Prates Fernanda Diniz, Araújo Max Roberto Batista, da Silva Sousa Jailan, de Oliveira Sant'Anna Lincoln, do Carmo Sant'Anna Cardoso Tayná, Silva Amanda Couto Calazans, de Castro Soares Siomar, Andrade Bruno Silva, Dos Santos Louisy Sanches, de Carvalho Azevedo Vasco Ariston
Operational Technical Nucleus, Microbiology, Hermes Pardini Institute, Vespasiano 33200-000, MG, Brazil.
Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte 31270-901, MG, Brazil.
Antibiotics (Basel). 2025 Aug 20;14(8):843. doi: 10.3390/antibiotics14080843.
is an emerging zoonotic pathogen capable of cau-sing diphtheria-like infections in humans.
we report, for the first time in Brazil, the detection and phenotypic/genomic characterization of three atoxigenic ST-339 strains isolated from domestic animals, including one with a ciprofloxacin resistance profile linked to double GyrA mutations (S89L, D93G).
species identification was performed by MALDI-TOF MS, followed by in vitro antimicrobial susceptibility testing, whole-genome sequencing, and bioinformatic analyses to predict virulence determinants, antimicrobial resistance genes, CRISPR-Cas systems, mobile genetic elements, and in silico structural analysis as well as phylogenetic reconstruction.
whole-genome sequencing confirmed species identity, revealed high genetic similarity, and identified distinct phylogenetic subclades, suggesting potential international dissemination. Genomic analyses showed conserved virulence determinants, such as incomplete pilus clusters, iron acquisition systems, and the gene, with the absence of the gene. Molecular modeling and dynamics simulations indicated that GyrA mutations disrupt critical ciprofloxacin-magnesium-water interactions, reducing binding stability. Mobile genetic elements, prophages, and CRISPR-Cas systems underscored the genomic plasticity of these isolates.
these findings document a little-studied antimicrobial resistance mechanism in zoonotic , highlighting the need for strengthened surveillance and further research on virulence and resistance, even in ato-xigenic strains.
是一种新兴的人畜共患病原体,能够在人类中引起类似白喉的感染。
我们首次在巴西报告了从家畜中分离出的三株无毒力的ST-339菌株的检测及表型/基因组特征,其中一株具有与双GyrA突变(S89L,D93G)相关的环丙沙星耐药谱。
通过基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)进行菌种鉴定,随后进行体外抗菌药物敏感性测试、全基因组测序和生物信息学分析,以预测毒力决定因素、抗菌药物耐药基因、CRISPR-Cas系统、移动遗传元件,并进行计算机模拟结构分析以及系统发育重建。
全基因组测序确认了菌种身份,揭示了高度的遗传相似性,并确定了不同的系统发育亚分支,表明可能存在国际传播。基因组分析显示了保守的毒力决定因素,如不完整的菌毛簇、铁获取系统和基因,且不存在基因。分子建模和动力学模拟表明,GyrA突变破坏了关键的环丙沙星-镁-水相互作用,降低了结合稳定性。移动遗传元件、前噬菌体和CRISPR-Cas系统强调了这些分离株的基因组可塑性。
这些发现记录了人畜共患病原体中一种研究较少的抗菌药物耐药机制,突出了加强监测以及对毒力和耐药性进行进一步研究的必要性,即使是针对无毒力菌株。