Abstract
Analysis of the sequence data obtained from the 5' portion of the Streptococcus pneumoniae type 19A capsular polysaccharide biosynthesis locus (cps19a) revealed that the first seven genes are homologous to the first seven genes in the type 19F (cps19f) locus. The former genes were designated cps19aA to -G and were 70 to 90% identical to their cps19f counterparts. Southern hybridization analysis of the cps loci from various S. pneumoniae serotypes with probes specific for the cps19aC, cps19aD, and cps19aE genes indicated a hybridization pattern complementary to that previously reported for cps19fC, cps19fD, and cps19fE. That is, all serotypes tested contained high-stringency homologues of either the cps19aC to -E genes or the cps19fC to -E genes, but not both. On this basis S. pneumoniae cps loci can be divided into two distinct classes. Long-range PCR was used to amplify the cps regions between cpsB and aliA from a variety of pneumococcal serotypes. Direct sequencing of the 5' end of these PCR products, and phylogenetic analysis of the sequence data, confirmed the presence of the two distinct classes of cpsC. Whereas members within one class are greater than 95% identical to each other, the DNA sequence identity between the two classes is only approximately 70%.
MeSH Terms
Bacterial Capsules/biosynthesis
Bacterial Proteins
Base Sequence
Blotting, Southern
Galactosyltransferases/chemistry,genetics
Genes, Bacterial/genetics
Genetic Variation/genetics
Molecular Sequence Data
Molecular Weight
Open Reading Frames/genetics
Phylogeny
Polymerase Chain Reaction
Sequence Analysis, DNA
Sequence Homology, Nucleic Acid
Streptococcus pneumoniae/classification,enzymology,genetics
Chemicals
Bacterial Proteins
CpsD protein, bacteria
Galactosyltransferases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Morona J K
Molecular Microbiology Unit, Women's and Children's Hospital, North Adelaide, South Australia 5006.
Morona R
Paton J C
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