Cargando…

Quantitative immunoassay for mink immunoglobulin in serum and milk

BACKGROUND: The significance of maternal immunoglobulin G (IgG) for the resistance against a number of infections affecting the health of young mink offspring is not known. Here, we present a validated immunoassay for quantification of mink IgG in serum and milk, using a commercially available polyc...

Descripción completa

Detalles Bibliográficos
Autores principales: Mathiesen, Ronja, Chriél, Mariann, Struve, Tina, Heegaard, Peter Mikael Helweg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6004692/
https://www.ncbi.nlm.nih.gov/pubmed/29914557
http://dx.doi.org/10.1186/s13028-018-0391-7
_version_ 1783332564615823360
author Mathiesen, Ronja
Chriél, Mariann
Struve, Tina
Heegaard, Peter Mikael Helweg
author_facet Mathiesen, Ronja
Chriél, Mariann
Struve, Tina
Heegaard, Peter Mikael Helweg
author_sort Mathiesen, Ronja
collection PubMed
description BACKGROUND: The significance of maternal immunoglobulin G (IgG) for the resistance against a number of infections affecting the health of young mink offspring is not known. Here, we present a validated immunoassay for quantification of mink IgG in serum and milk, using a commercially available polyclonal goat anti-ferret IgG antibody cross-reactive with mink IgG as both the catching and the detection antibody, in a sandwich format enzyme linked immunosorbent assay (ELISA). Using this ELISA, serum IgG concentrations was analyzed over time in both mothers and kits in order to establish a correlation between maternal IgG serum concentrations and those of the offspring. RESULTS: Intra-assay coefficient of variation (CV) for a serum sample ranged from 2.15 to 5.97% depending on the dilution, while the inter-assay CV ranged from 5.17 to 17.78%. In addition, the range of milk intra-assay CV was 2.71–5.92%, while the range of the inter-assay CV was 4.20–16.03%. Calibrating the ELISA with purified mink IgG (an in-house preparation purified from mink serum) the lower limit of detection was found to be 5 ng/mL for serum and 1 ng/mL for milk. Both serum and milk showed high precision and good linearity over a two-log dilution range. When comparing the serum IgG concentrations of the mink kits a clear within litter effect was seen, while the mean serum IgG concentrations of litters differed significantly between some of the litters (P = 0.0013). Mean maternal serum IgG concentrations correlated positively with the IgG serum concentration of the corresponding offspring sampled over a 3 week period (R(2) = 0.63). CONCLUSIONS: A calibrated and reproducible sandwich ELISA for quantifying mink IgG concentrations in both milk and serum with high analytical sensitivity was developed and validated. The results in this study corroborate previous investigations supporting the usability of the ELISA, paving the way for investigations into the importance of maternal IgG in milk and in serum for the welfare and health of the offspring.
format Online
Article
Text
id pubmed-6004692
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-60046922018-06-26 Quantitative immunoassay for mink immunoglobulin in serum and milk Mathiesen, Ronja Chriél, Mariann Struve, Tina Heegaard, Peter Mikael Helweg Acta Vet Scand Research BACKGROUND: The significance of maternal immunoglobulin G (IgG) for the resistance against a number of infections affecting the health of young mink offspring is not known. Here, we present a validated immunoassay for quantification of mink IgG in serum and milk, using a commercially available polyclonal goat anti-ferret IgG antibody cross-reactive with mink IgG as both the catching and the detection antibody, in a sandwich format enzyme linked immunosorbent assay (ELISA). Using this ELISA, serum IgG concentrations was analyzed over time in both mothers and kits in order to establish a correlation between maternal IgG serum concentrations and those of the offspring. RESULTS: Intra-assay coefficient of variation (CV) for a serum sample ranged from 2.15 to 5.97% depending on the dilution, while the inter-assay CV ranged from 5.17 to 17.78%. In addition, the range of milk intra-assay CV was 2.71–5.92%, while the range of the inter-assay CV was 4.20–16.03%. Calibrating the ELISA with purified mink IgG (an in-house preparation purified from mink serum) the lower limit of detection was found to be 5 ng/mL for serum and 1 ng/mL for milk. Both serum and milk showed high precision and good linearity over a two-log dilution range. When comparing the serum IgG concentrations of the mink kits a clear within litter effect was seen, while the mean serum IgG concentrations of litters differed significantly between some of the litters (P = 0.0013). Mean maternal serum IgG concentrations correlated positively with the IgG serum concentration of the corresponding offspring sampled over a 3 week period (R(2) = 0.63). CONCLUSIONS: A calibrated and reproducible sandwich ELISA for quantifying mink IgG concentrations in both milk and serum with high analytical sensitivity was developed and validated. The results in this study corroborate previous investigations supporting the usability of the ELISA, paving the way for investigations into the importance of maternal IgG in milk and in serum for the welfare and health of the offspring. BioMed Central 2018-06-18 /pmc/articles/PMC6004692/ /pubmed/29914557 http://dx.doi.org/10.1186/s13028-018-0391-7 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Mathiesen, Ronja
Chriél, Mariann
Struve, Tina
Heegaard, Peter Mikael Helweg
Quantitative immunoassay for mink immunoglobulin in serum and milk
title Quantitative immunoassay for mink immunoglobulin in serum and milk
title_full Quantitative immunoassay for mink immunoglobulin in serum and milk
title_fullStr Quantitative immunoassay for mink immunoglobulin in serum and milk
title_full_unstemmed Quantitative immunoassay for mink immunoglobulin in serum and milk
title_short Quantitative immunoassay for mink immunoglobulin in serum and milk
title_sort quantitative immunoassay for mink immunoglobulin in serum and milk
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6004692/
https://www.ncbi.nlm.nih.gov/pubmed/29914557
http://dx.doi.org/10.1186/s13028-018-0391-7
work_keys_str_mv AT mathiesenronja quantitativeimmunoassayforminkimmunoglobulininserumandmilk
AT chrielmariann quantitativeimmunoassayforminkimmunoglobulininserumandmilk
AT struvetina quantitativeimmunoassayforminkimmunoglobulininserumandmilk
AT heegaardpetermikaelhelweg quantitativeimmunoassayforminkimmunoglobulininserumandmilk