HETEROGENEITY OF CLOSTRIDIUM-DIFFICILE ISOLATES FROM INFANTS

被引:35
作者
COLLIGNON, A
TICCHI, L
DEPITRE, C
GAUDELUS, J
DELMEE, M
CORTHIER, G
机构
[1] UNIV PARIS 11,DEPT MICROBIOL,F-92296 CHATENAY MALABRY,FRANCE
[2] HOSP JEAN VERDIER,DEPT PAEDIAT,F-93143 BONDY,FRANCE
[3] INRA,CRJ,UEPSD,F-78352 JOUY EN JOSAS,FRANCE
[4] UNIV CATHOLIQUE LOUVAIN,MICROBIOL UNIT,B-1200 BRUSSELS,BELGIUM
关键词
CLOSTRIDIUM-DIFFICILE; TOXIN-A AND TOXIN-B; SEROGROUPS;
D O I
10.1007/BF01956743
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
In order to improve our understanding of the role of Clostridium difficile in infants we characterised the strains isolated from this population. The production of toxin A and toxin B was studied. The toxin A, playing a major role in the disease, was searched for in faecal samples. The serogroup of the isolates was determined because some serogroups have been shown to be more pathogenic than others. Over a 9-month period, 102 faecal samples from 102 hospitalised infants (0-12 months) were analysed and 26% of the children were colonised with C. difficile. Fifteen isolates secreted neither toxin A nor B (62.5%). Nine isolates were toxigenic and secreted both toxins (37.5%). Of the eight toxigenic strains tested, six were from serogroup H and two serogroup K. Of the 13 nontoxigenic strains tested, 8 belonged to serogroup D, 2 to serogroup X, and 1 each to serogroup A, serogroup B and serogroup C. Three infants out of 102 studied had toxin A in their faeces. In summary, the infants can be colonised by (1) nontoxigenic strains, most of them from nonpathogenic serogroup D, without toxin A in the faeces; (2) toxigenic strains of virulent serogroups H and K, with or without toxin A in the faeces. Although some infants had diarrhoea, none needed a specific treatment for C. difficile. No specific C. difficile pathology could be retained and different mechanisms are advanced to explain this absence of pathogenicity.
引用
收藏
页码:319 / 322
页数:4
相关论文
共 29 条
[21]   EFFECT OF VARIOUS DIETS ON TOXIN PRODUCTION BY 2 STRAINS OF CLOSTRIDIUM-DIFFICILE IN GNOTOBIOTIC MICE [J].
MAHE, S ;
CORTHIER, G ;
DUBOS, F .
INFECTION AND IMMUNITY, 1987, 55 (08) :1801-1805
[22]   COMPARISON OF 5 CULTURAL PROCEDURES FOR ISOLATION OF CLOSTRIDIUM-DIFFICILE FROM STOOLS [J].
MARLER, LM ;
SIDERS, JA ;
WOLTERS, LC ;
PETTIGREW, Y ;
SKITT, BL ;
ALLEN, SD .
JOURNAL OF CLINICAL MICROBIOLOGY, 1992, 30 (02) :514-516
[23]   SEROTYPING OF CLOSTRIDIUM-DIFFICILE [J].
TOMA, S ;
LESIAK, G ;
MAGUS, M ;
LO, HL ;
DELMEE, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (03) :426-428
[24]   PREVALENCE OF CLOSTRIDIUM-DIFFICILE AND ITS CYTO-TOXIN IN INFANTS IN MEXICO [J].
TORRES, JF ;
CEDILLO, R ;
SANCHEZ, J ;
DILLMAN, C ;
GIONO, S ;
MUNOZ, O .
JOURNAL OF CLINICAL MICROBIOLOGY, 1984, 20 (02) :274-275
[25]   INTESTINAL COLONIZATION WITH CLOSTRIDIUM-DIFFICILE IN INFANTS UP TO 18 MONTHS OF AGE [J].
TULLUS, K ;
ARONSSON, B ;
MARCUS, S ;
MOLLBY, R .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1989, 8 (05) :390-393
[26]   INCIDENCE OF CLOSTRIDIUM DIFFICILE IN HOSPITALIZED CHILDREN - A PROSPECTIVE-STUDY [J].
TVEDE, M ;
SCHIOTZ, PO ;
KRASILNIKOFF, PA .
ACTA PAEDIATRICA SCANDINAVICA, 1990, 79 (03) :292-299
[27]   RELATIONSHIP BETWEEN LEVELS OF CLOSTRIDIUM-DIFFICILE TOXIN-A AND TOXIN-B AND CECAL LESIONS IN GNOTOBIOTIC MICE [J].
VERNET, A ;
CORTHIER, G ;
DUBOSRAMARE, F ;
PARODI, AL .
INFECTION AND IMMUNITY, 1989, 57 (07) :2123-2127
[28]   ANTAGONISM OF TOXIGENIC CLOSTRIDIUM-DIFFICILE BY NONTOXIGENIC C-DIFFICILE [J].
WILSON, KH ;
SHEAGREN, JN .
JOURNAL OF INFECTIOUS DISEASES, 1983, 147 (04) :733-736
[29]   SEVERE PSEUDOMEMBRANOUS ENTEROCOLITIS IN A CHILD - CASE-REPORT AND LITERATURE-REVIEW [J].
ZWIENER, RJ ;
BELKNAP, WM ;
QUAN, R .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1989, 8 (12) :876-882