Background

Fluralaner is a new molecular entity of the isoxazoline class that has shown potent acaricidal and insecticidal activity through a dual mechanism of binding to neuronal GABA- and glutamate-gated chloride channels in susceptible invertebrates [1, 2]. Fluralaner has high selectivity for arthropods and a very favorable safety profile in vertebrates including dogs [3]. Oral fluralaner administration (Bravecto™) provides 12 weeks efficacy against tick and flea infestations on dogs [4, 5].

Flea-adulticide activity on infested dogs is important, but represents only part of the flea-control program needed to effectively eliminate the flea population. The adult population on the dog represents only approximately 5% of the total flea infestation in a dwelling, while the other 95% of the population consists of eggs, larvae and pupae in the dog’s home environment [6]. These maturing stages will re-infest the dog as they become adults.

Effective flea control needs to include highly potent adulticide activity that kills fleas quickly after treatment for immediate relief; maintenance of this high adulticide efficacy through the treatment period; and control of flea reproduction [7]. Fluralaner is a systemic insecticide that kills fleas that feed on treated dogs. The efficacy demonstrated in field trials for both flea control and reduction in signs of allergic flea dermatitis, suggests that treated dogs are exposed to fewer fleas developing from the environmental population of juvenile fleas [5]. Therefore, the objective of the in vitro study was to investigate if fluralaner concentrations below the instant flea-killing effect were able to inhibit flea reproduction and thus contribute to the control of environmental flea life stages.

Additionally, a simulated home-environment study was conducted to prove fluralaner’s flea-control properties not only on the dog but also the external flea population that would naturally occur in a household containing an infested animal.

Methods

In vitro membrane-feeding exposure

A membrane-feeding method [8] was modified to assess the impact of fluralaner exposure on flea reproduction. Defibrinated sheep blood was prepared in a series of dilutions with fluralaner to obtain concentrations between 50.0 and 0.09 ng/mL. Test solutions were prepared twice and each preparation was tested in duplicate resulting in a total of 4 replicates per concentration, along with a fluralaner-negative solvent control (a solvent concentration equivalent to that of the highest concentrated fluralaner test solution) and an untreated control.

Unfed adult fleas (C. felis; 20 males and 20 females) were placed into a plastic unit that was then closed with a gauze lid. A grid inside the plastic unit divided the unit into 2 chambers, an upper chamber for flea feeding and a lower chamber for egg collection [8]. Test or control-blood preparations (2 mL) were placed in an artificial membrane-closed glass tube that was then placed on the plastic unit as the food source. Feeding units were incubated (38°C and 60% RH) for 10 days. Test and negative-control-blood preparations were freshly prepared and exchanged (on days 1, 3, 5, and 8) to permit continuous flea feeding. Fleas were transferred into fresh plastic units on days 5 and 8 to facilitate egg collection. Collected eggs were mixed with flea nourishment medium and incubated (28°C and 80% RH) in darkness for 22 (±3) days to enable flea development. Parameters recorded were flea survival, oviposition control, egg hatchability, pupa control and flea-emergence control.

In vivo study to assess flea-control efficacy in a simulated home environment

Twenty healthy male and female mixed breed dogs ≥12 weeks old were housed in individual pens. Ten dogs per group were randomly assigned to receive either a fluralaner chewable tablet (Bravecto™) or no treatment. Each pen contained the bottom half of a dog carrier lined with carpet as bedding. Before treatment, each dog was infested twice, (28 and 21 days pre-treatment) with 100 adult, unfed C. felis to establish a flea population prior to treatment on each dog. Flea media was added to the carpet four weeks before the treatment date and weekly thereafter for the remainder of the study to encourage development of an active, developing population of juvenile flea stages in each pen. On the treatment day, dogs in the treated group received fluralaner at a dose close to 25 mg/kg body weight by oral administration of one or more flavored chewable tablets. The chewable tablet(s) were administered by placement in the back of the oral cavity over the tongue to initiate swallowing. Dogs in the negative-control group remained untreated.

