The nutritional status affects the complete blood count of goats experimentally infected with Haemonchus contortus

Springer Science and Business Media LLC - Tập 13 - Trang 1-10 - 2017
S. Cériac1, C. Jayles2, R. Arquet2, D. Feuillet1, Y. Félicité1, H. Archimède1, J.-C. Bambou1
1URZ, INRA, Petit-Bourg, France
2PTEA, INRA, Le Moule, France

Tóm tắt

Gastrointestinal nematode (GIN) remains the most important pathogenic constraint of small ruminant production worldwide. The improvement of the host immune response against GIN though breeding for improved animal resistance, vaccination and nutritional supplementation appear as very promising methods. The objective of this study was to investigate the effect of four nutritional status differing in protein and energy levels (Hay: 5.1 MJ/Kg of dry matter (DM) and 7.6% of crude protein (CP), Ban: 8.3 MJ/Kg of DM and 7.5% of CP, Soy: 7.6 MJ/Kg of DM and 17.3% of CP, BS: 12.7 MJ/Kg of DM and 7.4% of CP) on the haematological disturbances due to Haemonchus contortus infection in Creole kid goats. No significant effect of the nutritional status was observed for faecal egg count (FEC) but the experimental infection induced haematological disturbances whose intensity and lengthening were dependent on the nutritional status. A transient marked regenerative macrocytic hypochromic anaemia as revealed by a decrease of packed cell volume (PCV), red blood cells (RBC) and hemoglobin and an increase of reticulocytes was observed in all infected groups except Hay. In this latter, the anaemia settled until the end of the experiment. Furthermore, H. contortus induced a thrombocytopenia significantly more pronounced in the group under the lowest nutritional status in term of protein (Hay and Ban). A principal component analysis revealed that the variables that discriminated the nutritional status were the average daily gain (ADG) and the PCV, considered as measures of the level of resilience to H. contortus infection. Moreover, the variables that discriminated infected and non-infected animals were mostly related to the biology of RBC (i.e. size and hemoglobin content) and they were correlated with FEC. The severity and the lengthening of the regenerative anaemia and the thrombocytopenia induced by H. contortus have been affected by the nutritional status. The protein enriched diets induced resilience to the infection rather than resistance. This suggests that resilience is associated with an improved regenerative capacity of the bone marrow. However, this needs to be further investigated to understand the relationships between resistance, resilience and dietary supplementation.

