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In vivo validation of Aloe ferox (Mill). Elephantorrhiza elephantina Bruch. Skeels. and Leonotis leonurus (L) R. BR as potential anthelminthics and antiprotozoals against mixed infections of gastrointestinal nematodes in goats

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Abstract

Aloe ferox (Mill)., Elephantorrhiza elephantina Bruch. Skeels. and Leonotis leonurus (L) R. BR. are some of the plants used by farmers in the Eastern Cape Province to control worms in goats, but information on their efficacy is lacking. The study was conducted to determine efficacy of these plants on gastrointestinal nematodes in natural mixed infections in goats. Forty-eight male goats aged 8–12 months were divided into eight groups (Treatments A–H) of six animals each, balanced in terms of liveweight and worm egg count. Treatments A to F received plant extracts, three animals in each group receiving doses of 250 mg/kg and the other three receiving 500 mg/kg at concentration of 100 mg/ml, while those in G and H received Valbazen® (11.36% albendazole) at 10 mg/kg, and 0.5 ml/kg distilled water, respectively per os. Faecal samples were collected on days 0, 3, 6 and 9 for faecal egg counts (FEC), and body weights recorded on days 1 and 9. Results showed significant reductions (P < 0.05) in strongyle eggs by A. ferox extract at dose levels of 500 mg/kg on days 3, 6 and 9, while reductions in Eimeria spp. oocysts were observed on days 3, 6 and 9 for animals that received 500 mg/kg doses. E. elephantina caused significant reduction (P < 0.05) of Trichuris spp. eggs on days 3 and 6, respectively at 250 mg/kg dose level, whereas L. leonurus also caused significant reduction (P < 0.05) in FEC of Trichuris spp. and Eimeria spp. oocysts at 250 mg/kg dose level on day 9. Albendazole caused reductions (P < 0.05) in strongyle eggs on days 3 and 6, Trichuris spp. on days 3, 6 and 9, and on coccidia, it caused a reduction (P > 0.05) on day 1, whereas on days 6 and 9, there was an increase. On total mixed infections, highest FECR% were observed with the extract of A. ferox on days 3 (53%), 6 (54%) and 9 (58%) at 500 mg/kg,whereas albendazole had efficacy levels of 39%, 44% and 29% on days 3, 6 and 9, respectively. Body weight of goats from days 1 to 9 were not significant different from the control. The study revealed efficacy of A. ferox, E. elephantina and L. leonurus against gastrointestinal parasites at high doses (500 mg/kg), showing that the plants have the potential to be used as anthelminthics.

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References

  • Abdel-Ghaffar F, Semmler M, Al-Rasheid KAS, Strassen B, Fischer K, Aksu G, Klimpel S, Mehlhorn H (2011) The effects of different plant extracts on intestinal cestodes and on trematodes. Parasitol Res 108:979–984

    Article  PubMed  Google Scholar 

  • Akhtar MS, Iqbal Z, Khan MN, Lateef M (2000) Anthelmintic activity of medicinal plants with particular reference to their use in animals in Indo-Pakistan subcontinent. Small Rumin Res 38:99–107

    Article  Google Scholar 

  • Alawa CBI, Adamu AM, Gefu JO, Ajanusi OJ, Abdu PA, Chiezey NP, Alawa JN, Bowman DD (2003) In vitro screening of two Nigerian medicinal plants (Vernonia amygdalina and Annona senegalensis) for anthelmintic activity. Vet Parasitol 113:73–81

    Article  PubMed  CAS  Google Scholar 

  • Anthony JP, Fyfe L, Smith H (2005) Plant active components – a resource for antiparasitic agents? Trends Parasitol 21(10):462–468

    Article  PubMed  CAS  Google Scholar 

  • Arosemena NAE, Bevilaqua CML, Girão MD, Melo ACFL (1999) Seasonal variations of gastrointestinal nematodes in sheep and goats from semi-arid area in Brazil. Rev medecine veterinaire 150:873–876

    Google Scholar 

  • Bienvenu E, Amabeoku GJ, Eagles PK (2002) Anticonvulsant activity of aqueous extract of Leonotis leonorus. Phytomedicine 9:217–223

