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  • 1
    Publication Date: 2022-05-25
    Description: Author Posting. © Society of Systematic Biologists, 2004. This article is posted here by permission of Taylor and Francis for personal use, not for redistribution. The definitive version was published in Systematic Biology 53 (2004): 95-110, doi:10.1080/10635150490264842.
    Description: Bacterial endosymbionts are widespread across several insect orders and are involved in interactions ranging from obligate mutualism to reproductive parasitism. Candidatus Blochmannia gen. nov. (Blochmannia) is an obligate bacterial associate of Camponotus and related ant genera (Hymenoptera: Formicidae). The occurrence of Blochmannia in all Camponotus species sampled from field populations and its maternal transmission to host offspring suggest that this bacterium is engaged in a long-term, stable association with its ant hosts. However, evidence for cospeciation in this system is equivocal because previous phylogenetic studies were based on limited gene sampling, lacked statistical analysis of congruence, and have even suggested host switching. We compared phylogenies of host genes (the nuclear EF-1alphaF2 and mitochondrial COI/II) and Blochmannia genes (16S ribosomal DNA [rDNA], groEL, gidA, and rpsB), totaling more than 7 kilobases for each of 16 Camponotus species. Each data set was analyzed using maximum likelihood and Bayesian phylogenetic reconstruction methods. We found minimal conflict among host and symbiont phylogenies, and the few areas of discordance occurred at deep nodes that were poorly supported by individual data sets. Concatenated protein-coding genes produced a very well-resolved tree that, based on the Shimodaira-Hasegawa test, did not conflict with any host or symbiont data set. Correlated rates of synonymous substitution (dS) along corresponding branches of host and symbiont phylogenies further supported the hypothesis of cospeciation. These findings indicate that Blochmannia-Camponotus symbiosis has been evolutionarily stable throughout tens of millions of years. Based on inferred divergence times among the ant hosts, we estimated rates of sequence evolution of Blochmannia to be sim0.0024 substitutions per site per million years (s/s/MY) for the 16S rDNA gene and sim0.1094 s/s/MY at synonymous positions of the genes sampled. These rates are several-fold higher than those for related bacteria Buchnera aphidicola and Escherichia coli. Phylogenetic congruence among Blochmannia genes indicates genome stability that typifies primary endosymbionts of insects.
    Description: Funding for this research was provided by the NIH (R01 GM62626-01), the NSF (DEB 0089455 and associated REU supplement award), the NASA Astrobiology Institute (NCC2-1054), and the Josephine Bay Paul and C. Michael Paul Foundation.
    Keywords: Blochmannia ; Camponotus ; Cospeciation ; Endosymbiosis ; Molecular clock ; Phylogenetics
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 2
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    Public Library of Science (PLoS)
    Publication Date: 2022-05-25
    Description: © 2004 Jennifer J. Wernegreen. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The definitive version was published in PLoS Biology 2 (2004): e68, doi:10.1371/journal.pbio.0020068.
    Description: Symbiosis, an interdependent relationship between two species, is an important driver of evolutionary novelty and ecological diversity. Microbial symbionts in particular have been major evolutionary catalysts throughout the 4 billion years of life on earth and have largely shaped the evolution of complex organisms. Endosymbiosis is a specifi c type of symbiosis in which one—typically microbial—partner lives within its host and represents the most intimate contact between interacting organisms. Mitochondria and chloroplasts, for example, result from endosymbiotic events of lasting significance that extended the range of acceptable habitats for life. The wide distribution of intracellular bacteria across diverse hosts and marine and terrestrial habitats testifies to the continued importance of endosymbiosis in evolution. Among multicellular organisms, insects as a group form exceptionally diverse associations with microbial associates, including bacteria that live exclusively within host cells and undergo maternal transmission to offspring. These microbes have piqued the interest of evolutionary biologists because they represent a wide spectrum of evolutionary strategies, ranging from obligate mutualism to reproductive parasitism (Buchner 1965; Ishikawa 2003) (Box 1; Table 1).
    Description: JJW gratefully acknowledges the support of the National Institutes of Health (R01 GM62626-01), the National Science Foundation (DEB 0089455), the National Aeronautics and Space Administration Astrobiology Institute (NNA04CC04A), and the Josephine Bay Paul and C. Michael Paul Foundation.
    Keywords: Endosymbiosis ; Endosymbiosis manipulation
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 3
    Publication Date: 2022-05-26
    Description: Author Posting. © Inter-Research, 2009. This article is posted here by permission of Inter-Research for personal use, not for redistribution. The definitive version was published in Aquatic Microbial Ecology 57 (2009): 279-310, doi:10.3354/ame01340.
