Comparative genomics of Bacillus anthracis A and B-clades reveals genetic variation in genes responsible for spore germination
- PMID: 40633701
- DOI: 10.1016/j.ygeno.2025.111074
Comparative genomics of Bacillus anthracis A and B-clades reveals genetic variation in genes responsible for spore germination
Abstract
Bacillus anthracis, the causative agent of anthrax, is composed of three genetic clades (A, B, and C). Clade-A is the most common and distributed worldwide, B-clade has a narrow geographic distribution, and C-clade is rare. South Africa's Kruger National Park (KNP) has high diversity of B. anthracis, with strains from A and B clades described from its northernmost region, Pafuri. We employed whole genome sequencing to investigate the genomic diversity of B. anthracis strains isolated from animal carcasses (n = 34) during the 2012-2015 outbreaks. Whole-genome single-nucleotide polymorphism (wgSNP) analysis assigned the 2012-2015 B. anthracis genomes to the A-clade branch, distributed across the branch's two minor sub-clades A.Br.005/006. Additionally, pan-genomic analysis distinguished the A- and B-clade genomes, identifying unique accessory genes. Notable genetic differences include the biosynthetic spore cell wall genes; long-chain fatty acid CoA ligases (FaD13), Bacillus collagen-like protein of anthracis (BclA) involved in the exosporium germination, as well as a truncated murein DD-endopeptidase (mepH) found in the pXO2 plasmid of the B-clade strains. The tryptophan synthase subunit alpha gene (trpA), which results in a pseudogene in B-clade genomes separates the A- and B-clade genomes. These differences in biosynthetic cell wall genes suggest variation in adaptability or cell growth of the B-clade strains in the environment, further influenced by the truncation of the trpA gene involved in spore germination. The A.Br.005/006-clade strains in KNP exhibit higher genetic diversity, which may enhance their resilience to environmental stressors. In contrast, the KNP B-clade (B.Br.001/002) strains show limited genetic variation, potentially reducing their adaptability. This pattern is evident through whole-genome SNP analysis and pan-genomics investigating the evolution of B. anthracis.
Keywords: Bacillus anthracis; Bacillus collagen-like protein of anthracis; Single-nucleotide polymorphism (SNP); Tryptophan operon; Whole genome sequencing; pan-genomics.
Copyright © 2025 The Authors. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of competing interest The authors declare that they have no competing interests. The data (SSR files) are available and can be accessed on https://www.ncbi.nlm.nih.gov/search/all/?term=PRJNA1075343. The corresponding author, Sankwetea Prudent Mokgokong (prudent.mokgokong@nwu.ac.za), can be contacted with questions about the data used in this study. Any use of trade, firm, or product names is for descriptive purposes only and does not imply endorsement by the U.S. Government.
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