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Enrichment and Detection of Clostridium perfringens Toxinotypes in Retail Food Samples
Published on: October 18, 2019
Atypical cpb2 genes, encoding beta2-toxin in Clostridium perfringens isolates of nonporcine origin
B Helen Jost1, Stephen J Billington, Hien T Trinh
1Department of Veterinary Science and Microbiology, University of Arizona, 1117 East Lowell St., Tucson, AZ 85721, USA. jost@u.arizona.edu
Abstract:
Beta2-toxin, encoded by cpb2, is implicated in the pathogenesis of Clostridium perfringens enteritis. However, cpb2 genes from nonporcine C. perfringens isolates were not always expressed, at least in vitro. Nucleotide sequencing identified atypical cpb2 genes with 70.2 to 70.7% DNA identity to previously identified (consensus) cpb2. Atypical beta2-toxin displayed 62.3% identity and 80.4% similarity to consensus beta2-toxin. No porcine type C isolates (n = 16) and only 3.3% of porcine type A isolates (n = 60) carried atypical cpb2 genes. However, 88.5% of nonporcine isolates carried atypical cpb2 (n = 78), but beta2-toxin was not expressed. Almost half of the nonporcine consensus cpb2 genes (44.4%) carried a frameshift mutation (n = 9), resulting in an absence of beta2-toxin expression. These findings strengthen the role of beta2-toxin in the pathogenesis of enteritis in neonatal pigs. However, the identification of apparently nonexpressed, atypical cpb2 genes raises the question of whether this protein plays the same role in enteritis in other animal species.
Insights
Atypical Clostridium perfringens beta2-toxin genes are common in non-porcine isolates but often unexpressed due to mutations. This suggests beta2-toxin
Area of Science:
- Microbiology
- Veterinary Medicine
- Molecular Biology
Background:
- Beta2-toxin, encoded by cpb2, is linked to Clostridium perfringens enteritis.
- Expression of cpb2 genes varies among C. perfringens isolates, particularly non-porcine ones.
- Understanding beta2-toxin's role in enteritis across different animal species requires investigating gene variations.
Purpose of the Study:
- To investigate the prevalence and characteristics of atypical cpb2 genes in Clostridium perfringens.
- To determine the expression status of beta2-toxin from atypical cpb2 genes.
- To elucidate the role of beta2-toxin in enteritis pathogenesis in pigs versus other animals.
Main Methods:
- Nucleotide sequencing was used to identify and compare atypical and consensus cpb2 genes.
- DNA and protein sequence identities/similarities were analyzed between atypical and consensus beta2-toxins.
- Prevalence of atypical cpb2 genes was assessed in porcine and non-porcine C. perfringens isolates.
Main Results:
- Atypical cpb2 genes, with low DNA identity to consensus, were found in 88.5% of non-porcine isolates but rarely in porcine isolates.
- Atypical beta2-toxin showed significantly lower sequence identity and similarity to consensus beta2-toxin.
- Non-expressed beta2-toxin was observed in most non-porcine isolates carrying atypical cpb2, often due to frameshift mutations in consensus cpb2 genes.
Conclusions:
- Beta2-toxin plays a significant role in neonatal pig enteritis, supported by its presence in porcine isolates.
- The identification of non-expressed atypical cpb2 genes in non-porcine isolates questions beta2-toxin's universal role in enteritis across species.
- Further research is needed to understand the pathogenesis of enteritis in animals infected with C. perfringens strains carrying non-expressed beta2-toxin genes.
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