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Research Journal for Veterinary Practitioners

RJVP_9_2_12-17

 

 

Research Article

 

Evaluation of The Toxic Effect of Sarolaner on Earthworms (Eisenia foetida): A Pilot Study

 

Camilo Romero Núñez1*, Rafael Heredia Cárdenas1, Laura Miranda Contreras1, Galia Sheinberg Waisburd2, Alberto Martin Cordero3

1Dermavet Hospital Veterinario, José de la Luz Blanco, Mz. 187, Lt. 33, Col. Santa Martha Acatitla, Ciudad de México; 2Centro Veterinario México, Calle Cincinnati #22, Benito Juárez, Ciudad de los Deportes, 03710 Ciudad de México, México; 3Vetderm Dermatología Veterinaria Especializada Av Niños Héroes 1665, Guadalajara, México.

 

Abstract | There is a new class of insecticides/acaricides—isoxazolines—that shows good efficacy against several ectoparasites. Sarolaner belongs to this family of molecules, and its potency, safety and pharmacokinetics have been optimised for use in dogs and cats. Furthermore, it presents significant selectivity for insect neurons. Nevertheless, its negative effects on susceptible non-target microorganisms like earthworms (which can be indirectly affected by insecticides) are unknown. The present study examined the effect of sarolaner on earthworms via two methods. In the first experiment, faeces were collected from 24 rabbits, 18 of which were medicated with sarolaner. The faeces were applied to a compost with earthworms. In the second experiment, sarolaner was applied directly to the earthworms. For both experiments, the number of earthworms was evaluated on days 1, 15 and 30 post-treatment. There were no significant differences between the sarolaner-treated and control groups at 15 and 30 days. Thus, sarolaner exhibited no negative effects with regards to earthworm survival.

 

Keywords | Earthworm, Evaluation, Sarolaner, Toxicity

 

Received | April 21, 2021; Accepted | May 11, 2021; Published | June 25, 2021

*Correspondence | Camilo Romero Núñez, Dermavet Hospital Veterinario, José de la Luz Blanco Mz. 187, Lt.33, Santa Martha Acatitla, Iztapalapa, Ciudad de México; Email: mvzcamilo@yahoo.com.mx

Citation | Núñez CR, Cárdenas RH, Contreras LM, Waisburd GS, Cordero AM (2021). Evaluation of the toxic effect of sarolaner on earthworms (eisenia foetida): a pilot study. Res J. Vet. Pract. 9(2): 12-17.

DOI | http://dx.doi.org/10.17582/journal.rjvp/2021/9.2.12.17

ISSN | 2308-2798

Copyright © 2021 Núñez et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

 

Introduction

 

Since 2013, the use of isoxazolines in the veterinary market has increased. Recent studies demonstrated the efficacy of these molecules against several ectoparasites, including fleas, mites (Demodex sp., Sarcoptes scabiei, Otodectes cynotis, Caparinia tripilis and Psoroptes cuniculi), and ticks (McTier et al., 2016; Romero et al., 2016; Romero et al., 2017; Sheinberg et al., 2017). The γ-aminobutyric acid (GABA)-gated chloride channel and GABA receptor (GABA-R) are the targets for an expanding number and variety of insecticides, including the polychlorocycloalkanes (e.g., α-endosulfan), fiproles (e.g., fipronil), and avermectins. Like these, isoxazolines (the latest addition with outstanding potency on pests) exhibit insecticidal and miticidal activities by targeting arthropod chloride ions channels linked to GABA or glutamate receptors (Shoop et al., 2014; Zhao and Casida, 2014). They present significant selectivity for insect neurons (Kilp et al., 2016). However, the effect of these molecules on ecosystem functions is unknown. Isoxazolines can potentially accumulate in the soil and may affect the survival of key soil ecosystem microorganisms. Toxicological studies are highly important and essential for the evaluation of environmental effects. Several organisms may be involved in toxicity tests: terrestrial organisms, vertebrates, aquatic organisms and plants (Kolar and Eržen, 2006).

