Bradshaw David J, Marsh Philip D, Allison Clive, Schilling Kurt M
Research Division, CAMR, Salisbury SP4 OJG, UK.
Unilever Research Port Sunlight Laboratory, Bebington, Wirral L63 3JW, UK.
Microbiology (Reading). 1996 Mar;142 ( Pt 3):623-629. doi: 10.1099/13500872-142-3-623.
The effect of aeration on the development of a defined biofilm consortium of oral bacteria was investigated in a two-stage chemostat system. An inoculum comprising 10 species, including both facultatively anaerobic and obligately anaerobic bacteria, and species associated with oral health and disease, was inoculated into an anaerobic first-stage chemostat vessel. The effluent from this chemostat was linked to an aerated [200 ml CO2/air (5:95, v/v) min-1] second-stage vessel, in which removable hydroxyapatite discs were inserted to allow biofilm formation. Comparisons were made of planktonic and biofilm communities in the aerated second-stage vessel by means of viable counts. Both planktonic and early biofilm communities were dominated by Neisseria subflava, comprising > 40% of total c.f.u. in the fluid phase, and > 80% of c.f.u. in 2 h biofilms. Obligate anaerobes persisted in this mixed culture, and succession in biofilms led them to predominate only after 7 d. Despite the continuous addition of air, the dissolved oxygen tension (dO2) within the culture remained low (< 5% of air saturation), and the redox potential (Eh) was -275 mV. In order to assess the significance of the presence of N. subflava in community development, a subsequent experiment omitted this aerobe from the inoculum, to produce a nine-species culture. The planktonic phase was predominated by three streptococcal species, Prevotella nigrescens and Fusobacterium nucleatum. Biofilms again underwent successional changes, with anaerobes increasing in proportion with time. In contrast to the culture including N. subflava, dO2 was 50-60% of air saturation, and the Eh was +50 mV. In the final experiment, the rate of addition of first-stage culture was reduced to 1/10 of that in the previous experiment, in order to determine whether anaerobes were growing, rather than merely persisting in the aerated culture. The data for the planktonic phase indicated that the anaerobes were growing in aerated (dO2 40-50%, Eh +100 mV) conditions. Once again, anaerobes increased in proportion in older biofilms. The study indicates that mixed cultures can protect obligate anaerobes from the toxic effects of oxygen, both in the biofilm and planktonic modes of growth.
在两阶段恒化器系统中研究了曝气对口腔细菌特定生物膜群落发育的影响。将包含10个物种(包括兼性厌氧菌和专性厌氧菌以及与口腔健康和疾病相关的物种)的接种物接种到厌氧的第一阶段恒化器容器中。该恒化器的流出物连接到一个曝气的[200 ml CO₂/空气(5:95,v/v)min⁻¹]第二阶段容器,其中插入了可移除的羟基磷灰石圆盘以允许生物膜形成。通过活菌计数对曝气的第二阶段容器中的浮游生物和生物膜群落进行了比较。浮游生物和早期生物膜群落均以微黄奈瑟菌为主,在液相中占总菌落形成单位的>40%,在2小时生物膜中占菌落形成单位的>80%。专性厌氧菌在这种混合培养物中持续存在,生物膜中的演替导致它们仅在7天后占主导地位。尽管持续通入空气,但培养物中的溶解氧张力(dO₂)仍然很低(<空气饱和度的5%),氧化还原电位(Eh)为-275 mV。为了评估微黄奈瑟菌在群落发育中的存在意义,后续实验从接种物中省略了这种需氧菌,以产生九物种培养物。浮游阶段以三种链球菌、变黑普雷沃菌和具核梭杆菌为主。生物膜再次经历了演替变化,厌氧菌的比例随时间增加。与包含微黄奈瑟菌的培养物相比,dO₂为空气饱和度的50-60%,Eh为+50 mV。在最终实验中,将第一阶段培养物的添加速率降低到先前实验的1/10,以确定厌氧菌是在生长,而不仅仅是在曝气培养物中持续存在。浮游阶段的数据表明厌氧菌在曝气(dO₂ 40-50%,Eh +100 mV)条件下生长。厌氧菌在较老的生物膜中的比例再次增加。该研究表明,混合培养物可以在生物膜和浮游生长模式下保护专性厌氧菌免受氧气的毒性影响。