ABSTRACT
Mycobacterium abscessus subsp. bolletii is a rapidly growing mycobacterial organism for which the taxonomy is unclear. Here, we report the complete genome sequence of a Mycobacterium abscessus subsp. bolletii type strain. This sequence will provide essential information for future taxonomic and comparative genome studies of these mycobacteria.
GENOME ANNOUNCEMENT
The number of cases of nontuberculosis mycobacteria (NTM) is increasing, especially in developed countries. In our hospital-based survey of pulmonary NTM disease patients in Japan, the number of pulmonary Mycobacterium abscessus disease cases increased 5-fold relative to a survey conducted 7 years earlier (1). Moreover, the finding that the multidrug-resistant M. abscessus complex (MABC) is transmissible between patients with conditions such as cystic fibrosis provided a radical shift in thinking about MABC acquisition, which was previously thought to be environmental (2–4). Despite advances made in the genomics and documentation of clinical phenotypical differences among MABCs, discrepancies in conventional DNA-DNA hybridization (DDH) results led to debate about MABC taxonomic differentiation (3, 5–9).
Here, we report the complete genome sequence of M. abscessus subsp. bolletii BDT (=CIP108541T). The strain was grown in Middlebrook 7H9 medium, and DNA was extracted using a standard phenol-chloroform method. The genome sequence was determined using PacBio reads (112,992 reads) obtained with the RS II system (Pacific Biosciences, Menlo Park, CA, USA) (10–12). The reads were de novo assembled with Canu version 1.5 (13), and the assembled genome was circularized by manually trimming the repeated sequences. Illumina 2 × 300-bp paired-end reads (100,578,382 reads) were obtained with the MiSeq system (Illumina, San Diego, CA, USA) and mapped to the assembly using the Burrows-Wheeler aligner (14) for sequence and assembly error correction with Pilon (15). The DDBJ Fast Annotation and Submission Tool (DFAST) (https://dfast.nig.ac.jp/) was used for annotation (16). Average nucleotide identity (ANI), genome-to-genome distance (GGD), and genomic signature-delta distance (GS-DD) were calculated by JSpeciesWS, Genome-to-Genome Distance Calculator 2.1 (http://ggdc.dsmz.de/ggdc.php), and δ*-differences (http://www.cmbl.uga.edu/software/delta-differences.html), respectively (17–19).
The length of the M. abscessus subsp. bolletii BDT genome is 5,080,450 bp (64.1% G+C content). Mycobacterium-related ANI was 96.95% to M. abscessus subsp. abscessus (complete genome of strain ATCC_19977T [20]) and 96.73% to M. abscessus subsp. massiliense (complete genome of strain JCM_15300T [7]). GGD-estimated DDH values between strains BDT and ATCC_19977T, strains ATCC_19977T and JCM_15300, and strains JCM_15300 and BDT were 87.0%, 86.0%, and 88.1%, respectively. The GS-DD was 23 for these 3 comparisons. These values support the proposed taxonomic position of M. abscessus subsp. bolletii (3). The number of predicted protein-coding sequences in the genome (n = 4,976) is nearly equivalent to those of M. abscessus subsp. abscessus (n = 4,920) and M. abscessus subsp. massiliense (n = 4,857) (7, 20). The numbers of rRNA operons (n = 3) and tRNA genes (n = 49) are similar or equivalent to those of close relatives. Although a draft genome sequence for Mycobacterium abscessus subsp. bolletii BDT was previously determined (21), the number of predicted genes differed significantly from that obtained here. We also identified a 97.1-kb prophage that was longer than that seen in a previous study (63 kb) (21). The complete genome sequence of M. abscessus subsp. bolletii BDT represents essential data for future taxonomic and comparative genome studies.
Accession number(s).The chromosome sequence was deposited in DDBJ/ENA/GenBank under accession no. AP018436.
ACKNOWLEDGMENTS
This work was supported by a grant from the Japan Agency for Medical Research and Development/Japan International Cooperation Agency to Y. Hoshino and by a Grant-in-Aid for Scientific Research (C) from the Japan Society for the Promotion of Science (JSPS) to Y. Hoshino.
The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.
FOOTNOTES
- Received 14 December 2017.
- Accepted 21 December 2017.
- Published 1 February 2018.
- Copyright © 2018 Yoshida et al.
This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.
