- Open Access
Effectiveness and residual speed of flea kill of a novel spot on formulation of spinetoram (Cheristin®) for cats
Parasites & Vectors volume 10, Article number: 59 (2017)
A spot-on spinetoram formulation (Cheristin®) was developed to eliminate fleas from infested cats. This paper describes three spinetoram studies: two for registration (Studies 1 and 2), and one comparing residual speed of kill (SOK) with topically applied fipronil/(S)-methoprene (FSM) and imidacloprid (Study 3).
Cats were randomized to treatment based on flea counts from infestations placed within 2 weeks prior to treatment. In Studies 1 and 2, groups were untreated control and spinetoram; in Study 3, groups were untreated control, spinetoram, FSM and imidacloprid, all applied per label on Day 0. Cats were infested the day before treatment. In Studies 1 and 2, counts were completed 48 h post-treatment and after weekly challenges through 5 weeks. In Study 3, infestations were completed weekly through Day 28, with counts 1, 4, 8 and 12 h after treatment or post-infestation (PI). Efficacy was determined on geometric mean flea count reductions compared with controls, and in Study 3 mean flea counts in spinetoram-groups were compared with those in FSM and imidacloprid groups.
In Studies 1 and 2, spinetoram effectiveness was 100% against existing infestations, and at least 96% through Day 37. In Study 3 mean counts were not significantly different from controls in any group until 8 h post-treatment when imidacloprid counts were significantly lower than spinetoram counts, which were in turn significantly lower than FSM counts (P < 0.05). At 1 h PI spinetoram-group counts were significantly lower (P < 0.05) than counts in: controls, all days; imidacloprid, Days 7, 14, and 28; FSM, Days 14 and 28. At 4 h PI, spinetoram mean counts were significantly lower (P < 0.05) relative to: controls, all days; imidacloprid, Days 7, 14 and 21; FSM, Days 7, 14, 21 and 28 (P < 0.05). On multiple occasions, at 8 and 12 h PI, mean counts were significantly lower (P < 0.05) for spinetoram than for imidacloprid and FSM; at no point were FSM or imidacloprid significantly more effective than spinetoram against new infestations. All treatments were well tolerated.
Spinetoram was highly effective for at least 1 month post-treatment and provided more rapid month-long residual SOK than FSM or imidacloprid.
The spinosyns are a family of insecticidal fermentation products, derived from the actinomycete, Saccharopolyspora spinosa. These compounds exert their selective activity against insects primarily by allosterically activating nicotinic acetylcholine receptors (nAChRs), binding at receptor sites distinct from those at which other insecticides exert their activity. Some activity is also provided by spinosyns binding to γ-amino-butyric acid (GABA) receptors with an overall effect that leads to rapid insect paralysis and death [1–3]. The first of these compounds to be used to treat ectoparasitic infestations of animals was spinosad, which in different countries has approvals for use in or on cattle, sheep, dogs and cats, and also as a head lice treatment for humans.
The large and complex chemical structure of the spinosyns presented opportunities for modifications to enhance their chemical properties and biological activity. The outcome of the application of artificial neural networks to quantitative structure activity relationships was the discovery of spinetoram, a mixture of major (3’-ethoxy-5,6-dihydro spinetoram J) and minor (3’-ethoxy spinetoram L) components. Testing in agriculture systems demonstrated that spinetoram maintained the exceptional environmental and toxicological profile already established for the spinosyn class of chemistry . Like spinosad some years beforehand, spinetoram received the United States Presidential Green Chemistry award for 2008 (Environmental Protection Agency).
Anecdotal reports of the unreliable effectiveness of common topically applied products for cats were substantiated in a study in which three consecutive monthly treatments of client-owned cats with fipronil produced only a 46.1% reduction from baseline in geometric mean flea counts. In that study, an early formulation of spinetoram administered according to the same schedule produced geometric mean flea count reductions of 99.4% . Although that 39.6% w/v formulation of spinetoram was non-irritant, some field reports were received of focal hair loss from the application site in a small percentage of treated cats. This problem was attributed to the high viscosity of the formulation and so a formulation with a lower concentration and viscosity was developed . Preliminary laboratory effectiveness studies were completed, and tolerability studies in client-owned cats demonstrated the acceptability and safety of an 11.2% formulation (unpublished observations).
