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Effects of feed withdrawal duration on animal behaviour, rumen microbiota and blood chemistry in feedlot cattle: implications for rumen acidosis

Published online by Cambridge University Press:  18 July 2019

A. Rabaza
Affiliation:
Plataforma de Salud Animal , Instituto Nacional de Investigación Agropecuaria, La Estanzuela, Colonia 70000, Uruguay Departamento de Microbiología, Instituto de Investigaciones Biológicas Clemente Estable, Avenida Italia 3318, Montevideo 11600, Uruguay School of Veterinary Sciences, University of Bristol, Langford House, Langford, Bristol BS40 5DU, UK
G. Banchero
Affiliation:
Programa de Carne y Lana, Instituto Nacional de Investigación Agropecuaria, La Estanzuela, Colonia 70000, Uruguay
C. Cajarville
Affiliation:
Departamento de Nutrición Animal, Instituto de Producción Animal, Facultad de Veterinaria, Universidad de la República, Ruta 1 km 42.5, San José 80100, Uruguay
P. Zunino
Affiliation:
Departamento de Microbiología, Instituto de Investigaciones Biológicas Clemente Estable, Avenida Italia 3318, Montevideo 11600, Uruguay
A. Britos
Affiliation:
Departamento de Nutrición Animal, Instituto de Producción Animal, Facultad de Veterinaria, Universidad de la República, Ruta 1 km 42.5, San José 80100, Uruguay
J. L. Repetto
Affiliation:
Departamento de Producción de Bovinos, Instituto de Producción Animal, Facultad de Veterinaria, Universidad de la República, Ruta 1 km 42.5, San José 80100, Uruguay
M. Fraga*
Affiliation:
Plataforma de Salud Animal , Instituto Nacional de Investigación Agropecuaria, La Estanzuela, Colonia 70000, Uruguay
*
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Abstract

Feed withdrawal (FW) is a frequent issue in open outdoor feedlot systems, where unexpected circumstances can limit the animals’ access to food. The relationship among fasting period, animal behaviour during feed reintroduction (FR) and acidosis occurrence has not been completely elucidated. Twenty steers fitted with rumen catheters were fed a high-concentrate diet (concentrate : forage ratio 85 : 15) and were challenged by a protocol of FW followed by FR. The animals were randomly assigned to one of the four treatments: FW for 12 h (T12), 24 h (T24), 36 h (T36) or no FW (control group) followed by FR. The steers’ behaviour, ruminal chemistry, structure of the ruminal microbial community, blood enzymes and metabolites and ruminal acidosis status were assessed. Animal behaviour was affected by the FW–FR challenge ( P < 0.05). Steers from the T12, T24 and T36 treatments showed a higher ingestion rate and a lower frequency of rumination. Although all animals were suspected to have sub-acute ruminal acidosis (SARA) prior to treatment, a severe case of transient SARA arose after FR in the T12, T24 and T36 groups. The ruminal pH remained below the threshold adopted for SARA diagnosis ( pH value = 5.6) for more than three consecutive hours (24, 7 and 19 h in the T12, T24 and T36 treatments, respectively). The FW–FR challenge did not induce clinical acute ruminal acidosis even though steers from the T36 treatment presented ruminal pH values that were consistent with this metabolic disorder (pH threshold for acute acidosis = 5.2). Total mixed ration reintroduction after the withdrawal period reactivated ruminal fermentation as reflected by changes in the fermentation end-products. Ruminal lactic acid accumulation in steers from the T24 and T36 treatments probably led to the reduction of pH in these groups. Both the FW and the FR phases may have altered the structure of the ruminal microbiota community. Whereas fibrolytic bacterial groups decreased relative abundance in the restricted animals, both lactic acid producer and utiliser bacterial groups increased ( P < 0.05). The results demonstrated a synchronisation between Streptococcus (lactate producer) and Megasphaera (lactate utiliser), as the relative abundance of both groups increased, suggesting that bacterial resilience may be central for preventing the onset of metabolic disturbances such as ruminal acidosis. A long-FW period (36 h) produced rumen pH reductions well below and lactic acid concentration increased well above the accepted thresholds for acute acidosis without any perceptible clinical signs.

