A novel toxin homologous to large clostridial cytotoxins found in culture supernatant of Clostridium perfringens type C

被引:102
作者
Amimoto, Katsuhiko [1 ]
Noro, Taichi [1 ]
Oishi, Eiji [1 ]
Shimizu, Mitsugu [1 ]
机构
[1] Kyoto Biken Labs Inc, Uji, Kyoto 6110041, Japan
来源
MICROBIOLOGY-SGM | 2007年 / 153卷
关键词
D O I
10.1099/mic.0.2006/002287-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
An unknown cytotoxin was identified in the culture supernatant of Clostridium perfringens type C. The cytotoxin, named TpeL, which was purified using mAb-based affinity chromatography, had a lethal activity of 62 minimum lethal dose (MLD) mg(-1) in mice and a cytotoxic activity of 6.2 x 10(5) cytotoxic units (CU) mg(-1) in Vero cells. The nucleotide sequence of TpeL was determined. The entire ORF had a length of 4953 bases, and the same.nucleotide sequence was not recorded in the GenBank/EMBL/DDBJ databases. The molecular mass calculated from the deduced amino acid sequence was 191 kDa, and a signal peptide region was not found within the ORF. The deduced amino acid sequence exhibited 30-39 % homology to Clostridium difficile toxins A (TcdA) and B (TcdB), Clostridium sordellii lethal toxin (TcsL) and Clostridium novyi alpha-toxin (TcnA). The amino acid sequence of TpeL is shorter than these toxins, and the homologous region was located at the N-terminal site. Eighteen strains of C. perfringens types A, B and C were surveyed for the presence of the tpeL gene by PCR. The tpeL gene was detected in all type B (one strain) and C strains (five strains), but not in any type A strains (12 strains). TpeL was detected in culture filtrates of the five type C strains by dot-blot analysis, but not in the type B strain. It was concluded that TpeL is a novel toxin similar to the known large clostridial cytotoxins. Furthermore, the data indicated that TpeL is produced by many C. perfringens type C strains.
引用
收藏
页码:1198 / 1206
页数:9
相关论文
共 45 条
  • [21] HIGHLY SENSITIVE ASSAY FOR CLOSTRIDIUM-PERFRINGENS ENTERO-TOXIN THAT USES INHIBITION OF PLATING EFFICIENCY OF VERO CELLS GROWN IN CULTURE
    MCDONEL, JL
    MCCLANE, BA
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1981, 13 (05) : 940 - 946
  • [22] PRODUCTION OF PHOSPHOLIPASE-C (ALPHA-TOXIN), HEMOLYSINS AND LETHAL TOXINS BY CLOSTRIDIUM-PERFRINGENS TYPES A TO D
    MOLLBY, R
    HOLME, T
    NORD, CE
    SMYTH, CJ
    WADSTROM, T
    [J]. JOURNAL OF GENERAL MICROBIOLOGY, 1976, 96 (SEP): : 137 - 144
  • [23] Clostridium perfringens β-toxin is sensitive to thiol-group modification but does not require a thiol group for lethal activity
    Nagahama, M
    Kihara, A
    Miyawaki, T
    Mukai, M
    Sakaguchi, Y
    Ochi, S
    Sakurai, J
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1999, 1454 (01): : 97 - 105
  • [24] Biological activities and pore formation of Clostridium perfringens beta toxin in HL 60 cells
    Nagahama, M
    Hayashi, S
    Morimitsu, S
    Sakurai, J
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (38) : 36934 - 36941
  • [25] NAKAMURA S, 1984, MICROBIOL IMMUNOL, V28, P493, DOI 10.1111/j.1348-0421.1984.tb00700.x
  • [26] NIILO L, 1987, CAN J VET RES, V51, P224
  • [27] Effects of Clostridium perfringens alpha-toxin (PLC) and perfringolysin O (PFO) on cytotoxicity to macrophages, on escape from the phagosomes of macrophages, and on persistence of C-perfringens in host tissues
    O'Brien, DK
    Melville, SB
    [J]. INFECTION AND IMMUNITY, 2004, 72 (09) : 5204 - 5215
  • [29] REED L. J., 1938, AMER JOUR HYG, V27, P493
  • [30] AN IMPROVED COLORIMETRIC ASSAY FOR CELL-PROLIFERATION AND VIABILITY UTILIZING THE TETRAZOLIUM SALT XTT
    ROEHM, NW
    RODGERS, GH
    HATFIELD, SM
    GLASEBROOK, AL
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 1991, 142 (02) : 257 - 265