Characterization of Clostridium difficile isolates from foals with diarrhea:: 28 cases (1993-1997)

被引:52
作者
Magdesian, KG [1 ]
Hirsh, DC
Jang, SS
Hansen, LM
Madigan, JE
机构
[1] Univ Calif Davis, Sch Vet Med, Vet Med Teaching Hosp, Dept Med & Epidemiol, Davis, CA 95616 USA
[2] Univ Calif Davis, Sch Vet Med, Vet Med Teaching Hosp, Microbiol Diagnost Lab, Davis, CA 95616 USA
[3] Univ Calif Davis, Sch Vet Med, Dept Pathol Microbiol & Immunol, Davis, CA 95616 USA
来源
JOURNAL OF THE AMERICAN VETERINARY MEDICAL ASSOCIATION | 2002年 / 220卷 / 01期
关键词
D O I
10.2460/javma.2002.220.67
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Objective-To determine molecular characteristics of Clostridium difficile isolates from foals with diarrhea and identify clinical abnormalities in affected foals. Design-Retrospective study. Animals-28 foals with C difficile-associated diarrhea. Procedure-Toxigenicity, molecular fingerprinting, and antibiotic susceptibility patterns were determined. Information on signalment, clinical findings, results of clinicopathologic testing, whether antimicrobials had been administered prior to development of diarrhea, and outcome was obtained from the medical records. Results-Twenty-three (82%) foals survived. Toxin A and B gene sequences were detected in isolates from 24 of 27 foals, whereas the toxin B gene alone was detected in the isolate from 1 foal. Results of an ELISA for toxin A were positive for fecal samples from only 8 of 20 (40%) foals. Ten of 23 (43%) isolates were resistant to metronidazole. Molecular fingerprinting revealed marked heterogeneity among isolates, except for the metronidazole-resistant isolates. Sixteen foals had tachypnea. Hematologic abnormalities were indicative of inflammation. Common serum biochemical abnormalities included metabolic acidosis, hyponatremia, hypocalcemia, azotemia, hypoproteinemia, hyperglycemia, and high enzyme activities. Passive transfer of maternal antibodies was adequate in all 12 foals evaluated. Conclusions and Clinical Relevance-Results suggest that a large percentage of C difficile isolates from foals with diarrhea will have the toxin A and B gene sequences, Because of the possibility that Isolates will be resistant to metronidazole, susceptibility testing is warranted. Clostridium difficile isolates from foals may have a substantial amount of molecular heterogeneity. Clinical and hematologic findings in affected foals are similar to those for foals with diarrhea caused by other pathogens.
引用
收藏
页码:67 / 73
页数:7
相关论文
共 50 条
[1]   Characterization of a toxin A-negative, toxin B-positive strain of Clostridium difficile responsible for a nosocomial outbreak of Clostridium difficile-associated diarrhea [J].
Alfa, MJ ;
Kabani, A ;
Lyerly, D ;
Moncrief, S ;
Neville, LM ;
Al-Barrak, A ;
Harding, GKH ;
Dyck, B ;
Olekson, K ;
Embil, JM .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (07) :2706-2714
[2]   USE OF FATTY-ACID ANALYSIS (MICROBIAL IDENTIFICATION SYSTEM) FOR THE IDENTIFICATION OF CLOSTRIDIUM-DIFFICILE [J].
ANDERSON, J ;
KORVER, J ;
LUCHSINGER, I .
CLINICAL INFECTIOUS DISEASES, 1995, 20 :S202-S202
[3]   Usefulness of simultaneous detection of toxin A and glutamate dehydrogenase for the diagnosis of Clostridium difficile-associated diseases [J].
Barbut, F ;
Lalande, V ;
Daprey, G ;
Cohen, P ;
Marle, N ;
Burghoffer, B ;
Petit, JC .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2000, 19 (06) :481-484
[4]   Clostridium difficile associated with acute colitis in mares when their foals are treated with erythromycin and rifampicin for Rhodococcus equi pneumonia [J].
Båverud, V ;
Franklin, A ;
Gunnarsson, A ;
Gustafsson, A ;
Hellander-Edman, A .
EQUINE VETERINARY JOURNAL, 1998, 30 (06) :482-488
[5]  
Baverud V, 1997, EQUINE VET J, V29, P279, DOI 10.1111/j.2042-3306.1997.tb03124.x
[6]  
BOLTON RP, 1984, ARCH DIS CHILD, V59, P466, DOI 10.1136/adc.59.5.466
[7]   Detection of the ADP-ribosyltransferase toxin gene (cdtA) and its activity in Clostridium difficile isolates from Equidae [J].
Braun, M ;
Herholz, C ;
Straub, R ;
Choisat, B ;
Frey, J ;
Nicolet, J ;
Kuhnert, P .
FEMS MICROBIOLOGY LETTERS, 2000, 184 (01) :29-33
[8]   ANTIBIOTIC SUSCEPTIBILITY OF CLOSTRIDIUM-DIFFICILE [J].
BURDON, DW ;
BROWN, JD ;
YOUNGS, DJ ;
ARABI, Y ;
SHINAGAWA, N ;
ALEXANDERWILLIAMS, J ;
KEIGHLEY, MRB ;
GEORGE, RH .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1979, 5 (03) :307-310
[9]   Binding of Clostridium difficile toxin A to human milk secretory component [J].
Dallas, SD ;
Rolfe, RD .
JOURNAL OF MEDICAL MICROBIOLOGY, 1998, 47 (10) :879-888
[10]  
Davis MS, 1999, VET MED-US, V94, P363