Prophylactic treatment with flumethrin, a pyrethroid (Bayticol®, Bayer), against Anaplasma phagocytophilum infection in lambs
© Stuen et al.; licensee BioMed Central Ltd. 2012
Received: 2 March 2012
Accepted: 8 May 2012
Published: 23 May 2012
Anaplasma phagocytophilum (formerly Ehrlichia phagocytophila) causes the disease tick-borne fever (TBF) in domestic ruminants and has for decades been one of the main scourges for the sheep industry in the coastal areas of Norway. Current control strategies are based on reduction of tick infestation by chemical acaricides.
In the present study, we investigated if frequent pour-on applications of pyrethroids would reduce tick infestion rate and seroprevalence of A. phagocytophilum infection in sheep. Forty lambs, one month old, of the Norwegian White Sheep breed were used. The lambs belonged to the experimental sheep flock at the Department of Production Animal Clinical Sciences. None of the lambs had been on I. ricinus infested pasture before turnout (day 0). All lambs were twins and twenty lambs were treated with a pour-on pyrethroid (Bayticol®, Bayer A/S, DK-2300) with a dose of 5 ml on days 0, 14, 28, 42, 56, 70, 84, 98, 112 and 128. Twenty lambs were untreated controls. The lambs were collected every fourteen days on pasture for treatment. In addition, the lambs were examined for ticks, blood sampled, weighed, and rectal temperature was recorded.
Results and conclusion
A significant reduction in tick infestion rate was detected on treated lambs. However, the present results indicate that frequent acaricide treatment does not reduce the seroprevalence to A. phagocytophilum on tick-infested pasture.
KeywordsAnaplasma phagocytophilum Treatment Pyrethroids Lamb
The rickettsia Anaplasma phagocytophilum (formerly Ehrlichia phagocytophila) causes tick-borne fever (TBF) in domestic ruminants, a disease which has also been diagnosed in several other animal species and human beings [1–3]. In Europe, A. phagocytophilum is mainly transmitted by Ixodes ricinus ticks. TBF has for decades been one of the main scourges for the sheep industry in the coastal areas of Norway . A serological survey in sheep and wild cervids indicated that A. phagocytophilum infection was widespread along the coast of southern Norway [5, 6].
Sheep flocks on tick-infested pastures may suffer heavy losses due to direct mortality. The losses may vary from year to year and from area to area . In one study, 79% of the lambs that died one year on tick-infested pastures were infected with A. phagocytophilum. However, the severity of disease on I. ricinus infested pastures is influenced by several factors, such as questing activity of the ticks, variants of A. phagocytophilum in the tick population, prevalence of other tick-transmitted pathogens, and host factors such as age, immune status and body condition of the animal .
Current control strategies are based on the reduction of tick infestation by chemical acaricides. In Europe, this is mostly done by pour-on applications of pyrethroids. Normally this treatment has to be repeated several times during the grazing season. The most used pyrethroids in Norway are deltamethrin (Coopersect®, Intervet), flumethrin (Bayticol®, Bayer), cypermethrin (Crovect®, Young) and alphacypermethrin (Dysect®, Fort Dodge) (Legemiddelverket, personal information). Long-acting tetracycline is also used in the UK as a prophylactic measure given before animals are moved from tick-free environment into tick-infested pasture [9, 10]. However, there is a growing concern about the environmental safety and human health, increasing cost of chemical control and the increasing resistance of ticks to pesticides .
Treatment frequency of pyrethroids has been questioned by farmers and veterinary practitioners for several years. The main reason for the present study was to investigate if frequent treatment with pyrethroids will reduce the tick infestion rate, improve weight gain and lower the prevalence of A. phagocytophilum infection in lambs on I. ricinus infested pasture.
Material and methods
Animals, management and treatment
Forty lambs of the Norwegian White Sheep breed were used. The lambs belonged to the experimental sheep flock at the Department of Production Animal Clinical Sciences. The study was approved by the National Animal Research Authority (Norway). None of the lambs had been on I. ricinus infested pasture before turnout (day 0). The lambs were grouped in two according to equal distribution of sex and mean live weight. All lambs were twins and twenty lambs (10 twin couples) were treated with pour-on pyrethroids (Bayticol®, Bayer A/S, DK-2300) with a dose of 5 ml on days 0, 14, 28, 42, 56, 70, 84, 98, 112 and 126. The lambs were treated along the back from neck to tail of each lamb according to the manufacturers recommendation. The lambs were housed indoors for at least two hours post each treatment. In addition, twenty lambs were untreated controls.
