ROLE OF LIPOOLIGOSACCHARIDES IN EXPERIMENTAL DERMAL LESIONS CAUSED BY HAEMOPHILUS-DUCREYI

被引:97
作者
CAMPAGNARI, AA
WILD, LM
GRIFFITHS, GE
KARALUS, RJ
WIRTH, MA
SPINOLA, SM
机构
[1] SUNY BUFFALO, SCH MED, DEPT PATHOL, BUFFALO, NY 14215 USA
[2] SUNY BUFFALO, SCH MED, DEPT MICROBIOL, BUFFALO, NY 14215 USA
关键词
D O I
10.1128/IAI.59.8.2601-2608.1991
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The mouse and rabbit intradermal injection models have been used to define factors that may be important in Haemophilus ducreyi pathogenesis. We used H. ducreyi strains with diverse geographic origins and phenotypic characteristics to evaluate the experimental models. Injection of live and heat-killed bacteria caused skin abscesses in both models. Semiquantitative cultures of skin injected with live bacteria showed that H. ducreyi failed to replicate in animal tissue. These data suggested that the experimental lesions were caused by a heat-stable substance such as lipooligosaccharide (LOS). In mice, injection of H. ducreyi and Haemophilus influenzae LOS and Escherichia coli lipopolysaccharide caused mild to moderate inflammation. In rabbits, injection of H. ducreyi LOS caused intradermal abscesses that were histologically similar to those caused by live and heat-killed bacteria. H. ducreyi and Neisseria gonorrhoeae LOS caused significantly larger lesions than equivalent amounts of H. influenzae LOS and E. coli lipopolysaccharide in the rabbit model. We conclude that the intradermal injection models are not valid models to study the growth of H. ducreyi in vivo. However, these data indicate that H. ducreyi LOS may play an important role in the pathogenesis of chancroid and that the rabbit model should be useful in studying H. ducreyi LOS toxicity at the cellular level.
引用
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页码:2601 / 2608
页数:8
相关论文
共 31 条
[1]   MODIFICATION BY SIALIC-ACID OF NEISSERIA-GONORRHOEAE LIPOOLIGOSACCHARIDE EPITOPE EXPRESSION IN HUMAN URETHRAL EXUDATES - AN IMMUNOELECTRON MICROSCOPIC ANALYSIS [J].
APICELLA, MA ;
MANDRELL, RE ;
SHERO, M ;
WILSON, ME ;
GRIFFISS, JM ;
BROOKS, GF ;
LAMMEL, C ;
BREEN, JF ;
RICE, PA .
JOURNAL OF INFECTIOUS DISEASES, 1990, 162 (02) :506-512
[2]   COMPARATIVE STUDIES ON TOXICITY OF ESCHERICHIA COLI LIPOPOLYSACCHARIDE ENDOTOXIN IN VARIOUS ANIMAL SPECIES [J].
BERCZI, I ;
BERTOK, L ;
BEREZNAI, T .
CANADIAN JOURNAL OF MICROBIOLOGY, 1966, 12 (05) :1070-+
[3]   RISK-FACTORS ASSOCIATED WITH HIV INFECTION IN UGANDA [J].
BERKLEY, SF ;
WIDYWIRSKI, R ;
OKWARE, SI ;
DOWNING, R ;
LINNAN, MJ ;
WHITE, KE ;
SEMPALA, S .
JOURNAL OF INFECTIOUS DISEASES, 1989, 160 (01) :22-30
[4]   LIPOOLIGOSACCHARIDE EPITOPES SHARED AMONG GRAM-NEGATIVE NONENTERIC MUCOSAL PATHOGENS [J].
CAMPAGNARI, AA ;
SPINOLA, SM ;
LESSE, AJ ;
KWAIK, YA ;
MANDRELL, RE ;
APICELLA, MA .
MICROBIAL PATHOGENESIS, 1990, 8 (05) :353-362
[5]   ADVANCES IN THE DIAGNOSIS AND MANAGEMENT OF CHANCROID [J].
DCOSTA, LJ ;
BOWMER, I ;
NSANZE, H ;
DYLEWSKI, J ;
FRANSEN, L ;
PLUMMER, FA ;
PIOT, P ;
RONALD, AR .
SEXUALLY TRANSMITTED DISEASES, 1986, 13 (03) :189-191
[6]  
DIENST R B, 1948, Am J Syph Gonorrhea Vener Dis, V32, P289
[7]  
FEINER RR, 1945, AM J SYPH GON VD, V29, P71
[8]   HISTOLOGICAL ASPECTS OF SEXUALLY-TRANSMITTED GENITAL LESIONS [J].
FREINKEL, AL .
HISTOPATHOLOGY, 1987, 11 (08) :819-831
[9]  
GREENBLATT R. B., 1944, American Journal of Syphilis, V28, P165
[10]   TOXIC ACTIVITY OF PURIFIED LIPOPOLYSACCHARIDE OF NEISSERIA-GONORRHOEAE FOR HUMAN FALLOPIAN-TUBE MUCOSA [J].
GREGG, CR ;
MELLY, MA ;
HELLERQVIST, CG ;
CONIGLIO, JG ;
MCGEE, ZA .
JOURNAL OF INFECTIOUS DISEASES, 1981, 143 (03) :432-439