山东大学学报 (医学版) ›› 2018, Vol. 56 ›› Issue (1): 57-61.doi: 10.6040/j.issn.1671-7554.0.2017.418
• • 上一篇
周飞,刘璐,刘丽媛,王斐,于理想,相玉娟,马忠兵,余之刚
ZHOU Fei, LIU Lu, LIU Liyuan, WANG Fei, YU Lixiang, XIANG Yujuan, MA Zhongbing, YU Zhigang
摘要: 目的 探讨16S rDNA基因序列分析在非哺乳期乳腺炎患者病原菌检测中的应用价值。 方法 采集33份非哺乳期乳腺炎标本,分别进行传统的细菌镜检、微生物培养与鉴定,并提取其DNA进行PCR扩增及16S rDNA测序分析。 结果 革兰染色法41.18%(7/17)查见G+细菌,35.29%(6/17)查见G-细菌。微生物培养仅1例阳性(1/5)且呈现两种细菌生长。16S rDNA测序阳性率为100%,其中39.39%(13/33)为混合细菌感染,27.27%(9/33)为假单胞菌属,6.06%(2/33)为kroppenstedtii.棒状杆菌,6.06%(2/33)为屎肠球菌,3.03%(1/33)为坚硬芽孢杆菌,3.03%(1/33)为芽孢八叠球菌,3.03%(1/33)为金黄色葡萄球菌,12.12%(4/33)为宏基因组文库细菌。 结论 应用16S rDNA测序技术检测非哺乳期乳腺炎病原菌具有简便快速、灵敏度高、特异性强等优点,且可为临床合理选择抗生素提供线索。
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