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SRX1464764: GSM1964577: AB5075_LB; Acinetobacter baumannii AB5075; RNA-Seq
1 ION_TORRENT (Ion Torrent PGM) run: 4.3M spots, 526.8M bases, 415Mb downloads

Submitted by: NCBI (GEO)
Study: Towards the complete small RNome of Acinetobacter baumannii
show Abstracthide Abstract
In recent years, the Gram-negative bacterium Acinetobacter baumannii has garnered considerable attention for its unprecedented capacity to rapidly develop resistance to antibacterial therapeutics. This is coupled with the seemingly epidemic emergence of new hyper-virulent strains. Although strain-specific differences for A. baumannii isolates have been well described, these studies have primarily focused on proteinaceous factors. At present, only limited publications have investigated the presence and role of small regulatory RNA (sRNA) transcripts. Herein, we perform such an analysis, describing the RNA-seq-based identification of 78 A. baumannii sRNAs in the AB5075 background. Together with six previously identified elements, we include each of these in a new genome annotation file, which will serve as a tool to investigate regulatory events in this organism. Our work reveals that the sRNAs display high expression, accounting for >50 % of the 20 most strongly expressed genes. Through conservation analysis we identified six classes of similar sRNAs, with one found to be particularly abundant and homologous to regulatory, C4 antisense RNAs found in bacteriophages. These elements appear to be processed from larger transcripts in an analogous manner to the phage C4 molecule and are putatively controlled by two further sRNAs that are strongly antisense to them. Collectively, this study offers a detailed view of the sRNA content of A. baumannii, exposing sequence and structural conservation amongst these elements, and provides novel insight into the potential evolution, and role, of these understudied regulatory molecules. Overall design: This study is based on the annotation of novel sRNAs on basis of an Acinetobacter baumannii RNA sequencing dataset. Each sample was generated by pooling three independent biological replicate RNA preps
Sample: AB5075_LB
SAMN04317117 • SRS1191568 • All experiments • All runs
Library:
Instrument: Ion Torrent PGM
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Total bacterial RNA was isolated utilizing the Qiagen RNeasy mini kit and contaminating DNA was removed by treatment with Ambion DNA-free Library construction was performed using the Ion Total RNA-Seq v2 Kit from Life Technologies
Experiment attributes:
GEO Accession: GSM1964577
Links:
Runs: 1 run, 4.3M spots, 526.8M bases, 415Mb
Run# of Spots# of BasesSizePublished
SRR29754374,273,230526.8M415Mb2016-03-30

ID:
2069545

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