Mycoplasma Pneumoniae IgM ELISA

The Calbiotech, Inc. (CBI), Mycoplasma pneumoniae (M. pneumoniae) IgM ELISA test system is an enzyme linked immunosorbent assay (ELISA) for the detection of IgM class antibodies to M. pneumoniae in human serum or plasma.


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Product Catalog No: MP021M Pack Size: 96 Tests

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Summary

Mycoplasma pneumoniae is a pathogen with spectrum of clinical presentations ranging from asymptomatic to pronounced pneumonia. Symptoms start from 6 to 32 days after exposure with headache, malaise, cough, sore throat and fever. The illness can last from a few days to a month or more. Detection by ELISA of M. pneumoniae IgM antibodies or demonstration of a significant increase of specific IgG antibodies is strong evidence for recent infection in the appropriate clinical setting. Specific IgM antibodies typically increase significantly 1 week after clinical onset and specific IgG levels rise in the second week. M. pneumoniae IgM can, however, persist for more than two years after infection, and therefore, detection of specific IgM does not accurately indicate the time of infection. Primary infection and reinfection may be distinguished by the presence of elevated specific IgA and of specific IgM in primary infections and by the presence of elevated specific IgA in the absence of specific IgM in reinfections. In general, the absence of specific IgM in serum collected 10-20 days after onset is strong evidence against primary pneumonia due to M. pneumoniae.

Test Principle

Diluted patient serum (serum diluent contains sorbent to remove Rheumatoid Factor and human IgG interference) is added to wells coated with purified antigen. IgM specific antibody, if present, binds to the antigen. All unbound materials are washed away and the enzyme conjugate is added to bind to the antibody-antigen complex, if present. Excess enzyme conjugate is washed off and substrate is added. The plate is incubated to allow the hydrolysis of the substrate by the enzyme. The intensity of the color generated is proportional to the amount of IgM specific antibody in the sample.

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References
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  2. Cimolai N, Cheong ACH. An assessment of a new diagnostic indirect enzyme immunoassay for the detection of anti-Mycoplasma pneumoniae IgM. Am J Clin Pathol 1996;105:205-9.
  3. 5. Shearman MJ, Cubie HA, Inglis JM. Mycoplasma pneumoniae infection: early diagnosis by detection of specific IgM by immunofluorescence. Br J Biomed Sci 1993;50:305-8.
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  6. Aubert G, Pozzetto B, Gaudin OG, Hafid J, Mbida AD, Ros A. Evaluation of five commercial tests: complement fixation, microparticle agglutination, indirect immunofluorescence, enzyme-linked immunosorbent assay and latex agglutination, in comparison to immunoblotting for Mycoplasma pneumoniae serology. Ann Biol Clin 1992;50:593- 7.
  7. Kok T, Mickan LD, Burrell CJ. Routine diagnosis of seven respiratory viruses and Mycoplasma pneumoniae by enzyme immunoassay. J Virol Methods 1994;50:87-100.
  8. Kleemola M, Räty R, Karjalainen J, Schuy W, Gerstenecker B, Jacobs E. Evaluation of an antigen-capture enzyme immunoassay for rapid diagnosis of Mycoplasma pneumoniae infection. Eur J Clin Microbiol Infect Dis 1993;12:872-5.
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