 

Non-target sensitive microorganisms, like earthworms, may be undesirably affected by insecticides (Cang et al., 2017). Earthworms are a terrestrial invertebrate widely distributed in the soil environment (Zhang et al., 2020). They can absorb organic compounds through skin diffusion, as well as by ingesting soil particles (Miao et al., 2018). Eisenia foetida, also known as the red Californian earthworm, represents 60-80% of the total animal biomass of soils (Durán and Henríquez, 2009; Jouquet et al., 2010). This species is responsible for organic matter biotransformation, improves the soil structure and nutrient cycle and plays a key role in the evaluation of terrestrial ecotoxicity (Domínguez et al., 2009; Araneda, 2016; Zapata et al., 2016). Eisenia foetida has been recommended by the OECD (Organization for Economic Cooperation and Development) as a biomarker for toxicity studies with soil organisms due to its ease of cultivation, low cost and high sensitivity to environmental contaminants (Iturbe-Requena, et al., 2019).

 

Wang et al. (2012) showed 24 different insecticides cause toxicity in E. foetida. The highest toxicity is from neonicotinoids. Compared with antibiotics, carbamates and organophosphates, pyrethroids are less toxic. Similarly, ethyl carbamate causes E. foetida mortality and toxicity, data that reflect the importance of knowing the risks of ecotoxicity with different insecticide products (Iturbe, 2019). The effect of one of the isoxazolines has already been evaluated in non-target organisms such as fish and bees, showing from low toxicity to notable risk depending on the organism evaluated (Jia et al., 2018; Sheng et al., 2019). However, there are no studies on possible toxicity from sarolaner, a prominent isoxazoline compound. The objective of this study was to evaluate the impact of sarolaner on earthworm (E. foetida) survival.

 

Materials and Methods

 

The protocol used in this study was approved by the ethics committee of the UAEM Amecameca University Center, Mexico (CBE/CUA/2016/05). A compost was prepared with E. foetida according to OECD guideline 207 (1984). During the first 2 weeks, the worms were fed with organic matter (a mixture of fruits, vegetables, cereals and eggs; no citrus fruits, oils and meats). In the first experiment, 80% of the organic matter was then replaced with rabbit faeces. To collect faeces, 24 rabbits (13 males and 11 females) were randomly chosen. None of the rabbits were sterilized, and the females were not pregnant. Each rabbit was housed individually in separate cages to avoid excreta mixing; they were fed commercial feed. They were divided into four groups of 6 individuals each. Three groups were treated with 2.5 mg/kg sarolaner (Simparica®; Zoetis), and the fourth group was not treated with sarolaner (control group). Stool was collected for each rabbit group (with and without treatment). Stool administration was performed in each of the vermicompost sections: three compartments received sarolaner-treated rabbit faeces and one section received the control rabbit faeces. The morphology and number of earthworms in each section on days 1, 15 and 30 were compared.

 

In the second experiment, four more groups of 100 worms each were selected and fed with organic matter for 2 weeks. Subsequently, organic matter with 120 mg sarolaner was added to three groups; the fourth group served as the control and did not receive sarolaner. The number of worms was evaluated on days 1, 15 and 30 post-treatment by separating the worms from the organic matter.

 

Statistical analysis

The number of worms cultivated with rabbit faeces and the number of worms to which sarolaner was directly applied were analysed using a general linear model (Tukey’s standardised range test) with α = 0.05. Fisher’s exact test was used for statistical comparisons. Three replicates were performed for the sarolaner treatment in each experiment.

 

Results

 

For the earthworms exposed to rabbit faeces, there were no significant differences in the number of worms between sarolaner-treated and control groups at 15 and 30 days; there was an increase in the number of earthworms in all groups. These data indicate that sarolaner did not negatively affect the number of worms cultivated (Table 1). Table 2 shows the comparison of the control group and the average of the three sarolaner replicates. There were no significant differences at 15 and 30 days, during which the control and treatment groups exhibited similar behaviour.

 

For the second experiment, sarolaner was directly applied to the worms in culture. There were no significant differences in earthworm numbers at day 15 or 30 post-treatment between the control and the sarolaner groups (Table 3). These data again revealed that sarolaner treatment did not negatively affect the worms. The comparison between worms treated directly with sarolaner and the control (Table 4) showed no differences at 15 and 30 days post-treatment.

 

Table 1: Comparison of the number (N) of worms fed with faeces from sarolaner-treated rabbits (replicates I, II and III) and faeces from untreated rabbits (control) on days 15 and 30 post-treatment.

 

Treatments

Initial

(N)

Day 15

(N)

P

Day 30

(N)

P
Control 100 128   200  
Sarolaner I 100 120 0.73 187 0.69
Sarolaner II 100 134 0.80 250 0.18
Sarolaner III 100 171 0.11 195 0.88


P= > 0.05, determined using Fisher’s exact test.