The lambs were four-weeks old at turnout (first week of May). After turnout, the lambs were collected every fourteen days for inspection and treatment. On each sampling, all lambs were blood sampled (serum), weighed, and rectal temperature was obtained. In addition, each lamb was examined for ticks, especially on the head, axillae and inguinal regions [12, 13].
Gastrointestinal parasites are common on the actual pasture. In order to reduce the influence of Eimeria spp. and gastrointestinal nematodes, the lambs were treated with toltrazuril (Baycox®, Bayer) on day 7 and with fenbendazol (Valbazen®, Pfizer) on days 28, 56, 84 and 112. In order to monitor the parasite burden, fecal egg count reduction test (FECRT) was applied on ten randomly selected lambs every second week .
Blood samples and haematology
Full blood samples (EDTA) were collected if fever (≥ 40.5°C) was recorded. Haematological values including total and differential leucocyte counts were determined electronically (Technicon H1®, Miles Inc., USA) and blood smears were prepared and stained with May-Grünwald Giemsa. Four hundred neutrophils were examined on each smear by microscopy, and the number of cells containing Anaplasma inclusions was recorded.
Sera were collected within four days after birth, at turnout (day 0) and then every second week on pasture, i.e. on days 0, 14, 28, 42, 56, 70, 84, 98, 112 and 126. Sera were analysed using an indirect immunofluorescence antibody assay (IFA) to determine the antibody titre to an equine variant of A. phagocytophilum (formerly Ehrlichia equi) . Briefly, two-fold dilutions of sera were added to slides precoated with A. phagocytophilum antigen (Protatec, St. Paul, Minn.). Bound antibodies were visualized by fluorescein-isothiocyanate (FITC)-conjugated rabbit-anti-sheep immunoglobulin (Cappel, Organon Teknika, West Chester, PA). Sera were screened for antibodies at dilution 1:40. If positive, the serum was further diluted and retested. A titre of 1.6 (log10 reciprocal of 1:40) or more was regarded positive.
Statistical calculations were done using Statistix, version 4.0 (Analytical Software). Statistical analyses on ticks, seroconversion and treatment were performed using a chi-square test. A two sample t test was used to analyse the lamb weight. A P value of <0.05 was considered significant.
A low gastro-intestinal parasite burden was observed in the lambs during the grazing season (data not shown). Clinical disease or direct losses were not observed in any lamb during the study period, except for fever (>40.5°C) in 26 lambs, whereas high fever (≥41°C) was observed in three lambs. Of these 26 lambs only two and four lambs, including lambs with high fever, were found positive for an A. phagocytophilum infection by blood smear investigation in the treated and control group, respectively.
Number of ticks detected on pyrethroid-treated and control lambs after turn-out (day 0)
Comparison of the total number of ticks on pyrethroid-treated and control animals on pasture
Treatment against ticks
Number of seropositive (%) lambs and the antibody titre (mean ± SD) to A. phagocytophilum in treated (N = 20) and untreated (N = 20) lamb groups
2.3 ± 0.49
2.0 ± 0.35
1.6 ± 0.0
3.1 ± 0.0
2.7 ± 0.69
2.3 ± 0.32
1.9 ± 0.23
1.6 ± 0.0
2.3 ± 0.29
2.1 ± 0.15
2.2 ± 0.48
2.8 ± 0.46
Live weight (mean ± SD) of treated and untreated lambs on tick-infested pasture from turnout (day 0)
16.3 ± 2.12
26.4 ± 2.97
34.8 ± 3.03
43.2 ± 3.82
50.6 ± 4.42
52.6 ± 4.61
16.1 ± 2.54
26.2 ± 3.81
33.9 ± 5.24
41.7 ± 5.53
48.6 ± 6.04
50.8 ± 6.86
In the present study, clinical disease was not observed except for fever. Only a few lambs with high fever (≥41°C) typical for TBF were detected [1, 4]. This could be due to variants of A. phagocytophilum involved [15, 16]. However, the animals were only examined every fourteen days and the fever period in A. phagocytophilum infected sheep normally lasts around one week . In comparison, most primary infections in the field are not observed .
