[Abbas H., Hilmi A., Surakka J., Apajalahti P.E.J. (2007). Identification of the most abundant Lactobacillus species in the crop of 1- and 5-week-old broiler chickens. Appl. Environ. Microb., 73: 7867–7873.10.1128/AEM.01128-07]Search in Google Scholar
[Abdukalykova S.T., Zhao X., Ruiz-Feria C.A. (2008). Arginine and vitamin E modulate the subpopulations of T lymphocytes in broiler chickens. Poultry Sci., 87: 50–55.10.3382/ps.2007-00315]Search in Google Scholar
[Aguzey H.A., Gao Z., Wu H., Cheng G. (2018). Influence of feed form and particle size on gizzard, intestinal morphology and microbiota composition of broiler chicken. Poultry Fish Wild Sci., 6: 196.10.4172/2375-446X.1000196]Search in Google Scholar
[Al-Daraji H.J., Salih A.M. (2012). The influence of dietary arginine supplementation on blood traits of broiler chickens. Pak. J. Nutr., 11: 258–264.10.3923/pjn.2012.258.264]Search in Google Scholar
[Al-Hassani A.S. (2011). Effect of dietary supplementation with different levels of arginine on some blood traits of laying hens. Intern. J. Poult. Sci., 10: 705–709.10.3923/ijps.2011.705.709]Search in Google Scholar
[Allen P.C. (1999). Effects of daily oral doses of L-arginine on coccidiosis infections in chickens. Poultry Sci., 78: 1506–1509.10.1093/ps/78.11.1506]Search in Google Scholar
[Amin H.J., Zamora S.A., Mc Millan D.D., Fick G.H., Butzner J.D., Parsons H.G. (2002). Arginine supplementation prevents necrotizing enterocolitis in the premature infant. J. Pediatr., 140: 425–431.10.1067/mpd.2002.123289]Search in Google Scholar
[Apajalahti J., Kettunen A. (2006). Microbes of the chicken gastrointestinal tract. In: Avian gut function in health and disease, Perry G.C. (ed.). Poultry Sci. Symp. Series, 28, CABI Publishing, Wallingford, pp. 113–121.10.1079/9781845931803.0124]Search in Google Scholar
[Ball R.O., Urschel K.L., Pencharz P.B. (2007). Nutritional consequences of interspecies differences in arginine and lysine metabolism. J. Nutr., 137: 1626S–1641S.10.1093/jn/137.6.1626S]Search in Google Scholar
[Bistrain B.R. (2004). Practical recommendations for immune-enhancing diets. J. Nutr., 134: 2868–2872.10.1093/jn/134.10.2868S]Search in Google Scholar
[Bronte V., Zanovello P. (2005). Regulation of immune responses by L-arginine metabolism. Nat. Rev. Immunol., 5: 641–654.10.1038/nri1668]Search in Google Scholar
[Caly D.L., D‘Inca R., Auclair E., Drider D. (2015). Alternatives to antibiotics to prevent necrotic enteritis in broiler chickens: a microbiologist’s perspective. Front. Microb., 6: 1336.10.3389/fmicb.2015.01336]Search in Google Scholar
[Chen J., Wang M., Kong Y., Ma H., Zou S. (2011). Comparison of the novel compounds creatine and pyruvate on lipid and protein metabolism in broiler chickens. Animal, 5: 1082–1089.10.1017/S1751731111000085]Search in Google Scholar
[Coburn L.A., Gong X., Singh K., Asim M., Scull B.P., Allaman M.M., Williams C.S., Rosen M.J., Washington M.K., Barry D.P., Piazuelo M.B., Casero R.A., Chaturvedi R., Zhao Z., Wilson K.T. (2012). L-arginine supplementation improves responses to injury and inflammation in dextran sulfate sodium colitis. PLoS ONE, 7: e33546.10.1371/journal.pone.0033546]Search in Google Scholar
[Corzo A., Moran Jr.E.T., Hoehler D. (2003). Arginine needs of heavy broiler males: applying the ideal protein concept. Poultry Sci., 82: 402–407.10.1093/ps/82.3.402]Search in Google Scholar
