|Non-contiguous finished genome sequence and description of Clostridium senegalense sp. nov.|
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|PMID: 23408737 Owner: NLM Status: PubMed-not-MEDLINE|
|Clostridium senegalense strain JC122(T), is the type strain of Clostridium senegalense sp. nov., a new species within the genus Clostridium. This strain, whose genome is described here, was isolated from the fecal flora of a healthy patient. C. senegalense strain JC122(T) is an obligate anaerobic Gram-positive rod-shaped bacterium. Here we describe the features of this organism, together with the complete genome sequence and annotation. The 3,893,008 bp long genome (1 chromosome but no plasmid) exhibits a G+C content of 26.8% and contains 3,704 protein-coding and 57 RNA genes, including 6 rRNA genes.|
|Ajay Kumar Mishra; Jean-Christophe Lagier; Catherine Robert; Didier Raoult; Pierre-Edouard Fournier|
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|Type: Journal Article Date: 2012-07-20|
|Title: Standards in genomic sciences Volume: 6 ISSN: 1944-3277 ISO Abbreviation: Stand Genomic Sci Publication Date: 2012 Jul|
|Created Date: 2013-02-14 Completed Date: 2013-02-15 Revised Date: 2013-04-18|
Medline Journal Info:
|Nlm Unique ID: 101530505 Medline TA: Stand Genomic Sci Country: United States|
|Languages: eng Pagination: 386-95 Citation Subset: -|
|Unité de Recherche sur les Maladies Infectieuses et Tropicales Emergentes, UMR CNRS, Faculté de médecine, Aix-Marseille Université|
|APA/MLA Format Download EndNote Download BibTex|
Journal ID (nlm-ta): Stand Genomic Sci
Journal ID (iso-abbrev): Stand Genomic Sci
Journal ID (publisher-id): SIGS
Publisher: Michigan State University
Copyright © retained by original authors.
Electronic publication date: Day: 20 Month: 7 Year: 2012
collection publication date: Day: 30 Month: 7 Year: 2012
Volume: 6 Issue: 3
First Page: 386 Last Page: 395
PubMed Id: 23408737
Publisher Id: sigs.2766062
|Non-contiguous finished genome sequence and description of Clostridium senegalense sp. nov.|
|Ajay Kumar Mishra1|
1Unité de Recherche sur les Maladies Infectieuses et Tropicales Emergentes, UMR CNRS, Faculté de médecine, Aix-Marseille Université
|*Corresponding author: Pierre-Edouard Fournier (email@example.com)
Clostridium senegalense strain JC122T (= CSUR P152 = DSM 25507), is the type strain of Clostridium senegalense sp. nov. This bacterium is a Gram-positive, anaerobic, spore-forming, indole negative rod-shaped bacterium that was isolated from the stool of a healthy Senegalese patient as part of a “culturomics” study aiming at cultivating individually all species within human feces.
Since 1995 and the sequencing of the first bacterial genome, that of Haemophilus influenzae, more than 2,000 bacterial genomes have been sequenced . This was permitted by technical improvements as well as increased interest in having access to the complete genetic information encoded by bacteria. In the same time, biological tools for the definition of new bacterial species have not evolved, DNA-DNA hybridization still being considered as the gold standard  despite its drawbacks and the taxonomic revolution that has resulted from the comparison of 16S rDNA sequences . In this manuscript, we propose to use genomic data, in addition to phenotypic information , to describe a new Clostridium species.
Here we present a summary classification and a set of features for C. senegalense sp. nov. strain JC122T (= CSUR P152= DSM 25507) together with the description of the complete genomic sequencing and annotation. These characteristics support the circumscription of the species C. senegalense.
The genus Clostridium (Prazmowski, 1880) was created in 1880  and consists of obligate anaerobic rod-shaped bacilli capable of producing endospores . More than 180 species have been described to date. Members of the genus Clostridium are mostly environmental bacteria or associated with the commensal digestive flora of mammals. However, several are major human pathogens, including C. botulinum, C. difficile and C. tetani [6,7]. Few species, such as C. butyricum and C. pasteurianum, fix nitrogen and have gained importance in agricultural and industrial applications [8,9].
A stool sample was collected from a healthy 16-year-old male Senegalese volunteer patient living in Dielmo (a rural village in the Guinean-Sudanian zone in Senegal), who was included in a research protocol. The patient gave an informed and signed consent, and the agreement of the National Ethics Committee of Senegal and the local ethics committee of the IFR48 (Marseille, France) were obtained under agreements 09-022 and 11-017. The fecal specimen was preserved at -80°C after collection and sent to Marseille. Strain JC122 (Table 1) was isolated in June 2011 by anaerobic cultivation on 5% sheep blood-enriched Columbia agar (BioMerieux, Marcy l’Etoile, France). This strain exhibited a 95.6% nucleotide sequence similarity with C. subterminale , and occupied an intermediate phylogenetic position between C. cellulovorans and C. peptidivorans (Figure 1). Although sequence similarity of the 16S operon is not uniform across taxa, this value was lower than the 98.7% 16S rRNA gene sequence threshold recommended by Stackebrandt and Ebers to delineate a new species without carrying out DNA-DNA hybridization .
