Whole genome sequencing and identification of Bacillus endophyticus and B. anthracis isolated from anthrax outbreaks in South Africa
dc.contributor.author | Lekota, Kgaugelo Edward | |
dc.contributor.author | Bezuidt, Keoagile Ignatius Oliver | |
dc.contributor.author | Mafofo, Joseph | |
dc.contributor.author | Rees, Jasper | |
dc.contributor.author | Muchadeyi, Farai Catherine | |
dc.contributor.author | Madoroba, Evelyn | |
dc.contributor.author | Van Heerden, Henriette | |
dc.contributor.email | henriette.vanheerden@up.ac.za | en_ZA |
dc.date.accessioned | 2018-10-12T10:17:38Z | |
dc.date.available | 2018-10-12T10:17:38Z | |
dc.date.issued | 2018-07-09 | |
dc.description | Figure S1. (1) Colony morphology of (a) Bacillus endophyticus that is small circular, wet and non-mucoid and (b) B. anthracis appear circular, mucoid on nutrient agar supplemented with sodium bicarbonate at 5% CO2 after incubation at 37 °C. Colony morphology of B. endophyticus and B. anthracis on sheep blood agar incubated at 37 °C. B. anthracis shows the characteristic shiny, rough with ground-glass appearance compared to the white slimy and smooth colonies of B. endophyticus. | en_ZA |
dc.description | Figure S2. Phenotypic electron microscopic examination of the morphology of B. endophyticus strains after 24 h incubation on nutrient agar containing 0.8% sodium bicarbonate stained using copper sulphate. | en_ZA |
dc.description | Figure S3. Phylogenetic tree of 16S ribosomal RNA sequence of the Bacillus endophyticus 3618_1C, 3631_9D, 3617_2C and 3631_10C strains with related Bacillus species using maximum likelihood. Geobacillus thermoglucosidasius was used as an out-group. Bootstrap values > 60 are indicated at the internodes. | en_ZA |
dc.description | Table S1. Plasmid comparison of the four sequenced Bacillus endophyticus strains (3618_1C, 3631_9D, 3631_10C, 3617_2C) with B. endophyticus Hbe603 strain. | en_ZA |
dc.description.abstract | BACKGROUND : Bacillus endophyticus is a soil plant-endophytic bacterium, while B. anthracis is the causative agent of anthrax. The virulence factors of B. anthracis are the plasmid encoded tripartite toxins (pXO1) and poly-γ-glutamic acid (PGA) capsule (pXO2). B. endophyticus isolated alongside B. anthracis from animals that died of anthrax in Northern Cape Province (NCP), South Africa, harbored polyglutamate genes. The study compared the characteristics of B. anthracis and B. endophyticus with other Bacillus species with a focus on the presence of the PGA capsule or/and unbound PGA. The morphology and whole genome sequence analysis of B. endophyticus strains and B. anthracis were compared. RESULTS : In conventional microbiology, B. endophyticus showed gram-positive round-shaped rods in single/short chains, which were endospore-forming, non-motile, non-haemolytic with white and dry colonies, and γ-phage resistant. B. anthracis was differentiated from B. endophyticus based on the latter's box-shaped rods in pairs/long chains, white-grey and slimy colonies, encapsulated and γ-phage susceptible. The study identified a PGA polyglutamate synthase operon that consisted of pgsBCA, γ-glutamyltranspeptidase (ggt) and pgsE in B. endophyticus genomes. CONCLUSIONS : PGA regions of B. anthracis contain capBCADE genes located in the pXO2 required for capsulation formation, while B. endophyticus contain the pgsBCAE genes in the chromosome. Whole genome and microbiology analysis identified B. endophyticus, as a non-capsuled endospore-forming bacterium that consists of PGA required for biosynthesis. B. endophyticus strains do not synthesize surface associated PGA, therefore capsule visualization of B. anthracis is a key diagnostic characteristic. The study highlights the significance of using whole genome shotgun sequencing to identify virulence and other important genes that might be present amongst unknown samples from natural outbreaks. None of the B. anthracis related plasmids or virulence genes were found in the B. endophyticus genomes. | en_ZA |
dc.description.department | Veterinary Tropical Diseases | en_ZA |
dc.description.librarian | am2018 | en_ZA |
dc.description.sponsorship | The National Research Foundation (NRF), NRF-THRIP, Agricultural Research Council-Biotechnology Platform and AgriSETA. | en_ZA |
dc.description.uri | https://bmcmicrobiol.biomedcentral.com | en_ZA |
dc.identifier.citation | Lekota, K.E., Bezuidt, O.K.I., Mafofo, J. et al. 2018, 'Whole genome sequencing and identification of Bacillus endophyticus and B. anthracis isolated from anthrax outbreaks in South Africa', BMC Microbiology, vol. 18, art. 67, pp. 1-15. | en_ZA |
dc.identifier.issn | 1471-2180 (online) | |
dc.identifier.other | 10.1186/s12866-018-1205-9 | |
dc.identifier.uri | http://hdl.handle.net/2263/66863 | |
dc.language.iso | en | en_ZA |
dc.publisher | BioMed Central | en_ZA |
dc.rights | © The Author(s). 2018 Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License. | en_ZA |
dc.subject | Bacillus endophyticus | en_ZA |
dc.subject | Bacillus anthracis | en_ZA |
dc.subject | Poly-γ-glutamic acid (PGA) | en_ZA |
dc.subject | Whole genome sequencing (WGS) | en_ZA |
dc.subject | Strains | en_ZA |
dc.subject | Bacteria | en_ZA |
dc.subject | Cereus | en_ZA |
dc.subject | Alignment | en_ZA |
dc.subject | Subtilis | en_ZA |
dc.subject | Search tool | en_ZA |
dc.subject | Inhalation anthrax | en_ZA |
dc.subject | Molecular characterization | en_ZA |
dc.subject | Capsule synthesis | en_ZA |
dc.title | Whole genome sequencing and identification of Bacillus endophyticus and B. anthracis isolated from anthrax outbreaks in South Africa | en_ZA |
dc.type | Article | en_ZA |
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