Changes in gene expression in the rumen and colon epithelia during the dry period through lactation of dairy cows and effects of live yeast supplementation

Journal of Dairy Science

Volumn 101, Issue 3, 2018, Pages 2631-2640

  Bach, A ^a,b   Guasch, I ^c   Elcoso, G ^c   Chaucheyras Durand, F ^d,e   Castex, M ^d   Fabregas F ^b   Garcia Fruitos, E ^b   Aris, A ^b  

^a INSTITUCIÓ CATALANA DE RECERCA I ESTUDIS AVANÇATS ICREA   (Spain)

^b IRTA   (Spain)

^c Blanca from the Pyrenees   (Spain)

^d LALLEMAND SAS   (France)

^e UMR 454 MEDIS INRA UCA   (France)

Author keywords

colon; endoscope; epithelium; rumen

Indexed keywords

PROBIOTIC AGENT;

ANIMAL; BOVINE; COLON; DIET; DRIED YEAST; DRUG EFFECT; FEMALE; GENE EXPRESSION; INTESTINE MUCOSA; LACTATION; MAIZE; METABOLISM; MILK; PHYSIOLOGY; RUMEN; SACCHAROMYCES CEREVISIAE; VETERINARY;

ANIMALS; CATTLE; COLON; DIET; FEMALE; GENE EXPRESSION; INTESTINAL MUCOSA; LACTATION; MILK; PROBIOTICS; RUMEN; SACCHAROMYCES CEREVISIAE; YEAST, DRIED; ZEA MAYS;

EID: 85044861030     PISSN: 00220302     EISSN: 15253198     Source Type: Journal    
DOI: 10.3168/jds.2017-13212     Document Type: Article

References (55)

