Literature DB >> 27688330

Genome Sequences of Nine Gram-Negative Vaginal Bacterial Isolates.

Grace E Deitzler1, Maria J Ruiz2, Wendy Lu1, Cory Weimer1, SoEun Park1, Lloyd S Robinson1, Kymberlie Hallsworth-Pepin3, Aye Wollam3, Makedonka Mitreva4, Warren G Lewis5, Amanda L Lewis6.   

Abstract

The vagina is home to a wide variety of bacteria that have great potential to impact human health. Here, we announce reference strains (now available through BEI Resources) and draft genome sequences for 9 Gram-negative vaginal isolates from the taxa Citrobacter, Klebsiella, Fusobacterium, Proteus, and Prevotella.
Copyright © 2016 Deitzler et al.

Entities:  

Year:  2016        PMID: 27688330      PMCID: PMC5043548          DOI: 10.1128/genomeA.00889-16

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Reproductive and urinary tract infections are a major cause of morbidity and mortality for women worldwide (1, 2). Bacterial vaginosis (BV) is an imbalance of the vaginal microbiota that is associated with higher risks of sexually transmitted infections, urinary tract infections, and poor health outcomes among pregnant women (3–10). Women with BV have few lactic acid-producing bacteria (lactobacilli) and high levels of fastidious anaerobic bacteria. A variety of species within the Bacteroidetes and Fusobacteriales (among other taxa) have been isolated from women with BV, often from sites in the upper reproductive tract (e.g., placenta and amniotic fluid) (5, 11–14). Despite the widespread health complications associated with BV, its etiology is poorly characterized, and current treatment options are often met with recurrences (15). Urinary tract infection (UTI) is another recurrent urogenital condition that is common among women and associated with poor pregnancy outcomes (1). Escherichia coli is the most common cause of UTI (16), and there are many dozens of available isolates and genomes of E. coli available for study. Citrobacter and Klebsiella spp. are less common etiologic agents of UTI. It is thought that the vagina can sometimes act a reservoir for uropathogens; however, few vaginal isolates of uropathogenic bacterial species are available as fully sequenced deposited isolates. The lack of reference strains and corresponding reference genomes of urogenital bacteria hinders research progress aimed at understanding how bacteria cause infection in the genital and urinary tracts. Here, we present annotated genome sequences of nine Gram-negative vaginal isolates, which have been made available to the research community through BEI Resources. Vaginal swabs were collected from nonpregnant and pregnant women according to Washington University institutional review board (IRB)-approved protocols 201108155 and 201103082. Anaerobic vaginal swabs from reproductive-age pregnant and nonpregnant women were streaked onto agar medium and cultivated anaerobically. A detailed description of the isolation of these bacteria will be provided elsewhere. Genomes were assembled using the One Button Velvet (1.1.06) pipeline (17), with hash sizes of 31, 33, and 35 after downsizing the input data to 100× coverage. Postassembly, we set the minimum length for contigs to 200 bp, ran an internal core gene screen on the assembly (as defined by the Human Microbiome Project [HMP] [18]), removed adapters, trimmed low-quality regions, and screened for contamination. The gene annotation process included generating both ab initio and evidence-based (BLAST) predictions. Coding sequences were identified using GeneMark and Glimmer3 (19, 20). Loci were then defined by clustering predictions with the same reading frame. We evaluated predictions using the NR and Pfam databases (21) and resolved overlaps between adjacent coding genes. Intergenic regions not spanned by GeneMark and Glimmer3 were subjected to a BLAST search against NCBI’s nonredundant (NR) database, and predictions were generated based on protein alignments. tRNA genes and noncoding RNA genes were found using tRNAscan-SE, RNAmmer, and Rfam (22–24). The final gene set was annotated for metabolic pathway predictions using KEGG (25), subcellular localization using PSORTb (26), and functional domain associations using InterProScan (27).

Accession number(s).

