Repellent efficacy of a new combination of fipronil and permethrin against Lutzomyia longipalpis
Parasites & Vectors volume 11, Article number: 247 (2018)
Lutzomyia longipalpis is the main vector of Leishmania infantum, the agent of canine and human visceral leishmaniosis in the Americas. Considering that the dog is the main domestic host of the parasite, repellent treatment is a measure that might contribute to the prevention of canine visceral leishmaniosis. The repellent efficacy of a single treatment of a new spot-on topical combination of fipronil and permethrin (Frontline Tri-Act®, Merial, now part of Boehringer-Ingelheim) to repel Lu. longipalpis sand flies was evaluated.
Sixteen healthy Beagle dogs, eight females and eight males, weighing 8.4–14.4 kg, and 2 to 4 years-old were included in the study. Animals were blocked on decreasing body weight and randomly allocated within the blocks to one of two treatment groups of eight animals each. Dogs in Group 1 were untreated and Dogs in Group 2 were treated with a combination containing 67.6 mg/ml fipronil + 504.8 mg/ml permethrin (Frontline Tri-Act®) once on Day 0. Sand fly exposures were performed on Days 1, 14, 21 and 30 with Lu. longipalpis female sand flies. After 65 (± 15 min), sand flies were assessed for engorgement status.
The percent repellency of the treated group compared to the untreated control group was 95.7, 94.3, 81.7 and 72.2% for exposure days 1, 14, 21 and 30, respectively. The two treatment groups were significantly different for all exposure days (P ≤ 0.016 for days 1, 14, 21 and 30). No adverse reactions were observed during the study.
A single topical administration of a new combination of fipronil and permethrin demonstrated a significant repellent effect against Lu. longipalpis bites as soon as it was applied on the dogs and its repellent efficacy lasted for 4 weeks with results greater than 80% for 3 weeks. The results suggest that in endemic areas the regular application of the new combination could contribute to protect dogs from Leishmania infection and therefore serve as an additional tool for the prevention of canine visceral leishmaniosis.
Visceral leishmaniosis (VL) is a zoonotic protozoan vector-borne disease that affects humans, canine and other mammalian species. In the Neotropics its etiological agent is Leishmania infantum. The disease is potentially fatal if untreated and is endemic in Brazil, Argentina and Paraguay, where the number of cases is increasing and its geographical range is expanding [1,2,3,4]. VL also occurs in Mexico, Colombia, Venezuela, Costa Rica, Guatemala, Honduras, Nicaragua, Bolivia and Guyana . A total of 48,720 human VL cases have been reported in the Americas from 2001 to 2014 with an annual mean of 3480 cases. Most of these cases (46,976; 96.42%) have been reported in Brazil including 3690 human deaths from 2000 to 2015 .
Leishmania infantum parasites are transmitted by phlebotomine sand flies. In the New World the main vector is Lutzomyia longipalpis, a species adapted to sylvatic and rural , urban and peri-urban environments . This vector species occurs from Mexico to Argentina  and is progressively expanding its distributional range in Brazil, Paraguay, Argentina  and Uruguay , and consequently expanding the risk for human and canine VL cases in these areas .
The dog is the most important domestic reservoir of Leishmania infantum . Female sand flies may become infected after feeding on infected dogs and may then transmit the promastigote parasite to other mammals (mainly dogs and humans) through subsequent bites . One potential control measure to break the transmission cycle of VL is the prevention of Leishmania infection in dogs . The use of topical insecticides in dogs has been shown to be efficacious in preventing blood-feeding of phlebotomine sand flies [11,12,13,14].
This paper reports the results of a study conducted in Brazil assessing the repellent efficacy of a new spot-on topical combination of fipronil and permethrin (Frontline Tri-Act®, Merial, now part of Boehringer-Ingelheim) against the main vector of human and canine VL in the Americas, Lu. longipalpis. This combination is intended to provide both repellent and insecticidal-acaricidal effects against several ectoparasites of dogs such as fleas (Ctenocephalides felis and C. canis), ticks (Ixodes ricinus, Rhipicephalus sanguineus and Dermacentor reticulatus), sand flies (Phlebotomus perniciosus), stable flies (Stomoxys calcitrans) and mosquitoes (Aedes albopictus, Aedes aegypti and Culex pipiens) [12, 15,16,17,18,19,20].
