Cargando…

Analysis of complete genome sequence of Neorickettsia risticii: causative agent of Potomac horse fever

Neorickettsia risticii is an obligate intracellular bacterium of the trematodes and mammals. Horses develop Potomac horse fever (PHF) when they ingest aquatic insects containing encysted N. risticii-infected trematodes. The complete genome sequence of N. risticii Illinois consists of a single circul...

Descripción completa

Detalles Bibliográficos
Autores principales: Lin, Mingqun, Zhang, Chunbin, Gibson, Kathryn, Rikihisa, Yasuko
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2764437/
https://www.ncbi.nlm.nih.gov/pubmed/19661282
http://dx.doi.org/10.1093/nar/gkp642
_version_ 1782173082834698240
author Lin, Mingqun
Zhang, Chunbin
Gibson, Kathryn
Rikihisa, Yasuko
author_facet Lin, Mingqun
Zhang, Chunbin
Gibson, Kathryn
Rikihisa, Yasuko
author_sort Lin, Mingqun
collection PubMed
description Neorickettsia risticii is an obligate intracellular bacterium of the trematodes and mammals. Horses develop Potomac horse fever (PHF) when they ingest aquatic insects containing encysted N. risticii-infected trematodes. The complete genome sequence of N. risticii Illinois consists of a single circular chromosome of 879 977 bp and encodes 38 RNA species and 898 proteins. Although N. risticii has limited ability to synthesize amino acids and lacks many metabolic pathways, it is capable of making major vitamins, cofactors and nucleotides. Comparison with its closely related human pathogen N. sennetsu showed that 758 (88.2%) of protein-coding genes are conserved between N. risticii and N. sennetsu. Four-way comparison of genes among N. risticii and other Anaplasmataceae showed that most genes are either shared among Anaplasmataceae (525 orthologs that generally associated with housekeeping functions), or specific to each genome (>200 genes that are mostly hypothetical proteins). Genes potentially involved in the pathogenesis of N. risticii were identified, including those encoding putative outer membrane proteins, two-component systems and a type IV secretion system (T4SS). The bipolar localization of T4SS pilus protein VirB2 on the bacterial surface was demonstrated for the first time in obligate intracellular bacteria. These data provide insights toward genomic potential of N. risticii and intracellular parasitism, and facilitate our understanding of PHF pathogenesis.
format Text
id pubmed-2764437
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-27644372009-10-20 Analysis of complete genome sequence of Neorickettsia risticii: causative agent of Potomac horse fever Lin, Mingqun Zhang, Chunbin Gibson, Kathryn Rikihisa, Yasuko Nucleic Acids Res Genomics Neorickettsia risticii is an obligate intracellular bacterium of the trematodes and mammals. Horses develop Potomac horse fever (PHF) when they ingest aquatic insects containing encysted N. risticii-infected trematodes. The complete genome sequence of N. risticii Illinois consists of a single circular chromosome of 879 977 bp and encodes 38 RNA species and 898 proteins. Although N. risticii has limited ability to synthesize amino acids and lacks many metabolic pathways, it is capable of making major vitamins, cofactors and nucleotides. Comparison with its closely related human pathogen N. sennetsu showed that 758 (88.2%) of protein-coding genes are conserved between N. risticii and N. sennetsu. Four-way comparison of genes among N. risticii and other Anaplasmataceae showed that most genes are either shared among Anaplasmataceae (525 orthologs that generally associated with housekeeping functions), or specific to each genome (>200 genes that are mostly hypothetical proteins). Genes potentially involved in the pathogenesis of N. risticii were identified, including those encoding putative outer membrane proteins, two-component systems and a type IV secretion system (T4SS). The bipolar localization of T4SS pilus protein VirB2 on the bacterial surface was demonstrated for the first time in obligate intracellular bacteria. These data provide insights toward genomic potential of N. risticii and intracellular parasitism, and facilitate our understanding of PHF pathogenesis. Oxford University Press 2009-10 2009-08-06 /pmc/articles/PMC2764437/ /pubmed/19661282 http://dx.doi.org/10.1093/nar/gkp642 Text en © 2009 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genomics
Lin, Mingqun
Zhang, Chunbin
Gibson, Kathryn
Rikihisa, Yasuko
Analysis of complete genome sequence of Neorickettsia risticii: causative agent of Potomac horse fever
title Analysis of complete genome sequence of Neorickettsia risticii: causative agent of Potomac horse fever
title_full Analysis of complete genome sequence of Neorickettsia risticii: causative agent of Potomac horse fever
title_fullStr Analysis of complete genome sequence of Neorickettsia risticii: causative agent of Potomac horse fever
title_full_unstemmed Analysis of complete genome sequence of Neorickettsia risticii: causative agent of Potomac horse fever
title_short Analysis of complete genome sequence of Neorickettsia risticii: causative agent of Potomac horse fever
title_sort analysis of complete genome sequence of neorickettsia risticii: causative agent of potomac horse fever
topic Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2764437/
https://www.ncbi.nlm.nih.gov/pubmed/19661282
http://dx.doi.org/10.1093/nar/gkp642
work_keys_str_mv AT linmingqun analysisofcompletegenomesequenceofneorickettsiaristiciicausativeagentofpotomachorsefever
AT zhangchunbin analysisofcompletegenomesequenceofneorickettsiaristiciicausativeagentofpotomachorsefever
AT gibsonkathryn analysisofcompletegenomesequenceofneorickettsiaristiciicausativeagentofpotomachorsefever
AT rikihisayasuko analysisofcompletegenomesequenceofneorickettsiaristiciicausativeagentofpotomachorsefever