Parasitol Res. 2010, 107: 261-269. 10.1007/s00436-010-1915-x.PubMedView ArticleGoogle Scholar
Abdel-Ghaffar F, Semmler M, Al-Rasheid K, Mehlhorn H: In vitro efficacy of ByeMite and Mite-Stop on developmental stages of the red chicken mite Dermanyssus gallinae. Parasitol Res. 2009, 105: 1469-1471. 10.1007/s00436-009-1590-y.PubMedView ArticleGoogle Scholar
Abdel-Ghaffar F, Al-Quraishy S, Al-Rasheid KA, Mehlhorn H: Efficacy of a single treatment of head lice with a neem seed extract: an in vivo and in vitro study on nits and motile stages. Parasitol Res. 2012, 110: 277-280. 10.1007/s00436-011-2484-3.PubMedView ArticleGoogle Scholar
Heukelbach J, Oliveira FAS, Speare R: A new shampoo based on neem (Azadirachta indica) is highly effective against head lice in vitro. Parasitol Res. 2006, 99: 353-356. 10.1007/s00436-006-0146-7.PubMedView ArticleGoogle Scholar
Kiss T, Cadar D, Spinu M: Tick prevention at a crossroad: new and renewed solutions. Vet Parasitol. 2012, 187: 357-366. 10.1016/j.vetpar.2012.02.010.PubMedView ArticleGoogle Scholar
Benavides OE, Hernandez MG, Romero NA, Castro AH, Rodriguez BJL: Preliminary evaluation of neem (Azadirachta indica) extracts as alternative for cattle ticks Boophilus microplus. Rev Columb Entomol Rivista. 2001, 27: 1-8.Google Scholar
Srivastava R, Ghosh S, Mandal DB, Azhahianambi P, Singhal PS, Pandey NN, Swarup D: Efficacy of Azadirachta indicaextracts against Boophilus microplus. Parasitol Res. 2008, 104: 149-153. 10.1007/s00436-008-1173-3.PubMedView ArticleGoogle Scholar
Landau SY, Provenza FD, Gardner DR, Pfister JA, Knoppel EL, Peterson C, Kababya D, Needham GR, Villalba JJ: Neem-tree (Azadirachta indica Juss.) extract as a feed additive against the American dog tick (Dermacentor variabilis) in sheep (Ovis aries). Vet Parasitol. 2009, 165: 311-317. 10.1016/j.vetpar.2009.07.047.PubMedView ArticleGoogle Scholar
Pathak D, Mathur VC, Latha BR, John L: In vitro effect of indigenous plant extracts on ixodid ticks of small ruminants. Indian J Anim Sci. 2004, 74: 616-617.Google Scholar
Lundh J, Wiktelius D, Chirico J: Azadirachtin-impregnated traps for the control of Dermanyssus gallinae. Vet Parasitol. 2005, 130: 337-342. 10.1016/j.vetpar.2005.02.012.PubMedView ArticleGoogle Scholar
Shaalan EA, Canyon D, Younes MW, Abdel-Wahab H, Mansour AH: A review of botanical phytochemicals with mosquitocidal potential. Environ Int. 2005, 31: 1149-1166. 10.1016/j.envint.2005.03.003.PubMedView ArticleGoogle Scholar
Völlinger M: The possible development of resistance against neem seed kernel extract and deltamethrin in Plutella xylostella. Natural Pesticides from the Neem Tree (Azadirachta indica A. Juss) and Other Tropical Plants, Proceedings of the Third International Neem Conference: 10-15 July 1986; Nairobi. Edited by: Schmutterer H, S KR. 1987, Ascher: GTZ, 543-554.Google Scholar
Boeke SJ, Boersma MG, Alink GM, van Loon JJ, van Huis A, Dicke M, Rietjens IM: Safety evaluation of neem (Azadirachta indica) derived pesticides. J Ethnopharmacol. 2004, 94: 25-41. 10.1016/j.jep.2004.05.011.PubMedView ArticleGoogle Scholar
