Graduate School of Integrated Sciences for Life, Hiroshima University, Higashi-Hiroshima, Hiroshima, Japan.
Research Center for Subtropical Fisheries, Seikai National Fisheries Research Institute, Fisheries Research and Education Agency, Ishigaki, Okinawa, Japan.
PLoS One. 2019 Jul 19;14(7):e0220141. doi: 10.1371/journal.pone.0220141. eCollection 2019.
Unlike most bivalve shellfishes, giant clams (tridacnines) harbor symbiotic microalgae (zooxanthellae) in their fleshy bodies. Zooxanthellae are not maternally inherited by tridacnine offspring, hence, the larvae must acquire zooxanthellae from external sources, although such algal populations or sources in the environment are currently unknown. It is well known that giant clams expel fecal pellets that contain viable zooxanthellae cells, but whether these cells are infectious or just an expelled overpopulation from the giant clams has not been investigated. In this study, we observed the ultrastructural and photosynthetic competencies of zooxanthellae in the fecal pellets of Tridacna crocea and further tested the ability of these cells to infect T. squamosa juveniles. The ultrastructure of the zooxanthellae cells showed that the cells were intact and had not undergone digestion. Additionally, these zooxanthellae cells showed a maximum quantum yield of photosystem II (Fv/Fm) as high as those retained in the mantle of the giant clam. Under the assumption that feces might provide symbionts to the larvae of other giant clams, fecal pellets from Tridacna squamosa and T. crocea were given to artificially hatched 1-day-old T. squamosa larvae. On the 9th day, 15-34% of the larvae provided with the fecal pellets took up zooxanthellae in their stomach, and on the 14th day, zooxanthellae cells reached the larval margin, indicating the establishment of symbiosis. The rate reaching this stage was highest, ca. 5.3%, in the larvae given whole (nonhomogenized) pellets from T. crocea. The composition of zooxanthellae genera contained in the larvae were similar to those in the fecal pellets, although the abundance ratios were significantly different. This study is the first to demonstrate the potential of giant clam fecal pellets as symbiont vectors to giant clam larvae. These results also demonstrate the possibility that fecal pellets are a source of zooxanthellae in coral reefs.
与大多数双壳贝类不同,巨蛤(砗磲)的肉体中寄生着共生微藻(虫黄藻)。虫黄藻不是通过巨蛤后代的母系遗传获得的,因此幼虫必须从外部来源获得虫黄藻,尽管目前尚不清楚环境中的藻类种群或来源。众所周知,巨蛤会排出含有有活力的虫黄藻细胞的粪便颗粒,但这些细胞是否具有感染力,或者只是巨蛤过度繁殖而排出的,尚未进行研究。在这项研究中,我们观察了砗磲粪便中虫黄藻的超微结构和光合作用能力,并进一步测试了这些细胞感染 T. squamosa 幼虫的能力。虫黄藻细胞的超微结构表明,这些细胞完整无损,没有被消化。此外,这些虫黄藻细胞的最大光化学量子产量(Fv/Fm)与保留在巨蛤套膜中的虫黄藻相当。假设粪便可能为其他巨蛤的幼虫提供共生体,因此我们将来自 T. squamosa 和 T. crocea 的粪便给予人工孵化的 1 天大的 T. squamosa 幼虫。在第 9 天,有 15-34%的幼虫在胃中吸收了虫黄藻,在第 14 天,虫黄藻细胞到达幼虫边缘,表明共生关系建立。在给予来自 T. crocea 的完整(未均质化)粪便颗粒的幼虫中,达到这一阶段的比例最高,约为 5.3%。幼虫中虫黄藻属的组成与粪便中的相似,尽管丰度比有显著差异。本研究首次证明了巨蛤粪便作为共生体载体向巨蛤幼虫传播的潜力。这些结果还表明,粪便可能是珊瑚礁中虫黄藻的来源之一。