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. 2019 Jul 11;8(28):e00502-19. doi: 10.1128/MRA.00502-19

Draft Genomic Sequence of Multidrug-Resistant Klebsiella pneumoniae B8S35, Isolated from Retail Chicken Skin

Aixia Xu a, William Mackay b, Christopher H Sommers a,✉
Editor: David Raskoc
PMCID: PMC6624762  PMID: 31296679

Here, we report the draft genome sequence of Klebsiella pneumoniae strain B8S35, isolated from retail chicken skin. It carries genes for resistance to multiple antibiotics, as well as quaternary ammonium compounds used by the food and health care industries.

ABSTRACT

Here, we report the draft genome sequence of Klebsiella pneumoniae strain B8S35, isolated from retail chicken skin. It carries genes for resistance to multiple antibiotics, as well as quaternary ammonium compounds used by the food and health care industries.

ANNOUNCEMENT

Klebsiella pneumoniae is involved with gastrointestinal and extraintestinal diseases, including Crohn’s disease, sepsis, arthritis, and urinary tract infection (UTI) (1–5). K. pneumoniae is a common contaminant in retail meat (6). We report the draft genomic sequence of a K. pneumoniae strain isolated from retail chicken skin that is resistant to multiple antimicrobials.

B8S35 was isolated from chicken skin samples using the Food Safety and Inspection Service (FSIS) microbiology laboratory method (7). B8S35 was streaked onto a Trypticase soy agar (TSA) plate and incubated at 37°C for 24 h. DNA was isolated from a single colony scraped from the TSA plate. Genomic DNA was extracted using the DNeasy blood and tissue kit (Qiagen, Hilden, Germany) and quantified with a Qubit 3.0 fluorimeter (Life Technologies, Carlsbad, CA, USA). The genomic DNA library was prepared using the Nextera DNA flex library prep kit (Illumina, San Diego, CA, USA). Libraries were analyzed for concentration, pooled, and denatured for loading onto a flow cell for cluster generation. Denatured libraries were sequenced on an Illumina MiniSeq platform. A total of 8,153,078 sequencing reads using 150-bp paired-end sequencing were obtained.

Read quality was assessed with FastQC version 1.0.0 (Illumina BaseSpace Labs). The genome was assembled de novo using SPAdes (version 3.9.0), and 153 contigs (423-fold coverage) were obtained. Default parameters were used for all software unless otherwise specified. The B8S35 genome characteristics were as follows: genome size, 5,787,326 bp; N50, 172,984 bp; GC content, 56.74%; number of coding genes, 5,661; number of pseudogenes, 205; number of RNA genes, 120; number of rRNAs, 19; number of tRNAs, 88; number of noncoding RNAs (ncRNAs), 13; multilocus sequence type (MLST), ST37; and plasmid-MLST, K-:A10-like:B-, IncF. These characteristics were determined using the Bacterial Analysis Pipeline (version 1.0.4) and the NCBI Prokaryotic Genome Annotation Pipeline (PGAP; version 4.3). Based on the sequencing data, the strain was identified as Klebsiella pneumoniae using the Bacterial Analysis Pipeline.

K. pneumoniae ST37 is of clinical importance (6). The virulence factors of B8S35 include the BrkB superfamily protein, serine protease, type 1 fimbrial protein, capsule assembly protein Wzi, an iron-siderophore ABC transporter substrate-binding protein, and the CbtA toxin. The antimicrobial resistance of B8S35 includes fosfomycin (fosA), fluoroquinolones (oqxA and oqxB), tetracycline (tetD), beta-lactam (blaSHV-11), phenicol (catA2), and quaternary ammonium compound resistance (sugE). Decreasing the populations of K. pneumoniae in foods could lessen the risk of disease for at-risk populations.

Data availability.

This whole-genome shotgun project has been deposited in DDBJ/ENA/GenBank under BioProject number PRJNA474898 and accession number QKRJ00000000. The raw reads are available in the Sequence Read Archive (SRA) under accession number SRR8187417. The versions described in this paper are the first versions.

ACKNOWLEDGMENTS

This work was supported primarily by the U.S. Department of Agriculture (USDA) Agricultural Research Service National Program Project number 108 Food Safety Project 8072-42000-078-00D.

The mention of brand names, manufacturers, or trademarks is not considered an endorsement by the USDA.

We thank O. Joseph Scullen for technical assistance.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

This whole-genome shotgun project has been deposited in DDBJ/ENA/GenBank under BioProject number PRJNA474898 and accession number QKRJ00000000. The raw reads are available in the Sequence Read Archive (SRA) under accession number SRR8187417. The versions described in this paper are the first versions.


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