WITHANIA COAGULANS AS A POTENTIAL ANTHELMINTIC IN-VIVO AGAINST NEMATODES IN CHAKUR (ALECTORIS CHUKAR) HOSTS

Main Article Content

Ajmal Nisar Mengal
Muhammad Hassan Saleem
Aneela Zameer Durrani
Aftab Ahmad Anjum
Muhammad Oneeb

Keywords

Chukar partridge, Anthelmintic resistance, Withania coagulans, nematodes

Abstract

The Chukar partridge (Alectoris chukar), a prominent species in the Phasianidae family within the Galliformes order, stands as the national bird of Pakistan and Iraq. These birds, operating within a semi-scavenging system, contend with a diverse array of helminth parasites. To treat helminthiasis, the repeated utilization of anthelmintic has inadvertently nurtured a global prevalence of anthelmintic resistance. In response to this challenge, the trend of employing botanical anthelmintics has gained momentum as a viable strategy to counter anthelmintic resistance. A notable contender in this realm is Withania coagulans, a plant indigenous to Balochistan and other regions, member of the Solanaceae family. Following the procurement of fresh leaves and fruits, the subsequent drying process culminated in the transformation of the dried plants into a finely ground powder. A total of 50 birds were evaluated, out of which 15 Chakur birds with elevated egg per gram (EPG) counts exceeding 150 were selected. The unveiled compelling results, with mean efficacy rates of 87.43% for Fenbendazole, 98.2% for Piperazine, and 96.6% for Withania coagulans. Notably, nematodes such as Ascarids and Heterakis gallinarum exhibited susceptibility to Piperazine and Withania coagulans, while concurrently demonstrating resistance to Fenbendazole, indicative of the evolution of drug resistance over time. The core objective of the study centered on evaluating the effectiveness of Withania coagulans in combating nematodes within the native Chakur bird population of Pakistan. The research findings were fortified by the presence of withanolides in the methanolic extract of Withania coagulans, which demonstrated anti-nematodal activity. The observed decline in EPG counts following treatment with Withania coagulans hints at the plausible role of bioactive compounds such as withanolides and alkaloids. In light of these findings, the study calls for a more extensive exploration of the potential of Withania coagulans and analogous herbal products as a means of tackling helminth infestations. The insights gleaned from these herbal interventions could catalyze the development of robust, sustainable strategies to confront and overcome anthelmintic resistance among avian populations.