Flea counts were performed on all dogs 1 day before treatment, 1 day after treatment and then every 7 days until completion of the study 84 days later. All live fleas recovered were held and re-infested on the dog after the comb count was completed. Each dog was also infested with 50 newly emerged unfed adult fleas on days 22, 50 and 78 to simulate natural infestation post-treatment.

Statistical analysis

The individual dog was the experimental unit and data from each flea-count time point were analyzed separately. Flea-count data were transformed [Y = loge(x + 1)] and analyzed by a mixed linear model including treatment as the fixed effect and block as the random effect. Kenward-Rogers adjustment was used to determine the denominator degree of freedom. A two-tailed F-test was used within the mixed linear model for the comparison between treatment groups and statistical significance was declared when P ≤ 0.05. SAS version 9.3 was the primary software used for analysis.

Efficacy was calculated using arithmetic and geometric means with Abbott’s formula:

Efficacy (%) = 100 × (MC - MT)/MC, where MC was the arithmetic or geometric mean number of total adult live fleas on untreated dogs and MT the arithmetic or geometric mean number of total adult live fleas on treated dogs.

The study was conducted in California, USA in compliance with the Animal Welfare Act as overseen by the United States Department of Agriculture (USDA) and ethical approval was obtained before the start. The study was approved by the Institutional Animal Care and Use Committee (IACUC no. S11453-00).

Results

Impact on flea reproduction after in vitro membrane-feeding exposure

Feeding exposure to concentrations of 50 ng fluralaner/mL resulted in a flea survival of 78.1% (day 2), 20.0% (day 3), 8.7% (day 4) and 1.2% (day 5). At 25 ng/mL flea survival rates were 90.6% (day 2), 67.5% (day 3), 31.9% (day 4) and 11.3% (day 5). The flea survival rates increased at lower concentrations (Table 1). Concentrations of 50 and 25 ng fluralaner/mL achieved complete control of oviposition (100%), because fleas that survived 4 to 5 days of feeding at these concentrations did not produce any eggs. At lower concentrations of 12.5 and 6.25 ng fluralaner/mL, the oviposition was controlled by 99.6% and 80.6%, respectively (Table 2). Fluralaner did not affect the hatching of larvae, as hatch was observed in almost all flea groups that were able to lay eggs (Table 3). The pupal development was strongly reduced (85.1% at 12.5 ng fluralaner/mL, 88.7% at 6.25 ng fluralaner/mL) indicating that fluralaner exposure has a potent larvicidal effect (Table 4). The same effect continued through to 100% control of adult emergence at 12.5 ng fluralaner/mL (Table 5).

Table 1 Flea survival after feeding on blood containing fluralaner at sub-insecticidal concentrations
Full size table
Table 2 Flea oviposition control after feeding on blood containing fluralaner at sub-insecticidal concentrations
Full size table
Table 3 Flea larvae emergence from eggs of parent fleas fed on blood containing fluralaner at sub-insecticidal concentrations
Full size table
Table 4 Pupal development control from eggs of parent fleas fed on blood containing fluralaner at sub-insecticidal concentrations
Full size table
Table 5 Adult flea emergence control after parent fleas fed on blood containing fluralaner at sub-insectcidal concentrations
Full size table

In vivo flea-control efficacy in a simulated home environment

No adverse events were observed in any fluralaner (Bravecto™) treated dog following administration. Mean flea counts (arithmetic/geometric) on untreated-control dogs were 52.3/26.4 fleas before the day of treatment (day -1) and in the range of 5.1/1.8 to 57.1/40.6 fleas following treatment. Mean flea counts (arithmetic/geometric) on fluralaner-treated dogs were 35.0/14.1 fleas before treatment, 0/0 fleas on days 1, 7, 14, 21, 28, 35, 42, 63, 77 and 84, and 0.1/0.1 fleas on days 49, 56, and 70 after treatment. Compared to control, these counts were significantly different (P ≤0.021) on all post-treatment count days. Calculated efficacy results were either 100% or very close to 100% at all post-treatment time points (Table 6).

