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Reproduction, fertility, and development2001; 12(3-4); 183-189; doi: 10.1071/rd00062

A dipstick immunoassay to rapidly measure serum oestrone sulfate concentrations in horses.

Abstract: A dipstick, competitive immunoassay for rapidly measuring serum oestrone sulfate (OS) concentrations in horses was developed to distinguish mares 100 or more days pregnant from non-pregnant animals. 6-Ketoestrone 6-carboxymethyloxime conjugated to bovine serum albumin (oestrone CMO-BSA) was 'dotted' 25 mm from the bottom edge of 45 x 5 mm strips of polyester-film-supported cellulose nitrate membrane, pore size 3 microm. The strips were blocked, dried and a 15 x 5-mm cellulose absorbent sink attached 10 mm from the top of each strip. The manufactured dipsticks were stored with desiccant at room temperature until used. A monoclonal antibody recognizing OS was coated onto uniform, blue-dyed polystyrene microspheres (mean diameter, 0.31 microm) by adsorption. After blocking, several washes and resuspension by sonication, the antibody-coated microspheres were stored at 4 degrees C. The concentrations of oestrone CMO-BSA dotted onto the dipsticks and OS antibody coated onto the microspheres were optimized to produce a test that allowed maximum discrimination between the concentrations of OS found in serum of mares 100 or more days pregnant (i.e. >30 ng OS mL(-1)) relative to those found in non-pregnant mares (i.e. <10 ng OS mL(-1)). To perform the dipstick test, 30 microL of carrier buffer, 10 microL of OS antibody-coated microspheres and 10 microl of OS standard or serum sample were pipetted into a microwell and mixed. A dipstick was placed in the solution. All the liquid migrated up the dipstick into the absorbent sink within 15-20 min leaving a blue dot where the OCMO-BSA had been placed. The intensity of colour of the blue dot, which correlated inversely with the concentration of OS in the standard or serum sample, was assessed visually and by computer image analysis. An OS concentration less than 5 ng mL(-1) produced a deep blue dot, 20 ng/ml a light blue dot and a concentration greater than 50 ng mL(-1) a very faint blue dot, or none at all. Serum samples from 42 non-pregnant mares and 40 mares over 100 days pregnant were analysed by the dipstick test. All the serum samples from non-pregnant mares produced dipsticks with deep blue dots that ranged in intensity from 20 to 38 colour intensity units, equivalent to OS concentrations less than 7 ng mL(-1). Sera from all the pregnant mares generated dipsticks with either faint blue dots or none at all (i.e. 40 ng mL(-1). It is concluded that this novel, rapid dipstick immunoassay offers a practical, alternative means of analysing serum OS concentrations in horses, and enables mares that are 100 or more days pregnant to be distinguished from those that are not pregnant.
Publication Date: 2001-04-17 PubMed ID: 11302428DOI: 10.1071/rd00062Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research article focuses on the development of a dipstick immunoassay to rapidly measure serum oestrone sulfate concentrations in horses. The test can help distinguish between pregnant horses who are more than 100 days into their gestation and those who aren’t pregnant.

Objective of the Research

  • The key objective of the research was to formulate a swift, reliable, and efficient dipstick immunoassay capable of accurately measuring the serum oestrone sulfate (OS) concentrations in horses. This serves as a pivotal tool to differentiate pregnant mares that are more than 100 days pregnant from those that are not pregnant.

Methodology

  • First, a solution of Oestrone CMO-BSA was prepared and dotted on strips of polyester-film-supported cellulose nitrate membrane. These strips were left to dry and later attached to a cellulose absorbent sink.
  • A monoclonal antibody that could recognize OS was coated on uniform, blue-dyed polystyrene microspheres via adsorption. The coated microspheres were then washed, resuspended, and stored at 4 degrees Celsius.
  • The researchers optimized the concentrations of the Oestrone CMO-BSA dotted onto the dipsticks and the OS antibody-coated microspheres to distinguish between OS found in pregnant mares from that in non-pregnant ones.

Experiment and Results

  • To perform the assay, a dipstick was placed in a microwell solution containing buffer, antibody-coated microspheres, and an OS standard or serum sample. The solution migrated up the dipstick, leaving a specific color dot, which contrasted with the concentration of OS in the solution.
  • With increasing OS concentration, the dot intensity reduced i.e., from a deep blue dot (less than 5 ng mL(-1)) to a very faint blue or no dot (greater than 50 ng mL(-1)).
  • The research tested the assay on serum samples from 42 non-pregnant and 40 pregnant mares. In the case of non-pregnant mares, the resulting dipsticks produced deep blue dots, indicating OS concentrations less than 7 ng mL. For pregnant mares, the dots were either faint blue or none at all, signifying OS concentrations more than 40 ng mL(-1).

Conclusion

  • The study concluded that this innovative dipstick immunoassay serves as a practical alternative for analyzing serum OS concentrations in horses. This method can help to distinguish mares more than 100 days into their pregnancy from those that are not pregnant.

Cite This Article

APA
Henderson K, Stewart J. (2001). A dipstick immunoassay to rapidly measure serum oestrone sulfate concentrations in horses. Reprod Fertil Dev, 12(3-4), 183-189. https://doi.org/10.1071/rd00062

Publication

ISSN: 1031-3613
NlmUniqueID: 8907465
Country: Australia
Language: English
Volume: 12
Issue: 3-4
Pages: 183-189

Researcher Affiliations

Henderson, K
  • Reproductive Technologies Group, AgResearch, Wallaceville Animal Research Centre, Upper Hutt, New Zealand. keith.henderson@agresearch.cri.nz
Stewart, J

    MeSH Terms

    • Animals
    • Blood Chemical Analysis / methods
    • Blood Chemical Analysis / veterinary
    • Cattle
    • Estrone / analogs & derivatives
    • Estrone / blood
    • Female
    • Horses / blood
    • Immunoassay / methods
    • Immunoassay / veterinary
    • Pregnancy
    • Pregnancy, Animal / blood
    • Serum Albumin, Bovine

    Citations

    This article has been cited 1 times.
    1. Hsu HL, Chuang CC, Liang CC, Chiao DJ, Wu HL, Wu YP, Lin FP, Shyu RH. Rapid and sensitive detection of Yersinia pestis by lateral-flow assay in simulated clinical samples. BMC Infect Dis 2018 Aug 14;18(1):402.
      doi: 10.1186/s12879-018-3315-2pubmed: 30107826google scholar: lookup