Laboratory of Parasitology and Mycology, Aristide Le Dantec University Hospital, 3001, Dakar, Senegal.
Service of Parasitology-Mycology, Faculty of Medicine, Pharmacy and Odontology, Cheikh Anta Diop University of Dakar, 10700, Dakar, Senegal.
Mycopathologia. 2024 Sep 9;189(5):80. doi: 10.1007/s11046-024-00891-w.
Mycetoma can be caused either by fungi or aerobic Actinomycetes. A precise identification of the causal agents is critical for the therapeutic outcome. Thus, this study aimed to identify the pathogens of mycetoma using 16S/ITS rRNA gene polymerase chain reaction (PCR) followed by Sanger sequencing directly on grains. In sum, 32 samples including 15 black grains, 12 red grains, and five white/yellow grains collected from patients with mycetoma at the Aristide Le Dantec University Hospital in Dakar, Senegal, between October 2014 and September 2020 were submitted to PCR/sequencing. For black grain eumycetoma, the ITS rRNA region was targeted. Similarly, the 16S rRNA gene was targeted for red grain actinomycetoma. These two regions were targeted in parallel for white/yellow grains, which could be of either bacterial or fungal origin. The age of the patients ranged from 14 to 72 years with a mean age of 36 ± 14 years. Thirteen (86%) of the 15 samples with black grains, were successfully sequenced with only one established eumycetoma pathogen, Madurella mycetomatis identified in 11 (73%). Cladosporium sphaerospermum was identified in one sample. For the 16S rRNA sequencing of red grains, a 58.3% (7/12) success rate was obtained with Actinomadura pelletieri identified in six samples. Among the five samples sequenced twice, the 16S rRNA allowed us to identify the causative agent in 2 cases, A. madurae in one, and A. geliboluensis in the other. The ITS rRNA identified 3 fungi, of which none was a mycetoma agent. Overall, direct 16S/ITS rRNA sequencing of the grains for detecting and identifying mycetoma pathogens was successful in 59.4% of cases. Fungi, led by M. mycetomatis, were the predominant pathogens identified. Two probable new mycetoma agents, C. sphaerospermum, and A. geliboluensis were identified and both deserve to be confirmed in further studies.
足菌肿可以由真菌或需氧放线菌引起。明确致病因子对于治疗结果至关重要。因此,本研究旨在通过聚合酶链反应(PCR)直接对谷物进行 16S/ITS rRNA 基因测序,以鉴定足菌肿的病原体。本研究共纳入 2014 年 10 月至 2020 年 9 月间在塞内加尔达喀尔 Aristide Le Dantec 大学医院就诊的 32 例患者的 32 份样本,包括 15 份黑色颗粒、12 份红色颗粒和 5 份白色/黄色颗粒。对于黑色真菌性足菌肿,靶向 ITS rRNA 区域。同样,红色放线菌性足菌肿靶向 16S rRNA 基因。白色/黄色颗粒可能源自细菌或真菌,因此这两个区域同时靶向。患者年龄 14-72 岁,平均 36±14 岁。15 份黑色颗粒样本中,有 13 份(86%)成功测序,仅鉴定出一种真菌病原体,即米卡多毛孢菌(Madurella mycetomatis),11 份(73%)阳性。1 份样本鉴定为枝孢属(Cladosporium sphaerospermum)。红色颗粒的 16S rRNA 测序成功率为 58.3%(7/12),共鉴定出 6 份 Actinomadura pelletieri。5 份重复测序的样本中,16S rRNA 仅在 2 例中鉴定出病原体,1 例为马杜拉放线菌(A. madurae),1 例为格尔比洛乌斯放线菌(A. geliboluensis)。ITS rRNA 鉴定出 3 种真菌,但均非足菌肿病原体。总体而言,直接对谷物进行 16S/ITS rRNA 测序,用于检测和鉴定足菌肿病原体的成功率为 59.4%。真菌(主要是米卡多毛孢菌)是主要的病原体。鉴定出两种可能的新的足菌肿病原体,即枝孢属和格尔比洛乌斯放线菌,两者均有待进一步研究证实。