Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2023 Aug:22:102-106.
doi: 10.1016/j.ijpddr.2023.07.001. Epub 2023 Jul 20.

Multiple anthelmintic drug resistant Ancylostoma caninum in foxhounds

Affiliations

Multiple anthelmintic drug resistant Ancylostoma caninum in foxhounds

Jenna D Balk et al. Int J Parasitol Drugs Drug Resist. 2023 Aug.

Abstract

Ancylostoma caninum is the most common and important gastrointestinal nematode of dogs in the United States. Despite recent reports of A. caninum isolates resistant to all classes of anthelmintics, little is known about the frequency and extent of this anthelmintic resistance. The study aim was to evaluate the efficacy of three commercial anthelmintic products in the treatment of foxhound dogs with a history of persistent A. caninum infections. In the first phase of this study, 35 foxhounds were randomly divided into three treatment groups: moxidectin/imidacloprid (MI), pyrantel pamoate/febantel/praziquantel (PFP), and emodepside/praziquantel (EP). Fecal samples were collected on day 0, 11, and 33 post-treatment (PT), and hookworm eggs were quantified using the mini-FLOTAC technique with a multiplication factor of 5 eggs per gram (EPG). The fecal egg count reduction (FECR) on day 11 PT was 65% (95% CI: 62%-68%) for MI, 69% (95% CI: 66%-72%) for PFP, and 96% (95% CI: 94%-97%) for EP. On day 33 PT, the FEC in the MI and PFP groups returned to almost the same values as on day 0, while in the EP group, the FEC remained low. Since MI and PFP proved ineffective, 32 animals were randomly divided into two groups in the second phase. They were treated either with a combination of MI/PFP or EP. The FECR at day 13 PT for the combination MI/PFP was 89% (95% CI: 87%-91%) and 99% (95% CI: 98%-99%) for EP. These results suggest that this A. caninum population is resistant to multiple anthelmintics. Although the combination of MI/PFP improved the anthelmintic efficacy, the FECR remained below 90%. Future studies are indicated to evaluate further the epidemiology of persistent hookworm infections in dogs in the US and to identify more effective treatment protocols as they pose a significant health risk to canine and human health.

Keywords: Ancylostoma caninum; Anthelmintic resistance; Foxhounds; Hookworm.

PubMed Disclaimer

Figures

Image 1
Graphical abstract

References

    1. Al-Azzam S.I., Fleckenstein L., Cheng K.J., Dzimianski M.T., McCall J.W. Comparison of the pharmacokinetics of moxidectin and ivermectin after oral administration to beagle dogs. Biopharm. Drug Dispos. 2007;28:431–438. doi: 10.1002/BDD.572. - DOI - PubMed
    1. Bowman D.D., Grazette A.R., Basel C., Wang Y., Hostetler J.A. Protection of dogs against canine heartworm infection 28 days after four monthly treatments with Advantage Multi® for Dogs. Parasites Vectors. 2016;9 doi: 10.1186/S13071-016-1293-Z. - DOI - PMC - PubMed
    1. Bowman D.D., Montgomery S.P., Zajac A.M., Eberhard M.L., Kazacos K.R. Hookworms of dogs and cats as agents of cutaneous larva migrans. Trends Parasitol. 2010;26:162–167. doi: 10.1016/J.PT.2010.01.005. - DOI - PubMed
    1. Coles G.C., Jackson F., Pomroy W.E., Prichard R.K., Von Samson-Himmelstjerna G., Silvestre A., Taylor M.A., Vercruysse J. The detection of anthelmintic resistance in nematodes of veterinary importance. Vet. Parasitol. 2006;136:167–185. doi: 10.1016/J.VETPAR.2005.11.019. - DOI - PubMed
    1. Cringoli G., Maurelli M.P., Levecke B., Bosco A., Vercruysse J., Utzinger J., Rinaldi L. The Mini-FLOTAC technique for the diagnosis of helminth and protozoan infections in humans and animals. Nat. Protoc. 2017;12:1723–1732. doi: 10.1038/NPROT.2017.067. - DOI - PubMed

Publication types

LinkOut - more resources