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马伤口的生物膜证据及微生物多样性

Biofilm evidence and the microbial diversity of horse wounds.

作者信息

Freeman Karen, Woods Emma, Welsby Sarah, Percival Steven L, Cochrane Christine A

机构信息

University of Liverpool, Department of Veterinary Clinical Science, Leahurst, Neston, South Wirral-CH64-7TE, UK.

出版信息

Can J Microbiol. 2009 Feb;55(2):197-202. doi: 10.1139/w08-115.

DOI:10.1139/w08-115
PMID:19295652
Abstract

Evidence of biofilms in human chronic wounds are thought to be responsible for preventing healing in a timely manner. However, biofilm evidence in horse wounds has not yet been documented. Consequently, this study aimed to determine whether biofilms could be detected in wounds, and to investigate the microbiology of chronic wounds in horses. Prior to analysis, wound surfaces were irrigated with 5 mL of sterile saline to remove debris. All wounds were swabbed twice (1 cm2 area) using sterile cotton-tipped swabs. In addition to this, 2 tissue biopsies were taken to investigate evidence of biofilm and the microbiology richness of the wounds. All swabs and 1 biopsy sample were transported to the laboratory in Robertson's cooked meat broth. Traditional culturable techniques and denaturing gradient gel electrophoresis with PCR were utilized to identify common bacteria isolated in all wounds. Following analysis of a number of the biopsy samples, biofilms could be clearly seen. The most common bacteria isolated from each wound analysed included Pseudomonas aeruginosa, Staphylococcus epidermidis, Serratia marcescens, Enterococcus faecalis, and Providencia rettgeri. Sequencing of the 16S ribosmonal DNAs, selected on the basis of DGGE profiling, enabled identification of bacterial species not identified using culturable technology. This study is the first to identify biofilms in the chronic wounds of horses. In addition, this study also demonstrated the importance of combining DGGE-PCR with culture techniques to provide better microbiology analysis of chronic wounds.

摘要

人类慢性伤口中生物膜的存在被认为是导致伤口无法及时愈合的原因。然而,马伤口中的生物膜证据尚未见报道。因此,本研究旨在确定伤口中是否能检测到生物膜,并调查马慢性伤口的微生物学情况。在分析之前,用5毫升无菌盐水冲洗伤口表面以清除碎屑。使用无菌棉拭子对所有伤口进行两次擦拭(1平方厘米区域)。除此之外,还取了2份组织活检样本,以调查生物膜证据和伤口的微生物丰富度。所有拭子和1份活检样本均在罗伯逊熟肉培养基中运至实验室。采用传统可培养技术和聚合酶链反应变性梯度凝胶电泳来鉴定所有伤口中分离出的常见细菌。在对多个活检样本进行分析后,可以清楚地看到生物膜。从每个分析的伤口中分离出的最常见细菌包括铜绿假单胞菌、表皮葡萄球菌、粘质沙雷氏菌、粪肠球菌和雷氏普罗威登斯菌。基于变性梯度凝胶电泳图谱选择的16S核糖体DNA测序,能够鉴定出使用可培养技术未鉴定出的细菌种类。本研究首次在马的慢性伤口中鉴定出生物膜。此外,本研究还证明了将变性梯度凝胶电泳-聚合酶链反应与培养技术相结合,以更好地对慢性伤口进行微生物学分析的重要性。

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