Comparison of seven techniques for typing international epidemic strains of Clostfidium difficile:: Restriction endonuclease analysis, pulsed-field gel electrophoresis, PCR-ribotyping, multilocus sequence typing, multilocus variable-number tandem-repeat analysis, amplified fragment length polymorphism, and surface layer protein A gene sequence typing

被引:256
作者
Killgore, George [1 ]
Thompson, Angela [1 ]
Johnson, Stuart [2 ]
Brazier, Jon [3 ]
Kuijper, Ed [4 ]
Pepin, Jacques [5 ]
Frost, Eric H. [5 ]
Savelkoul, Paul [8 ]
Nicholson, Brad [6 ]
van den Berg, Renate J. [4 ]
Kato, Haru [7 ]
Sambol, Susan P. [2 ]
Zukowski, Walter [2 ]
Woods, Christopher [6 ]
Limbago, Brandi [1 ]
Gerding, Dale N. [2 ]
McDonald, L. Clifford [1 ]
机构
[1] Ctr Dis Control & Prevent, Atlanta, GA 30333 USA
[2] Hines VA Hosp, Hines, IL USA
[3] Microbiol Cardiff Univ Hosp Wales, Natl Publ Hlth Serv Wales, Anarobe Reference Lab, Cardiff, Wales
[4] Leiden Univ, Med Ctr, Ctr Infect Dis, Dept Med Microbiol, Leiden, Netherlands
[5] Univ Sherbrooke, Dept Microbiol & Infect Dis, Sherbrooke, PQ J1K 2R1, Canada
[6] Duke Univ, Sch Med, Dept Med, Div Infect Dis, Durham, NC 27706 USA
[7] Natl Inst Infect Dis, Dept Bacterial Pathogenesis & Infect Control, Tokyo, Japan
[8] Vrije Univ Amsterdam Med Ctr, Dept Med Microbiol & Infect Control, Amsterdam, Netherlands
关键词
D O I
10.1128/JCM.01484-07
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Using 42 isolates contributed by laboratories in Canada, The Netherlands, the United Kingdom, and the United States, we compared the results of analyses done with seven Clostridium difficile typing techniques: multilocus variable-number tandem-repeat analysis (MLVA), amplified fragment length polymorphism (AFLP), surface layer protein A gene sequence typing (slpAST), PCR-ribotyping, restriction endonuclease analysis (REA), multilocus sequence typing (MLST), and pulsed-field gel electrophoresis (PFGE). We assessed the discriminating ability and typeability of each technique as well as the agreement among techniques in grouping isolates by allele profile A (AP-A) through AP-F, which are defined by toxinotype, the presence of the binary toxin gene, and deletion in the tcdC gene. We found that all isolates were typeable by all techniques and that discrimination index scores for the techniques tested ranged from 0.964 to 0.631 in the following order. MLVA, REA, PFGE, slpAST, PCR-ribotyping, MLST, and AFLP. All the techniques were able to distinguish the current epidemic strain of C. difficile (BI/027/NAP1) from other strains. All of the techniques showed multiple types for AP-A (toxinotype 0, binary toxin negative, and no tcdC gene deletion). REA, slpAST, MLST, and PCR-ribotyping all included AP-B (toxinotype III, binary toxin positive, and an 18-bp deletion in WC) in a single group that excluded other APs. PFGE, AFLP, and MLVA grouped two, one, and two different non-AP-B isolates, respectively, with their AP-B isolates. All techniques appear to be capable of detecting outbreak strains, but only REA and MLVA showed sufficient discrimination to distinguish strains from different outbreaks.
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收藏
页码:431 / 437
页数:7
相关论文
共 34 条
  • [1] Clinical features of Clostridium difficile-associated infections and molecular characterization of strains:: Results of a retrospective study, 2000-2004
    Barbut, Frederic
    Gariazzo, Beatrice
    Bonne, Laetitia
    Lalande, Valerie
    Burghoffer, Beatrice
    Luiuz, Ralucca
    Petit, Jean-Claude
    [J]. INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 2007, 28 (02) : 131 - 139
  • [2] ANTIBIOTIC-ASSOCIATED PSEUDOMEMBRANOUS COLITIS DUE TO TOXIN-PRODUCING CLOSTRIDIA
    BARTLETT, JG
    CHANG, TW
    GURWITH, M
    GORBACH, SL
    ONDERDONK, AB
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1978, 298 (10) : 531 - 534
  • [3] Comparison of PCR-ribotyping, arbitrarily primed PCR, and pulsed-field gel electrophoresis for typing Clostridium difficile
    Bidet, P
    Lalande, V
    Salauze, B
    Burghoffer, B
    Avesani, V
    Delmée, M
    Rossier, A
    Barbut, F
    Petit, JC
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (07) : 2484 - 2487
  • [4] Development of a new PCR-ribotyping method for Clostridium difficile based on ribosomal RNA gene sequencing
    Bidet, P
    Barbut, F
    Lalande, V
    Burghoffer, B
    Petit, JC
    [J]. FEMS MICROBIOLOGY LETTERS, 1999, 175 (02) : 261 - 266
  • [5] BRAZIER JS, 1997, CLIN INFECT DIS S2, V25, P199
  • [6] DEVELOPMENT OF A RAPID AND EFFICIENT RESTRICTION-ENDONUCLEASE ANALYSIS TYPING SYSTEM FOR CLOSTRIDIUM-DIFFICILE AND CORRELATION WITH OTHER TYPING SYSTEMS
    CLABOTS, CR
    JOHNSON, S
    BETTIN, KM
    MATHIE, PA
    MULLIGAN, ME
    SCHABERG, DR
    PETERSON, LR
    GERDING, DN
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (07) : 1870 - 1875
  • [7] Pulsed-field gel electrophoresis of degradation-sensitive DNAs from Clostridium difficile PCR ribotype 1 strains
    Corkill, JE
    Graham, R
    Hart, CA
    Stubbs, S
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (07) : 2791 - 2792
  • [8] SEROGROUPING OF CLOSTRIDIUM-DIFFICILE STRAINS BY SLIDE AGGLUTINATION
    DELMEE, M
    HOMEL, M
    WAUTERS, G
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1985, 21 (03) : 323 - 327
  • [9] Pulsed-field gel electrophoresis can yield DNA fingerprints of degradation-susceptible Clostridium difficile strains
    Fawley, WN
    Wilcox, MH
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (09) : 3546 - 3547
  • [10] Determining confidence intervals when measuring genetic diversity and the discriminatory abilities of typing methods for microorganisms
    Grundmann, H
    Hori, S
    Tanner, G
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (11) : 4190 - 4192