Skip to main content
Log in

Impact of Eimeria tenella experimental Infection on intestinal and splenic reaction of broiler chickens

  • Original Article
  • Published:
Journal of Parasitic Diseases Aims and scope Submit manuscript

Abstract

This work assesses the cell-mediated immune reaction IL-6, TNF-α, and IFN-γ of experimentally challenged broiler chicken with Eimeria tenella (E. tenella). Therefore, ninety, 2-weeks-old healthy broiler chicks were allocated as eighty chicks infected orally with 2.5 × 104 E. tenella sporulated oocysts, and the other ten birds were kept as control negative birds. Post-challenge, mortality rate, symptoms, oocysts shedding, and lesion score were evaluated. Tissue samples (cecum and spleen) were collected at 0, 4, 8, and 12 days post-infection (dpi). Ten chickens were ethically slaughtered at 0, 4, 8, and 12 days post-infection, as well as two birds from the negative control group; parts from cecal and spleen samples were kept in cryopreservation containers, and other parts were preserved in formaline 10% for further investigation. The evaluated genes (IL-6, TNF-α, and IFN-γ) were normal at 0 days and upregulated at 4 and 8 days, which reached maximum upregulation at eight dpi. The histopathological examination of the ceca and spleen were evaluated before and after challenge. It could be concluded that E. tenella revealed direct severe macroscopic and microscopic changes in cecal tissues and indirectly induced alteration in splenic tissues, resulting in upregulation of different cell mediated immune response in cecum and spleen in relation to the experimental period.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7

Similar content being viewed by others

Data availability

Not applicable.

References

  • Al-Shaibani IRM, Al-Khadher AMA, AlHibah AZH (2020) Anticoccidial activity of Allium sativum and Punica granatum against experimentally induced Eimeria tenella infection in broiler chickens. Asian J Res Anim Vet Sci 5(4):20–29

    Google Scholar 

  • Attia MM, Salem HM (2022) Morphological and molecular characterization of Pseudolynchia canariensis (Diptera: Hippoboscidae) infesting domestic pigeons. Int J Trop Insect Sci 42:733–740

    Article  Google Scholar 

  • Attia MM, El-Gameel SM, Ismael E (2020) Evaluation of Tumor necrosis factor-alpha (TNF-α); gamma interferon (IFN-γ) genes and oxidative stress in sheep: immunological responses induced by Oestrus ovis (Diptera: Oestridae) infestation. J Parasit Dis 44(2):332–337. https://doi.org/10.1007/s12639-020-01220-w

    Article  PubMed  PubMed Central  Google Scholar 

  • Attia MM, Ibrahim MM, Mahmoud MA (2023) Heavy Infection of the orange-spotted grouper (Epinephelus coioides) with Huffmanela japonica: morphological, ultrastructural identification, tissue reactions and immunological analysis. Aquac Int. https://doi.org/10.1007/s10499-023-01124-5

    Article  Google Scholar 

  • Attia MM, Khalifa MM (2023) Virulence of Babesia bigemina in infected cattle (Bos taurus): olecular and immunological studies. Res Vet Sci 156:7–13. https://doi.org/10.1016/j.rvsc.2023.01.017

    Article  CAS  PubMed  Google Scholar 

  • Attia MM, Yehia N, Soliman MM, Shukry M, El-Saadony MT, Salem HM (2022) Evaluation of the antiparasitic activity of the chitosan-silver nanocomposites in the treatment of experimentally infested pigeons with Pseudolynchia canariensis. Saudi J Biol Sci 29:1644–1652

    Article  CAS  PubMed  Google Scholar 

  • Bancroft JD, Gamble M (eds) (2008) Theory and practice of histological techniques. Elsevier, Amsterdam

    Google Scholar 

  • Botwright NA, Mohamed AR, Slinger J, Lima PC, Wynne JW (2021) Host-parasite interaction of Atlantic salmon (Salmo salar) and the ectoparasite Neoparamoeba perurans in amoebic gill disease. Front Immunol 12:1900

