African relapsing fever borreliae genomospecies revealed by comparative genomics

Background:<br/>Relapsing fever borreliae are vector-borne bacteria responsible for febrile infection in humans in North America, Africa, Asia and in the Iberian Peninsula in Europe. Relapsing fever borreliae are phylogenetically closely related, yet they differ in pathogenicity and vectors. T...

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Main Authors: Haitham eElbir, Laurent eAbi-Rached, Pierre ePontarotti, Niayz eYoosuf, Michel eDRANCOURT
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-05-01
Series:Frontiers in Public Health
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fpubh.2014.00043/full
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spelling doaj-89d44cba0afb40f7b77f96e800c631692020-11-24T20:45:12ZengFrontiers Media S.A.Frontiers in Public Health2296-25652014-05-01210.3389/fpubh.2014.0004388982African relapsing fever borreliae genomospecies revealed by comparative genomicsHaitham eElbir0Laurent eAbi-Rached1Pierre ePontarotti2Niayz eYoosuf3Michel eDRANCOURT4Aix Marseille UniversitéAix Marseille UniversitéAix Marseille UniversitéAix Marseille UniversitéAix Marseille UniversitéBackground:<br/>Relapsing fever borreliae are vector-borne bacteria responsible for febrile infection in humans in North America, Africa, Asia and in the Iberian Peninsula in Europe. Relapsing fever borreliae are phylogenetically closely related, yet they differ in pathogenicity and vectors. Their long-term taxonomy, based on geography and vector grouping, needs a re-appraisal in the genomic area. We therefore embarked into genomic analyses of relapsing fever borreliae, focusing on species found in Africa. <br/><br/>Results:<br/>Genome-wide phylogenetic analyses group Old World Borrelia crocidurae, Borrelia hispanica, B. duttonii and B. recurrentis in one clade, and New World Borrelia turicatae and Borrelia hermsii in a second clade. Accordingly, average nucleotide identity is 99% among B. duttonii, B. recurrentis and B. crocidurae and 96% between latter borreliae and B. hispanica while the similarity is 86% between Old World and New World borreliae. Comparative genomics indicates that the Old World relapsing fever B. duttonii, B. recurrentis, B. crocidurae and B. hispanica have a 2,514-gene pan-genome and a 933-gene core genome that includes 788 chromosomal and 145 plasmidic genes. Analysing the role that natural selection has played in the evolution of Old World borreliae species revealed that 55 loci were under positive diversifying selection, including loci coding for membrane, flagellar and chemotaxis proteins, three categories associated with adaption to specific niches. <br/> <br/>Conclusions:<br/>Genomic analyses led to a reappraisal of the taxonomy of relapsing fever borreliae in Africa. These analyses suggest that B. crocidurae, B. duttonii and B. recurrentis are ecotypes of a unique genomospecies, while B. hispanica is a distinct species. <br/>http://journal.frontiersin.org/Journal/10.3389/fpubh.2014.00043/fullBorreliaGenomicsRelapsing Feverphylogenyspeciation
collection DOAJ
language English
format Article
sources DOAJ
author Haitham eElbir
Laurent eAbi-Rached
Pierre ePontarotti
Niayz eYoosuf
Michel eDRANCOURT
spellingShingle Haitham eElbir
Laurent eAbi-Rached
Pierre ePontarotti
Niayz eYoosuf
Michel eDRANCOURT
African relapsing fever borreliae genomospecies revealed by comparative genomics
Frontiers in Public Health
Borrelia
Genomics
Relapsing Fever
phylogeny
speciation
author_facet Haitham eElbir
Laurent eAbi-Rached
Pierre ePontarotti
Niayz eYoosuf
Michel eDRANCOURT
author_sort Haitham eElbir
title African relapsing fever borreliae genomospecies revealed by comparative genomics
title_short African relapsing fever borreliae genomospecies revealed by comparative genomics
title_full African relapsing fever borreliae genomospecies revealed by comparative genomics
title_fullStr African relapsing fever borreliae genomospecies revealed by comparative genomics
title_full_unstemmed African relapsing fever borreliae genomospecies revealed by comparative genomics
title_sort african relapsing fever borreliae genomospecies revealed by comparative genomics
publisher Frontiers Media S.A.
series Frontiers in Public Health
issn 2296-2565
publishDate 2014-05-01
description Background:<br/>Relapsing fever borreliae are vector-borne bacteria responsible for febrile infection in humans in North America, Africa, Asia and in the Iberian Peninsula in Europe. Relapsing fever borreliae are phylogenetically closely related, yet they differ in pathogenicity and vectors. Their long-term taxonomy, based on geography and vector grouping, needs a re-appraisal in the genomic area. We therefore embarked into genomic analyses of relapsing fever borreliae, focusing on species found in Africa. <br/><br/>Results:<br/>Genome-wide phylogenetic analyses group Old World Borrelia crocidurae, Borrelia hispanica, B. duttonii and B. recurrentis in one clade, and New World Borrelia turicatae and Borrelia hermsii in a second clade. Accordingly, average nucleotide identity is 99% among B. duttonii, B. recurrentis and B. crocidurae and 96% between latter borreliae and B. hispanica while the similarity is 86% between Old World and New World borreliae. Comparative genomics indicates that the Old World relapsing fever B. duttonii, B. recurrentis, B. crocidurae and B. hispanica have a 2,514-gene pan-genome and a 933-gene core genome that includes 788 chromosomal and 145 plasmidic genes. Analysing the role that natural selection has played in the evolution of Old World borreliae species revealed that 55 loci were under positive diversifying selection, including loci coding for membrane, flagellar and chemotaxis proteins, three categories associated with adaption to specific niches. <br/> <br/>Conclusions:<br/>Genomic analyses led to a reappraisal of the taxonomy of relapsing fever borreliae in Africa. These analyses suggest that B. crocidurae, B. duttonii and B. recurrentis are ecotypes of a unique genomospecies, while B. hispanica is a distinct species. <br/>
topic Borrelia
Genomics
Relapsing Fever
phylogeny
speciation
url http://journal.frontiersin.org/Journal/10.3389/fpubh.2014.00043/full
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