Nucleotide sequences have been deposited in GenBank under the accession numbers listed in Table 1. The sequences described in this paper are the first versions. We have also made the strains available to the research community by depositing them with the Biodefense and Emerging Infections (BEI) Research Resource Repository (see BEI numbers in Table 1).
TABLE 1 

Strain names and accession numbers

SpeciesStrain nameBEI catalog no.Nucleotide sequence accession no.
Citrobacter freundiiGED7749CHMS-1280LRPR00000000
Citrobacter koseriGED7778CHMS-1288LRPS00000000
Fusobacterium sp.CMW8396HMS-1274LRPX00000000
Fusobacterium nucleatumMJR7757BHMS-1289LRPY00000000
Klebsiella pneumoniaeMJR8396DHMS-1265LRQC00000000
Prevotella biviaGED7880HMS-1270LTAG00000000
Prevotella biviaGED7760CHMS-1286LRQF00000000
Prevotella corporisMJR7716HMS-1294LRQG00000000
Proteus mirabilisGED7834HMS-1271LSGS00000000
Strain names and accession numbers
  27 in total

1.  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

Review 2.  The global epidemiology of bacterial vaginosis: a systematic review.

Authors:  Chris Kenyon; Robert Colebunders; Tania Crucitti
Journal:  Am J Obstet Gynecol       Date:  2013-05-06       Impact factor: 8.661

3.  tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence.

Authors:  T M Lowe; S R Eddy
Journal:  Nucleic Acids Res       Date:  1997-03-01       Impact factor: 16.971

4.  Bacterial vaginosis is a strong predictor of Neisseria gonorrhoeae and Chlamydia trachomatis infection.

Authors:  Harold C Wiesenfeld; Sharon L Hillier; Marijane A Krohn; Daniel V Landers; Richard L Sweet
Journal:  Clin Infect Dis       Date:  2003-02-07       Impact factor: 9.079

5.  High recurrence rates of bacterial vaginosis over the course of 12 months after oral metronidazole therapy and factors associated with recurrence.

Authors:  Catriona S Bradshaw; Anna N Morton; Jane Hocking; Suzanne M Garland; Margaret B Morris; Lorna M Moss; Leonie B Horvath; Irene Kuzevska; Christopher K Fairley
Journal:  J Infect Dis       Date:  2006-04-26       Impact factor: 5.226

6.  Urinary tract infections in pregnant women with bacterial vaginosis.

Authors:  S H Sharami; M Afrakhteh; M Shakiba
Journal:  J Obstet Gynaecol       Date:  2007-04       Impact factor: 1.246

7.  Association between bacterial vaginosis and preterm delivery of a low-birth-weight infant. The Vaginal Infections and Prematurity Study Group.

Authors:  S L Hillier; R P Nugent; D A Eschenbach; M A Krohn; R S Gibbs; D H Martin; M F Cotch; R Edelman; J G Pastorek; A V Rao
Journal:  N Engl J Med       Date:  1995-12-28       Impact factor: 91.245

8.  Rfam: annotating non-coding RNAs in complete genomes.

Authors:  Sam Griffiths-Jones; Simon Moxon; Mhairi Marshall; Ajay Khanna; Sean R Eddy; Alex Bateman
Journal:  Nucleic Acids Res       Date:  2005-01-01       Impact factor: 16.971

9.  InterProScan: protein domains identifier.

Authors:  E Quevillon; V Silventoinen; S Pillai; N Harte; N Mulder; R Apweiler; R Lopez
Journal:  Nucleic Acids Res       Date:  2005-07-01       Impact factor: 16.971

10.  The Pfam protein families database.

Authors:  Robert D Finn; John Tate; Jaina Mistry; Penny C Coggill; Stephen John Sammut; Hans-Rudolf Hotz; Goran Ceric; Kristoffer Forslund; Sean R Eddy; Erik L L Sonnhammer; Alex Bateman
Journal:  Nucleic Acids Res       Date:  2007-11-26       Impact factor: 16.971

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