Abstract:Two species of the colonial green flagellate family Volvocaceae are worldwide in distribution yet exhibit contrasting species structure. Geographically disparate isolates of Gonium pectorale Mueller can interbreed while isolates of Pandorina morum Bory behave quite differently. More than 20 sexually isolated subpopulations occur within this species; these have been termed “syngens” (sensu Sonneborn). Because prezygotic barriers to mating cause intersyngen pairings to fail, breeding analyses cannot be used to e… Show more
“…was 4 to 7%, a level of variation similar to those observed among other algal ITS sequences used successfully for phylogenetic analysis (13,24,29). A limitation of the analysis of ITS sequence variation is the difficulty in defining suitable outgroups (relatives close enough that confident alignment is possible) for phylogenetic analyses.…”
The phylogenetic relationships of bacterial symbionts from three gall-bearing species in the marine red algal genus Prionitis (Rhodophyta) were inferred from 16S rDNA sequence analysis and compared to host phylogeny also inferred from sequence comparisons (nuclear ribosomal internal-transcribed-spacer region). Gall formation has been described previously on two species of Prionitis, P. lanceolata (from central California) and P. decipiens (from Peru). This investigation reports gall formation on a third related host, Prionitis filiformis. Phylogenetic analyses based on sequence comparisons place the bacteria as a single lineage within the Roseobacter grouping of the ␣ subclass of the division Proteobacteria (99.4 to 98.25% sequence identity among phylotypes). Comparison of symbiont and host molecular phylogenies confirms the presence of three gallbearing algal lineages and is consistent with the hypothesis that these red seaweeds and their bacterial symbionts are coevolving. The species specificity of these associations was investigated in nature by whole-cell hybridization of gall bacteria and in the laboratory by using cross-inoculation trials. Whole-cell in situ hybridization confirmed that a single bacterial symbiont phylotype is present in galls on each host. In laboratory trials, bacterial symbionts were incapable of inducing galls on alternate hosts (including two non-gall-bearing species). Symbiont-host specificity in Prionitis gall formation indicates an effective ecological separation between these closely related symbiont phylotypes and provides an example of a biological context in which to consider the organismic significance of 16S rDNA sequence variation.Marine bacteria are associated with gall formation (tumorigenesis) on a number of species of red algae, although only two reports detail the specific causation of an algal gall by an identified bacterium (5, 10). This probably reflects the general situation encountered when attempting to cultivate, or isolate in pure culture, symbiotic microbes (10,33,44). In the red algal genus Prionitis (Rhodophyta, Halymeniaceae, Gigartinales) gall formation is known from at least four species world wide and is, in the case of Prionitis lanceolata (from central California), associated with the presence of a specific microorganism (5). Despite attempts by several authors, this bacterium has yet to be cultivated or isolated in pure culture (3)(4)(5). No physiological function of these bacterially induced Prionitis galls has been determined, nor is it apparent what, if any, benefit is derived by algal host or bacterial invader. This organismic relationship is termed a symbiosis sensu DeBary as used by Smith, meaning simply the living together of differently named organisms (43). The 16S rDNA phylotype of this eubacterium has been determined from its complete small-subunit ribosomal DNA sequence and whole-cell hybridization used to confirm the inductive role of this symbiont in gall formation (5).The purpose of this investigation was to determine if bacterial gall ...
“…was 4 to 7%, a level of variation similar to those observed among other algal ITS sequences used successfully for phylogenetic analysis (13,24,29). A limitation of the analysis of ITS sequence variation is the difficulty in defining suitable outgroups (relatives close enough that confident alignment is possible) for phylogenetic analyses.…”
The phylogenetic relationships of bacterial symbionts from three gall-bearing species in the marine red algal genus Prionitis (Rhodophyta) were inferred from 16S rDNA sequence analysis and compared to host phylogeny also inferred from sequence comparisons (nuclear ribosomal internal-transcribed-spacer region). Gall formation has been described previously on two species of Prionitis, P. lanceolata (from central California) and P. decipiens (from Peru). This investigation reports gall formation on a third related host, Prionitis filiformis. Phylogenetic analyses based on sequence comparisons place the bacteria as a single lineage within the Roseobacter grouping of the ␣ subclass of the division Proteobacteria (99.4 to 98.25% sequence identity among phylotypes). Comparison of symbiont and host molecular phylogenies confirms the presence of three gallbearing algal lineages and is consistent with the hypothesis that these red seaweeds and their bacterial symbionts are coevolving. The species specificity of these associations was investigated in nature by whole-cell hybridization of gall bacteria and in the laboratory by using cross-inoculation trials. Whole-cell in situ hybridization confirmed that a single bacterial symbiont phylotype is present in galls on each host. In laboratory trials, bacterial symbionts were incapable of inducing galls on alternate hosts (including two non-gall-bearing species). Symbiont-host specificity in Prionitis gall formation indicates an effective ecological separation between these closely related symbiont phylotypes and provides an example of a biological context in which to consider the organismic significance of 16S rDNA sequence variation.Marine bacteria are associated with gall formation (tumorigenesis) on a number of species of red algae, although only two reports detail the specific causation of an algal gall by an identified bacterium (5, 10). This probably reflects the general situation encountered when attempting to cultivate, or isolate in pure culture, symbiotic microbes (10,33,44). In the red algal genus Prionitis (Rhodophyta, Halymeniaceae, Gigartinales) gall formation is known from at least four species world wide and is, in the case of Prionitis lanceolata (from central California), associated with the presence of a specific microorganism (5). Despite attempts by several authors, this bacterium has yet to be cultivated or isolated in pure culture (3)(4)(5). No physiological function of these bacterially induced Prionitis galls has been determined, nor is it apparent what, if any, benefit is derived by algal host or bacterial invader. This organismic relationship is termed a symbiosis sensu DeBary as used by Smith, meaning simply the living together of differently named organisms (43). The 16S rDNA phylotype of this eubacterium has been determined from its complete small-subunit ribosomal DNA sequence and whole-cell hybridization used to confirm the inductive role of this symbiont in gall formation (5).The purpose of this investigation was to determine if bacterial gall ...