Bakkali F, Averbeck S, Averbeck D, Idaomar M: Biological effects of essential oils - a review. Food Chemical Toxicol. 2008, 46: 446-475. 10.1016/j.fct.2007.09.106.View ArticleGoogle Scholar
George DR, Sparagano OA, Port G, Okello E, Shiel RS, Guy JH: Environmental interactions with the toxicity of plant essential oils to the poultry red mite Dermanyssus gallinae. Med Vet Entomol. 2010, 24: 1-8. 10.1111/j.1365-2915.2009.00855.x.PubMedView ArticleGoogle Scholar
Kweka EJ, Senthilkumar A, Venkatesalu V: Toxicity of essential oil from Indian borage on the larvae of the African malaria vector mosquito, Anopheles gambiae. Parasit Vectors. 2012, 5: 277-10.1186/1756-3305-5-277.PubMed CentralPubMedView ArticleGoogle Scholar
Kweka EJ, Nyindo M, Mosha F, Silva AG: Insecticidal activity of the essential oil from fruits and seeds of Schinus terebinthifolia Raddi against African malaria vectors. Parasit Vectors. 2011, 4: 129-10.1186/1756-3305-4-129.PubMed CentralPubMedView ArticleGoogle Scholar
Silva AG, Almeida DL, Ronchi SN, Bento AC, Scherer R, Ramos AC, Cruz ZM: The essential oil of Brazilian pepper, Schinus terebinthifolia Raddi in larval control of Stegomyia aegypti (Linnaeus, 1762). Parasit Vectors. 2010, 3: 79-10.1186/1756-3305-3-79.PubMed CentralPubMedView ArticleGoogle Scholar
Bossou AD, Mangelinckx S, Yedomonhan H, Boko PM, Akogbeto MC, De Kimpe N, Avlessi F, Sohounhloue DC: Chemical composition and insecticidal activity of plant essential oils from Benin against Anopheles gambiae (Giles). Parasit Vectors. 2013, 6: 337-10.1186/1756-3305-6-337.PubMed CentralPubMedView ArticleGoogle Scholar
Toloza AC, Zygadlo J, Cueto GM, Biurrun F, Zerba E, Picollo MI: Fumigant and repellent properties of essential oils and component compounds against permethrin-resistant Pediculus humanus capitis (Anoplura: Pediculidae) from Argentina. J Med Entomol. 2006, 43: 889-895. 10.1603/0022-2585(2006)43[889:FARPOE]2.0.CO;2.PubMedView ArticleGoogle Scholar
Toloza AC, Zygadlo J, Biurrun F, Rotman A, Picollo MI: Bioactivity of Argentinean essential oils against permethrin-resistant head lice, Pediculus humanus capitis. J Insect Sci. 2010, 10: 185-PubMed CentralPubMedView ArticleGoogle Scholar
George DR, Smith TJ, Shiel RS, Sparagano OA, Guy JH: Mode of action and variability in efficacy of plant essential oils showing toxicity against the poultry red mite, Dermanyssus gallinae. Vet Parasitol. 2009, 161: 276-282. 10.1016/j.vetpar.2009.01.010.PubMedView ArticleGoogle Scholar
Kim SI, Na YE, Yi JH, Kim BS, Ahn YJ: Contact and fumigant toxicity of oriental medicinal plant extracts againstDermanyssus gallinae (Acari: Dermanyssidae). Vet Parasitol. 2007, 145: 377-382. 10.1016/j.vetpar.2006.12.021.PubMedView ArticleGoogle Scholar
Sukumar K, Perich MJ, Boobar LR: Botanical derivatives in mosquito control: a review. J Am Mosquito Contr. 1991, 7: 210-237.Google Scholar
Ghosh A, Chowdhury N, Chandra G: Plant extracts as potential mosquito larvicides. Indian J Med Res. 2012, 135: 581-598.PubMed CentralPubMedGoogle Scholar
Macchioni F, Perrucci S, Cecchi F, Cioni PL, Morelli I, Pampiglione S: Acaricidal activity of aqueous extracts of camomile flowers, Matricaria chamomilla, against the mite Psoroptes cuniculi. Med Vet Entomol. 2004, 18: 205-207. 10.1111/j.0269-283X.2004.00488.x.PubMedView ArticleGoogle Scholar
