The Effect of Immune Selection on the Structure of the Meningococcal Opa Protein Repertoire

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Abstract
The opa genes of the Gram negative bacterium Neisseria meningitidis encode Opacity-associated outer membrane proteins whose role is to promote adhesion to the human host tissue during colonisation and invasion. Each meningococcus contains 3–4 opa loci, each of which may be occupied by one of a large number of alleles. We analysed the Opa repertoire structure in a large, well-characterised collection of asymptomatically carried meningococci. Our data show an association between Opa repertoire and meningococcal lineages similar to that observed previously for meningococci isolated from cases of invasive disease. Furthermore, these Opa repertoires exhibit discrete, non-overlapping structure at a population level, and yet low within-repertoire diversity. These data are consistent with the predictions of a mathematical model of strong immune selection upon a system where identical alleles may occupy different loci. Neisseria meningitidis is a globally important pathogen that causes 2,000–3,000 cases of invasive meningococcal disease annually in the United Kingdom. The meningococcal Opa proteins are important in mediating adhesion to and invasion of human tissues, and are important for evasion of the host immune response. They are encoded by a repertoire of 3–4 genomic loci in each meningococcus and exhibit high levels of sequence diversity. Here we analyzed the Opa repertoires of a large, well-characterised, asymptomatically carried meningococcal isolate collection. We found that the Opa repertoires were specific to individual meningococcal genotypes, similar to that observed in isolates from cases of invasive disease. These repertoires exhibited discrete, non-overlapping structure at a population level, and yet low within-repertoire diversity. These data were consistent with the predictions of a mathematical model of strong immune selection, suggesting that the collective immune response of the host population shapes the antigenic diversity of the meningococcal Opa repertoire. This study provides new insights into Opa-mediated meningococcal pathogenesis and the effect of host population immunity on the biodiversity and population structure of bacterial pathogens. These data may also have implications for the design of new meningococcal vaccines based on surface proteins.