“…In contrast, positive signals were obtained for both probes using the control algal total DNA. We chose the nuclear ribosomal DNA ITS region because of its rapid evolutionary change, which would prevent the V. litorea ITS probe from hybridizing to slug ITS and because of its presence in multiple copies (White et al, 1990;Coleman et al, 1994;Zechman et al, 1994;Manhart et al, 1995).…”
Early in its life cycle, the marine mollusc Elysia chlorotica Gould forms an intracellular endosymbiotic association with chloroplasts of the chromophytic alga Vaucheria litorea C. Agardh. As a result, the dark green sea slug can be sustained in culture solely by photoautotrophic CO 2 fixation for at least 9 months if provided with only light and a source of CO 2 . Here we demonstrate that the sea slug symbiont chloroplasts maintain photosynthetic oxygen evolution and electron transport activity through photosystems I and II for several months in the absence of any external algal food supply. This activity is correlated to the maintenance of functional levels of chloroplast-encoded photosystem proteins, due in part at least to de novo protein synthesis of chloroplast proteins in the sea slug. Levels of at least one putative algal nuclear encoded protein, a light-harvesting complex protein homolog, were also maintained throughout the 9-month culture period. The chloroplast genome of V. litorea was found to be 119.1 kb, similar to that of other chromophytic algae. Southern analysis and polymerase chain reaction did not detect an algal nuclear genome in the slug, in agreement with earlier microscopic observations. Therefore, the maintenance of photosynthetic activity in the captured chloroplasts is regulated solely by the algal chloroplast and animal nuclear genomes.
“…In addition, the internal transcribed spacer (ITS) regions of nuclear ribosomal DNA from three strains of E. unicocca (NIES-724, NIES-726 and UTEX 1221) and two aplanosporic strains (TKI-C-2 and 990601-IE-5) were sequenced, as described by Sakayama et al (2004), except for the primers used for polymerase chain reaction (PCR) and sequencing. The primers for the ITS regions were those of Coleman et al (1994) (Mai & Coleman, 1997;Coleman, 2002). The sequence alignment is available upon request from the corresponding author (H.N.).…”
Colonial volvocacean algae engage in two types of sexual reproduction: isogamy and anisogamy/oogamy with sperm packets. This difference is an important generic diagnosis within the Volvocaceae. Although Yamagishiella differs from the anisogamous genus Eudorina in its isogamous sexual reproduction, the vegetative morphology and asexual reproduction characteristics of the two genera are indistinguishable, especially between Eudorina unicocca G. M. Smith and Yamagishiella unicocca (Rayburn et Starr) Nozaki. We re-examined morphological characteristics of E. unicocca and related species, using multiple strains of E. unicocca and Y. unicocca and molecular phylogenetic analyses. Strains from two Japanese lakes, which produced aplanospores and were solely asexual, could be assigned to either E. unicocca or Y. unicocca, based on traditional morphological diagnoses. However, a new morphological diagnosis (the difference in the distribution and number of contractile vacuoles on the cell surface) and molecular phylogenetic analyses demonstrated that all were E. unicocca. Furthermore, E. unicocca can be divided into two species on the basis of the presence or absence of individual cellular sheaths in the colonial gelatinous matrix, which are observable with methylene blue staining. These two species, E. peripheralis (Goldstein) T. K. Yamada stat. nov. (¼ E. unicocca var. peripherialis Goldstein) and E. unicocca (including the Japanese aplanosporic strains), formed two robust monophyletic groups, based on chloroplast gene sequences for the large RuBisCO subunit and internal transcribed spacer regions of nuclear ribosomal DNA.
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