Togănel Radu Ovidiu, Coșeriu Razvan Lucian, Mare Anca Delia, Vintilă Camelia, Sîrbu Ioan-Ovidiu, Chis Aimée Rodica, Gîrbovan Cristina Elena, Man Adrian
Microbiology Department, George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Targu Mures, 540142 Targu Mures, Romania.
Doctoral School of Medicine and Pharmacy, George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Targu Mures, 540142 Targu Mures, Romania.
Infect Dis Rep. 2025 Sep 12;17(5):114. doi: 10.3390/idr17050114.
: Routine identification of common bacterial pathogens is typically efficient, utilizing standardized, cost-effective methods. However, the diagnostic process becomes significantly more complex when dealing with rare or unexpected microorganisms, especially as they can be considered colonizers in many cases. : This study presents diagnostic details of an uncommon pathogen, , isolated from auricular discharge in a patient with non-Hodgkin lymphoma diagnosed with persistent otitis externa and explores its identification through both conventional and modern laboratory approaches. Sequential ear discharge cultures resulted in phenotypically similar but genomically different isolates. We complemented classical methods like conventional culture (on Columbia agar and CLED agar), Vitek2 Compact identification, and EUCAST disk diffusion antimicrobial susceptibility testing (following the EUCAST version 12.0 guidelines) with MALDI-TOF mass spectrometry and Illumina/Nanopore whole genome sequencing. Comparative analysis of the genomes was performed with the PeGAS pipeline, Unicycler, and 1928Diagnostics SNP analysis. : The Vitek2 analysis identified both isolates as with 99% confidence, and this was supported by the MALDI-TOF MS results. The first isolate (A) was fully susceptible to the antibiotics tested, while the second (B) showed resistance to ciprofloxacin. Whole genome sequencing revealed 99.23% and 98.60% nucleotide identity to the reference genome for isolates A and B, respectively, with a 99.8% match between them. Isolate B acquired a (c.1870C>T) mutation that correlates with the ciprofloxacin resistance (MIC > 0.5 mg/L). Both genomes carry (hemolysin), (cholera toxin regulator), genes involved in biofilm formation (, , , ), (motility), , (virulence factors), and (oxytetracycline resistance). A core genome SNP distance of <100 indicates clonal relatedness. Our integrated (phenotypic and genomic) diagnostic approach confirmed and documented host resistance evolution, with a virulence repertoire that could explain the clinical evolution. : This case highlights the utility of molecular methods in confirming species identity, detecting resistance markers, characterizing virulence determinants, and differentiating a pathogen from a colonizer, supporting targeted clinical management.
常规鉴定常见细菌病原体通常效率较高,采用标准化且经济高效的方法。然而,在处理罕见或意外的微生物时,诊断过程会变得显著更加复杂,尤其是因为在许多情况下它们可能被视为定植菌。本研究展示了从一名被诊断为持续性外耳炎的非霍奇金淋巴瘤患者耳部分泌物中分离出的一种罕见病原体的诊断细节,并通过传统和现代实验室方法探索其鉴定过程。连续的耳部分泌物培养产生了表型相似但基因组不同的分离株。我们用基质辅助激光解吸电离飞行时间质谱(MALDI - TOF)和Illumina/Nanopore全基因组测序对传统培养(在哥伦比亚琼脂和CLED琼脂上)、Vitek2 Compact鉴定以及EUCAST纸片扩散法抗菌药敏试验(遵循EUCAST 12.0版指南)等经典方法进行了补充。使用PeGAS管道、Unicycler和1928Diagnostics SNP分析对基因组进行了比较分析。Vitek2分析以99%的置信度将两种分离株均鉴定为[具体菌种],MALDI - TOF MS结果也支持这一鉴定。第一个分离株(A)对所测试的抗生素完全敏感,而第二个(B)对环丙沙星耐药。全基因组测序显示,分离株A和B与[具体菌种]参考基因组的核苷酸同一性分别为99.23%和98.60%,它们之间的匹配度为99.8%。分离株B获得了一个[具体突变位点](c.1870C>T)突变,该突变与环丙沙星耐药性(最低抑菌浓度>0.5mg/L)相关。两个基因组都携带[溶血素相关基因](溶血素)、[霍乱毒素调节相关基因](霍乱毒素调节因子)、参与生物膜形成的基因([具体基因1]、[具体基因2]、[具体基因3]、[具体基因4])、[运动性相关基因](运动性)、[其他基因1]、[毒力因子相关基因](毒力因子)以及[土霉素耐药相关基因](土霉素耐药)。核心基因组SNP距离<100表明克隆相关性。我们的综合(表型和基因组)诊断方法确认并记录了宿主耐药性的演变,其毒力特征可以解释临床演变情况。该病例突出了分子方法在确认菌种身份、检测耐药标记、表征毒力决定因素以及区分病原体和定植菌方面的实用性,为有针对性的临床管理提供了支持。