Department of Applied Mathematics, School of Mathematics, University of Leeds, Leeds, UK.
CBR Division, Defence Science and Technology Laboratory, Salisbury, UK.
NPJ Syst Biol Appl. 2024 Mar 29;10(1):33. doi: 10.1038/s41540-024-00357-1.
Protective antigen (PA) is a protein produced by Bacillus anthracis. It forms part of the anthrax toxin and is a key immunogen in US and UK anthrax vaccines. In this study, we have conducted experiments to quantify PA in the supernatants of cultures of B. anthracis Sterne strain, which is the strain used in the manufacture of the UK anthrax vaccine. Then, for the first time, we quantify PA production and degradation via mathematical modelling and Bayesian statistical techniques, making use of this new experimental data as well as two other independent published data sets. We propose a single mathematical model, in terms of delay differential equations (DDEs), which can explain the in vitro dynamics of all three data sets. Since we did not heat activate the B. anthracis spores prior to inoculation, germination occurred much slower in our experiments, allowing us to calibrate two additional parameters with respect to the other data sets. Our model is able to distinguish between natural PA decay and that triggered by bacteria via proteases. There is promising consistency between the different independent data sets for most of the parameter estimates. The quantitative characterisation of B. anthracis PA production and degradation obtained here will contribute towards the ambition to include a realistic description of toxin dynamics, the host immune response, and anti-toxin treatments in future mechanistic models of anthrax infection.
保护性抗原(PA)是炭疽杆菌产生的一种蛋白质。它构成炭疽毒素的一部分,是美国和英国炭疽疫苗的关键免疫原。在这项研究中,我们进行了实验,定量分析了 UK 炭疽疫苗所使用的炭疽杆菌 Sterne 株培养物上清液中的 PA。然后,我们首次通过数学建模和贝叶斯统计技术来定量分析 PA 的产生和降解,利用这些新的实验数据以及另外两个独立的已发表数据集。我们提出了一个单一的数学模型,即时滞微分方程(DDE),可以解释所有三个数据集的体外动力学。由于我们在接种前没有加热激活炭疽杆菌孢子,因此在我们的实验中,萌发过程要慢得多,这使我们能够针对其他数据集校准两个额外的参数。我们的模型能够区分自然 PA 衰减和细菌通过蛋白酶触发的 PA 衰减。对于大多数参数估计值,不同独立数据集之间具有有希望的一致性。此处获得的炭疽杆菌 PA 产生和降解的定量特征将有助于在未来炭疽感染的机制模型中包含对毒素动力学、宿主免疫反应和抗毒素治疗的现实描述。