Acquisition of the capsule locus by horizontal gene transfer in Neisseria meningitidis is often accompanied by the loss of UDP-GalNAc synthesis
Year: 2017
Type: article
Abstract: Pathogenic meningococci have acquired a 24 kb capsule synthesis island (cps) by horizontal gene transfer which consists of a synthetic locus and associated capsule transport genes flanked by repetitive Regions D and D'. Regions D and D' contain an intact gene encoding a UDP-galactose epimerase (galE1) and a truncated remnant (galE2), respectively. In this study, GalE protein alleles were shown to be either mono-functional, synthesising UDP-galactose (UDP-Gal), or bi-functional, synthesising UDP-Gal and UDP-galactosamine (UDP-GalNAc). Meningococci possessing a capsule null locus (cnl) typically possessed a single bi-functional galE. Separation of functionality between galE1 and galE2 alleles in meningococcal isolates was retained for all serogroups except serogroup E which has a synthetic requirement for UDP-GalNAc. The truncated galE2 remnant in Region D' was also phylogenetically related to the bi-functional galE of the cnl locus suggesting common ancestry. A model is proposed in which the illegitimate recombination of the cps island into the galE allele of the cnl locus results in the formation of Region D' containing the truncated galE2 locus and the capture of the cps island en bloc. The retention of the duplicated Regions D and D' enables inversion of the synthetic locus within the cps island during bacterial growth.
Source: Scientific Reports
DOI: 10.1038/srep44442
Institutions: The University of Western Australia, University of Oxford
Language: English
Subfield: Microbiology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,690
Awards: PubMLST: Public databases for molecular typing and microbial genome diversity., Structure-based design of novel therapeutics for multi-drug resistant Neisseria gonorrhoeae, The development of tools to study carbohydrate-processing enzymes implicated in human disease, Interfering with lipid biosynthesis in bacterial pathogens, Population genomics of the Neisseria: evolution of commensalism and virulence., Investigations into how bacterial cell surface structures vary, and the effect this has on the ability to cause disease
OpenAlex ID: W2610813727
