Duodenal Histomorphological Changes in Broilers Administered poly d, l-lactic-coglycolic acid (PLGA ) Nanoparticles Encapsulated with Peptide
Main Article Content
Abstract
This research was carried out to evaluate the effect of poly d, l-lactic-coglycolic acid(PLGA) nanoparticles loaded with peptide (as vaccine) on histomorphological in duodenum of broiler chick. A total of ninety eight, one day old ,unsexed broiler( Rose) chicks were divided randomly into seven groups( 2 replicate in each group) as follows:G1-control,G2 - chicks received traditional vaccine of infectious bursal disease(Volvac@ IBD MLV) ,G3 – Chicks Received PLGA nanoparticles only, G4,G5,G6 and G7 – chicks were received prepared vaccine at 160, 80, 40,and 20 μg of peptide loaded PLGA respectively. At the end of the experiment histopathological examination of duodenum section and histomorphological changes were examined. The histopathological examination of duodenal sections shows an elongation and infiltration of lamina propria (LP) with increase villi height and crypt depth in groups that received PLGA alone and those received peptide loaded PLGA. At the same time these groups reveal an increase in mucosal thickness and in length and width of villi. The histomorphological examination in this study show thicker mucosal layer with deeper crypt in duodenum of broilers that subjected to PLGA administration alone or to different concentration of peptide loaded PLGA compared to G1 and G2. These findings are accompanied by a high density of goblet cells and lower villus hight/crypt depth (V/CD) ratio. All groups show mononuclear cells (MNCs) infiltration in submucosa ofduodenum. In-conclusion, the administration of PLGA nanoparticles is strongly linked to the improvement of the physiological and immunological features of the birds.
Downloads
Article Details
Section
How to Cite
Publication Dates
References
Rao JP, Geckeler KE. Polymer nanoparticles: preparation techniques and size-control parameters. Prog. Polym Sci. 2011; 36(7): 887-913. DOI: https://doi.org/10.1016/j.progpolymsci.2011.01.001
Hameed AH. Study of chrysin nanoparticles as antitumor agent in vitro. [Thesis]. Baghdad, Iraq: University of Technology; 2018.
Bolhassani A, Javanzad S, Saleh T, Hashemi M, Aghasadeghi M R, Sadat SM. Polymeric nanoparticles potent vectors for vaccine delivery targeting cancer and infectious diseases. Hum Vaccin Immunother.2014; 10:2, 321–332. DOI: https://doi.org/10.4161/hv.26796
Rauta P R.Immunological evaluation of biodegradable particle based nanoparticles encapsulating OMP antigen as potential vaccine candidate. [ Dissertation]. Rourkela. India: National Institute of Technology Rourkela; 2016
Thomas C, Rawat A, Hope-Weeks L. Aerosolized PLA and PLGA nanoparticles enhance humoral, mucosal and cytokine responses to hepatitis B vaccine. Mol Pharm. 2011; 8:405-415. DOI: https://doi.org/10.1021/mp100255c
Lü JM, Wang X, Marin-Muller C, Wang H, Lin PH, Yao Q. Current advances in research and clinical applications of PLGA-based nanotechnology. Expert Rev. Mol. Diagn. 2009; 9:325–41. DOI: https://doi.org/10.1586/erm.09.15
Akagi T, Baba M, Akashi M. Biodegradable nanoparticles as vaccine adjuvants and delivery systems: regulation of immune responses by nanoparticle-based vaccine. In: Kunugi S, Yamaoka T, editors. Polymers in nanomedicine. Berlin: Springer-Verlag Berlin;
p. 31–64.
Zhao K, Zhang Y, Zhang X, Shi C, Wang X, Wang X, et al. Chitosan-coated poly(lactic-co-glycolic) acid nanoparticles as an efficient delivery system for Newcastle disease virus DNA vaccine. Int J Nanomedicine. 2014; 9 :4609–4619. DOI: https://doi.org/10.2147/IJN.S70633
Danhier F, Ansorena E, Silva JM, s Coco R, Breton L, Préat V. PLGA-based nanoparticles. an overview of biomedical applications. J Control Release. 2012; 161 505–522. DOI: https://doi.org/10.1016/j.jconrel.2012.01.043
Manish M, Rahi A, Kaur M, Bhatnagar R, Singh S. A single-dose PLGA encapsulated protective antigen domain 4 nanoformulation protects mice against Bacillus anthracis spore challenge. PLoS ONE. 2013;8: e61885–90. DOI: https://doi.org/10.1371/journal.pone.0061885
Stevanovic M, Radulovic A, Jordovic B, Uskokovic D. “Poly (DL-lactide-co-glycolide) Nanospheres for the Sustained Release of Folic Acid,” J. Biomed. Nanotechnol. 2008; 4(3): 349–358. DOI: https://doi.org/10.1166/jbn.2008.321
McCall R, Sirianni R. PLGA nanoparticles formed by single- or double-emulsion with vitamin ETPGS. J Vis Exp. 2013:82:1-8. DOI: https://doi.org/10.3791/51015
Kumar V. Chitosan coated plg nanoparticles as delivery system for infectious bursal disease viral antigens. [Thesis]. Izatnagar, India: Deemed University Indian Veterinary Research Institute;2014.
