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Complete genome and methylome analysis of Neisseria meningitidis associated with increased serogroup Y disease
Örebro University, School of Medical Sciences. Örebro University Hospital. Department of Laboratory Medicine.ORCID iD: 0000-0003-4637-8626
Department of Zoology, University of Oxford, Oxford, United Kingdom.
Örebro University, School of Medical Sciences. Department of Laboratory Medicine.
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2020 (English)In: Scientific Reports, E-ISSN 2045-2322, Vol. 10, no 1, article id 3644Article in journal (Refereed) Published
Abstract [en]

Invasive meningococcal disease (IMD) due to serogroup Y Neisseria meningitidis emerged in Europe during the 2000s. Draft genomes of serogroup Y isolates in Sweden revealed that although the population structure of these isolates was similar to other serogroup Y isolates internationally, a distinct strain (YI) and more specifically a sublineage (1) of this strain was responsible for the increase of serogroup Y IMD in Sweden. We performed single molecule real-time (SMRT) sequencing on eight serogroup Y isolates from different sublineages to unravel the genetic and epigenetic factors delineating them, in order to understand the serogroup Y emergence. Extensive comparisons between the serogroup Y sublineages of all coding sequences, complex genomic regions, intergenic regions, and methylation motifs revealed small point mutations in genes mainly encoding hypothetical and metabolic proteins, and non-synonymous variants in genes involved in adhesion, iron acquisition, and endotoxin production. The methylation motif CACNNNNNTAC was only found in isolates of sublineage 2. Only seven genes were putatively differentially expressed, and another two genes encoding hypothetical proteins were only present in sublineage 2. These data suggest that the serogroup Y IMD increase in Sweden was most probably due to small changes in genes important for colonization and transmission.

Place, publisher, year, edition, pages
Nature Publishing Group, 2020. Vol. 10, no 1, article id 3644
National Category
Genetics
Identifiers
URN: urn:nbn:se:oru:diva-80302DOI: 10.1038/s41598-020-59509-yISI: 000563070300006PubMedID: 32108139Scopus ID: 2-s2.0-85080987210OAI: oai:DiVA.org:oru-80302DiVA, id: diva2:1411283
Funder
Wellcome trust, 218205/Z/19/Z 214374/Z/18/Z
Note

Funding Agencies:

"Functional Genomics" program of the Research Council of Norway  

"Infrastructure" program of the Research Council of Norway  

Southeastern Regional Health Authorities 

European Union (EU)

Örebro County Council Research Committee  

Nyckelfonden  

Örebro University 

Available from: 2020-03-03 Created: 2020-03-03 Last updated: 2022-09-15Bibliographically approved

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Stenmark, BiancaEriksson, Lorraine

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