Evrard Séverine, Minon Caroline, Lamtiri Laarif Mouhsine, De Backer Benjamin, Paridaens Henry, Hayette Marie-Pierre, Frère Julie, Senterre Jean-Marc, Minon Jean-Marc
Laboratory Medicine Department, Centre Hospitalier Régional de la Citadelle, 4000 Liege, Belgium.
Department of Clinical Microbiology, Centre Hospitalier Universitaire du Sart-Tilman, 4000 Liege, Belgium.
J Fungi (Basel). 2024 Jul 24;10(8):515. doi: 10.3390/jof10080515.
Onychomycosis (OM) is a widespread infection requiring prolonged treatment with potential side effects. Diagnostic certainty is therefore essential before initiating antifungal therapy. Molecular biology has already shown benefits in reducing the time to diagnosis, providing technical ease, and increasing sensitivity for the respective species that molecular tests can detect. Nevertheless, causative agents are numerous, and culture remains essential, particularly for detecting non-dermatophytes mold infections. This study compared the performance of three different diagnostic strategies: conventional culture technique, the multiplex DermaGenius 2.0 PCR (DG), and a mixed PCR/culture algorithm guided by the result of direct examination with calcofluor (DEC). The mixed algorithm (MA) prioritizes DG PCR and DEC as the primary diagnostic tools, supplemented by selective sample inoculation when mycelial elements are visualized in DEC and when DG PCR fails to detect any fungus or identifies a fungus with morphology differing from that observed in DEC (filamentous fungi versus yeasts). With only 13% of samples requiring inoculation, MA emerged as the most effective strategy, demonstrating significantly higher sensitivity (98.18%; < 0.001) compared to single-method approaches (78.18% for DG PCR alone and 74.55% for culture alone) while maintaining a specificity comparable to DG PCR (100%). This new approach saves time in result delivery, requires fewer human resources, and increases diagnostic accuracy to better meet the needs of clinicians.
甲癣(OM)是一种广泛传播的感染,需要长期治疗且存在潜在副作用。因此,在开始抗真菌治疗之前,明确诊断至关重要。分子生物学已显示出在缩短诊断时间、操作简便以及提高分子检测所能检测的相应菌种的敏感性方面具有优势。然而,致病原众多,培养仍然必不可少,尤其是对于检测非皮肤癣菌霉菌感染。本研究比较了三种不同诊断策略的性能:传统培养技术、多重DermaGenius 2.0 PCR(DG)以及一种由荧光增白剂直接检查(DEC)结果指导的PCR/培养混合算法。混合算法(MA)将DG PCR和DEC作为主要诊断工具,当在DEC中观察到菌丝成分且DG PCR未能检测到任何真菌或鉴定出与DEC中观察到的形态不同的真菌(丝状真菌与酵母)时,通过选择性样本接种进行补充。由于只有13%的样本需要接种,MA成为最有效的策略,与单一方法相比,其敏感性显著更高(98.18%;<0.001)(单独DG PCR为78.18%,单独培养为74.55%),同时保持了与DG PCR相当的特异性(100%)。这种新方法节省了结果交付时间,需要的人力资源更少,并提高了诊断准确性,以更好地满足临床医生的需求。