1. Abaker, J.A., Xu, T.L., Jin, D., Chang, G.J., Zhang, K., Shen, X.Z., Lipopolysaccharide derived from the digestive tract provokes oxidative stress in the liver of dairy cows fed a high-grain diet. J. Dairy Sci. 100 (2017), 666–678 10.3168/jds.2016-10871 27865500.
2. Abreu, M.T., Toll-like receptor signalling in the intestinal epithelium: How bacterial recognition shapes intestinal function. Nat. Rev. Immunol. 10 (2010), 131–144 10.1038/nri2707 20098461.
3. AOAC (Association of Official Analytical Chemists), Official Methods of Analysis. 15th ed., 1990, AOAC, Arlington, VA.
4. Aschenbach, J.R., Borau, T., Gäbel, G., Glucose uptake via SGLT-1 is stimulated by beta(2)-adrenoceptors in the ruminal epithelium of sheep. J. Nutr. 132 (2002), 1254–1257 12042442.
5. Ayabe, T., Satchell, D.P., Wilson, C.L., Parks, W.C., Selsted, M.E., Ouellette, A.J., Secretion of microbicidal alpha-defensins by intestinal Paneth cells in response to bacteria. Nat. Immunol. 1 (2000), 113–118 11248802.
6. Bach, A., Iglesias, C., Busto, I., Technical note: A computerized system for monitoring feeding behavior and individual feed intake of dairy cattle. J. Dairy Sci. 87 (2004), 4207–4209 10.3168/jds.S0022-0302(04)73565-1 15545384.
7. Bach, A., Iglesias, C., Devant, M., Daily rumen pH pattern of loose-housed dairy cattle as affected by feeding pattern and live yeast supplementation. Anim. Feed Sci. Technol. 136 (2007), 146–153 10.1016/j.anifeedsci.2006.09.011.
8. Bach, A., Yoon, I.K., Stern, M.D., Jung, H.G., Chester-Jones, H., Effects of type of carbohydrate supplementation to lush pasture on microbial fermentation in continuous culture. J. Dairy Sci. 82 (1999), 153–160 10.3168/jds.S0022-0302(99)75219-7 10022017.
9. Baldwin, R.L.V.I., The proliferative actions of insulin, insulin-like growth factor-I, epidermal growth factor, butyrate and propionate on ruminal epithelial cells in vitro. Small Rumin. Res. 32 (1999), 261–268.
10. Bannink, A., France, J., Lopez, S., Gerrits, W.J.J., Kebreab, E., Tamminga, S., Dijkstra, J., Modeling the implications of feeding strategy on rumen fermentation and functioning of the rumen wall. Anim. Feed Sci. Technol. 143 (2008), 3–26.
11. Bannink, A., Gerrits, W.J.J., France, J., Dijkstra, J., Variation in rumen fermentation and the rumen wall during the transition period in dairy cows. Anim. Feed Sci. Technol. 172 (2012), 80–94 10.1016/j.anifeedsci.2011.12.010.
12. Bauernfeind, F.G., Horvath, G., Stutz, A., Alnemri, E.S., MacDonald, K., Speert, D., Fernandes-Alnemri, T., Wu, J., Monks, B.G., Fitzgerald, K.A., Hornung, V., Latz, E., Cutting edge: NF-kappaB activating pattern recognition and cytokine receptors license NLRP3 inflammasome activation by regulating NLRP3 expression. J. Immunol. 183 (2009), 787–791 10.4049/jimmunol.0901363 19570822.
13. Beharka, A.A., Nagaraja, T.G., Morrill, J.L., Kennedy, G.A., Klemm, R.D., Effects of form of the diet on anatomical, microbial, and fermentative development of the rumen of neonatal calves. J. Dairy Sci. 81 (1998), 1946–1955 9710764.
14. Bevans, D.W., Beauchemin, K.A., Shwartzkopf-Genswein, K.S., McKinnon, J.J., McAllister, T.A., Effect of rapid or gradual grain adaptation on subacute acidosis and feed intake by feedlot cattle. J. Anim. Sci. 83 (2005), 1116–1132 15827257.
15. Brown, M.S., Ponce, C.H., Pulikanti, R., Adaptation of beef cattle to high-concentrate diets: Performance and ruminal metabolism. J. Anim. Sci. 84 (2006), E25–E33 16582090.
16. Castells, L., Bach, A., Aris, A., Terré, M., Effects of forage provision to young calves on rumen fermentation and development of the gastrointestinal tract. J. Dairy Sci. 96 (2013), 5226–5236 10.3168/jds.2012-6419 23706491.
17. Catalani, E., Amadori, M., Vitali, A., Bernabucci, U., Nardone, A., Lacetera, N., The Hsp72 response in periparturient dairy cows: Relationships with metabolic and immunological parameters. Cell Stress Chaperones 15 (2010), 781–790 10.1007/s12192-010-0186-x 20349286.
18. Chaucheyras-Durand, F., Walker, N.D., Bach, A., Effects of active dry yeasts on the rumen microbial ecosystem: Past, present and future. Anim. Feed Sci. Technol. 145 (2008), 5–26 10.1016/j.anifeedsci.2007.04.019.
19. de Ondarza, M.B., Sniffen, C.J., Dussert, L., Chevaux, E., Sulivan, J., Walker, N., Case study: Multiple-study analysis of the effect of live yeast on milk yield, milk component content and yield, and feed efficiency. Prof. Anim. Sci. 26 (2010), 661–666.