    Description: Acquisition of phototrophy is widely distributed in the eukaryotic tree of life and can involve algal endosymbiosis or plastid retention from green or red origins. Species with acquired phototrophy are important components of diversity in aquatic ecosystems, but there are major differences in host and algal taxa involved and in niches of protists with acquired phototrophy in marine and freshwater ecosystems. Organisms that carry out acquired phototrophy are usually mixotrophs, but the degree to which they depend on phototrophy is variable. Evidence suggests that ‘excess carbon’ provided by acquired phototrophy has been important in supporting major evolutionary innovations that are crucial to the current ecological roles of these protists in aquatic ecosystems. Acquired phototrophy occurs primarily among radiolaria, foraminifera, ciliates and dinoflagellates, but is most ecologically important among the first three. Acquired phototrophy in foraminifera and radiolaria is crucial to their contributions to carbonate, silicate, strontium, and carbon flux in subtropical and tropical oceans. Planktonic ciliates with algal kleptoplastids are important in marine and fresh waters, whereas ciliates with green algal endosymbionts are mostly important in freshwaters. The phototrophic ciliate Myrionecta rubra can be a major primary producer in coastal ecosystems. Our knowledge of how acquired phototrophy influences trophic dynamics and biogeochemical cycles is rudimentary; we need to go beyond traditional concepts of ‘plant’ and ‘animal’ functions to progress in our understanding of aquatic microbial ecology. This is a rich area for exploration using a combination of classical and molecular techniques, laboratory and field research, and physiological and ecosystem modeling.
    Description: F.N. and C.dV were supported by a SAD grant SYMFORAD from the Région Bretagne (France) and the BioMarKs project funded by the European ERA-net program BiodivERsA.
    Keywords: Mixotrophy ; Radiolaria ; Foraminifera ; Ciliates ; Dinoflagellates ; Kleptoplastidy ; Karyoklepty ; Endosymbiosis ; Myrionecta rubra
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 4
    Publication Date: 2022-05-26
    Description: Author Posting. © The Author(s), 2010. This is the author's version of the work. It is posted here by permission of Springer for personal use, not for redistribution. The definitive version was published in Photosynthesis Research 107 (2011): 117-132, doi:10.1007/s11120-010-9546-8.
    Description: Many non-photosynthetic species of protists and metazoans are capable of hosting viable algal endosymbionts or their organelles through adaptations of phagocytic pathways. A form of mixotrophy, acquired phototrophy (AcPh) encompasses a sweet of endosymbiotic and organelle retention interactions, that range from facultative to obligate. AcPh is a common phenomenon in aquatic ecosystems, with endosymbiotic associations generally more prevalent in nutrient poor environments, and organelle retention typically associated with more productive ones. All AcPhs benefit from enhanced growth due to access to photosynthetic products, however the degree of metabolic integration and dependency in the host varies widely. AcPhs are mixotrophic, using both heterotrophic and phototrophic carbon sources. AcPh is found in at least four of the major eukaryotic supergroups, and is the driving force in the evolution of secondary and tertiary plastid acquisitions. Mutualistic resource partitioning characterizes most algal endosymbiotic interactions, while organelle retention is a form of predation, characterized by nutrient flow (i.e. growth) in one direction. AcPh involves adaptations to recognize specific prey or endosymbionts and to house organelles or endosymbionts within the endomembrane system but free from digestion. In many cases, hosts depend upon AcPh for the production of essential nutrients, many of which remain obscure. The practice of AcPh has led to multiple independent secondary and tertiary plastid acquisition events among several eukaryote lineages, giving rise to the diverse array of algae found in modern aquatic ecosystems. This review highlights those AcPhs that are model research organisms for both metazoans and protists. Much of the basic biology of AcPhs remains enigmatic, particularly 1) which essential nutrients or factors make certain forms of AcPh obligatory, 2) how hosts regulate and manipulate endosymbionts or sequestered organelles, and 3) what genomic imprint, if any, AcPh leaves on non-photosynthetic host species.
    Description: Supported by NSF grant OCE-0851269
    Keywords: Acquired phototrophy ; Mixotrophy ; Kleptoplastidy ; Karyoklepty ; Endosymbiosis
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biosystems 28 (1992), S. 75-90 
    ISSN: 0303-2647
    Keywords: Algae ; Bacteria ; Endosymbiosis ; Land Plants ; Plastids
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biosystems 28 (1992), S. 47-55 
    ISSN: 0303-2647
    Keywords: Compatibility analysis ; Endosymbiosis ; Lateral transfer ; Variant filter
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biosystems 28 (1992), S. 91-106 
    ISSN: 0303-2647
    Keywords: Chlorarachnion ; Chloroplasts ; Chromista ; Cryptomonads ; Endosymbiosis ; Mitochondria
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0014-5793
    Keywords: (Brewer's yeast) ; Endosymbiosis ; Gram-posiitve bacteria ; Mitochondria, origin of ; Pyruvate dehydrogenase complex, type II
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biosystems 31 (1993), S. 85-92 
    ISSN: 0303-2647
    Keywords: Atmospherics ; Daisyworld ; Ecosystem ; Endosymbiosis ; Gaia ; James Lovelock ; Lynn Margulis
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1432-2048
    Keywords: Endosymbiosis ; Geosiphon ; Nostoc ; Photosynthesis in Geosiphon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Geosiphon pyriforme, an endosymbiotic association between a fungus and the cyanobacterium Nostoc, was shown by tracer studies to acquire carbon photosynthetically from CO2 or bicarbonate. The organism also fixes inorganic carbon in darkness, at lower rates than in the light. The patterns of label distribution are indicative of the operation of the reductive pentose-phosphate pathway in the light and of the phosphoenolpyruvate-carboxylase reaction in the dark. The results are discussed in relation to the evolution of photoautotrophic endosymbiotic associations.
    Type of Medium: Electronic Resource
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