Kim SI, Yi JH, Tak JH, Ahn YJ: Acaricidal activity of plant essential oils against Dermanyssus gallinae (Acari: Dermanyssidae). Vet Parasitol. 2004, 120: 297-304. 10.1016/j.vetpar.2003.12.016.PubMedView ArticleGoogle Scholar
George DR, Sparagano OA, Port G, Okello E, Shiel RS, Guy JH: Toxicity of plant essential oils to different life stages of the poultry red mite, Dermanyssus gallinae, and non-target invertebrates. Med Vet Entomol. 2010, 24: 9-15. 10.1111/j.1365-2915.2009.00856.x.PubMedView ArticleGoogle Scholar
Magano SR, Thembo KM, Ndlovu SM, Makhubela NFH: The anti-tick properties of the root extracts of Senna italicasubsp arachoides. Afr J Biotechnol. 2008, 7: 476-481.Google Scholar
Pitasawat B, Champakaew D, Choochote W, Jitpakdi A, Chaithong U, Kanjanapothi D, Rattanachanpichai E, Tippawangkosol P, Riyong D, Tuetun B, Chaiyasit D: Aromatic plant-derived essential oil: an alternative larvicide for mosquito control. Fitoterapia. 2007, 78: 205-210. 10.1016/j.fitote.2007.01.003.PubMedView ArticleGoogle Scholar
Oladimeji FA, Orafidiya OO, Ogunniyi TA, Adewunmi TA: Pediculocidal and scabicidal properties of Lippia multifloraessential oil. J Ethnopharmacol. 2000, 72: 305-311. 10.1016/S0378-8741(00)00229-4.PubMedView ArticleGoogle Scholar
Asenov A, Oliveira FA, Speare R, Liesenfeld O, Hengge UR, Heukelbach J: Efficacy of chemical and botanical over-the-counter pediculicides available in Brazil, and off-label treatments, against head lice ex vivo. Int J Dermatol. 2010, 49: 324-330. 10.1111/j.1365-4632.2009.04335.x.PubMedView ArticleGoogle Scholar
Heukelbach J, Canyon DV, Oliveira FA, Muller R, Speare R: In vitro efficacy of over-the-counter botanical pediculicides against the head louse Pediculus humanus var capitis based on a stringent standard for mortality assessment. Med Vet Entomol. 2008, 22: 264-272. 10.1111/j.1365-2915.2008.00738.x.PubMedView ArticleGoogle Scholar
Maia MF, Moore SJ: Plant-based insect repellents: a review of their efficacy, development and testing. Malaria J. 2011, 10 (Suppl 1): S11-10.1186/1475-2875-10-S1-S11.View ArticleGoogle Scholar
Nerio LS, Olivero-Verbel J, Stashenko E: Repellent activity of essential oils: a review. Bioresource Technol. 2010, 101: 372-378. 10.1016/j.biortech.2009.07.048.View ArticleGoogle Scholar
Trongtokit Y, Rongsriyam Y, Komalamisra N, Apiwathnasorn C: Comparative repellency of 38 essential oils against mosquito bites. Phytotherapy Res: PTR. 2005, 19: 303-309. 10.1002/ptr.1637.PubMedView ArticleGoogle Scholar
Dekker T, Ignell R, Ghebru M, Glinwood R, Hopkins R: Identification of mosquito repellent odours from Ocimum forskolei. Parasit Vectors. 2011, 4: 183-10.1186/1756-3305-4-183.PubMed CentralPubMedView ArticleGoogle Scholar
Bissinger BW, Roe RM: Tick repellents: past, present, and future. Pestic Biochem Phys. 2010, 96: 63-79. 10.1016/j.pestbp.2009.09.010.View ArticleGoogle Scholar
Lwande W, Ndakala AJ, Hassanali A, Moreka L, Nyandat E, Ndungu M, Amiani H, Gitu PM, Malonza MM, Punyua DK:Gynandropsis gynandra essential oil and its constituents as tick (Rhipicephalus appendiculatus) repellents. Phytochemistry. 1999, 50: 401-405. 10.1016/S0031-9422(98)00507-X.View ArticleGoogle Scholar