This report describes three studies undertaken to determine the effectiveness of this 11.2% spinetoram spot-on formulation (Cheristin®, Elanco, Greenfield, IN) against fleas on cats. Two studies (Studies 1 and 2) determined effectiveness when flea (Ctenocephalides felis) counts were completed at 48 h post-treatment, and at 48 h post-infestations applied over the 5 weeks after treatment. Study 3 focused on the residual speed of kill of spinetoram compared with that provided by imidacloprid (Advantage® II, Bayer Animal Health, Overland Park, KS) and by fipronil/(S)-methoprene (Frontline® Plus, Merial, Atlanta, GA).
Design of studies
All studies were controlled and utilized a blinded, randomized complete block design with pre-treatment live flea counts as a blocking factor. All protocols were approved by the relevant Institutional Animal Care and Use Committees. Uniquely identified domestic short-hair/cross bred cats, at least 7 months of age and weighing between 2.2 and 6.6 kg were acclimated in the trial facility for at least 14 days before the study began, and throughout each study cats were maintained in separate individual cages. Pre-treatment flea challenges (approximately 100 fleas per cat) and subsequent flea comb counts 48 h post-challenge were made at least once in each study, from 9 days to 7 days prior to treatment. These counts were used to verify that cats selected for the study would carry a burden of at least 30 adult fleas.
Cats meeting the inclusion/exclusion criteria with the highest counts were rank-ordered from highest to lowest. Blocks were formed by assigning the appropriate number of cats, based on the number of treatment groups, with the highest C. felis counts to the first block, the same number of cats with the next highest counts to the second block, and so on until the protocol-designated number of blocks was defined. Treatments were randomly assigned to cats within each block. Cats were housed individually in indoor stainless-steel cages. Treated cats were not housed over control cats, or over other treatment group cats where banks of cages (top/bottom arrangement) were used. In all three studies, the primary objective was the percent reduction in geometric mean live flea counts in treated groups when compared with counts from untreated or sham-treated control cats.
Treatments and groups
In all studies, treatments were administered once, on Day 0. In Studies 1 and 2 there were 8 cats per group, and in Study 3 six cats per group for each assessment point.
In Studies 1 and 2 cats were randomized among two treatment groups: Group 1: sham-treated topically with product vehicle without active ingredient (negative control); and Group 2: treated topically with the spinetoram 11.2% formulation (Cheristin).
In Study 3, 96 cats were randomized among four treatment groups, with three groups to receive commercially available formulations of topically applied products, all administered according to label: Group 1: Spinetoram 11.2% (Cheristin; Elanco); Group 2: Fipronil 9.8% w/v and (S)-methoprene 11.8% w/v (Frontline Plus for Cats); Group 3: Imidacloprid 9.1% w/v and pyriproxyfen 0.46% (Advantage II); Group 4: Untreated control.
Each treatment group was subdivided into 4 sub-groups, each of six cats, formed by ranking on the basis of Day -7 flea counts and randomizing to times of flea counts following treatment and after each subsequent flea infestation.
Flea infestations and counts
In all studies flea infestations were completed on Day -1, and then at weekly intervals from Days 7 to 28. In Studies 1 and 2 an additional infestation was completed on Day 35.
In Studies 1 and 2, flea counts were completed 48 h post-treatment and 48 h after each subsequent infestation. In Study 3, flea counts were completed 1, 4, 8 and 12 h after treatment and after each post-treatment infestation on Days 7, 14, 21 and 28. In all 3 studies, fleas removed during each flea count time point were not put back onto the cats. The effectiveness calculation for each product was based on reductions in mean live flea counts at 1, 4, 8 and 12 h after treatment or after subsequent infestations compared to mean live flea counts in untreated control cats infested according to the same schedule.
All flea infestations were completed using each facility’s in-house flea colonies which are periodically refreshed by the introduction of locally caught fleas. The infestation procedure involved placement of approximately 100 unfed, adult cat fleas onto each cat’s dorsum from the nuchal crest or shoulder area to the lumbar-sacral region, with the cat gently restrained in a standing or sternal recumbency position. Post-treatment infestations were made to avoid placing fleas near the area of highest insecticidal concentration. Live flea counts on each cat were obtained by thorough combing using a metal flea comb for a minimum of 5 min. If no fleas were found in this time, an additional 10 strokes of the flea comb were performed over each area of the body - dorsal, ventral, legs and thorax. If a flea was recovered, the 10-stroke routine was repeated until no fleas were recovered in any area. Care was taken to avoid the site of test substance application during the first 24 h after treatment. Combs were cleaned with alcohol after each use, and combs used for cats in the same treatment group were not used on cats in other treatment groups.
