Literature DB >> 25342679

Whole-Genome Yersinia sp. Assemblies from 10 Diverse Strains.

H E Daligault1, K W Davenport1, T D Minogue2, K A Bishop-Lilly, S M Broomall3, D C Bruce1, P S Chain1, S R Coyne2, K G Frey, H S Gibbons3, J Jaissle2, G I Koroleva4, J T Ladner4, C-C Lo1, C Munk1, G F Palacios4, C L Redden, C N Rosenzweig4, M B Scholz1, S L Johnson5.   

Abstract

Yersinia spp. are animal pathogens, some of which cause human disease. We sequenced 10 Yersinia isolates (from six species: Yersinia enterocolitica, Y. fredericksenii, Y. kristensenii, Y. pestis, Y. pseudotuberculosis, and Y. ruckeri) to high-quality draft or complete status. The genomes range in size from 3.77 to 4.94 Mbp.
Copyright © 2014 Daligault et al.

Entities:  

Year:  2014        PMID: 25342679      PMCID: PMC4208323          DOI: 10.1128/genomeA.01055-14

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Yersinia is a genus of Gram-negative facultative anaerobes belonging to the Enterobacteriaceae family, best known for its three main pathogens, Yersinia enterocolitica, Y. pestis, and Y. pseudotuberculosis. The genus was first described in 1894 by Alexandre Yersin (1), who isolated Y. pestis during the third plague pandemic. Generally, Yersinia spp. cause animal infections and humans are only incidental hosts (2). Y. enterocolitica and Y. pseudotuberculosis are both enteric pathogens while Y. pestis generally results in lymphadenitis (bubonic plague) and is derived from Y. pseudotuberculosis (2, 3). In this study, we sequenced and assembled 10 Yersinia strains, including 7 isolates of these 3 pathogenic species and 3 additional congeners. High-quality genomic DNA was extracted from purified isolates of each strain using a Qiagen Genomic-tip 500 at the USAMRIID Diagnostic Systems Division (DSD). Specifically, 100-mL bacterial cultures were grown to stationary phase and nucleic acid was extracted per the manufacturer’s recommendations with one minor variation. For BSL3 Yersinia pestis, all cultures were lysed overnight to ensure sterility of the resulting extracted material. If sterility was not achieved, the nucleic acid was passed through a 0.45-µM filter and rechecked for viable organisms before removal from the BSL3 suite. Sequence data for each draft genome were generated using a combination of Illumina and 454 technologies (4, 5). For each genome, we constructed and sequenced an Illumina library of 100-bp reads at high coverage (ranging from 119 to 733 bp) and a separate 454 library of long-insert paired-end reads (insert sizes ranging from 7.10 to 10.3 kb with 8- to 57-fold genome coverage). The two data sets were assembled together in Newbler (Roche) and the consensus sequences computationally shredded into 2-kbp overlapping fake reads (shreds). The raw reads were also assembled in Velvet and those consensus sequences computationally shredded into 1.5-kbp overlapping shreds (6). Draft data from all platforms were then assembled together with Allpaths, and the consensus sequences were computationally shredded into 10-kbp overlapping shreds (7). We then integrated the Newbler consensus shreds, Velvet consensus shreds, Allpaths consensus shreds, and a subset of the long-insert read pairs using parallel Phrap (High Performance Software, LLC). Possible misassemblies were corrected and some gap closure accomplished with manual editing in Consed (8–10). Automatic annotation for each genome utilized an Ergatis-based workflow at LANL with minor manual curation. Each genome is available in NCBI (accession numbers are listed in Table 1) and raw data can be provided upon request. In-depth comparative analyses of these and other genomes are under way and will be published in subsequent reports.
TABLE 1

Strain-identifying information and basic statistics on assemblies and annotations

Species and strainAlternate strain nameAccession no. (structure)Size (bp) (% G+C content)No. of CDSbNo. of rRNA genesNo. of tRNA genesPlasmida
pMT (pFra)pPCP (pPst)Pgm
Yersinia enterocolitica
ATCC 9610NCTC_12982JPDV00000000 (1 scaffold, 7 contigs)4,537,953 (47.3)4,0842281
DATRYE1013JPDU00000000 (2 scaffolds, 3 contigs)4,645,698 (47.3)4,2171979+
E265YE1012JPDW00000000 (3 scaffolds, 57 contigs)4,694,189 (46.9)4,2681878
YEANAcJPDX00000000 (2 scaffolds; 82 contigs)4,525,312 (47.0)4,0771473
Yersinia fredericksenii
ATCC 33641CDC1461 to CDC1481JPPS00000000 (2 scaffolds; 10 contigs)4,941,072 (47.0)4,3632280
Yersinia kristensenii
ATCC 33639CDC1459 to CDC1481CP008955 (single closed chromosome)4,442,328 (47.4)3,9462282+
Yersinia pestis
CO92YE0020CO92TAJPMB00000000 (7 scaffolds; 59 contigs)4,714,480 (47.6)4,2681369+++
Yersinia pseudotuberculosis
ATCC 4284447JPIY00000000 (4 scaffolds; 38 contigs)4,768,560 (47.6)4,1901578+
ATCC 6904NCTC 2476CP008943 (single closed chromosome)4,806,594 (47.6)4,1782281+
Yersinia ruckeri
ATCC 29473CDC 2396-61JPPT00000000 (2 scaffolds; 15 contigs)3,771,509 (47.4)3,377872

−, not present; +, present.

CDS, coding sequences.

NA, not applicable.

Strain-identifying information and basic statistics on assemblies and annotations −, not present; +, present. CDS, coding sequences. NA, not applicable.