Type
Research Article
Copyright
© The Animal Consortium 2019 

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References

Abrahamse, PA, Vlaeminck, B, Tamminga, S and Dijkstra, J 2008. The effect of silage and concentrate type on intake behavior, rumen function, and milk production in dairy cows in early and late lactation. Journal of Dairy Science 91, 47784792.CrossRefGoogle ScholarPubMed
Adams, RF, Jones, RL and Conway, PL 1984. High performance liquid chromatography of microbial acid metabolites. Journal of Chromatography 336, 125137.CrossRefGoogle ScholarPubMed
Brown, MS, Krehbiel, CR, Galyean, ML, Remmenga, MD, Peters, JP, Hibbard, B, Robinson, J and Moseley, WM 2000. Evaluation of models of acute and subacute acidosis on dry matter intake, ruminal fermentation, blood chemistry, and endocrine profiles of beef steers. Journal of Animal Science 78, 31553168.CrossRefGoogle ScholarPubMed
Caporaso, JG, Kuczynski, J, Stombaugh, J, Bittinger, K, Bushman, FD, Costello, EK, Fierer, N, Gonzalez-Pena, A, Goodrich, JK, Gordon, JI, Huttley, GA, Kelley, ST, Knights, D, Koenig, JE, Ley, RE, Lozupone, CA, McDonald, D, Muegge, BD, Pirrung, M, Reeder, J, Sevinsky, JR, Turnbaugh, PJ, Walters, WA, Widmann, J, Yatsunenko, T, Zaneveld, J and Knight, R 2010. QIIME allows analysis of high-throughput community sequencing data. Nature Methods 7, 335336.CrossRefGoogle ScholarPubMed
DePeters, EJ and Ferguson, JD 1992. Nonprotein nitrogen and protein distribution in the milk of cows. Journal of Dairy Science 75, 31923209.CrossRefGoogle ScholarPubMed
DeSantis, TZ, Hugenholtz, P, Larsen, N, Rojas, M, Brodie, EL, Keller, K, Huber, T, Dalevi, D, Hu, P and Andersen, GL 2006. Greengenes, a chimera-checked 16S rRNA gene database and workbench compatible with ARB. Applied and Environmental Microbiology 72, 50695072.CrossRefGoogle ScholarPubMed
Edgar, RC 2010. Search and clustering orders of magnitude faster than BLAST. Bioinformatics 26, 24602461.CrossRefGoogle ScholarPubMed
Félix, A, Repetto, JL, Hernández, N, Pérez-Ruchel, A and Cajarville, C 2017. Restricting the time of access to fresh forage reduces intake and energy balance but does not affect the digestive utilization of nutrients in beef heifers. Animal Feed Science and Technology 226,103112.CrossRefGoogle Scholar
Forbes, JM and Mayes, RW 2002. Food choice. In Sheep nutrition (ed. Freer, M and Dove, H), pp. 5169. CABI Publishing, Wallingford, UK.CrossRefGoogle Scholar
Galyean, ML, Malcom, KJ, Garcia, DR and Polsipher, GD 1992. Effects of varying the pattern of feed consumption on performance by programmed-fed steers. Clayton Livestock Research Center Progress Report 78, 13.Google Scholar
Garry, FB 2002. Indigestion in ruminants. In Large animal internal medicine (ed. Smith, BP), 3rd edition, pp. 722747.. Mosby Inc., St. Louis and Baltimore, MD, USA.Google Scholar
Ghorbani, GR, Morgavi, DP, Beauchemin, KA and Leedle, JA 2002. Effects of bacterial direct fed microbials on ruminal fermentation, blood variables, and the microbial populations of feedlot cattle. Journal of Animal Science 80, 19771985.CrossRefGoogle ScholarPubMed
Giger-Reverdin, S 2018. Recent advances in the understanding of subacute ruminal acidosis (SARA) in goats, with focus on the link to feeding behaviour. Small Ruminant Research 163, 2428.CrossRefGoogle Scholar
Gill, HS, Shu, Q and Leng, RA 2000. Immunization with Streptococcus bovis protects against lactic acidosis in sheep. Vaccine 18, 25412548.CrossRefGoogle Scholar
Golder, HM, Celi, P, Rabiee, AR, Heuer, C, Bramley, E, Miller, DW, King, R and Lean, IJ 2012. Effects of grain, fructose, and histidine on ruminal pH and fermentation products during an induced subacute acidosis protocol. Journal of Dairy Science 95, 19711982.CrossRefGoogle ScholarPubMed
Golder, HM, Thomson, JM, Denman, SE, McSweeney, CS and Lean, IJ 2018. Genetic markers are associated with the ruminal microbiome and metabolome in grain and sugar challenged dairy heifers. Frontiers in Genetics 9,110.CrossRefGoogle ScholarPubMed
