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Updated: Jul 22, 2026
Biosensor for Detection of Antibiotic Resistant Staphylococcus Bacteria
Published on: May 8, 2013
A novel diagnostic technique for diagnosis of Staphylococcus aureus subclinical mastitis using gold
Walaa A Gad1, Salama A Osman2, Khaled A Abd El-Razik1
1Department of Animal Reproduction, Veterinary Research Institute, National Research Centre, Giza, Egypt.
Background:
Bovine subclinical mastitis (SCM) is a significant cause of economic losses in dairy farms, primarily due to its asymptomatic nature and difficulty in early detection. The enzyme-linked immunosorbent assay (ELISA) is a widely used diagnostic tool in bioscience, facilitating antigen detection through antibody binding.
Aim:
The present study designed a gold nanoparticle (AuNPs)-based ELISA, to enhance the sensitivity of conventional ELISA by improving the binding efficiency of capture antibodies to purified antigens. This modified ELISA could enable more accurate detection of bovine SCM.
Methods:
A total of 200 milk samples from apparently healthy cows were screened for SCM using the California Mastitis Test (CMT). Positive samples were then subjected to bacteriological culture, biochemical testing, and polymerase chain reaction targeting the Nuc2 gene for confirmation of S. aureus. The purified fraction antigen of all 78 confirmed S. aureus isolates was extracted using sepharose 4B affinity column chromatography, described by SDS-polyacrylamide gel electrophoresis, and assessed for its sensitivity in S. aureus mastitis diagnosis compared with crude antigen and purified fraction antigen-conjugated gold nanoparticles within an indirect ELISA. Immunoglobulins (IGs) from positive cow serum were extracted and purified from all confirmed S. aureus. Gold nanoparticle-based indirect ELISA was used on 400 samples (200 milk and 200 serum) from the same cows.
Results:
Using CMT, out of 200 examined milk samples from apparently normal cows, 65% (130/200) were sub-clinically infected. Out of these 130 positive milk samples, 60% (78/130) were confirmed to be infected with S. aureus. Purified fraction antigen-conjugated gold nanoparticles achieved the highest sensitivity to ELISA at 97%, 94%, and 92% immediately before storage, 6 months at -20°C, and 1 year at -20°C, respectively. Gold nanoparticle-based indirect ELISA detected specific IgG antibodies in 97% (76/78) sera and milk samples related to confirmed S. aureus isolates.
Conclusion:
The utilization of purified fraction antigen with gold nanoparticles enhances the sensitivity of ELISA, increasing it from 83.3% to 97% (p < 0.01; CI: 99%). The current study establishes a valuable way for S. aureus mastitis diagnosis within the use of purified fraction antigen-conjugated gold nanoparticles instead of the classical way to improve the sensitivity and specificity of ELISA.
