Multipartite Genome of Lyme Disease Borrelia: Structure, Variation and Prophages

Current Issues in Molecular Biology ◽

10.21775/cimb.042.409 ◽

2022 ◽

pp. 409-454

Author(s):

Ira Schwartz ◽

Gabriele Margos ◽

Sherwood R. Casjens ◽

Wei-Gang Qiu ◽

Christian H. Eggers

Keyword(s):

Lyme Disease ◽

Structure Variation

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Multipartite Genome of Lyme Disease Borrelia: Structure, Variation and Prophages

Lyme Disease and Relapsing Fever Spirochetes: Genomics, Molecular Biology, Host Interactions and Disease Pathogenesis ◽

10.21775/9781913652616.02 ◽

2021 ◽

Author(s):

Ira Schwartz ◽

Gabriele Margos ◽

Sherwood R. Casjens ◽

Wei-Gang Qiu ◽

Christian H. Eggers

Keyword(s):

Lyme Disease ◽

Structure Variation

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New ultrastructural findings about Borrelia burgdorferi by cryofixation, negative staining, thin sectioning and scanning techniques

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100160467 ◽

1990 ◽

Vol 48 (3) ◽

pp. 582-583

Author(s):

S. F. Hayes ◽

M. D. Corwin ◽

T. G. Schwan ◽

D. W. Dorward ◽

W. Burgdorfer

Keyword(s):

Lyme Disease ◽

Borrelia Burgdorferi ◽

Structural Characterization ◽

Negative Staining ◽

Low Speed ◽

Thin Sectioning ◽

Ultrastructural Findings

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.

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