[Dahiya J.P., Hoehler D., Wilkie D.C., Van Kessel A.G., Drew M.D. (2005). Dietary glycine concentration affects intestinal Clostridium perfringens and lactobacilli populations in broiler chickens. Poultry Sci., 84: 1875–1885.10.1093/ps/84.12.1875]Search in Google Scholar
[Dalloul R.A., Lillehoj H.S. (2006). Poultry coccidiosis: recent advancements in control measures and vaccine development. Expert Rev. Vaccines, 5: 143–163.10.1586/14760584.5.1.143]Search in Google Scholar
[David L.A., Maurice C.F., Carmody R.N., Gootenberg D.B., Button J.E., Wolfe B.E. (2014). Diet rapidly and reproducibly alters the human gut microbiome. Nature, 505: 559–563.10.1038/nature12820]Search in Google Scholar
[De Gussem M. (2007). Coccidiosis in poultry: Review on diagnosis, control, prevention and interaction with overall gut health. Proc. 16th European Symposium on Poultry Nutrition, pp. 253–261.]Search in Google Scholar
[De Jonge W.J., Kwikkers K.L., te Velde A.A., van Deventer S.J.H., Nolte M.A., Mebius R.E., Ruijter J.M., Lamers M.C., Lamers W.H. (2002). Arginine deficiency affects early B cell maturation and lymphoid organ development in transgenic mice. J. Clin. Invest., 110: 1539–1548.10.1172/JCI0216143]Search in Google Scholar
[Dietert R.R., Austic R.E. (1994). Environment-immune interactions. Poultry Sci., 73: 1062–1076.10.3382/ps.0731062]Search in Google Scholar
[Ebrahimi M., Shahneh A.Z., Shivazad M., Pirsaraei Z.A., Tebianian M., Ruiz-Feria C.A., Adibmoradi M., Nourijelyani K., Mohamadnejad F. (2014). The effect of feeding excess arginine on lipogenic gene expression and growth performance in broilers. Brit. Poultry Sci., 55: 81–88.10.1080/00071668.2013.864381]Search in Google Scholar
[Efron D.T., Barbul A. (1998). Modulation of inflammation and immunity by arginine supplements. Curr. Opin. Clin. Nutr. Metab. Care, 1: 531–538.10.1097/00075197-199811000-00010]Search in Google Scholar
[Emadi M., Jahanshiri F., Kaveh K., Hair-Bejo M., Ideris A., Alimon A.R. (2011). Nutrition and immunity: The effects of the combination of arginine and tryptophan on growth performance, serum parameters and immune response in broiler chickens challenged with infectious bursal disease vaccine. Avian Pathol., 40: 63–72.10.1080/03079457.2010.539590]Search in Google Scholar
[Eriksson S., Chambers B.J., Rhen M. (2003). Nitric oxide produced by murine dendritic cells is cytotoxic for intracellular Salmonella enterica sv. Typhimurium. Scand. J. Immunol., 58: 493–502.10.1046/j.1365-3083.2003.01330.x]Search in Google Scholar
[Evoy D., Lieberman M.D., Fahey T.J., Daly J.M. (1998). Immunonutrition: The role of argi-nine. Nutrition, 14: 611–617.10.1016/S0899-9007(98)00005-7]Search in Google Scholar
[Fackelmayer F.O. (2005). Protein arginine methyltransferases: guardians of the Arg? Trends Biochem. Sci., 30: 666–671.10.1016/j.tibs.2005.10.002]Search in Google Scholar
[Fernandes J.I.M., Murakami A.E., Martins E.N., Sakamoto M.I., Garcia E.R.M. (2009). Effect of arginine on the development of the pectoralis muscle and the diameter and the protein: deoxyribonucleic acid rate of its skeletal myofibers in broilers. Poultry Sci., 88: 1399–1406.10.3382/ps.2008-00214]Search in Google Scholar
