Efficacy of spinosad against the poultry red mite, Dermanyssus gallinae (Mesostigmata: Dermanyssidae), in laboratory and field trials*

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Zoosymposia 6: 282 287 (2011) www.mapress.com/zoosymposia/ Copyright 2011. Magnolia Press ISSN 1178-9905 (print edition) ZOOSYMPOSIA ISSN 1178-9913 (online edition) Efficacy of spinosad against the poultry red mite, Dermanyssus gallinae (Mesostigmata: Dermanyssidae), in laboratory and field trials* GABRIELE LIEBISCH, RICHARD HACK & GOSSE SMID Laboratorium für klinische Diagnostik ZeckLab, Up n Kampe 3, D-30938, Germany * In: Moraes, G.J. de & Proctor, H. (eds) Acarology XIII: Proceedings of the International Congress. Zoosymposia, 6, 1 304. Abstract The poultry red mite, Dermanyssus gallinae (De Geer), is the most economically important ectoparasite in poultry houses in many countries around the world. The lack of efficacy of commercial products in its control results from poor application and/or from its resistance to active ingredients. A new insecticide, spinosad, was tested against mobile stages of the red mite in laboratory and field populations. Laboratory trials showed increasing efficacy five days (adults) and six days (nymphs) after exposure. Laboratory results were confirmed in a field trial conducted under commercial conditions. The trial was conducted in three separate houses on farms with high natural mite populations. The first and second houses were sprayed with concentrations of 2,000 and 4,000 ppm of spinosad (2 and 4 g/l), whereas the third house was used as an untreated control. Spraying was conducted using a sprayer (Stadikopumpe VAAR 252-200 LE, Dinklage, Germany) with a 200 L reservoir with permanent stirring, a 50 m long flexible tube with a double jet system, and jet size of 0.08 mm. The pressure used was 6 10 bar. Sampling was conducted immediately before the application and once a week for 56 days in the first house and 93 days in the second. In the first house, almost 100% reduction in mite numbers was observed until 28 days post treatment; 74.3% reduction was observed 49 days after treatment. In the second house, rates of reduction were higher than 90% until day 77. The untreated control house maintained high red mite infestations throughout the experimental period. The results showed effective control of all mobile stages of D. gallinae with spinosad. Key words: Red Mite, Dermanyssus gallinae, control, spinosad, elector. Introduction The poultry red mite, Dermanyssus gallinae (De Geer) (Acari: Mesostigmata), is a parasite with wide host-range, including wild and domestic birds. It is known from 30 bird and 10 mammal species (Moss, 1968). The most commonly recorded hosts are the domestic fowl (Gallus gallus), turkey (Meleagris gallopavo), duck (Anas platyrhynchos), pigeon (Columba livia), house sparrow (Passer domesticus), starling (Sturnus vulgaris) and canary (Serinus canarius) (Evans & Till, 1966). In the absence of birds, D. gallinae will also attack mammals such as rodents, dogs, cats, horses, as well as humans (Evans & Till, 1966; Brockis, 1980; Hoffmann, 1987). The nocturnal feeding behaviour of D. gallinae disturbs the sleep of birds, leading to irritation and apathy. Being able to ingest relatively large amounts of blood, it often causes anaemia and even death of the host (Kirkwood, 1967; Urquhart et al., 1996), resulting in major decrease in egg production (Jungmann et al., 1970). Dermanyssus gallinae is a potential vector of the causal agents of several viral diseases, such as Equine Encephalitis (Sulkin et al., 1955, Zeman et al., 1982, Durden et al., 1993) and St. Louis Encephalitis (Smith et al., 1947). It can be a vector of bacteria such as Salmonella spp. (Valiente Moro et al., 2007), Mycobacterium spp. and Erysipelothrix rhusiopathiae (Brooke & Riley, 1999; De Luna et al., 2008; Chirico et al., 2003). It is also known to cause itching dermatosis in humans (Baselga et al., 1996). The most frequently used acaricides against D. gallinae are organophosphates, carbamates and pyrethroids. Organophosphates and carbamates are toxic to arthropods and mammals by virtue of 282 Accepted by G. J. de Moraes: 30 Jul. 2011; Published: 20 Dec. 2011