Tài liệu tham khảo

Bishop SC, Morris CA. Genetics of disease resistance in sheep and goats. Small Rumin Res. 2007;70(1):48–59. Papadopoulos E. Anthelmintic resistance in sheep nematodes. Small Rumin Res. 2008;76(1–2):99–103. Beynon SA. Potential environmental consequences of administration of anthelmintics to sheep. Vet Parasitol. 2012;189(1):113–24. Baker RL, Gray GD. Worm control for small ruminants in tropical Asia. Australian Centre for International Agricultural Research (ACIAR). 2003;Monograph 113:63–95. van Wyk JA, Bath GF. The FAMACHA((c)) system for managing haemonchosis in sheep and goats by clinically identifying individual animals for treatment. Vet Res. 2002;33(5):509–29. Clunies Ross I, Gordon H. McL.: nutritional factors affecting reistance to haemonchosis. Aust Vet J. 1933;9:100–7. Gibson TE. The influence of nutrition on the relationships between gastro-intestinal parasites and their hosts. Proc Nutr Soc. 1963;22:15–20. Adams CA. Nutrition-based health in animal production. Nutr Res Rev. 2006;19(1):79–89. Colditz IG. Six costs of immunity to gastrointestinal nematode infections. Parasite Immunol. 2008;30(2):63–70. Lochmiller RL, Deerenberg C. Trade-offs in evolutionary immunology: just what is the cost of immunity? Oikos. 2000;88(1):87–98. Koski KG, Scott ME. Gastrointestinal nematodes, trace elements, and immunity. J Trace Elem Exp Med. 2003;16(4):237–51. McClure SJ. How minerals may influence the development and expression of immunity to endoparasites in livestock. Parasite Immunol. 2008;30(2):89–100. Torres-Acosta JFJ, Sandoval-Castro CA, Hoste H, Aguilar-Caballero AJ, Camara-Sarmiento R, Alonso-Diaz MA. Nutritional manipulation of sheep and goats for the control of gastrointestinal nematodes under hot humid and subhumid tropical conditions. Small Rumin Res. 2012;103(1):28–40. Walkden-Brown SW, Kahn LP. Nutritional modulation of resistance and resilience to gastrointestinal nematode infection - a review. Asian-Australas J Anim Sci. 2002;15(6):912–24. Knox MR, Torres-Acosta JFJ, Aguilar-Caballero AJ. Exploiting the effect of dietary supplementation of small ruminants on resilience and resistance against gastrointestinal nematodes. Vet Parasitol. 2006;139(4):385–93. Houdijk JGM. Differential effects of protein and energy scarcity on resistance to nematode parasites. Small Rumin Res. 2012;103(1):41–9. Bambou JC, de la Chevrotiere C, Varo H, Arquet R, Kooyman FNJ, Mandonnet N. Serum antibody responses in Creole kids experimentally infected with Haemonchus contortus. Vet Parasitol. 2008;158(4):311–8. Aumont G, R. Pouillot, Mandonnet N: Le dénombrement des éléments parasitaires: Un outil pour l'étude de la résistance génétique aux endo-parasites chez les petits ruminants. Workshop final de l’AT CIRAD-MIPA 72/94, Guadeloupe 1997. Dawkins HJS, Windon RG, Eagleson GK. Eosinophil responses in sheep selected for high and low responsiveness to Trichostrongylus colubriformis. Int J Parasitol. 1989;19(2):199–205. Le S, Josse J, Husson F. FactoMineR: an R package for multivariate analysis. J Stat Softw. 2008;25(1):1–18. Sykes AR, Coop RL. Interaction between nutrition and gastrointestinal parasitism in sheep. New Zeal Vet J. 2001;49(6):222–6. Walkden-Brown SW, Kahn LP: Nutritional modulation of resistance and resilience to gastrointestinal nematode infection - a review. In: International symposium on new challenges for animal science in a new century 2001; Sendai, Japan; 2001: 912-924. Andronicos NM, Henshall JM, Le Jambre LF, Hunt PW, Ingham AB. A one shot blood phenotype can identify sheep that resist Haemonchus contortus challenge. Vet Parasitol. 2014;205(3–4):595–605. Khan FA, Sahoo A, Sonawane GG, Karim SA, Dhakad S, Pareek AK, Tripathi BN. Effect of dietary protein on responses of lambs to repeated Haemonchus contortus infection. Livest Sci. 2012;150(1–3):143–51. Abbott EM, Parkins JJ, Holmes PH. The effect of dietary-protein on the pathogenesis of acute ovine haemonchosis. Vet Parasitol. 1986;20(4):275–89. Crab A, Noppe W, Pelicaen C, Van Hoorelbeke K, Deckmyn H. The parasitic hematophagous worm Haemonchus contortus inhibits human platelet aggregation and adhesion: partial purification of a platelet inhibitor. Thromb Haemost. 2002;87(5):899–904. Meeusen E, Balic A, Bowles V. Cells, cytokines and other molecules associated with rejection of gastrointestinal nematode parasites. Vet Immunol Immunopathol. 2005;108(1–2):121–5. Gill HS. Genetic control of acquired resistance to haemonchosis in merino lambs. Parasite Immunol. 1991;13:617–28. Adams DB. Systemic responses to challenge infection with Haemonchus contortus in immune merino sheep. Vet Res Commun. 1993;17(1):25–35. Woolaston RR, Manueli P, Eady SJ, Barger IA, LeJambre LF, Banks DJD, Windon RG. The value of circulating eosinophil count as a selection criterion for resistance of sheep to trichostrongyle parasites. Int J Parasitol. 1996;26(1):123–6. Bambou JC, Archimede H, Arquet R, Mahieu M, Alexandre G, Gonzalez-Garcia E, Mandonnet N. Effect of dietary supplementation on resistance to experimental infection with Haemonchus contortus in Creole kids. Vet Parasitol. 2011;178(3–4):279–85. Rowe A, McMaster K, Emery D, Sangster N. Haemonchus contortus infection in sheep: parasite fecundity correlates with worm size and host lymphocyte counts. Vet Parasitol. 2008;153(3–4):285–93. Ortolani EL, Leal MLD, Minervino AHH, Aires AR, Coop RL, Jackson F, Suttle NF. Effects of parasitism on cellular immune response in sheep experimentally infected with Haemonchus contortus. Vet Parasitol. 2013;196(1–2):230–4. Bambou JC, Gonzalez-Garcia E, de la Chevrotiere C, Arquet R, Vachiery N, Mandonnet N. Peripheral immune response in resistant and susceptible Creole kids experimentally infected with Haemonchus contortus. Small Rumin Res. 2009;82(1):34–9. Wallace DS, Bairden K, Duncan JL, Fishwick G, Holmes PH, McKellar QA, Murray M, Parkins JJ, Stear M: Influence of soyabean meal supplementation on the resistance of Scottish blackface lambs to haemonchosis. Res Vet Sci 1996, 60(2):138-143. Datta FU, Nolan JV, Rowe JB, Gray GD. Protein supplementation improves the performance of parasitised sheep fed a straw-based diet. Int J Parasitol. 1998;28(8):1269–78. Louvandini H, Veloso CFM, Paludo GR, Dell'Porto A, Gennari SM, McManus CM. Influence of protein supplementation on the resistance and resilience on young hair sheep naturally infected with gastrointestinal nematodes during rainy and dry seasons. Vet Parasitol. 2006;137(1–2):103–11. Nnadi PA, Kamalu TN, Onah DN. The effect of dietary protein on the productivity of west African dwarf (WAD) goats infected with Haemonchus contortus. Vet Parasitol. 2009;161(3–4):232–8. Rauw W. Immune response from a resource allocation perspective. Front Genet. 2012;3(267)