Nucleotide sequence accession numbers.

Genome accession numbers to public databases are listed in Table 1.
  10 in total

1.  Solexa Ltd.

Authors:  Simon Bennett
Journal:  Pharmacogenomics       Date:  2004-06       Impact factor: 2.533

2.  Genome sequencing in microfabricated high-density picolitre reactors.

Authors:  Marcel Margulies; Michael Egholm; William E Altman; Said Attiya; Joel S Bader; Lisa A Bemben; Jan Berka; Michael S Braverman; Yi-Ju Chen; Zhoutao Chen; Scott B Dewell; Lei Du; Joseph M Fierro; Xavier V Gomes; Brian C Godwin; Wen He; Scott Helgesen; Chun Heen Ho; Chun He Ho; Gerard P Irzyk; Szilveszter C Jando; Maria L I Alenquer; Thomas P Jarvie; Kshama B Jirage; Jong-Bum Kim; James R Knight; Janna R Lanza; John H Leamon; Steven M Lefkowitz; Ming Lei; Jing Li; Kenton L Lohman; Hong Lu; Vinod B Makhijani; Keith E McDade; Michael P McKenna; Eugene W Myers; Elizabeth Nickerson; John R Nobile; Ramona Plant; Bernard P Puc; Michael T Ronan; George T Roth; Gary J Sarkis; Jan Fredrik Simons; John W Simpson; Maithreyan Srinivasan; Karrie R Tartaro; Alexander Tomasz; Kari A Vogt; Greg A Volkmer; Shally H Wang; Yong Wang; Michael P Weiner; Pengguang Yu; Richard F Begley; Jonathan M Rothberg
Journal:  Nature       Date:  2005-07-31       Impact factor: 49.962

3.  Velvet: algorithms for de novo short read assembly using de Bruijn graphs.

Authors:  Daniel R Zerbino; Ewan Birney
Journal:  Genome Res       Date:  2008-03-18       Impact factor: 9.043

4.  Base-calling of automated sequencer traces using phred. I. Accuracy assessment.

Authors:  B Ewing; L Hillier; M C Wendl; P Green
Journal:  Genome Res       Date:  1998-03       Impact factor: 9.043

5.  Base-calling of automated sequencer traces using phred. II. Error probabilities.

Authors:  B Ewing; P Green
Journal:  Genome Res       Date:  1998-03       Impact factor: 9.043

6.  Consed: a graphical tool for sequence finishing.

Authors:  D Gordon; C Abajian; P Green
Journal:  Genome Res       Date:  1998-03       Impact factor: 9.043

7.  Yersinia pestis, the cause of plague, is a recently emerged clone of Yersinia pseudotuberculosis.

Authors:  M Achtman; K Zurth; G Morelli; G Torrea; A Guiyoule; E Carniel
Journal:  Proc Natl Acad Sci U S A       Date:  1999-11-23       Impact factor: 11.205

Review 8.  Yersinia pestis--etiologic agent of plague.

Authors:  R D Perry; J D Fetherston
Journal:  Clin Microbiol Rev       Date:  1997-01       Impact factor: 26.132

9.  ALLPATHS: de novo assembly of whole-genome shotgun microreads.

Authors:  Jonathan Butler; Iain MacCallum; Michael Kleber; Ilya A Shlyakhter; Matthew K Belmonte; Eric S Lander; Chad Nusbaum; David B Jaffe
Journal:  Genome Res       Date:  2008-03-13       Impact factor: 9.043

Review 10.  Plague.

Authors:  Michael B Prentice; Lila Rahalison
Journal:  Lancet       Date:  2007-04-07       Impact factor: 79.321

  10 in total
  5 in total

1.  Yersinia enterocolitica-Specific Infection by Bacteriophages TG1 and ϕR1-RT Is Dependent on Temperature-Regulated Expression of the Phage Host Receptor OmpF.

Authors:  Carlos G Leon-Velarde; Lotta Happonen; Maria Pajunen; Katarzyna Leskinen; Andrew M Kropinski; Laura Mattinen; Monika Rajtor; Joanna Zur; Darren Smith; Shu Chen; Ayesha Nawaz; Roger P Johnson; Joseph A Odumeru; Mansel W Griffiths; Mikael Skurnik
Journal:  Appl Environ Microbiol       Date:  2016-08-15       Impact factor: 4.792

2.  Deeplasmid: deep learning accurately separates plasmids from bacterial chromosomes.

Authors:  William B Andreopoulos; Alexander M Geller; Miriam Lucke; Jan Balewski; Alicia Clum; Natalia N Ivanova; Asaf Levy
Journal:  Nucleic Acids Res       Date:  2022-02-22       Impact factor: 16.971

3.  Comparative bioinformatic and proteomic approaches to evaluate the outer membrane proteome of the fish pathogen Yersinia ruckeri.

Authors:  Michael J Ormsby; Edward Grahame; Richard Burchmore; Robert L Davies
Journal:  J Proteomics       Date:  2019-03-01       Impact factor: 4.044

4.  Biotyping reveals loss of motility in two distinct Yersinia ruckeri lineages exclusive to Norwegian aquaculture.

Authors:  Andreas Riborg; Duncan J Colquhoun; Snorre Gulla
Journal:  J Fish Dis       Date:  2022-02-18       Impact factor: 2.580

Review 5.  Yersinia ruckeri, the causative agent of enteric redmouth disease in fish.

Authors:  Gokhlesh Kumar; Simon Menanteau-Ledouble; Mona Saleh; Mansour El-Matbouli
Journal:  Vet Res       Date:  2015-09-24       Impact factor: 3.683

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.