Biological basis for syphilis

被引:379
作者
LaFond, RE
Lukehart, SA
机构
[1] Univ Washington, Dept Pathobiol, Seattle, WA 98195 USA
[2] Univ Washington, Dept Med, Seattle, WA 98195 USA
关键词
D O I
10.1128/CMR.19.1.29-49.2006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Syphilis is a chronic sexually transmitted disease caused by Treponema pallidum subsp. pallidum. Clinical manifestations separate the disease into stages; late stages of disease are uncommon now compared to the case in the preantibiotic era. T pallidum has an unusually small genome and lacks genes that encode many metabolic functions and classical virulence factors. The organism is extremely sensitive to environmental conditions and has not been continuously cultivated in vitro. Nonetheless, T pallidum is highly infectious and survives for decades in the untreated host. Early syphilis lesions result from the host's immune response to the treponemes. Bacterial clearance and resolution of early lesions results from a delayed hypersensitivity response, although some organisms escape to cause persistent infection. One factor contributing to T pallidum's chronicity is the paucity of integral outer membrane proteins, rendering intact organisms virtually invisible to the immune system. Antigenic variation of TprK, a putative surface-exposed protein, is likely to contribute to immune evasion. T pallidum remains exquisitely sensitive to penicillin, but macrolide resistance has recently been identified in a number of geographic regions. The development of a syphilis vaccine, thus far elusive, would have a significant positive impact on global health.
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页码:29 / +
页数:23
相关论文
共 340 条
[91]  
ESCOBAR MR, 1970, AM J CLIN PATHOL, V53, P886
[92]  
FEHER J, 1975, LANCET, V2, P896
[93]   NATIVE SURFACE ASSOCIATION OF A RECOMBINANT 38-KILODALTON TREPONEMA-PALLIDUM ANTIGEN ISOLATED FROM THE ESCHERICHIA-COLI OUTER-MEMBRANE [J].
FEHNIGER, TE ;
RADOLF, JD ;
WALFIELD, AM ;
CUNNINGHAM, TM ;
MILLER, JN ;
LOVETT, MA .
INFECTION AND IMMUNITY, 1986, 52 (02) :586-593
[94]   Sequence analysis, expression, and binding activity of recombinant major outer sheath protein (Msp) of Treponema denticola [J].
Fenno, JC ;
Muller, KH ;
McBride, BC .
JOURNAL OF BACTERIOLOGY, 1996, 178 (09) :2489-2497
[95]   FURTHER-STUDIES ON REPLICATION OF VIRULENT TREPONEMA-PALLIDUM IN TISSUE-CULTURES OF SFLEP CELLS [J].
FIELDSTEEL, AH ;
COX, DL ;
MOECKLI, RA .
INFECTION AND IMMUNITY, 1982, 35 (02) :449-455
[96]   CULTIVATION OF VIRULENT TREPONEMA-PALLIDUM IN TISSUE-CULTURE [J].
FIELDSTEEL, AH ;
COX, DL ;
MOECKLI, RA .
INFECTION AND IMMUNITY, 1981, 32 (02) :908-915
[97]   Common themes in microbial pathogenicity revisited [J].
Finlay, BB ;
Falkow, S .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 1997, 61 (02) :136-+
[98]   CHARACTERIZATION OF ATTACHMENT OF TREPONEMA-PALLIDUM (NICHOLS STRAIN) TO CULTURED MAMMALIAN-CELLS AND POTENTIAL RELATIONSHIP OF ATTACHMENT TO PATHOGENICITY [J].
FITZGERALD, TJ ;
JOHNSON, RC ;
MILLER, JN ;
SYKES, JA .
INFECTION AND IMMUNITY, 1977, 18 (02) :467-478
[99]  
FITZGERALD TJ, 1984, BRIT J VENER DIS, V60, P357
[100]  
FITZGERALD TJ, 1975, INFECT IMMUN, V11, P1133