[Gao T., Zhao M.M., Zhang L., Li J.L., Yu L.L., Lv P.A., Gao F., Zhou G.H. (2017). Effects of in ovo feeding of L-arginine on the development of lymphoid organs and small intestinal immune barrier function in posthatch broilers. Anim. Feed Sci. Technol., 225: 8–19.10.1016/j.anifeedsci.2017.01.004]Search in Google Scholar
[Gill S.R., Pop M., Deboy R.T., Eckburg B., Turnbaugh P.J., Samuel B.S. (2006). Metagenomic analysis of the human distal gut microbiome. Science, 312: 1355–1359.10.1126/science.1124234]Search in Google Scholar
[Guo Y.W., Shi B.L., Yan S.M., Xu Y.Q., Li J.L., Li T.Y. (2015). Effects of arginine on cytokines and nitric oxide synthesis in broilers. J. Anim. Plant. Sci., 25: 366–371.]Search in Google Scholar
[Hamer H.M., De Preter D., Windey K., Verbeke K. (2011). Functional analysis of colonic bacterial metabolism: relevant to health. Am. J. Physiol. Gastr. L., 302: G1–G9.10.1152/ajpgi.00048.2011]Search in Google Scholar
[Hanew K. (2000). The mechanism of arginine- and insulin-induced GH release in humans. Endocrinol. J., 47: 23–27.10.1507/endocrj.47.SupplMarch_S23]Search in Google Scholar
[Harley J.P., Prescott L.M. (1998). Laboratory exercises in microbiology (2nd ed.). W.M.C. Brown Publishers, New York, US.]Search in Google Scholar
[He Q., Tang H., Ren P., Kong X., Wu G., Yin Y., Wang Y. (2011). Dietary supplementation with L-arginine partially counteracts serum metabonome induced by weaning stress in piglets. J. Proteome Res., 10: 5214–5221.10.1021/pr200688u]Search in Google Scholar
[Humphrey B.D., Klasing K.C. (2004). Modulation of nutrient metabolism and homeostasis by the immune system. World Poultry Sci. J., 60: 90–100.10.1079/WPS20037]Search in Google Scholar
[Jahanian R. (2009). Immunological responses as affected by dietary protein and arginine concentrations in starting broiler chicks. Poultry Sci., 88: 1818–1824.10.3382/ps.2008-00386]Search in Google Scholar
[Jiao P., Guo Y., Yang X., Long F. (2010). Effects of dietary arginine and methionine levels on broiler carcass traits and meat quality. J. Anim. Vet. Adv., 9: 1546–1551.10.3923/javaa.2010.1546.1551]Search in Google Scholar
[Khajali F., Wideman R.F. (2010). Dietary arginine: metabolic, environmental, immunological and physiological interrelationships. World Poultry Sci. J., 66: 751–766.10.1017/S0043933910000711]Search in Google Scholar
[Khajali F., Tahmasebi M., Hassanpour H., Akbari M.R., Qujeq D., Wideman R.F. (2011). Effects of supplementation of canola meal-based diets with arginine on performance, plasma nitric oxide, and carcass characteristics of broiler chickens grown at high altitude. Poultry Sci., 90: 2287–2294.10.3382/ps.2011-01618]Search in Google Scholar
[Kidd M.T., Peebles E.D., Whitmarsh S.K., Yeatman J.B., Wideman R.F. (2001). Growth and immunity of broiler chicks as affected by dietary arginine. Poultry Sci., 80: 1535–1542.10.1093/ps/80.11.1535]Search in Google Scholar
[Kim S.W., Mc Pherson R.L., Wu G. (2004). Dietary arginine supplementation enhances the growth of milk-fed young pigs. J. Nutr., 134: 625–630.10.1093/jn/134.3.625]Search in Google Scholar
[Klasing K.C. (2007). Nutrition and the immune system. Brit. Poultry Sci., 48: 525–537.10.1080/00071660701671336]Search in Google Scholar
[Kwak H., Austic R.E., Dietert R.R. (1999). Influence of dietary arginine concentration on lymphoid organ growth in chickens. Poultry Sci., 78: 1536–154.10.1093/ps/78.11.1536]Search in Google Scholar
