Efficacy of ERL-4221 as an ovotoxin for feral pigs (Sus scrofa)
Dustin L. Sanders A , Fang Xie B , Richard E. Mauldin C , Jerome C. Hurley C , Lowell A. Miller C , Michelle R. Garcia B , Randy W. DeYoung A , David B. Long D and Tyler A. Campbell D EA Caesar Kleberg Wildlife Research Institute, Texas A&M University-Kingsville, Kingsville, TX 78363, USA.
B Department of Animal and Wildlife Sciences, Texas A&M University-Kingsville, Kingsville, TX 78363, USA.
C United States Department of Agriculture, Animal and Plant Health Inspection Service, Wildlife Services, National Wildlife Research Center, Fort Collins, CO 80521, USA.
D United States Department of Agriculture, Animal and Plant Health Inspection Service, Wildlife Services, National Wildlife Research Center, Texas A&M University-Kingsville, Kingsville, TX 78363, USA.
E Corresponding author. Email: tyler.a.campbell@aphis.usda.gov
Wildlife Research 38(2) 168-172 https://doi.org/10.1071/WR10179
Submitted: 29 September 2010 Accepted: 21 March 2011 Published: 20 April 2011
Abstract
Context: The expansion of feral pig populations across the United States has increased the occurrence of damage and damage complaints. New techniques are needed to more effectively manage feral pig damage, including the development of fertility control agents.
Aims: We aimed to assess the ovotoxic properties of ERL-4221 as a candidate fertility control agent for feral pigs.
Methods: We conducted two palatability trials to determine ERL-4221 acceptance and one experimental trial with ERL-4221 at the captive wildlife facility of Texas A&M University-Kingsville during 2008. Our experimental trial had three treatments, a control containing no ERL-4221, baits containing 16.0 mg ERL-4221 kg–1 bodyweight for 10 days, and baits containing 16.0 mg ERL-4221 kg–1 bodyweight for 20 days.
Key results: Final body mass, total ovary mass, number of follicles and number of corpora lutea did not differ between treatments.
Conclusions: We did not find it efficacious to orally deliver ERL-4221 to feral pigs to reduce fertility. Oral delivery is the most practical, cost-effective means of delivering fertility control agents to feral pigs and development of additional fertility control strategies are needed.
Implications: Unless ovotoxic effects of ERL-4221 can be identified in feral pigs, along with a successful means of administration, other fertility control strategies may need to be explored, such as oocyte-secreted proteins that regulate follicular development.
Additional keywords: ERL-4221, fertility control, oocyte, ovary, toxicity.
References
Adams, C. E., Higginbotham, B. J., Rollins, D., Taylor, R. B., Skiles, R., Mapston, M., and Turman, S. (2005). Regional perspectives and opportunities for feral hog management in Texas. Wildlife Society Bulletin 33, 1312–1320.| Regional perspectives and opportunities for feral hog management in Texas.Crossref | GoogleScholarGoogle Scholar |
American Veterinary Medical Association (AVMA) (2007). ‘AVMA Guidelines on Euthanasia.’ (American Veterinary Medical Association: Schraumburg, IL.)
Campbell, T. A., and Long, D. B. (2008). Mammalian visitation to candidate feral swine attractants. The Journal of Wildlife Management 72, 305–309.
| Mammalian visitation to candidate feral swine attractants.Crossref | GoogleScholarGoogle Scholar |
Campbell, T. A., and Long, D. B. (2009). Feral swine damage and damage management in forested ecosystems. Forest Ecology and Management 257, 2319–2326.
| Feral swine damage and damage management in forested ecosystems.Crossref | GoogleScholarGoogle Scholar |
Campbell, T. A., Garcia, M. E., Miller, L. A., Ramirez, M. A., Long, D. B., Marchand, J., and Hill, F. (2010). Immunocontraception of male feral swine with a recombinant GnRH vaccine. Journal of Swine Health and Production 18, 118–124.