20. Devant, M., Penner, G.B., Marti, S., Quintana, B., Fàbregas, F., Bach, A., Aris, A., Behavior and inflammation of the rumen and cecum in Holstein bulls fed high-concentrate diets with different concentrate presentation forms with or without straw supplementation. J. Anim. Sci. 94 (2016), 3902–3917 10.2527/jas.2016-0594 27898891.
21. Dieho, K., Dijkstra, J., Schonewille, J.T., Bannink, A., Changes in ruminal volatile fatty acid production and absorption rate during the dry period and early lactation as affected by rate of increase of concentrate allowance. J. Dairy Sci. 99 (2016), 5370–5384 10.3168/jds.2015-10819 27157578.
22. Dirksen, G.U., Liebich, H.-G., Mayer, E., Adaptive changes of the ruminal mucosa and their functional and clinical significance. Bov. Pract. 20 (1985), 116–120.
23. Durand-Chaucheyras, F., Fonty, G., Bertin, G., Théveniot, M., Gout, P., Fate of Levucell SC I-1077 yeast additive during digestive transit in lambs. Reprod. Nutr. Dev. 38 (1998), 275–280 9698278.
24. Emenaker, N.J., Calaf, G.M., Cox, D., Basson, M.D., Qureshi, N., Short-chain fatty acids inhibit invasive human colon cancer by modulating uPA, TIMP-1, TIMP-2, mutant p53, Bcl-2, Bax, p21 and PCNA protein expression in an in vitro cell culture model. J. Nutr. 131 (2001), 3041S–3046S 11694645.
25. Fernando, S.C., Purvis, H.T., Najar, F.Z., Sukharnikov, L.O., Krehbiel, C.R., Nagaraja, T.G., Roe, B.A., DeSilva, U., Rumen microbial population dynamics during adaptation to a high-grain diet. Appl. Environ. Microbiol. 76 (2010), 7482–7490 10.1128/AEM.00388-10 20851965.
26. Franchi, L., Eigenbrod, T., Núñez, G., Cutting edge: TNF-alpha mediates sensitization to ATP and silica via the NLRP3 inflammasome in the absence of microbial stimulation. J. Immunol. 183 (2009), 792–796 19542372.
27. Genís, S., Sánchez-Chardi, A., Bach, A., Fàbregas, F., Arís, A., A combination of lactic acid bacteria regulates Escherichia coli infection and inflammation of the bovine endometrium. J. Dairy Sci. 100 (2017), 479–492 10.3168/jds.2016-11671 27837977.
28. Górka, P., Kowalski, Z.M., Pietrzak, P., Kotunia, A., Jagusiak, W., Holst, J.J., Guilloteau, P., Zabielski, R., Effect of method of delivery of sodium butyrate on rumen development in newborn calves. J. Dairy Sci. 94 (2011), 5578–5588 10.3168/jds.2011-4166 22032381.
29. Graham, C., Simmons, N.L., Functional organization of the bovine rumen epithelium. Am. J. Physiol. Regul. Integr. Comp. Physiol. 288 (2005), R173–R181 15319221.
30. Jouany, J.P., Optimizing rumen functions in the close-up transition period and early lactation to drive dry matter intake and energy balance in cows. Anim. Reprod. Sci. 96 (2006), 250–264 10.1016/j.anireprosci.2006.08.005 16996704.
31. Kern, R.J., Zarek, C.M., Lindholm-Perry, A.K., Kuehn, L.A., Snelling, W.M., Freetly, H.C., Cunningham, H.C., Meyer, A.M., Ruminal expression of the NQO1, RGS5, and ACAT1 genes may be indicators of feed efficiency in beef steers. Anim. Genet. 48 (2017), 90–92 10.1111/age.12490 27611366.
32. Kirat, D., Masuoka, J., Hayashi, H., Iwano, H., Yokota, H., Taniyama, H., Kato, S., Monocarboxylate transporter 1 (MCT1) plays a direct role in short-chain fatty acids absorption in caprine rumen. J. Physiol. 576 (2006), 635–647 10.1113/jphysiol.2006.115931 16901943.
33. Malmuthuge, N., Li, M., Goonewardene, L.A., Oba, M., Guan, L.L., Effect of calf starter feeding on gut microbial diversity and expression of genes involved in host immune responses and tight junctions in dairy calves during weaning transition. J. Dairy Sci. 96 (2013), 3189–3200 10.3168/jds.2012-6200 23498024.
34. Martens, H., Rabbani, I., Shen, Z., Stumpff, F., Deiner, C., Changes in rumen absorption processes during transition. Anim. Feed Sci. Technol. 172 (2012), 95–102 10.1016/j.anifeedsci.2011.12.011.
35. Mentschel, J., Leiser, R., Mulling, C., Pfarrer, C., Claus, R., Butyric acid stimulates rumen mucosa development in the calf mainly by a reduction of apoptosis. Arch. Tierernahr. 55 (2001), 85–102 12068484.
36. Metzler-Zebeli, B.U., Hollmann, M., Epithelial response to high-grain diets involves alteration in nutrient transporters and Na/K-ATPase mRNA expression in rumen and colon of goats. J. Anim. Sci. 91 (2013), 4256–4266 10.2527/jas.2012-5570 23825322.
37. Minuti, A., Palladino, A., Khan, M.J., Alqarni, S., Agrawal, A., Piccioli-Capelli, F., Hidalgo, F., Cardoso, F.C., Trevisi, E., Loor, J.J., Abundance of ruminal bacteria, epithelial gene expression, and systemic biomarkers of metabolism and inflammation are altered during the peripartal period in dairy cows. J. Dairy Sci. 98 (2015), 8940–8951 10.3168/jds.2015-9722 26409956.
