Back to Search
Start Over
Identifying the Genes Responsible for Iron-Limited Condition in Riemerella anatipestifer CH-1 through RNA-Seq-Based Analysis.
- Source :
-
BioMed research international [Biomed Res Int] 2017; Vol. 2017, pp. 8682057. Date of Electronic Publication: 2017 Apr 30. - Publication Year :
- 2017
-
Abstract
- One of the important elements for most bacterial growth is iron, the bioavailability of which is limited in hosts. Riemerella anatipestifer ( R. anatipestifer , RA), an important duck pathogen, requires iron to live. However, the genes involved in iron metabolism and the mechanisms of iron transport are largely unknown. Here, we investigated the transcriptomic effects of iron limitation condition on R. anatipestifer CH-1 using the RNA-Seq and RNA-Seq-based analysis. Data analysis revealed genes encoding functions related to iron homeostasis, including a number of putative TonB-dependent receptor systems, a HmuY-like protein-dependent hemin (an iron-containing porphyrin) uptake system, a Feo system, a gene cluster related to starch utilization, and genes encoding hypothetical proteins that were significantly upregulated in response to iron limitation. Compared to the number of upregulated genes, more genes were significantly downregulated in response to iron limitation. The downregulated genes mainly encoded a number of outer membrane receptors, DNA-binding proteins, phage-related proteins, and many hypothetical proteins. This information suggested that RNA-Seq-based analysis in iron-limited medium is an effective and fast method for identifying genes involved in iron uptake in R. anatipestifer CH-1.
- Subjects :
- Animals
Ducks microbiology
High-Throughput Nucleotide Sequencing
Iron Metabolism Disorders metabolism
Iron Metabolism Disorders microbiology
Poultry Diseases metabolism
Poultry Diseases microbiology
Riemerella metabolism
Riemerella pathogenicity
Iron metabolism
Iron Metabolism Disorders genetics
Riemerella genetics
Transcriptome genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2314-6141
- Volume :
- 2017
- Database :
- MEDLINE
- Journal :
- BioMed research international
- Publication Type :
- Academic Journal
- Accession number :
- 28540303
- Full Text :
- https://doi.org/10.1155/2017/8682057