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沙罗拉纳(Simparica)和阿福拉纳(NexGard)对犬诱导感染的血红扇头蜱(Rhipicephalus sanguineus s.l.)的杀蜱速度比较。

Comparative speed of kill of sarolaner (Simparica) and afoxolaner (NexGard) against induced infestations of Rhipicephalus sanguineus s.l. on dogs.

作者信息

Six Robert H, Young David R, Holzmer Susan J, Mahabir Sean P

机构信息

Zoetis, Veterinary Medicine Research and Development, 333 Portage St., Kalamazoo, MI, 49007, USA.

YVRS, 7243 East Ave, Turlock, CA, 95380, USA.

出版信息

Parasit Vectors. 2016 Feb 19;9:91. doi: 10.1186/s13071-016-1375-y.

Abstract

BACKGROUND

The brown dog tick, Rhipicephalus sanguineus sensu lato, commonly infests dogs globally, is the major vector of the pathogen that causes canine monocytic ehrlichiosis and also transmits Babesia vogeli. A rapid speed of kill of a parasiticide is essential to reduce the direct deleterious effects of tick infestation and the risk of tick-borne pathogen transmission. The speed of kill of a novel orally administered isoxazoline parasiticide, sarolaner (Simparica), against R. sanguineus sensu lato on dogs was evaluated and compared with afoxolaner (NexGard) for 5 weeks after a single oral dose.

METHODS

Based on pretreatment tick counts, 24 dogs were randomly allocated to oral treatment with either placebo, or label doses of sarolaner (2-4 mg/kg) or afoxolaner (2.5-6.8 mg/kg). Dogs were examined and live ticks counted at 8, 12, and 24 h after treatment and subsequent re-infestations on Days 7, 14, 21, 28, and 35. Efficacy was determined at each time point relative to counts for placebo dogs.

RESULTS

There were no adverse reactions to treatment. Based on geometric means, sarolaner provided >94 % efficacy within 8 h of treatment, and >99 % after 12 and 24 h. Against subsequent weekly re-infestations of ticks, sarolaner achieved ≥91.7 % efficacy (based on geometric means) to Day 35 at 24 h. Sarolaner significantly reduced tick counts versus placebo on Days 0 and 28 at 8 h (P ≤ 0.0390), on Days 0 to 14 and 28 at 12 h (P ≤ 0.0142), and on all days at 24 h (P < 0.0001). By comparison, tick counts for afoxolaner were significantly lower than placebo at 8 h on Days 0 and 28 (P ≤ 0.0117), at 12 h on Day 0 only (P < 0.0001), and on all days at 24 h (P ≤ 0.0078). Significantly more live ticks were recovered from afoxolaner-treated dogs than from sarolaner-treated dogs at 8 and 12 h after treatment (P ≤ 0.0286), at 12 h after re-infestation on Days 7 and 28 (P ≤ 0.04630), and at 24 h after re-infestations from Day 7 to Day 35 (P ≤ 0.0119). At 24 h, efficacy (based on geometric mean counts) of afoxolaner was less than 90 % from Day 7 onwards, and declined to less than 45 % by Day 35, while efficacy for sarolaner was >90 % for 35 days.

CONCLUSIONS

In this controlled laboratory evaluation, sarolaner had a faster speed of kill against R. sanguineus sensu lato than afoxolaner. The rapid and consistent kill of ticks within 24 h after a single oral dose of sarolaner over 35 days indicates that this treatment will provide highly effective and reliable control of ticks over the entire treatment interval and should reduce the risk of tick-borne pathogen transmission.

摘要

背景

棕狗蜱,即广义上的血红扇头蜱,在全球范围内普遍寄生于犬类身上,是导致犬单核细胞埃立克体病的病原体的主要传播媒介,还能传播伏氏巴贝斯虫。杀虫剂的快速杀灭效果对于降低蜱虫寄生的直接有害影响以及蜱传病原体传播风险至关重要。评估了一种新型口服异恶唑啉类杀虫剂沙罗拉纳(Simparica)对犬身上广义血红扇头蜱的杀灭速度,并与阿福拉纳(NexGard)在单次口服给药后的5周内进行了比较。

方法

根据治疗前蜱虫计数,将24只犬随机分配至口服安慰剂、标签剂量的沙罗拉纳(2 - 4毫克/千克)或阿福拉纳(2.5 - 6.8毫克/千克)进行治疗。在治疗后8、12和24小时以及后续第7、14、21、28和35天再次感染后对犬进行检查并计数存活蜱虫。相对于安慰剂组犬的计数,在每个时间点确定疗效。

结果

治疗无不良反应。基于几何平均数,沙罗拉纳在治疗后8小时内提供了>94%的疗效,12和24小时后>99%。针对随后每周再次感染的蜱虫,沙罗拉纳在第35天24小时时达到了≥91.7%的疗效(基于几何平均数)。沙罗拉纳在第0天和第28天8小时(P≤0.0390)、第0天至第14天和第28天12小时(P≤0.0142)以及所有天数24小时(P<0.0001)时与安慰剂相比显著减少了蜱虫计数。相比之下,阿福拉纳在第0天和第28天8小时(P≤0.0117)、仅在第0天12小时(P<0.0001)以及所有天数24小时(P≤0.0078)时蜱虫计数显著低于安慰剂。在治疗后8和12小时(P≤0.0286)、第7和28天再次感染后12小时(P≤0.04630)以及第7天至第35天再次感染后24小时(P≤0.0119),从阿福拉纳治疗的犬身上回收的存活蜱虫明显多于沙罗拉纳治疗的犬。在24小时时,从第7天起阿福拉纳的疗效(基于几何平均计数)低于90%,到第35天降至低于45%,而沙罗拉纳的疗效在35天内>90%。

结论

在这项对照实验室评估中,沙罗拉纳对广义血红扇头蜱的杀灭速度比阿福拉纳快。单次口服沙罗拉纳后在35天内24小时内迅速且持续地杀灭蜱虫表明该治疗在整个治疗期间将提供高效且可靠的蜱虫控制,并应降低蜱传病原体传播风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04c2/4759861/69e0289ad217/13071_2016_1375_Fig1_HTML.jpg

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