@article{mbs:/content/journal/jmm/10.1099/jmm.0.018663-0, author = "Jefferies, J. M. C. and Tocheva, A. S. and Rubery, H. and Bennett, J. and Garland, J. and Christodoulides, M. and Faust, S. N. and Smith, A. and Mitchell, T. J. and Clarke, S. C.", title = "Identification of novel pneumolysin alleles from paediatric carriage isolates of Streptococcus pneumoniae", journal= "Journal of Medical Microbiology", year = "2010", volume = "59", number = "7", pages = "808-814", doi = "https://doi.org/10.1099/jmm.0.018663-0", url = "https://www.microbiologyresearch.org/content/journal/jmm/10.1099/jmm.0.018663-0", publisher = "Microbiology Society", issn = "1473-5644", type = "Journal Article", keywords = "gDNA, genomic DNA", keywords = "MLST, multilocus sequence typing", keywords = "ST, sequence type", abstract = "Pneumolysin (Ply) is a major virulence factor of Streptococcus pneumoniae and is produced by all known clinical isolates of pneumococci. Pneumolysin toxoids are being considered as vaccine candidates. We investigated the diversity of pneumolysin among 194 nasopharyngeal pneumococci characterized by serotyping and multilocus sequence typing (MLST). Eight Ply protein alleles were identified, four of which were novel. The 4 novel alleles varied at 10 different amino acid positions, from a total of 147, 3 of these substitutions have been previously reported in different combinations. The protein allele correlated closely with MLST. It is critical that the presence of pneumolysin variants is considered with regards to the potential use of Ply in future vaccine formulations, as variation in Ply amino acid sequence may influence the immunogenicity of vaccines based on the presence of an individual Ply allele.", }