 

Table 2: Comparison of the number of worms grown with faeces from sarolaner-treated rabbits and worms grown with faeces from untreated rabbits (control) on days 15 and 30 post-treatment.

 

Day 15

Number of worms

Day 15

Number of worms

Day 30

Number of worms

128a

128a

200a

141.63a

141.63a

210a

694.3 694.3 1176.3


Statistical analysis performed with GLM Tukey’s staged range test; columns with the different letter were significantly different. * mean of the 3 replicates

 

Table 3: Comparison of the number (N) of worms treated directly with Sarolaner (replicates I, II and III) and worms without treatment (control) on days 15 and 30 post-treatment.

 

Treatments

Initiation

(N)

Day 15

(N)

P

Day 30

(N)

P
Control 100 141   198  
Sarolaner I 100 133 0.75 187 0.74
Sarolaner II 100 126 0.54 160 0.22
Sarolaner III 100 136 0.84 201 0.93


P= > 0.05, determined using Fisher’s exact test.

 

Table 4: Comparison of the number (N) of worms treated directly with sarolaner and worms without treatment (control) on days 15 and 30 post-treatment.

 

 

Day 15

(N)

Day 30

(N)

Control

141.0a

198.0a

Sarolaner*

131.6a

182.6a

EE 26.3 434.3


Statistical analysis performed with GLM Tukey’s staged range test; columns with the different letter were significantly different. * mean of the 3 replicates

 

Discussion

 

Earthworms are dominant fauna in most temperate terrestrial ecosystems (Shi et al., 2017). They play a crucial role in modifying soil structure and accelerating the breakdown of organic matter and nutrient recycling (Domínguez et al., 2009). Thus, their abundance in soil is an indicator of the soil health (Ouina et al., 2016). With the emergence of increased resistance of insects to insecticides, the application of higher doses of these can increase adverse effects for non-target organisms. The effects of toxic substances on reproduction, growth rates and behavioral traits of E. fetida have been reported. Therefore, it is important to assess the ecological risks of insecticides for ecosystems (Wang et al., 2015).

 

Isoxazolines (sarolaner, fluralaner, afoxolaner and lotilaner) are a new class of oral ectoparasiticides for pets. These compounds have demonstrated remarkable activity against the most common dog ectoparasites, namely fleas and ticks. They have several advantages over first-generation oral parasiticides, which have a limited ability to effectively kill both fleas and ticks in dogs (Beugnet and Franc, 2012). The sarolaner mechanism of action in insects and mites involves blocking chloride channels linked to GABA and glutamate receptors. This blockage prevents chloride ion entry into nerve cells and consequently increases nerve stimulation and leads to the death of the parasites. Sarolaner was shown to exhibit a greater potential for blocking insect receptors compared to the mammalian receptors (McTier et al., 2016). Furthermore, it does not interact with insecticidal nicotinic receptors or other GABAergic insecticidal receptors like other insecticide classes, including neonicotinoids, fiproles, milbemycins, avermectins and cyclodienes (Shoop, 2014). However, there are no reports of the effect of isoxazolines, including sarolaner, on other microorganisms, including those that belong to the Lumbricidae family.

 

In dogs, sarolaner has been shown to provide rapid killing of existing fleas, as well as newly infested fleas, for 35 days (Six et al., 2016a). Reduction of 94% was seen in 8 hours after oral administration, and fleas were eliminated from all dogs during the 35-day assessment period (Six et al., 2016a). Sarolaner has been reported to be effective against 5 species of ticks infesting dogs in United States America (Six et al., 2016b), and 4 species infecting dogs in Europe (Geurden et al., 2016). Newer publications show efficacy against the Australian paralysis tick (Packianathan et al., 2017) and the Asian long horn tick (Oda et al., 2019). For multiple tick species, killing of > 90% of ticks in 24 hours persists for 28 days. By contrast, in this study, neither the feces of rabbits treated with sarolaner not the direct administration killed earthworms at 15 and 30 days post-treatment. This data is consistent with a previous observation that direct administration to earthworms did not cause harmful effects (Shoop, 2014).