Thorsell W, Mikiver A, Tunon H: Repelling properties of some plant materials on the tick Ixodes ricinus L. Phytomedicine. 2006, 13: 132-134. 10.1016/j.phymed.2004.04.008.PubMedView ArticleGoogle Scholar
Jaenson TG, Garboui S, Palsson K: Repellency of oils of lemon eucalyptus, geranium, and lavender and the mosquito repellent MyggA natural to Ixodes ricinus (Acari: Ixodidae) in the laboratory and field. J Med Entomol. 2006, 43: 731-736. 10.1603/0022-2585(2006)43[731:ROOOLE]2.0.CO;2.PubMedView ArticleGoogle Scholar
George DR, Sparagano OA, Port G, Okello E, Shiel RS, Guy JH: Repellence of plant essential oils to Dermanyssus gallinaeand toxicity to the non-target invertebrate Tenebrio molitor. Vet Parasitol. 2009, 162: 129-134. 10.1016/j.vetpar.2009.02.009.PubMedView ArticleGoogle Scholar
Birkett MA, Hassanali A, Hoglund S, Pettersson J, Pickett JA: Repellent activity of catmint, Nepeta cataria, and iridoid nepetalactone isomers against Afro-tropical mosquitoes, ixodid ticks and red poultry mites. Phytochemistry. 2011, 72: 109-114. 10.1016/j.phytochem.2010.09.016.PubMedView ArticleGoogle Scholar
Canyon DV, Speare R: A comparison of botanical and synthetic substances commonly used to prevent head lice (Pediculus humanus var. capitis) infestation. Int J Dermatol. 2007, 46: 422-426. 10.1111/j.1365-4632.2007.03132.x.PubMedView ArticleGoogle Scholar
Eyres GT, Marriott PJ, Dufour JP: Comparison of odor-active compounds in the spicy fraction of hop (Humulus lupulus L.) essential oil from four different varieties. J Agric Food Chem. 2007, 55: 6252-6261. 10.1021/jf070739t.PubMedView ArticleGoogle Scholar
Moreno PRH, Lima MEL, Sobral M, Young MCM, Cordeiro I, Apel MA, Limberger RP, Henriques AT: Essential oil composition of fruit colour varieties of Eugenia brasiliensis Lam. Sci Agr. 2007, 64: 428-432.View ArticleGoogle Scholar
Talal A, Mohammad H, Vanni C: Chemical composition of the essential oil from different aerial parts of lavender (Lavandula coronopofolia Poiert) grown in Jordan. J Essent Oil Res. 2005, 17: 49-51. 10.1080/10412905.2005.9698827.View ArticleGoogle Scholar
Munoz-Bertomeu J, Arrillaga I, Segura J: Essential oil variation within and among natural populations of Lavendula latifolia and its relation to their ecological areas. Biochem Systemat Ecol. 2007, 35: 479-488. 10.1016/j.bse.2007.03.006.View ArticleGoogle Scholar
Raal A, Orav A, Arak E: Composition of the essential oil of Salvia officinalis L. from various European countries. Nat Prod Res. 2007, 21: 406-411. 10.1080/14786410500528478.PubMedView ArticleGoogle Scholar
Barra A, Coroneo V, Dessi S, Cabras P, Angioni A: Characterisation of the volatile constituents in the essential oil ofPistacea lentiscus L. from different origins and its antifungal and antioxidant activity. J Agric Food Chem. 2007, 55: 7093-7098. 10.1021/jf071129w.PubMedView ArticleGoogle Scholar
Flamini G, Cioni PL: Seasonal variation of the chemical constituents of the essential oil of Santolina etrusca from Italy. Che Biodivers. 2007, 4: 1008-1019. 10.1002/cbdv.200790069.View ArticleGoogle Scholar
