Detection of hypogammaglobulinaemia in neonatal foals using the glutaraldehyde coagulation test.
Abstract: The glutaraldehyde coagulation test was adapted to foal serum to determine adequacy of the colostral-intestinal transfusion of IgG. The test is performed simply by mixing one volume of reagent with 10 volumes of serum and observing the coagulation time. The required glutaraldehyde concentration was established for various threshold levels of IgG as determined by radial immunodiffusion. The analysis consisted of 140 serum samples from foals. Sera with low IgG levels require high glutaraldehyde concentrations and vice versa. The 4 g/l threshold generally accepted for IgG adequacy, was achieved at the optimum diagnostic sensitivity and specificity level by using 10% solution of glutaraldehyde and observing the coagulation at 20 minutes. The use of a 5% glutaraldehyde solution resulted in a cut off level at 5.5 g/l, respectively. The glutaraldehyde test is the cheapest field test for IgG-adequacy.
Publication Date: 1989-05-01 PubMed ID: 2503956DOI: 10.1111/j.1439-0450.1989.tb00587.xGoogle Scholar: Lookup
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- Journal Article
Summary
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The research article discusses the adaptation of the glutaraldehyde coagulation test to assess the concentration of IgG in the serum of neonatal foals. The test is important in determining whether the neonatal foals received adequate colostral-intestinal transfusion of IgG.
Introduction to the Research Objective
- The research aimed to adapt the glutaraldehyde coagulation test for measuring immunoglobulin G (IgG) concentration in the serum of neonatal foals. IgG is a type of antibody that is crucial for the immunity of foals.
- This research was critical as it helps in determining whether a newborn foal has received sufficient amounts of IgG, indicating a successful colostral-intestinal transfusion. This can directly influence the foal’s health and immunity in the early stages of life.
Test Methodology
- The glutaraldehyde coagulation test involves mixing one volume of the reagent (glutaraldehyde) with ten volumes of serum to observe how long it takes for coagulation to occur.
- The required concentration of glutaraldehyde is established by calculating different threshold levels of IgG using radial immunodiffusion.
- It is important to note that serum with low IgG levels requires higher concentrations of glutaraldehyde and vice versa.
Findings from the Research
- From a total of 140 serum samples from foals analyzed, the researchers determined the 4 grams per litre (g/l) threshold, which is the generally accepted level signifying adequate IgG.
- This threshold was achieved optimally by using a 10% solution of glutaraldehyde and observing coagulation at 20 minutes, providing the diagnostic sensitivity and specificity needed.
- A 5% solution of glutaraldehyde resulted in a cut-off level at 5.5 g/l, indicating that different concentration levels of the reagent can lead to variations in the IgG reading.
Significance of the Findings
- A significant conclusion from this research is that the adapted glutaraldehyde test provides an economical method to assess IgG levels in foals, proving valuable for vets and animal-health workers.
- This cost-effective test should offer a helpful diagnostic tool in veterinary medicine, especially in the field where resources for advanced analysis may be limited.
Cite This Article
APA
Saikku A, Koskinen E, Sandholm M.
(1989).
Detection of hypogammaglobulinaemia in neonatal foals using the glutaraldehyde coagulation test.
Zentralbl Veterinarmed B, 36(3), 168-174.
https://doi.org/10.1111/j.1439-0450.1989.tb00587.x Publication
Researcher Affiliations
MeSH Terms
- Agammaglobulinemia / diagnosis
- Agammaglobulinemia / veterinary
- Animals
- Animals, Newborn
- Blood Coagulation Tests
- Glutaral
- Horse Diseases / diagnosis
- Horses
- Immunoglobulin G / analysis
Citations
This article has been cited 1 times.- Brink P, Wright JC, Schumacher J. An investigation of the ability of the glutaraldehyde test to distinguish between acute and chronic inflammatory disease in horses.. Acta Vet Scand 2005;46(1-2):69-78.
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