[Labadan M.C., Hsu K.N., Austic R.E. (2001). Lysine and arginine requirements of broiler chickens at two- to three-week intervals to eight weeks of age. Poultry Sci., 80: 599–606.10.1093/ps/80.5.599]Search in Google Scholar
[Laika M., Jahanian R. (2017). Increase in dietary arginine level could ameliorate detrimental impacts of coccidial infection in broiler chickens. Livest. Sci., 195: 38–44.10.1016/j.livsci.2016.11.002]Search in Google Scholar
[Laparra J.M., Sanz Y. (2010). Interactions of gut microbiota with functional food components and nutraceuticals. Pharmacol. Res., 61: 219–225.10.1016/j.phrs.2009.11.001]Search in Google Scholar
[Lewis S. (1996). Avian biochemistry and molecular biology. Cambridge University Press, New Jersey, New York City, USA.]Search in Google Scholar
[Li P., Yin Y.L., Li D., Kim S.W., Wu G. (2007). Amino acids and immune function. Brit. J. Nutr., 98: 237–252.10.1017/S000711450769936X]Search in Google Scholar
[Liu D., Guo S., Guo Y. (2012 a). Xylanase supplementation to a wheatbased diet alleviated the intestinal mucosal barrier impairment of broiler chickens challenged by Clostridium perfringens. Avian Pathol., 41: 291–298.10.1080/03079457.2012.68408922702457]Search in Google Scholar
[Liu X., Wu X., Yin Y., Liu Y., Geng M., Yang H., Wu G. (2012 b). Effects of dietary L-argi- nine or N-carbamylglutamate supplementation during late gestation of sows on the miR-15b/16, miR-221/222, VEGFA and eNOS expression in umbilical vein. Amino Acids, 42: 2111–2119.10.1007/s00726-011-0948-5335160521638020]Search in Google Scholar
[Lu J., Idris U., Harmon B., Hofacre C., Maurer J.J., Lee M.D. (2003). Diversity and succession of the intestinal bacterial community of the maturing broiler chicken. Appl. Env. Microb., 69: 6816–6824.10.1128/AEM.69.11.6816-6824.2003]Search in Google Scholar
[Luiking Y.C., Ten Have G.A., Wolfe R.R., Deutz N.E. (2012). Arginine de novo and nitric oxide production in disease states. Am. J. Physiol. Endocrinol. Metab., 303: e1177–1189.10.1152/ajpendo.00284.2012]Search in Google Scholar
[Luo Y., Zhang L., Li H., Smidt H., Wright A.G., Zhang K. (2017). Different types of dietary fibers trigger specific alterations in composition and predicted functions of colonic bacterial communities in BALB/c Mice. Front. Microbiol., 8: 966.10.3389/fmicb.2017.00966]Search in Google Scholar
[Ma C.S., Nichols K.E., Tangye S.G. (2007). Regulation of cellular and humoral immune responses by the SLAM and SAP families of molecules. Annu. Rev. Immunol., 25: 337–379.10.1146/annurev.immunol.25.022106.141651]Search in Google Scholar
[Mantis N.J., Rol N., Corthésy B. (2011). Secretory IgA’s complex roles in immunity and mucosal homeostasis in the gut mucosal. Immunology, 4: 603–611.10.1038/mi.2011.41]Search in Google Scholar
[Masoud A., Marziyeh E., Ahmad Z.S., Mahmoud S., Zarbakht A.P., Majid T., Keramat Y.Q. (2014). The effects of L-arginine on growth, small intestine, and immune system of broilers in starter period. Annu. New York Acad. Sci., 521: 72–87.]Search in Google Scholar
[Metzler-Zebeli B.U., Eklund M., Mosenthin R. (2009). Impact of osmoregulatory and methyl donor functions of betaine on intestinal health and performance in poultry. World Poultry Sci. J., 65: 419–442.10.1017/S0043933909000300]Search in Google Scholar