Different growth temperatures (25, 30, 37, 45°C) were tested; no growth occurred at 45°C, growth occurred at 25° and 30°C, and optimal growth was observed at 37°C. Colonies were 2 mm in diameter on blood-enriched Columbia agar and Brain Heart Infusion (BHI) agar. Growth of the strain was tested under anaerobic and microaerophilic conditions using GENbag anaer and GENbag microaer systems, respectively (BioMérieux), and in the presence of air, with or without 5% CO2. Growth was achieved only anaerobically. Gram staining showed rod-shaped Gram-positive bacilli able to form spores (Figure 2). The motility test was positive. Cells grown on agar have a mean diameter of 1.1 µm (Figure 3).
Strain JC122T exhibited neither catalase nor oxidase activities. Using API Rapid ID 32A, a positive reaction was observed for arginine dihydrolase, N-acetyl-β-glucosanimidase and pyroglutamic acid arylamidase. Negative reactions were observed for urease, indole and nitrate reduction. C. senegalense is susceptible to amoxicillin, imipenem, metronidazole, rifampicin and vancomycin but resistant to trimethoprim/sulfamethoxazole.
Matrix-assisted laser-desorption/ionization time-of-flight (MALDI-TOF) MS protein analysis was carried out as previously described . Briefly, a pipette tip was used to pick one isolated bacterial colony from a culture agar plate and spread it as a thin film on a MTP 384 MALDI-TOF target plate (Bruker Daltonics, Germany). Twelve distinct deposits were done for strain JC122T from twelve isolated colonies. Each smear was overlaid with 2µL of matrix solution (saturated solution of alpha-cyano-4-hydroxycinnamic acid) in 50% acetonitrile, 2.5% tri-fluoracetic acid, and allowed to dry for five minutes. Measurements were performed with a Microflex spectrometer (Bruker). Spectra were recorded in the positive linear mode for the mass range of 2,000 to 20,000 Da (parameter settings: ion source 1 (ISI), 20kV; IS2, 18.5 kV; lens, 7 kV). A spectrum was obtained after 675 shots at a variable laser power. The time of acquisition was between 30 seconds and 1 minute per spot. The twelve JC122T spectra were imported into the MALDI Bio Typer software (version 2.0, Bruker) and analyzed by standard pattern matching (with default parameter settings) against the main spectra of 3,769 bacteria, including spectra from 59 validated Clostridium species used as reference data, in the Bio Typer database (updated March 15th, 2012). The method of identification includes the m/z from 3,000 to 15,000 Da. For every spectrum, 100 peaks at most were taken into account and compared with the spectra in database. A score enabled the presumptive identification and discrimination of the tested species: a score ≥ 2 with a validated species enabled the identification at the species level; a score ≥ 1.7 but < 2 enabled the identification at the genus level; and a score < 1.7 did not enable any identification. For strain JC122T, the obtained score was 1.3, thus suggesting that our isolate was not a member of a known species. We incremented our database with the spectrum from strain JC122T (Figure 4).
The organism was selected for sequencing on the basis of its phylogenetic position and 16S rRNA similarity to other members of the genus Clostridium, and is part of a “culturomics” study of the human digestive flora aiming at isolating all bacterial species within human feces. It was the 74th genome of a Clostridium species and the first genome of Clostridium senegalense sp. nov. The Genbank accession number is CAEV00000000 and consists of 191 contigs. Table 2 shows the project information and its association with MIGS version 2.0 compliance.
C. senegalense sp. nov. strain JC122T, CSUR P152 = DSM 25507, was grown on blood agar medium at 37°C. Five petri dishes were spread and resuspended in 5x100µl of G2 buffer (EZ1 DNA Tissue kit, Qiagen). A first mechanical lysis was performed by glass powder on the Fastprep-24 device (Sample Preparation system) from MP Biomedicals, USA) using 2x20 seconds cycles. DNA was then treated with 2.5 µg/µL lysozyme (30 minutes at 37°C) and extracted through the BioRobot EZ 1 Advanced XL (Qiagen). The DNA was then concentrated and purified on a Qiamp kit (Qiagen). The yield and the concentration was measured by the Quant-it Picogreen kit (Invitrogen) on a Genios_Tecan fluorometer at 70.7 ng/µl.
