Passage through Ixodes scapularis Ticks Enhances the Virulence of a Weakly Pathogenic Isolate of Borrelia burgdorferi

被引:4
作者
Adusumilli, Sarojini [1 ]
Booth, Carmen J. [2 ]
Anguita, Juan [3 ]
Fikrig, Erol [1 ]
机构
[1] Yale Univ, Infect Dis Sect, Dept Internal Med, Sch Med, New Haven, CT 06520 USA
[2] Yale Univ, Comparat Med Sect, Sch Med, New Haven, CT 06520 USA
[3] Univ Massachusetts, Dept Vet & Anim Sci, Amherst, MA 01003 USA
基金
美国国家卫生研究院;
关键词
LYME-DISEASE SPIROCHETE; FIBRONECTIN-BINDING PROTEIN; SURFACE PROTEIN; GENE-EXPRESSION; IMMUNODEFICIENT MICE; INFECTION; SURVIVAL; BBK32; CYCLE;
D O I
10.1128/IAI.00470-09
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lyme disease is the most common tick-borne illness in the United States. In this paper we explore the contribution of Ixodes scapularis ticks to the pathogenicity of Borrelia burgdorferi in mice. Previously we demonstrated that an isolate of B. burgdorferi sensu stricto (designated N40), passaged 75 times in vitro (N40-75), was infectious but was no longer able to cause arthritis and carditis in C3H mice. We now show that N40-75 spirochetes can readily colonize I. scapularis and multiply during tick engorgement. Remarkably, tick-transmitted N40-75 spirochetes cause disease in mice. N40-75 spirochetes isolated from these animals also retained their pathogenicity when subsequently administered to mice via syringe inoculation. Array analysis revealed that several genes associated with virulence, including bba25, bba65, bba66, bbj09, and bbk32, had higher expression levels in the tick-passaged N40-75 spirochete. These data suggest that transmission of a high-passage attenuated isolate of B. burgdorferi by the arthropod vector results in the generation of spirochetes that have enhanced pathogenesis in mice.
引用
收藏
页码:138 / 144
页数:7
相关论文
共 37 条
[1]   Borrelia burgdorferi gene expression in vivo and spirochete pathogenicity [J].
Anguita, J ;
Samanta, S ;
Revilla, B ;
Suk, K ;
Das, S ;
Barthold, SW ;
Fikrig, E .
INFECTION AND IMMUNITY, 2000, 68 (03) :1222-1230
[2]   Borrelia burgdorferi-induced inflammation facilitates spirochete adaptation and variable major protein-like sequence locus recombination [J].
Anguita, J ;
Thomas, V ;
Samanta, S ;
Persinski, R ;
Hernanz, C ;
Barthold, SW ;
Fikrig, E .
JOURNAL OF IMMUNOLOGY, 2001, 167 (06) :3383-3390
[3]   Protective and arthritis-resolving activity in sera of mice infected with Borrelia burgdorferi [J].
Barthold, SW ;
Feng, SL ;
Bockenstedt, LK ;
Fikrig, E ;
Feen, K .
CLINICAL INFECTIOUS DISEASES, 1997, 25 :S9-S17
[4]   Assessment of decorin-binding protein A to the infectivity of Borrelia burgdorferi in the murine models of needle and tick infection [J].
Blevins, Jon S. ;
Hagman, Kayla E. ;
Norgard, Michael V. .
BMC MICROBIOLOGY, 2008, 8 (1)
[5]   Protection elicited by native outer membrane protein Oms66 (p66) against host-adapted Borrelia burgdorferi:: Conformational nature of bactericidal epitopes [J].
Exner, MM ;
Wu, XY ;
Blanco, DR ;
Miller, JN ;
Lovett, MA .
INFECTION AND IMMUNITY, 2000, 68 (05) :2647-2654
[6]   Current concepts - A critical appraisal of "chronic Lyme disease'' [J].
Feder, Henry M., Jr. ;
Johnson, Barbara J. B. ;
O'Connell, Susan ;
Shapiro, Eugene D. ;
Steere, Allen C. ;
Wormser, Gary P. .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 357 (14) :1422-1430
[7]   Arthropod- and host-specific Borrelia burgdorferi bbk32 expression and the inhibition of spirochete transmission [J].
Fikrig, E ;
Feng, W ;
Barthold, SW ;
Telford, SR ;
Flavell, RA .
JOURNAL OF IMMUNOLOGY, 2000, 164 (10) :5344-5351
[8]   Fibronectin binding protein BBK32 of the Lyme disease spirochete promotes bacterial attachment to glycosaminoglycans [J].
Fischer, JR ;
LeBlanc, KT ;
Leong, JM .
INFECTION AND IMMUNITY, 2006, 74 (01) :435-441
[9]   Temporal expression analysis of the Borrelia burgdorferi paralogous gene [J].
Gilmore, Robert D., Jr. ;
Howison, Rebekah R. ;
Schmit, Virginia L. ;
Nowalk, Andrew J. ;
Clifton, Dawn R. ;
Nolder, Christi ;
Hughes, Jessica L. ;
Carroll, James A. .
INFECTION AND IMMUNITY, 2007, 75 (06) :2753-2764
[10]   Borrelia burgdorferi expression of the bba64, bba65, bba66, and bba73 genes in tissues during persistent infection in mice [J].
Gilmore, Robert D., Jr. ;
Howison, Rebekah R. ;
Schmit, Virginia L. ;
Carroll, James A. .
MICROBIAL PATHOGENESIS, 2008, 45 (5-6) :355-360