Botan Alexandru, Campisciano Giuseppina, Zerbato Verena, Di Bella Stefano, Simonetti Omar, Busetti Marina, Toc Dan Alexandru, Luzzati Roberto, Comar Manola
Faculty of Medicine, "Iuliu Hațieganu" University of Medicine and Pharmacy, 400012 Cluj-Napoca, Romania.
Laboratory of Advanced Microbiology Diagnosis and Translational Research, Institute for Maternal and Child Health IRCCS Burlo Garofolo, 34137 Trieste, Italy.
Diagnostics (Basel). 2024 Jun 21;14(13):1318. doi: 10.3390/diagnostics14131318.
Effective treatment of infectious diseases requires prompt and accurate bacterial identification and tailored antimicrobial treatments. Traditional culture methods are considered the gold standard, but their effectiveness diminishes for fastidious and hard-to-grow microorganisms. In recent years, molecular diagnostic tools such as 16S rRNA gene next-generation sequencing (16S NGS) have gained popularity in the field. We analysed data from samples submitted for 16S NGS between July 2022 and July 2023 at the Department of Advanced Translational Microbiology in Trieste, Italy. The study included samples submitted for both culture-based identification and 16S NGS. Conventional media were used for culture, and bacterial identification was performed using MALDI-TOF mass spectrometry. The V3 region of the 16S rRNA gene was sequenced using the Ion PGM platform. Among the 123 samples submitted, drainage fluids (38%) and blood (23%) were the most common, with requests predominantly from the Infectious Diseases (31.7%) and Orthopedic (21.13%) Units. In samples collected from patients with confirmed infections, 16S NGS demonstrated diagnostic utility in over 60% of cases, either by confirming culture results in 21% or providing enhanced detection in 40% of instances. Among the 71 patients who had received antibiotic therapies before sampling (mean 2.3 prior antibiotic days), pre-sampling antibiotic consumption did not significantly affect the sensitivity of 16S NGS. In routine microbiology laboratories, combining 16S NGS with culture method enhances the sensitivity of microbiological diagnostics, even when sampling is conducted during antibiotic therapy.
有效治疗传染病需要迅速准确地鉴定细菌并进行针对性的抗菌治疗。传统培养方法被视为金标准,但对于苛求难养的微生物,其有效性会降低。近年来,诸如16S rRNA基因下一代测序(16S NGS)等分子诊断工具在该领域颇受欢迎。我们分析了2022年7月至2023年7月间提交至意大利的里雅斯特高级转化微生物学系进行16S NGS检测的样本数据。该研究纳入了同时提交进行基于培养的鉴定和16S NGS检测的样本。使用传统培养基进行培养,并采用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF质谱)进行细菌鉴定。使用Ion PGM平台对16S rRNA基因的V3区域进行测序。在提交的123份样本中,引流液(38%)和血液(23%)最为常见,主要来自传染病科(31.7%)和骨科(21.13%)。在确诊感染患者采集的样本中,16S NGS在超过60%的病例中显示出诊断效用,其中21%的病例证实了培养结果,40%的病例检测能力得到增强。在采样前接受过抗生素治疗的71例患者中(平均提前2.3天使用抗生素),采样前使用抗生素并未显著影响16S NGS的敏感性。在常规微生物实验室中,即使在抗生素治疗期间进行采样,将16S NGS与培养方法相结合也能提高微生物诊断的敏感性。