    Article  PubMed  CAS  Google Scholar 

  • Chapman MR, Klei TR, French DD (1991) Identification of thiabendazole-resistant cyathostome species in Louisiana. Vet Parasitol 39:293–299

    Article  PubMed  CAS  Google Scholar 

  • Chiejina SN (2001) The epidemiology of helminthes infections of domesticated animals in the tropics with emphasis on fascioliasis and parasitic gastroenteritis. In: Chowdhury N, Tada I (eds) Perspectives. Helminthol Science Publishers Inc., Enfield, pp 41–87

    Google Scholar 

  • Doerfler RL, Peters KJ (2006) The relativity of ethical issues in animal agriculture related to different cultures and production conditions. Liv Scie 103(3):257–262

    Article  Google Scholar 

  • Dold AP, Cocks ML (2001) Traditional veterinary medicine in the Alice district of the Eastern Cape Province, South Africa. S Afr J Sci 97:1–5

    Google Scholar 

  • Eguale T, Tilahun G, Debella A, Feleke A, Makonnen E (2007) Haemonchus contortus: In vitro and in vivo anthelmintic activity of aqueous and hydro-alcoholic extracts of Hedera helix. Exp Parasitol 116:340–345

    Article  PubMed  CAS  Google Scholar 

  • Fajmi AK, Taiwo AA (2005) Herbal remedies in animal parasitic diseases in Nigeria: a review. Afr J Biotech 4:303–307

    Google Scholar 

  • Gasbarre CL, Stou LW, Leighton AE (2001) Gastrointestinal nematodes of cattle in the North Eastern US: results of a producer survey. Vet Parasitol 101:29–44

    Article  PubMed  CAS  Google Scholar 

  • Gibbs HC (1986) Hypobiosis in parasitic nematodes. In: Epidemiology, diagnosis and control of gastrointestinal parasitism. A handbook. ILRAD, Kenya, pp 121

  • Githiori JB, Athanasiadou S, Thamsborg SM (2006) Use of plants in novel approaches for control of gastrointestinal helminths in livestock with emphasis on small ruminants. Vet Parasitol 139:308–320

    Article  PubMed  Google Scholar 

  • Guarrera MP (1999) Traditional anthelmintic, antiparasitic and repellent uses of plants in central Italy. J Ethnopharmacol 68:183–192

    Article  PubMed  CAS  Google Scholar 

  • Hansen J, Perry B (1994) The epidemiology, diagnosis and control of helminth parasites of ruminants. International Laboratory for Research on Animal Diseases, Nairobi, Kenya

    Google Scholar 

  • Horak GE, Ursula PRE (2004) Parasites of domestic and wild animals in South Africa. XLV. Helminths of dairy calves on dry-land Kikuyu grass pastures in the Eastern Cape Province. Onderstepoort J Vet Res 71:291–306

    PubMed  CAS  Google Scholar 

  • Hutchings A, Scott AH, Lewis G, Cunningham AB (1996) Zulu medicinal plants: an inventory. University of Natal Press, Pietermaritzburg, p 66

    Google Scholar 

  • Jackson F, Miller J (2006) Alternative approaches to control—Quo vadit? Vet Parasitol 139:371–384

    Article  PubMed  Google Scholar 

  • Klimpel S, Abdel-Ghaffar F, Al-Rasheid KAS, Aksu G, Fischer K, Strassen B, Mehlhorn Res H (2011) The effects of different plant extracts on nematodes. Parasitol Res 108:1047–1054

    Article  PubMed  Google Scholar 

  • Mabusela WT, Stephen AM, Botha MC (1990) Carbohydrate polymers from Aloe ferox leaves. Phytochem 29(11):3555–3558

    Article  CAS  Google Scholar 

  • Maphosa V, Masika PJ (2010) Ethnoveterinary uses of medicinal plants: a survey of plants used in the ethnoveterinary control of gastro-intestinal parasites of goats in the Eastern Cape Province, South Africa. Pharm Biol 48(6):697–702