their ability to inactivate the enzyme acetylcholinesterase (Fukuto, 1990). Pyrethroids are neurotoxins, interacting with the sodium channel in the cell membrane (Salish, 1989). Organic farmers commonly use non-chemical methods, as chalk spraying of the walls and ceiling, to combat this mite. Other options involve mite desiccation with sorptive dusts (Kirkwood, 1974; Maurer & Perler, 2006; Saucke, 1998). The effect of entomopathogenic fungi is another approach under investigation (Steenberg & Kilpinen, 2003). There are reports of D. gallinae resistance to permethrin and organophosphates (Murphy et al., 2002; Beugnet et al., 1997; Liebisch & Liebisch, 1998, 2001a, b). In order to prevent the development of resistance, groups of acaricides are suggested to be used in rotation (Chauve, 1998). Spinosad is a new compound shown to be potentially effective against insects. This compound corresponds to a fermented product of the bacterium Saccharopolyspora spinosa (Mertz & Yao, 1990). The formulation of this compound contains a mixture of two of the most active metabolites, designated as spinosyn A and spinosyn D. In insects, the mode of action of spinosad is associated with excitation of the nervous system (Salgado, 1998), altering the function of nicotinic and GABA-gated ion channels, in a manner consistent with that observed in neuronal excitation. Spinosad does not interact with known binding sites for other nicotinic or GABAergic insecticides. The objective of this research was to evaluate the efficacy of spinosad for controlling D. gallinae under laboratory and field conditions. Materials and Methods Laboratory trials The adopted experimental procedure for engorged nymphs and adults corresponded to the Mite-Package-Test (MPT), an adaptation of the Larval-Package-Test used to test resistance of the tick Rhipicephalus (Boophilus) microplus (Canestrini), Ixodidae (Stone & Haydock, 1962; Anonymous, 1971). The experimental unit for this procedure consisted of a bag made with a piece of filter paper (10 x 7.5 cm). The paper was folded across its mid length and then closed tightly along the margins, leaving the top open. For each test, 100 nymphs or adults of D. gallinae were placed in the bag through the open top. A total of 10 ml spinosad solution was then sprayed in the bag with a 10 ml bottle sprayer (Köhler, Art. No. 5024001, OMNILAB, Munich, Germany); two concentrations (2 and 4 g/l) of Elector (480 g of spinosad/l, Elanco Animal Health), corresponding to 2,000 and 4,000 ppm, were used. The top of the bag was then closed with clips and placed onto a floating platform inside a bowl with water plus detergent, to prevent the mites from escaping. The test with adults had three replicates and a 5-day exposure period, while the test with nymphs had two replicates and a 6-day exposure period. At the end of each exposure period, the numbers of mites that were live and apparently healthy, moribund or dead were counted under a stereomicroscope. Response data of adults to spinosad were subjected to ANOVA. Field trials The study was conducted in two poultry layer houses of a commercial facility, where spinosad was applied; a third layer house in a different commercial facility was used as an untreated control. The first two houses were located in Immensen and the third in Lindhorst (Germany); the study was conducted between July and November 2009. The houses were of the aviary style or cage free birds, each 8.5 x 10.5 m in the first facility and 6.0 x 12.0 m in the second. Spinosad was applied once using a commercial application equipment (Stadikopumpe VA AR 252-200 LE, Dinklage, Germany) having a 200 L reservoir with stirring, a 50 m flexible tube with a double jet system, and jet size of 0.08 mm. The concentrations used were 2g/L in the first house and 4 g/l EFFICACY OF SPINOSAD AGAINST THE POULTRY RED MITE Zoosymposia 6 2011 Magnolia Press 283

