Extraction of stress hormones by fecal sampling of big cats, ungulates and mammals in captivity and wild by using enzyme linked immunoabsorbant assay (ELISA)

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Research Paper 01/11/2020
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Extraction of stress hormones by fecal sampling of big cats, ungulates and mammals in captivity and wild by using enzyme linked immunoabsorbant assay (ELISA)

Jahanzeb Sarwer, Saqafat Ahmed, Maryam Khan, Sikander Hayat, Bushra Nisar Khan, Arif Malik, Saba Shamim
Int. J. Biosci.17( 5), 176-183, November 2020.
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Abstract

The determination of fecal cortisol and steroids via immunoassay and extraction techniques is a widely accepted and used phenomena with respect to both captive and field study for the provision of the estimation of the regulating concentration of hormones in animals, which was achieved through non-invasive procedures. The reposition of fecal samples is a significant matter of concern due to the metabolism of fecal steroids by bacteria present in the feces of animals only after a few hours of deposition. In this study, the estimation of fecal hormones like estrogen (fE) and glucocorticoid (fGC) metabolites was carried out in big cats of the wild in captivity, such as lions, tigers, African lions, puma, jaguar, few ungulates, mouflon sheep, deer, chinkara, zebra and Punjab urial. The fecal samples (n=106) were collected from these wild animals and were treated with methanol to curb the metabolism of fecal hormones by bacteria. The expression of stress hormone levels in different animals as obtained by ELISA is given as 0.644±0.03 for Punjab urial followed by 0.619±0.02 for deer, 0.614±0.05 for Chinkara, 0.606±0.01 for tiger and Puma, 0.579±0.02 for lion and 0.061±0.04 for Jaguar. Much stress hormone was observed in Punjab urial whereas Jaguar was least affected by the stress. It showed that animals living in small and noisy environment are more affected by any disturbance in their surroundings as compared to the animals living in quiet and less noisy environment.

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Aziz MH, Anjum KM, Javed K, Samiullah K, Ali Z, Khan SA, Suleman S. 2018. Evaluation of social and breeding behaviour of Chinkara (Gazella bennettii) in wild and captivity. Journal of Animal and Plant Sciences 28(2), 616-622.

Behringer V, Deschner T. 2017. Non-invasive monitoring of physiological markers in primates. Hormones and Behavior 91, 3-18. http://dx.doi.org/10.1016/j.yhbeh.2017.02.001

Bourne A, Cunningham S. 2019. Non-invasive physiological measurements in wild animals: no touching please! Quest 15(4), 32-35.

Caslini C, Comin A, Peric T, Prandi A, Pedrotti L, Mattiello S. 2016. Use of hair cortisol analysis for comparing population status in wild red deer (Cervus elaphus) living in areas with different characteristics. European Journal of Wildlife Research 62(6), 713-723. http://dx.doi.org/10.1007/s10344-016-1049-2

Ciliberti MG, Albenzio M, Inghese C, Santillo A, Marino R, Sevi A, Caroprese M. 2017. Peripheral blood mononuclear cell proliferation and cytokine production in sheep as affected by cortisol level and duration of stress. Journal of Dairy Science 100(1), 750-756. http://dx.doi.org/10.3168/jds.2016-11688

Claxton AM. 2011. The potential of the human–animal relationship as an environmental enrichment for the welfare of zoo-housed animals. Applied Animal Behaviour Science 133(1-2), 1-10. http://dx.doi.org/10.1016/j.applanim.2011.03.002

Conforti VA, Morato RG, Augusto MA, de Oliveira e Sousa L, de Avila DM, Brown JL, Reeves JJ. 2012. Noninvasive monitoring of adrenocortical function in captive jaguars (Panthera onca). Zoo Biology 31(4), 426-441. http://dx.doi.org/10.1002/zoo.20409

Conte C. 2014. Do visitors affect zebra behavior in zoos? University of Connecticut, Department of Biology.

Cook NJ. 2012. Minimally invasive sampling media and the measurement of corticosteroids as biomarkers of stress in animals. Canadian Journal of Animal Sciences 92, 227-259.

Dantzer B, Fletcher QE, Boonstra R, Sheriff MJ. 2014. Measures of physiological stress: a transparent or opaque window into the status, management and conservation of species? Conservation Physiology 2(1), 1-18. http://dx.doi.org/10.1093/conphys/cou023

DeRango EJ, Schwarz JF, Kalberer S, Piedrahita P, Páez-Rosas D, Krüger O. 2019. Intrinsic and maternal traits influence personality during early life in Galápagos sea lion, Zalophus wollebaeki, pups. Animal Behaviour 154, 111-120. http://dx.doi.org/10.1016/j.anbehav.2019.06.011

Din S, Masood S, Zaneb H, ur Rehman H, Ashraf S, Khan I, Shah M, Hadi SA. 2020. Gross and clinical anatomy of the skull of adult Chinkara (Gazella bennettii). Pakistan Journal of Zoology 52(5), 1-12. http://dx.doi.org/10.17582/journal.pjz/20190207070209

Fischer A, Kaiser T, Pickert J, Behrendt A. 2017. Studies on drinking water intake of fallow deer, sheep and mouflon under semi‐natural pasture conditions. Grassland Science 63(1), 46-53. http://dx.doi.org/10.1111/grs.12149

Fourie CE. 2012. Vigilance behaviour and its endocrine correlates in Plains zebra (Equus burchelli) living in a predator-free landscape. Doctoral dissertation, University of Pretoria.