The study was conducted according to Good Clinical Practices (GCP) as described in the International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products (VICH) guideline 9 .
Adult Beagle dogs were used in the study and had not been exposed to ectoparasiticides for at least three months prior to enrollment in the study. Eight males and eight females, weighing 8.4–14.4 kg, two- to four-years-old, were included in the study. The dogs were housed in groups until Day -1 (i.e. until the day immediately preceding the start of the experiment) and then individually until the end of the study. No concurrent medication, except for the anesthetics used during the sand fly exposures were given during the study. The dogs were managed similarly and with due regard for their well-being. Animals were handled in compliance with Nowavet and Merial Animal Care and Use Guidelines, and in compliance with the Brazilian regulatory requirements. The dogs were acclimated to the study conditions prior to treatment and were observed at least once a day for general health conditions throughout the study. No susceptibility test to sand flies was performed pre-treatment so it was assumed dogs which were from the same breed were equally susceptible.
Allocation and treatment
To allocate the dogs, blocks were formed based on decreasing body weight, with the two dogs with the highest body weight forming block 1, the next two forming block 2, and so on, until all dogs were assigned to a block. Within blocks, each dog was randomly allocated to one of the two treatment groups. Six additional dogs (three treated and three untreated) were kept as spare animals. Dogs in Group 1 served as untreated control animals. Dogs in Group 2 were treated on Day 0 with the topical combination of permethrin and fipronil, at the recommended commercial dose (1.0 ml for dogs < 10.0 kg, and 2.0 ml for dogs > 10.0 to 20 kg, delivering a minimum dose of 6.76 mg/kg fipronil and 50.48 mg/kg permethrin). The dose was applied by parting the hair and applying the formulation directly onto the skin on the dorsal midline of the neck. The total volume was divided into two approximately equal portions. One fraction was applied between the base of the skull and the shoulder blades and the other fraction was applied at the front of the shoulder blades. The dogs were observed prior to treatment and hourly for approximately 4 h following treatment administration.
Sand fly exposures
Lutzomyia longipalpis sand flies used in the study were laboratory-reared and came from a colony located at Departamento de Parasitologia, Instituto de Ciências Biológicas (ICB), Universidade Federal de Belo Horizonte (UFMG), Belo Horizonte, MG, Brazil. The colony has been active for approximately five years and the original parental insects were obtained from the city of Teresina, Piauí State, Brazil.
Sand fly exposures were performed on Days 1, 14, 21 and 30. Prior to each exposure, animals were anesthetized with an intramuscular combination of acepromazine (0.1 mg/kg), ketamine (11 mg/kg) and midazolam (0.5 mg/kg), or ketamine (22 mg/kg) and xylazine (1.1 mg/kg) and placed individually into sand fly proof exposure cages. Exposures on control and treated dogs were performed in separate areas of the building and handled by different personnel to avoid potential contamination. An average of 79.0 three-to-five-day-old female phlebotomine sand flies were released into the exposure cages, per dog, per exposure, together with an average of 58.2 males to stimulate biting and landing behavior. Exposures were done during the night period in total darkness in order to maximize the natural nocturnal biting behavior of phlebotomine sand flies. After 65 (± 15) min, all sand flies (live and dead) were recovered and placed in a container, then counted and categorized as engorged or non-engorged.
Percent sand fly repellency was calculated using the proportion of engorged (alive + dead) sand flies at the end of each post-treatment exposure period transforming to the natural logarithm of (count + 1) for calculation of geometric means (GM) of the proportions by treatment group. Percent repellency was expressed as the percent reduction in fed sand flies of the treated group compared to the control group at each post-treatment exposure day: 100 × [(C-T)/C], where C is the GM of the control group and T is the GM of the treated group. The individual dogs’ proportions of engorged sand flies from the two groups were compared using the nonparametric aligned rank test  that adjusted for the body-weight-blocks. SAS Version 9.4 was used for all testing, which was two-sided and used a significance level of 5%.