Chiasson H, Belanger A, Bostanian N, Vincent C, Poliquin A: Acaricidal properties of Artemisia absinthium andTanacetum vulgare (Asteraceae) essential oils obtained by three methods of extraction. J Econ Entomol. 2001, 94: 167-171. 10.1603/0022-0493-94.1.167.PubMedView ArticleGoogle Scholar
Chalchat JC, Ozcan MM, Dagdelen A, Akgul A: Variability of essential oil composition of Echinophora tenuifolia subspsibthorpiana tutin by harvest location and year and oil storage. Chem Nat Compd. 2007, 43: 225-227. 10.1007/s10600-007-0087-0.View ArticleGoogle Scholar
Loziene K, Venskutonis PR: Influence of environmental and genetic factors on the stability of essential oil composition ofThymus pulegioides. Biochem Syst Ecol. 2005, 33: 517-525. 10.1016/j.bse.2004.10.004.View ArticleGoogle Scholar
George DR, Biron JM, Jolly G, Duvallet G, Sparagano OAE: Toxicity of geraniol solution in vitro to the poultry red mite,Dermanyssus gallinae. Parasite. 2009, 16: 319-321. 10.1051/parasite/2009164319.PubMedView ArticleGoogle Scholar
Pasay C, Mounsey K, Stevenson G, Davis R, Arlian L, Morgan M, Vyszenski-Moher D, Andrews K, McCarthy J: Acaricidal activity of eugenol based compounds against scabies mites. PloS one. 2010, 5: e12079-10.1371/journal.pone.0012079.PubMed CentralPubMedView ArticleGoogle Scholar
Traboulsi AF, El-Haj S, Tueni M, Taoubi K, Nader NA, Mrad A: Repellency and toxicity of aromatic plant extracts against the mosquito Culex pipiens molestus (Diptera: Culicidae). Pest Manag Sci. 2005, 61: 597-604. 10.1002/ps.1017.PubMedView ArticleGoogle Scholar
Bissinger BW, Schmidt JP, Owens JJ, Mitchell SM, Kennedy MK: Activity of the plant-based repellent, TT-4302 against the ticks Amblyomma americanum, Dermacentor variabilis, Ixodes scapularis and Rhipicephalus sanguineus (Acari: Ixodidae). Exp Appl Acarol. 2014, 62: 105-113. 10.1007/s10493-013-9719-1.PubMedView ArticleGoogle Scholar
Turek C, Stintzing FC: Impact of different storage conditions on the quality of selected essential oils. Food Res Int. 2012, 46: 341-353. 10.1016/j.foodres.2011.12.028.View ArticleGoogle Scholar
George DR, Callaghan K, Guy JH, Sparagano OAE: Lack of prolonged activity of lavender essential oils as acaricides against the poultry red mite (Dermanyssus gallinae) under laboratory conditions. Res Vet Sci. 2008, 85: 540-542. 10.1016/j.rvsc.2008.02.001.PubMedView ArticleGoogle Scholar
Specos MM, Garcia JJ, Tornesello J, Marino P, Vecchia MD, Tesoriero MV, Hermida LG: Microencapsulated citronella oil for mosquito repellent finishing of cotton textiles. T Roy Soc Trop Med H. 2010, 104: 653-658. 10.1016/j.trstmh.2010.06.004.View ArticleGoogle Scholar
Saha S, Walia S, Parmar BS: Exploring the diversity of neem bioactives as eco-benign pesticides: a reappraisal. Toxicol Environ Chem. 2011, 93: 1508-1546. 10.1080/02772248.2011.585761.View ArticleGoogle Scholar
George DR, Olatunji G, Guy JH, Sparagano OAE: Effect of plant essential oils as acaricides against the poultry red mite,Dermanyssus gallinae, with special focus on exposure time. Vet Parasitol. 2010, 169: 222-225. 10.1016/j.vetpar.2009.12.038.PubMedView ArticleGoogle Scholar
