The Arcanobacterium (Actinomyces) pyogenes hemolysin, pyolysin, is a novel member of the thiol-activated cytolysin family

被引:94
作者
Billington, SJ [1 ]
Jost, BH [1 ]
Cuevas, WA [1 ]
Bright, KR [1 ]
Songer, JG [1 ]
机构
[1] UNIV ARIZONA,DEPT VET SCI,TUCSON,AZ 85721
关键词
D O I
10.1128/jb.179.19.6100-6106.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Arcanobacterium (Actinomyces) pyogenes, an animal pathogen, produces a hemolytic exotoxin, pyolysin (PLO), The gene encoding PLO was cloned, and sequence analysis revealed an open reading frame of 1,605 bp encoding a protein of 57.9 kDa. PLO has 30 to 40% identity with the thiol-activated cytolysins (TACYs) of a number of gram-positive bacteria, The activity of PLO was found to be very similar to allose of other TACYs, except that it was not thiol activated, The highly conserved TACY undecapeptide is divergent in PLO; in particular, the cysteine residue required for thiol activation has been replaced with alanine, However, mutagenesis of the alanine residue to cysteine did not confer thiol activation on PLO, suggesting a conformational difference in thf undecapeptide region of this toxin, Specific antibodies against purified, recombinant PLO completely neutralized the hemolytic activity of A. pyogenes, suggesting that this organism produces a single hemolysin. Furthermore, these antibodies could passively protect mice against lethal challenge with A, pyogenes, suggesting that like other TACYs PLO is an important virulence factor in the pathogenesis of this organism.
引用
收藏
页码:6100 / 6106
页数:7
相关论文
共 47 条
[1]   STREPTOCOCCAL TOXINS (STREPTOLYSIN-O, STREPTOLYSIN-S, ERYTHROGENIC TOXIN) [J].
ALOUF, JE .
PHARMACOLOGY & THERAPEUTICS, 1980, 11 (03) :661-717
[2]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[3]  
[Anonymous], CURRENT PROTOCOLS MO
[4]   VIRULENCE STUDIES ON CHROMOSOMAL ALPHA-TOXIN AND THETA-TOXIN MUTANTS CONSTRUCTED BY ALLELIC EXCHANGE PROVIDE GENETIC-EVIDENCE FOR THE ESSENTIAL ROLE OF ALPHA-TOXIN IN CLOSTRIDIUM PERFRINGENS-MEDIATED GAS-GANGRENE [J].
AWAD, MM ;
BRYANT, AE ;
STEVENS, DL ;
ROOD, JI .
MOLECULAR MICROBIOLOGY, 1995, 15 (02) :191-202
[5]   REDUCED VIRULENCE OF A DEFINED PNEUMOLYSIN-NEGATIVE MUTANT OF STREPTOCOCCUS-PNEUMONIAE [J].
BERRY, AM ;
YOTHER, J ;
BRILES, DE ;
HANSMAN, D ;
PATON, JC .
INFECTION AND IMMUNITY, 1989, 57 (07) :2037-2042
[6]   COMPLEMENT ACTIVATION AND ATTACK ON AUTOLOGOUS CELL-MEMBRANES INDUCED BY STREPTOLYSIN-O [J].
BHAKDI, S ;
TRANUMJENSEN, J .
INFECTION AND IMMUNITY, 1985, 48 (03) :713-719
[7]   ISOLATION AND IDENTIFICATION OF 2 HEMOLYTIC FORMS OF STREPTOLYSIN-O [J].
BHAKDI, S ;
ROTH, M ;
SZIEGOLEIT, A ;
TRANUMJENSEN, J .
INFECTION AND IMMUNITY, 1984, 46 (02) :394-400
[8]   STRUCTURE AND FUNCTION OF PNEUMOLYSIN, THE MULTIFUNCTIONAL, THIOL-ACTIVATED TOXIN OF STREPTOCOCCUS-PNEUMONIAE [J].
BOULNOIS, GJ ;
PATON, JC ;
MITCHELL, TJ ;
ANDREW, PW .
MOLECULAR MICROBIOLOGY, 1991, 5 (11) :2611-2616
[9]  
CARTER GR, 1991, ESSENTIALS VET BACTE
[10]  
CHAPMAN AJ, 1987, ZBL BAKT-INT J MED M, V264, P279