Department of Ecology, Evolution, & Behavior, University of Minnesota-Twin Cities, 100 Ecology Building, 1987 Upper Buford Circle, Saint Paul, MN, 55108, USA,
Microb Ecol. 2014 Apr;67(3):700-21. doi: 10.1007/s00248-013-0356-3. Epub 2014 Jan 9.
Vibrio fischeri isolated from Euprymna scolopes (Cephalopoda: Sepiolidae) was used to create 24 lines that were serially passaged through the non-native host Euprymna tasmanica for 500 generations. These derived lines were characterized for biofilm formation, swarming motility, carbon source utilization, and in vitro bioluminescence. Phenotypic assays were compared between "ES" (E. scolopes) and "ET" (E. tasmanica) V. fischeri wild isolates to determine if convergent evolution was apparent between E. tasmanica evolved lines and ET V. fischeri. Ecological diversification was observed in utilization of most carbon sources examined. Convergent evolution was evident in motility, biofilm formation, and select carbon sources displaying hyperpolymorphic usage in V. fischeri. Convergence in bioluminescence (a 2.5-fold increase in brightness) was collectively evident in the derived lines relative to the ancestor. However, dramatic changes in other properties--time points and cell densities of first light emission and maximal light output and emergence of a lag phase in growth curves of derived lines--suggest that increased light intensity per se was not the only important factor. Convergent evolution implies that gnotobiotic squid light organs subject colonizing V. fischeri to similar selection pressures. Adaptation to novel hosts appears to involve flexible microbial metabolism, establishment of biofilm and swarmer V. fischeri ecotypes, and complex changes in bioluminescence. Our data demonstrate that numerous alternate fitness optima or peaks are available to V. fischeri in host adaptive landscapes, where novel host squids serve as habitat islands. Thus, V. fischeri founder flushes occur during the initiation of light organ colonization that ultimately trigger founder effect diversification.
从文昌鱼(头足纲:枪乌贼科)中分离出的 Fischeri 弧菌被用于创建 24 条连续通过非本地宿主文昌鱼 Tasmanica 传代 500 代的衍生系。这些衍生系的生物膜形成、群集运动、碳源利用和体外生物发光特性进行了表征。在 ES(E. scolopes)和 ET(E. tasmanica)V. fischeri 野生分离株之间比较表型测定,以确定 ET V. fischeri 进化系之间是否出现趋同进化。在大多数检查的碳源利用方面观察到生态多样化。在运动、生物膜形成和选择碳源方面观察到趋同进化,在 V. fischeri 中表现出超多态性使用。生物发光(亮度增加 2.5 倍)在衍生系中相对于祖先表现出明显的趋同。然而,其他特性的剧烈变化——首次发光和最大光输出的时间点和细胞密度以及衍生系生长曲线中出现的滞后期——表明光强度本身并不是唯一的重要因素。趋同进化表明,无菌鱿鱼光器官使定植的 Fischeri 弧菌受到类似的选择压力。对新宿主的适应似乎涉及微生物代谢的灵活性、生物膜和游动 Fischeri 弧菌生态型的建立,以及生物发光的复杂变化。我们的数据表明,在宿主适应性景观中,Fischeri 弧菌有许多替代的适应度最优值或峰值,其中新型宿主鱿鱼作为栖息地岛屿。因此,在光器官定植开始时会发生 Fischeri 弧菌的奠基者冲洗,最终引发奠基者效应多样化。