[Moncada S., Higgs A. (1993). The L-arginine-nitric oxide pathway. New Engl. J. Med., 329: 2002–2012.10.1056/NEJM199312303292706]Search in Google Scholar
[Moncada S., Palmer R.M.J., Higgs E.A. (1991). Nitric oxide: physiology, pathophysiology and pharmacology. Pharmacol. Rev., 43: 109–142.]Search in Google Scholar
[Mountzouris K.C., Tsirtsikos P., Kalamara E., Nitsch S., Schatzmayr G., Fegeros K. (2007). Evaluation of the efficacy of a probiotic containing Lactobacillus, Bifidobacterium, Enterococcus, and Pediococcus strains in promoting broiler performance and modulating cecal microflora composition and metabolic activities. Poultry Sci., 86: 309–317.10.1093/ps/86.2.309]Search in Google Scholar
[Munir K., Muneer M.A., Masaoud E., Tiwari A., Mahmud A., Chaudhry R.M., Rashid A. (2009). Dietary arginine stimulates humoral and cell-mediated immunity in chickens vaccinated and challenged against hydropericardium syndrome virus. Poultry Sci., 88: 1629–1638.10.3382/ps.2009-00152]Search in Google Scholar
[Newsholme P., Brennan L., Rubi B., Maechler P. (2005). New insights into amino acid metabolism, β-cell function and diabetes. Clin. Sci., 108: 185–194.10.1042/CS20040290]Search in Google Scholar
[NRC (1994). Nutrient Requirements of Poultry, 9th ed. National Academy Press, Washington, DC, USA.]Search in Google Scholar
[O‘Keefe S.J. (2008). Nutrition and colonic health: the critical role of the microbiota. Curr. Opin. Gastroen., 24: 51–58.10.1007/978-1-59745-112-3]Search in Google Scholar
[Ochoa J.B., Strange J., Kearney P., Gellin G., Endean E., Fitzpatrick E. (2001). Effects of L-arginine on the proliferation of T lymphocyte subpopulations. J.-Parenter. Enter. Nutr., 25: 23–29.10.1177/014860710102500123]Search in Google Scholar
[Ovington K.S., Smith N.C. (1992). Cytokines, free radicals and resistance to Eimeria. Parasitol. Today, 8: 422–426.10.1016/0169-4758(92)90196-9]Search in Google Scholar
[Perez-Carbajal C., Caldwell D., Farnell M., Stringfellow K., Pohl S., Casco G., Pro-Martinez A., Ruiz-Feria C.A. (2010). Immune response of broiler chickens fed different levels of arginine and vitamin E to a coccidiosis vaccine and Eimeria challenge. Poultry Sci., 89: 1870–1877.10.3382/ps.2010-00753]Search in Google Scholar
[Persia M.E., Young E.L., Utterback P.L., Parsons C.M. (2006). Effects of dietary ingredients and Eimeria acervulina infection on chick performance, apparent metabolizable energy, and amino acid digestibility. Poultry Sci., 85: 48–55.10.1093/ps/85.1.48]Search in Google Scholar
[Ravindran V. (2016). Feed-induced specific ileal endogenous amino acid losses: measurement and significance in the protein nutrition of monogastric animals. Anim. Feed Sci. Technol., 221: 304–313.10.1016/j.anifeedsci.2016.05.013]Search in Google Scholar
[Ren W., Yin Y., Liu G., Yu X., Li Y., Yang G., Li T., Wu G. (2012). Effect of dietary arginine supplementation on reproductive performance of mice with porcine circovirus type 2 (PCV2) infection. Amino Acids, 42: 2089–2094.10.1007/s00726-011-0942-y]Search in Google Scholar
[Ren W., Chen S., Yin J., Duan J., Li T., Liu G., Feng Z., Tan B., Yin Y., Wu G. (2014 a). Dietary arginine supplementation of mice alters the microbial population and activates intestinal innate immunity. J. Nutr., 166: 988–995.10.3945/jn.114.19212024670969]Search in Google Scholar
