Emergence of Anaplasma marginale antigenic variants during persistent rickettsemia

被引:126
作者
French, DM [1 ]
Brown, WC [1 ]
Palmer, GH [1 ]
机构
[1] Washington State Univ, Dept Vet Microbiol & Pathol, Program Vector Borne Dis, Pullman, WA 99164 USA
关键词
D O I
10.1128/IAI.67.11.5834-5840.1999
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Anaplasma marginale is an ehrlichial pathogen of cattle, in the order Rickettsiales, that establishes persistent cyclic rickettsemia in the infected host. Within each rickettsemic cycle, A. marginale expressing antigenically variant major surface protein 2 (MSP2) emerge. By cloning 17 full-length msp2 transcripts expressed during cyclic rickettsemia, we determined that emergent variants have a single, central hypervariable region encoding variant B-cell epitopes, The N- and C-terminal regions are highly conserved among the expressed A. marginale variants, and similar sequences define the MSP2 homologues in the agent of human granulocytic ehrlichiosis (FIGE). This is in contrast to the MSP2 homologues in ehrlichial genogroup I pathogens, Ehrlichia chaffeensis, Ehrlichia canis, and Cowdria ruminantium, that have multiple hypervariable regions. By defining the variable and conserved regions, we were able to show that the single hypervariable region of A. marginale MSP2 encodes epitopes that are immunogenic and induce variant-specific antibody responses during persistent infection. These findings demonstrate that the MSP2 structural variants that emerge during each cycle of persistent rickettsemia are true antigenic variants, consistent with MSP2 antigenic variation as a mechanism of A. marginale persistence.
引用
收藏
页码:5834 / 5840
页数:7
相关论文
共 29 条
  • [1] CD4+ T-lymphocyte and immunoglobulin G2 responses in calves immunized with Anaplasma marginale outer membranes and protected against homologous challenge
    Brown, WC
    Shkap, V
    Zhu, DM
    McGuire, TC
    Tuo, WB
    McElwain, TF
    Palmer, GH
    [J]. INFECTION AND IMMUNITY, 1998, 66 (11) : 5406 - 5413
  • [2] The repertoire of Anaplasma marginale antigens recognized by CD4+ T-lymphocyte clones from protectively immunized cattle is diverse and includes major surface protein 2 (MSP-2) and MSP-3
    Brown, WC
    Zhu, DM
    Shkap, V
    McGuire, TC
    Blouin, EF
    Kocan, KM
    Palmer, GH
    [J]. INFECTION AND IMMUNITY, 1998, 66 (11) : 5414 - 5422
  • [3] Expression of major surface protein 2 antigenic variants during acute Anaplasma marginale Rickettsemia
    Eid, G
    French, DM
    Lundgren, AM
    Barbet, AF
    McElwain, TF
    Palmer, GH
    [J]. INFECTION AND IMMUNITY, 1996, 64 (03) : 836 - 841
  • [4] DETECTION AND QUANTITATION OF ANAPLASMA-MARGINALE IN CARRIER CATTLE BY USING A NUCLEIC-ACID PROBE
    ERIKS, IS
    PALMER, GH
    MCGUIRE, TC
    ALLRED, DR
    BARBET, AF
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1989, 27 (02) : 279 - 284
  • [5] IMPACT OF PERSISTENT ANAPLASMA-MARGINALE RICKETTSEMIA ON TICK INFECTION AND TRANSMISSION
    ERIKS, IS
    STILLER, D
    PALMER, GH
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (08) : 2091 - 2096
  • [6] Expression of Anaplasma marginale major surface protein 2 variants during persistent cyclic rickettsemia
    French, DM
    McElwain, TF
    McGuire, TC
    Palmer, GH
    [J]. INFECTION AND IMMUNITY, 1998, 66 (03) : 1200 - 1207
  • [7] *GEN COMP GROUP, 1994, PROGR MAN GCG PACK
  • [8] Cloning of the gene encoding the 44-kilodalton antigen of the agent of human granulocytic ehrlichiosis and characterization of the humoral response
    Ijdo, JW
    Sun, W
    Zhang, Y
    Magnarelli, LA
    Fikrig, E
    [J]. INFECTION AND IMMUNITY, 1998, 66 (07) : 3264 - 3269
  • [9] CYCLIC RICKETTSEMIA DURING PERSISTENT ANAPLASMA-MARGINALE INFECTION OF CATTLE
    KIESER, ST
    ERIKS, IS
    PALMER, GH
    [J]. INFECTION AND IMMUNITY, 1990, 58 (04) : 1117 - 1119
  • [10] A SIMPLE METHOD FOR DISPLAYING THE HYDROPATHIC CHARACTER OF A PROTEIN
    KYTE, J
    DOOLITTLE, RF
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1982, 157 (01) : 105 - 132