    Article  Google Scholar 

  • Breed DG, Dorrestein J, Schetters TP, Waart LV, Rijke E, Vermeulen AN (1997) Peripheral blood lymphocytes from Eimeria tenella infected chickens produce gamma interferon after stimulation in vitro. Parasite Immunol 19(3):127–135

    Article  CAS  PubMed  Google Scholar 

  • Cornelissen JBWJ, Swinkels WJC, Boersma WA, Rebel JMJ (2009) Host response to simultaneous Infections with Eimeria acervulina, maxima and tenella: a cumulation of single responses. Vet Parasitol 162(1–2):58–66

    Article  CAS  PubMed  Google Scholar 

  • Cribillero G, Molina D, Reyna P, Salgado V, Gonzalez R, Icochea VME (2014) Comparison of two infection dosage of Eimeria tenella in broiler chickens for anticoccidials efficacy trials. In: Conference: annual meeting American Association of Avian Pathologist at Denver-Colorado, USA

  • del Cacho E, Gallego M, Lee SH, Lillehoj HS, Quilez J, Lillehoj EP, Sánchez-Acedo C (2012) Induction of protective immunity against Eimeria tenella, Eimeria maxima, and Eimeria acervulina infections using dendritic cell-derived exosomes. Infect Immun 80(5):1909–1916

    Article  PubMed  PubMed Central  Google Scholar 

  • Ding X, Lillehoj HS, Quiroz MA, Bevensee E, Lillehoj EP (2004) Protective immunity against Eimeria acervulina following in ovo immunization with a recombinant subunit vaccine and cytokine genes. Infect Immun 72(12):6939–6944. https://doi.org/10.1016/j.psj.2021.101542

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • El-Shall NA, El-Hack A, Albaqami ME, Khafaga NM, Taha AF, Swelum AE, El-Saadony AA, Salem MT, El-Tahan HM, AbuQamar AM, El-Tarabily SF, Elbestawy KA (2021) Phytochemical control of poultry coccidiosis: a review. Poult, Sci

    Google Scholar 

  • Gu Y, Cui L, Chen H, Li W, Li S, Jin G, Liu D (2010) Effect on serum antioxidase of the same age chicken inoculated with different doses E. tenella. Chin J Vet Sci 30(4):462–464

    CAS  Google Scholar 

  • Hong YH, Lillehoj HS, Lee SH, Dalloul RA, Lillehoj EP (2006) Analysis of chicken cytokine and chemokine gene expression following Eimeria acervulina and Eimeria tenella infections. Vet Immunol Immunopathol 114(3–4):209–223

    Article  CAS  PubMed  Google Scholar 

  • Jeong J, Kim WH, Yoo J, Lee C, Kim S, Cho JH, Min W (2012) Identification and comparative expression analysis of interleukin 2/15 receptor β chain in chickens infected with E. tenella. PLoS ONE 7(5):e37704

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Jiao J, Yang Y, Liu M, Li J, Cui Y, Yin S, Tao J (2018) Artemisinin and Artemisia annua leaves alleviate Eimeria tenella infection by facilitating apoptosis of host cells and suppressing inflammatory response. Vet Parasitol 254:172–177

    Article  CAS  PubMed  Google Scholar 

  • Kogut MH, Rothwell L, Kaiser P (2003) Differential regulation of cytokine gene expression by avian heterophils during receptor-mediated phagocytosis of opsonized and nonopsonized Salmonella enteritidis. J Interferon Cytokine Res 23(6):319–327

    Article  CAS  PubMed  Google Scholar 

  • Laurent F, Mancassola R, Lacroix S, Menezes R, Naciri M (2001) Analysis of chicken mucosal immune response to Eimeria tenella and Eimeria maxima infection by quantitative reverse transcription-PCR. Infect Immun 69(4):2527–2534

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Long PL, Rose ME (1976) Growth of Eimeria tenelIa in vitro in macrophages from chicken peritoneal exudates. Z Parasitenk 48:291–294

