Moxidectin: A Viable Alternative for the Control of Ivermectin-Resistant Gastrointestinal Nematodes in Beef Cattle
The increasing prevalence of anthelmintic resistance in cattle especially for avermectins, is a challenge for controlling parasites in some herds. Thus, field studies demonstrating the increase in productivity by the use of anthelmintic formulations, even when a suboptimal treatment (efficacy below...
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Veröffentlicht in: | Acta veterinaria (Beograd) 2022-03, Vol.72 (1), p.16-29 |
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Sprache: | eng |
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Zusammenfassung: | The increasing prevalence of anthelmintic resistance in cattle especially for avermectins, is a challenge for controlling parasites in some herds. Thus, field studies demonstrating the increase in productivity by the use of anthelmintic formulations, even when a suboptimal treatment (efficacy below 95%), can contribute to the development of gastrointestinal nematodes control programs in beef cattle. The objective of the present study was to evaluate the anthelmintic efficacy and productive performance in pasture-raised beef calves, treated with macrocyclic lactones. A Split plot in time randomized block design was used to assess weight gain and reduction in fecal egg count (FECs) of treatments: 1% moxidectin (1% MOX), ivermectin (IVM) and abamectin (ABM) (2.25% IVM+1.25% ABM), 4% IVM, 3.15% IVM and placebo. For the evaluation of FECs and weight gain of the animals, individual samples were collected seven days before treatment and, +14, +30, +56, +91 and +118 days post-treatment (DPT). The efficacies in the 14th DPT were: 72.3% (1% MOX), 22.1% (4% IVM), 22% (2.25% IVM + 1.25% ABM) and 0% (3.15% ivermectin). 1% MOX was the only treatment that resulted in a significant increase in weight gain of the animals compared to the placebo group after 118 days of treatment, with a difference of 7.6 kg. Therefore, MOX remains a viable alternative for the control of helminths resistant to avermectins and still capable of resulting in significant productive gains, even with an efficacy below 95%. |
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ISSN: | 1820-7448 1820-7448 |
DOI: | 10.2478/acve-2022-0002 |