Significance of Limosilactobacillus fermentum and Saccharomyces cerevisiae on the Growth Performance, Haematological Traits, Serum Biochemistry, Faecal and Caeca Microbiota of Broiler Chickens

References

• Lutful Kabir SM. The role of probiotics in the poultry industry. Int J Mol Sci. 2009;10(8):3531–46. doi:10.3390/ijms10083531
   PubMed Web of Science ®Google Scholar
• Gao P, Ma C, Sun Z, Wang L, Huang S, Su X, Xu J, Zhang H. Feed-additive probiotics accelerate yet antibiotics delay intestinal microbiota maturation in broiler chicken. Microbiome. 2017;5(1):1–4. doi:10.1186/s40168-017-0315-1
   PubMedGoogle Scholar
• Abdel-Raheem SM, Abd-Allah SM, Hassanein KM. The effects of prebiotic, probiotic and synbiotic supplementation on intestinal microbial ecology and histomorphology of broiler chickens. IJAVMS. 2012;6(4):277–89. doi:10.5455/ijavms.156
   Google Scholar
• Rowghani E, Arab M, Akbarian A. Effects of a probiotic and other feed additives on performance and immune response of broiler chicks. Int J of Poult Sci. 2007;6(4):261–5. doi:10.3923/ijps.2007.261.265
   Google Scholar
• Ahiwe EU, Dos Santos TT, Graham H, Iji PA. Can probiotic or prebiotic yeast (Saccharomyces cerevisiae) serve as alternatives to in-feed antibiotics for healthy or disease-challenged broiler chickens?: a review. J Appl Poult Res. 2021;30(3):100164. doi:10.1016/j.japr.2021.100164
   Web of Science ®Google Scholar
• Alkhalf A, Alhaj M, Al-Homidan I. Influence of probiotic supplementation on blood parameters and growth performance in broiler chickens. Saudi J Biol Sci. 2010;17(3):219–25. doi:10.1016/j.sjbs.2010.04.005
   PubMedGoogle Scholar
• Van den Bogaard AE, Stobberingh EE. Epidemiology of resistance to antibiotics: links between animals and humans. Int J Antimicrob Agents. 2000;14(4):327–35. doi:10.1016/S0924-8579(00)00145-X
   PubMed Web of Science ®Google Scholar
• Khomayezi R, Adewole D. Probiotics, prebiotics, and synbiotics: an overview of their delivery routes and effects on growth and health of broiler chickens. Worlds Poult Sci J. 2022;78(1):57–81. doi:10.1080/00439339.2022.1988804
   Web of Science ®Google Scholar
• Pakroo S, Tarrah A, Takur R, Wu M, Corich V, Giacomini A. Limosilactobacillus fermentum ING8, a potential multifunctional non-starter strain with relevant technological properties and antimicrobial activity. Foods. 2022;11(5):703. doi:10.3390/foods11050703
   PubMed Web of Science ®Google Scholar
• Rodríguez-Sojo MJ, Ruiz-Malagón AJ, Rodríguez-Cabezas ME, Gálvez J, Rodríguez-Nogales A. Limosilactobacillus fermentum CECT5716: mechanisms and therapeutic insights. Nutrients. 2021;13(3):1016. doi:10.3390/nu13031016
   PubMed Web of Science ®Google Scholar
• Zheng J, Wittouck S, Salvetti E, Franz CMAP, Harris HMB, Mattarelli P, O'Toole PW, Pot B, Vandamme P, Walter J, et al. A taxonomic note on the genus Lactobacillus: description of 23 novel genera, emended description of the genus Lactobacillus Beijerinck 1901, and union of Lactobacillaceae and Leuconostocaceae. Int J Syst Evol Microbiol. 2020;70(4):2782–858. doi:10.1099/ijsem.0.004107
   PubMed Web of Science ®Google Scholar
• Khan I, Nawaz M, Anjum AA, Ahmad MU, Mehmood A, Rabbani M, Mustafa A, Ali MA. Effect of indigenous probiotics on gut morphology and intestinal absorption capacity in broiler chicken challenged with Salmonella enteritidis. PJZ. 2020;52(5):1825. doi:10.17582/journal.pjz/20190518090547
   Web of Science ®Google Scholar
• Sorescu I, Dumitru M, Ciurescu G. Lactobacillus spp. Strains isolation, identification, preservation and quantitative determinations from gut content of 45-day-old chickens broilers. Braz J Poultry Sci. 2021;23:1–7. doi:10.1590/1806-9061-2020-1378
   Web of Science ®Google Scholar
• Jadhav K, Sharma KS, Katoch S, Sharma VK, Mane BG. Probiotics in broiler poultry feeds: a review. J Anim Nutr Physiol. 2015;1:4–16.
