The Early Effects of Clostridium perfringens Type D Epsilon Toxin in Ligated Intestinal Loops of Goats and Sheep

被引:0
作者
M.E. Fernandez Miyakawa
F.A. Uzal
机构
[1] Animal Health Unit,
[2] The National Institute of Agricultural Technology,undefined
来源
Veterinary Research Communications | 2003年 / 27卷
关键词
colon; enterotoxaemia; epsilon toxin; flux; goat; histopathology; ileum; sheep;
D O I
暂无
中图分类号
学科分类号
摘要
Clostridium perfringens type D produces enterotoxaemia in goats, sheep and other animals. The disease is caused by C. perfringens epsilon toxin and, while enterotoxaemia in goats is usually characterized by enterocolitis, the disease in sheep is characterized by systemic lesions (such as lung and brain oedema) with minor and inconsistent changes observed in the intestine. A possible explanation for these differences is that epsilon toxin is more promptly absorbed by the ovine than by the caprine intestine. In an attempt to clarify this, we examined the early effects of epsilon toxin on caprine and ovine intestine. Intestinal loop assays were performed to analyse the physiological and morphological changes induced by epsilon toxin in the intestine of these species. Fluid accumulation was observed in caprine and ovine ileum and colon treated with epsilon toxin. Ileal loops from goats treated with epsilon toxin retained sodium and water earlier than ovine ileal loops treated with the same toxin. Histological analysis showed morphological alterations in the colon of both species as early as 2 h after the commencement of epsilon toxin treatment; these changes were more marked in goats than in sheep. No morphological changes were observed in the ileum of either species after 4 h incubation with epsilon toxin. These results suggest that epsilon toxin modifies ion and water transport in the small and the large intestine of goats and sheep through different mechanisms.
引用
收藏
页码:231 / 241
页数:10
相关论文
共 50 条
  • [1] The early effects of Clostridium perfringens type D epsilon toxin in ligated intestinal loops of goats and sheep
    Miyakawa, MEF
    Uzal, FA
    VETERINARY RESEARCH COMMUNICATIONS, 2003, 27 (03) : 231 - 241
  • [2] Diagnosis of Clostridium perfringens intestinal infections in sheep and goats
    Uzal, FA
    ANAEROBE, 2004, 10 (02) : 135 - 143
  • [3] Evaluation of different fluids for detection of Clostridium perfringens type D epsilon toxin in sheep with experimental enterotoxemia
    Layana, Jorge E.
    Miyakawa, Mariano E. Fernandez
    Uzal, Francisco A.
    ANAEROBE, 2006, 12 (04) : 204 - 206
  • [4] Clostridium perfringens type-D enterotoxaemia in cattle: the diagnostic significance of intestinal epsilon toxin
    Jones, A. L.
    Dagleish, M. P.
    Caldow, G. L.
    VETERINARY RECORD, 2015, 177 (15) : 390
  • [5] Neurological disorders produced by Clostridium perfringens type D epsilon toxin
    Finnie, JW
    ANAEROBE, 2004, 10 (02) : 145 - 150
  • [6] Diagnosis of Clostridium perfringens intestinal infections in sheep and goats
    Uzal, Francisco A.
    Songer, J. Glenn
    JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2008, 20 (03) : 253 - 265
  • [7] Resistance of Ovine, Caprine and Bovine Endothelial Cells to Clostridium perfringens Type D Epsilon Toxin In Vitro
    F.A. Uzal
    B.E. Rolfe
    N.J. Smith
    A.C. Thomas
    W.R. Kelly
    Veterinary Research Communications, 1999, 23 : 275 - 284
  • [8] Resistance of ovine, caprine and bovine endothelial cells to Clostridium perfringens type D epsilon toxin in vitro
    Uzal, FA
    Rolfe, BE
    Smith, NJ
    Thomas, AC
    Kelly, WR
    VETERINARY RESEARCH COMMUNICATIONS, 1999, 23 (05) : 275 - 284
  • [9] Pathology and Pathogenesis of Brain Lesions Produced by Clostridium perfringens Type D Epsilon Toxin
    Finnie, John W.
    Uzal, Francisco A.
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (16)
  • [10] Naturally acquired antibodies against Clostridium perfringens epsilon toxin in goats
    Veschi, Josir Laine A.
    Bruzzone, Octavio A.
    Losada-Eaton, Daniela M.
    Dutra, Iveraldo S.
    Fernandez-Miyakawa, Mariano E.
    VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2008, 125 (1-2) : 198 - 202