Brucellosis: An overview

被引:963
作者
Corbel, MJ
机构
[1] Natl. Inst. of Biol. Std. and Contr., Hertfordshire
[2] Natl. Inst. of Biol. Std. and Contr., Potters Bar, Hertfordshire ENG 3QG, Blamche Lane, South Mimms
关键词
D O I
10.3201/eid0302.970219
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Brucellosis remains a major zoonosis worldwide. Although many countries have eradicated Brucella abortus from cattle, in some areas Brucella melitensis has emerged as a cause of infection in this species as well as in sheep and goats. Despite vaccination campaigns with the Rev 1 strain, B. melitensis remains the principal cause of human brucellosis. Brucella suis is also emerging as an agent of infection in cattle, thus extending its opportunities to infect humans. The recent isolation of distinctive strains of Brucella from marine mammals has extended its ecologic range. Molecular genetic studies have demonstrated the phylogenetic affiliation to Agrobacterium, Phyllobacterium, Ochrobactrum, and Rhizobium. Polymerase chain reaction and gene probe development may provide more effective typing methods. Pathogenicity is related to production of lipopolysaccharides containing a poly N-formyl perosamine O chain, Cu-Zn superoxide dismutase, erythrulose phosphate dehydrogenase, stress-induced proteins related to intracellular survival, and adenine and guanine monophosphate inhibitors of phagocyte functions. Protective immunity is conferred by antibody to lipopolysaccharide and T-cell-mediated macrophage activation triggered by protein antigens. Diagnosis still centers on isolation of the organism and serologic test results, especially enzyme immunoassay, which is replacing other methods. Polymerase chain reaction is also under evaluation. Therapy is based on tetracyclines with or without rifampicin, aminoglycosides, or quinolones. No satisfactory vaccines against human brucellosis are available, although attenuated purE mutants appear promising.
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页码:213 / 221
页数:9
相关论文
共 68 条
  • [1] QUINOLONES IN TREATMENT OF HUMAN BRUCELLOSIS - COMPARATIVE TRIAL OF OFLOXACIN-RIFAMPIN VERSUS DOXYCYCLINE-RIFAMPIN
    AKOVA, M
    UZUN, O
    AKALIN, HE
    HAYRAN, M
    UNAL, S
    GUR, D
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (09) : 1831 - 1834
  • [2] DNA POLYMORPHISM IN STRAINS OF THE GENUS BRUCELLA
    ALLARDETSERVENT, A
    BOURG, G
    RAMUZ, M
    PAGES, M
    BELLIS, M
    ROIZES, G
    [J]. JOURNAL OF BACTERIOLOGY, 1988, 170 (10) : 4603 - 4607
  • [3] ALTON GG, 1975, LAB TECHNIAUES BRUCE
  • [4] EVALUATION OF ELISA IN THE DIAGNOSIS OF ACUTE AND CHRONIC BRUCELLOSIS IN HUMAN-BEINGS
    ARAJ, GF
    LULU, AR
    MUSTAFA, MY
    KHATEEB, MI
    [J]. JOURNAL OF HYGIENE, 1986, 97 (03) : 457 - 469
  • [5] SPECIFIC ANTIBODY PROFILE IN HUMAN BRUCELLOSIS
    ARIZA, J
    PELLICER, T
    PALLARES, R
    FOZ, A
    GUDIOL, F
    [J]. CLINICAL INFECTIOUS DISEASES, 1992, 14 (01) : 131 - 140
  • [6] COMPARATIVE TRIAL OF RIFAMPIN-DOXYCYCLINE VERSUS TETRACYCLINE-STREPTOMYCIN IN THE THERAPY OF HUMAN BRUCELLOSIS
    ARIZA, J
    GUDIOL, F
    PALLARES, R
    RUFI, G
    FERNANDEZVILADRICH, P
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1985, 28 (04) : 548 - 551
  • [7] BRUCELLA RIBOSOMAL-PROTEIN L7/L12 IS A MAJOR COMPONENT IN THE ANTIGENICITY OF BRUCELLIN INRA FOR DELAYED-TYPE HYPERSENSITIVITY IN BRUCELLA-SENSITIZED GUINEA-PIGS
    BACHRACH, G
    BANAI, M
    BARDENSTEIN, S
    HOIDA, G
    GENIZI, A
    BERCOVIER, H
    [J]. INFECTION AND IMMUNITY, 1994, 62 (12) : 5361 - 5366
  • [8] ISOLATION, IDENTIFICATION, AND CHARACTERIZATION IN ISRAEL OF BRUCELLA-MELITENSIS BIOVAR-1 ATYPICAL STRAINS SUSCEPTIBLE TO DYES AND PENICILLIN, INDICATING THE EVOLUTION OF A NEW VARIANT
    BANAI, M
    MAYER, I
    COHEN, A
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (05) : 1057 - 1059
  • [9] BRICKER BJ, 1990, INFECT IMMUN, V58, P2933
  • [10] DEFINITION OF BRUCELLA-A AND BRUCELLA-M EPITOPES BY MONOCLONAL TYPING REAGENTS AND SYNTHETIC OLIGOSACCHARIDES
    BUNDLE, DR
    CHERWONOGRODZKY, JW
    GIDNEY, MAJ
    MEIKLE, PJ
    PERRY, MB
    PETERS, T
    [J]. INFECTION AND IMMUNITY, 1989, 57 (09) : 2829 - 2836