   Google Scholar
• Shojadoost B, Vince AR, Prescott JF. The successful experimental induction of necrotic enteritis in chickens by Clostridium perfringens: a critical review. Vet Res. 2012;43(1):74. doi:10.1186/1297-9716-43-74
   PubMedGoogle Scholar
• Cao L, Li C, Yang XJ, Li ZJ, Sun FF, Wu XH, Yao JH. Reduced lesions in chickens with Clostridium perfringens-induced necrotic enteritis by Lactobacillus fermentum 1.2029. Poult Sci. 2012;91(12):3065–71. doi:10.3382/ps.2012-02548
   PubMed Web of Science ®Google Scholar
• Ezema C, Ugwu CC. Yeast (Saccharomyces cerevisiae) as a probiotic of choice for broiler production. In Beneficial microorganisms in agriculture, aquaculture and other areas. Cham: Springer; 2015. p. 59–79. doi:10.1007/978-3-319-23183-9_4
   Google Scholar
• Yang Y, Iji PA, Kocher A, Mikkelsen LL, Choct M. Effects of dietary mannanoligosaccharide on growth performance, nutrient digestibility and gut development of broilers given different cereal‐based diets. J Anim Physiol Anim Nutr (Berl). 2008;92(6):650–9. doi:10.1111/j.1439-0396.2007.00761.x
   PubMed Web of Science ®Google Scholar
• Gunal M, Yayli G, Kaya O, Karahan N, Sulak O. The effects of antibiotic growth promoter, probiotic or organic acid supplementation on performance, intestinal microflora and tissue of broilers. Int J Poult Sci. 2006;5(2):149–55. doi:10.3923/ijps.2006.149.155
   Google Scholar
• Martin SA, Nisbet DJ, Dean RG. Influence of a commerical yeast supplement on the in vitro ruminal fermentation. Nutrition Reports International (USA); 1989.
   Google Scholar
• Froebel LK, Jalukar S, Lavergne TA, Lee JT, Duong T. Administration of dietary prebiotics improves growth performance and reduces pathogen colonization in broiler chickens. Poult Sci. 2019;98(12):6668–76. doi:10.3382/ps/pez537
   PubMed Web of Science ®Google Scholar
• Elghandour MM, Tan ZL, Abu Hafsa SH, Adegbeye MJ, Greiner R, Ugbogu EA, Cedillo Monroy J, Salem AZ. Saccharomyces cerevisiae as a probiotic feed additive to non and pseudo‐ruminant feeding: a review. J Appl Microbiol. 2020;128(3):658–74. doi:10.1111/jam.14416
   PubMed Web of Science ®Google Scholar
• Mishra BK, Hati S, Brahma J, Das S. Evaluation of probiotic potentials of yeast isolates from traditional fermented rice beverages of Meghalaya, India. Rev Med Microbiol. 2021;32(1):28–38. doi:10.1097/MRM.0000000000000230
   Web of Science ®Google Scholar
• Mishra BK, Das S, Prajapati JB, Hati S. Bio-functional properties and storage study of ‘Chubitchi’ - a fermented rice beverage of Garo Hills, Meghalaya. Indian J Tradit Knowl. 2021;20(2):498–511. http://op.niscair.res.in/index.php/IJTK/article/view/31946.
