Chen Li, Shi Guo-You, Wang Mei-Mei, Zhao Lin-Lin, Huang Yuan-Yong, Chen Xiao-Lei, Yuan Li-Jie, Xiong Ya-Nan, Si Dao-Wen, Zhu Li-Hua
College of Clinical Medicine, Hebei United University, Tangshan, 063000, China.
Jitang College, Hebei United University, Tangshan, 063000, China.
J Huazhong Univ Sci Technolog Med Sci. 2013 Dec;33(6):917-922. doi: 10.1007/s11596-013-1222-8. Epub 2013 Dec 13.
In this study, we used traditional morphological and molecular identification methods to preliminarily identify two strains of dermatophytes. The two strains were observed under the microscope. And then the dermatophytes were cultured on Sabouraud's dextrose agar (SDA). The 18S rRNA regions of the two dermatophyte strains were amplified by polymerase chain reaction (PCR), and the PCR products were sequenced and compared with GenBank data. BLAST tools and DNAMAN software were used to analyze the sequences. To further determine highly homologous sequences, a phylogenetic tree was constructed using the Neighbor-Joining method. The two strains of dermatophytes were identified by traditional morphological identification as Epidermophyton floccosum and Microsporum ferrugineum. The 18S rRNA sequence analyses showed high similarities to Cladosporium cladosporioides isolate C115LM-UFPR and Ascomycete sp. LB68A1A2. Epidermophyton and Cladosporium belong to dermatophyte, while Microsporum ferrugineum and Ascomycete belong to microsporum. The two novel strains of dermatophytes were therefore identified as Cladosporium cladosporioides isolate C115LM-UFPR (JN650537, Cladosporium) and Ascomycete sp. LB68A1A2 (AY770409, Ascomycete sp).
在本研究中,我们使用传统的形态学和分子鉴定方法对两株皮肤癣菌进行了初步鉴定。在显微镜下观察这两株菌株。然后将皮肤癣菌接种在沙氏葡萄糖琼脂(SDA)上进行培养。通过聚合酶链反应(PCR)扩增两株皮肤癣菌菌株的18S rRNA区域,并对PCR产物进行测序,与GenBank数据进行比较。使用BLAST工具和DNAMAN软件对序列进行分析。为进一步确定高度同源的序列,采用邻接法构建系统发育树。通过传统形态学鉴定,这两株皮肤癣菌分别被鉴定为絮状表皮癣菌和铁锈色小孢子菌。18S rRNA序列分析显示,它们与枝孢霉菌株C115LM-UFPR和子囊菌LB68A1A2具有高度相似性。表皮癣菌属和枝孢霉属属于皮肤癣菌,而铁锈色小孢子菌和子囊菌属于小孢子菌。因此,这两株新型皮肤癣菌被鉴定为枝孢霉菌株C115LM-UFPR(JN650537,枝孢霉属)和子囊菌LB68A1A2(AY770409,子囊菌属)。