Geometric mean counts were used to assess the primary objective of reductions in flea counts when treated groups were compared to controls. Percent efficacy at each time point was calculated using the formula:
Logarithmic transformation of flea counts was performed using the logarithm of flea count + 1 to account for zero values. Geometric mean values were obtained via back-transformation of transformed mean counts and subtracting one. Arithmetic means were also calculated.
For each time point, repeated measures analysis of variance was generated. The model included treatment group, study day and treatment group by study day interaction as fixed effects and case id as a random effect. The percent reduction compared to control was obtained from the least squares means of each model. Pairwise comparisons between all treatment groups was also obtained from these models. Primary objective assessments were based on geometric mean count reductions.
All treatments were well tolerated in each study and, other than for occasional mild and transient cosmetic changes typical of products applied topically to cats (e.g. hair clumping), there were no treatment-related adverse events. Post-treatment application-site observations indicated that any wetness and/or hair clumping in spinetoram-treated cats on the day of, or the day after treatment had disappeared during the following days.
In Studies 1 and 2, when flea counts were completed 48 h post-treatment and after each subsequent infestation, the percentage effectiveness was 100% against infestations present at the time of treatment, with at least 96% effectiveness based on geometric mean counts maintained through Day 37 (Tables 1 and 2; Fig. 1). The least squares mean differences between the transformed flea counts in the treated and control groups were statistically significant (P < 0.0001) for each study day.
In Study 3, the comparative speed of flea kill study, no product demonstrated significant reductions from the control group in mean flea counts at 1 and 4 h post- treatment (Day 0) (Tables 3 and 4). At the 1-h post-infestation time point only the spinetoram group showed a significant reduction from controls on Day 7 (t-test: t (80) = -3.03, P = 0.0033), when mean flea counts were significantly lower than in the imidacloprid group (t-test: t (80) = -2.06, P = 0.0428) (Table 3). At this 1-h time point the spinetoram group also had significantly lower mean counts than the imidacloprid group on Days 14 (t-test: t (80) = -5.19, P < 0.0001), and 28 (t-test: t (80) = -3.64, P = 0.0005), and the fipronil/(S)-methoprene group on Days 14 (t-test: t (80) = -3.85, P = 0.0002), 21 (t-test: t (80) = -3.01, P = 0.0035) and 28 (t-test: t (80) = -2.58, P = 0.0116). At 4 h post-infestation, spinetoram provided significantly greater effectiveness than imidacloprid on Days 7 (t-test: t (80) = -2.93, P = 0.0044), 14 (t-test: t (80) = -2.10, P = 0.0388) and 21 (t-test: t (80) = -3.21, P 0.0019) and fipronil/(S)-methoprene on Days 7 (t-test: t (80) = -5.83, P < 0.0001), 14 (t-test: t (80) = -6.18, P < 0.0001), 21 (t-test: t (80) = -5.54, P < 0.0001) and 28 (t-test: t (80) = -2.76, P = 0.0072) (Table 4).
At 8 h post-treatment, only the fipronil/(S)-methoprene group failed to achieve significant reductions in mean flea counts from the control group. Mean counts in the spinetoram group were significantly lower (P < 0.05) than in the fipronil/(S)-methoprene group but significantly higher (P < 0.05) than in the imidacloprid group (Table 5). For all counts completed 8 h after each infestation timepoint, mean flea burdens in the spinetoram group were significantly lower than in the control group (Day 7: t-test: t (80) = -5.60, P < 0.0001; Day 14: t (80) = -8.62, P < 0.0001; Day 21: t (80) = -5.58, P < 0.0001; Day 28: t (80) = -4.36, P < 0.0001) and significantly lower than in the fipronil/(S)-methoprene group on Days 7 (t-test: t (80) = -2.61, P = 0.0108), 14 (t-test: t (80) = -4.37, P < 0.0001) and 28 (t-test: t (80) = -2.52, P = 0.0138).
At 12 h post-treatment and on all days post-infestation, flea counts in all treated groups were significantly lower than those of the control groups. At 12 h post-treatment, mean flea counts in the imidacloprid and fipronil/(S)-methoprene groups were significantly lower than those of the spinetoram group (t-test: t (80) = 2.29, P = 0.0245 and t (80) = 2.19, P = 0.0315, respectively) (Table 6). At 12 h post-infestation mean flea counts in the spinetoram group were significantly lower than in the imidacloprid group on Days 7 (t-test: t (80) = -2.55, P = 0.0126) and 21 (t-test: t (80) = -3.21, P = 0.0019), and significantly lower than the fipronil/(S)-methoprene group on Day 21 (t-test: t (80) = -2.49, P = 0.0148).