Table 6 Flea-control efficacy on treated dogs (25 mg fluranaler/kg body weight) compared with untreated dogs in a simulated home environment
Full size table

Discussion

Fluralaner has potent inhibitory effects on C. felis fleas as demonstrated in the aforementioned in vitro and in vivo experiments. The control of flea reproduction prevents the formation of a flea population within a household. In addition to a field study that showed fluralaner (Bravecto™) to be effective against fleas on dogs for 12 weeks [5], an in vitro study was performed to investigate the effect of fluralaner on flea reproduction using sub-insecticidal concentrations.

The fluralaner concentrations tested in this study were sufficiently low that fleas survived for 2 to 10 days. This survival duration allows for flea reproduction, as viable eggs can be produced 24 hours after fleas start feeding. Fluralaner concentrations tested correlated with the effects on the reproduction cycle. 50 to 25 ng fluralaner/mL effectively controlled the oviposition (egg laying), and 12.5 to 6.25 ng/mL largely reduced the pupal development (indicating a strong larvicidal effect). Overall, sub-insecticidal concentrations as low as 12.5 ng fluralaner/mL achieved 100% cessation of flea reproduction, illustrating that fluralaner provides dog owners’ with additional protection against re-infestation of their pets in the home environment.

The potent in vitro effects on flea reproduction substantiate the results of the in vivo study where dogs were treated with oral fluralaner (Bravecto™) compared to untreated-control dogs in a simulated home environment. The environment was created by allowing the dogs access to a carpeted bedding area and heavy flea-challenges during the month preceding the fluralaner treatment. This resulted in an environment with a thriving flea population including all developmental stages before treatment administration, leading to an increased flea burden on untreated-control dogs throughout the study duration. Thus, fleas were permanently present on control dogs during the study, however, some variability was observed in flea numbers although the study design should have provided a high flea burden on controls at all assessment times. Following treatment, the flea populations were effectively controlled on the fluralaner (Bravecto™) -treated dogs, with efficacy at, or near, 100% throughout the 12-week post-treatment period.

The long-lasting adulticidal activity of fluralaner (Bravecto™) provides two benefits with respect to flea control: first, it prevents a sustainable re-infestation of dogs by offspring from the environment, and second, it prevents new flea eggs from being added to the environment as female fleas are killed within 8 hours (before they produce eggs) [9]. Both effects lead to the depletion of the environmental flea population. The studies described here indicate that fluralaner’s flea-control capabilities combine an adulticidal effect with long-term efficacy and, additionally, effective prevention of flea reproduction. This is an advantage over pure adulticides which are often combined with an insect-growth regulator (IGR) to provide the same effect.

Highly effective control of environmental flea populations has been recorded with topically applied insecticides [7], but is not reliably achieved with previously evaluated systemically administered insecticides [10]. Taken together the results of both the in vitro and in vivo studies support the claims of fluralaner’s effective flea control properties. In addition to the fast flea killing effect within 8 hours [9] the studies indicate that fluralaner, a systemic flea treatment, is successful in controlling developing flea populations in the environment.

The efficacy of monthly treatments is dependent on dog owner compliance. It has recently been shown that owner compliance with monthly re-treatment recommendations is weak [11] which may jeopardize flea control. The results reported here provide evidence that a single systemic fluralaner treatment (Bravecto™) provides 12 weeks of flea-population control and is a valuable new tool for achieving effective and long-term flea control for dogs and their homes.

Conclusions

Fluralaner is a potent inhibitor of flea reproduction at various developmental stages and at exposure levels that are far below its immediate insecticidal activity. Thus, fluralaner treatment disrupts the flea-breeding cycle and protects dogs and their homes from flea infestations over a 12-week period without additional premise treatment.