Abstract
In August 2011, an anthrax outbreak occurred among Hippopotamus amphibius hippopotamuses and humans in Zambia. Here, we report the draft genome sequence of the Bacillus anthracis outbreak strain CZC5, isolated from tissues of H. amphibius hippopotamuses that had died in the outbreak area.
GENOME ANNOUNCEMENT
Anthrax is a life-threatening disease caused by the Gram-positive spore-forming bacterium Bacillus anthracis (1). The disease occurs worldwide, and outbreaks and epidemics of the disease in both humans and animals have been reported in Zambia (2, 3). In August 2011, an anthrax outbreak occurred among Hippopotamus amphibius hippopotamuses in the Chama district of the eastern province of Zambia (4). Over 80 hippopotamuses died after showing signs of infection with B. anthracis. Following the deaths of the hippopotamuses, 521 suspected human cases resulting in 6 deaths were reported. As of January 2014, 7 completed genome sequences and 23 draft genome sequences for B. anthracis had been deposited in GenBank. However, most of these belong to strains that were isolated in the United States; there have been no reports on the genome sequences of B. anthracis strains isolated in central Africa. Here, we report the draft genome sequence of a B. anthracis strain associated with an outbreak linked to unnatural deaths of hippopotamuses in Zambia in 2011.
The genomic DNA was extracted from overnight cultures using a Qiagen DNeasy blood and tissue kit, according to the supplied protocol. A library for sequencing was prepared from the extracted genomic DNA using a Nextera XT sample preparation kit (Illumina), and paired-end sequencing with a read length of 2 × 300 bp was performed on an Illumina MiSeq platform. The total amount of read data comprises 1,223,422,928 bases, representing 234-fold coverage of the genome. After obtaining reads that passed the quality threshold with the Trimmomatic-0.20 tool (5) and merging overlapping paired-end reads with FastqJoin (https://code.google.com/p/ea-utils/), a mapping assembly was carried out with Newbler version 2.9 (Roche). The assembled genome consists of 25 contigs of >301 bp (N50 contig size, 195,537 bp), with an average G+C content of 35.12%. The draft genome was structurally and functionally annotated using the Rapid Annotations using Subsystems Technology (RAST) annotation server (6). A total of 5,841 putative coding sequences (CDS), 11 rRNA operons, and 91 tRNA genes were identified. The quality-passed reads were aligned to the reference B. anthracis strain Ames Ancestor (taxonomy ID 261594) using SSAHA2 (7) as part of the Breseq pipeline version 0.24rc4 (8), resulting in only 1 missing gene (that for aspartate ammonia-lyase [aspA-3]) in this strain.
We believe that a detailed comparative genomic analysis of this B. anthracis strain, designated CZC5, with more genome sequences of this species obtained in Zambia might lead to new insights into its evolutionary history and pathogenicity. The results of such studies combined with data for worldwide lineages will be included in a future publication.
Nucleotide sequence accession number.
This whole-genome shotgun project for B. anthracis strain CZC5 has been deposited at DDBJ/ENA/GenBank under the accession no. BAVT00000000. The version described in this paper is the first version.
ACKNOWLEDGMENTS
We thank the Zambia Wildlife Authority for supporting the anthrax research in Zambia. We also thank H. Sawa for useful discussions and help.
This work was supported by the Government of the Republic of Zambia, the Japan Initiative for Global Research Network on Infectious Diseases (J-GRID) of the Ministry of Education, Culture, Sports, Science and Technology (MEXT), and JSPS Grants-in-Aid for Scientific Research 25670206 (N. Ohnishi) and 23390076 (H. Higashi).
Footnotes
Citation Ohnishi N, Maruyama F, Ogawa H, Kachi H, Yamada S, Fujikura D, Nakagawa I, Hang’ombe MB, Thomas Y, Mweene AS, Higashi H. 2014. Genome sequence of a Bacillus anthracis outbreak strain from Zambia, 2011. Genome Announc. 2(2):e00116-14. doi:10.1128/genomeA.00116-14.
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