 

Fipronil, a phenylpyrazole insecticide, has been widely used for insect control and plant protection; it is effective against a wide range of insect pests (Qin et al., 2014). Fipronil is a chronic pesticide that binds with organic matter and is detrimental to earthworms in shallow soil (Yu et al., 2013). It can reduce the earthworm reproduction rate, as does imidacloprid, a neonicotinoid insecticide (Alves et al., 2013). Although fipronil does not promote acute toxicity in earthworms (Mostert et al., 2002), earthworms can accumulate fipronil and its soil metabolites. These compounds can then be transferred and/or bioaccumulate in predatory organisms that feed on earthworms (Qin et al., 2014).

 

Although organophosphates and carbamates have different structures, both inhibit acetylcholinesterase (AChE) activity (Carmo et al., 2010). The toxicity of organophosphates for earthworms depends on the evaluated parameter. These chemicals will certainly show a very high toxicity if AChE inhibition and the consequent physiological damage are evaluated (Reddy and Rao, 2008).

 

Neonicotinoids are among the most effective insecticides for pest control. They act as competitive inhibitors of nicotinic acetylcholine receptors (nAChR) in the central nervous system (Elbert et al., 2008). These compounds can endanger soil organisms, including earthworms (Ishaaya and Degheele, 1998). In a study by Wang et al. (2012), among the different chemical classes evaluated, neonicotinoids, such as imidacloprid and nitenpyram, show the highest toxicity towards E. foetida through direct contact. Soil toxicity was also tested, namely by assessing mortality at 7 and 14 days post-treatment. The neonicotinoids again exhibit the highest toxicity. Even a more recent study, in addition to affirming the toxicity on physiological and biochemical indicators of earthworms, indicated possibilities of damage at the genetic level after application of nitenpyram (Zhang et al., 2020).

 

In contrast, the current study showed that soil-level and direct sarolaner administration to the vermicompost had no effect on earthworm reproduction. Imidacloprid, in comparison with carbaryl, cyfluthrin, chlorpyrifos and fipronil, exhibits a negative effect on the earthworm (Mostert et al., 2002) that was not observed with sarolaner. Luo et al (1999) also found adverse effects and developed the sperm deformity test to detect possible adverse influences of pesticides on earthworm reproduction. These deficits occur for imidacloprid concentrations greater than 0.5 mg/kg dry soil.

 

Pyrethroid insecticides bind to a distinct receptor site in the sodium channel and are relatively less toxic to mammals because they are rapidly metabolised in those animals as well as ecosystems (Narahashi, 2000). Most of these compounds are not toxic to earthworms in soil toxicity tests (Inglesfield, 1984). These results are similar to the current study with regards to the lack of sarolaner toxic effects.

 

The adverse effect of subchronic or chronic exposure is also important in ecological risk assessments (Liu et al., 2011). Isoxazoline toxicity has been examined in zebrafish and honeybee. Fluralaner exhibits low toxicity in this fish, but it can rapidly bioaccumulate (Jia et al., 2017). Instead, after exposure of fluralaner to the honeybee, high toxicity risk was reported (Sheng et al., 2019); other isoxazolines have not been tested in this model.

 

The growth and reproduction of earthworms are important measures used in environmental ecotoxicity (Wu et al., 2011). Thus, the relative lack of a toxic sarolaner effect on earthworms provides crucial information about the potential environmental safety of this compound.

 

In the present investigation, sarolaner was not toxic to earthworms (E. foetida) through either indirect exposure (through the faeces of rabbits medicated with this isoxazoline) or direct administration of sarolaner to the vermicompost. Sarolaner did not affect the reproduction and growth of earthworms up to 30 days post-administration.

 

Conflict of Interest

 

There are no conflict of interests.

 

authors contribution

 

Camilo Romero Núñez: Conceptualization, Methodology, Software, Validation, Formal Analysis, Data Curation, Writing – Original Draft, Supervision, Project Administration. Rafael Heredia Cárdenas: Resources, Software, Validation, Formal Analysis, Data Curation, Writing – Review & Editing. Laura Miranda Contreras: Investigation, Writing – Original Draft, Writing – Review & Editing, Visualization. Galia Sheinberg Waisburd: Resources, Methodology, Review & Editing, Visualization. Alberto Martin Cordero: Resources, Methodology, Review & Editing, Visualization.