FIGURE 1. Lower surface of feeding racks with aggregations of Dermanyssus gallinae. in the second house. The pressure used was 6 10 bar. A total of 140 liters of solution was sprayed in each house. Efficacy evaluations were done weekly over a period of 56 days after treatment in the first house and 93 days after treatment in the second. For such, a sample of substrate was randomly taken from each of ten points from throughout each of the three houses immediately before the application of spinosad and every seven days afterwards. Each sample consisted of mites and debris collected from an area of approximately 10 x 10 cm at three locations (conveyer belt that carries the eggs, connecting sites and the lower surface of the feeding racks) (Fig. 1), with the help of a 2 cm wide paint brush. Each sample was transferred into a container which was then sealed and immediately taken to the lab. Mites of each sample were then separated from the debris under stereomicroscope. All mites from samples with apparently up to 1,000 mites were slide mounted in polyvinyl-lactophenol. In the case of samples containing more than 1,000 mites after a rough estimate, all mites were placed in a container with 100 ml of 70% alcohol and then an aliquot of 10 ml was taken to filter out all mites, which were mounted as previously indicated. All mites were counted and all mounted mites were identified. The efficacy of the treatments was calculated by Abbott s formula (Abbott, 1925). Results Laboratory trials The laboratory trials showed the efficacy of spinosad against nymphs and adults of D. gallinae at both concentrations. Average nymph mortalities, including dead and moribund mites, were very similar, namely 91.6 and 97.4% for concentrations of 2 and 4 g/l, respectively (Table 1). TABLE 1. Response to spinosad in engorged nymphs (6-day exposure period) and adults (5-day exposure period) of Dermanyssus gallinae under laboratory conditions. Nymphs Adults Treatment Total number % dead % (dead + Total number % dead % (dead + of mites moribund) of mites moribund) Spinosad 2 g/l 202 89.6 91.6 327 62.1 65.7 Spinosad 4 g/l 196 95.4 97.4 321 90.3 93.1 Control 194 3.1 3.1 335 2.4 2.4 284 Zoosymposia 6 2011 Magnolia Press LIEBISCH ET AL.

TABLE 2. Descriptive data analysis with ANOVA for trials with adults of Dermanyssus gallinae to spinosad. N Mean Standard Deviation Min Max Untreated 3 0.83865 0.48419 1.50 3.00 2 g/l 3 11.47519 6.62520 53.00 73.80 4 g/l 3 9.70000 5.60030 81.40 98.30 total 9 40.82870 13.60957 1.50 98.30 TABLE 3. Efficacy of spinosad against Dermanyssus gallinae (all mobile stages) after treatments of two poultry layer houses in farm Hattenbach (house 1 at 2 g of spinosad/l, house 2 at 4 g of spinosad/l) and farm Brunkhorst (untreated control). Total number of mites Days after (all mobile stages) Efficacy (%) treatment house 1 house 2 control house 1 house2 (2 g/l) (4 g/l) (2 g/l) (4 g/l) 0 12010 10260 12300 - - 7 241 71 15720 98.5 99.5 14 38 0 14980 99.7 100 21 263 1 8750 97.0 99.9 28 81 1 18749 99.6 99.9 35 1117 16 16880 93.4 99.9 42 2248 7 10800 79.2 99.9 49 3110 1 12090 74.3 99.9 56 10310 196 14080 26.8 98.6 63 n.c. 280 13870 n.c. 98.0 70 n.c. 444 6410 n.c. 93.1 77 n.c. 565 9450 n.c. 94.0 84 n.c. 3066 7090 n.c. 56.8 93 n.c. 11510 7560 n.c. 0 n.c. not counted Average adult mortality, also including dead and moribund mites, was 65.7 and 90.3% for concentrations of 2 and 4 g/l, respectively; in this case, statistical differences were observed between treatments (p= 0.0001), with no overlapping between ranges of mortality rates (Table 2). Field trials In the house sprayed with 2 g/l, almost 100% mite mortality was observed until 28 