[Ren W., Yin J., Wu M., Liu G., Yang G., Xion Y., Su D., Wu L., Li T., Chen S., Duan J., Yin Y., Wu G. (2014 b). Serum amino acids profile and the beneficial effects of L-arginine or L-glutamine supplementation in Dextran Sulfate Sodium Colitis. PLoS One, 9: e88335.10.1371/journal.pone.0088335391499224505477]Search in Google Scholar
[Rhoads J.M., Liu Y., Niu X., Surendran S., Wu G. (2008). Arginine stimulates cdx2-transformed intestinal epithelial cell migration via a mechanism requiring both nitric oxide and phosphorylation of p70 S6 kinase. J. Nutr., 138: 1652–1657.10.1093/jn/138.9.1652]Search in Google Scholar
[Round J.L., Mazmanian S.K. (2009). The gut microbiota shapes intestinal immune responses during health and disease. Nat. Rev. Immunol., 9: 313–323.10.1038/nri2515]Search in Google Scholar
[Ruiz-Feria C.A. (2009). Concurrent supplementation of arginine, vitamin E, and vitamin C improve cardiopulmonary performance in broilers chickens. Poultry Sci., 88: 526–535.10.3382/ps.2008-00401]Search in Google Scholar
[Ruiz-Feria C.A., Kidd M.T., Wideman R.F. (2001). Plasma levels of arginine, ornithine, and urea and growth performance of broilers fed supplemental L-arginine during cool temperature exposure. Poultry Sci., 80: 358–369.10.1093/ps/80.3.358]Search in Google Scholar
[Ruiz-Feria C.A., Abdukalykova S.T. (2009). Arginine and vitamin E improve the antibody response to infectious bursal disease virus (IBDV) and sheep red blood cells in broiler chickens. Brit. Poultry Sci., 50: 291–297.10.1080/00071660902942759]Search in Google Scholar
[Shao Y., Guo Y., Wang Z. (2013). β-1, 3/1, 6-glucan alleviated intestinal mucosal barrier impairment of broiler chickens challenged with Salmonella enterica serovar Typhimurium. Poultry Sci., 92: 1764–1773.10.3382/ps.2013-03029]Search in Google Scholar
[Sharma J.M., Kim I.J., Rautenschlein S., Yeh H-Y. (2000). Infectious bursal disease virus of chickens: Pathogenesis and immunosuppression. Dev. Comp. Immunol., 24: 223–235.10.1016/S0145-305X(99)00074-9]Search in Google Scholar
[Stechmiller J.K., Langkamp-Henken B., Childress B., Herrlinger-Garcia K.A., Hudgens B., Tian J. (2005). Arginine supplementation does not enhance serum nitric oxide levels in elderly nursing home residents with pressure ulcers. Biol. Res. Nurs., 6: 289–299.10.1177/1099800405274732]Search in Google Scholar
[Sung Y.J., Hotchkiss J.H., Austic R.E., Dietert R.R. (1991). L-arginine dependent production of a reactive nitrogen intermediate by macrophages of a uricotelic species. J. Leukocyte Biol., 50: 49–56.10.1002/jlb.50.1.49]Search in Google Scholar
[Tan B., Li X.G., Kong X., Huang R., Ruan Z., Yao K., Deng Z., Xie M., Shinzato I., Yin Y., Wu G. (2009 a). Dietary L-arginine supplementation enhances the immune status in early-weaned piglets. Amino Acids, 37: 323–331.10.1007/s00726-008-0155-118712273]Search in Google Scholar
[Tan B., Yin Y., Liu Z., Li X., Xu H., Kong X., Huang R., Tang W., Shinzato I., Smith S., Wu G. (2009 b). Dietary L-arginine supplementation increases muscle gain and reduces body fat mass in growing-finishing pigs. Amino Acids, 37: 169–175.10.1007/s00726-008-0148-018683021]Search in Google Scholar