 

References

 

  • Alves PR, Cardoso EJ, Martines AM, Sousa JP, Pasini A (2013). Earthworm ecotoxicological assessments of pesticides used to treat seeds under tropical conditions. Chemosphere. 90: 2674-2682. https://doi.org/10.1016/j.chemosphere.2012.11.046
  • Araneda GA (2016). Uso de la lombriz de tierra como organismo indicador del impacto de pesticidas en el agrosistema. Tesis Doctoral. Universidad de Concepción, Facultad de Ciencias Ambientales, Chile.
  • Beugnet F, Franc M (2012). Insecticide and acaricide molecules and/or combinations to prevent pet infestation by ectoparasites. Trends Parasitol. 28(7): 267–279. https://doi.org/10.1016/j.pt.2012.04.004
  • Cang T, Dai D, Yang G, Yu Y, Lv L, Cai L, Wang Q, Wang Y (2017). Combined toxicity of imidacloprid and three insecticides to the earthworm, Eisenia fetida (Annelida, Oligochaeta). Environ. Sci. Pollut. Res. 24(9): 8722–8730. https://doi.org/10.1007/s11356-017-8627-z
  • Carmo EL, Bueno AF, Bueno RCOF (2010). Pesticide selectivity for the insect egg parasitoid Telenomus remus. BioControl. 55: 455–464. https://doi.org/10.1007/s10526-010-9269-y
  • Domínguez J, Aira M, Gómez-Brandón M (2009). El papel de las lombrices de tierra en la descomposición de la materia orgánica y el ciclo de nutrientes. Ecosistemas. 18: 20-31.
  • Durán L, Henríquez C (2009). Crecimiento y reproducción de la lombriz roja (Eisenia foetida) en cinco sustratos orgánicos. Agronomía Costarricense. 33(2): 275-281.
  • Elbert A, Haas M, Springer B, Thielert W, Nauen R (2008). Applied aspects of neonicotinoid uses in crop protection. Pest. Manage. Sci. 64(11): 1099–1105. https://doi.org/10.1002/ps.1616
  • Geurden T, Becskei C, Grace S, Strube C, Doherty P, Liebenberg J, Mahabir SP, Slootmans N, Lloyd A, Six RH (2016). Efficacy of a novel oral formulation of sarolaner (Simparica™) against four common tick species infesting dogs in Europe. Vet. Parasitol. 222:33-36. https://doi.org/10.1016/j.vetpar.2016.03.024
  • Inglesfield C (1984). Toxicity of the pyrethroid insecticides cypermethrin and WL85871 to the earthworm, Eisenia fetida (Savigny). Bull. Environ. Contam. Toxicol. 33: 568–570. https://doi.org/10.1007/BF01625585
  • Ishaaya I, Degheele D (1998). Mechanism and resistance management. In: Insecticides with Novel Modes of Action. Narosa Publishing House, London. https://doi.org/10.1007/978-3-662-03565-8
  • Iturbe-Requena SL, Prado-Ochoa MG, Muñoz-Guzmán MA, Velázquez-Sánchez AM, Ángeles E, Alba-Hurtado F (2019). Toxic effects of new ethyl-carbamates on the morphology, mortality and acetylcholinesterase activity of Eisenia foetida. Ecotoxicol. Environmen. Safety. 176: 219-225. https://doi.org/10.1016/j.ecoenv.2019.03.094
  • Jia ZQ, Liu D, Sheng CW, Casida JE, Wang C, Song PP, Chen YM, Han ZJ, Zhao CQ (2018). Acute toxicity, bioconcentration, elimination and antioxidant effects of fluralaner in zebrafish, Danio rerio. Environ. Pollut, 232: 183–190. https://doi.org/10.1016/j.envpol.2017.09.032
  • Jouquet P, Plumere T, Thu TD, Rumpel C, Duc TT, Orange T (2010). The rehabilitation of tropical soils using compost and vermicompost is affected by the presence of endogeic earthworms. Appl. Soil Ecol. 46: 125–133. https://doi.org/10.1016/j.apsoil.2010.07.002
  • Kilp S, Ramirez D, Allan MJ, Roepke RK (2016). Comparative pharmacokinetics of fluralaner in dogs and cats following single topical or intravenous administration. Parasit. Vectors. 9(1): 296. https://doi.org/10.1186/s13071-016-1564-8
