» Articles » PMID: 12198612

Disease Severity in a Murine Model of Lyme Borreliosis is Associated with the Genotype of the Infecting Borrelia Burgdorferi Sensu Stricto Strain

Overview
Journal J Infect Dis
Date 2002 Aug 29
PMID 12198612
Citations 97
Authors
Affiliations
Soon will be listed here.
Abstract

The pathogenicity of Borrelia burgdorferi sensu stricto clinical isolates representing 2 distinct ribosomal DNA spacer restriction fragment-length polymorphism genotypes (RSTs) was assessed in a murine model of Lyme disease. B. burgdorferi was recovered from 71.5% and 26.6% of specimens from mice infected with RST1 and RST3 isolates, respectively (P<.0001). The average ankle diameter and histologic scores for carditis and arthritis were significantly higher after 2 weeks of infection among mice infected with RST1 isolates than among those infected with RST3 isolates (P<.001). These clinical manifestations were associated with larger numbers of spirochetes in target tissues but not with the serum sensitivity of the individual isolates. Thus, the development and severity of disease in genetically identical susceptible hosts is determined mainly by the pathogenic properties of the infecting B. burgdorferi isolate. The RST1 genotype is genetically homogeneous and thus may represent a recently evolved clonal lineage that is highly pathogenic in humans and animals.

Citing Articles

Mouse Models for the Study of Borrelia burgdorferi Infection.

Olsen K, Sachan S, Baumgarth N Curr Protoc. 2024; 4(8):e1127.

PMID: 39193882 PMC: 11361713. DOI: 10.1002/cpz1.1127.


Development and validation of systems for genetic manipulation of the Old World tick-borne relapsing fever spirochete, Borrelia duttonii.

Jackson-Litteken C, Guo W, Hogland B, Ratliff C, McFadden L, Fullerton M PLoS Negl Trop Dis. 2024; 18(7):e0012348.

PMID: 39038047 PMC: 11293673. DOI: 10.1371/journal.pntd.0012348.


Cellular and transcriptome signatures unveiled by single-cell RNA-Seq following infection of murine splenocytes with .

Kumaresan V, Ingle T, Kilgore N, Zhang G, Hermann B, Seshu J Front Immunol. 2023; 14:1296580.

PMID: 38149246 PMC: 10749944. DOI: 10.3389/fimmu.2023.1296580.


Diversity and host specificity of 's outer surface protein C () alleles in synanthropic mammals, with a notable allele U absence from mixed infections.

Shifflett S, Ferreira F, Gonzalez J, Toledo A, Fonseca D, Ellis V Infect Immun. 2023; 92(1):e0024423.

PMID: 38099660 PMC: 10790820. DOI: 10.1128/iai.00244-23.


Differential Resistance of Clones to Human Serum-Mediated Killing Does Not Correspond to Their Predicted Invasiveness.

Pearson P, Rich C, Siegel E, Brisson D, Rich S Pathogens. 2023; 12(10).

PMID: 37887754 PMC: 10609869. DOI: 10.3390/pathogens12101238.


References
1.
Liveris D, Gazumyan A, Schwartz I . Molecular typing of Borrelia burgdorferi sensu lato by PCR-restriction fragment length polymorphism analysis. J Clin Microbiol. 1995; 33(3):589-95. PMC: 227995. DOI: 10.1128/jcm.33.3.589-595.1995. View

2.
Yang L, Weis J, Eichwald E, Kolbert C, Persing D, Weis J . Heritable susceptibility to severe Borrelia burgdorferi-induced arthritis is dominant and is associated with persistence of large numbers of spirochetes in tissues. Infect Immun. 1994; 62(2):492-500. PMC: 186134. DOI: 10.1128/iai.62.2.492-500.1994. View

3.
Liveris D, Wormser G, Nowakowski J, Nadelman R, Bittker S, Cooper D . Molecular typing of Borrelia burgdorferi from Lyme disease patients by PCR-restriction fragment length polymorphism analysis. J Clin Microbiol. 1996; 34(5):1306-9. PMC: 229006. DOI: 10.1128/jcm.34.5.1306-1309.1996. View

4.
Livey I, Gibbs C, Schuster R, Dorner F . Evidence for lateral transfer and recombination in OspC variation in Lyme disease Borrelia. Mol Microbiol. 1995; 18(2):257-69. DOI: 10.1111/j.1365-2958.1995.mmi_18020257.x. View

5.
Peavey C, Lane R . Comparison of infectivities of six tick-derived isolates of Borrelia burgdorferi for rodents and ticks. J Clin Microbiol. 1996; 34(1):71-5. PMC: 228733. DOI: 10.1128/jcm.34.1.71-75.1996. View