Protective effects of lactoferrin chimera and bovine lactoferrin in a mouse model of enterohaemorrhagic Escherichia coli O157:H7 infection1This article is part of a Special Issue entitled Lactoferrin and has undergone the Journal's usual peer review process.

Author:

Flores-Villaseñor Héctor1,Canizalez-Román Adrian2,Velazquez-Roman Jorge3,Nazmi Kamran4,Bolscher Jan G.M.4,Leon-Sicairos Nidia25

Affiliation:

1. Programa Regional para el Doctorado en Biotecnología. Facultad de Ciencias Químico-Biológicas. Universidad Autónoma de Sinaloa. Culiacán Sinaloa, México.

2. Unidad de Investigación de la Facultad de Medicina, Universidad Autónoma de Sinaloa, Culiacán Sinaloa, México.

3. Escuela Superior de Medicina Instituto Politécnico Nacional, México D.F, México.

4. Department of Oral Biochemistry ACTA, Amsterdam, The Netherlands.

5. Departamento de Investigación, Hospital Pediátrico de Sinaloa, Culiacán Sinaloa, México.

Abstract

Mice orally infected with enterohaemorrhagic Escherichia coli (EHEC) O157:H7 were used to evaluate the activity of bovine lactoferrin (bLF) and the synthetic peptide LFchimera. Groups of BALB/c mice inoculated intragastrically with EHEC O157:H7 showed chronic intestinal infection with the pathogen that persisted over 6 days and resulted in a high mortality rate (90%). LFchimera and kanamycin significantly decreased (40%) this mortality rate (P = 0.028). On the other hand, although mice administered with bLF showed an important reduction in mortality (50%), this was not statistically significant (P = 0.070). In infected and untreated mice, severe tubular necrosis, glomerular lesions, and moderate intratubular hyaline casts were found in the kidney. However, in the bLF and LFchimera groups we found a reduction in the damage and a substantial decrease in the bacterial concentration excreted in feces 48 h after infection. Furthermore, sepsis caused by EHEC was reduced by the treatments, evidenced by the fact that bacteria were not detected in the kidney or liver 72 h after infection. The results suggest the bLF and LFchimera could have potential as therapeutics in EHEC infections.

Publisher

Canadian Science Publishing

Subject

Cell Biology,Molecular Biology,Biochemistry

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