Grimmett R, Roberts TJ, Inskipp T, Byers C. 2008. Birds of Pakistan (Ed. Christopher Helm). Publisher, A & C Black.

Ivanov EA, Rozhnov VV, Naidenko SV. 2017. The effect of ambient temperature on glucocorticoid level in the Amur tiger (Panthera tigris altaica). Russian Journal of Ecology 48(3), 294-297.

Jachowski DS, Kauffman MJ, Jesmer BR, Sawyer H, Millspaugh JJ. 2018. Integrating physiological stress into the movement ecology of migratory ungulates: a spatial analysis with mule deer. Conservation Physiology 6(1), 1-12. http://dx.doi.org/10.1093/conphys/coy054

Khattak RH, Liu Z, Teng L. 2019. Development and implementation of baseline welfare assessment protocol for captive breeding of wild ungulate—Punjab Urial (Ovis vignei punjabiensis, Lydekker 1913). Animals 9(12), 1102-1116. http://dx.doi.org/10.3390/ani9121102

le Saout S, Massouh M, Martin JL, Presseault-Gauvin H, Poilvé E, Côté SD, Picot D, Verheyden H, Chamaillé-Jammes S. 2016. Levels of fecal glucocorticoid metabolites do not reflect environmental contrasts across islands in black-tailed deer (Odocoileus hemionus sitkensis) populations. Mammal Research 61(4), 391-398. http://dx.doi.org/10.1007/s13364-016-0294-9

Marino L, Merskin D. 2019. Intelligence, complexity, and individuality in sheep. Animal Sentience 4(25), 1.

Mesa-Cruz JB, Brown JL, Waits LP, Kelly MJ. 2016. Non-invasive genetic sampling reveals diet shifts, but little difference in endoparasite richness and faecal glucocorticoids, in Belizean felids inside and outside protected areas. Journal of Tropical Ecology 32(3), 226-239. http://dx.doi.org/10.1017/S0266467416000213

Mittal SK, Rao RJ, Shakya S, Tripathi SM. 2019. Modern naturalistic enclosures: comparatively an enhanced management practice of captive felids in the Zoological Park. Journal of Animal Research 9(1), 103-113.

Möstl E, Palme R. 2002. Hormones as indicators of stress. Domestic Animal Endocrinology 23(1-2), 67-74. http://dx.doi.org/10.1016/S0739-7240(02)00146-7

Putman SB, Brown LJ, Saffoe CJ, Franklin AD, Pukazhenthi BS. 2019. Linkage between fecal androgen and glucocorticoid metabolites, spermaturia, body weight and onset of puberty in male African lions (Panthera leo). PLoS One 14(7), 1-16. http://dx.doi.org/10.1371/journal.pone.0217986

Rimbau LM. 2019. The influence of enclosure conditions and social interactions of faecal glucocorticoid levels in African lions (Panthera leo bleyenberghi). Universitat Autònoma de Barcelona. Poster displayed on June 25, 2019.

Sajjad S, Farooq U, Anwar M, Khurshid A, Bukhari SA. 2011. Effect of captive environment on plasma cortisol level and behavioral pattern of Bengal tigers (Panthera tigris tigris). Pakistan Veterinary Journal 31(3), 195-198.

Schildkraut R. 2016. Characterisation of positive welfare indices in captive African lions (Panthera leo). Master’s thesis, University of Sydney.

Seeber PA, Franz M, Dehnhard M, Ganswindt A, Greenwood AD, East ML. 2018. Plains zebra (Equus quagga) adrenocortical activity increases during times of large aggregations in the Serengeti ecosystem. Hormones and Behavior 102, 1-9. http://dx.doi.org/10.1016/j.yhbeh.2018.04.005

Vaz J, Narayan JR, Kumar RD, Thenmozhi K, Thiyagesan K, Baskaran N. 2017. Prevalence and determinants of stereotypic behaviours and physiological stress among tigers and leopards in Indian zoos. PLoS One 12(4), 1-27. http://dx.doi.org/10.1371/journal.pone.0174711

Vaz MJ. 2015. Evaluation of stereotypic behaviours and faecal corticosterone levels of captive felids in six Indian zoos. Doctoral dissertation, AVC College.

Webster AB, Burroughs RE, Laver P, Ganswindt A. 2018. Non-invasive assessment of adrenocortical activity as a measure of stress in leopards Panthera pardus. African Zoology 53(2), 53-60. http://dx.doi.org/10.1080/15627020.2018.1467280

Yalçintan H, Ekiz EE, Ekiz B, Koçak Ö, Bala DA, Yilmaz A. 2018. Certain behavioral characteristics and stress responses of out-of-breeding ewes and rams during an intensive fattening program. Turkish Journal of Veterinary and Animal Sciences 42(2), 97-102. http://dx.doi.org/10.3906/vet-1707-95

Zbyryt A, Bubnicki JW, Kuijper DP, Dehnhard M, Churski M, Schmidt K. 2018. Do wild ungulates experience higher stress with humans than with large carnivores? Behavioral Ecology 29(1), 19-30. http://dx.doi.org/10.1093/beheco/arx142