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1.
Vet Parasitol ; 223: 26-9, 2016 Jun 15.
Article in English | MEDLINE | ID: mdl-27198772

ABSTRACT

Anthelmintic resistance (AR) of gastrointestinal nematodes to macrocyclic lactones is an increasingly common worldwide phenomenon limiting cattle production. This has motivated the search for alternatives, such as new active compounds, added drug synergisms, different doses, and alternate administration routes. The aim of this study was the assessment of moxidectin (MXD) performance in feedlot calves with a history of AR to ivermectin (IVM). Crossbred female calves aged 6-7 months and weighing 163kg (SD=34kg) were divided into 3 groups of 35 animals each. They were assigned to the following antiparasitic treatment groups: IVM group (0.2mg/kg IVM); MXD group (0.2mg/kg MXD), and ricobendazole+levamisole (RBZ+LEV) group (7.5mg/kg RBZ+8mg/kg LEV). On days 0, 26, and 47, fecal samples were taken and the weight of each animal was registered. Anthelmintic efficacy (by fecal egg count reduction), total weight gain (TWG) and average daily weight gain (AWG) were compared between the groups. A mixed SAS procedure was used for statistical analysis. Fecal egg count reduction 26 days post-treatment (PT) was calculated at 28% for the IVM group, 85% for the MXD group, and 99% for the RBZ+LEV group. AWGs (Standard Error) of 1.095g (56), 1.264g (49), and 1.340g (52) were registered for the IVM, MXD, and RBZ+LEV groups, respectively (p<0.05). Coprocultures revealed that MXD more effectively reduced Haemonchus spp. and Cooperia spp. egg counts than IVM. This resulted in higher AWGs and TWGs for this group; similar results were seen for the RBZ+LEV group as well. In this study, animals treated with MXD gained about 160 more g/day than animals treated with IVM. This represents a gain of 16 USD per animal over the 47 day trial.


Subject(s)
Cattle Diseases/parasitology , Drug Resistance , Ivermectin/pharmacology , Macrolides/therapeutic use , Nematoda/drug effects , Nematode Infections/veterinary , Albendazole/administration & dosage , Albendazole/analogs & derivatives , Albendazole/therapeutic use , Animals , Cattle , Cattle Diseases/drug therapy , Female , Levamisole/administration & dosage , Levamisole/therapeutic use , Nematode Infections/drug therapy , Nematode Infections/parasitology
2.
Vet Parasitol ; 206(3-4): 240-5, 2014 Dec 15.
Article in English | MEDLINE | ID: mdl-25468022

ABSTRACT

The aim of this study was to evaluate, in a commercial feedlot, the effect of different anthelmintic drugs on the productivity of naturally infected calves from a cow-calf operation, where resistance to ivermectin (IVM) has been previously detected. The study began with the random selection of 80 calves whose weight was 132 ± 12 kg. Four groups were made: IVM, ricobendazole (RBZ), ricobendazole plus levamisol (RBZ + LEV) and a control group (CG) without treatment. On days 0, 21, 42, 70, 98 and 126, manual collection of fecal matter and individual weight were registered. Mixed SAS procedure was used for statistical analysis. The percentages of fecal egg count reduction test (FECRT) calculated 21 days post treatment (PT) were 18%, 96% and 100% for the IVM, RBZ and RBZ + LEV groups, respectively. Body weight (± SEM) at the end of the trial was 266 kg (± 0.9), 269 kg (± 1.1), 276 kg (± 1.3), 280 kg (± 1.9) for CG, IVM, RBZ and RBZ + LEV groups, respectively. The effect on live weight was highly significant (p < 0001). After 126 days of fattening, the deleterious effect of the combination of Cooperia and Haemonchus in the IVM group on body weight was evident. Undetected animals carrying anthelmintic resistant (AR) worms entering the feedlot, could cause major productivity losses.


Subject(s)
Anthelmintics/pharmacology , Cattle Diseases/parasitology , Drug Resistance , Trichostrongyloidea/drug effects , Trichostrongyloidiasis/veterinary , Albendazole/analogs & derivatives , Albendazole/pharmacology , Animals , Cattle , Cattle Diseases/drug therapy , Feces/parasitology , Ivermectin/pharmacology , Levamisole/pharmacology , Parasite Egg Count/veterinary , Trichostrongyloidiasis/drug therapy , Trichostrongyloidiasis/parasitology
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