Literature DB >> 31649088

Genome Sequences of Novel Azospirillum sp. Strains B21 and Sh1, Isolated from Raised Sphagnum Bogs, and Type Strains Azospirillum lipoferum 59b and Azospirillum oryzae COC8.

Denis S Grouzdev1, Ekaterina N Tikhonova2, Irina K Kravchenko2.   

Abstract

Here, we report the genomic sequences of the novel Azospirillum sp. strains B21 and Sh1, isolated from raised bogs, along with the genome sequences of Azospirillum lipoferum 59bT, the type species of the genus, and Azospirillum oryzae COC8T, which were analyzed to get more knowledge about the genus Azospirillum.
Copyright © 2019 Grouzdev et al.

Entities:  

Year:  2019        PMID: 31649088      PMCID: PMC6813400          DOI: 10.1128/MRA.01174-19

Source DB:  PubMed          Journal:  Microbiol Resour Announc        ISSN: 2576-098X


ANNOUNCEMENT

Bacteria of the genus Azospirillum, belonging to the order Rhodospirillales and the family Rhodospirillaceae, are well-characterized plant growth-promoting rhizobacteria (PGPR) due to their capacity for fixing atmospheric nitrogen and their ability to colonize roots of cereals and other grasses and to produce phytohormones. Recently Azospirillum palustre, a novel methylotrophic bacterium isolated from raised bog, was described (1). Azospirillum sp. strains B21 and Sh1 were isolated from acidic Sphagnum-dominated peat soil in the Russian Federation. Strain B21 was isolated from the Sosvyatskoye peatland in the Tver region in 2000 (2). Strain Sh1 was isolated in 2018 from the upper 0- to 5-cm layer of a typical raised bog in the Shatura region, Moscow Oblast, which was afforested, i.e., drained and planted with trees. Pure cultures were obtained by serial 10-fold dilutions on N-free NFb agar medium (1.5%) (3). The plates were incubated at 29°C for 72 h, and the isolates were kept as pure cultures. DNA was purified from the cell biomass using the DNeasy PowerSoil kit (Qiagen, Germany) following the manufacturer’s instructions. The 16S rRNA gene was amplified with the 27F and 1492R primers (4), and purified PCR products were sequenced with an ABI Prism 3730 DNA analyzer (Applied Biosystems, USA). The 16S rRNA sequence analysis conducted using the online tool EzBioCloud (5) revealed that B21 shares 99.2% similarity with Azospirillum oryzae COC8T (6), and Sh1 shares 99.0% similarity with Azospirillum palustre B2T (1, 7). Both bacteria were assigned to clade L (Azospirillum lipoferum) (8). Despite the fact that Azospirillum lipoferum 59bT (9) and Azospirillum oryzae COC8T (6) have been described for a long time, genome-wide studies for these organisms were absent, which prevented a detailed comparison with newly isolated azospirilla. The strains Azospirillum lipoferum 59bT (IBPPM 173 = VKM B-1519 = ATCC 29707) and Azospirillum oryzae COC8T (IBPPM 548 = LMG 23844 = IAM 15130) were provided by the Collection of Rhizosphere Microorganisms (collection.ibppm.ru) in the framework of scientific cooperation. To perform whole-genome sequencing, all strains were cultivated on the NFb agar medium for 72 h at 29°C. Colonies were washed from the plate with liquid NFb medium and centrifuged. The genomic DNA was extracted using the DNeasy PowerSoil kit (Qiagen, Germany), following the manufacturer’s instructions. The libraries were constructed with the NEBNext DNA library prep reagent set for Illumina according to the protocol for the kit. The genomes were sequenced using the HiSeq 2500 platform (Illumina, Inc., USA) with 150-bp (Azospirillum lipoferum 59bT, Azospirillum oryzae COC8T, and Azospirillum sp. strain Sh1) and 100-bp (Azospirillum sp. strain B21) paired-end reads. Low-quality reads were trimmed using Trimmomatic v. 0.36 (10) with the default settings for paired-end reads. Subsequently, the quality-filtered reads were de novo assembled with SPAdes v. 3.13.0 using the default settings (11). The resulting assemblies were quality assessed with QUAST v. 5.0 (12). Identification of protein-coding sequences and primary annotation were performed using the NCBI Prokaryotic Genome Annotation Pipeline (PGAP) (13). Summary statistics and characteristic features of the whole-genome sequencing, assembly, and annotation of the four strains are given in Table 1. These genome sequences provide valuable data to study the ecology, evolution, and physiology of Azospirillum species.
TABLE 1

Characteristics of draft genome sequences and accession numbers of Azospirillum oryzae COC8T, Azospirillum lipoferum 59bT, and Azospirillum sp. strains Sh1 and B21

