Journal of Bacteriology, September 1999, p. 5551-5556, Vol. 181, No. 18
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Division of Bacteriology,
Received 11 January 1999/Accepted 8 July 1999
Periodically, new disease-associated variants of the human pathogen
Neisseria meningitidis arise. These meningococci diversify during spread, and related isolates recovered from different parts of
the world have different genetic and antigenic characteristics. An
example is the ET-5 complex, members of which were isolated globally
from the mid-1970s onwards. Isolates from a hyperendemic outbreak of
meningococcal disease in Worcester, England, during the late 1980s were
characterized by multilocus sequence typing and sequence determination
of antigen genes. These data established that the Worcester outbreak
was caused by ET-5 complex meningococci which were not closely related
to the ET-5 complex bacteria responsible for a hyperendemic outbreak in
the nearby town of Stroud during the years preceding the Worcester
outbreak. A comparison with other ET-5 complex meningococci established
that there were at least three distinct globally distributed
subpopulations within the ET-5 complex, characterized by particular
housekeeping and antigen gene alleles. The Worcester isolates belonged
to one of these subpopulations, the Stroud isolates belonged to
another, and at least one representative of the third subpopulation
identified in this work was isolated elsewhere in the United Kingdom.
The sequence data demonstrated that ET-5 variants have arisen by
multiple complex pathways involving the recombination of antigen and
housekeeping genes and de novo mutation of antigen genes. The data
further suggest that either the ET-5 complex has been in existence for many years, evolving and spreading relatively slowly until its disease-causing potential was recognized, or it has evolved and spread
rapidly since its first identification in the 1970s, with each of the
subpopulations attaining a distribution spanning several continents.
*
Corresponding author. Mailing address: Wellcome Trust
Centre for the Epidemiology of Infectious Disease, Department of
Zoology, University of Oxford, South Parks Rd., Oxford OX1 2PS, United Kingdom. Phone: 44 (1865) 271284. Fax: 44 (1865) 271284.
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