At no post-treatment time point was the residual speed of kill of fipronil/(S)-methoprene or imidacloprid significantly greater than that of spinetoram against new flea infestations. Percent effectiveness for spinetoram was greater than for fipronil/(S)-methoprene or imidacloprid at multiple post-treatment timepoints.
As a combination of two semi-synthetic spinosyns (spinosyns J and L), spinetoram shares a common fermentation background and mode of action with spinosad, a mixture of spinosyns A and D. Spinosad delivered orally to dogs has been shown in laboratory flea infestation studies to have a rapid onset of activity that is sustained over a month following treatment [7–9]. This effectiveness has translated to high levels of flea control on dogs under field conditions in which monthly treatment with spinosad provided significant improvement in flea control and in signs of FAD, including owner-scored pruritus, when compared with other topically applied products [5, 9–11]. Similar findings have been reported for an oral formulation of spinosad administered to client-owned cats . The results of the studies presented in this paper validate the potential value that a single topical application of 0.7 ml of this spinetoram formulation can bring to flea control in cats.
The two registration studies reported here, in which counts were completed 48 h after treatment and after each new infestation, demonstrated that spinetoram eliminated virtually all (98 to 100%) fleas through the month following treatment, with efficacy of 96.0 to 97.9% still apparent 5 weeks after treatment. However, flea egg production may begin within 24 to 36 h of the first blood meal, with 25% of fleas having fed within 5 min of finding a feline host and 97% within 1 h [13, 14]. Thus while the 48-h count can demonstrate the potential value of reducing egg output, and with repeated monthly treatments potentially solve the long term flea infestation problem in a local environment, a faster speed of kill is desirable to accelerate the epidemiological cure, to alleviate the irritation caused by flea bites and to reduce the risk of transmission of the cestode, Dipylidium caninum, and disease causing organisms such as Bartonella henselae.
Given the excellent speed of kill that orally administered spinosad has demonstrated in laboratory studies by killing more than 50% of fleas infesting dogs within 1 h and achieving 100% efficacy within 4 h of treatment, it had been anticipated that the similarly acting spinetoram applied topically to cats would match this rapid onset of effectiveness . In fact, none of the topical products in this study achieved such a rapid onset of efficacy, and only imidacloprid and spinetoram showed significant differences from control at 8 h post-treatment. It would therefore seem that an interval of 12 to 24 h after treatment may be needed for topical products to achieve complete effectiveness against flea burdens present on cats at the time of treatment, and that systemically acting products may have a more rapid onset of activity. Support for this is provided in a report in which systemically acting products, by more effectively reducing the amount of blood fleas consume before dying, appeared to affect fleas infesting cats more quickly than treatments that act topically .
There are two possible explanations, not necessarily mutually exclusive, for the speed of flea knockdown of topical products to be quicker against new infestations than against flea burdens already established at the time of treatment. First, fleas that have established on the cat, having already taken a blood meal, may be more robust and so do not succumb as quickly to contact insecticidal activity. Secondly, topically applied products may require some amount of time to disperse from the site of application to ensure that fleas are exposed to lethal concentrations that will provide a rapid residual speed of kill. Importantly, the results of this study demonstrate that the residual speed of flea kill of spinetoram, applied topically, was at least equal to and at multiple times greater than that of fipronil/(S)-methoprene or imidacloprid for at least 4 weeks following application.
In conclusion, the results of the three studies reported here show that this 11.2% spot-on formulation of spinetoram provides a high level of flea killing effectiveness that lasts beyond 1 month, and that a rapid speed of flea kill is maintained through at least 1 month. The rapid month-long residual speed of kill was more sustained for spinetoram than for fipronil/(S)-methoprene or imidacloprid, and demonstrates that this novel spinetoram formulation addresses the need for rapidly acting products that can substantially and quickly help to reduce irritation arising from flea bites, and break the flea life cycle by killing fleas before egg laying can begin.
Speed of kill
Insecticide Resistance Action Committee. 2016. URL http://www.irac-online.org/modes-of-action/. Accessed 26 Jan 2017.
