Draft Genome Sequence of Pseudomonas aeruginosa ATCC 9027, Originally Isolated from an Outer Ear Infection

ABSTRACT Pseudomonas aeruginosa ATCC 9027 was isolated in 1943 from a case of otitis externa and is commonly employed as a quality control strain for sterility, assessment of antibiofilm agents, and in vitro study of wound infection. Here, we present the 6.34-Mb draft genome sequence and highlight some pertinent genes that are associated with virulence.

P seudomonas aeruginosa ATCC 9027 was originally isolated from a case of otitis externa and is used as a quality control organism (https://www.lgcstandards-atcc .org/Products/Cells_and_Microorganisms/Bacteria.aspx). Despite its origin as a skin pathogen, this strain has been regarded as avirulent and has been utilized to produce rhamnolipid surfactants (1,2). Nonetheless, P. aeruginosa ATCC 9027 has been used extensively to study wound infection in vitro, because it is an excellent biofilm former (3). P. aeruginosa ATCC 9027 is closely related to PA7, a taxonomic outlier which exhibits numerous multidrug resistance mechanisms (4). PA7 lacks several factors associated with virulence, including a 36-gene cluster encoding the type III secretory system (5).
Genomic DNA derived from a biofilm of P. aeruginosa ATCC 9027 was purified using the GenElute bacterial genomic DNA extraction kit (Sigma-Aldrich). The sample library was prepared using an Illumina Nextera XT before DNA sequencing using an Illumina MiSeq system. The genomic data were transferred to and stored in Illumina BaseSpace. The raw reads were processed for quality using Trimmomatic version 0.36 (6) and quality reports generated using FastQC (7). A 6,340,907-bp assembly with 126-fold coverage was constructed using SPAdes version 3.8 (8) and run remotely using Cloud Infrastructure for Microbial Bioinformatics (CLIMB) (9,10). Quality assessment of assembly was done using QUAST (11). The assembly consists of 53 contigs (500 bp or more) with a mean GϩC content of 66.65%. The N 50 and N 75 values of the assembly were 290,774 bp and 197,962 bp, respectively. The L 50 and L 75 values of the assembly were 8 and 15, respectively. The annotation was performed with the NCBI Prokaryotic Genome Annotation Pipeline (http://www.ncbi.nlm.nih.gov/genome/annotation_prok), which predicted a total of 5,841 protein-coding genes and 58 tRNAs.

Accession number(s).
This whole-genome shotgun project has been deposited at DDBJ/ENA/GenBank under the accession number PDLX00000000. The version described in this paper is version PDLX01000000. Unassembled reads are also available from the NCBI Sequence Read Archive (SRA) under the accession number SRP120030.

ACKNOWLEDGMENTS
This study was funded by a Cardiff Metropolitan University Research Innovation Award to S.E.M. This study has also used many resources from the Cloud Infrastructure for Microbial Bioinformatics (CLIMB) project, which is funded by UK's Medical Research Council and provides free cloud-based computing resources for analyzing microbial genomics data.
We gratefully acknowledge Lesley Ward and University of Warwick for performing Illumina MiSeq sequencing. We gratefully acknowledge the support provided by the CLIMB project and would like to thank the team managing and funding the CLIMB project.