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Type: Journal article
Title: Laboratory diagnosis of Mycoplasma pneumoniae infection. 4. Antigen capture and PCR-gene amplification for detection of the mycoplasma: problems of clinical correlation
Author: Williamson, J.
Marmion, B.
Worswick, D.
Kok, T.
Tannock, G.
Herd, R.
Harris, R.
Citation: Epidemiology and Infection, 1992; 109(3):519-537
Publisher: Cambridge University Press
Issue Date: 1992
ISSN: 0950-2688
Statement of
J. Williamson, B. P. Marmion, D. A. Worswick, T.-W. Kok, G. Tannock, R. Herd, and R. J. Harris
Abstract: Direct detection assays for Mycoplasma pneumoniae were established by PCR amplification of short sequences within the foot protein/adhesin (P1) gene and the 16S ribosomal RNA gene. Specificity and sensitivity was excellent, no hybridization was observed with M. genitalium and other human Mycoplasma species. In nose and throat washings from subjects with respiratory infection a pattern of high counts (c.f.u./ml) of M. pneumoniae (deduced from the amount of amplified PCR product), and a positive antigen capture assay, was found in 83% of subjects with serological evidence of current infection with M. pneumoniae. A small proportion of subjects with serological patterns suggesting infection in the more distant past had positive PCR assays. This was considered to represent either persistence of the organism from a previous infection or perhaps transient carriage during a reinfection, without substantial change in antibody response. PCR-based assay of M. pneumoniae offers a powerful, rapid, and sensitive substitute for culture of the mycoplasma. Antigen capture, while less sensitive than PCR, offers the advantage that it is more often positive with samples from current infection and requires less stringent laboratory organization to contain false positive results. We conclude however that the laboratory diagnosis of a chosen clinical episode should not rest on the PCR or Ag-EIA assays alone, but must also include antibody assays to confirm whether infection is current or represents persistence from past exposure.
Keywords: Mycoplasma pneumoniae; RNA, Bacterial; RNA, Ribosomal, 16S
Rights: © Cambridge University Press 1992
RMID: 0030075260
DOI: 10.1017/S0950268800050512
Appears in Collections:Medicine publications

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