No health abnormalities were observed on the animals after treatment during the whole period of the study, including observations conducted for 4 h immediately after treatment. One dog presented intolerance to anesthesia during exposure to phlebotomine sand flies on Day 1. The exposure on Day 1 was completed but the dog was then removed from the study and replaced by one of the spare animals from the same treatment group, same gender, same breed and similar weight for the following exposures (Days 14, 21 and 30).
Untreated control dogs had high numbers of engorged sand flies at the end of the exposure period at all time points, with engorgement percentage means among the total exposed females of 84.6, 98.8, 98.7 and 99.4% for Days 1, 14, 21 and 30, respectively (Table 1). This feeding behaviour on control dogs shows a robust and aggressive phlebotomine sand fly strain population.
The percent repellency of the treated group compared to the untreated control group was 95.7, 94.3, 81.7 and 72.2% for exposure Days 1, 14, 21 and 30, respectively. The two treatment groups were significantly different for all exposure days (χ2 ≥ 5.8454, df=1, P ≤ 0.016) (Table 2).
The results of this study demonstrate the high repellent effect of the new spot-on topical combination of fipronil and permethrin (Frontline Tri-Act®) against the sand fly Lu. longipalpis. Previous studies demonstrated that the topical combination of permethrin and fipronil provides repellency against several species of insects and ticks in dogs. Regarding the mosquito species of the Culicidae Meigen, 1818, repellency against Ae. albopictus was ≥ 93.4% through Day 21 and 86.9% on Day 28; for Ae. aegypti it was ≥ 91.0% through Day 35, and for Cu. pipiens, repellency was ≥ 90.4% through Day 28 . Excellent repellency was also demonstrated against St. calcitrans stable flies with ≥ 96.6% repellency through Day 28, and 88.7% on Day 35 . The product also showed good results versus Ph. perniciosus, an important vector of VL in the Old World with repellency results of 98.2, 98.5, 99.2, 90.9 and 90.3%, for Days 1, 7, 14, 21, and 29, respectively, post-treatment .
Topical application of pyrethroid-based insecticides to dogs in aqueous baths  or top spot pour-on formulations [13, 24,25,26,27] and impregnated collars [28, 29] have been described and have been shown to protect dogs against bites of phlebotomine sand flies and/or to demonstrate a prevention of transmission effect on arthropod borne agents, including leishmaniosis in the Old World. Molina et al.  evaluated the efficacy of a 65% topical permethrin formulation on two dogs challenged with Ph. perniciosus on days -8, 0, 7, 14, 21, 28, 35, 49, 70 and 91 and observed an anti-feeding effect higher than 90% until day 28. On day 35 the efficacy was 79.8%. However, there are few studies reported in peer reviewed journals evaluating the repellent and/or insecticidal efficacy of commercial veterinary products versus New World’s phlebotomine sand flies. Anti-feeding efficacy has been evaluated versus the main vector of canine visceral leishmaniosis, Lu. longipalpis  and also for vector species of cutaneous leishmaniosis (CL) like Migonemyia migonei  and Nyssomyia intermedia (sensu lato) .
David et al.  reported good results on the anti-feeding efficacy of a deltamethrin 4% impregnated collar on four treated versus three untreated dogs exposed for two hours to colony-reared Lu. longipalpis and Mi. migonei sand flies. Exposures to sand flies were performed on weeks 3–4, 7–8, 11–12, 15–16, 22, 26–27 and 35–36 with anti-feeding efficacy results against Lu. longipalpis of 99.3, 100, 100, 96, 96, 90 and 96%, respectively, and 98.3, 100, 100, 99.3, 94.3, 91.8%, respectively, for Mi. migonei.
Percentage of engorgement of female sand flies that fed on untreated dogs, considering all exposures during the study were 83% (1737/2,094) for Lu. longipalpis and 76% (1555/2035) for Mi. migonei.