days post treatment; on day 49, reduction was 74.3% (Table 3). Mortality dropped to only 26.8% at this concentration on day 56, when monitoring was discontinued. In the house sprayed with 4 g/l, mortality was at least 93.1% up to day 77 post treatment, dropping to 56.8% on day 84 and no mortality on day 93, when monitoring was discontinued (Table 3). The untreated control house maintained high red mite infestations throughout the experimental period. Discussion The results showed that spinosad is effective against all mobile stages of the poultry red mite. The 4 g/l dose provided a greater reduction in mite numbers and for longer duration than the 2 g/l dose. Present issues in controlling D. gallinae are that there are no approved acaricide that can be used because of residues in meat and eggs. Carbamate, organophosphate and pyrethroid acaricides can only be used in the service period between flocks, when hens are absent from the houses. Another major issue is the high resistance against available acaricides. Therefore, it is important to find new substances to control this parasite. EFFICACY OF SPINOSAD AGAINST THE POULTRY RED MITE Zoosymposia 6 2011 Magnolia Press 285

Elector (spinosad) is registered in the Germany, UK, France and Italy for the control of the poultry red mite, darkling beetles (Alphitobius diaperinus) and house flies (Musca domestica). Registration is pending in other countries of Western Europe. Field evaluations have been conducted in all countries where it is registered as well as in the countries pending approvals, always with good results. References Abbott, W.S. (1925) A method of computing the effectiveness of an insecticide. Journal of Economic Entomology, 18, 265 267. Anonymous (1971) Recommended methods for the detection and measurement of resistance of agricultural pests to pesticides. Tentative method for larvae of cattle tick, Boophilus sp.. FAO Method No. 7, Plant Protection Bulletin, FAO 19, pp. 15. Baselga, E., Drolet, B.A. & Esterly, N.B. (1996) Avian mite dermatitis. Pediatrics, 97, 743 745. Beugnet, F., Chauve, C., Gauthey, M. & Beert, L. (1997) Resistance of the red poultry mite to pyrethroids in France. Veterinary Record, 140, 577 579. Brockis, D.C. (1980) Mite infestations. Veterinary Record, 107, 315 316. Brooke, C.J. & Riley, T.V. (1999) Erysipelothrix rhusiopathiae: bacteriology, epidemiology and clinical manifestations of an occupational pathogen. Journal of Medicine Microbiology, 48, 789 799. Chauve, C. (1998) The poultry red mite Dermanyssus gallinae (De Geer, 1778): current situation and future prospects for control. Veterinary Parasitology, 79, 239 245. Chirico, J., Eriksson, H., Fossum, O. & Jansson, D. (2003) The poultry red mite, Dermanyssus gallinae, a potential vector of Erysipelothrix rhusiopathiae causing erysipelas in hens. Medical and Veterinary Entomology, 17, 232 234. De Luna, C.J., Arkle, S., Chapman, P., Harrington, A.S., George, D.R., Guy, J.H. & Sparagano, O.A. (2008) The poultry red mite Dermanyssus gallinae as a potential carrier of vector-borne disease. Annals of the New York Academy of Sciences, 1149, 255 258. Durden, L.A., Linthicum, K.J. & Monath, T.P. (1993) Laboratory transmission of eastern equine encephalomyelitis virus to chickens by chicken mites (Acari: Dermanyssidae). Journal of Medical Entomology, 30, 281 285. Evans, G.O. & Till, W.M. (1966) Studies on the British Dermanyssidae (Acari: Mesostigmata). Part II, Classification. Bulletin of the British Museum (Natural History), 14, 109 370. Fukuto, T.R. (1990) Mechanism of action of organophosphorus and carbamate insecticides. Environmental Health Perspectives, 87, 245 254. Hoffmann, G. (1987) Vogelmilben als Lästlinge, Krankheitserzeuger und Vektoren bei Mensch und Nutztier. Deutsche Tierärztliche Woschenzeitschrift, 95, 7 10. Jungmann, R., Ribbeck, R., Eisenblätter, S. & Schematus, H. (1970) Zur Schadwirkung und Bekämpfung des Dermanyssus gallinae- und Federlingsbefalls bei Legehennen. Monatsheft Veterinärmed, 25, 28 31. Kirkwood, A.C. (1967) Anemia in poultry infested with the red mite Dermanyssus gallinae. Veterinary Record, 80, 514 516. Kirkwood, A.C. (1974) Sorptive dusts for the control of the poultry red mite Dermanyssus gallinae. International Pest Control, 16, 12 15. Liebisch, G. & Liebisch, A. (1998) Zur Untersuchung von Resistenzen bei der Bekämpfung der Roten Vogelmilbe (Dermanyssus gallinae). Tag. Fachgr. Geflügelkrankheiten (DVG), 54. Fachgespräch 07.