Epidemiology and Infection



Clonal analysis of the serogroup B meningococci causing New Zealand's epidemic


K. H. DYET a1 and D. R. MARTIN a1c1
a1 Communicable Disease Group, Institute of Environmental Science and Research, Porirua, New Zealand

Article author query
dyet kh   [PubMed][Google Scholar] 
martin dr   [PubMed][Google Scholar] 

Abstract

An epidemic of meningococcal disease caused by serogroup B meningococci expressing the P1.7-2,4 PorA protein began in New Zealand in 1991. The PorA type has remained stable. Different porB have been found in association with the P1.7-2,4 PorA, although type 4 has been most common. The clonal origins of B:P1.7-2,4 meningococci isolated from cases during 1990 to the end of 2003 were analysed. In 1990, the year immediately preceding the recognized increase in disease rates, all three subclones (ST-41, ST-42, and ST-154) of the ST-41/44 clonal complex occurred among the five isolates of B:P1.7-2,4. The two sequence types, ST-42 and ST-154, continued to cause most disease throughout New Zealand. Isolates belonging to subclone ST-41 were mostly identified early in the epidemic and in the South Island. 16S rRNA typing indicated that isolates belonging to the subclones ST-41 and ST-154 share a common ancestor, with those typing as ST-42 more distantly related with some genetically ambiguous. It is possible that ST-41 and ST-154 may have evolved one from the other but evolution to ST-42 is more difficult to explain. It is possible that one or more of the ST types could have been introduced into New Zealand prior to the first detection of clinical cases in 1990. Genetic diversity may have occurred during carriage in the community.

(Published Online September 5 2005)
(Accepted May 27 2005)
(September 5 2005)


Correspondence:
c1 Communicable Disease Group, Institute of Environmental Science and Research, PO Box 50 348, Porirua, New Zealand. (Email: diana.martin@esr.cri.nz)


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