Literature DB >> 8300208

Heritable susceptibility to severe Borrelia burgdorferi-induced arthritis is dominant and is associated with persistence of large numbers of spirochetes in tissues.

L Yang1, J H Weis, E Eichwald, C P Kolbert, D H Persing, J J Weis.   

Abstract

In human Lyme disease, symptoms with widely varying levels of severity have been observed. A mouse model of Lyme disease has been developed which allows analysis of mice with mild, moderate, and severe pathologies after inoculation with the spirochete Borrelia burgdorferi. To determine whether the differences in symptoms reflect differences in the number of spirochetes persisting in affected tissues, a sensitive PCR technique was developed to detect B. burgdorferi DNA in virtually any tissue of an infected mouse. This analysis, which detects DNA from as few as three spirochetes, revealed the presence of B. burgdorferi DNA in many tissues from severely arthritic C3H/HeJ mice as early as 1 week postinfection. The heart, ear, and ankle were particularly heavily infected, although B. burgdorferi DNA was also detected in spleen, liver, brain, kidney, bladder, uterus, and lymph nodes. In contrast, much lower levels of spirochete DNA were detected in tissues of infected BALB/c mice, which develop less severe arthritis when infected with B. burgdorferi than do C3H/HeJ mice. This difference was evident throughout the 5-week analysis. A competitive PCR method allowed determination of the absolute number of spirochete gene sequences in infected tissues. Ankles and hearts from C3H/HeJ mice were found to harbor 10(7) copies of the B. burgdorferi ospA gene, while these tissues from BALB/c mice contained 5- and 10-fold less B. burgdorferi DNA, respectively. The genetic regulation of severe pathology was analyzed by infecting the offspring of a cross between C3H/HeJ and BALB/c mice. The F1 mice developed severe arthritis and contained high levels of Borrelia DNA in the heart and ankle, similar to the C3H/HeJ parent. These findings indicate that susceptibility to severe arthritis is a dominant trait and suggest that it may correlate with high levels of persisting spirochetes. Models of pathology in Lyme disease should take into consideration the fact that severity of pathology may be directly related to the number of organisms in infected tissues.

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Year:  1994        PMID: 8300208      PMCID: PMC186134          DOI: 10.1128/iai.62.2.492-500.1994

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  35 in total

Review 1.  Lyme disease, 1988: immunologic manifestations and possible immunopathogenetic mechanisms.

Authors:  L H Sigal
Journal:  Semin Arthritis Rheum       Date:  1989-02       Impact factor: 5.532

2.  Nucleotide sequence of a gene encoding the Borrelia burgdorferi flagellin.

Authors:  G S Gassmann; M Kramer; U B Göbel; R Wallich
Journal:  Nucleic Acids Res       Date:  1989-05-11       Impact factor: 16.971

3.  Demonstration of spirochetes in cardiac biopsies of patients with Lyme disease.

Authors:  J de Koning; J A Hoogkamp-Korstanje; M R van der Linde; H J Crijns
Journal:  J Infect Dis       Date:  1989-07       Impact factor: 5.226

4.  In vivo and in vitro evidence of B cell hyperactivity during Lyme disease.

Authors:  L H Sigal; A C Steere; J M Dwyer
Journal:  J Rheumatol       Date:  1988-04       Impact factor: 4.666

5.  Lack of responsiveness of C3H/HeJ macrophages to lipopolysaccharide: the cellular basis of LPS-stimulated metabolism.

Authors:  J L Ryan; L M Glode; D L Rosenstreich
Journal:  J Immunol       Date:  1979-03       Impact factor: 5.422

6.  Specific and nonspecific responses of murine B cells to membrane blebs of Borrelia burgdorferi.

Authors:  W M Whitmire; C F Garon
Journal:  Infect Immun       Date:  1993-04       Impact factor: 3.441

7.  Molecular analysis of linear plasmid-encoded major surface proteins, OspA and OspB, of the Lyme disease spirochaete Borrelia burgdorferi.

