Sotiraki Smaragda, Kantzoura Vaia, Ligda Panagiota, Baka Ourania, Saratsis Anastasios, Fankhauser Becky, Kley Katrin, Rehbein Steffen
Laboratory of Parasitology, Veterinary Research Institute, Hellenic Agricultural Organization (ELGO) - DIMITRA, Campus ELGO, Thermi, Thessaloniki 57001, Greece.
Laboratory of Parasitology, Veterinary Research Institute, Hellenic Agricultural Organization (ELGO) - DIMITRA, Campus ELGO, Thermi, Thessaloniki 57001, Greece.
Vet Parasitol. 2025 Jul;337:110489. doi: 10.1016/j.vetpar.2025.110489. Epub 2025 May 2.
Sarcoptic mange of sheep is a skin disease which compromises the health and welfare of the animals, impacts their productivity and is zoonotic. In Europe, sarcoptic mange appears to be the prevailing type of mange affecting sheep kept for milk production in the Mediterranean countries. Eprinomectin 5 mg/mL topical solution (EPRINEX® Multi, Boehringer Ingelheim) was recently authorized for the treatment of gastrointestinal and pulmonary nematodes and Oestrus ovis in sheep with zero hours milk withdrawal in several countries in Europe. As the product in cattle has claims against a broad range of parasites including sarcoptic mange mites, the therapeutic efficacy of the product was evaluated in dairy sheep with naturally acquired S. scabiei infestation in two field efficacy study (25 sheep per study) and one controlled, masked clinical study (22 sheep) conducted in Greece. In the field studies, all animals were administered twice, two weeks apart (Days 0 and 14), eprinomectin 5 mg/mL topical solution at 14 mL per animal pour on, based on the body weight measured for the visually estimated heaviest five animals in each study. In the controlled study, animals were ranked by decreasing pre-treatment live mite count, formed in blocks of two animals and randomly assigned to one of two groups to remain untreated (control) or to be administered twice, two weeks apart, eprinomectin 5 mg/mL topical solution at 1 mL per 5 kg body weight pour on. Skin scrapings were collected prior to treatment and at intervals for eight weeks after the first treatment to establish live Sarcoptes mite counts. A 'Mange Clinical Score' was established for each animal using a 5-category scoring system at each sampling. Mite counts of the eprinomectin 5 mg/mL topical solution-treated animals were significantly (p < 0.0001) lower than the pre-treatment counts in the field studies or those of the controls in the controlled study, on all occasions post-treatment. All treated animals had zero live mite counts at 28 days after the first treatment and at the subsequent occasions until the end of the studies (Day 56). All untreated animals in the controlled study remained infested throughout the study. The 'Mange Clinical Score' of the eprinomectin 5 mg/mL topical solution-treated animals, compared either to the pre-treatment scores in the animals in the field studies or to the scores of the controls in the controlled study, improved significantly (p < 0.05) from Day 7 or Day 14, respectively. At the end of the studies, 56 of the 61 treated sheep had healthy skin and did not show clinical symptoms associated with sarcoptic mange, while five animals still presented small, reddened skin areas and some itching despite demonstrating zero mite counts over four weeks. The administration of the treatments was well accepted by all animals and no health problems were observed throughout the studies. This series of studies demonstrated eprinomectin 5 mg/mL topical solution when administered twice, two weeks apart, to be an efficacious and safe treatment against ovine sarcoptic mange.
绵羊疥螨病是一种影响动物健康和福利、降低其生产力且人畜共患的皮肤病。在欧洲,疥螨病似乎是影响地中海国家产奶绵羊的主要螨病类型。依普菌素5mg/mL外用溶液(EPRINEX® Multi,勃林格殷格翰公司)最近在欧洲多个国家被批准用于治疗绵羊的胃肠道和肺部线虫以及羊狂蝇,且无需停药即可产奶。由于该产品在牛身上可用于治疗包括疥螨在内的多种寄生虫,因此在希腊进行了两项田间药效试验(每项试验25只绵羊)和一项对照、双盲临床研究(22只绵羊),以评估其对自然感染疥螨的奶羊的治疗效果。在田间试验中,根据每项试验中目测估计最重的5只动物的体重,每只动物按14mL的剂量浇淋5mg/mL依普菌素外用溶液,所有动物均给药两次,间隔两周(第0天和第14天)。在对照研究中,根据治疗前活螨数量从高到低对动物进行排序,每两只动物分为一组,随机分配到两个组之一,一组不治疗(对照组),另一组按每5kg体重1mL的剂量浇淋5mg/mL依普菌素外用溶液,给药两次,间隔两周。在治疗前以及首次治疗后的八周内定期采集皮肤刮屑,以确定活疥螨数量。在每次采样时,使用5级评分系统为每只动物建立一个“螨病临床评分”。在所有治疗后的时间点,依普菌素5mg/mL外用溶液治疗的动物的螨数量均显著低于田间试验中的治疗前数量或对照研究中的对照组数量(p<0.0001)。所有治疗的动物在首次治疗后28天以及直至研究结束(第56天)的后续时间点活螨数量均为零。对照研究中所有未治疗的动物在整个研究过程中均受到感染。与田间试验中动物的治疗前评分或对照研究中对照组的评分相比,依普菌素溶液治疗的动物的“螨病临床评分”分别从第7天或第14天开始显著改善(p<0.05)。在研究结束时,61只接受治疗绵羊中有56只皮肤健康,未表现出与疥螨病相关的临床症状,而另外5只动物尽管在四周内螨数量为零,但仍有小面积皮肤发红和一些瘙痒症状。所有动物对治疗的接受度良好,在整个研究过程中未观察到健康问题。这一系列研究表明,间隔两周给药两次的依普菌素5mg/mL外用溶液是治疗绵羊疥螨病的一种有效且安全的方法。