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Contribution to laboratory diagnosis of mumps and parainfluenza

V Franková1, J Holubová, L Grubhoffer

  • 1Institute for Medical Microbiology and Immunology, Faculty of Medicine, Charles University, Prague, Czechoslovakia.

Acta Virologica
|November 1, 1988
PubMed

Insights

This study shows that ELISA can detect mumps virus (MV) antibodies, but cross-reactivity with parainfluenza virus (PiV) can occur. Specific MV antigens help eliminate these cross-reactions in diagnostic tests.

Area of Science:

  • Virology
  • Immunology
  • Diagnostic Microbiology

Background:

  • Mumps virus (MV) and parainfluenza virus (PiV) are common respiratory pathogens.
  • Accurate serological diagnosis is crucial for differentiating MV and PiV infections.
  • Enzyme-Linked Immunosorbent Assay (ELISA) is a widely used method for antibody detection.

Purpose of the Study:

  • To evaluate the efficacy of ELISA in detecting specific IgM and IgG antibodies to mumps virus (MV).
  • To investigate cross-reactivity between MV and parainfluenza virus (PiV) T3 antigens in ELISA.
  • To identify methods for eliminating cross-reactions in serological assays.

Main Methods:

  • Detection of specific IgM and IgG antibodies to MV using ELISA and indirect immunofluorescence (IF).
  • Assessment of cross-reactivity with PiV T3 antigens in patient sera.
  • Utilizing MV-nucleocapsid antigen and peroxidase-labelled whole virion antigen to eliminate cross-reactions.

Main Results:

  • ELISA results for MV antibodies agreed with indirect immunofluorescence (IF).
  • 37.5% of sera showed IgM cross-reactivity with PiV T3 antigens.
  • Cross-reactions with MV antigens were observed in 30.7% of patients with respiratory illness; these were eliminated using specific MV antigens.

Conclusions:

  • ELISA is effective for detecting MV antibodies, but cross-reactivity with PiV must be considered.
  • Using specific MV-nucleocapsid or whole virion antigens in ELISA can resolve cross-reactivity issues.
  • Discrepancies in antibody detection in young children may be due to low-avidity antibodies.

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