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BMC Genomics. 2016 Oct 28;17(1):843.

In-silico prediction and deep-DNA sequencing validation indicate phase variation in 115 Neisseria meningitidis genes.

Author information

1
GSK Vaccines, 53100, Siena, Italy. emilio.x.siena@gsk.com.
2
GSK Vaccines, 53100, Siena, Italy.
3
Present address: Institute of Informatics and Telematics and Institute of Clinical Physiology, National Research Council, 56124, Pisa, Italy.
4
Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD, 21201, USA.
5
Present address: Personal Genome Disgnostics inc., Baltimore, MD, 21224, USA.
6
Medical Sciences Division, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Oxford, OX3 9DS, UK.
7
GSK Vaccines, 53100, Siena, Italy. duccio.x.medini@gsk.com.

Abstract

BACKGROUND:

The Neisseria meningitidis (Nm) chromosome shows a high abundance of simple sequence DNA repeats (SSRs) that undergo stochastic, reversible mutations at high frequency. This mechanism is reflected in an extensive phenotypic diversity that facilitates Nm adaptation to dynamic environmental changes. To date, phase-variable phenotypes mediated by SSRs variation have been experimentally confirmed for 26 Nm genes.

RESULTS:

Here we present a population-scale comparative genomic analysis that identified 277 genes and classified them into 52 strong, 60 moderate and 165 weak candidates for phase variation. Deep-coverage DNA sequencing of single colonies grown overnight under non-selective conditions confirmed the presence of high-frequency, stochastic variation in 115 of them, providing circumstantial evidence for their phase variability. We confirmed previous observations of a predominance of variable SSRs within genes for components located on the cell surface or DNA metabolism. However, in addition we identified an unexpectedly broad spectrum of other metabolic functions, and most of the variable SSRs were predicted to induce phenotypic changes by modulating gene expression at a transcriptional level or by producing different protein isoforms rather than mediating on/off translational switching through frameshifts. Investigation of the evolutionary history of SSR contingency loci revealed that these loci were inherited from a Nm ancestor, evolved independently within Nm, or were acquired by Nm through lateral DNA exchange.

CONCLUSIONS:

Overall, our results have identified a broader and qualitatively different phenotypic diversification of SSRs-mediated stochastic variation than previously documented, including its impact on central Nm metabolism.

KEYWORDS:

Comparative genomics; Contingency loci; Host-pathogen interaction; Neisseria meningitidis; Phase variation

PMID:
27793092
PMCID:
PMC5084427
DOI:
10.1186/s12864-016-3185-1
[Indexed for MEDLINE]
Free PMC Article

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