Reithinger et al.  tested different commercial products versus Ny. intermedia (s.l.), a vector of Leishmania braziliensis in dogs, in a rural area of southern Brazil in which CL is endemic . On Day 0, five dogs received deltamethrin (DM) 4% impregnated collars, three dogs received diazinon (DZ) 15% impregnated collars, three dogs were treated with 65% permethrin (P) pour-on, three dogs with 15% fenthion (F) topical formulations, and three dogs were untreated controls. Non-anesthetized dogs were exposed overnight to wild caught sand flies on three different occasions [5 to 12, 32 to 36 and 58 to 65 days post-treatment (PT)]. Percent reduction in sand fly blood-feeding for the three exposures was 44.1, 31.6 and 49.2% for P; 37.6, 56.7 and 68.5% for DM; 4.2, 41.4 and 43.1% for F; and 37, 1.4 and 3.4% for DZ. In the absence of treatment, the mean engorgement rate of the female sand flies was 42%. During the first exposure, the most effective product was topical permethrin reaching only 44.1% efficacy, however there was no significant difference at the 5% significance level between the number of blood-fed sand flies from treated versus non-treated dogs. The deltamethrin collar had the highest efficacy overall, reaching maximum anti-feeding efficacy of 68.5% around 60 days PT.
Pour-on formulations containing pyrethroids have an important benefit since an immediate repellent effect is obtained, thus protecting the animal with the maximum efficacy within a few hours after treatment as shown in the present study. Results of the present study show that by 24 h post-treatment an efficacy of 95.7% is obtained. This is in contrast to deltamethrin-impregnated collars  for which the maximum repellent efficacy occurs two to three weeks after initial treatment. Since potential protection against sand fly transmitted diseases to individual dogs depends solely on their anti-feeding effect, adequate repellent efficacy is mandatory for the prevention of Leishmania infection in susceptible dogs. This new combination product showed rapid onset of effect with maximum repellent action within 24 h after treatment.
It is important to highlight that the anti-feeding efficacy results observed in the present study were obtained under a high challenge situation, on a study design sufficiently powered using eight animals per group, whereas other efficacy studies versus Neotropical sand flies had three or four animals per group [24, 30]. The level of engorgement observed on the females in the control group considering the four different exposure periods was 95.63% (2669/2791). That means phlebotomine sand flies presented an aggressive feeding behavior, which provided a strong challenge for the product. This value was higher than engorgement results observed in other studies conducted in Brazil with Lu. longipalpis like those reported by David et al.  with 83% (1737/2094) or other New World’s sand flies such as Mi. migonei with 76% (1555/2035)  and Ny. intermedia (s.l.) with 42% .
High biting rates of Lu. longipalpis in dogs, as observed in this study, are an important component of the vector capacity of this sand fly species and is directly related to its zoonotic ability to transmit Leishmania infantum on VL endemic areas . The use of insecticide products in the dog population has been suggested as an important measure that could aid in the prevention and control of VL [30, 32,33,34]. Here, we demonstrate the anti-feeding effect of a topical combination of fipronil and permethrin (Frontline Tri-Act®) with high protection rates for 28 days. Considering the VL dynamics, our results demonstrate that this product could protect dogs from the bites of Lu. longipalpis and so could be integrated into canine leishmaniosis control and prevention programs in the Americas.
The new combination of fipronil and permethrin demonstrated a significant repellent effect against Lutzomyia longipalpis bites as soon as it was applied on the dogs, and its repellent efficacy lasted for 4 weeks, with results greater than 80% for 3 weeks. The results suggest that in VL endemic areas, the regular application of the new combination can contribute to the prevention of canine visceral leishmaniosis.
canine visceral leishmaniosis
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The authors are sincerely grateful to investigators and the staff of the study location either linked to the authors or serving as independent Contract Research Organizations who took part in the study and ensured that Good Clinical Practice standards were adhered to. FRONTECT® and FRONTLINE TRI-ACT™, registered trademarks of Boehringer Ingelheim.
The work reported herein was funded by Boehringer Ingelheim GA, USA.
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All relevant data are provided within the paper.
The study was approved by Nowavet Institutional Animal Care and Use Committee (IACUC) with the concurrence of Boehringer Ingelheim.
AAC, FOS and BF are current employees of Boehringer Ingelheim. STC is a former employee of Boehringer Ingelheim.
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Cutolo, A.A., Galvis-Ovallos, F., de Souza Neves, E. et al. Repellent efficacy of a new combination of fipronil and permethrin against Lutzomyia longipalpis. Parasites Vectors 11, 247 (2018). https://doi.org/10.1186/s13071-018-2831-7