Construction and virulence testing of a collagenase mutant of Clostridium perfringens

被引:32
作者
Awad, MM
Ellemor, DM
Bryant, AE
Matsushita, O
Boyd, RL
Stevens, DL
Emmins, JJ
Rood, JI [1 ]
机构
[1] Monash Univ, Bacterial Pathogenesis Res Grp, Dept Microbiol, Clayton, Vic 3800, Australia
[2] Monash Med Sch, Dept Pathol & Immunol, Prahran, Vic 3181, Australia
[3] Vet Adm Med Ctr, Infect Dis Res Unit, Boise, ID 83702 USA
[4] Univ Washington, Sch Med, Dept Med, Seattle, WA 98195 USA
[5] Kagawa Med Univ, Dept Microbiol, Kagawa 7610793, Japan
基金
英国医学研究理事会;
关键词
Clostridium perfringens; collagenase; myonecrosis; gas gangrene; virulence; pathogenesis;
D O I
10.1006/mpat.1999.0328
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Clostridium perfringens produces several extracellular toxins and enzymes, including an extracellular collagenase or kappa toxin that is encoded by the colA gene. To determine if the ability to produce collagenase was a significant virulence factor in cases of gas gangrene or clostridial myonecrosis that are caused by C. perfringens, a chromosomal colA mutant was constructed by homologous recombination and subsequently virulence tested in the mouse myonecrosis model. The results clearly indicate that loss of the ability to produce collagenase does not alter the ability of the mutant to establish a virulent infection. By contrast, infection with a mutant unable to produce alpha-toxin led to a marked decrease in virulence. These results indicate that collagenase is not a major determinant of virulence in C. perfringens-mediated clostridial myonecrosis. (C) 2000 Academic Press.
引用
收藏
页码:107 / 117
页数:11
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