Min K R, Rickard A H
Department of Biological Sciences, Binghamton University, NY 13902, USA.
Appl Environ Microbiol. 2009 Jun;75(12):3987-97. doi: 10.1128/AEM.02843-08. Epub 2009 Apr 17.
Coaggregation is hypothesized to enhance freshwater biofilm development. To investigate this hypothesis, the ability of the coaggregating bacterium Sphingomonas natatoria to form single- and dual-species biofilms was studied and compared to that of a naturally occurring spontaneous coaggregation-deficient variant. Attachment assays using metabolically inactive cells were performed using epifluorescence and confocal laser scanning microscopy. Under static and flowing conditions, coaggregating S. natatoria 2.1gfp cells adhered to glass surfaces to form diaphanous single-species biofilms. When glass surfaces were precoated with coaggregation partner Micrococcus luteus 2.13 cells, S. natatoria 2.1gfp cells formed densely packed dual-species biofilms. The addition of 80 mM galactosamine, which reverses coaggregation, mildly reduced adhesion to glass but inhibited the interaction and attachment to glass-surface-attached M. luteus 2.13 cells. As opposed to wild-type coaggregating cells, coaggregation-deficient S. natatoria 2.1COGgfp variant cells were retarded in colonizing glass and did not interact with glass-surface-attached M. luteus 2.13 cells. To determine if coaggregation enhances biofilm growth and expansion, viable coaggregating S. natatoria 2.1gfp cells or the coaggregation-deficient variant S. natatoria 2.1COGgfp cells were coinoculated in flow cells with viable M. luteus 2.13 cells and allowed to grow together for 96 h. Coaggregating S. natatoria 2.1gfp cells outcompeted M. luteus 2.13 cells, and 96-h biofilms were composed predominantly of S. natatoria 2.1gfp cells. Conversely, when coaggregation-deficient S. natatoria 2.1COGgfp cells were coinoculated with M. luteus 2.13 cells, the 96-h biofilm contained few coaggregation-deficient S. natatoria 2.1 cells. Thus, coaggregation promotes biofilm integration by facilitating attachment to partner species and likely contributes to the expansion of coaggregating S. natatoria 2.1 populations in dual-species biofilms through competitive interactions.
据推测,共聚集作用可促进淡水生物膜的形成。为了验证这一假设,研究了共聚集细菌游泳鞘氨醇单胞菌形成单物种和双物种生物膜的能力,并将其与天然存在的自发共聚集缺陷变体进行了比较。使用代谢不活跃的细胞进行附着试验,采用落射荧光显微镜和共聚焦激光扫描显微镜。在静态和流动条件下,共聚集的游泳鞘氨醇单胞菌2.1gfp细胞附着在玻璃表面,形成透明的单物种生物膜。当玻璃表面预先包被有共聚集伙伴藤黄微球菌2.13细胞时,游泳鞘氨醇单胞菌2.1gfp细胞形成密集堆积的双物种生物膜。添加80 mM半乳糖胺可逆转共聚集作用,轻微降低对玻璃的附着力,但抑制与玻璃表面附着的藤黄微球菌2.13细胞的相互作用和附着。与野生型共聚集细胞不同,共聚集缺陷的游泳鞘氨醇单胞菌2.1COGgfp变体细胞在定殖于玻璃时受到阻碍,并且不与玻璃表面附着的藤黄微球菌2.13细胞相互作用。为了确定共聚集是否增强生物膜的生长和扩展,将有活力的共聚集游泳鞘氨醇单胞菌2.1gfp细胞或共聚集缺陷变体游泳鞘氨醇单胞菌2.1COGgfp细胞与有活力的藤黄微球菌2.13细胞一起接种到流动池中,共同培养96小时。共聚集的游泳鞘氨醇单胞菌2.1gfp细胞胜过藤黄微球菌2.13细胞,96小时的生物膜主要由游泳鞘氨醇单胞菌2.1gfp细胞组成。相反,当共聚集缺陷的游泳鞘氨醇单胞菌2.1COGgfp细胞与藤黄微球菌2.13细胞一起接种时,96小时的生物膜中几乎没有共聚集缺陷的游泳鞘氨醇单胞菌2.1细胞。因此,共聚集通过促进与伙伴物种的附着来促进生物膜整合,并可能通过竞争相互作用有助于双物种生物膜中共聚集的游泳鞘氨醇单胞菌2.1种群的扩展。