Isman MB, Miresmailli S, Machial C: Commercial opportunities for pesticides based on plant essential oils in agriculture, industry and consumer products. Phytochem Rev. 2011, 10: 197-204. 10.1007/s11101-010-9170-4.View ArticleGoogle Scholar
Sherer TB, Betarbet R, Testa CM, Seo BB, Richardson JR, Kim JH, Miller GW, Yagi T, Matsuno-Yagi A, Greenamyre JT: Mechanism of toxicity in rotenone models of Parkinson’s disease. J Neurosci. 2003, 23: 10756-10764.PubMedGoogle Scholar
Tanner CM, Kamel F, Ross GW, Hoppin JA, Goldman SM, Korell M, Marras C, Bhudhikanok GS, Kasten M, Chade AR: Rotenone, paraquat, and Parkinson’s disease. Environ Health Persp. 2011, 119: 866-872. 10.1289/ehp.1002839.View ArticleGoogle Scholar
George DR, Sparagano OAE, Port G, Okello E, Shiel RS, Guy JH: The effect of essential oils on laying hen welfare when deployed as acaricides for the poultry red mite, Dermanyssus gallinae. Anim Welf. 2010, 19: 265-273.Google Scholar
Genovese AG, McLean MK, Khan SA: Adverse reactions from essential oil-containing natural flea products exempted from Environmental Protection Agency regulations in dogs and cats. J Vet Emerg Crit Care. 2012, 22: 470-475. 10.1111/j.1476-4431.2012.00780.x.View ArticleGoogle Scholar
Koul O, Walia S, Dhaliwal GS: Essential oils as green pesticides: potential and constraints. Biopestic Int. 2008, 4: 63-84.Google Scholar
Qi BY, Gordon G, Gimme W: Effects of neem-fed prey on the predacious insects Harmonia conformis (Boisduval) (Coleoptera: Coccinellidae) and Mallada signatus (Schneider) (Neuroptera: Chrysopidae). Biol Control. 2001, 22: 185-190. 10.1006/bcon.2001.0965.View ArticleGoogle Scholar
Tedeschi R, Alma A, Tavella L: Side-effects of three neem (Azadirachta indica A. Juss) products on the predatorMacrolophus caliginosus Wagner (Het., Miridae). J Appl Entomol. 2001, 125: 397-402. 10.1046/j.1439-0418.2001.00563.x.View ArticleGoogle Scholar
Naumann K, Isman MB: Toxicity of a neem (Azadirachta indica A. Juss) insecticide to larval honey bees. Am Bee J. 1996, 136: 518-520.Google Scholar
Abudulai M, Shepard BM, Mitchell PL: Effects of neem (Azadirachta indica A. Juss) on predators of Nezara viridula (L.) (Hemiptera: Heteroptera: Pentatomidae). J Agr Urban Entomol. 2004, 21: 9-13.Google Scholar
Clemente MA, de Oliveira Monteiro CM, Scoralik MG, Gomes FT, de Azevedo Prata MC, Daemon E: Acaricidal activity of the essential oils from Eucalyptus citriodora and Cymbopogon nardus on larvae of Amblyomma cajennense (Acari: Ixodidae) and Anocentor nitens (Acari: Ixodidae). Parasitol Res. 2010, 107: 987-992. 10.1007/s00436-010-1965-0.PubMedView ArticleGoogle Scholar
Schmutterer H: Properties and potential of natural pesticides from the neem tree, Azadirachta indica. Ann Rev Entomol. 1990, 35: 271-297. 10.1146/annurev.en.35.010190.001415.View ArticleGoogle Scholar
Rattan RS: Mechanism of action of insecticidal secondary metabolites of plant origin. Crop Prot. 2010, 29: 913-920. 10.1016/j.cropro.2010.05.008.View ArticleGoogle Scholar
Salehzadeh A, Akhkha A, Cushley W, Adams RL, Kusel JR, Strang RH: The antimitotic effect of the neem terpenoid azadirachtin on cultured insect cells. Insect Biochem Mol Biol. 2003, 33: 681-689. 10.1016/S0965-1748(03)00057-2.PubMedView ArticleGoogle Scholar
