About: Borrelia burgdorferi is a research topic. Over the lifetime, 7906 publications have been published within this topic receiving 295557 citations.
TL;DR: Spirochete dissemination and disease severity vary significantly in mice infected with distinct genotypes of B. burgdorferi, suggesting that genotypic differences in the infecting spirochetes play a key role in the pathogenesis and development of clinical disease.
Abstract: Various genotypes of Borrelia burgdorferi sensu stricto have been previously identified among a large collection of isolates cultured from patients with Lyme disease in the United States. Furthermore, association of specific genotypes with hematogenous dissemination early in the disease course has been observed. The present study assessed kinetics of spirochete dissemination and disease severity in C3H/HeJ mice infected with two different genotypes of B. burgdorferi. Spirochete load in plasma and ear and other tissue samples of infected mice was measured by quantitative PCR, and these data were compared to those obtained by culture and histopathologic analysis. In mice infected with isolate BL206 (a type 1 strain), the peak number of spirochetes was observed in plasma between day 4 and 7, in heart and ear tissue on day 14, and in joints on day 28 postinoculation. There was a correlation between the peak number of spirochetes in plasma on day 4 or 7 and that in ear biopsy and joint specimens on day 14. By contrast, spirochete burdens in plasma of mice infected with isolate B356 (a type 3 strain) were 16- and 5-fold lower than those of BL206-infected mice on days 7 and 14 of infection, respectively. Similarly, approximately 6- and 13-fold fewer spirochetes were detected in the heart tissues of B356-infected mice compared to BL206-infected mice. Histopathologically, severe arthritis and aortitis were noted only in mice infected with isolate BL206. Spirochete dissemination and disease severity vary significantly in mice infected with distinct genotypes of B. burgdorferi, suggesting that genotypic differences in the infecting spirochetes play a key role in the pathogenesis and development of clinical disease.
TL;DR: It is shown that homologous chromosomal loci from several North American and European isolates of the Lyme disease spirochete Borrelia burgdorferi, as well as from the relapsing fever spiroCHE hermsii, may have a clinical correlate reflected in differences between "typical" Lyme borreliosis in North America and Europe.
Abstract: We sequenced homologous chromosomal loci from several North American and European isolates of the Lyme disease spirochete Borrelia burgdorferi, as well as from the relapsing fever spirochete Borrelia hermsii. Inter- and intraspecies sequence comparisons permitted the design of B. burgdorferi-specific polymerase chain reaction primers that detected all strains tested (n = 31) from diverse geographical and biological origins. Polymerase chain reaction "typing" with other unique sets of primers subdivided B. burgdorferi isolates into two groups: all North American isolates and a few European isolates made up one group, while the majority of the European and Asian isolates made up the second group. This classification may have a clinical correlate reflected in differences between "typical" Lyme borreliosis in North America and Europe.
TL;DR: The presence of antibodies against the Lyme disease agent Borrelia burgdorferi sensu lato, a spirochaete transmitted by the seabird tick Ixodes uriae, in the eggs of kittiwakes Rissa tridactyla suggests that mothers can alter investment in their young depending on local conditions.
Abstract: Mothers are predicted to invest in their offspring depending on the quality of their mate, their opportunity to invest in future reproduction and the characteristics of the habitat in which their offspring will be born. Recent studies have suggested a transfer of maternal immunity to offspring as an induced response to the local presence of parasites in the environment, but evidence has been indirect. Here, we show the presence of antibodies against the Lyme disease agent Borrelia burgdorferi sensu lato, a spirochaete transmitted by the seabird tick Ixodes uriae, in the eggs of kittiwakes Rissa tridactyla. We report higher prevalence of antibodies against Borrelia in eggs from breeding areas with higher prevalence and abundance of ticks. Further, high repeatabilities of antibody-positive eggs within clutches and between first and replacement clutches show that, within a breeding season, females differ consistently with respect to the expression of this induced maternal response. Our results suggest that mothers can alter investment in their young depending on local conditions. Such maternal effects clearly have implications for the ecology and evolution of host-parasite interactions.
TL;DR: In this paper, the distribution, conservation, expression and potential global regulatory capability of Rrp1 were assessed for Borrelia burgdorferi, a causative agent of Lyme disease, comprised of open reading frames (ORFs) BB0419 and BB0420.
Abstract: Two-component systems (TCS) are universal among bacteria and play critical roles in gene regulation. Our understanding of the contributions of TCS in the biology of the Borrelia is just now beginning to develop. Borrelia burgdorferi, a causative agent of Lyme disease, harbours a TCS comprised of open reading frames (ORFs) BB0419 and BB0420. BB0419 encodes a response regulator designated Rrp1, and BB0420 encodes a hybrid histidine kinase-response regulator designated Hpk1. Rrp1, which contains a conserved GGDEF domain, undergoes phosphorylation and produces the secondary messenger, cyclic diguanylate (c-di-GMP), a critical signaling molecule in numerous organisms. However, the regulatory role of the Rrp1-Hpk1 TCS and c-di-GMP signaling in Borrelia biology are unexplored. In this study, the distribution, conservation, expression and potential global regulatory capability of Rrp1 were assessed. rrp1 was found to be universal and highly conserved among isolates, co-transcribed with hpk1, constitutively expressed during in vitro cultivation, and significantly upregulated upon tick feeding. Allelic exchange replacement and microarray analyses revealed that the Rrp1 regulon consists of a large number of genes encoded by the core Borrelia genome (linear chromosome, linear plasmid 54 and circular plasmid 26) that encode for proteins involved in central metabolic processes and virulence mechanisms including immune evasion.
TL;DR: The whole-genome sequences of 13 additional B. burgdorferi isolates are determined to allow improved understanding of pathogenesis and provide a foundation for novel detection, diagnosis, and prevention strategies.
Abstract: Borrelia burgdorferi is a causative agent of Lyme disease in North America and Eurasia. The first complete genome sequence of B. burgdorferi strain 31, available for more than a decade, has assisted research on the pathogenesis of Lyme disease. Because a single genome sequence is not sufficient to understand the relationship between genotypic and geographic variation and disease phenotype, we determined the whole-genome sequences of 13 additional B. burgdorferi isolates that span the range of natural variation. These sequences should allow improved understanding of pathogenesis and provide a foundation for novel detection, diagnosis, and prevention strategies.