Abstract
Pseudomonas strain WCHP16 recovered from hospital sewage in West China Hospital, Chengdu, China was found to carry two carbapenemase genes blaIMP-25 and blaVIM-2. Here, we report its 5.7-Mb draft genome sequence, comprising 141 contigs and an average 59.53% G+C content. The genome contained 5,504 coding sequences and 67 tRNA genes.
GENOME ANNOUNCEMENT
The genus Pseudomonas comprises 231 species (http://www.bacterio.net/pseudomonas.html), many of which are important opportunistic pathogens for plants and animals. Pseudomonas sp. strain WCHP16 was recovered from the influx mainstream of the wastewater treatment plant in West China Hospital, Chengdu, western China, in January 2015. Strain WCHP16 exhibited high-level resistance to meropenem (MIC, >512 µg/ml). Screening for acquired carbapenem-hydrolyzing β-lactamase (carbapenemase) genes blaGES (including noncarbapenemase variants), blaIMP, blaIMI, blaKPC, blaNDM, blaOXA-48-like, and blaVIM was performed using PCR as described previously (1–4). Strain WCHP16 was positive to both blaIMP and blaVIM and was therefore subjected to whole-genome sequencing.
Genomic DNA of strain WCHP16 was prepared using the QIAamp DNA minikit (Qiagen, Hilden, Germany) and then was sequenced using the Hiseq 2500 Sequencer (Illumina, San Diego, CA, USA) with the 150-bp paired-end protocol and 100× coverage. A total of 4,244,316 reads and 636,647,400 clean bases were generated. The Spades program (version 2.8) (5) was used for de novo assembly and generated 141 contigs ≥1,000 bp in length (N50, 111,079 bp) with a 59.53% G+C content. The genome size was about 5.7 Mb. Annotation of the genomic sequence was carried out using the Prokka program (version 1.11) (6). The genome of strain WCHP16 contained 5,504 coding sequences and 67 tRNA genes. Antimicrobial resistance genes were predicted using ResFinder from the Center for Genomic Epidemiology (http://genomicepidemiology.org/). Strain WCHP16 had two carbapenemase genes, i.e., blaIMP-25 and blaVIM-2. blaIMP-25 was a variant of blaIMP-1 and was first found in a Pseudomonas aeruginosa from South Korea (GenBank accession number EU541448). blaIMP-25 was rarely reported and had only been identified in P. aeruginosa in China and South Korea before (7). Furthermore, to our knowledge, the co-existence of blaIMP-25 and blaVIM-2 in a single strain has not been reported before.
Other antimicrobial resistance genes identified in strain WCHP16 included aacA4 (mediating resistance to aminoglycosides), arr-2 (to rifampin), blaOXA-1 (to penicillins), catB3 (to phenicol), dfrA22 and dfrB1 (to trimethoprim), qnrVC1 (to quinolones), and sul1 (to sulfonamides).
The 16S rRNA gene sequence of strain WCHP16 had the highest identity with those of Pseudomonas sp. 5 (GenBank accession number NZ_JYOC00000000; 99.48% identity), Pseudomonas putida UASWS0946 (NZ_JXOG00000000; 99.35% identity), and Pseudomonas sp. NBRC 111117 (NZ_BCAT00000000; 99.35% identity).
Average nucleotide identity (ANI) has been increasingly employed to determine bacterial species and the ≥95% ANI cutoff has been proposed to define Pseudomonas species (8, 9) previously. The ≥95% ANI cutoff corresponds to the ≥70% DNA-DNA hybridization value for defining a bacterial species (10). Pair-wise ANI between strain WCHP16 and the three Pseudomonas strains was therefore determined using the JSpecies web program (http://imedea.uib-csic.es/jspecies/) with the default settings (11). The genome of strain WCHP16 shared only 79.99% to 81.06% ANI with the three Pseudomonas strains, which were far below the ≥95% ANI cutoff. The ANI results suggest that strain WCHP16 is likely to belong to a new species of the Pseudomonas genus.
Accession number(s).
This whole-genome shotgun project has been deposited at DDBJ/EMBL/GenBank under the accession number MBPN00000000. The version described in this paper is the first version, MBPN01000000.
ACKNOWLEDGMENTS
The work was supported by grants from the National Natural Science Foundation of China (project no. 81222025 and 81572030).
