Cary S C
Department of Microbiology, Oregon State University, Corvallis 97331.
Mol Mar Biol Biotechnol. 1994 Jun;3(3):121-30.
Invertebrates that contain endosymbiotic chemoautotrophic bacteria are widely distributed in a variety of reducing marine habitats (i.e., hydrothermal vents and cold seeps). The mechanisms of symbiont transmission and incorporation during early host development are poorly understood primarily because these critical early life stages have not been procured. Solemya reidi is a gutless protobranch bivalve found inhabiting pulpmill effluent and sewage outfall sites. Endosymbiotic sulfur oxidizing bacteria are contained within specialized host cells of the gill filaments. These bivalves have the advantage over their deep-sea counterparts in that they can be spawned and cultured axenically, providing the opportunity to examine the ontogenetic process of symbiont incorporation. The 16S rDNA of the symbiont from Solemya reidi was sequenced from a PCR product obtained using two bacterial-specific primers. Phylogenetic analysis of this sequence identified a hypervariable region of the molecule that was unique to this symbiont. An 18-base oligonucleotide probe was synthesized and tested for specificity and sensitivity to detect its symbiont-specific target. Immobilized cellular RNAs from a range of taxa were used to screen the specificity of the Solemya probe. At high stringency, the symbiont-specific probe hybridized only to RNA extracted from gill tissue of S. reidi. When matched with a bacterial-specific forward primer in PCR amplifications, the symbiont-specific probe successfully amplified S. reidi symbiont 16S rDNA genes in genomic DNA isolated from the host ovary, eggs, and 1- and 4-day-old larvae. Amplifications detected the presence of symbiont target in the germ tissue and larvae. Nonradioactive in situ hybridizations were performed on 3-day-old larvae with the symbiont-specific probe. Detection of hybrids localized the symbionts to the epithelial test cells of the larvae. These results suggest that the symbionts are vertically transmitted with the egg and are incorporated as a post-metamorphosis event.
含有内共生化学自养细菌的无脊椎动物广泛分布于各种还原性海洋栖息地(如热液喷口和冷泉)。共生体在宿主早期发育过程中的传播和整合机制目前了解甚少,主要原因是这些关键的早期生命阶段难以获得。里氏索足蛤是一种无肠的原鳃双壳类动物,栖息于纸浆厂废水排放口和污水排放口。内共生硫氧化细菌存在于鳃丝的特殊宿主细胞内。这些双壳类动物比它们的深海同类具有优势,因为它们可以无菌产卵和培养,这为研究共生体整合的个体发育过程提供了机会。使用两种细菌特异性引物从里氏索足蛤共生体的PCR产物中对其16S rDNA进行测序。对该序列的系统发育分析确定了该分子的一个高变区,该高变区是该共生体所特有的。合成了一个18碱基的寡核苷酸探针,并对其特异性和敏感性进行了测试,以检测其共生体特异性靶标。使用来自一系列分类群的固定化细胞RNA来筛选索足蛤探针的特异性。在高严谨度下,共生体特异性探针仅与从里氏索足蛤鳃组织中提取的RNA杂交。当在PCR扩增中与细菌特异性正向引物匹配时,共生体特异性探针成功地从宿主卵巢、卵以及1日龄和4日龄幼虫中分离的基因组DNA中扩增出里氏索足蛤共生体16S rDNA基因。扩增检测到生殖组织和幼虫中存在共生体靶标。使用共生体特异性探针对3日龄幼虫进行了非放射性原位杂交。杂交体的检测将共生体定位到幼虫的上皮测试细胞中。这些结果表明,共生体通过卵垂直传播,并在变态后事件中整合。