Only a few ticks were found on the animals. The reason for this is unknown, but tick may have attached and detached unnoticeably, since the attachment period on animals for all stages of I. ricinus ticks is normally less than 14 days . In the present study, ticks were not observed on 20% of the lambs that seroconverted to A. phagocytophilum. Attached ticks may also have been overlooked, since a detailed inspection of the whole animal was not performed. However, most I. ricinus ticks on sheep are attached on the head, axillae and inguinal regions [12, 13]. In addition, most ticks were found in May/June and in August/September. Earlier studies indicate that cases of TBF in the same county have a similar distribution with 60.4% occurring in May/June and 27.7% in September/October .
Maternal antibodies were found in 88% of the lambs. In the previous year, maternal antibodies were found in 89% of the lambs (Stuen, unpublished results), indicating that A. phagocytophilum infection is common on the actual pasture. However, the infection seems to occur mainly in the autumn, since the seroprevalence in medio September was only 35%. In the pyrethroid treated group, 30% of lambs were seropositive, which was slightly less than in the control group (40%), although a significantly higher number of ticks were found on the control lambs. The reason for this apparent discrepancy between tick infestation rate and infection prevalence may be due to an unknown number of infested ticks involved (the lambs were only observed every fourteen days) or variation in both A. phagocytophilum variants and infection prevalence in the actual tick population. In an earlier study from the same county in Norway, 24 msp-4 gene variants of A. phagocytophilum were found among 16 lambs during the first grazing season . Serological response may differ significantly between variants of the bacterium , whereas some variants may not even give a detectable serological titre (Stuen, unpublished result). Unfortunately, variants of A. phagocytophilum were not investigated in the present study.
Ticks were found on pyrethroid-treated lambs. This indicates that frequent treatment every second week is not 100% efficient against tick infestation. The present result is in accordance with earlier studies indicating that ticks can be found on animals already 13–14 days after treatment with either cypermethrin or deltamethrin [7, 13]. An earlier field study also supports the present results, since most lambs seroconverted already three weeks after pyrethroid treatment . The main reason for this lack of efficiency is unknown. According to the manufacturer, it may take 1–2 days after tick attachment until therapeutic concentration of pyrethroids in the tick is reached (Enemark, personal information). In addition, an earlier study indicated that sheep infested with ticks at the time of pour-on treatment lost their ticks within two days, which may indicate the kill time and the time for the tick to become detached . Furthermore, treatment of young lambs (≤4 weeks) with flumethrin (Bayticol®, Bayer) may be less effective due to lack of skin fat which in turn impairs the distribution of the compound (Enemark, personal communication). However, the present lambs were more than four weeks old when they were treated.
Acute cases of anaplasmosis were detected in both the control and the treatment group. Transmission of A. phagocytophilum from vector to host generally occurs between 24–48 hours after tick attachment [21–23], but the pathogen have been detected in the salivary glands of questing ticks and may therefore be transmitted immediately when ticks start feeding [24, 25]. The results indicate that Anaplasma can be transmitted by I. ricinus ticks in the time window between attachment and therapeutic concentration of pyrethroids. However, acaricide resistance cannot be ruled out and must be further elucidated. In the present study, resistance seems rather unlikely since pyrethroids have only been used for one grazing season.
No significant weight difference was observed between treated and untreated lambs or between seropositive and seronegative lambs. In contrast, earlier studies indicate a weight reduction of 1.4-3.8 kg in the autumn between seropositive and seronegative lambs [26, 27]. An earlier report also indicates that spring treatment of ewes and lambs with cypermectin pour-on produced 6% more lambs at weaning and the treated lambs were 1.5 kg heavier than untreated lambs . The reason for this discrepancy is unknown, but may be due to small sample size, variants of A. phagocytophilum involved, infection rate in ticks, other tick-borne pathogens, immune status and conditions of the lambs, management and environmental factors such as for instance variation in temperature and rainfall [4, 29].
