Comparative genomics and transcriptomics of trait-gene association

<p>Abstract</p> <p>Background</p> <p>The Order <it>Rickettsiales</it> includes important tick-borne pathogens, from <it>Rickettsia rickettsii</it>, which causes Rocky Mountain spotted fever, to <it>Anaplasma marginale</it>, the most p...

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Main Authors: Pierlé Sebastián, Dark Michael J, Dahmen Dani, Palmer Guy H, Brayton Kelly A
Format: Article
Language:English
Published: BMC 2012-11-01
Series:BMC Genomics
Subjects:
Online Access:http://www.biomedcentral.com/1471-2164/13/669
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author Pierlé Sebastián
Dark Michael J
Dahmen Dani
Palmer Guy H
Brayton Kelly A
author_facet Pierlé Sebastián
Dark Michael J
Dahmen Dani
Palmer Guy H
Brayton Kelly A
author_sort Pierlé Sebastián
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>The Order <it>Rickettsiales</it> includes important tick-borne pathogens, from <it>Rickettsia rickettsii</it>, which causes Rocky Mountain spotted fever, to <it>Anaplasma marginale</it>, the most prevalent vector-borne pathogen of cattle. Although most pathogens in this Order are transmitted by arthropod vectors, little is known about the microbial determinants of transmission. <it>A. marginale</it> provides unique tools for studying the determinants of transmission, with multiple strain sequences available that display distinct and reproducible transmission phenotypes. The closed core <it>A. marginale</it> genome suggests that any phenotypic differences are due to single nucleotide polymorphisms (SNPs). We combined DNA/RNA comparative genomic approaches using strains with different tick transmission phenotypes and identified genes that segregate with transmissibility.</p> <p>Results</p> <p>Comparison of seven strains with different transmission phenotypes generated a list of SNPs affecting 18 genes and nine promoters. Transcriptional analysis found two candidate genes downstream from promoter SNPs that were differentially transcribed. To corroborate the comparative genomics approach we used three RNA-seq platforms to analyze the transcriptomes from two <it>A. marginale</it> strains with different transmission phenotypes. RNA-seq analysis confirmed the comparative genomics data and found 10 additional genes whose transcription between strains with distinct transmission efficiencies was significantly different. Six regions of the genome that contained no annotation were found to be transcriptionally active, and two of these newly identified transcripts were differentially transcribed.</p> <p>Conclusions</p> <p>This approach identified 30 genes and two novel transcripts potentially involved in tick transmission. We describe the transcriptome of an obligate intracellular bacterium in depth, while employing massive parallel sequencing to dissect an important trait in bacterial pathogenesis.</p>
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spelling doaj.art-c1398e0189c34a7f8088b691fc465dd12022-12-21T20:56:26ZengBMCBMC Genomics1471-21642012-11-0113166910.1186/1471-2164-13-669Comparative genomics and transcriptomics of trait-gene associationPierlé SebastiánDark Michael JDahmen DaniPalmer Guy HBrayton Kelly A<p>Abstract</p> <p>Background</p> <p>The Order <it>Rickettsiales</it> includes important tick-borne pathogens, from <it>Rickettsia rickettsii</it>, which causes Rocky Mountain spotted fever, to <it>Anaplasma marginale</it>, the most prevalent vector-borne pathogen of cattle. Although most pathogens in this Order are transmitted by arthropod vectors, little is known about the microbial determinants of transmission. <it>A. marginale</it> provides unique tools for studying the determinants of transmission, with multiple strain sequences available that display distinct and reproducible transmission phenotypes. The closed core <it>A. marginale</it> genome suggests that any phenotypic differences are due to single nucleotide polymorphisms (SNPs). We combined DNA/RNA comparative genomic approaches using strains with different tick transmission phenotypes and identified genes that segregate with transmissibility.</p> <p>Results</p> <p>Comparison of seven strains with different transmission phenotypes generated a list of SNPs affecting 18 genes and nine promoters. Transcriptional analysis found two candidate genes downstream from promoter SNPs that were differentially transcribed. To corroborate the comparative genomics approach we used three RNA-seq platforms to analyze the transcriptomes from two <it>A. marginale</it> strains with different transmission phenotypes. RNA-seq analysis confirmed the comparative genomics data and found 10 additional genes whose transcription between strains with distinct transmission efficiencies was significantly different. Six regions of the genome that contained no annotation were found to be transcriptionally active, and two of these newly identified transcripts were differentially transcribed.</p> <p>Conclusions</p> <p>This approach identified 30 genes and two novel transcripts potentially involved in tick transmission. We describe the transcriptome of an obligate intracellular bacterium in depth, while employing massive parallel sequencing to dissect an important trait in bacterial pathogenesis.</p>http://www.biomedcentral.com/1471-2164/13/669BacteriaRickettsiaSNPRNA-seqAnaplasma
spellingShingle Pierlé Sebastián
Dark Michael J
Dahmen Dani
Palmer Guy H
Brayton Kelly A
Comparative genomics and transcriptomics of trait-gene association
BMC Genomics
Bacteria
Rickettsia
SNP
RNA-seq
Anaplasma
title Comparative genomics and transcriptomics of trait-gene association
title_full Comparative genomics and transcriptomics of trait-gene association
title_fullStr Comparative genomics and transcriptomics of trait-gene association
title_full_unstemmed Comparative genomics and transcriptomics of trait-gene association
title_short Comparative genomics and transcriptomics of trait-gene association
title_sort comparative genomics and transcriptomics of trait gene association
topic Bacteria
Rickettsia
SNP
RNA-seq
Anaplasma
url http://www.biomedcentral.com/1471-2164/13/669
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AT darkmichaelj comparativegenomicsandtranscriptomicsoftraitgeneassociation
AT dahmendani comparativegenomicsandtranscriptomicsoftraitgeneassociation
AT palmerguyh comparativegenomicsandtranscriptomicsoftraitgeneassociation
AT braytonkellya comparativegenomicsandtranscriptomicsoftraitgeneassociation