Priyadarsini RV, Murugan RS, Sripriya P, Karunagaran D, Nagini S: The neem limonoids azadirachtin and nimbolide induce cell cycle arrest and mitochondria-mediated apoptosis in human cervical cancer (HeLa) cells. Free Radic Res. 2010, 44: 624-634. 10.3109/10715761003692503.PubMedView ArticleGoogle Scholar
Tewary DK, Bhardwaj A, Sharma A, Sinha AK, Shanker A: Bioactivity and structure–activity relationship of natural methoxylated phenylpropenes and their derivatives against Aphis craccivora Koch (Hemiptera: Aphididae). J Pest Sci. 2006, 79: 209-214. 10.1007/s10340-006-0135-8.View ArticleGoogle Scholar
Blenau W, Rademacher E, Baumann A: Plant essential oils and formamidines as insecticides/acaricides: what are the molecular targets?. Apidologie. 2012, 43: 334-347. 10.1007/s13592-011-0108-7.View ArticleGoogle Scholar
Dua VK, Kumar A, Pandey AC, Kumar S: Insecticidal and genotoxic activity of Psoralea corylifolia Linn. (Fabaceae) against Culex quinquefasciatus Say, 1823. Parasit Vectors. 2013, 6: 30-10.1186/1756-3305-6-30.PubMed CentralPubMedView ArticleGoogle Scholar
Enan E: Insecticidal activity of essential oils: octopaminergic sites of action. Comp Biochem Physiol C Toxicol Pharmacol. 2001, 130: 325-337. 10.1016/S1532-0456(01)00255-1.PubMedView ArticleGoogle Scholar
Sparagano O, George DR, Harrington D, Giangaspero A: Biology, epidemiology, management and risk related to the poultry red mite, Dermanyssus gallinae. Annu Rev Entomol. 2014, 59: 447-466. 10.1146/annurev-ento-011613-162101.PubMedView ArticleGoogle Scholar
McAllister JC, Adams MF: Mode of action for natural products isolated from essential oils of two trees is different from available mosquito adulticides. J Med Entomol. 2010, 47: 1123-1126. 10.1603/ME10098.PubMedView ArticleGoogle Scholar
Anderson JA, Coates JR: Acetylcholinesterase inhibition by nootkatone and carvacrol in arthropods. Pestic Biochem Phys. 2012, 102: 124-128. 10.1016/j.pestbp.2011.12.002.View ArticleGoogle Scholar
Tong F, Gross AD, Dolan MC, Coats JR: The phenolic monoterpenoid carvacrol inhibits the binding of nicotine to the housefly nicotinic acetylcholine receptor. Pest Manag Sci. 2013, 69: 775-780. 10.1002/ps.3443.PubMedView ArticleGoogle Scholar
Oliveira MS, Morais SM, Magalhaes DV, Batista WP, Vieira IG, Craveiro AA, de Manezes JE, Carvalho AF, de Lima GP: Antioxidant, larvicidal and antiacetylcholinesterase activities of cashew nut shell liquid constituents. Acta Trop. 2011, 117: 165-170. 10.1016/j.actatropica.2010.08.003.PubMedView ArticleGoogle Scholar
Bullangpoti V, Wajnberg E, Audant P, Feyereisen R: Antifeedant activity of Jatropha gossypifolia and Melia azedarachsenescent leaf extracts on Spodoptera frugiperda (Lepidoptera: Noctuidae) and their potential use as synergists. Pest Manag Sci. 2012, 68: 1255-1264. 10.1002/ps.3291.PubMedView ArticleGoogle Scholar
Yadav S, Mittal PK, Saxena PN, Singh RK: Effect of synergist piperonyl butoxide (PBO) on the toxicity of some essential oils against mosquito larvae. J Commun Dis. 2009, 41: 33-38.PubMedGoogle Scholar