The present study indicates that the effect of acaricides on the prevalence of A. phagocytophilum is limited. However, acaricide treatment may reduce the losses due to secondary infections. For instance, the incidence of lambs with lameness (tick pyaemia) or sudden death (Bibersteinia/Mannheimia septicaemia) has been reduced due to pour-on treatment . The reason for this effect is unknown. Ticks may carry several infectious agents or several variants of the same agent . Animals treated with acaricides may have reduced infection pressure due to a reduced number of ticks on each animal . For instance, microorganisms not already present in the salivary glands of newly attached ticks may be more vulnerable to hosts treated with acaricides. In order to examine the beneficial effect of acaricides on tick infested pastures, the distribution of A. phagocytophilum variants and other tick-borne pathogens in I. ricinus ticks has to be further elucidated.
The present results indicate that frequent acaricide treatment do not reduce the seroprevalence to A. phagocytophilum on tick-infested pasture, although it reduced the number of ticks on treated lambs.
- Foggie A: Studies on the infectious agent of tick-borne fever in sheep. J Pathol Bacteriol. 1951, 63: 1-15. 10.1002/path.1700630103.View ArticlePubMedGoogle Scholar
- Bakken JS, Dumler JS, Chen S-M, Eckman MR, Van Etta LL, Walker DH: Human granulocytic ehrlichiosis in the upper Midwest United States. A new species emerging?. JAMA. 1994, 272: 212-218. 10.1001/jama.1994.03520030054028.View ArticlePubMedGoogle Scholar
- Foley JE, Foley P, Jecker M, Swift PK, Madigan JE: Granulocytic ehrlichiosis and tick infestation in mountain lions in California. J Wild Dis. 1999, 35: 703-709.View ArticleGoogle Scholar
- Stuen S: Anaplasma phagocytophilum(formerlyEhrlichia phagocytophila) infection in sheep and wild ruminants in Norway. A study on clinical manifestation, distribution and persistence. Dr. Philosophiae Thesis. 2003, Oslo: Norwegian School of Veterinary ScienceGoogle Scholar
- Stuen S, Bergström K: Serological investigation of granulocyticEhrlichiainfection in sheep in Norway. Acta Vet Scand. 2001, 42: 331-338. 10.1186/1751-0147-42-331.PubMed CentralView ArticlePubMedGoogle Scholar
- Stuen S, Åkerstedt J, Bergström K, Handeland K: Antibodies to granulocyticEhrlichiain moose, red deer, and roe deer in Norway. J Wild Dis. 2002, 38: 1-6.View ArticleGoogle Scholar
- Mitchell GBB, Webster KA, Wright CL: Use of deltamethrin „pour-on“ for control of the sheep tickIxodes ricinus. Vet Rec. 1986, 119: 156-157.View ArticlePubMedGoogle Scholar
- Stuen S, Kjølleberg K: An investigation of lamb deaths on tick pastures in Norway. Proceedings of the third International Conference on Ticks and Tick-borne pathogens: Into the 21st century. Edited by: Kazimirová M, Labuda M, Nuttall PA. 2000, Slovakia: Slovak Academy of Sciences, Bratislava, 111-115.Google Scholar
- Brodie TA, Holmes PH, Urquhart GM: Some aspects of tick-borne diseases of British sheep. Vet Rec. 1986, 118: 415-418. 10.1136/vr.118.15.415.View ArticlePubMedGoogle Scholar
- Brodie TA, Holmes PH, Urquhart GM: Prophylactic use of long-acting tetracycline against tick-borne fever (Cytoecetes phagocytophila) in sheep. Vet Rec. 1988, 122: 43-44. 10.1136/vr.122.2.43.View ArticlePubMedGoogle Scholar
- Samish M, Ginsberg H, Glazer I: Biological control of ticks. Parasitology. 2004, 129: S389-S403. 10.1017/S0031182004005219.View ArticlePubMedGoogle Scholar
- Arthur DR: Ticks and diseases. 1962, Oxford: Pergamon Press, 236-269.Google Scholar
