scholarly journals Lyme Disease Pathogenesis

2022 ◽  
pp. 473-518
Author(s):  
Jenifer Coburn ◽  
Brandon Garcia ◽  
Linden T. Hu ◽  
Mollie W. Jewett ◽  
Peter Kraiczy ◽  
...  
Author(s):  
Jenifer Coburn ◽  
Brandon Garcia ◽  
Linden T. Hu ◽  
Mollie W. Jewett ◽  
Peter Kraiczy ◽  
...  

2005 ◽  
Vol 11 (3) ◽  
pp. 114-120 ◽  
Author(s):  
Mireia Guerau-de-Arellano ◽  
Brigitte T. Huber

1994 ◽  
Vol 2 (11) ◽  
pp. 431-437 ◽  
Author(s):  
Mario T. Philipp ◽  
Barbara J.B. Johnson

1999 ◽  
Vol 289 (5-7) ◽  
pp. 690-695 ◽  
Author(s):  
Markus M. Simon ◽  
Yvonne Bauer ◽  
Weimin Zhong ◽  
Heidelore Hofmann ◽  
Reinhard Wallich

2006 ◽  
Vol 74 (3) ◽  
pp. 1967-1972 ◽  
Author(s):  
Kelley M. Hovis ◽  
Emily Tran ◽  
Christina M. Sundy ◽  
Eric Buckles ◽  
John V. McDowell ◽  
...  

ABSTRACT The binding of Borrelia burgdorferi OspE, OspF, and family 163 (Elp) proteins to factor H/factor H-like protein 1 (FHL-1) and other serum proteins from different animals was assessed. OspE paralogs bound factor H and unidentified serum proteins from a subset of animals, while OspF and Elp proteins did not. These data advance our understanding of factor H binding, the host range of the Lyme spirochetes, and the expanding role of OspE in pathogenesis.


Author(s):  
S. F. Hayes ◽  
M. D. Corwin ◽  
T. G. Schwan ◽  
D. W. Dorward ◽  
W. Burgdorfer

Characterization of Borrelia burgdorferi strains by means of negative staining EM has become an integral part of many studies related to the biology of the Lyme disease organism. However, relying solely upon negative staining to compare new isolates with prototype B31 or other borreliae is often unsatisfactory. To obtain more satisfactory results, we have relied upon a correlative approach encompassing a variety EM techniques, i.e., scanning for topographical features and cryotomy, negative staining and thin sectioning to provide a more complete structural characterization of B. burgdorferi.For characterization, isolates of B. burgdorferi were cultured in BSK II media from which they were removed by low speed centrifugation. The sedimented borrelia were carefully resuspended in stabilizing buffer so as to preserve their features for scanning and negative staining. Alternatively, others were prepared for conventional thin sectioning and for cryotomy using modified procedures. For thin sectioning, the fixative described by Ito, et al.


2014 ◽  
Vol 56 ◽  
pp. 69-83 ◽  
Author(s):  
Ko-Fan Chen ◽  
Damian C. Crowther

The formation of amyloid aggregates is a feature of most, if not all, polypeptide chains. In vivo modelling of this process has been undertaken in the fruitfly Drosophila melanogaster with remarkable success. Models of both neurological and systemic amyloid diseases have been generated and have informed our understanding of disease pathogenesis in two main ways. First, the toxic amyloid species have been at least partially characterized, for example in the case of the Aβ (amyloid β-peptide) associated with Alzheimer's disease. Secondly, the genetic underpinning of model disease-linked phenotypes has been characterized for a number of neurodegenerative disorders. The current challenge is to integrate our understanding of disease-linked processes in the fly with our growing knowledge of human disease, for the benefit of patients.


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