Luna LG. Manual of Histology Staining. Methods of Armed Forces. Institute of Pathology. 3rd ed. New York and London: McGraw-Hill Book Company1;968.
Burkholder KM, Thompson KL, Einstein ME, Applegate TJ, Patterson JA. Influence of stressors on normal intestinal microbiota, intestinal morphology, and susceptibility to Salmonella enteridis colonization in broilers. Poult.Sci. 2008;87(9):1734-1741. DOI: https://doi.org/10.3382/ps.2008-00107
SAS. SAS/STAT Users guide for personal computer. release 9.13.SAS Institute, Inc., Cary, N.C., USA. 2010.
Lei XJ, Ru YJ, Zhang HF. Effect of Bacillus amyloliquefaciens- based direct-fed microbials and antibiotic on performance, nutrient digestibility, ceca microflora and intestinal morphology in broiler chickens. J Appl Poult Res. 2014; 23:1-8. DOI: https://doi.org/10.3382/japr.2014-00965
Xu Y, Shi B, Yan S, Li T, Guo Y, Li J. Effects of chitosan on body weight gain, growth hormone and intestinal morphology in weaned pigs. Asian Australas. J. Anim. Sci. 2013 ;26(10): 1484-1489. DOI: https://doi.org/10.5713/ajas.2013.13085
Wang C, Zhang L, Su W, Ying Z, He J, Zhang L, et al. Zinc oxide nanoparticles as a substitute for zinc oxide or colistin sulfate: Effects on growth, serum enzymes, zinc deposition, intestinal morphology and epithelial barrier in weaned piglets. PLoS ONE.
; 12(7): e0181136.
Hu C H, Gu ZS, Luan J, Zhu K. Effects of montmorillonite-zinc oxide hybrid on performance, diarrhea, intestinal permeability and morphology of weanling pigs. Anim. Feed Sci. Technol. 2012; 177:108-115. DOI: https://doi.org/10.1016/j.anifeedsci.2012.07.028
Montagne L, Pluske J R, Hampson DJ. A review of interactions between dietary fibre and the intestinal mucosa, and their consequences on digestive health in young non-ruminant animals. Anim. Feed Sci. Technol. 2003; 108:95-117. DOI: https://doi.org/10.1016/S0377-8401(03)00163-9
Awad W, Ghareeb K, Böhm J. Intestinal structure and function of broiler chickens on diets supplemented with a symbiotic containing Enterococcus faecium and oligosaccharides. Int J MolSci. 2008; 9:2205-16. DOI: https://doi.org/10.3390/ijms9112205
Baurhoo B, Phillip L, Ruiz-Feria CA. Effects of purified lignin and mannan oligosaccharides on intestinal integrity and microbial populations in the ceca and litter of broiler chickens. PoultSci.2007; 86:1070-78. DOI: https://doi.org/10.1093/ps/86.6.1070
Han XY, Du WL, Huang QC, Xu ZR, Wang YZ. Changes in small intestinal morphology and digestive enzyme activity with oral administration of copper-loaded chitosan nanoparticles in rats. Biol. Trace Elem. Res. 2012; 145:355-360. DOI: https://doi.org/10.1007/s12011-011-9191-x
Ali S, Masood S, Zaneb H,Rehman HFU, Masood S, Khan MUR, et al . Supplementation of zinc oxide nanoparticles has beneficial effects on intestinal morphology in broiler chicken. Pak Vet J. 2017; 37(3): 335-339.
Dailey L, Jekel N, Fink L, Gessler T, Schmehl T, Wittmar M, et al. Investigation of the proinflammatory potential of biodegradable nanoparticle drug delivery systems in the lung. Toxicol Appl Pharmacol. 2006; 215:100-108. DOI: https://doi.org/10.1016/j.taap.2006.01.016
Shakweh M, Ponchel G, Fattal E. Particle uptake by peyers patches: a pathway for drug and vaccine delivery. Drug Deliv.
;1(1):141-163.
Lundquist P, Artursson P. Oral absorption of peptides and nanoparticles across the human intestine: opportunities, limitations and studies in human tissue.Adv. Drug Deliv. Rev. 2016; 106 :256–276. DOI: https://doi.org/10.1016/j.addr.2016.07.007
Uni Z, Smirnov A, Sklan D. Pre- and pos thatch development of goblet cells in the broiler small intestine: effects of delayed access to feed.J.Poult.Sci. 2003;82:320-327. DOI: https://doi.org/10.1093/ps/82.2.320
Kim JJ, Khan WI. Goblet cells and mucins: Role in innate defense in enteric Infections. J Pathog. 2013; 2: 55-70. DOI: https://doi.org/10.3390/pathogens2010055
Bar-Shira E, Friedman A. Innate immune functions of avian intestinal epithelial cells: Response to bacterial stimuli and localization of responding cells in the developing avian digestive tract. PLoS One. 2018; 13(7): e0200393. DOI: https://doi.org/10.1371/journal.pone.0200393
Duritis I, Mugurevics A. Distribution and characterization of goblet cells in the large intestine of Ostriches during the pre‐and post‐hatch period. Anat Histol Embryol. 2015; 45:457-62 DOI: https://doi.org/10.1111/ahe.12221