Authors:  S Bergström; V G Bundoc; A G Barbour
Journal:  Mol Microbiol       Date:  1989-04       Impact factor: 3.501

8.  Murine Lyme borreliosis: route of inoculation determines immune response and infectivity.

Authors:  A R Pachner; E Delaney; N S Ricalton
Journal:  Reg Immunol       Date:  1992 Nov-Dec

9.  Amino acid sequence of mouse nidogen, a multidomain basement membrane protein with binding activity for laminin, collagen IV and cells.

Authors:  K Mann; R Deutzmann; M Aumailley; R Timpl; L Raimondi; Y Yamada; T C Pan; D Conway; M L Chu
Journal:  EMBO J       Date:  1989-01       Impact factor: 11.598

10.  Isolation and cultivation of Lyme disease spirochetes.

Authors:  A G Barbour
Journal:  Yale J Biol Med       Date:  1984 Jul-Aug
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  80 in total

1.  PCR-Based quantification of Borrelia burgdorferi organisms in canine tissues over a 500-Day postinfection period.

Authors:  R K Straubinger
Journal:  J Clin Microbiol       Date:  2000-06       Impact factor: 5.948

Review 2.  Host-pathogen interactions in the immunopathogenesis of Lyme disease.

Authors:  L T Hu; M S Klempner
Journal:  J Clin Immunol       Date:  1997-09       Impact factor: 8.317

3.  Relative contributions of innate and acquired host responses to bacterial control and arthritis development in Lyme disease.

Authors:  Xiaohui Wang; Ying Ma; John H Weis; James F Zachary; Carsten J Kirschning; Janis J Weis
Journal:  Infect Immun       Date:  2005-01       Impact factor: 3.441

4.  Inhibition of neutrophil function by two tick salivary proteins.

Authors:  Xiuyang Guo; Carmen J Booth; Michael A Paley; Xiaomei Wang; Kathleen DePonte; Erol Fikrig; Sukanya Narasimhan; Ruth R Montgomery
Journal:  Infect Immun       Date:  2009-03-30       Impact factor: 3.441

5.  Induction of pro- and anti-inflammatory cytokines by Borrelia burgdorferi lipoproteins in monocytes is mediated by CD14.

Authors:  G H Giambartolomei; V A Dennis; B L Lasater; M T Philipp
Journal:  Infect Immun       Date:  1999-01       Impact factor: 3.441

6.  Interleukin-4 (IL-4) and IL-13 signaling pathways do not regulate Borrelia burgdorferi-induced arthritis in mice: IgG1 is not required for host control of tissue spirochetes.

Authors:  M R Potter; N Noben-Trauth; J H Weis; C Teuscher; J J Weis
Journal:  Infect Immun       Date:  2000-10       Impact factor: 3.441

7.  Ablation of interleukin-12 exacerbates Lyme arthritis in SCID mice.

Authors:  J Anguita; S Samanta; S W Barthold; E Fikrig
Journal:  Infect Immun       Date:  1997-10       Impact factor: 3.441

8.  E and P selectins are not required for resistance to severe murine lyme arthritis.

Authors:  K P Seiler; Y Ma; J H Weis; P S Frenette; R O Hynes; D D Wagner; J J Weis
Journal:  Infect Immun       Date:  1998-09       Impact factor: 3.441

9.  Treatment of mice with the neutrophil-depleting antibody RB6-8C5 results in early development of experimental lyme arthritis via the recruitment of Gr-1- polymorphonuclear leukocyte-like cells.

Authors:  Charles R Brown; Victoria A Blaho; Christie M Loiacono
Journal:  Infect Immun       Date:  2004-09       Impact factor: 3.441

10.  A critical role for type I IFN in arthritis development following Borrelia burgdorferi infection of mice.

Authors:  Jennifer C Miller; Ying Ma; Jiantao Bian; Kathleen C F Sheehan; James F Zachary; John H Weis; Robert D Schreiber; Janis J Weis
Journal:  J Immunol       Date:  2008-12-15       Impact factor: 5.422

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