Cowled, B. D., Elsworth, P., and Lapidge, S. J. (2008). Additional toxins for feral pig (Sus scrofa) control: identifying and testing Achilles’ heels. Wildlife Research 35, 651–662.
| Additional toxins for feral pig (Sus scrofa) control: identifying and testing Achilles’ heels.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXhtlyjsLjO&md5=54ea48dc98b63d2c6d3123bf0b65f064CAS |
Delgado-Acevedo, J., Zamorano, A., DeYoung, R. W., Campbell, T. A., Hewitt, D. G., and Long, D. B. (2010). Promiscuous mating in feral pigs (Sus scrofa) from Texas, USA. Wildlife Research 37, 539–546.
| Promiscuous mating in feral pigs (Sus scrofa) from Texas, USA.Crossref | GoogleScholarGoogle Scholar |
Devine, P. J., Sipes, I. G., and Hoyer, P. B. (2004). Initiation of delayed ovotoxicity by in vitro and in vivo exposure of rat ovaries to 4-vinylcyclohexene diepoxide. Reproductive Toxicology (Elmsford, N.Y.) 19, 71–77.
| Initiation of delayed ovotoxicity by in vitro and in vivo exposure of rat ovaries to 4-vinylcyclohexene diepoxide.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXntFSlt70%3D&md5=0f5278ea390ea85ebb5be47fa5983043CAS | 15336714PubMed |
Fagerstone, K. A., Miller, L. A., Bynum, K. S., Eisemann, J. D., and Yoder, C. (2006). When, where and for what wildlife species will contraception be a useful management approach? Proceedings of the Vertebrate Pest Conference 22, 45–54.
Griffin, J., Emery, B. R., Huang, I., Peterson, C. M., and Carrell, D. T. (2006). Comparative analysis of follicle morphology and oocyte diameter in four mammalian species (mouse, hamster, pig, and human). Journal of Experimental & Clinical Assisted Reproduction 3, 2.
| Comparative analysis of follicle morphology and oocyte diameter in four mammalian species (mouse, hamster, pig, and human).Crossref | GoogleScholarGoogle Scholar | 16509981PubMed |
Hoyer, P. B., Devine, P. J., Hu, X., Thompson, K. E., and Sipes, I. G. (2001). Ovarian toxicity of 4-vinylcyclohexene diepoxide: a mechanistic model. Toxicologic Pathology 29, 91–99.
| Ovarian toxicity of 4-vinylcyclohexene diepoxide: a mechanistic model.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXhtl2mtbw%3D&md5=150b6a47a95679a81fd1e1689502c231CAS | 11215690PubMed |
Mauldin, R. E., and Miller, L. A. (2007). Wildlife contraception: targeting the oocyte. In ‘Managing Vertebrate Invasive Species: Proceedings of an International Symposium’. (Eds G. W. Witmer, W. C. Pitt and K. A. Fagerstone.) pp. 434–444. (National Wildlife Research Center: Fort Collins, CO.)
Mayer, L. P., Devine, P. J., Dyer, C. A., and Hoyer, P. B. (2004). The follicle-depleted mouse ovary produces androgen. Biology of Reproduction 71, 130–138.
| The follicle-depleted mouse ovary produces androgen.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXltFKktbg%3D&md5=3b3b3b06f52353a2b38d2ba2bf5eb37bCAS | 14998904PubMed |
Miers, H., Dyer, C., Craig, R., Kalleco, D., Karr, K., Robinson, Z., Marion, S., Hoyer, P., Blalock, C., and Mayer, L. (2005). 4-Vinylcyclohexene diepoxide-induced primordial follicle depletion in canine ovaries. In ‘Proceedings of the Symposium of the 38th Annual Meeting of the Society of the Study of Reproduction’. (The Society of the Study of Reproduction: Quebec City, Canada.)
Oxender, W. D., Colenbrander, B., Van de Wiel, D. F. M., and Wensing, C. J. G. (1979). Ovarian development in fetal and prepubertal pigs. Biology of Reproduction 21, 715–721.
| Ovarian development in fetal and prepubertal pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL3cXjsl2r&md5=00877d83790f16aab2c754ef68f1c8ddCAS | 497327PubMed |
Thompson, K. E., Bourguet, S. M., Christian, P. J., Benedict, J. C., Snipes, I. G., Flaws, J. A., and Hoyer, P. B. (2005). Differences between rats and mice in the involvement of the aryl hydrocarbon receptor in 4-vinylcyclohexene diepoxide-induced ovarian follicle loss. Toxicology and Applied Pharmacology 203, 114–123.
| Differences between rats and mice in the involvement of the aryl hydrocarbon receptor in 4-vinylcyclohexene diepoxide-induced ovarian follicle loss.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXhtlelsLk%3D&md5=30bf21d11ec371fda6028f9969353601CAS | 15710172PubMed |