Literature DB >> 24233592

Draft Genome Sequence of a Plant Growth-Promoting Rhizobacterium, Serratia fonticola Strain AU-P3(3).

Usha Devi1, Indu Khatri, Navinder Kumar, Lalit Kumar, Deepak Sharma, Srikrishna Subramanian, Adesh K Saini.   

Abstract

Plant growth-promoting rhizobacteria (PGPR), found in the rhizospheric region of plants, not only suppress plant disease, but also directly improve plant health by improving the availability of nutrients and by providing phytostimulants. Herein, we report the high-quality genome sequence of Serratia fonticola strain AU-P3(3), a PGPR of the pea plant, which confers phosphate solubilization, indole-3-acetic acid production, ammonia production, hydrogen cyanide (HCN) production, and siderophore production and also confers activity against Rhizoctonia species. The 5.02-Mb genome sequence contains genes related to plant growth promotion and biocontrol activities.

Entities:  

Year:  2013        PMID: 24233592      PMCID: PMC3828316          DOI: 10.1128/genomeA.00946-13

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

The rhizosphere, the layer of soil under the influence of roots, is richer in bacteria than the surrounding soil (1). Many of the microbes present in the rhizosphere work symbiotically to improve plant growth and, thus, are referred to as plant growth-promoting rhizobacteria (PGPR) (1). PGPR exhibit biofertilization and rhizoremediation, stimulate growth of roots, control plant stresses, and reduce plant diseases to augment plant growth (1). Many members of the Serratia genus have been shown to confer PGPR traits, including solubilization of inorganic phosphate (2) and phytohormone production and phytoremediation (3), and protect plants from flood-induced damage (4). They also improve plant health indirectly by reducing plant pathogens of bacterial, fungal, and nematodal origin (3, 5–8). We isolated Serratia fonticola AU-P3(3), a Gram-negative motile rod from the rhizosphere of pea roots, which confers activity against Rhizoctonia species (U. Devi, I. Khatri, N. Kumar, L. Kumar, D. Sharma, S. Subramanian, and A. K. Saini, unpublished results), fungal plant pathogens of the pea (9). AU-P3(3) produces HCN and siderophores that may account for its antifungal activity. AU-P3(3) also produces ammonia and indole-3-acetic acid and exhibits phosphate solubilization (Devi et al., unpublished). Importantly, AU-P3(3) also utilizes insecticides and fungicides as carbon sources, suggesting its role in bioremediation (L. Kumar, U. Devi, I. Khatri, N. Kumar, D. Sharma, S. Subramanian, and A. K. Saini, unpublished results). Considering the broader biotechnological application of S. fonticola AU-P3(3), we went on to sequence its genome. The genome of S. fonticola AU-P3(3) was sequenced using the Illumina-HiSeq 1000 technology. Sequencing resulted in 34,600,774 paired-end reads (insert size of 350 bp) of 101 bp. A total of 34,322,211 high-quality reads with approximately 690× coverage were assembled with CLCbio wb6 (word size 35 and bubble size 55) to obtain 49 contigs (N50, 318,463 bp). The genome finishing module of CLCbio, followed by SSPACE v2.0 scaffolder (10) and GapFiller v1-10 (11), was used. The gap-filled scaffolds thus obtained were broken at the gaps to obtain 44 contigs (N50, 318,901 bp) of 5,023,127 bp, with an average G+C content of 54%. The functional annotation was carried out by RAST (Rapid Annotations using Subsystems Technology) (12), tRNA was predicted by tRNAscan-SE 1.23 (13), and rRNA genes were predicted by RNAmmer 1.2 (14). The genome contains 3 rRNA genes (5S, 23S, and 16S) and 72 aminoacyl-tRNA synthetase genes. A total of 4,483 coding regions (2,340 genes transcribed from the positive strand and 2,143 from the negative strand) were found in the genome, of which 3,669 (82%) were functionally annotated. The genome coding density is 85%, with an average gene length of 923 bp. The annotated genome has 78 genes responsible for motility and chemotaxis, including 14 genes for flagellar motility. Fifty-three genes are responsible for phosphorus metabolism. Twenty-one genes are osmotic stress response genes, including 5 for osmoregulation and 53 for oxidative stress, to make a total of 139 genes responsible for stress response in this organism. The functional comparison of the genome sequences available on the RAST server revealed the closest neighbor of S. fonticola AU-P3(3) to be Serratia odorifera 4Rx13 (score, 502), followed by S. proteamaculans 568 (score, 490), S. odorifera DSM 4582 (score, 489), and S. marcescens Db11 (score, 464).