- Henderson D, Stevens DP: Cypermethrin pour-on for the control of ticks (Ixodes ricinus) on sheep. Vet Rec. 1987, 121: 317-319. 10.1136/vr.121.14.317.View ArticlePubMedGoogle Scholar
- Domke A, Chartier C, Gjerde B, Höglund J, Leine N, Vatn S, Stuen S: Prevalence of anthelmintic resistance in gastrointestinal nematodes of sheep and goats in Norway. Parasitol Res. 2012, In pressGoogle Scholar
- Stuen S, Bergström K, Petrovec M, Van de Pol I, Schouls LM: Differences in clinical manifestations and hematological and serological responses after experimental infection with genetic variants ofAnaplasma phagocytophilumin sheep. Clin Diagn Lab Immunol. 2003, 10: 692-695.PubMed CentralPubMedGoogle Scholar
- Ladbury GAF, Stuen S, Thomas R, Bown KJ, Woldehiwet Z, Granquist EG, Birtles RJ: Dynamic transmission of numerousAnaplasma phagocytophilumgenotypes among lambs in an infected sheep flock in an area of anaplasmosis endemicity. J Clin Microbiol. 2008, 46 (5): 1686-91. 10.1128/JCM.02068-07.PubMed CentralView ArticlePubMedGoogle Scholar
- Scott GR: Tick-borne infections. Diseases of sheep. Edited by: Martin WB, Aitken ID. 1991, Oxford: Blackwell Scientific Publications, 327-336. 2Google Scholar
- MacLeod J: The bionomics ofIxodes ricinusL. the “sheep tick” of Scotland. Parasitology. 1932, 24: 382-400. 10.1017/S0031182000020795.View ArticleGoogle Scholar
- Stuen S: Utbredelsen av sjodogg (tick-borne fever) i Norge [In Norwegian]. Nor Vet Tidsskr. 1997, 109: 83-87.Google Scholar
- Hardeng F, Baalsrud KJ, Øvernes G: Controlling tick infestations and diseases in sheep by pour-on formulations of synthetic pyrethroids. A field study. Vet Res Commun. 1992, 16: 429-436. 10.1007/BF01839020.View ArticlePubMedGoogle Scholar
- MacLeod J: Studies on tick-borne fever in sheep. II. Experiments on transmission and distribution of the disease. Parasitology. 1936, 28: 321-329.Google Scholar
- Hodzic E, Fish D, Maretzki CM, De Silva AM, Feng S, Barthold SW: Acquisition and transmission of the agent of human granulocytic ehrlichiosis byIxodes scapularisticks. J Clin Microbiol. 1998, 36: 3574-3578.PubMed CentralPubMedGoogle Scholar
- Katavolos P, Armstrong PM, Dawson JE, Telford SR: Duration of tick attachment required for transmission of granulocytic ehrlichiosis. J Infect Dis. 1998, 177: 1422-1425. 10.1086/517829.View ArticlePubMedGoogle Scholar
- Des Vignes F, Piesman J, Heffernan R, Schulze TL, Stafford KC, Fish D: Effect of tick removal on transmission ofBorrelia burgdorferiandEhrlichia phagocytophilabyIxodes scapularisnymphs. J Inf Dis. 2001, 183: 773-778. 10.1086/318818.View ArticleGoogle Scholar
- Neelakanta G, Sultana H, Fish D, Anderson JF, Fikrig E: Anaplasma phagocytophiluminducesIxodes scapularisticks to express an antifreeze glucoprotein gene that enhances their survival in the cold. J Clin Invest. 2010, 120: 3179-3190. 10.1172/JCI42868.PubMed CentralView ArticlePubMedGoogle Scholar
- Stuen S, Bergström K, Palmér E: Reduced weight gain due to subclinicalAnaplasma phagocytophilum(formerlyEhrlichia phagocytophila) infection. Exp Appl Acarol. 2002, 28: 209-215.View ArticlePubMedGoogle Scholar
- Grøva L, Olesen I, Steinshamn H, Stuen S: Prevalence ofAnaplasma phagocytophiluminfection and effect on lamb growth. Acta Vet Scand. 2011, 13: 53,30-Google Scholar
- Hunt J: Farmers weekly. 1986, April 25:24Google Scholar
- Stuen S, Longbottom D: Treatment and control of chlamydial and rickettsial infections in sheep and goats. Vet Clin North Am Food Anim Pract. 2010, 27: 213-233.View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.