[Tan B.E., Yin Y.L., Liu Z.Q., Tang W.J., Xu H.J., Konga X.F., Li X.G., Yao K., Gu W., Smith S.B., Wu G. (2011). Dietary L-arginine supplementation differentially regulates expression of fat-metabolic genes in porcine adipose tissue and skeletal muscle. J. Nutr. Biochem., 22: 441–445.10.1016/j.jnutbio.2010.03.012]Search in Google Scholar
[Tan J., Applegate T.J., Liu S., Guo Y., Eicher S.D. (2014). Supplemental dietary L-arginine attenuates intestinal mucosal disruption during coccidial vaccine challenge in broiler chickens. Brit. J. Nutr., 112:1098–109.10.1017/S0007114514001846]Search in Google Scholar
[Tan J.Z., Guo Y.M., Applegate T.J., Du E.C., Zhao X. (2015). Dietary L-arginine modulates immunosuppression in broilers inoculated with an intermediate strain of infectious bursa disease virus. J. Sci. Food Agric., 95: 126–135.10.1002/jsfa.6692]Search in Google Scholar
[Tayade C., Jaiswal T., Mishra S., Koti M. (2006 a). L-arginine stimulates immune response in chickens immunized with intermediate plus strain of infectious bursal disease vaccine. Vaccine, 24: 552–560.10.1016/j.vaccine.2005.08.05916168528]Search in Google Scholar
[Tayade C., Koti M., Mishra S.C. (2006 b). L-arginine stimulates intestinal intraepithelial lymphocyte functions and immune response in chickens orally immunized with live intermediate plus strain of infectious bursal disease vaccine. Vaccine, 24: 5473–5480.10.1016/j.vaccine.2006.03.086712647616723175]Search in Google Scholar
[Tomasello G., Tralongo P., Damiani P., Sinagra E., Di Trapani B., Zeenny M.N. (2014). Dismicrobism in inflammatory bowel disease and colorectal cancer: changes in response of colocytes. World J. Gastroenterol., 20: 18121–18130.10.3748/wjg.v20.i48.18121]Search in Google Scholar
[Uni Z., Ferket P. (2003). Enhancement of development of oviparous species by in ovo feeding. U.S. Regular Patent US 6,592,878 B2, Washington, DC., US.]Search in Google Scholar
[Van Den Berg T.P. (2000). Acute infectious bursal disease in poultry: A review. Avian Pathol., 29: 175–194.10.1080/03079450050045431]Search in Google Scholar
[Van Immerseel F., Rood J.I., Moore R.J., Titball R.W. (2009). Rethinking our understanding of the pathogenesis of necrotic enteritis in chickens. Trends Microbiol., 17: 32–36.10.1016/j.tim.2008.09.005]Search in Google Scholar
[Vermeulen A.N., Schaap D.C., Schetters T.M. (2001). Control of coccidiosis in chickens by vaccination. Vet. Parasitol., 100: 13–20.10.1016/S0304-4017(01)00479-4]Search in Google Scholar
[Wershil B.K., Furuta G.T. (2008). 4: Gastrointestinal mucosal immunity. J. Allergy Clin. Immunol., 121: S380–S383.10.1016/j.jaci.2007.10.023]Search in Google Scholar
[Williams R.B. (2005). Intercurrent coccidiosis and necrotic enteritis of chickens: rational, integrated disease management by maintenance of gut integrity. Avian Pathol., 34: 159–180.10.1080/03079450500112195]Search in Google Scholar
[Wu G. (2009). Amino acids: metabolism, functions, and nutrition. Amino Acids, 37: 1–17.10.1007/s00726-009-0269-0]Search in Google Scholar
[Wu L.Y., Fang Y.J., Guo X.Y. (2011). Dietary L-arginine supplementation beneficially regulates body fat deposition of meat-type ducks. Brit. Poultry Sci., 52: 221–226.10.1080/00071668.2011.559452]Search in Google Scholar
[Wu X., Wu Y.L., Yin Y.Q., Liu X.D., Liu Z.Q., Liu T.J., Li R., Huang L., Ruan Z., Deng Z. (2012). Effect of dietary arginine and N-carbamoylglutamate supplementation reproduction and gene expression of eNOS, VEGFA and PlGF1 in on in late pregnancy of sow placenta. Anim. Reprod. Sci., 132: 187–192.10.1016/j.anireprosci.2012.05.002]Search in Google Scholar