   Web of Science ®Google Scholar
• Ashokbhai JK, Basaiawmoit B, Das S, Sakure A, Maurya R, Bishnoi M, Kondepudi KK, Padhi S, Rai AK, Liu Z, et al. Antioxidative, antimicrobial and anti-inflammatory activities and release of ultra-filtered antioxidative and antimicrobial peptides during fermentation of sheep milk: in-vitro, in-silico and molecular interaction studies. Food Biosci. 2022;47:101666. doi:10.1016/j.fbio.2022.101666
   Web of Science ®Google Scholar
• Dineshbhai CK, Basaiawmoit B, Sakure AA, Maurya R, Bishnoi M, Kondepudi KK, Patil GB, Mankad M, Liu Z, Hati S. Exploring the potential of Lactobacillus and Saccharomyces for biofunctionalities and the release of bioactive peptides from whey protein fermentate. FoodBiosci. 2022;48:101758. 10.1016/j.fbio.2022.101666
   Google Scholar
• Patel D, Sakure A, Lodha D, Basaiawmoit B, Maurya R, Das S, Bishnoi M, Kondepudi KK, Hati S. Significance of lactobacillus fermentum on antioxidative and anti-inflammatory activities and ultrafiltration peptide fractions as potential sources of antioxidative peptides from fermented camel milk (Indian breed). J Am Coll Nutr. 2021;1–10. doi:10.1080/07315724.2021.1983485
   PubMed Web of Science ®Google Scholar
• Hati S, Mishra BK, Patel M, Prajapati JB. Indigenous Lactobacillus strains improve growth performance and high-density cholesterol levels in broilers. Indian J Exp Biol. 2021;59:556–63. http://op.niscpr.res.in/index.php/IJEB/article/view/54439/0.
   Web of Science ®Google Scholar
• Luna LG. Manual of histologic staining methods of the Armed Forces Institute of Pathology; 1968.
   Google Scholar
• Jia G, Rao Z, Zhang J, Li Z, Chen F. Tetraether biomarker records from a loess-paleosol sequence in the western Chinese Loess Plateau. Front Microbiol. 2013;4:199. doi:10.3389/fmicb.2013.00199
   PubMed Web of Science ®Google Scholar
• Callahan BJ, McMurdie PJ, Rosen MJ, Han AW, Johnson AJ, Holmes SP. DADA2: high-resolution sample inference from Illumina amplicon data. Nat Methods. 2016;13(7):581–3. doi:10.1038/nmeth.3869
   PubMed Web of Science ®Google Scholar
• Parks DH, Chuvochina M, Chaumeil PA, Rinke C, Mussig AJ, Hugenholtz PA. Complete domain-to-species taxonomy for Bacteria and Archaea. Nat Biotechnol. 2020;38(9):1079–86. doi:10.1038/s41587-020-0501-8
   PubMed Web of Science ®Google Scholar
• McMurdie PJ, Holmes S. phyloseq: an R package for reproducible interactive analysis and graphics of microbiome census data. PLoS One. 2013;8(4):e61217. doi:10.1371/journal.pone.0061217
   PubMed Web of Science ®Google Scholar
• Oksanen J, Blanchet FG, Kindt R, Legendre P, Minchin PR, O’hara RB, Simpson GL, Solymos P, Stevens MH, Wagner H, et al. Package ‘vegan’. Community Ecology Package, Version. 2013;2(9):1–295. http://CRAN.Rproject.org/package=vegan
   Google Scholar
• Lahti L, Shetty S, Blake T, Salojarvi J. Tools for microbiome analysis in R version 2.1.26; 2020.
   Google Scholar
• Kassambara A. ggpubr: ‘ggplot2’ based publication ready plots. R package version 0.4.0. Computer software; 2020. https://cran-r-project.org/web/packages/ggpubr/indes.html.
   Google Scholar
• Wickham H. Data analysis. Inggplot2. Cham: Springer; 2016. p. 189–201.
