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Using single-nucleotide polymorphisms to discriminate disease-associated from carried genomes of Neisseria
Lee S Katz1, Nitya V Sharma, Brian H Harcourt
1School of Biology, Georgia Institute of Technology, Atlanta, GA 30332, USA.
Abstract:
Neisseria meningitidis is one of the main agents of bacterial meningitis, causing substantial morbidity and mortality worldwide. However, most of the time N. meningitidis is carried as a commensal not associated with invasive disease. The genomic basis of the difference between disease-associated and carried isolates of N. meningitidis may provide critical insight into mechanisms of virulence, yet it has remained elusive. Here, we have taken a comparative genomics approach to interrogate the difference between disease-associated and carried isolates of N. meningitidis at the level of individual nucleotide variations (i.e., single nucleotide polymorphisms [SNPs]). We aligned complete genome sequences of 8 disease-associated and 4 carried isolates of N. meningitidis to search for SNPs that show mutually exclusive patterns of variation between the two groups. We found 63 SNPs that distinguish the 8 disease-associated genomes from the 4 carried genomes of N. meningitidis, which is far more than can be expected by chance alone given the level of nucleotide variation among the genomes. The putative list of SNPs that discriminate between disease-associated and carriage genomes may be expected to change with increased sampling or changes in the identities of the isolates being compared. Nevertheless, we show that these discriminating SNPs are more likely to reflect phenotypic differences than shared evolutionary history. Discriminating SNPs were mapped to genes, and the functions of the genes were evaluated for possible connections to virulence mechanisms. A number of overrepresented functional categories related to virulence were uncovered among SNP-associated genes, including genes related to the category "symbiosis, encompassing mutualism through parasitism."
Insights
Genomic analysis identified 63 single nucleotide polymorphisms (SNPs) distinguishing disease-causing Neisseria meningitidis from carriage strains. These SNPs offer insights into bacterial meningitis virulence mechanisms.
Area of Science:
- Genomics
- Microbiology
- Infectious Diseases
Background:
- Neisseria meningitidis causes bacterial meningitis, a significant global health concern.
- Most N. meningitidis strains are carried asymptomatically, with the genomic basis for virulence remaining unclear.
Purpose of the Study:
- To investigate the genomic differences between disease-associated and carried Neisseria meningitidis isolates.
- To identify single nucleotide polymorphisms (SNPs) that discriminate between virulent and commensal strains.
Main Methods:
- Comparative genomics approach.
- Alignment of complete genome sequences from 8 disease-associated and 4 carried N. meningitidis isolates.
- Identification and analysis of single nucleotide polymorphisms (SNPs).
Main Results:
- Identified 63 SNPs that exclusively differentiate disease-associated from carried N. meningitidis genomes.
- These discriminating SNPs are more indicative of phenotypic differences related to virulence than evolutionary history.
- SNP-associated genes revealed overrepresented functional categories linked to virulence, including symbiosis and parasitism.
Conclusions:
- Comparative genomics can identify genetic markers distinguishing virulent from commensal N. meningitidis.
- SNPs in specific genes may play a role in the transition from carriage to invasive disease.
- Further research with larger sample sizes may refine the list of discriminating SNPs and their functional implications.
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