Funding Statement
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
Footnotes
Citation Hu Y, Wu W, Feng Y, Zhang X, Zong Z. 2016. Draft genome sequence of a Pseudomonas sp. strain carrying blaIMP-25 and blaVIM-2 carbapenemase genes from hospital sewage. Genome Announc 4(5):e01027-16. doi:10.1128/genomeA.01027-16.
REFERENCES
- 1.Zong Z, Zhang X. 2013. blaNDM-1-carrying Acinetobacter johnsonii detected in hospital sewage. J Antimicrob Chemother 68:1007–1010. doi: 10.1093/jac/dks505. [DOI] [PubMed] [Google Scholar]
- 2.Mendes RE, Kiyota KA, Monteiro J, Castanheira M, Andrade SS, Gales AC, Pignatari AC, Tufik S. 2007. Rapid detection and identification of metallo-β-lactamase-encoding genes by multiplex real-time PCR assay and melt curve analysis. J Clin Microbiol 45:544–547. doi: 10.1128/JCM.01728-06. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Poirel L, Le Thomas I, Naas T, Karim A, Nordmann P. 2000. Biochemical sequence analyses of GES-1, a novel class A extended-spectrum β-lactamase, and the class 1 integron In52 from Klebsiella pneumoniae. Antimicrob Agents Chemother 44:622–632. doi: 10.1128/AAC.44.3.622-632.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Bradford PA, Bratu S, Urban C, Visalli M, Mariano N, Landman D, Rahal JJ, Brooks S, Cebular S, Quale J. 2004. Emergence of carbapenem-resistant Klebsiella species possessing the class A carbapenem-hydrolyzing KPC-2 and inhibitor-resistant TEM-30 β-lactamases in New York City. Clin Infect Dis 39:55–60. doi: 10.1086/421495. [DOI] [PubMed] [Google Scholar]
- 5.Bankevich A, Nurk S, Antipov D, Gurevich AA, Dvorkin M, Kulikov AS, Lesin VM, Nikolenko SI, Pham S, Prjibelski AD, Pyshkin AV, Sirotkin AV, Vyahhi N, Tesler G, Alekseyev MA, Pevzner PA. 2012. SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. J Comput Biol 19:455–477. doi: 10.1089/cmb.2012.0021. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Seemann T. 2014. Prokka: rapid prokaryotic genome annotation. BioInformatics 30:2068–2069. doi: 10.1093/bioinformatics/btu153. [DOI] [PubMed] [Google Scholar]
- 7.Yu G, Wen W, Peters BM, Liu J, Ye C, Che Y, Liu J, Cao K, Xu Z, Shirtliff ME. 2016. First report of novel genetic array aacA4-blaIMP-25-oxa30-catB3 and identification of novel metallo-β-lactamase gene blaIMP-25: A retrospective study of antibiotic resistance surveillance on Psuedomonas aeruginosa in Guangzhou of South China, 2003–2007. Microb Pathog 95:62–67. doi: 10.1016/j.micpath.2016.02.021. [DOI] [PubMed] [Google Scholar]
- 8.Scortichini M, Marcelletti S, Ferrante P, Firrao G. 2013. A genomic redefinition of Pseudomonas avellanae species. PLoS One 8:e75794. doi: 10.1371/journal.pone.0075794. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Marcelletti S, Scortichini M. 2014. Definition of plant-pathogenic Pseudomonas genomospecies of the Pseudomonas syringae complex through multiple comparative approaches. Phytopathology 104:1274–1282. doi: 10.1094/PHYTO-12-13-0344-R. [DOI] [PubMed] [Google Scholar]
- 10.Goris J, Konstantinidis KT, Klappenbach JA, Coenye T, Vandamme P, Tiedje JM. 2007. DNA-DNA hybridization values and their relationship to whole-genome sequence similarities. Int J Syst Evol Microbiol 57:81–91. doi: 10.1099/ijs.0.64483-0. [DOI] [PubMed] [Google Scholar]
- 11.Richter M, Rosselló-Móra R. 2009. Shifting the genomic gold standard for the prokaryotic species definition. Proc Natl Acad Sci U S A 106:19126–19131. doi: 10.1073/pnas.0906412106. [DOI] [PMC free article] [PubMed] [Google Scholar]