Literature DB >> 19684139

tISCpe8, an IS1595-family lincomycin resistance element located on a conjugative plasmid in Clostridium perfringens.

Dena Lyras1, Vicki Adams, Susan A Ballard, Wee L Teng, Pauline M Howarth, Paul K Crellin, Trudi L Bannam, J Glenn Songer, Julian I Rood.   

Abstract

Clostridium perfringens is a normal gastrointestinal organism that is a reservoir for antibiotic resistance genes and can potentially act as a source from which mobile elements and their associated resistance determinants can be transferred to other bacterial pathogens. Lincomycin resistance in C. perfringens is common and is usually encoded by erm genes that confer macrolide-lincosamide-streptogramin B resistance. In this study we identified strains that are lincomycin resistant but erythromycin sensitive and showed that the lincomycin resistance determinant was plasmid borne and could be transferred to other C. perfringens isolates by conjugation. The plasmid, pJIR2774, is the first conjugative C. perfringens R-plasmid to be identified that does not confer tetracycline resistance. Further analysis showed that resistance was encoded by the lnuP gene, which encoded a putative lincosamide nucleotidyltransferase and was located on tISCpe8, a functional transposable genetic element that was a member of the IS1595 family of transposon-like insertion sequences. This element had significant similarity to the mobilizable lincomycin resistance element tISSag10 from Streptococcus agalactiae. Like tISSag10, tISCpe8 carries a functional origin of transfer within the resistance gene, allowing the element to be mobilized by the conjugative transposon Tn916. The similarity of these elements and the finding that they both contain an oriT-like region support the hypothesis that conjugation may result in the movement of DNA modules that are not obviously mobile since they are not linked to conjugation or mobilization functions. This process likely plays a significant role in bacterial adaptation and evolution.

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Year:  2009        PMID: 19684139      PMCID: PMC2753038          DOI: 10.1128/JB.00668-09

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  44 in total

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Authors:  Jaroslav Spízek; Jitka Novotná; Tomás Rezanka
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Review 2.  Emergent antibiotic resistance: health risks and economic impact.

Authors:  G H Cassell
Journal:  FEMS Immunol Med Microbiol       Date:  1997-08

3.  Isolation of alpha-toxin, theta-toxin and kappa-toxin mutants of Clostridium perfringens by Tn916 mutagenesis.

Authors:  M M Awad; J I Rood
Journal:  Microb Pathog       Date:  1997-05       Impact factor: 3.738

Review 4.  Erythromycin resistance by ribosome modification.

Authors:  B Weisblum
Journal:  Antimicrob Agents Chemother       Date:  1995-03       Impact factor: 5.191

5.  Genetic organization and distribution of tetracycline resistance determinants in Clostridium perfringens.

Authors:  D Lyras; J I Rood
Journal:  Antimicrob Agents Chemother       Date:  1996-11       Impact factor: 5.191

6.  New lnu(C) gene conferring resistance to lincomycin by nucleotidylation in Streptococcus agalactiae UCN36.

Authors:  Adeline Achard; Corinne Villers; Vianney Pichereau; Roland Leclercq
Journal:  Antimicrob Agents Chemother       Date:  2005-07       Impact factor: 5.191

7.  Mosaic structure of a multiple-drug-resistant, conjugative plasmid from Campylobacter jejuni.

Authors:  Warawadee Nirdnoy; Carl J Mason; Patricia Guerry
Journal:  Antimicrob Agents Chemother       Date:  2005-06       Impact factor: 5.191

8.  Electroporation-mediated transformation of lysostaphin-treated Clostridium perfringens.

Authors:  P T Scott; J I Rood
Journal:  Gene       Date:  1989-10-30       Impact factor: 3.688

9.  High-level chloramphenicol resistance in Neisseria meningitidis.

Authors:  M Galimand; G Gerbaud; M Guibourdenche; J Y Riou; P Courvalin
Journal:  N Engl J Med       Date:  1998-09-24       Impact factor: 91.245

10.  The closely related ermB-ermAM genes from Clostridium perfringens, Enterococcus faecalis (pAM beta 1), and Streptococcus agalactiae (pIP501) are flanked by variants of a directly repeated sequence.

Authors:  D I Berryman; J I Rood
Journal:  Antimicrob Agents Chemother       Date:  1995-08       Impact factor: 5.191

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