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Comparative genomics of Riemerella anatipestifer reveals genetic diversity
BACKGROUND: Riemerella anatipestifer is one of the most important pathogens of ducks. However, the molecular mechanisms of R. anatipestifer infection are poorly understood. In particular, the lack of genomic information from a variety of R. anatipestifer strains has proved severely limiting. RESULTS...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103989/ https://www.ncbi.nlm.nih.gov/pubmed/24935762 http://dx.doi.org/10.1186/1471-2164-15-479 |
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author | Wang, Xiaojia Liu, Wenbin Zhu, Dekang Yang, LinFeng Liu, MaFeng Yin, Sanjun Wang, MingShu Jia, RenYong Chen, Shun Sun, KunFeng Cheng, Anchun Chen, Xiaoyue |
author_facet | Wang, Xiaojia Liu, Wenbin Zhu, Dekang Yang, LinFeng Liu, MaFeng Yin, Sanjun Wang, MingShu Jia, RenYong Chen, Shun Sun, KunFeng Cheng, Anchun Chen, Xiaoyue |
author_sort | Wang, Xiaojia |
collection | PubMed |
description | BACKGROUND: Riemerella anatipestifer is one of the most important pathogens of ducks. However, the molecular mechanisms of R. anatipestifer infection are poorly understood. In particular, the lack of genomic information from a variety of R. anatipestifer strains has proved severely limiting. RESULTS: In this study, we present the complete genomes of two R. anatipestifer strains, RA-CH-1 (2,309,519 bp, Genbank accession CP003787) and RA-CH-2 (2,166,321 bp, Genbank accession CP004020). Both strains are from isolates taken from two different sick ducks in the SiChuang province of China. A comparative genomics approach was used to identify similarities and key differences between RA-CH-1 and RA-CH-2 and the previously sequenced strain RA-GD, a clinical isolate from GuangDong, China, and ATCC11845. CONCLUSION: The genomes of RA-CH-2 and RA-GD were extremely similar, while RA-CH-1 was significantly different than ATCC11845. RA-CH-1 is 140,000 bp larger than the three other strains and has 16 unique gene families. Evolutionary analysis shows that RA-CH-1 and RA-CH-2 are closed and in a branch with ATCC11845, while RA-GD is located in another branch. Additionally, the detection of several iron/heme-transport related proteins and motility mechanisms will be useful in elucidating factors important in pathogenicity. This information will allow a better understanding of the phenotype of different R. anatipestifer strains and molecular mechanisms of infection. |
format | Online Article Text |
id | pubmed-4103989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41039892014-07-30 Comparative genomics of Riemerella anatipestifer reveals genetic diversity Wang, Xiaojia Liu, Wenbin Zhu, Dekang Yang, LinFeng Liu, MaFeng Yin, Sanjun Wang, MingShu Jia, RenYong Chen, Shun Sun, KunFeng Cheng, Anchun Chen, Xiaoyue BMC Genomics Research Article BACKGROUND: Riemerella anatipestifer is one of the most important pathogens of ducks. However, the molecular mechanisms of R. anatipestifer infection are poorly understood. In particular, the lack of genomic information from a variety of R. anatipestifer strains has proved severely limiting. RESULTS: In this study, we present the complete genomes of two R. anatipestifer strains, RA-CH-1 (2,309,519 bp, Genbank accession CP003787) and RA-CH-2 (2,166,321 bp, Genbank accession CP004020). Both strains are from isolates taken from two different sick ducks in the SiChuang province of China. A comparative genomics approach was used to identify similarities and key differences between RA-CH-1 and RA-CH-2 and the previously sequenced strain RA-GD, a clinical isolate from GuangDong, China, and ATCC11845. CONCLUSION: The genomes of RA-CH-2 and RA-GD were extremely similar, while RA-CH-1 was significantly different than ATCC11845. RA-CH-1 is 140,000 bp larger than the three other strains and has 16 unique gene families. Evolutionary analysis shows that RA-CH-1 and RA-CH-2 are closed and in a branch with ATCC11845, while RA-GD is located in another branch. Additionally, the detection of several iron/heme-transport related proteins and motility mechanisms will be useful in elucidating factors important in pathogenicity. This information will allow a better understanding of the phenotype of different R. anatipestifer strains and molecular mechanisms of infection. BioMed Central 2014-06-17 /pmc/articles/PMC4103989/ /pubmed/24935762 http://dx.doi.org/10.1186/1471-2164-15-479 Text en © Wang et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Wang, Xiaojia Liu, Wenbin Zhu, Dekang Yang, LinFeng Liu, MaFeng Yin, Sanjun Wang, MingShu Jia, RenYong Chen, Shun Sun, KunFeng Cheng, Anchun Chen, Xiaoyue Comparative genomics of Riemerella anatipestifer reveals genetic diversity |
title | Comparative genomics of Riemerella anatipestifer reveals genetic diversity |
title_full | Comparative genomics of Riemerella anatipestifer reveals genetic diversity |
title_fullStr | Comparative genomics of Riemerella anatipestifer reveals genetic diversity |
title_full_unstemmed | Comparative genomics of Riemerella anatipestifer reveals genetic diversity |
title_short | Comparative genomics of Riemerella anatipestifer reveals genetic diversity |
title_sort | comparative genomics of riemerella anatipestifer reveals genetic diversity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103989/ https://www.ncbi.nlm.nih.gov/pubmed/24935762 http://dx.doi.org/10.1186/1471-2164-15-479 |
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