This project was loaded twice on a 1/4 region for the paired end application and once on a 1/8 region for the shotgun on PTP Picotiterplates. The shotgun library was constructed with 500ng of DNA as described by the manufacturer Roche with the GS Rapid library Prep kit. For the paired-end sequencing, DNA (5µg) was mechanically fragmented on the Hydroshear device (Digilab, Holliston, MA, USA) with an enrichment size of 3-4kb. The DNA fragmentation was visualized using an Agilent 2100 BioAnalyzer on a DNA labchip 7500 to yield an optimal size of 3.6 kb. The library was constructed according to the 454_Titanium paired end protocol and manufacturer. Circularization and nebulization were performed and generated a pattern with an optimum at 561 bp. After PCR amplification through 15 cycles followed by double size selection, the single stranded paired end library was then quantified on the Quant-it Ribogreen kit (Invitrogen) on the Genios_Tecan fluorometer at 52pg/µL. The library concentration equivalence was calculated as 1.7E+08 molecules/µL. The library was held at -20°C until use.
The shotgun library was clonally amplified with 3cpb in 3 emPCR reactions and the paired end library was amplified with lower cpb (1cpb) in 4 emPCR reactions with the GS Titanium SV emPCR Kit (Lib-L) v2. The yield of the emPCR was 5.37% for the shotgun and 19.27% for the paired end according to the quality expected by the range of 5 to 20% from the Roche procedure. A total of 340,000 beads for the 1/8 region for the shotgun and 790,000 beads on the 1/4 region for the paired end were loaded on the GS Titanium PicoTiterPlates (PTP Kit 70×75) and sequenced with the GS Titanium Sequencing Kit XLR70.
The runs were performed overnight and then analyzed on the cluster through the gsRunBrowser and gsAssembler_Roche. The global 383,079 passed filter sequences generated 96.50 Mb with a length average of 277bp. These sequences were assembled using the Newbler software from Roche with 90% identity and 40 bp as overlap. Fourteen scaffolds and 120 large contigs (>1500bp) were obtained, for a genome size of 3,893,008 bp.
Open Reading Frames (ORFs) were predicted using Prodigal  with default parameters but the predicted ORFs were excluded if they were spanning a sequencing gap region. The predicted bacterial protein sequences were searched against the GenBank database  and the Clusters of Orthologous Groups (COG) database using BLASTP. The tRNAScanSE tool  was used to find tRNA genes, whereas ribosomal RNAs were found by using RNAmmer  and BLASTn against the GenBank database. ORFans were identified if their BLASTP E-value was lower than 1e-03 for alignment length greater than 80 amino acids. If alignment lengths were smaller than 80 amino acids, we used an E-value of 1e-05. Such parameter thresholds have already been used in previous works to define ORFans.
To estimate the mean level of nucleotide sequence similarity at the genome level between Clostridium species, we compared the ORFs only using BLASTN and the following parameters: a query coverage of ≥ 70% and a minimum nucleotide length of 100 bp.
The genome of C. senegalense sp. nov. strain JC122T is 3,893,008 bp long (1 chromosome, but no plasmid) with a 26.8% G + C content of (Figure 5 and Table 3). Of the 3,761 predicted genes, 3,704 were protein-coding genes, and 57 were RNAs. Six rRNA genes (one 16S rRNA, one 23S rRNA and four 5S rRNA) and 51 predicted tRNA genes were identified in the genome. A total of 2,560 genes (68.06%) were assigned a putative function. Four hundred forty-three genes were identified as ORFans (12%). The remaining genes were annotated as hypothetical proteins. The properties and the statistics of the genome are summarized in Table 3.The distribution of genes into COGs functional categories is presented in Table 4.
Seventy-three genomes are currently available for Clostridium species. Here, we compared the genome sequence of C. senegalense strain JC122T with those of C. botulinum strain ATCC 19397 and C. cellulovorans strain, ATCC 35296.
The draft genome sequence of C. senegalense strain JC122T has a similar size to that of C. botulinum (3.89 and 3.94 Mb, respectively), but a smaller size than C. cellulovorans (5.2 Mb). The G+C content of C. senegalense was lower than C. botulinum and C. cellulovorans (26.8% vs 28.2 and 31.2%, respectively). The gene content of C. senegalense is comparable to that of C. botulinum (3,761 and 3,750, respectively) but is smaller to that of C. cellulovorans (4,500). The ratios of genes per Mb and numbers of genes assigned to COGs of C. senegalense and C. botulinum are similar (974 vs 946 and 2,560 vs 2,549, respectively), but larger than the ratio of genes per Mb (844) and smaller than the number of genes assigned to COGs of C. cellulovorans (2,927). However, the distribution of genes into COG categories (Table 4) was similar in all the three compared genomes.
In addition, C. senegalense shared a mean 84.9% (range 77.4-95%) and 82.79% (range 77.2-92.3%) sequence similarity with C. botulinum and C. cellulovorans respectively at the genome level.