Nucleotide sequence accession numbers.

This whole-genome shotgun project has been deposited at DDBJ/EMBL/GenBank under the accession number ASZB00000000. The version described in this paper is the first version, ASZB01000000.
  14 in total

1.  Broad-range antagonistic rhizobacteria Pseudomonas fluorescens and Serratia plymuthica suppress Agrobacterium crown gall tumours on tomato plants.

Authors:  N Dandurishvili; N Toklikishvili; M Ovadis; P Eliashvili; N Giorgobiani; R Keshelava; M Tediashvili; A Vainstein; I Khmel; E Szegedi; L Chernin
Journal:  J Appl Microbiol       Date:  2010-11-23       Impact factor: 3.772

2.  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

3.  Assessment of mineral phosphate-solubilizing properties and molecular characterization of zinc-tolerant bacteria.

Authors:  Neha Misra; Garima Gupta; Prabhat N Jha
Journal:  J Basic Microbiol       Date:  2012-02-23       Impact factor: 2.281

4.  1-Aminocyclopropane-1-carboxylic acid (ACC) deaminase-containing rhizobacteria protect Ocimum sanctum plants during waterlogging stress via reduced ethylene generation.

Authors:  Deepti Barnawal; Nidhi Bharti; Deepamala Maji; Chandan Singh Chanotiya; Alok Kalra
Journal:  Plant Physiol Biochem       Date:  2012-07-20       Impact factor: 4.270

5.  Quantitative and specific detection of the biocontrol agent, Serratia plymuthica, in plant extracts using a real-time TaqMan® assay.

Authors:  Robert Czajkowski; Jan M van der Wolf
Journal:  J Appl Genet       Date:  2012-08-11       Impact factor: 3.240

6.  Development of Multi-Component Transplant Mixes for Suppression of Meloidogyne incognita on Tomato (Lycopersicon esculentum).

Authors:  N Kokalis-Burelle; N Martinez-Ochoa; R Rodríguez-Kábana; J W Kloepper
Journal:  J Nematol       Date:  2002-12       Impact factor: 1.402

7.  Biological Control of Pathogens Causing Root Rot Complex in Field Pea Using Clonostachys rosea Strain ACM941.

Authors:  Allen G Xue
Journal:  Phytopathology       Date:  2003-03       Impact factor: 4.025

8.  Differential effectiveness of Serratia plymuthica IC1270-induced systemic resistance against hemibiotrophic and necrotrophic leaf pathogens in rice.

Authors:  David De Vleesschauwer; Leonid Chernin; Monica M Höfte
Journal:  BMC Plant Biol       Date:  2009-01-22       Impact factor: 4.215

9.  GapFiller: a de novo assembly approach to fill the gap within paired reads.

Authors:  Francesca Nadalin; Francesco Vezzi; Alberto Policriti
Journal:  BMC Bioinformatics       Date:  2012-09-07       Impact factor: 3.169

10.  The RAST Server: rapid annotations using subsystems technology.

Authors:  Ramy K Aziz; Daniela Bartels; Aaron A Best; Matthew DeJongh; Terrence Disz; Robert A Edwards; Kevin Formsma; Svetlana Gerdes; Elizabeth M Glass; Michael Kubal; Folker Meyer; Gary J Olsen; Robert Olson; Andrei L Osterman; Ross A Overbeek; Leslie K McNeil; Daniel Paarmann; Tobias Paczian; Bruce Parrello; Gordon D Pusch; Claudia Reich; Rick Stevens; Olga Vassieva; Veronika Vonstein; Andreas Wilke; Olga Zagnitko
Journal:  BMC Genomics       Date:  2008-02-08       Impact factor: 3.969

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  2 in total

Review 1.  Winding paths to simplicity: genome evolution in facultative insect symbionts.

Authors:  Wen-Sui Lo; Ya-Yi Huang; Chih-Horng Kuo
Journal:  FEMS Microbiol Rev       Date:  2016-11-01       Impact factor: 16.408

2.  Bacterial Microbiota of Rice Roots: 16S-Based Taxonomic Profiling of Endophytic and Rhizospheric Diversity, Endophytes Isolation and Simplified Endophytic Community.

Authors:  Felix Moronta-Barrios; Fabrizia Gionechetti; Alberto Pallavicini; Edgloris Marys; Vittorio Venturi
Journal:  Microorganisms       Date:  2018-02-11
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