Infection of hamsters with historical and epidemic BI types of Clostridium difficile

被引:44
作者
Razaq, Nadia [1 ]
Sambol, Susan [2 ]
Nagaro, Kristin [2 ]
Zukowski, Walter [2 ]
Cheknis, Adam [2 ]
Johnson, Stuart [1 ,2 ]
Gerding, Dale N. [1 ,2 ]
机构
[1] Loyola Univ, Stritch Sch Med, Maywood, IL 60153 USA
[2] Vet Affairs Edward Hines Jr Hosp, Hines, IL USA
关键词
D O I
10.1086/523106
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. North American and European hospitals have reported outbreaks of Clostridium difficile-associated disease with unexpectedly high mortality caused by a newly recognized group of C. difficile strains, group BI. Our objective was to compare, in hamsters, the virulence of a historical nonepidemic BI type, BI1, with that of 2 recent epidemic BI types, BI6 and BI17, and with that of 2 standard toxigenic strains, K14 and 630. Methods. For each strain, 10 hamsters were given 1 dose of clindamycin, followed 5 days later with 100 C. difficile spores administered by gastric inoculation. Outcomes were recorded. Results. The hamster model demonstrated variations in mean times from inoculation to death (for BI6, 40 h; for BI1, 48 h; for K14, 49 h; for BI17, 69 h; for 630, 102 h; for BI6, BI1, and K14 vs. 630, P < .01; for BI17 vs. 630, P < .05) and from colonization to death (for BI1, 7 h; for BI17, 13 h; for BI6, 16 h; for K14, 17 h; for 630, 52 h; for BI1, BI17, BI6, and K14 vs. 630, P < .01). Conclusion. Group BI strains were not more rapidly fatal than the standard toxinotype 0 strain K14 but were more rapidly fatal than the standard toxinotype 0 strain 630. BI6, the most common BI type in our collection, was particularly virulent in hamsters, consistently causing death within 48 h of inoculation.
引用
收藏
页码:1813 / 1819
页数:7
相关论文
共 18 条
[1]   Risk factors for Clostridium difficile infection [J].
Bignardi, GE .
JOURNAL OF HOSPITAL INFECTION, 1998, 40 (01) :1-15
[2]   CLOSTRIDIUM-DIFFICILE - A SPECTRUM OF VIRULENCE AND ANALYSIS OF PUTATIVE VIRULENCE DETERMINANTS IN THE HAMSTER MODEL OF ANTIBIOTIC-ASSOCIATED COLITIS [J].
BORRIELLO, SP ;
KETLEY, JM ;
MITCHELL, TJ ;
BARCLAY, FE ;
WELCH, AR ;
PRICE, AB ;
STEPHEN, J .
JOURNAL OF MEDICAL MICROBIOLOGY, 1987, 24 (01) :53-64
[3]   DEVELOPMENT OF A RAPID AND EFFICIENT RESTRICTION-ENDONUCLEASE ANALYSIS TYPING SYSTEM FOR CLOSTRIDIUM-DIFFICILE AND CORRELATION WITH OTHER TYPING SYSTEMS [J].
CLABOTS, CR ;
JOHNSON, S ;
BETTIN, KM ;
MATHIE, PA ;
MULLIGAN, ME ;
SCHABERG, DR ;
PETERSON, LR ;
GERDING, DN .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (07) :1870-1875
[4]  
*HLTH PROT AG, 2005, COMMUN DIS REP CDR W, V15, P2
[5]  
Klaassen CHW, 2002, J CLIN MICROBIOL, V40, P3547
[6]   A predominantly clonal multi-institutional outbreak of Clostridium difficile-associated diarrhea with high morbidity and mortality [J].
Loo, VG ;
Poirier, L ;
Miller, MA ;
Oughton, M ;
Libman, MD ;
Michaud, S ;
Bourgault, AM ;
Nguyen, T ;
Frenette, C ;
Kelly, M ;
Vibien, A ;
Brassard, P ;
Fenn, S ;
Dewar, K ;
Hudson, TJ ;
Horn, R ;
René, P ;
Monczak, Y ;
Dascal, A .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (23) :2442-2449
[7]   An epidemic, toxin gene-variant strain of Clostridium difficile [J].
McDonald, LC ;
Killgore, GE ;
Thompson, A ;
Owens, RC ;
Kazakova, SV ;
Sambol, SP ;
Johnson, S ;
Gerding, DN .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (23) :2433-2441
[8]  
MCDONALD LC, 2004, 42 ANN M INF DIS SOC
[9]  
MEKONEN E, 1996, INFECT CONT HOSP E S, V17, P32
[10]  
*NNCLS, 2004, METH ANT SUSC TEST A