Expression of cytolethal distending toxin and hemolysin is not required for pustule formation by Haemophilus ducreyi in human volunteers

被引:46
作者
Young, RS
Fortney, KR
Gelfanova, V
Phillips, CL
Katz, BP
Hood, AF
Latimer, JL
Munson, RS
Hansen, EJ
Spinola, SM
机构
[1] Indiana Univ, Sch Med, Dept Med, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Dept Microbiol & Immunol, Indianapolis, IN 46202 USA
[3] Indiana Univ, Sch Med, Dept Pathol & Lab Med, Indianapolis, IN 46202 USA
[4] Indiana Univ, Sch Med, Dept Dermatol, Indianapolis, IN 46202 USA
[5] Ohio State Univ, Childrens Res Inst, Columbus, OH 43205 USA
[6] Ohio State Univ, Dept Pediat, Columbus, OH 43205 USA
[7] Ohio State Univ, Dept Microbiol, Columbus, OH 43205 USA
[8] Univ Texas, SW Med Ctr, Dept Microbiol, Dallas, TX 75235 USA
关键词
D O I
10.1128/IAI.69.3.1938-1942.2001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Haemophilus ducreyi makes cytolethal distending toxin (CDT) and hemolysin. In a previous human challenge trial, an isogenic hemolysin-deficient mutant caused pustules with a rate similar to that of its parent. To test whether CDT was required for pustule formation, six human subjects were inoculated,vith a CDT mutant and parent at multiple sites. The pustule formation rates were similar at both parent and mutant sites. A CDT and hemolysin double mutant was constructed and tested in five additional subjects. The pustule formation rates were similar for the parent and double mutant. These results indicate that neither the expression of CDT, nor that of hemolysin, nor both are required for pustule formation by H. ducreyi in humans.
引用
收藏
页码:1938 / 1942
页数:5
相关论文
共 34 条
[1]   Immunohistochemical investigations of genital ulcers caused by Haemophilus ducreyi [J].
Abeck, D ;
Freinkel, AL ;
Korting, HC ;
Szeimis, RM ;
Ballard, RC .
INTERNATIONAL JOURNAL OF STD & AIDS, 1997, 8 (09) :585-588
[2]   An isogenic hemoglobin receptor-deficient mutant of Haemophilus ducreyi is attenuated in the human model of experimental infection [J].
Al-Tawfiq, JA ;
Fortney, KR ;
Katz, BP ;
Hood, AF ;
Elkins, C ;
Spinola, SM .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (03) :1049-1054
[3]   Standardization of the experimental model of Haemophilus ducreyi infection in human subjects [J].
Al-Tawfiq, JA ;
Thornton, AC ;
Katz, BP ;
Fortney, KR ;
Todd, KD ;
Hood, AF ;
Spinola, SM .
JOURNAL OF INFECTIOUS DISEASES, 1998, 178 (06) :1684-1687
[4]   Experimental infection of human volunteers with Haemophilus ducreyi does not confer protection against subsequent challenge [J].
Al-Tawfiq, JA ;
Palmer, KL ;
Chen, CY ;
Haley, JC ;
Katz, BP ;
Hood, AF ;
Spinola, SM .
JOURNAL OF INFECTIOUS DISEASES, 1999, 179 (05) :1283-1287
[5]   Cumulative experience with Haemophilus ducreyi 35000 in the human model of experimental infection [J].
Al-Tawfiq, JA ;
Harezlak, J ;
Katz, BP ;
Spinola, SM .
SEXUALLY TRANSMITTED DISEASES, 2000, 27 (02) :111-114
[6]   Haemophilus ducreyi hemolysin acts as a contact cytotoxin and damages human foreskin fibroblasts in cell culture [J].
Alfa, MJ ;
DeGagne, P ;
Totten, PA .
INFECTION AND IMMUNITY, 1996, 64 (06) :2349-2352
[7]   Localization of Haemophilus ducreyi at the pustular stage of disease in the human model of infection [J].
Bauer, ME ;
Spinola, SM .
INFECTION AND IMMUNITY, 2000, 68 (04) :2309-2314
[8]  
BLACKMORE CA, 1985, J INFECT DIS, V151, P840, DOI 10.1093/infdis/151.5.840
[9]   DsrA-deficient mutant of Haemophilus ducreyi is impaired in its ability to infect human volunteers [J].
Bong, CTH ;
Throm, RE ;
Fortney, KR ;
Katz, BP ;
Hood, AF ;
Elkins, C ;
Spinola, SM .
INFECTION AND IMMUNITY, 2001, 69 (03) :1488-1491
[10]   Facile construction of mutations in Haemophilus ducreyi using lacZ as a counter-selectable marker [J].
Bozue, JA ;
Tarantino, L ;
Munson, RS .
FEMS MICROBIOLOGY LETTERS, 1998, 164 (02) :269-273