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Enrichment and Detection of Clostridium perfringens Toxinotypes in Retail Food Samples
Published on: October 18, 2019
[Morphologic changes in cultures of different tissues exposed to the toxins of C1. perfringens types B, C, E and F]
Abstract:
There were revealed morphological peculiarities of the action of C1. perfringens toxins, types B, C, D, E and F on the cultures of fibroblasts of chick embryo, amniotic cells and intestinal tissue. The toxin type B was characterized by a marked vocuolization of the cell cytoplasm; the action of the toxin of type C was expressed in the swelling of the nuclei and the lysis of the chromatine substance, the toxin of type E casued kariorhexis, and the toxin of type F--hyperchromatosis of the nuclei. All the cultures proved to be insensitive to the toxin of type D. Peculiarity of the morphological affection of the cells permitted to differentiate toxin of type B in the cultures of the fibroblasts of chick embryo, whereas the toxins of types C, E and F--in the cultures of the amniotic cells under control of the reaction of neutralization with the homologous antitoxic sera.
Insights
Morphological effects of Clostridium perfringens toxins (types B, C, E, F) on cell cultures were identified. These distinct cellular changes allow for toxin differentiation using neutralization assays.
Area of Science:
- Veterinary Microbiology
- Cell Biology
- Toxicology
Background:
- Clostridium perfringens produces various toxins implicated in animal diseases.
- Understanding toxin-specific cellular effects is crucial for diagnosis and treatment.
Purpose of the Study:
- To investigate and characterize the distinct morphological effects of Clostridium perfringens toxins (types B, C, D, E, and F) on different cell cultures.
- To evaluate the potential of these morphological changes for differentiating toxin types.
Main Methods:
- Exposure of chick embryo fibroblasts, amniotic cells, and intestinal tissue cultures to purified Clostridium perfringens toxins.
- Microscopic observation of cellular alterations, including vacuolization, nuclear swelling, chromatin lysis, kariorhexis, and hyperchromatosis.
- Neutralization assays using homologous antitoxic sera to confirm toxin identification.
Main Results:
- Clostridium perfringens toxin type B induced significant cytoplasmic vacuolization in fibroblasts.
- Toxin type C caused nuclear swelling and chromatin lysis.
- Toxin type E led to kariorhexis, and toxin type F resulted in nuclear hyperchromatosis.
- All tested cell cultures were insensitive to toxin type D.
- Distinct morphological patterns enabled differentiation of toxin type B in fibroblasts and types C, E, and F in amniotic cells.
Conclusions:
- Specific morphological changes in cell cultures correlate with different Clostridium perfringens toxin types.
- Cellular morphology serves as a basis for differentiating Clostridium perfringens toxins B, C, E, and F.
- Neutralization assays combined with morphological analysis provide a reliable method for toxin identification.
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