Alexander, Kathleen A.Larsen, Michelle H.Robbe-Austerman, SueleeStuber, Tod P.Camp, Patrick M.2019-11-132019-11-132016Alexander KA, Larsen MH, Robbe-Austerman S, Stuber TP, Camp PM. 2016. Draft genome sequence of the Mycobacterium tuberculosis complex pathogen M. mungi, identified in a banded mongoose (Mungos mungo) in northern Botswana. Genome Announc 4(4):e00471-16. doi:10.1128/genomeA.00471-16.http://hdl.handle.net/10919/95516Mycobacterium mungi, a member of the Mycobacterium tuberculosis complex, has emerged in wild banded mongoose in northern Botswana (1). Molecular examinations place the organism in wildlife-associated lineage six of the M. tuberculosis complex, which includes M. suricattae, infecting meerkats (Suricata suricatta) (2), and the dassie bacillus, infecting rock hyraxes (Procavia capensis) (3), with one reported case of infection in West Africa in a chimpanzee (Pan troglodytes) caused by a member of this complex (chimpanzee bacillus) (4). The pathogen is primarily transmitted between mongoose through an environmental pathway where infected secretions used in olfactory communication behaviors expose and invade the mongoose host through abrasions or injuries to the skin and/or nasal planum (5). In northern Botswana, banded mongoose have been the subject of intensive study since the pathogen emerged in 1999 (IACUC 13-164-FIW and Botswana Ministry of Environment, Wildlife and Tourism EWT 8/36/4 XXVI [24]). In 2013, postmortem samples were obtained opportunistically from a severely infected male mongoose. Because this Mycobacterium tuberculosis complex (MTBC) pathogen has not been successfully cultivated in vitro, wholegenome shotgun sequencing was performed directly from affected tissue. Several tissues from this mongoose were screened with a real-time IS6110 MTBC PCR (6), and a small portion (3 g) of the severely diseased liver with the lowest threshold cycle (CT) value (13.8) was homogenized thoroughly using a gentleMACSMtube (Milteny Biotec, San Diego, CA, USA). After hominization, 200 mg was placed in a 2.0-ml O-ring sealed microcentrifuge tube with a mixture of 1.0- and 0.1-mm glass beads, along with 400 µl of 1x Tris-EDTA buffer, and heated at 100°C for 30 min. Bead disruption was performed on a Mini-Beadbeater-96 (BioSpec Products, Bartlesville, OK, USA) for 2 min, the supernatant was purified with phenol-chloroform-isoamyl alcohol, and the aqueous layer was further purified through a spin column (Zymo Research, Irvine, CA, USA). Libraries were prepared using the Nextera XT kit and sequenced on a MiSeq for 2 x 250 paired-end reads. The total number of reads obtained was 1,324,968, with 1,208,783 (91.2%) reads mapping to M. tuberculosis H37Rv (GenBank accession no. NC_000962.3), for an estimated average depth of coverage of 120X. De novo alignments were performed using SeqMan NGen (DNAStar Lasergene, USA), and the reads were reduced to 130 contigs, for an estimated genome size of 4.4 Mb. We report here the first draft genome of the only knownMTBC species that has not been successfully cultured in vitro. Comparing this sequence to publicly available genomes, M. mungi has diverged by at least 623 single-nucleotide polymorphisms (SNPs) since sharing a common ancestor with M. suricattae (7).2 pagesapplication/pdfenCreative Commons Attribution 4.0 InternationalArticle - Refereedhttps://doi.org/10.1128/genomea.00471-1644