Authors
Ignacio J Gamietea, Maria V Rossner, Adrian L Lifschitz, Oscar S Anziani, Santiago Nava
Published in
Tropical animal health and production. Volume 58. Issue 8. Oct 10, 2026. Epub Oct 10, 2026.
Abstract
The aim of this study was to evaluate the efficacy of pour-on fluralaner formulations for the prevention of cutaneous myiasis caused by Cochliomyia hominivorax in newborn calves under field conditions. Three field trials were conducted in Argentina, including subtropical and temperate regions. In Trial 1, calves with unhealed navels were assigned to two fluralaner-treated groups with different commercial pour-on formulations and an untreated control group. In Trial 2, two groups of newborn calves were treated either with fluralaner pour-on or injectable doramectin. Trial 3, where 84 calves were also treated with a pour-on formulation of fluralaner, was performed in an island livestock farming systems located along the Paraná River, where extensive grazing conditions are extreme, and the operational difficulties associated with providing meticulous animal husbandry practices to prevent parasitic diseases in cattle are amplified. Animals were monitored daily for the occurrence of myiasis. In Trial 1, no cases of myiasis were recorded in fluralaner-treated calves, whereas all control animals became infested. In Trial 2, no infestations were observed in the fluralaner-treated group, while myiasis was recorded in 3.5% of calves treated with doramectin. In Trial 3, the prevalence of myiasis in fluralaner-treated calves was 7.1%, with most cases associated with treatments applied under rainy conditions. In contrast, a prevalence of 34.5% was recorded in the previous year in the same herd when treatment consisted of insecticidal formulations based on organophosphates and pyrethroid. No adverse effects associated with fluralaner treatment were observed in all treated calves. These results demonstrate the high efficacy of fluralaner pour-on formulations for the prevention of C. hominivorax myiasis in newborn calves under extensive production systems.
PMID:
42859311
Bibliographic data and abstract were imported from PubMed on 11 Oct 2026.
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