Analysis of a Clostridium difficile PCR ribotype 078 100 kilobase island reveals the presence of a novel transposon, Tn6164

被引:29
作者
Corver, Jeroen [1 ,4 ]
Bakker, Dennis [1 ]
Brouwer, Michael S. M. [2 ]
Harmanus, Celine [1 ]
Hensgens, Marjolein P. [1 ]
Roberts, Adam P. [2 ]
Lipman, Len J. A. [3 ]
Kuijper, Ed J. [1 ]
van Leeuwen, Hans C. [1 ]
机构
[1] Leiden Univ, Med Ctr, Ctr Infect Dis, Dept Med Microbiol,Sect Expt Microbiol, Leiden, Netherlands
[2] UCL, UCL Eastman Dent Inst, Div Microbial Dis, London, England
[3] Univ Utrecht, Fac Vet Med, Inst Risk Assessment Sci, Div Vet Publ Hlth, Utrecht, Netherlands
[4] LUMC, NL-2300 RC Leiden, Netherlands
基金
英国医学研究理事会;
关键词
Clostridium difficile; Transposable element; Phage; Antimicrobial resistance; Virulence; TANDEM-REPEAT ANALYSIS; TETRACYCLINE RESISTANCE; HYPERVIRULENT STRAIN; GENOME; PATHOGENICITY; DETERMINANT; SEQUENCE; DISEASE; MOBILE; GENE;
D O I
10.1186/1471-2180-12-130
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Clostridium difficile is the main cause of antibiotic associated diarrhea. In the past decade, the number of C. difficile patients has increased dramatically, coinciding with the emergence of two PCR ribotypes 027 and 078. PCR ribotype 078 is also frequently found during C. difficile outbreaks in pigfarms. Previously, the genome of the PCR ribotype 078 strain M120, a human isolate, was described to contain a unique insert of 100 kilobases. Results: Analysis of this insert revealed over 90 open reading frames, encoding proteins originating from transposons, phages and plasmids. The insert was shown to be a transposon (Tn6164), as evidenced by the presence of an excised and circularised molecule, containing the ligated 5' and 3' ends of the insert. Transfer of the element could not be shown through filter-mating experiments. Whole genome sequencing of PCR ribotype 078 strain 31618, isolated from a diarrheic piglet, showed that Tn6164 was not present in this strain. To test the prevalence of Tn6164, a collection of 231 Clostridium difficile PCR ribotype 078 isolates from human (n = 173) and porcine (n = 58) origin was tested for the presence of this element by PCR. The transposon was present in 9 human, tetracycline resistant isolates, originating from various countries in Europe, and none of the pig strains. Nine other strains, also tetracycline resistant human isolates, contained half of the transposon, suggesting multiple insertion steps yielding the full Tn6164. Other PCR ribotypes (n = 66) were all negative for the presence of the transposon. Multi locus variable tandem repeat analysis revealed genetic relatedness among transposon containing isolates. Although the element contained several potential antibiotic resistance genes, it did not yield a readily distinguishable phenotype. Conclusions: Tn6164 is a newly described transposon, occurring sporadically in C. difficile PCR ribotype 078 strains. Although no transfer of the element could be shown, we hypothesize that the element could serve as a reservoir of antibiotic resistance genes for other bacteria. Further research is needed to investigate the transfer capabilities of the element and to substantiate the possible role of Tn6164 as a source of antibiotic resistance genes for other gut pathogens.
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共 46 条
[1]   Two Novel Antibiotic Resistance Genes, tet(44) and ant(6)-Ib, Are Located within a Transferable Pathogenicity Island in Campylobacter fetus subsp fetus [J].
Abril, Carlos ;
Brodard, Isabelle ;
Perreten, Vincent .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2010, 54 (07) :3052-3055
[2]   The clostridial mobilisable transposons [J].
Adams, V ;
Lyras, D ;
Farrow, KA ;
Rood, JI .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2002, 59 (12) :2033-2043
[3]   Relatedness of Human and Animal Clostridium difficile PCR Ribotype 078 Isolates Determined on the Basis of Multilocus Variable-Number Tandem-Repeat Analysis and Tetracycline Resistance [J].
Bakker, D. ;
Corver, J. ;
Harmanus, C. ;
Goorhuis, A. ;
Keessen, E. C. ;
Fawley, W. N. ;
Wilcox, M. H. ;
Kuijper, E. J. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2010, 48 (10) :3744-3749
[4]   Clostridium difficile infection in Europe: a hospital-based survey [J].
Bauer, Martijn P. ;
Notermans, Daan W. ;
van Benthem, Birgit H. B. ;
Brazier, Jon S. ;
Wilcox, Mark H. ;
Rupnik, Maja ;
Monnet, Dominique L. ;
van Dissel, Jaap T. ;
Kuijper, Ed J. .
LANCET, 2011, 377 (9759) :63-73
[5]   Development of a new PCR-ribotyping method for Clostridium difficile based on ribosomal RNA gene sequencing [J].
Bidet, P ;
Barbut, F ;
Lalande, V ;
Burghoffer, B ;
Petit, JC .
FEMS MICROBIOLOGY LETTERS, 1999, 175 (02) :261-266
[6]   Definition of the single integration site of the pathogenicity locus in Clostridium difficile [J].
Braun, V ;
Hundsberger, T ;
Leukel, P ;
Sauerborn, M ;
vonEichelStreiber, C .
GENE, 1996, 181 (1-2) :29-38
[7]   Draft Genome Sequence of the Nontoxigenic Clostridium difficile Strain CD37 [J].
Brouwer, Michael S. M. ;
Allan, Elaine ;
Mullany, Peter ;
Roberts, Adam P. .
JOURNAL OF BACTERIOLOGY, 2012, 194 (08) :2125-2126
[8]   Genetic Organisation, Mobility and Predicted Functions of Genes on Integrated, Mobile Genetic Elements in Sequenced Strains of Clostridium difficile [J].
Brouwer, Michael S. M. ;
Warburton, Philip J. ;
Roberts, Adam P. ;
Mullany, Peter ;
Allan, Elaine .
PLOS ONE, 2011, 6 (08)
[9]  
Brouwer MSM, 2012, MOBILE GENETIC ELEME, V2
[10]   New genetic element carrying the erythromycin resistance determinant erm (TR) in Streptococcus pneumoniae [J].
Carnilli, Rornina ;
Del Grosso, Maria ;
Lannelli, Francesco ;
Pantostil, Annalisa .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2008, 52 (02) :619-625