Waliwitiya R, Kennedy CJ, Lowenberger CA: Larvicidal and oviposition-altering activity of monoterpenoids, trans-anithole and rosemary oil to the yellow fever mosquito Aedes aegypti (Diptera: Culicidae). Pest Manag Sci. 2009, 65: 241-248. 10.1002/ps.1675.PubMedView ArticleGoogle Scholar
Joffe T, Gunning RV, Allen GR, Kristensen M, Alptekin S, Field LM, Moores GD: Investigating the potential of selected natural compounds to increase the potency of pyrethrum against houseflies Musca domestica (Diptera: Muscidae). Pest Manag Sci. 2012, 68: 178-184. 10.1002/ps.2241.PubMedView ArticleGoogle Scholar
Rossi YE, Palacios SM: Fumigant toxicity of Citrus sinensis essential oil on Musca domestica L. adults in the absence and presence of a P450 inhibitor. Acta Trop. 2013, 127: 33-37. 10.1016/j.actatropica.2013.03.009.PubMedView ArticleGoogle Scholar
David JP, Ismail HM, Chandor-Proust A, Paine MJ: Role of cytochrome P450s in insecticide resistance: impact on the control of mosquito-borne diseases and use of insecticides on Earth. Philos Trans R Soc Lond B Biol Sci. 2013, 368: 20120429-10.1098/rstb.2012.0429.PubMed CentralPubMedView ArticleGoogle Scholar
Mounsey KE, Pasay CJ, Arlian LG, Morgan MS, Holt DC, Currie BJ, Walton SF, McCarthy JS: Increased transcription of Glutathione S-transferases in acaricide exposed scabies mites. Parasit Vectors. 2010, 3: 43-10.1186/1756-3305-3-43.PubMed CentralPubMedView ArticleGoogle Scholar
Rossi YE, Canavoso L, Palacios SM: Molecular response of Musca domestica L. to Mintostachys verticillata essential oil, (4R)+-pulegone and menthone. Fitoterapia. 2012, 83: 336-342. 10.1016/j.fitote.2011.11.019.PubMedView ArticleGoogle Scholar
Kusamran WR, Ratanavila A, Tepsuwan A: Effects of neem flowers, Thai and Chinese bitter gourd fruits and sweet basil leaves on hepatic monooxygenases and glutathione S-transferase activities, and in vitro metabolic activation of chemical carcinogens in rats. Food Chem Toxicol. 1998, 36: 475-484. 10.1016/S0278-6915(98)00011-8.PubMedView ArticleGoogle Scholar
Subapriya R, Velmurugan B, Nagini S: Modulation of xenobiotic-metabolizing enzymes by ethanolic neem leaf extract during hamster buccal pouch carcinogenesis. J Exp Clin Cancer Res. 2005, 24: 223-230.PubMedGoogle Scholar
McLaughlin LA, Niazi U, Bibby J, David JP, Vontas J, Hemingway J, Ranson H, Sutcliffe MJ, Paine MJ: Characterization of inhibitors and substrates of Anopheles gambiae CYP6Z2. Insect Mol Biol. 2008, 17: 125-135. 10.1111/j.1365-2583.2007.00788.x.PubMedView ArticleGoogle Scholar
Waliwitiya R, Nicholson RA, Kennedy CJ, Lowenberger CA: The synergistic effects of insecticidal essential oils and piperonyl butoxide on biotransformational enzyme activities in Aedes aegypti (Diptera: Culicidae). J Med Entomol. 2012, 49: 614-623. 10.1603/ME10272.PubMedView ArticleGoogle Scholar
Jaramillo Ramirez GI, Logan JG, Loza-Reyes E, Stashenko E, Moores GD: Repellents inhibit P450 enzymes in Stegomyia (Aedes) aegypti. PloS one. 2012, 7: e48698-10.1371/journal.pone.0048698.PubMed CentralPubMedView ArticleGoogle Scholar
Shinde GN, Biswas B: An environ-economic backbone in the economic resurgence of barren and semi-arid regions:Azadirachta Indica. J Nat Prod Plant Resour. 2011, 1: 8-13.Google Scholar