  • Kolar L, Eržen, NK (2006). Veterinary parasiticides – are they posing an environmental risk? Slov. Vet. Res. 43(2): 85-96.
  • Liu S, Zhou Q, Wang Y (2011). Ecotoxicological responses of the earthworm Eisenia fetida exposed to soil contaminated with HHCB. Chemosphere. 83(8): 1080–1086. https://doi.org/10.1016/j.chemosphere.2011.01.046
  • Luo Y, Zang Y, Zhong Y, Kong Z (1999). Toxicological study of two novel pesticides on earthworm Eisenia foetida. Chemosphere. 39: 2347-2356. https://doi.org/10.1016/S0045-6535(99)00142-3
  • McTier TL, Chubb N, Curtis MP, Hedges L, Inskeep GA, Knauer CS, Menon S, Mills B, Pullins A, Zinser E, Woods DJ, Meeus P (2016). Discovery of sarolaner: a novel, orally administered, broad spectrum, isoxazoline ectoparasiticide for dogs. Vet. Parasitol. 222: 3–11. https://doi.org/10.1016/j.vetpar.2016.02.019
  • Miao J, Chen X, Xu T, Yin D, Hu X, Sheng GD (2018). Bioaccumulation, distribution and elimination of lindane in Eisenia foetida: The aging effect. Chemosphere. 190: 350–357. https://doi.org/10.1016/j.chemosphere.2017.09.138
  • Mostert MA, Schoeman\ AS, van der Merwe M (2002). The relative toxicities of insecticides to earthworms of the Pheretima group (Oligochaeta). Pest Manage. Sci. 58: 446–450. https://doi.org/10.1002/ps.473
  • Narahashi T (2000). Neuroreceptors and ion channels as the basis for drug action: past, present, and future. J. Pharmacol. Exp. Ther. 294: 1–26.
  • Oda K, Yonetake W, Fuji T, Hodge A, Six RH, Maeder S, Rugg D (2019). Efficacy of sarolaner (Simparica®) against induced infestations of Haemaphysalis longicornis on dogs. Parasit Vectors. 12: 509. https://doi.org/10.1186/s13071-019-3765-4
  • OECD, Organization for Economic Co-operation and Development (1984). Test 207: earthworm, acute toxicity tests, in: Organization for Economic Co-operationand Development (Ed.), OECD Guidelines for testing of chemicals, (1984).
  • Ouina TS, Panoff Jean-M, Koussémon M, Gonnety JT (2017). Effect of pesticides and micro-organisms on earthworm Eisenia fetida (Savigny, 1826). Afri. J. Agric. Res. 12: 706-715. https://doi.org/10.5897/AJAR2016.11844
  • Packianathan R, Hodge A, Bruelke N, Davis K, Maeder S (2017). Comparative speed of kill of sarolaner (Simparica®) and afoxolaner (NexGard®) against induced infestations of Ixodes holocyclus on dogs. Parasit Vectors. 10:98. https://doi.org/10.1186/s13071-017-2024-9
  • Qi S, Wang D, Zhu L, Teng M, Wang C, Xue X, Wu L (2018). Effects of a novel neonicotinoid insecticide cycloxaprid on earthworm, Eisenia fetida. Environ. Sci. Pollut. Res. 25: 14138–14147. https://doi.org/10.1007/s11356-018-1624-z
  • Qin F, Gao Y, Xu P, Guo B, Li J, Wang H (2014). Enantioselective bioaccumulation and toxic effects of fipronil in the earthworm Eisenia foetida following soil exposure. Pest Manag. Sci. 71(4): 553–561. https://doi.org/10.1002/ps.3841
  • Reddy NC, Rao JV (2008). Biological response of earthworm, Eisenia foetida (Savigny) to an organophosphorous pesticide, profenofos. Ecotoxicol. Environ. Saf. 71: 574–582. https://doi.org/10.1016/j.ecoenv.2008.01.003
  • Romero C, Heredia R, Pineda J, Serrano JA, Mendoza GD, Trápala P, Cordero AM (2016). Efficacy of fluralaner in 17 dogs with sarcoptic mange. Vet. Dermatol. 27: 353–e88. https://doi.org/10.1111/vde.12363
  • Romero C, Sheinberg G, Pineda J, Heredia R, Yarto E, Cordero AM (2017). Fluralaner as a single dose oral treatment for Caparinia tripilis in a pygmy African hedgehog. Vet. Dermatol. 28(6): 622-e152. https://doi.org/10.1111/vde.12465