Gozho, GN, Krause, DO and Plaizier, JC 2007. Ruminal lipopolysaccharide concentration and inflammatory response during grain-induced subacute ruminal acidosis in dairy cows. Journal of Dairy Science 90, 856866.CrossRefGoogle ScholarPubMed
Gozho, GN, Plaizier, JC, Krause, DO, Kennedy, AD and Wittenberg, KM 2005. Subacute ruminal acidosis induces ruminal lipopolysaccharide endotoxin release and triggers an inflammatory response. Journal of Dairy Science 88, 13991403.CrossRefGoogle ScholarPubMed
Khafipour, E, Li, S, Plaizier, JC and Krause, DO 2009. Rumen microbiome composition determined using two nutritional models of subacute ruminal acidosis. Applied and Environmental Microbiology 75, 71157124.CrossRefGoogle ScholarPubMed
Kim, YH, Nagata, R, Ohkubo, A, Ohtani, N, Kushibiki, S, Ichijo, T and Sato, S 2018. Changes in ruminal and reticular pH and bacterial communities in Holstein cattle fed a high-grain diet. BMC Veterinary Research 14, 310.CrossRefGoogle ScholarPubMed
Lean, I, Annison, F, Bramley, E, Browning, C and Cusack, P 2007. Ruminal acidosis-understandings, prevention and treatment. A review for veterinarians and nutritional professionals. Australian Veterinary Association 3, 46.Google Scholar
McCann, JC, Luan, S, Cardoso, FC, Derakhshani, H, Khafipour, E and Loor, JJ 2016. Induction of subacute ruminal acidosis affects the ruminal microbiome and epithelium. Frontiers in Microbiology 7, 118.CrossRefGoogle ScholarPubMed
Mutsvangwa, T, Walton, JD, Plaizier, JC, Duffield, TF, Bagg, R, Dick, P, Vessie, G and McBride, BW 2002. Effects of a monensin controlled-release capsule or premix on attenuation of subacute ruminal acidosis in dairy cows. Journal of Dairy Science 85, 34543461.CrossRefGoogle ScholarPubMed
Nagaraja, TG and Titgemeyer, EC 2007. Ruminal acidosis in beef cattle: the current microbiological and nutritional outlook. Journal of Dairy Science 90, E17E38.CrossRefGoogle ScholarPubMed
National Research Council (NRC) 2000. Nutrient requirements of beef cattle, 7th revised edition. National Academy Press, Washington, DC, USA.Google Scholar
Oetzel, GR 2003. Subacute ruminal acidosis in dairy cattle. Advanced Dairy Science and Technology 15, 307317.Google Scholar
Olson, KC and Hollis, LC 2007. Topics in nutritional management of feedlot cattle. Saunders, Philadelphia, PA, USA.Google Scholar
Owens, FN, Secrist, DS, Hill, WJ and Gill, DR 1998. Acidosis in cattle: a review. Journal of Animal Science 76, 275286.CrossRefGoogle ScholarPubMed
Patra, RC, Lal, SB and Swamp, D 1996. Biochemical profile of rumen liquor, blood and urine in experimental acidosis in sheep. Small Ruminant Research 19, 177180.CrossRefGoogle Scholar
Plaizier, JC, Khafipour, E, Li, S, Gozho, GN and Krause, DO 2012. Subacute ruminal acidosis (SARA), endotoxins and health consequences. Animal Feed Science and Technology 172, 921.CrossRefGoogle Scholar
Plaizier, JC, Li, S, Tun, HM and Khafipour, E 2017. Nutritional models of experimentally-induced subacute ruminal acidosis (SARA) differ in their impact on rumen and hindgut bacterial communities in dairy cows. Frontiers in Microbiology 7, 2128.CrossRefGoogle ScholarPubMed
Schwartzkopf-Genswein, KS, Beauchemin, KA, McAllister, TA, Gibb, DJ, Streeter, M and Kennedy, AD 2004. Effect of feed delivery fluctuations and feeding time on ruminal acidosis, growth performance, and feeding behavior of feedlot cattle. Journal of Animal Science 82, 33573365.CrossRefGoogle ScholarPubMed
Van Harmelen, V, Reynisdottir, S, Cianflone, K, Degerman, E, Hoffstedt, J, Nilsell, K, Sniderman, A and Arner, P 1999. Mechanisms involved in the regulation of free fatty acid release from isolated human fat cells by acylation-stimulating protein and insulin. Journal of Biological Chemistry 274, 1824318251.CrossRefGoogle ScholarPubMed
Wassell, J 2000. Haptoglobin: function and polymorphism. Clinical Laboratory 46, 547552.Google ScholarPubMed
Weatherburn, MW 1967. Phenol-hypochlorite reaction for determination of ammonia. Analytical Chemistry 39, 971974.CrossRefGoogle Scholar
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