Draft Genome Sequences of 13 Plant-Associated Actinobacteria of the Family Microbacteriaceae

Draft genome sequences of 13 bacterial strains from the family Microbacteriaceae were generated using Illumina technology. The genome sizes varied from 3.0 to 4.8 Mb, and the DNA G+C content was 68.1 to 72.5%. The sequences obtained will contribute to the development of genome-based taxonomy and understanding of molecular interactions between bacteria and plants.

M embers of the family Microbacteriaceae (class Actinobacteria) are widely distributed in various terrestrial and aquatic ecosystems and often occur in association with plants as endophytes and pathogens (1)(2)(3).
Novel strains of Microbacteriaceae were recovered from eight different plants of five families (Table 1) collected in various sites in California. Rathayibacter sp. strain VKM Ac-2835 was isolated from a Malus sp. with symptoms of bacterial wetwood disease by macerating several pieces of symptomatic superficial bark tissue in a sterile aqueous solution and then plating it onto Pseudomonas F agar (Becton, Dickinson, USA) amended with cycloheximide (100 mg/liter). The remaining strains were isolated from plants without visible symptoms of diseases, as described (3,4), but Reasoner's 2A (R2A) agar (Fluka Analytical, USA) was used as the plating medium for isolation. Rathayibacter agropyri CA-4 T (ϭVKM Ac-2828 T ) was kindly provided by T. D. Murray. For preservation, strains were grown on R2A agar and lyophilized using standard techniques. All strains were deposited in the All-Russian Collection of Microorganisms (VKM; http://www .vkm.ru).
Biomass for DNA extraction was grown in liquid peptone-yeast medium (5) inoculated with cells from a single colony, followed by cultivation at 28°C for 18 to 20 h on a rotary shaker. Genomic DNA was extracted using a QIAamp DNA minikit (Qiagen, Germany). DNA libraries for strains VKM Ac-2828 T , VKM Ac-2835, and VKM Ac-2836 were prepared in-house using a NEBNext Ultra II FS DNA library prep kit for Illumina (New England Biolabs, USA) following the protocol for use with inputs of Ն100 ng with modifications as described previously (6). Pooled DNA libraries were sequenced by Novogene Co., Ltd., on an Illumina HiSeq X Ten instrument to obtain 150-bp paired-end reads. For the remaining strains, DNA library construction and sequencing were conducted by Novogene Co., Ltd. Libraries were generated using a NEBNext DNA library prep kit for Illumina (New England Biolabs) following the manufacturer's recommendations. Pooled DNA libraries were sequenced on an Illumina NovaSeq 6000 instrument to obtain 150-bp paired-end reads. Default parameters were used for all software unless otherwise specified. The quality of the reads was checked with FastQC 0.11.8 (7). Adapter sequences and lowquality regions in the raw reads were cut with Trimmomatic 0.39 (8) with the following options: ILLUMINACLIP:TruSeq3-PE-2.fa:2:30:10, SLIDINGWINDOW:4:15, and MINLEN:50. Trimmed reads were assembled using SPAdes 3.14.1 (9) with the following options: --cov-cutoff, auto; and --careful. The quality of assembly was assessed with QUAST 5.0.2 (10). Assemblies were annotated with NCBI PGAP (11) and the RAST Web server (12,13). The pairwise similarity between the 16S rRNA gene sequences was determined using TaxonDC 1.3.1 (14). The average nucleotide identity (ANI) and digital DNA-DNA hybridization (dDDH) values were calculated using the JSpecies 1.2.1 (15) and GGDC 2.1 (16) tools, respectively.
Accession numbers and characteristics of the genomes are provided in Table 1. Figure 1 shows the phylogenomic positions of Rathayibacter strains sequenced here within the genus Rathayibacter. Four newly isolated strains clustered with Rathayibacter festucae but exhibited average nucleotide identity values (90.6 to 93.4%) and digital DNA-DNA hybridization levels (41.7 to 52.1%) to R. festucae DSM 15932 T not exceeding the thresholds for species delineation (17). No genome sequences of relevant type strains of the Curtobacterium, Frigoribacterium, and Herbiconiux species are available to precisely determine the phylogenomic positions of the remaining strains sequenced in this work (Table 1).
A BLAST search confirmed the presence of a genomic cluster comprising a complete suite of tunicaminyluracil-related biosynthetic genes in R. agropyri CA-4 T as already reported by Tancos et al. (18) for this strain. This gene cluster is not present in any other genomes sequenced in this work. Further whole-genome sequencing of other Microbacteriaceae along with comparative genomic and phenotypic analyses of putative and known species with validly published names will result in valid descriptions of the revealed new taxa, contributing to the development of the genome-based taxonomy of prokaryotes.
Data availability. These whole-genome shotgun projects have been deposited in DDBJ/ENA/GenBank under the accession numbers listed in Table 1.