Literature DB >> 31323290

Expanding the repertoire of conservative site-specific recombination in Clostridioides difficile.

Ognjen Sekulovic1, Jacob Bourgeois2, Aimee Shen3, Andrew Camilli4.   

Abstract

Recent genomic analysis of an epidemic ribotype 027 (RT027) Clostridioides difficile strain revealed the presence of several chromosomal site-specific invertible sites hypothesized to control the expression of adjacent genes in a bimodal on-off mode. This process, named phase variation, is thought to enhance phenotypic variability under homogeneous conditions ultimately increasing population fitness in unpredictable environmental fluctuations. The full extent of phase variation mediated by DNA-inversions in C. difficile is currently unknown. Here, we sought to expand our previous analysis by screening for site-specific inversions in isolates that belong to the rapidly emerging ribotypes RT017 and RT078. We report the finding of one novel inversion site for which we demonstrate the inversion potential and quantify inversion proportions during exponential and stationary growth in both historic and modern isolates of the same ribotype. We then employ a computational approach to assess the prevalence of all sites identified so far in a large collection of sequenced C. difficile isolates. We show that phase-variable loci are widespread with some sites being present in virtually all analyzed strains. Furthermore, in our small subset of RT017 and RT078 strains, we detect no evidence of gain or loss of invertible sites in historic versus modern isolates demonstrating the relative stability of those genomic elements. Overall, our results support the idea that C. difficile has adopted phase variation mediated by DNA inversions as its major generator of diversity which could be beneficial during the pathogenesis process.
Copyright © 2019 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Genomic inversions; Phase variation; Site-specific recombination

Mesh:

Year:  2019        PMID: 31323290      PMCID: PMC6917912          DOI: 10.1016/j.anaerobe.2019.102073

Source DB:  PubMed          Journal:  Anaerobe        ISSN: 1075-9964            Impact factor:   3.331


  30 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  1980-12       Impact factor: 11.205

4.  Multiple factors contribute to bimodal toxin gene expression in Clostridioides (Clostridium) difficile.

Authors:  Eric M Ransom; Gabriela M Kaus; Phuong M Tran; Craig D Ellermeier; David S Weiss
Journal:  Mol Microbiol       Date:  2018-10-14       Impact factor: 3.501

5.  Update of Clostridium difficile-associated disease due to PCR ribotype 027 in Europe.

Authors:  E J Kuijper; B Coignard; J S Brazier; C Suetens; D Drudy; C Wiuff; H Pituch; P Reichert; F Schneider; A F Widmer; K E Olsen; F Allerberger; D W Notermans; F Barbut; M Delmée; M Wilcox; A Pearson; B C Patel; D J Brown; R Frei; T Akerlund; I R Poxton; P Tüll
Journal:  Euro Surveill       Date:  2007-06-01

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Authors:  D Drudy; N Harnedy; S Fanning; R O'Mahony; L Kyne
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7.  High Prevalence and Genetic Diversity of Large phiCD211 (phiCDIF1296T)-Like Prophages in Clostridioides difficile.

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9.  Genome-wide detection of conservative site-specific recombination in bacteria.

Authors:  Ognjen Sekulovic; Elizabeth Mathias Garrett; Jacob Bourgeois; Rita Tamayo; Aimee Shen; Andrew Camilli
Journal:  PLoS Genet       Date:  2018-04-05       Impact factor: 5.917

10.  Fast and accurate short read alignment with Burrows-Wheeler transform.

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2.  Flagellum and toxin phase variation impacts intestinal colonization and disease development in a mouse model of Clostridioides difficile infection.

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Journal:  PLoS Biol       Date:  2019-10-28       Impact factor: 8.029

4.  Rho factor mediates flagellum and toxin phase variation and impacts virulence in Clostridioides difficile.

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