{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,21]],"date-time":"2026-02-21T06:29:10Z","timestamp":1771655350317,"version":"3.50.1"},"reference-count":51,"publisher":"Microbiology Society","issue":"7","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2003,7,1]]},"abstract":"<jats:p>Meningococcal FetA (FrpB), an iron-regulated outer-membrane protein and vaccine component, was shown to be highly diverse: a total of 60<jats:italic>fetA<\/jats:italic>alleles, encoding 56 protein sequences, were identified from 107 representative<jats:italic>Neisseria meningitidis<\/jats:italic>isolates. Phylogenetic analysis established that the allelic variants had been generated by both point mutation and horizontal genetic exchange. Nucleotide substitution was unevenly distributed in the gene, which contained both conserved and variable sequence regions. The most conserved region of the translated peptide sequence corresponded to an amino-terminal domain of the protein and the most diverse region to a previously identified variable region (VR). A nomenclature system for the peptides encoded by the VR was devised which classified 24 variants into 5 FetA variant families. On the basis of these data, murine polyclonal sera specific for four FetA variants were generated. The reactivities of these sera in whole-cell ELISA experiments were consistent with the hypothesis that the VR encoded an immunodominant epitope and indicated that the sera reacted mainly with variants against which they were raised. The diversity of this protein is likely to limit its effectiveness as a vaccine component.<\/jats:p>","DOI":"10.1099\/mic.0.26131-0","type":"journal-article","created":{"date-parts":[[2003,7,10]],"date-time":"2003-07-10T17:23:48Z","timestamp":1057857828000},"page":"1849-1858","source":"Crossref","is-referenced-by-count":134,"title":["Antigenic diversity of meningococcal enterobactin receptor FetA, a vaccine component"],"prefix":"10.1099","volume":"149","author":[{"given":"Emily A. 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