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Journal of veterinary internal medicine2007; 21(4); 797-805; doi: 10.1892/0891-6640(2007)21[797:socpao]2.0.co;2

Serum opsonization capacity, phagocytosis, and oxidative burst activity in neonatal foals in the intensive care unit.

Abstract: Phagocytic activity of neonatal foals has been reported to be similar to that of adult horses, but serum opsonization capacity develops with age and may be further altered when opsonins are consumed during infection. Objective: Phagocytosis, oxidative burst activity, and serum opsonization capacity in neonatal foals admitted to an intensive care unit are reduced in comparison with control foals. Methods: Blood samples were collected from hospitalized neonatal foals and from control foals. Hospitalized foals were characterized as sick or septic on the basis of a sepsis score and received intravenous plasma transfusion. Methods: Phagocytosis, oxidative burst activity, and serum opsonization capacity were tested with flow cytometric analysis. Serum immunoglobulin and complement component 3 concentrations were determined with radial immunodiffusion. Serum amyloid A concentration was assayed with a commercially available solid-phase Sandwich ELISA Kit. Data were analyzed with nonparametric and regression methods. Alpha was set at P = .05. Results: Phagocytic functions of septic and sick foals were lower than control foals in the initial phase of the study (P = .01). Opsonization capacity was significantly higher when bacteria were opsonized with serum from septic (P = .029) and sick (P = .006) foals than from control foals on day 1. Opsonization capacity in septic foals was comparable with control foals on days 2 and 5. This effect was not accompanied by an increase in serum complement C3 or immunoglobulin G concentrations independently. Conclusions: Our results suggest that phagocytic function could be decreased in hospitalized foals. The synergistic effect of opsonic elements provided by plasma transfusion may sustain opsonization capacity during sepsis.
Publication Date: 2007-08-22 PubMed ID: 17708402DOI: 10.1892/0891-6640(2007)21[797:socpao]2.0.co;2Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research article deals with the study of the reduced capacity for phagocytosis (a process where cells engulf and ingest harmful particles), oxidative burst activity (a rapid release of reactive oxygen species from cells), and serum opsonization (the process by which pathogens are marked for ingestion and elimination) in newborn foals in an intensive care unit compared to healthy, control foals.

Study Methodology

  • The researchers collected blood samples from both hospitalized newborn foals and healthy, control foals for experimentation.
  • The hospitalized foals were categorized as either sick or septic (a severe infection that spreads through the bloodstream) based on a sepsis score, and they were subjected to intravenous plasma transfusion.
  • Phagocytosis, oxidative burst activity, and serum opsonization capacity were examined using flow cytometric analysis, a method that can analyze the physical and chemical characteristics of particles in a fluid as it passes through a laser.
  • The amount of serum immunoglobulin (a type of antibody) and complement component 3 (a protein that plays a role in the immune response) was determined using radial immunodiffusion, a method to measure the concentration of proteins in a solution.
  • The concentration of Serum amyloid A, a marker for inflammation in horses, was measured using a commercial solid-phase Sandwich ELISA Kit.
  • All data collected from the experiment was analyzed using nonparametric and regression methods with an alpha value set at P = .05 (this means that a result is statistically significant if the p-value is less than or equal to 0.05.)

Research Findings

  • Phagocytic functions of septic and sick foals were found to be lower than control foals in the beginning phase of the study.
  • The serum opsonization capacity was significantly higher when bacteria were marked for elimination with serum from septic and sick foals than with serum from control foals on the first day of the study.
  • The serum opsonization capacity for septic foals was similar to control foals on the second and fifth days of the study.
  • The increase in serum opsonization capacity was not associated with an increase in serum complement C3 or immunoglobulin G concentrations independently.

Conclusions

The findings of this research suggest that the ability of cells to engulf and ingest harmful particles could be compromised in hospitalized foals. However, the results also suggest that the combined effect of opsonic elements provided by plasma transfusion may help to maintain the process by which pathogens are marked for ingestion and elimination during sepsis in these foals.

Cite This Article

APA
Gardner RB, Nydam DV, Luna JA, Bicalho ML, Matychak MB, Flaminio MJ. (2007). Serum opsonization capacity, phagocytosis, and oxidative burst activity in neonatal foals in the intensive care unit. J Vet Intern Med, 21(4), 797-805. https://doi.org/10.1892/0891-6640(2007)21[797:socpao]2.0.co;2

Publication

ISSN: 0891-6640
NlmUniqueID: 8708660
Country: United States
Language: English
Volume: 21
Issue: 4
Pages: 797-805

Researcher Affiliations

Gardner, Rachel B
  • Department of Clinical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.
Nydam, Daryl V
    Luna, Jennifer A
      Bicalho, Marcela L S
        Matychak, Mary Beth
          Flaminio, M Julia B F

            MeSH Terms

            • Animals
            • Animals, Newborn
            • Complement C3 / metabolism
            • Female
            • Horse Diseases / blood
            • Horse Diseases / metabolism
            • Horses
            • Immunoglobulins / blood
            • Intensive Care Units
            • Male
            • Opsonin Proteins / blood
            • Opsonin Proteins / metabolism
            • Phagocytosis
            • Respiratory Burst / physiology
            • Sepsis / blood
            • Sepsis / metabolism
            • Serum Amyloid A Protein / metabolism

            Citations

            This article has been cited 1 times.
            1. Long A, Nolen-Walston R. Equine Inflammatory Markers in the Twenty-First Century: A Focus on Serum Amyloid A.. Vet Clin North Am Equine Pract 2020 Apr;36(1):147-160.
              doi: 10.1016/j.cveq.2019.12.005pubmed: 32007299google scholar: lookup