Elongated versions of Vlp surface lipoproteins protect Mycoplasma hyorhinis escape variants from growth-inhibiting host antibodies

被引:64
作者
Citti, C [1 ]
Kim, MF [1 ]
Wise, KS [1 ]
机构
[1] UNIV MISSOURI, SCH MED, DEPT MOL MICROBIOL & IMMUNOL, COLUMBIA, MO 65212 USA
关键词
D O I
10.1128/IAI.65.5.1773-1785.1997
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Variation in Vlp surface proteins of Mycoplasma hyorhinis was evaluated in terms of its role in determining susceptibility of organisms to growth inhibition by host antibodies (Abs), High-frequency switching of Vip surface lipoproteins has been studied in isogenic lineages of M. hyorhinis SK76, In these lineages, the products of three genes, vlpA, vlpB, and vlpC, are subject to phase and size variation in vitro, which occur through distinct mutator elements that independently govern the expression of each vlp gene (promoter mutations) or the size of the rip gene product (by intragenic expansion or contraction of a 3' region containing tandem repeats), Isogenic clonal variants of M. hyorhinis SK76 expressing distinct profiles of Vip products were assessed for their susceptibility to complement-independent growth inhibition by serum Abs of swine experimentally infected with the arthritigenic SK76 strain, Invariably, variants expressing longer versions of VlpA, VlpB, or VlpC (each expressed individually) were completely resistant to host immune serum Abs, whereas variants expressing shorter allelic versions of each Vlp were susceptible, The target of growth-inhibiting Abs was not the Vip products, since removal of anti-Vlp Abs had no effect on the inhibitory activity of the host immune serum on susceptible variants, Escape variant populations derived by propagating susceptible variants in an immune (versus control) host serum revealed a strong selection for the long-Vlp phenotype, irrespective of the identity of the Vlp expressed. Apparent mutational pathways of acquiring the protective phenotype included mutational switches to express long rip genes that had been transcriptionally silent or switches to elongate expressed vlp genes, These results suggest that a major function of the Vip system is to shield the wall-less mycoplasma surface from host Abs capable of binding vital (and as-yet-unidentified) surface antigens of this organism.
引用
收藏
页码:1773 / 1785
页数:13
相关论文
共 59 条
[1]   METABOLISM INHIBITION AS A RESULT OF INTERACTION OF ANTIBODY WITH A MEMBRANE-PROTEIN OF MYCOPLASMA-BOVOCULI [J].
AWUMBILA, B ;
ROSENBUSCH, RF .
CURRENT MICROBIOLOGY, 1991, 22 (04) :221-224
[2]   BORRELIA-BURGDORFERI ANTIGENS THAT ARE TARGETED BY ANTIBODY-DEPENDENT, COMPLEMENT-MEDIATED KILLING IN THE RHESUS-MONKEY [J].
AYDINTUG, MK ;
GU, Y ;
PHILIPP, MT .
INFECTION AND IMMUNITY, 1994, 62 (11) :4929-4937
[3]   ANTIGENIC VARIATION OF A RELAPSING FEVER BORRELIA SPECIES [J].
BARBOUR, AG .
ANNUAL REVIEW OF MICROBIOLOGY, 1990, 44 :155-171
[4]   INTERPLAY BETWEEN MYCOPLASMAS AND HOST TARGET-CELLS [J].
BASEMAN, JB ;
LANGE, M ;
CRISCIMAGNA, NL ;
GIRON, JA ;
THOMAS, CA .
MICROBIAL PATHOGENESIS, 1995, 19 (02) :105-116
[5]  
Beveridge T J., 1995, ASM News, V61, P125
[6]   Mechanism of antigenic variation in Mycoplasma pulmonis: Interwoven, site-specific DNA inversions [J].
Bhugra, B ;
Voelker, LL ;
Zou, NX ;
Yu, HL ;
Dybvig, K .
MOLECULAR MICROBIOLOGY, 1995, 18 (04) :703-714
[7]   MODIFICATIONS OF GROWTH INHIBITION TEST AND ITS APPLICATION TO HUMAN T-MYCOPLASMAS [J].
BLACK, FT .
APPLIED MICROBIOLOGY, 1973, 25 (04) :528-533
[8]   EXPLORING THE MYCOPLASMA-CAPRICOLUM GENOME - A MINIMAL CELL REVEALS ITS PHYSIOLOGY [J].
BORK, P ;
OUZOUNIS, C ;
CASARI, G ;
SCHNEIDER, R ;
SANDER, C ;
DOLAN, M ;
GILBERT, W ;
GILLEVET, PM .
MOLECULAR MICROBIOLOGY, 1995, 16 (05) :955-967
[9]   PROGRAMMED GENE REARRANGEMENTS ALTERING GENE-EXPRESSION [J].
BORST, P ;
GREAVES, DR .
SCIENCE, 1987, 235 (4789) :658-667
[10]  
BORST P, 1992, Current Biology, V2, P304, DOI 10.1016/0960-9822(92)90878-E