On the basis of phenotypic, phylogenetic and genomic analyses, we formally propose the creation of Clostridium senegalense sp. nov. which contains the strain JC122T. This bacterium has been found in Senegal.
Clostridium senegalense (se.ne.gal.e′n.sis. L. gen. masc. n. senegalensis, pertaining to, or originating from Senegal, the country from which the specimen was isolated).
Colonies are 2 mm in diameter on blood-enriched Columbia agar and Brain Heart Infusion (BHI) agar. Cells are rod-shaped with a mean diameter of 1.1 μm. Optimal growth is achieved anaerobically. No growth is observed in aerobic conditions. Growth occurs between 25-37°C, with optimal growth observed at 37°C, in BHI medium + 5% NaCl. Cells stain Gram-positive, are endospore-forming, and motile. Catalase, oxidase, urease, indole and nitrate reduction activity are absent. Arginine dihydrolase, N-acetyl-β-glucosanimidase and pyroglutamic acid arylamidase activity are present. Cells are susceptible to amoxicillin, imipenem, metronidazole, rifampicin and vancomycin but resistant to trimethoprim/sulfamethoxazole. The G+C content of the genome is 26.8%.
The type strain is JC122T (= CSUR P152 = DSM 25507) was isolated from the fecal flora of a healthy patient in Senegal.
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|MIGS ID||Property||Term||Evidence codea|
|Current classification||Domain Bacteria||TAS |
|Phylum Firmicutes||TAS [11-13]|
|Class Clostridia||TAS [14,15]|
|Order Clostridiales||TAS [16,17]|
|Family Clostridiaceae||TAS [16,18]|
|Genus Clostridium||TAS [16,19,20]|
|Species Clostridium senegalense||IDA|
|Type strain JC122T||IDA|
|MIGS-6.3||Salinity||growth in BHI medium + 5% NaCl||IDA|
|MIGS-15||Biotic relationship||free living||IDA|
|MIGS-5||Sample collection time||September 2010||IDA|
|MIGS-4.4||Altitude||51 m above sea level||IDA|
aEvidence codes - IDA: Inferred from Direct Assay; TAS: Traceable Author Statement (i.e., a direct report exists in the literature); NAS: Non-traceable Author Statement (i.e., not directly observed for the living, isolated sample, but based on a generally accepted property for the species, or anecdotal evidence). These evidence codes are from the Gene Ontology project . If the evidence is IDA, then the property was directly observed for a live isolate by one of the authors or an expert mentioned in the acknowledgements.
|MIGS-31||Finishing quality||High-quality draft|
|MIGS-28||Libraries used||One 454 paired end 3-kb library|
|MIGS-29||Sequencing platforms||454 GS FLX Titanium|
|MIGS-30||Assemblers||Newbler version 2.5.3|
|MIGS-32||Gene calling method||Prodigal|
|Genbank Date of Release||July 25, 2011|
|MIGS-13||Project relevance||Study of the human gut microbiome|
|Attribute||Value||% of totala|
|Genome size (bp)||3,893,008||100|
|DNA coding region (bp)||3,126,069||80.30|
|DNA G+C content (bp)||1,043,326||26.8|
|Genes with function prediction||2,677||71.17|
|Genes assigned to COGs||2,560||68.06|
|Genes with peptide signals||169||4.49|
|Genes with transmembrane helices||973||25.87|
a The total is based on either the size of the genome in base pairs or the total number of protein coding genes in the annotated genome
|J||183||4.94||Translation, ribosomal structure and biogenesis|
|A||0||0||RNA processing and modification|
|L||165||4.45||Replication, recombination and repair|
|B||1||0.03||Chromatin structure and dynamics|
|D||28||0.75||Cell cycle control, mitosis and meiosis|
|T||202||5.45||Signal transduction mechanisms|
|M||134||3.62||Cell wall/membrane biogenesis|
|U||37||0.99||Intracellular trafficking and secretion|
|O||74||1.99||Posttranslational modification, protein turnover, chaperones|
|C||170||4.59||Energy production and conversion|
|G||102||2.75||Carbohydrate transport and metabolism|
|E||226||6.10||Amino acid transport and metabolism|
|F||79||2.13||Nucleotide transport and metabolism|
|H||104||2.80||Coenzyme transport and metabolism|
|I||64||1.73||Lipid transport and metabolism|
|P||136||3.67||Inorganic ion transport and metabolism|
|Q||61||1.65||Secondary metabolites biosynthesis, transport and catabolism|
|R||426||11.50||General function prediction only|
|-||1,198||32.34||Not in COGs|
a The total is based on the total number of protein coding genes in the annotated genome.
Keywords: Key words: Clostridium senegalense, genome.
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