   Google Scholar
• Conway JR, Lex A, Gehlenborg N. UpSetR: an R package for the visualization of intersecting sets and their properties. Bioinformatics. 2017;33(18):2938–40. doi:10.1093/bioinformatics/btx364
   PubMed Web of Science ®Google Scholar
• Sugiharto S, Isroli I, Yudiarti T, Widiastuti E. The effect of supplementation of multistrain probiotic preparation in combination with vitamins and minerals to the basal diet on the growth performance, carcass traits, and physiological response of broilers. Vet World. 2018;11(2):240–7. doi:10.14202/vetworld.2018.240-247
   PubMed Web of Science ®Google Scholar
• Khoobani M, Hasheminezhad SH, Javandel F, Nosrati M, Seidavi A, Kadim IT, Laudadio V, Tufarelli V. Effects of dietary chicory (Chicorium intybus L.) and probiotic blend as natural feed additives on performance traits, blood biochemistry, and gut microbiota of broiler chickens. Antibiotics. 2019;9(1):5. doi:10.3390/antibiotics9010005
   Google Scholar
• Zhang ZF, Kim IH. Effects of multistrain probiotics on growth performance, apparent ileal nutrient digestibility, blood characteristics, cecal microbial shedding, and excreta odor contents in broilers. Poult Sci. 2014;93(2):364–70. doi:10.3382/ps.2013-03314
   PubMed Web of Science ®Google Scholar
• Mountzouris KC, Tsirtsikos P, Kalamara E, Nitsch S, Schatzmayr G, Fegeros K. 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. Poult Sci. 2007;86(2):309–17. doi:10.1093/ps/86.2.309
   PubMed Web of Science ®Google Scholar
• Panda AK, Rao SV, Raju MV, Sharma SR. Dietary supplementation of Lactobacillus sporogenes on performance and serum biochemico-lipid profile of broiler chickens. J Poult Sci. 2006;43(3):235–40. doi:10.2141/jpsa.43.235
   Google Scholar
• Gheorghe A, Hăbeanu M, Dumitru M, Lefter NA, Idriceanu L. Performance and intestinal microflora response of broilers to a probiotic mixture supplementation. Arch. zootech. 2021;24(1):53–65. doi:10.2478/azibna-2021-0005
   Google Scholar
• Wang H, Ni X, Qing X, Zeng D, Luo M, Liu L, Li G, Pan K, Jing B. Live probiotic Lactobacillus johnsonii BS15 promotes growth performance and lowers fat deposition by improving lipid metabolism, intestinal development, and gut microflora in broilers. Front Microbiol. 2017;8:1073. doi:10.3389/fmicb.2017.01073
   PubMed Web of Science ®Google Scholar
• Yun W, Lee DH, Choi YI, Kim IH, Cho JH. Effects of supplementation of probiotics and prebiotics on growth performance, nutrient digestibility, organ weight, fecal microbiota, blood profile, and excreta noxious gas emissions in broilers. Appl Poult Res. 2017;26(4):584–92. doi:10.3382/japr/pfx033
   Web of Science ®Google Scholar
• Shen X, Yi D, Ni X, Zeng D, Jing B, Lei M, Bian Z, Zeng Y, Li T, Xin J. Effects of Lactobacillus plantarum on production performance, immune characteristics, antioxidant status, and intestinal microflora of bursin-immunized broilers. Can J Microbiol. 2014;60(4):193–202. doi:10.1139/cjm-2013-0680
   PubMed Web of Science ®Google Scholar
• Obamedo TN, Duru S, Omage J, Olugbemi TS, Olutunmogun AK. Effect of Bacillus subtilis and Lactobacillus acidophilus as probiotic feed supplements on growth performance, haematology, biochemistry and lipid profile of starter broiler chickens during the wet season. Niger J Anim Sci T Echnol (NJAST). 2021;4(4):1–10. http://www.njast.com.ng/index.php/home/article/view/167.
   Google Scholar
• Deraz SF. Synergetic effects of multispecies probiotic supplementation on certain blood parameters and serum biochemical profile of broiler chickens. J Anim Health Prod. 2018;6(1):27–34. doi:10.17582/journal.jahp/2018/6.1.27.34
   Google Scholar
• Mulatu K, Ameha N, Girma M. Effects of feeding different levels of baker’s yeast on performance and hematological parameters in broiler chickens. JWPR. 2019;9(2):38–49. doi:10.36380/jwpr.2019.5
   Google Scholar
• Khalil KK, Islam MA, Islam MM, Sujan KM, Islam MK, Miah MA. Effects of selected probiotics and synbiotics on growth performance and blood-biochemical changes in broiler chickens. J Bangladesh Agril Univ. 2021;19:1–6. doi:10.5455/JBAU.120923
   Google Scholar
• Siddiqui SH, Howlader MM, Begum S, Rahman MM, Islam S, Hasan MM. Biological effects of commercial enzymes, probiotics and liver tonic on live weight and hematobiochemical parameters in broiler. Cell. 2017;88:56–60.