Salgado VL. Studies on the mode of action of spinosad: insect symptoms and physiological correlates. J Pest Biochem Physiol. 1998;60:91–102.
Sparks TC, Crouse GD, Durst G. Natural products as insecticides: the biology, biochemistry and quantitative structure-activity relationships of spinosyns and spinosoids. Pest Manag Sci. 2001;57:896–905.
Sparks TC, Crouse GD, Dripps JE, Anzeveno P, Martynow J, Deamicis CV, Gifford J. Neural network-based QSAR and insecticide discovery: spinetoram. J Comput Aided Mol Des. 2008;22:393–401.
Dryden MW, Ryan WG, Bell M, Rumschlag AJ, Young LM, Snyder DE. Assessment of owner-administered monthly treatments with oral spinosad or topical spot-on fipronil/(S)-methoprene in controlling fleas and associated pruritus in dogs. Vet Parasitol. 2013;191:340–6.
Credille KM, Thompson LA, Young LM, Meyer JA, Winkle JR. Evaluation of hair loss in cats occurring after treatment with a topical flea control product. Vet Dermatol. 2013;24:602–5.
Snyder DE, Meyer J, Zimmermann AG, Qiao M, Gissendanner SJ, Cruthers LR, et al. Preliminary studies on the effectiveness of the novel pulicide, spinosad, for the treatment and control of fleas on dogs. Vet Parasitol. 2007;150:345–51.
Blagburn BL, Young DR, Moran C, Meyer JA, Leigh-Heffron A, Paarlberg T, et al. Effects of orally administered spinosad (Comfortis) in dogs on adult and immature stages of the cat flea (Ctenocephalides felis). Vet Parasitol. 2010;168:312–7.
Snyder DE, Rumschlag AJ, Young LM, Ryan WG. Speed of flea knockdown of spinosad compared to afoxolaner, and of spinosad through 28 days post-treatment in controlled laboratory studies. Parasit Vectors. 2015;8:578.
Robertson-Plouch C, Baker KA, Hozak RR, Zimmermann AG, Parks SC, Herr C, et al. Clinical field study of the safety and efficacy of spinosad chewable tablets for controlling fleas on dogs. Vet Ther. 2008;9:26–36.
Wolken S, Franc M, Bouhsira E, Wiseman S, Hayes B, Schnitzler B, Jacobs DE. Evaluation of spinosad for the oral treatment and control of flea infestations on dogs in Europe. Vet Rec. 2012;170:99–103.
Paarlberg TE, Wiseman S, Trout CM, Kee EA, Snyder DE. Safety and efficacy of spinosad chewable tablets for treatment of flea infestations of cats. J Am Vet Med Assoc. 2013;242:1092–8.
Cadiergues MC, Hourcq B, Cantaloube B, Franc M. First blood meal of Ctenocephalides felis felis (Siphonaptera: Pulicidae) on cats: Time to initiation and duration of feeding. J Med Entomol. 2000;37:634–6.
Dryden MW. Host association, on-host longevity and egg production of Ctenocephalides felis felis. Vet Parasitol. 1989;34:117–22.
McCoy C, Broce AB, Dryden MW. Flea blood feeding patterns in cats treated with oral nitenpyram and the topical insecticides imidacloprid, fipronil and selamectin. Vet Parasitol. 2008;156:293–301.
The authors acknowledge Drs. David Young of Young Veterinary Research Services and William Russell Everett of BerTek Inc for their contribution in acquiring data for these studies, and Dr Caryn M. Thompson of Elanco and Ms Margie Bell for their statistical analyses.
All studies were funded by Elanco.
Availability of data and materials
The datasets supporting the conclusions of this article are included within the article.
All authors participated in the design and completion of at least one of the reported studies and were involved in drafting of the manuscript. All authors read and approved the final manuscript.
Drs. Snyder, Rumschlag and Young and Ms. Paarlberg are all employees of Elanco. Dr. Ryan acted as a paid advisor for Elanco in the design and completion of the speed of kill study and manuscript.
Consent for publication
All protocols were approved by the study site Institutional Animal Care and Use Committees.
About this article
Cite this article
Paarlberg, T., Winkle, J., Rumschlag, A.J. et al. Effectiveness and residual speed of flea kill of a novel spot on formulation of spinetoram (Cheristin®) for cats. Parasites Vectors 10, 59 (2017). https://doi.org/10.1186/s13071-017-1996-9