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J Bacteriol. Jun 2011; 193(11): 2890–2891.
PMCID: PMC3133108

Genome Sequence of Streptomyces griseus Strain XylebKG-1, an Ambrosia Beetle-Associated Actinomycete[down-pointing small open triangle]

Abstract

Streptomyces griseus strain XylebKG-1 is an insect-associated strain of the well-studied actinobacterial species S. griseus. Here, we present the genome of XylebKG-1 and discuss its similarity to the genome of S. griseus subsp. griseus NBRC13350. XylebKG-1 was isolated from the fungus-cultivating Xyleborinus saxesenii system. Given its similarity to free-living S. griseus subsp. griseus NBRC13350, comparative genomics will elucidate critical components of bacterial interactions with insects.

TEXT

Streptomyces griseus is a soil bacterium known for its production of secondary metabolites, including streptomycin, the first effective antibiotic for tuberculosis (19). Here, we present the genome sequence of Streptomyces griseus strain XylebKG-1, which, to our knowledge, is the first strain of S. griseus associated with an insect. XylebKG-1 was isolated from the ambrosia beetle Xyleborinus saxeseni, which cultivates a fungus for food (2). Actinobacteria-specific isolations from both beetles and their fungal galleries resulted in isolation of XylebKG-1.

DNA from pure isolates was extracted using a bead-beating protocol (10), and the genome was sequenced at the DOE Joint Genome Institute (JGI). A noncontiguous finished genome of XylebKG-1 was generated using a shotgun approach employing a combination of Illumina (3) and 454 sequencing technologies (15). An Illumina shotgun library (69,927,062 reads totaling ~5.3 Gbp) and two 454 GS (FLX Titanium) shotgun libraries (688,595 standard reads and 172,566 20-kbp paired-end reads totaling ~352 Mbp) were sequenced and assembled. The 454 data were assembled using Newbler, version 2.3 (Roche), and Illumina sequencing data were assembled with Velvet, version 0.7.63 (20). All assemblies were integrated using parallel Phrap, version SPS D 4.24 (High Performance Software, LLC). Illumina data were used to correct potential base errors and increase consensus quality using the software program Polisher, developed at the JGI (Alla Lapidus, unpublished). Possible misassembled regions were corrected using gapResolution (Cliff Han, unpublished) or Dupfinisher (11) or by sequencing cloned bridging PCR fragments with subcloning. Gaps between contigs were closed by editing in Consed (68), by PCR, and by Bubble PCR (J.-F. Cheng, unpublished) primer walks. The total size of the genome is 8,727,768 bp, and the final assembly is based on 352.4 Mbp of 454 sequence (38× coverage) and 5.3 Gbp of Illumina sequence (257× coverage).

The overall genome G+C content is 72.1%. Generation (http://compbio.ornl.gov/generation/), Glimmer (5), and Critica (version 1.05) (1) were used to predict a total of 7,265 candidate protein-encoding gene models. RNAmmer (13) annotated six 16S rRNAs and six 23S rRNAs. A tRNAscan-SE (14) search revealed 66 tRNAs corresponding to all 20 standard amino acids. Additional PRIAM (4), KEGG (12), and COG (18) analyses were completed, and the results can be accessed at http://genome.ornl.gov/microbial/streACT1.

Evidence for XylebKG-1 as a strain of S. griseus is based on similarity between the genomes of XylebKG-1 and the type strain S. griseus subsp. griseus NBRC13350 (16). Both have similar genome sizes (8.7 Mbp to 8.5 Mbp) and G+C contents (72.1% to 72.2%), six rRNA operons, and 66 tRNAs. An average nucleotide identity analysis conducted between both genomes using Jspecies (version 1.2.1) (17) revealed a 98.98 ANIb value (91.68% genome alignment) and a 98.95 ANIm value (94.13% genome alignment), indicating a species level degree of similarity (9). Given this similarity, XylebKG-1 represents a unique opportunity to study genetic elements involved in Actinobacteria-insect associations.

Nucleotide sequence accession number.

The genome sequence of Streptomyces griseus strain XylebKG-1 has been deposited in GenBank under accession no. ADFC00000000.

Acknowledgments

This work was funded by the DOE Great Lakes Bioenergy Research Center (DOE BER Office of Science DE-FC02-07ER64494), supporting G.S., S.M.A., J.A.M., and C.R.C. This work was also funded by the National Institute of Food and Agriculture, U.S. Department of Agriculture, under identification number WISO1321, supporting K.J.G. P.H.W.B. was partly supported by a DOC fellowship of the Austrian Academy of Sciences at the Department of Behavioral Ecology, University of Bern. The work conducted by the U.S. Department of Energy Joint Genome Institute is supported by the Office of Science of the U.S. Department of Energy under contract no. DE-AC02-05CH11231. Additional support was provided by the National Science Foundation (MCB-0702025). Support for J.L.K. comes from an NSERC postdoctoral fellowship.

Footnotes

[down-pointing small open triangle]Published ahead of print on 1 April 2011.

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