应用16S rRNA基因及培养法综合分析术后上颌囊肿液细菌菌群。

ISRN dentistry Pub Date : 2012-01-01 Epub Date: 2012-05-22 DOI:10.5402/2012/840483
Naoto Sano, Yoshio Yamashita, Kazumasa Fukuda, Hatsumi Taniguchi, Masaaki Goto, Hiroshi Miyamoto
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引用次数: 7

摘要

对11例术后上颌囊肿(POMC)患者进行无菌收集囊内液,并从POMC液中提取DNA。在克隆16S rRNA基因约580 bp后,通过测序鉴定了细菌种类。采用培养法对病原菌进行鉴定。通过对1139个16S rRNA基因克隆进行517-596 bp的测序,确定了系统发育的同一性。共鉴定出1114个无性系,其余25个无性系未鉴定。通过16S rRNA基因分析,在POMC液样中鉴定出42属103种细菌。普雷沃菌属(91%)、奈瑟菌属(73%)、梭杆菌属(73%)、卟啉单胞菌属(73%)和丙酸杆菌属(73%)在所有患者中高度流行。11例患者中有6例以上检出mitis(64%)、Fusobacterium nucleatum(55%)、acnes丙酸杆菌(55%)、Staphylococcus capitis(55%)和Streptococcus salivarius(55%)。培养法得到的结果与16S rRNA基因分析得到的结果不同,但这两种方法对于鉴定病原菌,特别是培养法难以检测到的细菌,以及为POMC患者制定合理的治疗方案可能是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comprehensive Analysis of Bacterial Flora in Postoperative Maxillary Cyst Fluid by 16S rRNA Gene and Culture Methods.

Comprehensive Analysis of Bacterial Flora in Postoperative Maxillary Cyst Fluid by 16S rRNA Gene and Culture Methods.

Comprehensive Analysis of Bacterial Flora in Postoperative Maxillary Cyst Fluid by 16S rRNA Gene and Culture Methods.

Comprehensive Analysis of Bacterial Flora in Postoperative Maxillary Cyst Fluid by 16S rRNA Gene and Culture Methods.

Intracystic fluid was aseptically collected from 11 patients with postoperative maxillary cyst (POMC), and DNA was extracted from the POMC fluid. Bacterial species were identified by sequencing after cloning of approximately 580 bp of the 16S rRNA gene. Identification of pathogenic bacteria was also performed by culture methods. The phylogenetic identity was determined by sequencing 517-596 bp in each of the 1139 16S rRNA gene clones. A total of 1114 clones were classified while the remaining 25 clones were unclassified. A total of 103 bacterial species belonging to 42 genera were identified in POMC fluid samples by 16S rRNA gene analysis. Species of Prevotella (91%), Neisseria (73%), Fusobacterium (73%), Porphyromonas (73%), and Propionibacterium (73%) were found to be highly prevalent in all patients. Streptococcus mitis (64%), Fusobacterium nucleatum (55%), Propionibacterium acnes (55%), Staphylococcus capitis (55%), and Streptococcus salivarius (55%) were detected in more than 6 of the 11 patients. The results obtained by the culture method were different from those obtained by 16S rRNA gene analysis, but both approaches may be necessary for the identification of pathogens, especially of bacteria that are difficult to detect by culture methods, and the development of rational treatments for patients with POMC.

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