Abstract 174 | pdf Downloads 89

References

Afrasiab SR, Mohammad MK, Ali HH, Al-Moussawi AA and Abdul-Rassoul M. 2013. Fauna and flora of Hawraman mountain (part one) Hawraman lowest zone, Kurdistan province north east of Iraq. Bulletin of the Iraq Natural History Museum (P-ISSN: 1017-8678, E-ISSN: 2311-9799). 12(4): 7-34.
2. Akhtar M, Iqbal Z, Khan M, Lateef M. 2000. Anthelmintic activity of medicinal plants with particular reference to their use in animals in the Indo–Pakistan subcontinent. Small Rumin Res. 38(2): 99-107.
3. Alawa C, Adamu A, Gefu J, Ajanusi O, Abdu P, Chiezey N, Alawa J and Bowman D. 2003. In vitro screening of two Nigerian medicinal plants (Vernonia amygdalina and Annona senegalensis) for anthelmintic activity. Vet Parasitol. 113(1): 73-81.
4. APVMA. 2020. Details of the Registration of Agricultural and Veterinary Chemical Products and Other Approvals Granted by the APVMA.
5. Asuzu I and Onu U. 1994. Anthelmintic activity of the ethanolic extract of Piliostigma thonningii bark in Ascaridia galli infected chickens. Fitoterapia (Milano). 65(4): 291-297.
6. Choudhary MI, Parveen Z, Jabbar A and Ali I. 1995. Antifungal steroidal lactones from Withania coagulance. Phytochem. 40(4): 1243-1246.
7. Coles G, Bauer C, Borgsteede F, Geerts S, Klei T, Taylor M, Waller P. 1992. World Association for the Advancement of Veterinary Parasitology (WAAVP) methods for the detection of anthelmintic resistance in nematodes of veterinary importance. Vet. Parasitol. 44: 35-44.
8. Coles G, Jackson F, Pomroy W, Prichard R, von Samson-Himmelstjerna G, Silvestre A, Taylor M, Vercruysse J. 2006. The detection of anthelmintic resistance in nematodes of veterinary importance. Vet. Parasitol. 136: 167-185.
9. Cringoli G, Rinaldi L, Maurelli MP and Utzinger J. 2010. FLOTAC: new multivalent techniques for qualitative and quantitative copromicroscopic diagnosis of parasites in animals and humans. Nat. Protoc. 5(3): 503-515.
10. Desta B. 1995. Ethiopian traditional herbal drugs. Part I: Studies on the toxicity and therapeutic activity of local taenicidal medications. J. Ethnopharmacol. 45(1): 27-33.
11. Fajimi A and Taiwo A. 2005. Herbal remedies in animal parasitic diseases in Nigeria: a review. Afr J Biotech. 4(4): 303-307
12. Farooq Z, Baboo I, Wajid M, Sadia H, Abrar M, Iqbal K, Javid A and Hussain D. 2019. Hematological and Plasma biochemical reference values in Chukar Partridge (Alectoris chukar) under captive facilities. Biol Pak. 65.
13. Gaind K and Budhiraja R. 1967. Antibacterial and anthelmintic activity of Withania coagulans Dunal. Indian J. Pharm. 29: 185-186.
14. Hammond J, Fielding D and Bishop S. 1997. Prospects for plant anthelmintics in tropical veterinary medicine. Vet Res Communs. 21(3): 213-228
15. Hawramany S. 2007. Ecology, behavior, reproduction, and classification of Alectoris chukar (Gray) with a comparison between sub-species found in Iraq [master’s thesis]. Baghdad: Univercity of Baghdad.
16. Jabbar A, Raza MA, Iqbal Z and Khan MN. 2006. An inventory of the ethnobotanicals used as anthelmintics in the southern Punjab (Pakistan). J Ethnopharmacol. 108(1): 152-154.
17. Jaeger LH and Carvalho-Costa FA. 2017. Status of benzimidazole resistance in intestinal nematode populations of livestock in Brazil: a systematic review. BMC Vet. Res. 13: 1-10.
18. Kaufmann F, Daş G, Sohnrey B and Gauly M. 2011. Helminth infections in laying hens kept in organic free range systems in Germany. Livest. Sci. 141(2-3): 182-187.
19. Khan M, Ashraf M, Tehniyat S, Bukhtair M, Ashraf S and Ahmad W. 1993. Antibacterial activity of Withania coagulans. Fitoterapia 64:367.
20. Khan MN, Sajid MS, Rizwan HM, Qudoos A, Abbas RZ, Riaz M and Khan MK. 2017. Comparative Efficacy of Six Anthelmintic Treatments against Natural Infection of Fasciola Species in Sheep. Pak Vet J. 37(1): 65-68.
21. Khan RU, Sadam A and Mahmood S. 2021. Population ecology of chakor partridge (Alectoris chukar) in district Bajaur, Khyber Pakhtunkhwa, Pakistan. Pak J Zool. 52.
22. Khare CP. 2008. Indian medicinal plants: an illustrated dictionary. Springer Science & Business Media. p.
23. Khodaei M, Jafari M and Noori M. 2012. Remedial use of withanolides from Withania coagolans (Stocks) Dunal. Adv Life Sci. 2(1): 6-19.
24. Khoshnaw ZO and Abdullah SM. 2013. Study on the parasites of chukar partridge Alectoris chukar from Shaqlawa district, Kurdistan region, Iraq. Tikrit Journal of Pure Science. 18(3): 26-30.
25. Köhler P (2001). The biochemical basis of anthelmintic action and resistance. Elsevier.34(4):336-345
26. Kuroyanagi M, Murata M, Nakane T, Shirota O, Sekita S, Fuchino H and Shinwari ZK. 2012. Leishmanicidal active withanolides from a pakistani medicinal plant, Withania coagulans. Chem Pharm Bull. 60(7): 892-897.
27. Lalchhandama K. 2010. Anthelmintic resistance: the song remains the same. Sci Vis. 10(4): 111-122.
28. Maurya R. 2010. Chemistry and pharmacology of Withania coagulans: an Ayurvedic remedy. J Pharm Pharmacol. 62(2): 153-160.
29. Mitchell G. 2002. Update on fasciolosis in cattle and sheep. In Prac. 24(7): 378.
30. Mooney L, Good B, Hanrahan J, Mulcahy G and De Waal T. 2009. The comparative efficacy of four anthelmintics against a natural acquired Fasciola hepatica infection in hill sheep flock in the west of Ireland. Vet Parasitol. 164(2): 201-205.
31. Overend D and Bowen F. 1995. Resistance of Fasciola hepatica to Triclabendazole. Aus vet Jl. 72(7): 275-276.
32. Shifaw A, Feyera T, Walkden-Brown SW, Sharpe B, Elliott T and Ruhnke I. 2021. Global and regional prevalence of helminth infection in chickens over time: a systematic review and meta-analysis. Poult. Sci. 100(5): 101082.
33. Shivambu N, Shivambu CT and Downs CT. 2020. Chukar Partridge (Alectoris chukar Gray, 1830). In: Invasive birds: global trends and impacts pp. 132-137. CABI Wallingford UK.
34. Pandey VS and Demey F (1993). Village poultry production in Africa. Proceedings of an international workshop. Held at Rabat (Morocco), 7-11 May 1992. In Village poultry production in Africa. International workshop, Rabat (Morocco), 7-11 May 1992.
35. Rahman M, Mondal M and Huq M. 1989. A note on the occurrences of parasitic mites of domestic fowls (Gallus gallus) in Bangladesh. Bang. Vet. 6: 45-47.
36. Terefe D, Demissie D, Beyene D, Haile S. 2012. A prevalence study of internal parasites infecting Boer goats at Adami Tulu agricultural research center, Ethiopia. J. Vet. Med. Anim. Health. 4: 12-16.
37. Thapa S, Hinrichsen LK, Brenninkmeyer C, Gunnarsson S, Heerkens JL, Verwer C, Niebuhr K, Willett A, Grilli G and Thamsborg SM. 2015. Prevalence and magnitude of helminth infections in organic laying hens (Gallus gallus domesticus) across Europe. Vet. Parasitol. 214(1-2): 118-124.
38. Ullah A, Khan K, Bibi N, Ahmad S, Khan A, Ali M, Ali H, Khan M, Ghayyur S and Yasmin S. 2022. New Parasitic records of Aves: Phasianidae () in Malakand division northern, Pakistan. Helminthologia. 59(4): 398-403.
39. Waller P. 2003. The future of anthelmintics in sustainable parasite control programs for livestock. Helminthologia. 40(2): 97-102.
40. Zajac AM. 2006. Gastrointestinal nematodes of small ruminants: life cycle, anthelmintics, and diagnosis. Veterinary Clinics of North America: Food Animal Practice. 22: 529-541.