Complete Genome Sequence of the Attenuated Corynebacterium pseudotuberculosis Strain T1

We present here the genome sequence of the attenuated Corynebacterium pseudotuberculosis strain T1. The sequencing was performed with an Ion Torrent Personal Genome Machine platform. The genome is a circular chromosome of 2,337,201 bp, with a G+C content of 52.85% and a total of 2,125 coding sequences (CDSs), 12 rRNAs, 49 tRNAs, and 24 pseudogenes.

seous lymphadenitis, a chronic disease that affects small ruminants worldwide. C. pseudotuberculosis is a Gram-positive bacterium that belongs to the Corynebacterium, Mycobacterium, Nocardia, and Rhodococcus (CMNR) group (1). Here, we present the complete genome sequence of C. pseudotuberculosis strain T1. This strain was isolated from a goat lymph node in Bahia State, Brazil, and belongs to C. pseudotuberculosis bv. ovis; after several passages in culture, it was considered to present low virulence and was used as an attenuated immunogen in goats, producing 33.3% protection against caseous lymphadenitis clinical signs (2). It was described that the secreted/excreted antigens of the T1 strain showed 89% sensitivity and 99% specificity in the detection of specific anti-C. pseudotuberculosis IgG antibodies in sheep (1). Later, it was found that these T1 strain antigens were able to stimulate the production of gamma interferon by peripheral blood mononuclear cells of goats and sheep infected with the bacteria (3). The T1 strain could be used as an antigenic model for the detection of specific anti-C. pseudotuberculosis IgM antibodies in sheep (4).
The genome was sequenced using the Ion Torrent Personal Genome Machine (PGM) system, a 200-bp-fragment library kit, and a coverage of 110-fold. The quality of the reads was analyzed using the FastQC software (http://www.bioinformatics.babraham .ac.uk/projects/fastqc), and de novo assembly was performed using Newbler 2.9 (Roche, USA). The assembly process produced seven contigs with an N 50 value of 367,637 bp. The contigs were oriented and positioned based on an optical map. The optical mapping system measures the lengths of DNA fragments after digestion with restriction enzymes. This high-resolution technique can generate ordered maps of whole genomes and can also be used in the discrimination of closely related bacterial strains (5). Last, the Argus MapSolver software (OpGen, Inc., Gaithersburg, MD) was employed to import the DNA sequence and convert to in silico map data. For adjacent contigs with overlapping edges, SIMBA (http://ufmg-simba.sourceforge.net) was used. Repetitive regions were mapped with the CLC Genomics Workbench 7.0 software from Qiagen, USA (CLC bio), using as a reference the genome of C. pseudotuberculosis strain 1002. The gap-filling process was done with SIMBA (http://ufmg-simba.sourceforge.net), CLC Genomics Workbench 7.0, and in-house scripts. Automatic annotation was performed by transferring information from a curated database using in-house scripts. Genes encoding tRNAs, rRNAs, and some coding sequences (CDSs) that were absent following the transfer by in-house scripts were predicted using RAST (http: //rast.nmpdr.org). All CDSs were manually curated using the Artemis software (6) and the UniProt database (http://www.uniprot .org).
The complete genome of C. pseudotuberculosis T1 includes one circular chromosome with a length of 2,337,201 bp, a GϩC content of 52.85%, and a total of 2,125 CDSs, 12 rRNAs (5S, 16S, and 23S), 49 tRNAs, and 24 pseudogenes.
Accession number(s). The complete genome sequence has been deposited in GenBank under the accession no. CP015100.

ACKNOWLEDGMENTS
This work was supported by the Conselho Nacional de Desenvolvimento Científico e Tecnoló gico (CNPq), Fundação de Apoio à Pesquisa e Extensão (FAPEX), Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG), and Fundação de Apoio à Pesquisa do Estado da Bahia (FAPESB). The funders had no role in the study design, data collection and interpretation, or the decision to submit the work for publication.
We declare that we do not have any conflict of interest in the publication of this work.