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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1989-3-9
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pubmed:abstractText |
The efficiency of the direct detection of Mycoplasma pneumoniae in respiratory exudates by an antigen capture, indirect enzyme immunoassay (Ag-EIA), has been compared with its detection with a cDNA probe ('Gen-Probe assay') directed against the specific ribosomal RNA sequences of the organism ('Mycoplasma pneumoniae Rapid Diagnostic System', Gen-Probe, San Diego, California). Both assays showed excellent specificity against a range of mycoplasma species suspended in negative nasopharyngeal aspirates; only M. pneumoniae and M. genitalium reacted. In experiments with graded doses of viable M. pneumoniae cells suspended in negative nasopharyngeal aspirate, the Gen-Probe assay was more sensitive than Ag-EIA; detection limits were respectively 2 X 10(3) c.f.u./ml (3.2 X 10(5) genomes) and 2.5 X 10(4) c.f.u./ml (4 X 10(6) genomes); detection levels 10-100 times less sensitive than culture. The two assays were also tested on nasopharyngeal aspirates or sputum specimens from 90 patients with respiratory infection; 67 of these were culture- or seronegative for M. pneumoniae and 23 were culture- or seropositive. Ag-EIA detected 21 (91%) of the latter but the Gen-Probe assay detected only 5 (22%). Both assays were negative with the 67 culture-/sero-negatives; there were no Gen-Probe assay positive/Ag-EIA negatives. Overall, it is concluded that although Ag-EIA and the Gen-Probe assay are effective substitutes for culture as a diagnostic procedure, there is a significant problem with samples which are culture-negative and from patients who have good serological evidence of current infection. Possible reasons for the disparity between the two assays are advanced.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/3145892-2417956,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3145892-3106412,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3145892-3133385,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3145892-3145891,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3145892-3893219,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3145892-4429272,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3145892-4925209,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3145892-5358346,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3145892-6210265,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3145892-6440905
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0950-2688
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
101
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
685-94
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pubmed:dateRevised |
2010-9-7
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pubmed:meshHeading |
pubmed-meshheading:3145892-Antigens, Bacterial,
pubmed-meshheading:3145892-DNA Probes,
pubmed-meshheading:3145892-Humans,
pubmed-meshheading:3145892-Immunoenzyme Techniques,
pubmed-meshheading:3145892-Mycoplasma pneumoniae,
pubmed-meshheading:3145892-Nucleic Acid Hybridization,
pubmed-meshheading:3145892-Pneumonia, Mycoplasma,
pubmed-meshheading:3145892-RNA, Ribosomal,
pubmed-meshheading:3145892-Serologic Tests,
pubmed-meshheading:3145892-Species Specificity
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pubmed:year |
1988
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pubmed:articleTitle |
Laboratory diagnosis of Mycoplasma pneumoniae infection. 2. Comparison of methods for the direct detection of specific antigen or nucleic acid sequences in respiratory exudates.
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pubmed:affiliation |
School of Pharmacy, S.A. Institute of Technology, Adelaide.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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