- 08. Mai 1998, Hannover, pp 37 41. Liebisch, A. & Liebisch, G. (2001a) Teil 1: Resistenzen und Prüfung neuer Mittel bei der Bekämpfung von Roten Vogelmilben (Dermanyssus gallinae). Der praktische Schädlingsbekämpfer, 3, 11 15. Liebisch, G. & Liebisch, A. (2001b) Dermanyssus gallinae. Testing acaricide resistance and new products for control in Germany. 18 th International Conference of the World Association for the advanced of Veterinary Parasitology, Stresa, 26 30. Maurer, V. & Perler, E. (2006) Kontrolle der Roten Vogelmilbe Dermanyssus gallinae mit Silikaten. DVG, Tag. Fachgruppe Parasitologie und parasitäre Krankheiten, zum Thema Diagnostik, Epidemiologie und Bekämpfung von Parasitosen bei Nutz-, und Haus- und Heimtieren, 07.06.-09.06.2006, Wetzlar, pp. 78. Mertz, F.P. & Yao, R.C. (1990) Saccharopolyspora spinosa sp. nov. isolated from soil collected in a sugar mill rum still. International Journal of Systematic Bacteriology, 40, 34 39. 286 Zoosymposia 6 2011 Magnolia Press LIEBISCH ET AL.

Moss, W.W. (1968) An illustrated key to the species of the acarine genus Dermanyssus (Mesostigmata: Laelapoidea: Dermanyssidae). Journal of Medical Entomology, 5, 67 84. Murphy, T.M., McAuliffe, A., Clegg, T. & O Brien, D.J. (2002) Resistance of Dermanyssus gallinae, the poultry red mite, to insecticides on Irish farms. In: Good, M., Hall, M.J., Losson, B., O Brien, D., Pithan, K. & Sol, J. (eds) Mange and myiasis of livestock. University of Bari, pp. 44 46. Salgado, V.L. (1998) Studies on the mode of action of spinosad: insect symptoms and physiological correlates. Pesticide Biochemistry and Physiology, 60, 91 102. Salish, H. (1989) Recent developments in the chemotherapy of parasitic infections of poultry. World s Poultry Science Journal, 45, 115 124. Saucke, H. (1998) Bekämpfung der Roten Vogelmilbe: Erfolg mit einem neuen Staub aus Kieselalgen. DGS Magazine, 6, 10 12. Smith, M.G., Blattner, R.J. & Heys, F.M. (1947) Transmission of virus to chickens by infected mites Dermanyssus gallinae and resulting viremia as a source of virus for infection of mites. Journal of Experimental Medicine, 86, 229 237. Steenberg, T. & Kilpinen, O. (2003) Fungus infection of the chicken mite Dermanyssus gallinae. In: Papierok, B. (ed) Insect pathogens and insect parasitic nematodes. IOBC/WPRS Bulletin, 26, 27 30. Stone, B.F. & Haydock, K.P. (1962) A method for measuring the acaricide-susceptibility of the cattle tick Boophilus microplus (Can.). Bulletin of Entomological Research, 53, 563 578. Sulkin, S.E., Wissemann, C.L., Izumi, E.M. & Zarafonetis, C. (1955) Mites as possible vectors or reservoirs of equine encephalomyelitis in Texas. American Journal of Tropical Medicine and Hygiene, 4, 119 135. Urquhart, G.M., Armour, J., Duncan, J.L., Dunn, A.M. & Jennings, F.W. (1996) Veterinary Parasitology. Blackwell Science Ltd, Oxford. Valiente Moro, C., Chauve, C. & Zenner, L. (2007) Experimental infection of Salmonella enteritidis by the poultry red mite, Dermanyssus gallinae. Veterinary Parasitology, 146, 329 336. Zeman, P., Stika, V., Skalka, B., Bartik, M., Dusbabek, F. & Lavickova, M. (1982) Potential role of Dermanyssus gallinae De Geer, 1778 in the circulation of the agent of pullurosis-typhus in hens. Folia Parastologica, 29, 371 374. EFFICACY OF SPINOSAD AGAINST THE POULTRY RED MITE Zoosymposia 6 2011 Magnolia Press 287

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