    Article  CAS  PubMed  Google Scholar 

  • Ogbe AO, Mgbojikwe LO, Abdu PA, Atawodi SE (2008) Organ and carcass weight variation and histopathological changes in Eimeria tenella infected broiler chickens treated with aqueous extract of a wild mushroom (Ganoderma Lucidum). Electron J Environ Agric Food Chem 7(5):2906–2913

    Google Scholar 

  • Pham HHS, Matsubayashi M, Tsuji N, Hatabu T (2021) Relationship between Eimeria tenella associated-early clinical signs and molecular changes in the intestinal barrier function. Vet Immunol Immunopathol 240:110321

    Article  CAS  PubMed  Google Scholar 

  • Razzaq A, Ali T, Saghir A, Arshad S, Cheema A (2011) Training needs assessment of poultry farmers in tehsil Faisalabad. J Anim Plant Sci 21(3):629–631

    Google Scholar 

  • Salem HM, Khattab MS, Yehia N, Abd El-Hack ME, El-Saadony MT, Alhimaidi AR, Swelum AA, Attia MM (2022b) Morphological and molecular characterization of Ascaridia columbae in the domestic pigeon (Columba livia domestica) and the assessment of its immunological responses. Poult Sci 101(2):101596

    Article  CAS  PubMed  Google Scholar 

  • Salem HM, Salem MA, Soliman MM, Althobaiti SA, Khafaga AK, El-Tahan AM, El-Saadony MT, Attia MM (2022) Parasitological and histopathological examination of Cocktail love birds infected with Eimeria aratinga (Apicomplexa: Eimeriidae). Poult Sci. https://doi.org/10.1016/j.psj.2022.101781

    Article  PubMed  PubMed Central  Google Scholar 

  • Wang X, Zou W, Yu H, Lin Y, Dai G, Zhang T, Zhang G, Xie K, Wang J, Shi H (2019) RNA sequencing analysis of chicken cecum tissues following Eimeria tenella Infection in vivo. Genes (Basel) 10:E420

    Article  Google Scholar 

  • Xu ZY, Zheng MX, Zhang L, Gong X, Xi R, Cui XZ, Bai R (2017) Dynamic expression of death receptor adapter proteins tradd and fadd in Eimeria tenella-induced host cell apoptosis. Poult Sci 96(5):1438–1444

    Article  CAS  PubMed  Google Scholar 

  • Ye C, You J, Li X, You R, Weng Y, Li J, Wang Y (2010) Design, synthesis and anticoccidial activity of a series of 3-(2-(2-methoxyphenyl)-2-oxoethyl) quinazolinone derivatives. Pestic Biochem Physiol 97(3):194–198

    Article  CAS  Google Scholar 

  • Younis NA, Thabit H, El-Samannoudy SI et al (2023) The immune responses of Oreochromis niloticus against Prohemistomum Vivax encysted metacercariae infection with the evaluation of different biomarkers stressors. Sci Rep 13:11885. https://doi.org/10.1038/s41598-023-38809-z

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Yu Y, Zhao Q, Zhu S, Dong H, Huang B, Liang S, Han H (2020) Molecular characterization of serine/threonine protein phosphatase of Eimeria tenella. J Eukaryot Microbiol 67(5):510–520

    Article  CAS  PubMed  Google Scholar 

  • Yu H, Zou W, Mi C, Wang Q, Dai G, Zhang T, Shi H (2021) Research note: expression of T cell-related cytokines in chicken cecal and spleen tissues following Eimeria tenella infection in vivo. Poult Sci 100(7):101161

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Funding

This research received no external funding.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Marwa M. Attia.

Ethics declarations

Conflict of interest

The authors declare that there is no conflict of interest in this paper.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Attia, M.M., Mohamed, R.I. & Salem, H.M. Impact of Eimeria tenella experimental Infection on intestinal and splenic reaction of broiler chickens. J Parasit Dis 47, 829–836 (2023). https://doi.org/10.1007/s12639-023-01629-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12639-023-01629-z

Keywords

Navigation