Belda-Baillie Carmen A, Baillie Brett K, Maruyama Tadashi
Marine Biotechnology Institute Co., Ltd., Kamaishi Laboratories, Heita, Kamaishi City, Iwate 026-0001, Japan.
Biol Bull. 2002 Feb;202(1):74-85. doi: 10.2307/1543224.
To understand the flexibility of symbiotic associations in coral reefs, we investigated the specificity of the Aiptasia (cf. insignis)-Symbiodinium association in the laboratory by rendering the anemones aposymbiotic and inoculating them with different isolates of SYMBIODINIUM: Infective algal symbionts were monitored over 3 months by re-isolation and identification using denaturing-gradient gel electrophoresis and sequence comparison of their amplified 18S rRNA hypervariable V1 + V2 gene region. Despite similarity in their external morphology, the algal isolates differed in their infectivity towards the host. Within days of single-isolate inoculation, aposymbiotic anemones formed associations with fresh or cultured isolates (clade B) from the anemones Aiptasia sp. or A. tagetes, respectively. They associated to a limited extent with cultured isolates (clade A) from the tridacnids Tridacna crocea or Hippopus hippopus, and not at all with a cultured isolate (clade C) from the stony coral Montipora verrucosa, nor with a free-living isolate (clade A) from subtidal sands. Aposymbiotic anemones inoculated with a mixture of all isolates had only the anemone taxon as their detectable symbionts. Re-inoculation of induced symbioses with a mixture of all isolates and incubation with wild anemones showed that the initial induced symbioses with the anemone taxon were stable. Anemones originally infected with tridacnid isolates either additionally acquired the anemone taxon or had the former outgrown by the latter. These results demonstrate the presence of a host-symbiont recognition mechanism, and possibly competition among potential algal symbionts in the Aiptasia-Symbiodinium association. Here we present a method that may be useful in monitoring the algal population dynamics in symbiotic corals in the field, along with an efficient method of rendering Aiptasia aposymbiotic for further laboratory investigation of Aiptasia-Symbiodinium symbioses.
为了解珊瑚礁中共生关系的灵活性,我们在实验室中通过使海葵成为无共生体状态并接种不同的共生藻分离株,研究了艾氏海葵(cf. insignis)与共生藻之间关系的特异性:通过变性梯度凝胶电泳重新分离和鉴定,并对其扩增的18S rRNA高变V1 + V2基因区域进行序列比较,在3个月内监测感染性藻类共生体。尽管这些藻类分离株的外部形态相似,但它们对宿主的感染性却有所不同。在单株接种后的几天内,无共生体海葵分别与来自艾氏海葵属或塔氏艾氏海葵的新鲜或培养分离株(B类群)形成了共生关系。它们与来自长砗磲或平濑马氏贝的培养分离株(A类群)有一定程度的共生,而与来自疣状棘豆珊瑚的培养分离株(C类群)以及来自潮下沙的自由生活分离株(A类群)完全没有共生。接种了所有分离株混合物的无共生体海葵,其可检测到的共生体只有海葵类群。用所有分离株的混合物对诱导的共生体进行重新接种,并与野生海葵一起培养,结果表明最初与海葵类群诱导的共生体是稳定的。最初感染了砗磲分离株的海葵,要么额外获得了海葵类群,要么前者被后者取代。这些结果证明了宿主 - 共生体识别机制的存在,以及在艾氏海葵 - 共生藻共生关系中潜在藻类共生体之间可能存在的竞争。在这里,我们提出了一种可能有助于监测野外共生珊瑚中藻类种群动态的方法,以及一种使艾氏海葵成为无共生体状态的有效方法,以便进一步在实验室研究艾氏海葵 - 共生藻共生关系。