Hemolysis in human erythrocytes by Clostridium perfringens epsilon toxin requires activation of P2 receptors. Issue 1 (31st December 2018)

• Record Type: Journal Article
• Authors: Gao, Jie; Xin, Wenwen; Huang, Jing; Ji, Bin; Gao, Shan; Chen, Liang; Kang, Lin; Yang, Hao; Shen, Xin; Zhao, Baohua; Wang, Jinglin
• Is Part Of: Virulence. Volume 9:Issue 1(2018)
• Page Start: 1601
• Page End: 1614
• Publication Date: 2018-12-31
• Subjects: Clostridium perfringens -- ε-toxin -- erythrocytes -- hemolysis -- P2 receptors; Virulence (Microbiology) -- Periodicals; Bacterial diseases -- Periodicals; Molecular microbiology -- Periodicals; 579.05
• DOI: 10.1080/21505594.2018.1528842
• Languages: English
• ISSNs: 2150-5608

Abstract

ABSTRACT: Epsilon-toxin (ETX) is produced by types B and D strains of Clostridium perfringens, which cause fatal enterotoxaemia in sheep, goats and cattle. Previous studies showed that only a restricted number of cell lines are sensitive to ETX and ETX-induced hemolysis has not previously been reported. In this study, the hemolytic ability of ETX was examined using erythrocytes from 10 species including murine, rabbit, sheep, monkey and human. We found that ETX caused hemolysis in human erythrocytes (HC50 = 0.2 μM) but not erythrocytes from the other test species. Moreover, the mechanism of ETX-induced hemolysis was further explored. Recent studies showed that some bacterial toxins induce hemolysis through purinergic receptor (P2) activation. Hence, the function of purinergic receptors in ETX-induced hemolysis was tested, and we found that the non-selective P2 receptor antagonists PPADS inhibited ETX-induced lysis of human erythrocytes in a concentration-dependent manner, indicating that ETX-induced hemolysis requires activation of purinergic receptors. P2 receptors comprise seven P2X (P2X1–7) and eight P2Y (P2Y1, P2Y2, P2Y4, P2Y6, and P2Y11–P2Y14) receptor subtypes. The pattern of responsiveness to more selective P2-antagonists implies that both P2Y13 and P2X7 receptors are involved in ETX-induced hemolysis in human species. Furthermore, we demonstrated that extracellular ATP is likely not involved in ETX-induced hemolysis and the activation of P2 receptors. These findings clarified the mechanism of ETX-induced hemolysis and provided new insight into the activities and ETX mode of action.