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Typing African Relapsing Fever Spirochetes

Relapsing fever Borrelia spp. challenge microbiologic typing because they possess segmented genomes that maintain essential genes on large linear plasmids. Antigenic variation further complicates typing. Intergenic spacer (IGS, between 16S–23S genes) heterogeneity provides resolution among Lyme dise...

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Detalles Bibliográficos
Autores principales: Scott, Julie Christine, Wright, David Julian Maurice, Cutler, Sally Jane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Centers for Disease Control and Prevention 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3367362/
https://www.ncbi.nlm.nih.gov/pubmed/16318724
http://dx.doi.org/10.3201/eid1111.050483
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author Scott, Julie Christine
Wright, David Julian Maurice
Cutler, Sally Jane
author_facet Scott, Julie Christine
Wright, David Julian Maurice
Cutler, Sally Jane
author_sort Scott, Julie Christine
collection PubMed
description Relapsing fever Borrelia spp. challenge microbiologic typing because they possess segmented genomes that maintain essential genes on large linear plasmids. Antigenic variation further complicates typing. Intergenic spacer (IGS, between 16S–23S genes) heterogeneity provides resolution among Lyme disease–associated and some relapsing fever spirochetes. We used an IGS fragment for typing East African relapsing fever Borrelia spp. Borrelia recurrentis and their louse vectors showed 2 sequence types, while 4 B. duttonii and their tick vectors had 4 types. IGS typing was unable to discriminate between the tick- and louseborne forms of disease. B. crocidurae, also present in Africa, was clearly resolved from the B. recurrentis/B. duttonii complex. IGS analysis of ticks showed relapsing fever Borrelia spp. and a unique clade, distant from those associated with relapsing fever, possibly equivalent to a novel species in ticks from this region. Clinical significance of this spirochete is undetermined.
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spelling pubmed-33673622012-06-07 Typing African Relapsing Fever Spirochetes Scott, Julie Christine Wright, David Julian Maurice Cutler, Sally Jane Emerg Infect Dis Research Relapsing fever Borrelia spp. challenge microbiologic typing because they possess segmented genomes that maintain essential genes on large linear plasmids. Antigenic variation further complicates typing. Intergenic spacer (IGS, between 16S–23S genes) heterogeneity provides resolution among Lyme disease–associated and some relapsing fever spirochetes. We used an IGS fragment for typing East African relapsing fever Borrelia spp. Borrelia recurrentis and their louse vectors showed 2 sequence types, while 4 B. duttonii and their tick vectors had 4 types. IGS typing was unable to discriminate between the tick- and louseborne forms of disease. B. crocidurae, also present in Africa, was clearly resolved from the B. recurrentis/B. duttonii complex. IGS analysis of ticks showed relapsing fever Borrelia spp. and a unique clade, distant from those associated with relapsing fever, possibly equivalent to a novel species in ticks from this region. Clinical significance of this spirochete is undetermined. Centers for Disease Control and Prevention 2005-11 /pmc/articles/PMC3367362/ /pubmed/16318724 http://dx.doi.org/10.3201/eid1111.050483 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited.
spellingShingle Research
Scott, Julie Christine
Wright, David Julian Maurice
Cutler, Sally Jane
Typing African Relapsing Fever Spirochetes
title Typing African Relapsing Fever Spirochetes
title_full Typing African Relapsing Fever Spirochetes
title_fullStr Typing African Relapsing Fever Spirochetes
title_full_unstemmed Typing African Relapsing Fever Spirochetes
title_short Typing African Relapsing Fever Spirochetes
title_sort typing african relapsing fever spirochetes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3367362/
https://www.ncbi.nlm.nih.gov/pubmed/16318724
http://dx.doi.org/10.3201/eid1111.050483
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