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Journal of Clinical Microbiology, 06 1996, 1468-1473, Vol 34, No. 6
B Swaminathan, GM Matar, MW Reeves, LM Graves, G Ajello, WF Bibb, LO Helsel, M Morales, H Dronavalli, M el-Swify, W DeWitt and SB Hunter
In order to compare methods for subtyping Neisseria meningitidis serogroup
B isolates, 96 isolates obtained from various locations in the United
States and northwestern Europe were subtyped by five methods: monoclonal
antibody (MAb)-based serotyping and serosubtyping, DNA macrorestriction
analysis by pulsed-field gel electrophoresis (PFGE), multilocus enzyme
electrophoresis (MEE), ribotyping, and PCR- restriction fragment length
polymorphism of the internally transcribed spacer region of the rRNA operon
(ITS PCR-RFLP). All N. meningitidis serogroup B isolates were typeable by
PFGE, MEE, ribotyping, and ITS PCR-RFLP. Only 44.8% of the isolates were
completely typeable (both serotype and serosubtype determination) by
MAb-based serotyping and serosubtyping. 60.4% of the isolates could be
serotyped but not serosubtyped, and 90.6% of the isolates could be either
serotyped or serosubtyped. Simpson's discrimination indices of diversity
for the methods were as follows: PFGE, 99.7%; MEE, 99.4%; ribotyping,
98.8%; MAb serotyping, 75.8%; MAb serotyping and/or serosubtyping 97.5%;
and ITS PCR-RFLP, 84.2%. The high degree of diversity observed by PFGE,
MEE, and ribotyping can be explained by the fact that isolates were
collected from different geographic locations at various times. PFGE, MEE,
and ribotyping showed greater discriminatory abilities than MAb- based
serotyping and serosubtyping or ITS PCR-RFLP.
Copyright © 1996 by the American Society for Microbiology. All rights reserved.
Molecular subtyping of Neisseria meningitidis serogroup B: comparison of five methods
Division of Bacterial and Mycotic Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA. BAS5@CIDDBD2.EM.CDC.GOV
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