» Articles » PMID: 35755604

Histopathological, Immunohistochemical and Biochemical Studies of Murine Hepatosplenic Tissues Affected by Chronic Toxoplasmosis

Overview
Journal J Parasitol Res
Publisher Wiley
Specialty Parasitology
Date 2022 Jun 27
PMID 35755604
Authors
Affiliations
Soon will be listed here.
Abstract

Toxoplasmosis is a serious health problem in humans and animals resulting from obligatory intracellular invasion of reticuloendothelial tissue by . The profound pathologic effect of toxoplasmosis is confined to nervous tissue, but many other organs, including the liver and spleen, are insulted. Many molecules like caspase-3, CD3, and CD138 are implicated in the tissue immune response in a trial to alleviate hazardous toxoplasmosis impact. This study aimed to investigate the effect of chronic toxoplasmosis on the liver and spleen tissues of mice using biochemical and histopathological techniques and to detect the activity and level of expression of caspase-3, CD3, and CD138 in these tissues using immunohistochemical labeling. Compared with normal control, altered normal histological features accompanied by inflammatory reaction were recorded in hepatosplenic reticuloendothelial tissues in chronically infected mice. The biochemical profile of the liver has been changed in the form of increased liver enzymes, and oxidative stress has been evidenced by elevated nitric oxide (NO) concentration in liver homogenate. The levels of caspase3, CD3, and CD138 were markedly expressed in the liver and spleen of infected mice. Our findings revealed the persistent effect of latent toxoplasmosis on the host's histological architecture, metabolic, and immunological profile, creating a continued challenging host-parasite relationship.

Citing Articles

Nanospheres as the delivery vehicle: novel application of ribosomal protein S2 in PLGA and chitosan nanospheres against acute toxoplasmosis.

Qi W, Yu Y, Yang C, Wang X, Jiang Y, Zhang L Front Immunol. 2024; 15:1475280.

PMID: 39416787 PMC: 11480959. DOI: 10.3389/fimmu.2024.1475280.


Spiramycin-loaded maltodextrin nanoparticles as a promising treatment of toxoplasmosis on murine model.

Abdel-Wahab A, Shafey D, Selim S, Sharaf S, Mohsen K, Allam D Parasitol Res. 2024; 123(7):286.

PMID: 39046555 PMC: 11269460. DOI: 10.1007/s00436-024-08280-4.

References
1.
El-Sayad M, Abdel Rahman M, Hussein N, Abdel Aziz R, El-Taweel H, El-Latif N . microRNA-155 Expression and Butyrylcholinesterase Activity in the Liver Tissue of Mice Infected with Toxoplasma gondii (Avirulent and Virulent Strains). Acta Parasitol. 2021; 66(4):1167-1176. DOI: 10.1007/s11686-021-00383-7. View

2.
Chen X, Zhou C, Elsheikha H, He S, Hu G, Zhu X . Profiling of the perturbed metabolomic state of mouse spleen during acute and chronic toxoplasmosis. Parasit Vectors. 2017; 10(1):339. PMC: 5516376. DOI: 10.1186/s13071-017-2282-6. View

3.
Dincel G, Atmaca H . Nitric oxide production increases during Toxoplasma gondii encephalitis in mice. Exp Parasitol. 2015; 156:104-12. DOI: 10.1016/j.exppara.2015.06.009. View

4.
Zorgi N, Jimenez Galisteo Jr A, Sato M, Nascimento N, de Andrade Jr H . Immunity in the spleen and blood of mice immunized with irradiated Toxoplasma gondii tachyzoites. Med Microbiol Immunol. 2016; 205(4):297-314. DOI: 10.1007/s00430-015-0447-5. View

5.
Elsheikha H, El-Motayam M, Abouel-Nour M, Morsy A . Oxidative stress and immune-suppression in Toxoplasma gondii positive blood donors: implications for safe blood transfusion. J Egypt Soc Parasitol. 2009; 39(2):421-8. View