   Google Scholar
• Nyamagonda H, Swamy MN, Veena T, Swamy HD, Jayakumar K. Effect of prebiotic, probiotic and G-probiotic SPL on certain haematological parameters in broiler chickens. Vet. World. 2009;2(9):344–6.
   Google Scholar
• Hasan S, Hossain MM, Alam J, Bhuiyan MER. Benificial effects of probiotic on growth performance and hemato-biochemical parameters in broilers during heat stress. Int J Res Sci Innov Appl Sci. 2015;10(1):244–9.
   Google Scholar
• Zuhra FT, Paul AK, Riad MM, Ahmed MS. Effects of probiotics and phytoextracts on growth and immunomodulating performances of broiler chickens. Bangl J Vet Med. 2018;16(1):13–21. doi:10.3329/bjvm.v16i1.37368
   Google Scholar
• Kumar S, Yadav SP, Chandra G, Sahu DS, Kumar R, Maurya PS, Yadav DK, Jaiswal V, Ranjan K. Effect of dietary supplementation of yeast (Saccharomyces cerevisiae) on performance and hemato-biochemical status of broilers. India J Poul Sci. 2019;54(1):15–9. doi:10.5958/0974-8180.2019.00002.3
   Google Scholar
• Yazhini P, Visha P, Selvaraj P, Vasanthakumar P, Chandran V. Dietary encapsulated probiotic effect on broiler serum biochemical parameters. Vet World. 2018;11(9):1344–8. doi:10.14202/vetworld.2018.1344-1348
   PubMed Web of Science ®Google Scholar
• Banu LA, Mustari A, Ahmad N. Efficacy of probiotics on growth performance and hemato-biochemical parameters in broiler. Res Agric Livest Fish. 2019;6(1):91–100. doi:10.3329/ralf.v6i1.41390
   Google Scholar
• Hung AT, Lin SY, Yang TY, Chou CK, Liu HC, Lu JJ, Wang B, Chen SY, Lien TF. Effects of Bacillus coagulans ATCC 7050 on growth performance, intestinal morphology, and microflora composition in broiler chickens. Anim Prod Sci. 2012;52(9):874–9. doi:10.1071/AN11332
   Google Scholar
• Haque MI, Ahmad N, Miah MA. Comparative analysis of body weight and serum biochemistry in broilers supplemented with some selected probiotics and antibiotic growth promoters. J Adv Vet Anim Res. 2017;4(3):288–94. doi:10.5455/javar.2017.d226
   Web of Science ®Google Scholar
• Abbas G, Asif-Iqbal M, Riaz M, Sajid M, Zahid O, Wasim-Abbas S, Saeed H, Imran-Raza A, Zohaib M. Comparative effect of different levels of probiotics (protexin) on hemato-chemical profile in broilers. AZB. 2018;6(3):84–7. doi:10.13189/azb.2018.060302
   Google Scholar
• Aluwong T, Hassan F, Dzenda T, Kawu M, Ayo J. Effect of different levels of supplemental yeast on body weight, thyroid hormone metabolism and lipid profile of broiler chickens. J Vet Med Sci. 2013;75(3):291–8. doi:10.1292/jvms.12-0368
   PubMed Web of Science ®Google Scholar
• Mansoub NH. Comparison of effects of using nettle (Urtica dioica) and probiotic on performance and serum composition of broiler chickens. Glob Vet. 2011;6(3):247–50.
