Antigenic variation of Anaplasma marginale by expression of MSP2 mosaics

被引:99
作者
Barbet, AF
Lundgren, A
Yi, J
Rurangirwa, FR
Palmer, GH
机构
[1] Univ Florida, Coll Vet Med, Dept Pathobiol, Gainesville, FL 32611 USA
[2] Washington State Univ, Dept Vet Microbiol & Pathol, Program Vector Borne Dis, Pullman, WA 99164 USA
关键词
D O I
10.1128/IAI.68.11.6133-6138.2000
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 a tick-borne pathogen, one of several closely related ehrlichial organisms that cause disease in animals and humans. These Ehrlichia species have complex life cycles that require, in addition to replication and development within the tick vector, evasion of the immune system in order to persist in the mammalian reservoir host. This complexity requires efficient use of the small ehrlichial genome, A. marginale and related ehrlichiae express immunoprotective, variable outer membrane proteins that have similar structures and are encoded by polymorphic multigene families. We show here that the major outer membrane protein of A. marginale, MSP2, is encoded on a polycistronic mRNA, The genomic expression site for this mRNA is polymorphic and encodes numerous amino acid sequence variants in bloodstream populations of A. marginale. A potential mechanism for persistence is segmental gene conversion of the expression site to link hypervariable msp2 sequences to the promoter and polycistron.
引用
收藏
页码:6133 / 6138
页数:6
相关论文
共 33 条
  • [1] ALLEMAN AR, 1993, J GEN MICROBIOL, V139, P2439
  • [2] Anaplasma marginale major surface protein 3 is encoded by a polymorphic, multigene family
    Alleman, AR
    Palmer, GH
    McGuire, TC
    McElwain, TF
    Perryman, LE
    Barbet, AF
    [J]. INFECTION AND IMMUNITY, 1997, 65 (01) : 156 - 163
  • [3] The genome sequence of Rickettsia prowazekii and the origin of mitochondria
    Andersson, SGE
    Zomorodipour, A
    Andersson, JO
    Sicheritz-Pontén, T
    Alsmark, UCM
    Podowski, RM
    Näslund, AK
    Eriksson, AS
    Winkler, HH
    Kurland, CG
    [J]. NATURE, 1998, 396 (6707) : 133 - 140
  • [4] CHARACTERIZATION OF AN IMMUNOPROTECTIVE PROTEIN COMPLEX OF ANAPLASMA-MARGINALE BY CLONING AND EXPRESSION OF THE GENE CODING FOR POLYPEPTIDE AM105L
    BARBET, AF
    PALMER, GH
    MYLER, PJ
    MCGUIRE, TC
    [J]. INFECTION AND IMMUNITY, 1987, 55 (10) : 2428 - 2435
  • [5] THE IMPORTANCE OF MOSAIC GENES TO TRYPANOSOME SURVIVAL
    BARBET, AF
    KAMPER, SM
    [J]. PARASITOLOGY TODAY, 1993, 9 (02): : 63 - 66
  • [6] Dumler JS, 1998, ANNU REV MED, V49, P201, DOI 10.1146/annurev.med.49.1.201
  • [7] 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
  • [8] Expression of Anaplasma marginale major surface protein 2 variants during persistent cyclic rickettsemia (vol 66, pg 1202, 1998)
    French, DM
    McElwain, TF
    McGuire, TC
    Palmer, GH
    [J]. INFECTION AND IMMUNITY, 1998, 66 (05) : 2400 - 2400
  • [9] Emergence of Anaplasma marginale antigenic variants during persistent rickettsemia
    French, DM
    Brown, WC
    Palmer, GH
    [J]. INFECTION AND IMMUNITY, 1999, 67 (11) : 5834 - 5840
  • [10] 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