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培养和检测以前未培养微生物的新策略。

New strategies for cultivation and detection of previously uncultured microbes.

作者信息

Stevenson Bradley S, Eichorst Stephanie A, Wertz John T, Schmidt Thomas M, Breznak John A

机构信息

Department of Microbiology and Molecular Genetics, Michigan State University, 2209 Biomedical Physical Sciences, East Lansing, MI 48824-4320, USA.

出版信息

Appl Environ Microbiol. 2004 Aug;70(8):4748-55. doi: 10.1128/AEM.70.8.4748-4755.2004.

Abstract

An integrative approach was used to obtain pure cultures of previously uncultivated members of the divisions Acidobacteria and Verrucomicrobia from agricultural soil and from the guts of wood-feeding termites. Some elements of the cultivation procedure included the following: the use of agar media with little or no added nutrients; relatively long periods of incubation (more than 30 days); protection of cells from exogenous peroxides; and inclusion of humic acids or a humic acid analogue (anthraquinone disulfonate) and quorum-signaling compounds (acyl homoserine lactones) in growth media. The bacteria were incubated in the presence of air and in hypoxic (1 to 2% O(2) [vol/vol]) and anoxic atmospheres. Some bacteria were incubated with elevated concentrations of CO(2) (5% [vol/vol]). Significantly more Acidobacteria were found on isolation plates that had been incubated with 5% CO(2). A simple, high-throughput, PCR-based surveillance method (plate wash PCR) was developed. This method greatly facilitated detection and ultimate isolation of target bacteria from as many as 1,000 colonies of nontarget microbes growing on the same agar plates. Results illustrate the power of integrating culture methods with molecular techniques to isolate bacteria from phylogenetic groups underrepresented in culture.

摘要

采用综合方法从农业土壤和以木材为食的白蚁肠道中获取酸杆菌门和疣微菌门中以前未培养的成员的纯培养物。培养过程的一些要素如下:使用添加很少或不添加营养成分的琼脂培养基;较长的培养时间(超过30天);保护细胞免受外源过氧化物的影响;在生长培养基中加入腐殖酸或腐殖酸类似物(蒽醌二磺酸盐)和群体感应化合物(酰基高丝氨酸内酯)。细菌在有空气、低氧(1%至2% O₂[体积/体积])和无氧环境中培养。一些细菌在CO₂浓度升高(5%[体积/体积])的条件下培养。在含有5% CO₂培养的分离平板上发现的酸杆菌明显更多。开发了一种简单的、基于PCR的高通量监测方法(平板冲洗PCR)。该方法极大地促进了从生长在同一琼脂平板上多达1000个非目标微生物菌落中检测和最终分离目标细菌。结果表明将培养方法与分子技术相结合对于从培养中代表性不足的系统发育群体中分离细菌的强大作用。

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