The influence of an innovative antibacterial drug of the thiadiazinone class on the virulence factors of bacteria of the phylum Pseudomonadota, which chronically infect patients with cystic fibrosis

O. Voronina, E. A. Koroleva, M. Kunda, N. Ryzhova, E. Aksenova, L. N. Kapotina, S. A. Nelubina, Anna V. Lazareva, Nailya A. Zigangirova
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Abstract

Introduction. Infections of the lower respiratory tract by bacteria of the Pseudomonadota phylum: Pseudomonas aeruginosa, Burkholderia spp., Achromobacter spp. are critical to the quality and life expectancy of patients with cystic fibrosis (CF). When the infection is chronic, eradication of bacteria with existing antibacterial drugs is practically impossible. To explore alternative drugs, trials are needed on bacteria isolated from CF patients and characterized using genomic approaches. The objective of our study was a comparative analysis of virulence factors of 6 isolates of bacteria of the Pseudomonadota phylum and testing the efficacy of the innovative drug Fluorothiazinone (FT) in suppressing the pathogenicity of bacteria in vitro. Materials and methods. Isolates of A. ruhlandii ST36, A. xylosoxidans ST555, B. cepacia ST2140, B. gladioli ST2141, P. aeruginosa ST859 and ST198 were examined using whole-genome sequencing and bioinformatics analysis to search for resistance and virulence determinants. The FT drug was tested for its effect on bacteria in in vitro experiments on cytotoxicity on HeLa cells, motility and biofilm formation. Results. Genomic studies have confirmed the arsenal of resistance determinants, especially the efflux systems of bacteria isolated from patients with CF, and the diversity of virulence factors, among which we identified factors in the categories of motility, signals of quorum-sensing systems, secretion systems, exotoxins, as the most essential for the adaptation of bacteria to conditions of the lower respiratory tract. In vitro tests of the FT drug showed its effectiveness in suppressing cytotoxicity (2.6–4.0 times), motility (2.0–3.6 times) and the process of biofilm formation (2.0–7.7 times). Conclusion. For the first time, the effectiveness of the innovative antibacterial drug Fluorothiazinone has been shown against bacteria of the Pseudomonadota phylum, isolated from chronically infected patients with CF, with the described potential of virulence factors.
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噻二嗪酮类创新抗菌药对长期感染囊性纤维化患者的假单胞菌门细菌毒力因子的影响
导言。假单胞菌门细菌(铜绿假单胞菌、伯克霍尔德氏菌属、阿克罗莫氏菌属)感染下呼吸道对囊性纤维化(CF)患者的生活质量和预期寿命至关重要。如果是慢性感染,用现有的抗菌药物根除细菌几乎是不可能的。为了探索替代药物,需要对从 CF 患者体内分离出来的细菌进行试验,并利用基因组学方法对其进行鉴定。我们的研究目的是比较分析假单胞菌门 6 株分离细菌的致病因子,并测试创新药物氟噻嗪酮(FT)在体外抑制细菌致病性的功效。材料和方法通过全基因组测序和生物信息学分析,对 A. ruhlandii ST36、A. xylosoxidans ST555、B. cepacia ST2140、B. gladioli ST2141、P. aeruginosa ST859 和 ST198 的分离株进行了检测,以寻找耐药性和毒力决定因素。在体外实验中测试了 FT 药物对 HeLa 细胞的细胞毒性、运动性和生物膜形成对细菌的影响。结果。基因组研究证实了抗药性决定因素的多样性,特别是从 CF 患者体内分离出的细菌的外排系统,以及毒力因子的多样性,其中我们确定了运动性、定量感应系统信号、分泌系统、外毒素等类别的因子是细菌适应下呼吸道条件的最基本要素。对 FT 药物的体外测试表明,它能有效抑制细胞毒性(2.6-4.0 倍)、运动性(2.0-3.6 倍)和生物膜形成过程(2.0-7.7 倍)。结论创新抗菌药物氟噻嗪酮对从慢性感染的 CF 患者体内分离出的假单胞菌门细菌的有效性首次得到证实。
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