Comparison of two methods for serotyping Ureaplasma urealyticum clinical isolates

被引:6
|
作者
Echahidi, F [1 ]
van Geel, K [1 ]
Lauwers, S [1 ]
Naessens, A [1 ]
机构
[1] Free Univ Brussels, Dept Microbiol, Acad Ziekenhuis, B-1090 Brussels, Belgium
关键词
ELISA; immunofluorescence; Ureaplasma urealyticum;
D O I
10.1016/S0167-7012(01)00359-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A newly developed enzyme linked immunosorbent assay (ELISA) method using monoclonal antibodies (MAbs) to the 14 serotypes of Ureaplasma urealyticum was compared to immunofluorescence assay (IFA) for serotyping U. urealyticum clinical isolates. Of the 102 vaginal isolates of U. urealyticum, five strains were lost and were excluded from analysis. Of the 97 strains analysed, a total of 86 (89%) strains were typeable by ELISA and a total of 89 (92%) strains were typeable by IFA. Eighty-six strains were typeable by both methods, three by IFA only and eight strains were not typeable neither by ELISA nor by IFA. Of the 86 strains typeable by both methods, complete concordance in serotyping results was found. The three strains not typeable by ELISA were typeable as serotype 4 by IFA. These three strains were reanalysed by ELISA after major modifications of the antigen preparation and were typeable as serotype 4. In conclusion, the ELISA was found suitable for serotyping clinical isolates. However, since the ELISA had a somewhat lower performance than IFA, strains not typeable by ELISA, should be retested by another technique such as IFA. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
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页码:157 / 161
页数:5
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