   Google Scholar
• Peng Q, Zeng XF, Zhu JL, Wang S, Liu XT, Hou CL, Thacker PA, Qiao SY. Effects of dietary Lactobacillus plantarum B1 on growth performance, intestinal microbiota, and short chain fatty acid profiles in broiler chickens. Poult Sci. 2016;95(4):893–900. doi:10.3382/ps/pev435
   PubMed Web of Science ®Google Scholar
• Khonyoung D, Yamauchi KE. Effects of heat-killed Lactobacillus plantarum L-137 on morphology of intestinal villi and epithelial cells in broiler chickens. J Appl Anim Res. 2012;40(2):140–7. doi:10.1080/09712119.2011.640208
   Web of Science ®Google Scholar
• Shokryazdan P, Faseleh Jahromi M, Liang JB, Ramasamy K, Sieo CC, Ho YW. Effects of a Lactobacillus salivarius mixture on performance, intestinal health and serum lipids of broiler chickens. PLoS One. 2017;12(5):e0175959. doi:10.1371/journal.pone.0175959
   PubMed Web of Science ®Google Scholar
• Mountzouris KC, Tsitrsikos P, Palamidi I, Arvaniti A, Mohnl M, Schatzmayr G, Fegeros K. Effects of probiotic inclusion levels in broiler nutrition on growth performance, nutrient digestibility, plasma immunoglobulins, and cecal microflora composition. Poult Sci. 2010;89(1):58–67. doi:10.3382/ps.2009-00308
   PubMed Web of Science ®Google Scholar
• Biernasiak J, Slizewska K. The effect of a new probiotic preparation on the performance and faecal microflora of broiler chickens. Vet Med. 2009;54(11):525–31. doi:10.17221/3075-VETMED
   Web of Science ®Google Scholar
• Geeta AS, Pradhan S, Rajoria R, Kumar A, Gopi M, Navani NK, Pathania R. Probiotic attributes of Lactobacillus fermentum NKN51 isolated from yak cottage cheese and the impact of its feeding on growth, immunity, caecal microbiology and jejunal histology in the starter phase of broiler birds. Indian J. Anim. Res. 2021;55(4):451–6. https://arccjournals.com/journal/indian-journal-of-animal-research/B-3970
   Google Scholar
• Jin LZ, Ho YW, Abdullah N, Ali MA, Jalaludin S. Effects of adherent Lactobacillus cultures on growth, weight of organs and intestinal microflora and volatile fatty acids in broilers. Anim Feed Sci Technol. 1998;70(3):197–209. doi:10.1016/S0377-8401(97)00080-1
   Web of Science ®Google Scholar
• Jin LZ, Ho YW, Abdullah N, Jalaludin S. Growth performance, intestinal microbial populations, and serum cholesterol of broilers fed diets containing Lactobacillus cultures. Poult Sci. 1998;77(9):1259–65. doi:10.1093/ps/77.9.1259
   PubMed Web of Science ®Google Scholar
• Lan PT, Le TB, Benno Y. Impact of two probiotic Lactobacillus strains feeding on fecal lactobacilli and weight gains in chicken. J Gen Appl Microbiol. 2003;49(1):29–36. doi:10.2323/jgam.49.29
   PubMed Web of Science ®Google Scholar
• Mohd Shaufi MA, Sieo CC, Chong CW, Gan HM, Ho YW. Deciphering chicken gut microbial dynamics based on high-throughput 16S rRNA metagenomics analyses. Gut Pathog. 2015;7(1):1–2. doi:10.1186/s13099-015-0051-7
   PubMedGoogle Scholar
• Wei S, Lilburn M, Yu Z. The bacteriomes of ileal mucosa and cecal content of broiler chickens and turkeys as revealed by metagenomic analysis. Int J Microbiol. 2016;2016:4320412. doi:10.1155/2016/4320412
   PubMedGoogle Scholar
• Corrigan A, Horgan K, Clipson N, Murphy RA. Effect of dietary supplementation with a Saccharomyces cerevisiae mannan oligosaccharide on the bacterial community structure of broiler cecal contents. Appl Environ Microbiol. 2011;77(18):6653–62. doi:10.1128/AEM.05028-11
   PubMed Web of Science ®Google Scholar
• J, Scupham A, Patton TG, Bent E, Bayles DO. Comparison of the cecal microbiota of domestic and wild turkeys. Microb Ecol. 2008;56(2):322–31. doi:10.1007/s00248-007-9349-4
   PubMed Web of Science ®Google Scholar
• Wang W, Zijlstra RT, Ganzle MG. Feeding Limosilactobacillus fermentum K9-2 and Lacticaseibacillus casei K9-1, or Limosilactobacillus reuteri TMW1. 656 reduces pathogen load in weanling pigs. Front Microbiol. 2020;11:1–14. doi:10.3389/fmicb.2020.608293
   PubMed Web of Science ®Google Scholar