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Research Article


Effects of giardiasis on iron, hepcidin, and gut microbiota metabolites in young rats: Evidence for systemic inflammation and malabsorptive metabolic reprogramming

Zahraa Fadhil Abbas, Osama Hadi Al-obaidy, Monyer Abdulameir Abd Alfatlawi.


Abstract
Background:
Giardiasis is one of the most common intestinal parasites affecting young mammals, birds, and humans. Giardiasis is also frequently associated with the malabsorption of nutrients, particularly iron. However, the effects of Giardia lamblia on iron metabolism and overall inflammation in the host have not been fully understood.

Aim:
This study aimed to investigate giardiasis in experimentally infected young rats and its impact on the systemic response of the host following the parasite clearance from the intestine. More specifically, this study focuses on the body’s iron regulation, the response of the protein hepcidin, and the body’s metabolites.

Methods:
A total of 36 weaned, young male Wistar rats were assigned to one of the following 3 groups: uninfected control, infected with G. lamblia in the acute phase (day 7), and post-infected phase (day 21). All rats in the infected groups received 1×106 G. lamblia trophozoites by oral gavage. Biochemical parameters of interest in the blood and serum of all rats were determined. These were iron, total iron binding capacity (TIBC), transferrin saturation, ferritin, hepcidin, erythropoietin (EPO), C-reactive protein (CRP), interleukin 6 (IL-6), tumor necrosis factor (TNF-α), albumin, and prealbumin. The metabolites of interest were kynurenine, citrulline, trimethylamine oxide (TMAO), lactate, succinate, and SCFAs. The metabolites were determined by high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS).

Results:
The infected groups had significantly lower serum iron, transferrin saturation, albumin, and citrulline (p<0.01). Levels of ferritin and hepcidin decreased significantly post infection (p<0.001) and were associated with increased IL-6 and CRP levels. The metabolites kynurenine and TMAO were significantly increased, whereas the SCFAs (especially butyrate and acetate) were significantly lower. These results suggest an imbalance in the gut microbiota and metabolic reprogramming. A drop in EPO levels was also observed, which, together with the lower levels of MCV and MCH, indicates that the host was in the early stages of anemia.

Conclusion:
Infection with G. lamblia in younger rats causes systemic inflammation, and the iron in the body is sequestered. Significant disruption of the host’s microflora and the metabolites derived from the host and the microbes is also observed. These findings support the role of post-infectious metabolic dysregulation in giardiasis and the risk of damage restricted to the intestinal tract alone.

Key words: Cobalamin; Enterocyte function; Erythropoiesis; Hypoferremia; Mitochondrial stress.


 
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How to Cite this Article
Pubmed Style

Abbas ZF, Al-obaidy OH, Alfatlawi MAA. Effects of giardiasis on iron, hepcidin, and gut microbiota metabolites in young rats: Evidence for systemic inflammation and malabsorptive metabolic reprogramming. Open Vet. J.. 2026; 16(5): 3104-3120. doi:10.5455/OVJ.2026.v16.i5.52


Web Style

Abbas ZF, Al-obaidy OH, Alfatlawi MAA. Effects of giardiasis on iron, hepcidin, and gut microbiota metabolites in young rats: Evidence for systemic inflammation and malabsorptive metabolic reprogramming. https://www.openveterinaryjournal.com/?mno=298577 [Access: May 31, 2026]. doi:10.5455/OVJ.2026.v16.i5.52


AMA (American Medical Association) Style

Abbas ZF, Al-obaidy OH, Alfatlawi MAA. Effects of giardiasis on iron, hepcidin, and gut microbiota metabolites in young rats: Evidence for systemic inflammation and malabsorptive metabolic reprogramming. Open Vet. J.. 2026; 16(5): 3104-3120. doi:10.5455/OVJ.2026.v16.i5.52



Vancouver/ICMJE Style

Abbas ZF, Al-obaidy OH, Alfatlawi MAA. Effects of giardiasis on iron, hepcidin, and gut microbiota metabolites in young rats: Evidence for systemic inflammation and malabsorptive metabolic reprogramming. Open Vet. J.. (2026), [cited May 31, 2026]; 16(5): 3104-3120. doi:10.5455/OVJ.2026.v16.i5.52



Harvard Style

Abbas, Z. F., Al-obaidy, . O. H. & Alfatlawi, . M. A. A. (2026) Effects of giardiasis on iron, hepcidin, and gut microbiota metabolites in young rats: Evidence for systemic inflammation and malabsorptive metabolic reprogramming. Open Vet. J., 16 (5), 3104-3120. doi:10.5455/OVJ.2026.v16.i5.52



Turabian Style

Abbas, Zahraa Fadhil, Osama Hadi Al-obaidy, and Monyer Abdulameir Abd Alfatlawi. 2026. Effects of giardiasis on iron, hepcidin, and gut microbiota metabolites in young rats: Evidence for systemic inflammation and malabsorptive metabolic reprogramming. Open Veterinary Journal, 16 (5), 3104-3120. doi:10.5455/OVJ.2026.v16.i5.52



Chicago Style

Abbas, Zahraa Fadhil, Osama Hadi Al-obaidy, and Monyer Abdulameir Abd Alfatlawi. "Effects of giardiasis on iron, hepcidin, and gut microbiota metabolites in young rats: Evidence for systemic inflammation and malabsorptive metabolic reprogramming." Open Veterinary Journal 16 (2026), 3104-3120. doi:10.5455/OVJ.2026.v16.i5.52



MLA (The Modern Language Association) Style

Abbas, Zahraa Fadhil, Osama Hadi Al-obaidy, and Monyer Abdulameir Abd Alfatlawi. "Effects of giardiasis on iron, hepcidin, and gut microbiota metabolites in young rats: Evidence for systemic inflammation and malabsorptive metabolic reprogramming." Open Veterinary Journal 16.5 (2026), 3104-3120. Print. doi:10.5455/OVJ.2026.v16.i5.52



APA (American Psychological Association) Style

Abbas, Z. F., Al-obaidy, . O. H. & Alfatlawi, . M. A. A. (2026) Effects of giardiasis on iron, hepcidin, and gut microbiota metabolites in young rats: Evidence for systemic inflammation and malabsorptive metabolic reprogramming. Open Veterinary Journal, 16 (5), 3104-3120. doi:10.5455/OVJ.2026.v16.i5.52