Evidence map›Paper›PMID 39558410›Full record

ArticleParasites & vectors2024

Novel insights into antioxidant status, gene expression, and immunohistochemistry in an animal model infected with camel-derived Trypanosoma evansi and Theileria annulata.

Reem M Ramadan, Alaa F Bakr, Esraa Fouad, Faten F Mohammed, Azza M Abdel-Wahab, Sahar Z Abdel-Maogood, Mohamed M El-Bahy, Mai A Salem

Abstract read
In one paragraph

Article in Parasites & vectors, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
  2. Determination of the efficacy of red ginger (Open veterinary journal · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. The impact of parasitic diseases on dromedary camel (Frontiers in veterinary science · 2025
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Reem M RamadanDepartment of Parasitology, Faculty of Veterinary Medicine, Cairo University, Giza, 1221, Egypt. reem.montaser@cu.edu.eg.
Alaa F BakrDepartment of Pathology, Faculty of Veterinary Medicine, Cairo University, Giza, 1221, Egypt.
Esraa FouadThe Central Laboratory for Evaluation of Veterinary Biologics (CLEVB), Agriculture Research Centre (ARC), Cairo, Egypt.
Faten F MohammedDepartment of Pathology, Faculty of Veterinary Medicine, Cairo University, Giza, 1221, Egypt.
Azza M Abdel-WahabDepartment of Parasitology, Faculty of Veterinary Medicine, Cairo University, Giza, 1221, Egypt.
Sahar Z Abdel-MaogoodDepartment of Parasitology, Faculty of Veterinary Medicine, Cairo University, Giza, 1221, Egypt.
Mohamed M El-BahyDepartment of Parasitology, Faculty of Veterinary Medicine, Cairo University, Giza, 1221, Egypt.
Mai A SalemDepartment of Parasitology, Faculty of Veterinary Medicine, Cairo University, Giza, 1221, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHemoprotozoan diseases, especially trypanosomosis and theileriosis, adversely affect the productivity, growth, and performance of camels. Regular sampling and investigation of camels are challenging due to several factors. Consequently, there is a lack of knowledge on camel parasite genotyping, cytokine production, and oxidative stress parameters during infection.

methodsThe present study investigated two critical blood protozoa infecting camels in Egypt, Trypanosoma evansi and Theileria annulata, using molecular methods, specifically 18S rRNA gene analysis. Following molecular confirmation, experimental infections were induced in Swiss albino mice to assess the expression of immune response genes and oxidative stress parameters. The study further explored the correlation between histopathological alterations and inflammatory reactions in the kidney, spleen, and liver of infected mice, alongside the immunohistochemical expression of caspase-3, proliferating cell nuclear antigen (PCNA), and tumor necrosis factor (TNF).

resultsTrypanosoma evansi and T. annulata isolated from naturally infected camels were molecularly identified and deposited in GenBank under accession numbers OR116429 and OR103130, respectively. Infection with T. evansi and T. annulata caused significant adverse effects on the immune condition of infected mice, increasing the pathogenicity of the infection. This was evidenced by a significant increase in oxidative stress parameter levels in both naturally infected camels and experimentally infected mice compared to healthy controls. Furthermore, the expression of immune response genes was significantly elevated in infected mice. Immunohistochemistry analysis showed a pronounced upregulation of caspase-3, PCNA, and TNF in the infected groups relative to the control group. These findings are the first to be reported in Egypt.

conclusionsThis study successfully identified and genotyped two economically important blood protozoa, T. evansi and T. annulata, from camels in Egypt. Additionally, the experimental animal model provided valuable insights into the immune response, oxidative stress, and histopathological changes induced by these parasites, demonstrating comparable results to naturally infected camels. These findings highlight the potential of this model to study parasite-host interactions and immune responses, contributing to a better understanding of the pathogenic mechanisms of T. evansi and T. annulata infections. This model may be useful for future studies focused on disease control and therapeutic interventions.

Indexed as

CamelusDisease Models, AnimalImmunohistochemistryOxidative StressTheileria annulataTheileriasisTrypanosomaTrypanosomiasisAnimalsAntioxidantsEgyptGene ExpressionLiverMiceRNA, Ribosomal, 18SSpleenAntioxidantsRNA, Ribosomal, 18SCamelsGene expressionImmunohistochemistryStress markersTheileria annulataTrypanosoma evansi

Identifiers

PMID39558410
PMCPMC11575088

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.