  • Sheinberg G, Romero C, Heredia R, Capulin M, Yarto E, Carpio J (2017). Use of oral fluralaner for the treatment of Psoroptes cuniculi in 15 naturally infested rabbits. Vet. Dermatol. 28: 393–395. https://doi.org/10.1111/vde.12429
  • Sheng C, Huang Q, Liu G, Ren X, Jiang J, Jia Z, Han ZJ, Zhao, C (2019). Neurotoxicity and mode of action of fluralaner on honeybee Apis mellifera L. Pest Manag. Sci. 75(11): 2901-2909. https://doi.org/10.1002/ps.5483
  • Shi Z, Tang Z, Wang C (2017). A brief review and evaluation of earthworm biomarkers in soil pollution assessment. Environ. Sci. Pollut. Res. 24: 13284–13294. https://doi.org/10.1007/s11356-017-8784-0
  • Shoop WL, Hartline EJ, Gould BR, Waddell ME, McDowell RG, Kinney JB, Lahm GP, Long JK, Xu M, Wagerle T, Jones GS, Dietrich RF, Cordova D, Schroeder ME, Rhoades DF, Benner EA, Confalone PN (2014). Discovery and mode of action of afoxolaner, a new isoxazoline parasiticide for dogs. Vet. Parasitol. 201(3-4): 179–189. https://doi.org/10.1016/j.vetpar.2014.02.020
  • Six RH, Everett WR, Myers MR, Mahabir SP (2016a). Comparative speed of kill of sarolaner (Simparica™) and spinosad plus milbemycin oxime (Trifexis®) against induced infestations of Ctenocephalides felis on dogs. Parasit Vectors. 9: 93. https://doi.org/10.1186/s13071-016-1374-z
  • Six RH, Everett WR, Young DR, Carter L, Mahabir SP, Honsberger NA, Myers MR, Holzmer S, Chapin S, Rugg JJ (2016b). Efficacy of a novel oral formulation of sarolaner (Simparica TM) against five common tick species infesting dogs in the United States. Vet. Parasitol. 222: 28-32. https://doi.org/10.1016/j.vetpar.2015.12.023
  • Wang Y, Cang T, Zhao X, Yu R, Chen L, Wu C, Wang Q (2012). Comparative acute toxicity of twenty-four insecticides to earthworm, Eisenia fetida. Ecotoxicol. Environ. Saf. 79: 122-128. https://doi.org/10.1016/j.ecoenv.2011.12.016
  • Wang K, Pang S, Mu X, Qi S, Li D, Cui F, Wang C (2015). Biological response of earthworm, Eisenia fetida, to five neonicotinoid insecticides. Chemosphere. 132: 120–126. https://doi.org/10.1016/j.chemosphere.2015.03.002
  • Wu SJ, Wu E, Qiu L, Zhong W, Chen J (2011). Effects of phenanthrene on the mortality, growth, and anti-oxidant system of earthworms (Eisenia fetida) under laboratory conditions. Chemosphere. 83: 429–434. https://doi.org/10.1016/j.chemosphere.2010.12.082
  • Yu Z, Meng W, Ya-jun T, Yan-ping L, Zheng Fu-c, Ye Y, Chao-hua Z (2013). Leaching patterns of fipronil in 3 kinds of soil in Hainan province, China. Afri J. Agric. Res. 8: 1725-1730 https://doi.org/10.5897/AJAR12.2190.
  • Zapata IC, Martínez L, Posada E, González ME, Saldarriaga JF (2016). Efectos de la lombriz roja californiana (Eisenia foetida), sobre el crecimiento de microorganismos en suelos contaminados con mercurio de segovia, Antioquia. Cien. Ing. Neogranad. 27(1): 77-90. https://doi.org/10.18359/rcin.1911
  • Zhang W, Xia X, Wang J, Zhu L, Wang J, Wang G, Chen Y, Kim YM (2020). Oxidative stress and genotoxicity of nitenpyram to earthworms (Eisenia foetida). Chemosphere. 264 (2): 128493. https://doi.org/10.1016/j.chemosphere.2020.128493
  • Zhao C, Casida, JE (2014). Insect γ-Aminobutyric Acid Receptors and Isoxazoline Insecticides: Toxicological Profiles Relative to the Binding Sites of [3H] Fluralaner, [3H]-4-Ethynyl-4-n-propylbicycloorthobenzoate, and [3H] Avermectin. J. Agric. Food Chemi. 62(5): 10191024. https://doi.org/10.1021/jf4050809
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