Data for strain:
CharacteristicA. oryzae COC8TA. lipoferum 59bTAzospirillum sp. Sh1Azospirillum sp. B21
BioProject no.PRJNA563036PRJNA563039PRJNA562938PRJNA563053
GenBank accession no.VTTM00000000VTTN00000000VTTK00000000VTTO00000000
BioSample no.SAMN12661881SAMN12661906SAMN12660160SAMN12662157
SRA no.SRR10092265SRR10092045SRR10092256SRR10103333
Genome size (bp)6,755,2017,987,1837,274,6037,463,459
G+C content (%)67.3667.2767.7167.33
No. of scaffolds397210357
No. of pair-end reads4,606,9764,476,8964,770,14623,572,400
L50 value57146
N50 value (bp)405,582372,840158,668465,063
Coverage (×)154127141236
Total no. of genes6,0777,1526,5616,781
No. of protein-coding genes5,8596,9036,3196,534
No. of RNAs74767476
Characteristics of draft genome sequences and accession numbers of Azospirillum oryzae COC8T, Azospirillum lipoferum 59bT, and Azospirillum sp. strains Sh1 and B21

Data availability.

These whole-genome projects have been deposited at DDBJ/ENA/GenBank under the accession numbers listed in Table 1. The versions described in this paper are the first versions.
  12 in total

1.  SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing.

Authors:  Anton Bankevich; Sergey Nurk; Dmitry Antipov; Alexey A Gurevich; Mikhail Dvorkin; Alexander S Kulikov; Valery M Lesin; Sergey I Nikolenko; Son Pham; Andrey D Prjibelski; Alexey V Pyshkin; Alexander V Sirotkin; Nikolay Vyahhi; Glenn Tesler; Max A Alekseyev; Pavel A Pevzner
Journal:  J Comput Biol       Date:  2012-04-16       Impact factor: 1.479

2.  Azospirillum palustre sp. nov., a methylotrophic nitrogen-fixing species isolated from raised bog.

Authors:  Ekaterina N Tikhonova; Denis S Grouzdev; Irina K Kravchenko
Journal:  Int J Syst Evol Microbiol       Date:  2019-09       Impact factor: 2.747

3.  Rapid determination of 16S ribosomal RNA sequences for phylogenetic analyses.

Authors:  D J Lane; B Pace; G J Olsen; D A Stahl; M L Sogin; N R Pace
Journal:  Proc Natl Acad Sci U S A       Date:  1985-10       Impact factor: 11.205

4.  Molecular identification of Azospirillum spp.: Limitations of 16S rRNA and qualities of rpoD as genetic markers.

Authors:  Guillermo A Maroniche; Julia E García; Florencia Salcedo; Cecilia M Creus
Journal:  Microbiol Res       Date:  2016-11-16       Impact factor: 5.415

5.  QUAST: quality assessment tool for genome assemblies.

Authors:  Alexey Gurevich; Vladislav Saveliev; Nikolay Vyahhi; Glenn Tesler
Journal:  Bioinformatics       Date:  2013-02-19       Impact factor: 6.937

6.  [Isolation and characterization of nitrogen-fixing bacteria of the genus Azospirillum from the soil of a Sphagnum peat bog].

Authors:  E V Doroshenko; E S Bulygina; E M Spiridonova; T P Turova; I K Kravchenko
Journal:  Mikrobiologiia       Date:  2007 Jan-Feb

7.  Introducing EzBioCloud: a taxonomically united database of 16S rRNA gene sequences and whole-genome assemblies.

Authors:  Seok-Hwan Yoon; Sung-Min Ha; Soonjae Kwon; Jeongmin Lim; Yeseul Kim; Hyungseok Seo; Jongsik Chun
Journal:  Int J Syst Evol Microbiol       Date:  2017-05-30       Impact factor: 2.747

8.  Genome Sequence of Methylotrophic Azospirillum sp. Strain B2, Isolated from a Raised Sphagnum Bog.

Authors:  Denis S Grouzdev; Ekaterina N Tikhonova; Maria S Krutkina; Irina K Kravchenko
Journal:  Genome Announc       Date:  2018-06-07

9.  Trimmomatic: a flexible trimmer for Illumina sequence data.

Authors:  Anthony M Bolger; Marc Lohse; Bjoern Usadel
Journal:  Bioinformatics       Date:  2014-04-01       Impact factor: 6.937

10.  NCBI prokaryotic genome annotation pipeline.

Authors:  Tatiana Tatusova; Michael DiCuccio; Azat Badretdin; Vyacheslav Chetvernin; Eric P Nawrocki; Leonid Zaslavsky; Alexandre Lomsadze; Kim D Pruitt; Mark Borodovsky; James Ostell
Journal:  Nucleic Acids Res       Date:  2016-06-24       Impact factor: 16.971

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