Papadopoulos Elias, Angelou Athanasios, Madder Maxime, Lebon Wilfried, Beugnet Frederic
Laboratory of Parasitology and Parasitic Diseases, School of Veterinary Medicine, Aristotle University of Thessaloniki, Greece.
Clinglobal, The Tamarin Commercial Hub, Jacaranda Avenue, Tamarin, 90903, Mauritius.
Vet Parasitol X. 2020 May 18;3:100026. doi: 10.1016/j.vpoa.2020.100026. eCollection 2020 May.
Canine vector-borne disease transmission can be reduced with regular use of repellent insecticides. The objective of this year-long experimental study was to assess the efficacy of a topical formulation of fipronil/permethrin (Frontline Tri-Act®) in preventing transmission of by sandflies. This clinical field trial was conducted in Xanthi (Northern Greece), an area highly endemic for canine leishmaniosis, from April 2018 to March 2019. Forty purpose-bred Beagle dogs, testing negative for prior to study initiation, were enrolled in the study, which consisted of three phases: Phase 1 (field exposure phase) took place from Day 0-196. The dogs were randomly allocated to two groups, group 1 (sham-treated topically with sterile water) and group 2 (treated topically with Frontline Tri-Act®). Dogs in both groups were housed in two subunits of an open-air kennel for a period of 7 months, spanning the transmission season. All dogs were treated or sham-treated on Days 0, 28, 56, 84, 112, 140 and 168. Clinical examinations, PCR analysis of conjunctival swabs, and serological tests were performed on a monthly basis. Sandflies were collected every 2 weeks, during a 12 -h period overnight using light traps. Each collection was placed in a container and kept refrigerated until speciation and PCR analysis could be performed. In the second phase of the study, from Day 197 to 252, the dogs were moved into a protected environment (insect-proof protected environment phase). CDC light traps were activated every 2 weeks inside and outside the kennels to ensure the vector-free status of the facility. Monthly clinical examinations, including PCR analysis of conjunctival swabs, and serological tests continued. At the end of the phase 2, bone marrow samples were collected on all dogs. Phase 3 (the final post-winter check) took place from Day 253 to 350. Dogs were released and adopted by individual private owners on Day 253. Follow up analyses included blood collection for SNAP tests and conjunctival swaps for PCR analysis on Days 304 and 350. Additionally, bone marrow collections were also performed on Day 350. Presence of sandflies was observed only in the phase 1 exposure period, and 1714 sandflies were collected (1427 females and 287 males). Two species were identified, var and . Out of the 62 pooled samples of sandflies assessed by PCR, three were considered positive (4.8 %). By the end of the study, 35 % of the Group 1 dogs (7/20) became positive based on PCR (conjunctival swab and bone marrow) and 30 % (6/20) based on SNAP/IFAT and ELISA tests, while all the dogs in the Frontline Tri-Act® treated group 2 remained negative for all tests (G1 vs G2, p = 0.008). All tests identified the same positive animals, and PCR allowed the detection of one additional infected dog. This clinical field trial demonstrated that monthly administration of Frontline Tri-Act® to dogs exposed to infection in a high endemic area provided 100 % preventive efficacy against transmission of .
定期使用驱虫杀虫剂可减少犬类媒介传播疾病的传播。这项为期一年的实验研究的目的是评估氟虫腈/氯菊酯局部用制剂(福来恩三效驱虫滴剂®)预防白蛉传播疾病的效果。这项临床现场试验于2018年4月至2019年3月在希腊北部的克桑西进行,该地区是犬利什曼病的高流行区。40只专门培育的比格犬在研究开始前检测为阴性,被纳入该研究,研究包括三个阶段:第一阶段(野外暴露阶段)从第0天至196天。将狗随机分为两组,第1组(用无菌水进行假处理)和第2组(用福来恩三效驱虫滴剂®进行局部处理)。两组狗被安置在露天犬舍的两个子单元中7个月,跨越疾病传播季节。所有狗在第0、28、56、84、112、140和168天接受处理或假处理。每月进行临床检查、结膜拭子的PCR分析和血清学检测。每2周在夜间12小时期间使用诱虫灯收集白蛉。每次收集的白蛉被放入一个容器中并冷藏,直到可以进行物种鉴定和PCR分析。在研究的第二阶段,从第197天至252天,狗被转移到一个受保护的环境(防虫保护环境阶段)。犬舍内外每2周启动一次疾控中心诱虫灯,以确保设施无媒介。每月继续进行临床检查,包括结膜拭子的PCR分析和血清学检测。在第二阶段结束时,对所有狗采集骨髓样本。第三阶段(冬季后最终检查)从第253天至350天。狗在第253天被释放并由个体私人主人领养。后续分析包括在第304天和350天采集血液进行SNAP检测以及采集结膜拭子进行PCR分析。此外,在第350天也进行骨髓采集。仅在第一阶段暴露期观察到白蛉,共收集到1714只白蛉(1427只雌性和287只雄性)。鉴定出两个物种,即长管白蛉和中华白蛉。在通过PCR评估的62个白蛉混合样本中,3个被认为呈阳性(4.8%)。到研究结束时,第1组中35%的狗(7/20)基于PCR(结膜拭子和骨髓)呈阳性,30%(6/20)基于SNAP/间接荧光抗体试验和酶联免疫吸附测定呈阳性,而福来恩三效驱虫滴剂®处理的第2组中的所有狗在所有检测中均为阴性(第1组与第2组,p = 0.008)。所有检测都识别出相同的阳性动物,并且PCR还检测出另外一只感染狗。这项临床现场试验表明,在高流行地区每月给暴露于疾病感染的狗施用福来恩三效驱虫滴剂®可提供100%预防疾病传播的效果。