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莫昔克丁长效注射制剂(1 毫克/千克体重)对自然感染绵羊的捻转血矛线虫第一期幼虫的疗效。

Efficacy of moxidectin long-acting injectable formulation (1 mg/kg bodyweight) against first instar larvae of Oestrus ovis in naturally infected sheep.

机构信息

Departamento de Sanidad Animal, Instituto de Ganadería de Montaña, CSIC-ULE, 24346 Grulleros, León, Spain.

出版信息

Vet Parasitol. 2013 Mar 31;193(1-3):320-4. doi: 10.1016/j.vetpar.2012.10.006. Epub 2012 Oct 17.

DOI:10.1016/j.vetpar.2012.10.006
PMID:23333136
Abstract

The objective of the current study was to evaluate the efficacy of a single treatment with a long-acting injectable formulation of moxidectin (MOX) at 1.0 mg/kg bodyweight (b.w.) against natural infection by nasal bots (Oestrus ovis) in sheep with special attention to first instar larvae (L1). Firstly, a local farm with clinical history of oestrosis was chosen to conduct the assay. A total of 49 sheep were pre-selected at the end of the summer according to the presence of evident clinical signs of infection and confirmed later by means of an indirect ELISA against excretory-secretory products from L1 to detect IgG antibodies. After that, 24 sheep were chosen to carry out the study on the basis of positive serology and age since the oldest ones were selected. The day 0 of the assay, the treatment group was administered with the MOX formulation by subcutaneous injection at the base of the left ear and the control group was administered with a saline solution in the same way. All sheep were slaughtered on day 28 post-treatment (pt). At the necropsy, the head of all sheep were cut off and split into two sagital sections and all larvae from nasal passages, septum, middle meatus, conchae and sinuses were recovered. After the necropsy, a significant number of L1 was only found in the control group and therefore the efficacy of the MOX formulation was only calculated against this stage. As a result, the formulation was 90.2% effective against L1 for sheep slaughtered at day 28 pt.

摘要

本研究的目的是评估 1.0mg/kg 体重(BW)的莫昔克丁长效注射制剂单次治疗对绵羊自然感染鼻蝇幼虫(Oestrus ovis)的疗效,特别关注第一期幼虫(L1)。首先,选择一家具有临床鼻蝇病史的当地农场进行试验。在夏季末,根据感染的明显临床症状并通过间接 ELISA 检测 L1 的排泄-分泌产物检测 IgG 抗体来确认,总共选择了 49 只绵羊作为预筛选。之后,根据血清学和年龄选择了 24 只绵羊进行研究,因为选择了最年长的绵羊。试验第 0 天,治疗组在左耳基部皮下注射莫昔克丁制剂,对照组以同样方式注射生理盐水。所有绵羊均于治疗后第 28 天(pt)进行屠宰。在剖检时,将所有绵羊的头部剪下并分为两个矢状切片,从鼻腔、鼻中隔、中鼻甲、鼻甲和鼻窦中回收所有幼虫。剖检后,仅在对照组中发现了大量的 L1,因此仅针对这一阶段计算了莫昔克丁制剂的疗效。结果,该制剂对第 28 天 pt 屠宰的绵羊的 L1 有效率为 90.2%。

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