    Article  PubMed  Google Scholar 

  • Maphosa V, Masika PJ, Bizimenyera ES, Eloff JN (2009) In-vitro anthelminthic activity of crude aqueous extracts of Aloe ferox, Leonotis leonurus and Elephantorrhiza elephantina against Haemonchus contortus. Trop Anim Health Prod 42:301–307

    Article  PubMed  Google Scholar 

  • Mathius-Mundy E, McCorkle CM (1989) Ethnoveterinary medicine: an annotated bibliography. Bibliographies in Technology and Social Change, No 6. Technology and Social Change Program, Iowa State University, Ames, Iowa 50011. USA. ISBN 0-945271- pp 16–6. 199.

  • McCorkle M, Mathias E, van Veen TW Schillhorn (1996) Ethnoveterinary research and development. IT studies in indigenous knowledge & development. Intermediate Technology Publications, Southampton Row, London, pp 1–450

    Google Scholar 

  • McGaw LJ, van Jäger AK, Staden J (2000) Antibacterial, anthelmintic and anti-amoebic activity in South African medicinal plants. J Ethnopharmacol 72:247–263

    Article  PubMed  CAS  Google Scholar 

  • Mehlhorn H, Al-Quraishy S, Al-Rasheid KA, Jatzlau A, Abdel-Ghaffar F (2011) Addition of a combination of onion (Allium cepa) and coconut (Cocos nucifera) to food of sheep stops gastrointestinal helminthic infections. Parasitol Res 108:1041–1046

    Article  PubMed  Google Scholar 

  • Mutsabisa M (2006) Traditional medicines. http://www.sahealthinfo.org/traditionalmeds/aboutuwc.htm [accessed 23.08.2010],

  • Naidoo V (2005) Screening of four plants commonly used in ethnoveterinary medicine for antimicrobial, anti-protozoal and anti-oxidant activity. MSc dissertation. University of Pretoria. pp 1–130

  • Naidoo V, Zweygarth E, Eloff JN, Swan GE (2005) Identification of anti-babesial activity for four ethnoveterinary plants in vitro. Vet Parasitol 130:9–13

    Article  PubMed  CAS  Google Scholar 

  • Perry B, Randolph T, McDermott J, Sones K, Tornton PK (2002) Investing in animal health research to alleviate poverty. International Livestock Research Institute, Nairobi, Kenya, p 148

    Google Scholar 

  • Schillhorn van Veen TW (1997) Sense or nonsense? Traditional methods of animal parasitic disease control. Vet Parasitol 71:177–194

    Article  PubMed  CAS  Google Scholar 

  • Statistical Analysis Systems Institute (2003) SAS user's guide: statistics, version 6. SAS Institute Inc., Cary, NC, USA

    Google Scholar 

  • Van Shalkwyk PP, Schröder J (1989) Benzimidazole resistant Ostertagia circumcincta in Angora goats. J S Afr Vet Assoc 60(2):76–78

    Google Scholar 

  • Van Wyk E, Malan S (1988) Field guide to the wild flowers of the Witwatersrand and Pretoria region. Struik Publishers, Cape Town, South Africa

    Google Scholar 

  • Van Wyk B-E, Van Ousdtshoorn B, Gericke N (2002) Medicinal plants of South Africa. Pretoria, Briza, pp 1–304

    Google Scholar 

  • Waller PJ (2003) The future of anthelmintics in sustainable parasite control programs for livestock. Helminthologia 40:97–102

    CAS  Google Scholar 

Download references

Acknowledgements

The authors would like to acknowledge the Govan Mbeki Research and Development Centre (GMRDC) and the National Research Foundation (NRF) for the funding.

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Correspondence to Patrick J. Masika.

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Maphosa, V., Masika, P.J. In vivo validation of Aloe ferox (Mill). Elephantorrhiza elephantina Bruch. Skeels. and Leonotis leonurus (L) R. BR as potential anthelminthics and antiprotozoals against mixed infections of gastrointestinal nematodes in goats. Parasitol Res 110, 103–108 (2012). https://doi.org/10.1007/s00436-011-2455-8

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