38. Nagaraja, T.G., Titgemeyer, E.C., Ruminal acidosis in beef cattle: The current microbiological and nutritional outlook. J. Dairy Sci. 90 (2007), E17–E38 10.3168/jds.2006-478 17517750.
39. NRC, Nutrient Requirements of Dairy Cattle. 7th rev. ed., 2001, National Academy Press, Washington, DC.
40. Offner, A., Bach, A., Sauvant, D., Quantitative review of in situ starch degradation in the rumen. Anim. Feed Sci. Technol. 106 (2003), 81–93 10.1016/S0377-8401(03)00038-5.
41. Penner, G.B., Beauchemin, K.A., Mutsvangwa, T., Severity of ruminal acidosis in primiparous Holstein cows during the periparturient period. J. Dairy Sci. 90 (2007), 365–375 17183105.
42. Pfaffl, M.W., Tichopad, A., Prgomet, C., Neuvians, T.P., Determination of stable housekeeping genes, differentially regulated target genes and sample integrity: BestKeeper–Excel-based tool using pair-wise correlations. Biotechnol. Lett. 26 (2004), 509–515 15127793.
43. Rajput, I.R., Li, L.Y., Xin, X., Wu, B.B., Juan, Z.L., Cui, Z.W., Yu, D.Y., Li, W.F., Effect of Saccharomyces boulardii and Bacillus subtilis B10 on intestinal ultrastructure modulation and mucosal immunity development mechanism in broiler chickens. Poult. Sci. 92 (2013), 956–965 10.3382/ps.2012-02845 23472019.
44. Rakoff-Nahoum, S., Paglino, J., Eslami-Varzaneh, F., Edberg, S., Medzhitov, R., Recognition of commensal microflora by toll-like receptors is required for intestinal homeostasis. Cell 118 (2004), 229–241 15260992.
45. Reynolds, C.K., Dürst, B., Lupoli, B., Humphries, D.J., Beever, D.E., Visceral tissue mass and rumen volume in dairy cows during the transition from late gestation to early lactation. J. Dairy Sci. 87 (2004), 961–971 10.3168/jds.S0022-0302(04)73240-3 15259230.
46. Steele, M.A., Croom, J., Kahler, M., AlZahal, O., Hook, S.E., Plaizier, K., McBride, B.W., Bovine rumen epithelium undergoes rapid structural adaptations during grain-induced subacute ruminal acidosis. Am. J. Physiol. Regul. Integr. Comp. Physiol. 300 (2011), R1515–R1523 10.1152/ajpregu.00120.2010 21451145.
47. Steele, M.A., Vandervoort, G., AlZahal, O., Hook, S.E., Matthews, J.C., Mcbride, B.W., Rumen epithelial adaptation to high-grain diets involves the coordinated regulation of genes involved in cholesterol homeostasis. Physiol. Genomics 43 (2011), 308–316 10.1152/physiolgenomics.00117.2010 21245418.
48. Terré, M., Maynou, G., Bach, A., Gauthier, M., Effect of Saccharomyces cerevisiae CNCM I-1077 supplementation on performance and rumen microbiota of dairy calves. Prof. Anim. Sci. 31 (2015), 153–158 10.15232/pas.2014-01384.
49. Thrune, M., Bach, A., Ruiz Moreno, M., Stern, M.D., Linn, J.G., Effects of Saccharomyces cerevisiae on ruminal pH and microbial fermentation in dairy cows: Yeast supplementation on rumen fermentation. Livest. Sci. 124 (2009), 261–265 10.1016/j.livsci.2009.02.007.
50. Ulluwishewa, D., Anderson, R., McNabb, W., Moughan, P., Wells, J., Roy, N., Regulation of tight junction permeability by intestinal bacteria and dietary components. J. Nutr. 141 (2011), 769–776 21430248.
51. Vandesompele, J., De Preter, K., Pattyn, F., Poppe, B., Van Roy, N., De Paepe, A., Spelema, F., Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol., 3, 2002 research0034.
52. Van Soest, P.J., Robertson, J.B., Lewis, B.I., Methods for dietary fiber, neutral detergent fiber and non-starch polysaccharide in relation to animal nutrition. J. Dairy Sci. 74 (1991), 3583–3597 1660498.
53. Yang, F., Wang, A., Zeng, X., Hou, C., Liu, H., Qiao, S., Lactobacillus reuteri I5007 modulates tight junction protein expression in IPEC-J2 cells with LPS stimulation and in newborn piglets under normal conditions. BMC Microbiol., 15, 2015, 32 10.1186/s12866-015-0372-1 25888437.
54. Yuan, K., Mendonça, L.G.D., Hulbert, L.E., Mamedova, L.K., Muckey, M.B., Shen, Y., Elrod, C.C., Bradford, B.J., Yeast product supplementation modulated humoral and mucosal immunity and uterine inflammatory signals in transition dairy cows. J. Dairy Sci. 98 (2015), 3236–3246 10.3168/jds.2014-8469 25726103.
55. Zhao, G.-Y., Sun, Y.-B., Effects of volatile fatty acids on IGF-I, IGFBP-3, GH, insulin and glucagon in plasma, and IGF-I and IGFBP-3 in different tissues of growing sheep nourished by total intragastric infusions. Asian-Australas. J. Anim. Sci. 23 (2010), 366–371.