Soie Chung, Jun Sik Kim, Sang Won Seo, Eun Kyung Ra, Sei-Ick Joo, So Yeon Kim, Sung Sup Park, Eui-Chong Kim
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The API Rapid ID 32A test (bioMérieux, France) was performed using a colony, but an unacceptable profile was obtained. Then, the pus was transferred into the enrichment broths of the BACTEC FX (Becton Dickinson, USA) and BacT/Alert 3D (bioMérieux, Organon Teknika, USA) systems, but only the BACTEC FX system could detect growth after 5 days. We performed 16S rRNA gene sequencing and API Rapid 32A profiling with a colony recovered from Brucella agar, which was inoculated with the microbial growth in the enrichment broth from the BACTEC FX system. The organism was identified as P. acnes by both methods. 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引用次数: 14
摘要
痤疮丙酸杆菌是革兰氏阳性厌氧杆菌,是皮肤的正常居民。虽然它通常被认为是血液培养物的污染物,但它偶尔会引起严重的感染,包括术后中枢神经系统感染。在这里,我们报告一例70岁的男性在神经外科手术后13个月发生由痤疮疱疮引起的脑脓肿。脑内脓液的立即革兰氏染色显示存在革兰氏阳性球菌。然而,培养5天后才观察到菌落生长。因此,我们对脓标本进行16S rRNA基因测序。分离物经鉴定为痤疮假单胞菌。菌落在初始培养后9天发育。使用菌落进行API Rapid ID 32A测试(biomrieux, France),但获得不可接受的轮廓。然后,将脓液转移到BACTEC FX (Becton Dickinson, USA)和bacact /Alert 3D (biomacrieux, Organon Teknika, USA)系统的富集液中,但5天后只有BACTEC FX系统可以检测到生长。我们对从布鲁氏菌琼脂中回收的菌落进行了16S rRNA基因测序和API Rapid 32A分析,该菌落接种于BACTEC FX系统的富集肉汤中的微生物生长。两种方法鉴定该菌为痤疮假单胞杆菌。该病例表明,16S rRNA基因测序可能是一种有用的替代方法,用于从培养5天后未显示生长的标本中鉴定生长缓慢的痤疮假单胞菌。
A case of brain abscess caused by Propionibacterium acnes 13 months after neurosurgery and confirmed by 16S rRNA gene sequencing.
Propionibacterium acnes is a gram-positive anaerobic bacillus and a normal inhabitant of the skin. Although it is often considered a contaminant of blood cultures, it can occasionally cause serious infections, including postoperative central nervous system infections. Here, we report the case of a 70-yr-old man who developed a large cerebral abscess caused by P. acnes 13 months after neurosurgery. Immediate gram staining of the pus from his brain revealed the presence of gram-positive coccobacilli. However, colony growth was observed only after 5 days of culture. Therefore, we performed 16S rRNA gene sequencing of the pus specimen. The isolate was identified as P. acnes. The colonies developed 9 days after the initial culture. The API Rapid ID 32A test (bioMérieux, France) was performed using a colony, but an unacceptable profile was obtained. Then, the pus was transferred into the enrichment broths of the BACTEC FX (Becton Dickinson, USA) and BacT/Alert 3D (bioMérieux, Organon Teknika, USA) systems, but only the BACTEC FX system could detect growth after 5 days. We performed 16S rRNA gene sequencing and API Rapid 32A profiling with a colony recovered from Brucella agar, which was inoculated with the microbial growth in the enrichment broth from the BACTEC FX system. The organism was identified as P. acnes by both methods. This case suggests that 16S rRNA gene sequencing may be a useful alternative for identifying slowly growing P. acnes from specimens that do not show growth after 5 days of culture.