Literature DB >> 11577151

Genomic analysis of the erythromycin resistance element Tn5398 from Clostridium difficile.

Kylie A Farrow1, Dena Lyras1, Julian I Rood1.   

Abstract

Clostridium difficile is a nosocomial pathogen that causes a range of chronic intestinal diseases, usually as a result of antimicrobial therapy. Macrolide-lincosamide-streptogramin B (MLS) resistance in C. difficile is encoded by the Erm B resistance determinant, which is thought to be located on a conjugative transposon, Tn5398. The 9630 bp Tn5398 element has been cloned and completely sequenced and its insertion site determined. Analysis of the resultant data reveals that Tn5398 is not a classical conjugative transposon but appears to be a mobilizable non-conjugative element. It does not carry any transposase or site-specific recombinase genes, nor any genes likely to be involved in conjugation. Furthermore, using PCR analysis it has been shown that isolates of C. difficile obtained from different geographical locations exhibit heterogeneity in the genetic arrangement of both Tn5398 and their Erm B determinants. These results indicate that genetic exchange and recombination between these determinants occurs in the clinical and natural environment.

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Year:  2001        PMID: 11577151     DOI: 10.1099/00221287-147-10-2717

Source DB:  PubMed          Journal:  Microbiology        ISSN: 1350-0872            Impact factor:   2.777


  35 in total

1.  Utility of the clostridial site-specific recombinase TnpX to clone toxic-product-encoding genes and selectively remove genomic DNA fragments.

Authors:  Vicki Adams; Radhika Bantwal; Lauren Stevenson; Jackie K Cheung; Milena M Awad; Joel Nicholson; Glen P Carter; Kate E Mackin; Julian I Rood; Dena Lyras
Journal:  Appl Environ Microbiol       Date:  2014-06       Impact factor: 4.792

2.  Horizontal transfer of erythromycin resistance from Clostridium difficile to Butyrivibrio fibrisolvens.

Authors:  Patrizia Spigaglia; Fabrizio Barbanti; Paola Mastrantonio
Journal:  Antimicrob Agents Chemother       Date:  2005-12       Impact factor: 5.191

Review 3.  The TetR family of transcriptional repressors.

Authors:  Juan L Ramos; Manuel Martínez-Bueno; Antonio J Molina-Henares; Wilson Terán; Kazuya Watanabe; Xiaodong Zhang; María Trinidad Gallegos; Richard Brennan; Raquel Tobes
Journal:  Microbiol Mol Biol Rev       Date:  2005-06       Impact factor: 11.056

4.  Molecular analysis of Clostridium difficile PCR ribotype 027 isolates from Eastern and Western Canada.

Authors:  Duncan R MacCannell; Thomas J Louie; Dan B Gregson; Michel Laverdiere; Annie-Claude Labbe; Felicia Laing; Scott Henwick
Journal:  J Clin Microbiol       Date:  2006-06       Impact factor: 5.948

5.  Interaction of related Tn916-like transposons: analysis of excision events promoted by Tn916 and Tn5386 integrases.

Authors:  Louis B Rice; Lenore L Carias; Rebecca Hutton-Thomas; Susan Rudin
Journal:  J Bacteriol       Date:  2007-02-23       Impact factor: 3.490

6.  Characterization of a small mobilizable transposon, MTnSag1, in Streptococcus agalactiae.

Authors:  Adeline Achard; Roland Leclercq
Journal:  J Bacteriol       Date:  2007-04-06       Impact factor: 3.490

7.  Streptococcus pneumoniae transposon Tn1545/Tn6003 changes to Tn6002 due to spontaneous excision in circular form of the erm(B)- and aphA3-containing macrolide-aminoglycoside-streptothricin (MAS) element.

Authors:  Claudio Palmieri; Marina Mingoia; Orietta Massidda; Eleonora Giovanetti; Pietro E Varaldo
Journal:  Antimicrob Agents Chemother       Date:  2012-08-13       Impact factor: 5.191

8.  Unconventional circularizable bacterial genetic structures carrying antibiotic resistance determinants.

Authors:  Claudio Palmieri; Marina Mingoia; Pietro E Varaldo
Journal:  Antimicrob Agents Chemother       Date:  2013-05       Impact factor: 5.191

Review 9.  Recent advances in the understanding of antibiotic resistance in Clostridium difficile infection.

Authors:  Patrizia Spigaglia
Journal:  Ther Adv Infect Dis       Date:  2016-02

10.  Characterization of toxin A-negative, toxin B-positive Clostridium difficile isolates from outbreaks in different countries by amplified fragment length polymorphism and PCR ribotyping.

Authors:  Renate J van den Berg; Eric C J Claas; Duddy H Oyib; Corné H W Klaassen; Lenie Dijkshoorn; Jon S Brazier; Ed J Kuijper
Journal:  J Clin Microbiol       Date:  2004-03       Impact factor: 5.948

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