[Wylie K.M., Truty R.M., Sharpton T.J., Mihindukulasuriya K.A., Zhou Y., Gao H. (2012). Novel bacterial taxa in the human microbiome. PLoS ONE, 7: e35294.10.1371/journal.pone.0035294]Search in Google Scholar
[Xia Y., Dawson V.L., Dawson T.M., Snyder S.H., Zweier J.L. (1996). Nitric oxide synthase generates superoxide and nitric oxide in arginine-depleted cells leading to peroxynitrite-mediated cellular injury. Proc. Natl. Acad. Sci., 93: 6770–6774.10.1073/pnas.93.13.6770]Search in Google Scholar
[Xu S., Lin Y., Zeng D., Zhou M., Zeng Y., Wang H. (2018). Bacillus licheniformis normalize the ileum microbiota of chickens infected with necrotic enteritis. Sci. Rep., 8: 17–44.10.1038/s41598-018-20059-z]Search in Google Scholar
[Yang H., Lin B.Q., Zhang L., Wang T., Du H.J. (2012). Effects of L-arginine and lactobacillus on growth performance, blood biochemical indexes and intestinal mucosal morphology of weanling piglets (in Chinese). J. Fujian Agric. Forestry Univ. (Nat. Sci. Ed.), 4: 515–519.]Search in Google Scholar
[Yao K., Yin Y.L., Chu W.Y., Liu Z.Q., Deng D., Li T.J., Huang R.L., Zhang J.S., Tan B., Wang W.C., Wu G.Y. (2008). Dietary arginine supplementation increases mTOR signaling activity in skeletal muscle of neonatal pigs. J. Nutr., 138: 867–872.10.1093/jn/138.5.867]Search in Google Scholar
[Yao K., Guan S., Li T., Huang R., Wu G., Ruan Z., Yin Y. (2011). Dietary L-arginine supplementation enhances intestinal development and expression of vascular endothelial growth factor in weanling piglets. Brit. J. Nutr., 105: 703–709.10.1017/S000711451000365X]Search in Google Scholar
[Yin J., Ren W., Duan J., Wu L., Chen S., Li T., Yin Y., Wu G. (2014). Dietary arginine supplementation enhances intestinal expression of SLC7A7 and SLC7A1 and ameliorates growth depression in mycotoxin challenged pigs. Amino Acids, 46: 883–892.10.1007/s00726-013-1643-5]Search in Google Scholar
[Yu T.K., Caudell E.G., Smid C., Grimm E.A. (2000). IL-2 activation of NK cells: involvement of MKK1/2/ERK but not p38 kinase pathway. J. Immunol., 164: 6244–6251.10.4049/jimmunol.164.12.6244]Search in Google Scholar
[Zavarize K.C., Sartori J.R., Gonzales E., Pezzato A.C. (2012). Morphological changes of the intestinal mucosa of broilers and layers as affected by fasting before sample collection. Rev. Bras. Cienc. Avic., 14: 2002–2012.10.1590/S1516-635X2012000100004]Search in Google Scholar
[Zhang B., Lv Z., Li H., Guo S., Liu D., Guo Y. (2017). Dietary L-arginine inhibits intestinal Clostridium perfringens colonisation and attenuates intestinal mucosal injury in broiler chickens. Brit. J. Nutr., 118: 321–332.10.1017/S0007114517002094]Search in Google Scholar
[Zhang B., Lv Z., Li Z., Wang W., Li G., Guo Y. (2018). Dietary L-arginine supplementation alleviates the intestinal injury and modulates the gut microbiota in broiler chickens challenged by Clostridium perfringens. Front. Microbiol., 9: 1716.10.3389/fmicb.2018.01716]Search in Google Scholar
[Ziegler T.R., Evans M.E., Fernandez-Estivariz C., Jones D.P. (2013). Trophic and cyto-protective nutrition for intestinal adaptation, mucosal repair, and barrier function. Annu. Rev. Nutr., 23: 229–261.]Search in Google Scholar