Cellular dialogues in the holobiont
This book examines how the growing knowledge of the huge range of protist-, animal-, and plant-bacterial interactions, whether in shared ecosystems or intimate symbioses, is fundamentally altering our understanding of biology. The establishment and maintenance of these interactions and their contrib...
Autor principal: | |
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Otros Autores: | , |
Formato: | Libro electrónico |
Idioma: | Inglés |
Publicado: |
Boca Raton, Florida ; London ; New York :
CRC Press
2020.
[2021] |
Edición: | 1st ed |
Colección: | Evolutionary cell biology.
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Materias: | |
Ver en Biblioteca Universitat Ramon Llull: | https://discovery.url.edu/permalink/34CSUC_URL/1im36ta/alma991009781183506719 |
Tabla de Contenidos:
- Cover
- Half Title
- Series Page
- Title Page
- Copyright Page
- Contents
- Series Preface
- Preface
- Contributors
- Chapter 1: When does symbiosis begin? Bacterial cues necessary for metamorphosis in the marine polychaete Hydroides elegans
- 1.1 The symbiosis space
- 1.2 Chemical cues mediate symbiotic interactions
- 1.3 How do specific symbiotic interactions begin? Examples from the pre-symbiosis space
- 1.4 Bacterially induced metamorphosis of marine invertebrate animals
- 1.5 Bacterial induction of metamorphosis in Hydroides elegans
- 1.6 Identification of larval metamorphic cues from biofilm bacteria
- 1.7 How variability of inductive bacteria and identified settlement cues relate to variable larval settlement and recruitment
- 1.8 Lipopolysaccharide mediates both symbiotic and pre-symbiotic interactions
- 1.9 Conclusion
- References
- Chapter 2: The language of symbiosis: Insights from protist biology
- 2.1 Introduction
- 2.2 Cytoplasm as microcosm
- 2.3 Eukaryotes inside eukaryotes (inside other eukaryotes)
- 2.4 Ectosymbiosis: It's a jungle out there
- 2.5 Microbial symbioses: Power struggles in time and space
- 2.6 Conclusion
- Acknowledgments
- References
- Chapter 3: Trichoplax and its bacteria: How many are there? Are they speaking?
- 3.1 Introduction
- 3.2 How many symbionts are known to be present and where do they occur?
- 3.3 Do all placozoans harbor both G. incantans and R. eludens?
- 3.4 Intracellular locations of the placozoan symbionts
- 3.5 Unusual mitochondria in placozoan fiber cells and their possible relationship to symbiosis
- 3.6 Molecular inferences on the nature of the Trichoplax-bacteria symbioses
- 3.7 How are the bacterial symbionts of placozoans transmitted between generations?
- 3.8 Some big questions remaining and suggestions for their resolution
- Acknowledgments.
- References
- Chapter 4: Decoding cellular dialogues between sponges, bacteria, and phages
- 4.1 Introduction
- 4.2 Host-bacteria dialogue
- 4.2.1 Sponge immune receptors
- 4.2.2 Microbe associated molecular patterns (MAMPs)
- 4.3 Bacteria-bacteria dialogue
- 4.3.1 Quorum sensing
- 4.3.2 Quorum quenching
- 4.4 Phage-bacteria-host dialogue
- 4.4.1 Phage diversity and host-specificity
- 4.4.2 Ankyphages aid symbionts in immune evasion
- 4.5 Conclusions and future perspectives
- Acknowledgments
- References
- Chapter 5: Symbiotic interactions in the holobiont Hydra
- 5.1 Introduction
- 5.2 Interactions between Hydra viridissima and the Chlorella photobiont
- 5.2.1 Location and transmission of the photobiont
- 5.2.2 Mutual benefits
- 5.2.3 Establishment and maintenance of the Chlorella-Hydra symbiosis
- 5.2.4 Molecular mechanisms involved in maintaining the symbiosis
- 5.3 Interactions between Hydra and symbiotic bacteria
- 5.3.1 Spatial localization of the bacteria in the Hydra host
- 5.3.2 Bacteria provide protection against fungal infection
- 5.3.3 The innate immune system shapes the host microbiome
- 5.3.4 Crosstalk between innate immunity and stem cell factors
- 5.3.5 Crosstalk between the microbiota and the nervous system
- 5.3.6 Effect of bacteria on host physiology
- 5.4 Conclusion: Hydra, an excellent model to understand inter-species interactions
- Acknowledgments
- References
- Chapter 6: Hydra and Curvibacter: An intimate crosstalk at the epithelial interface
- 6.1 Introduction
- 6.2 Hydra and Curvibacter: The ideal duo to understand inter-kingdom communications
- 6.3 Spatial localization and transmission of Curvibacter
- 6.4 Establishment and carrying capacity of Curvibacter colonization
- 6.5 Curvibacter function in the Hydra metaorganism
- 6.6 Inter-kingdom communication between Hydra and Curvibacter.
- 6.7 Outlook
- Acknowledgments
- References
- Chapter 7: The coral holobiont highlights the dependence of cnidarian animal hosts on their associated microbes
- 7.1 Introduction: The coral holobiont as an ecosystem engineer and its reliance on associated microbes
- 7.2 The coral-Symbiodiniaceae relationship
- 7.2.1 Symbiodiniaceae: Micro-algal engines of the coral holobiont machinery
- 7.2.2 Innate immunity, symbiosis sensing, and cell signaling
- 7.2.3 Coral bleaching: The breakdown of the coral-Symbiodiniaceae relationship
- 7.3 Symbiodiniaceae-bacteria relationships
- 7.4 Diversity and function of microbes associated with the coral host
- 7.4.1 The host as a habitat
- 7.4.2 Diversity of coral-associated bacteria and interspecies interactions
- 7.4.3 Acquisition of bacterial associates and their roles in early coral life-stages
- 7.4.4 Coral probiotics
- 7.4.5 Contribution of bacteria to holobiont nutrient cycling
- 7.4.6 Archaea associated with the coral holobiont
- 7.4.7 Protists and fungi associated with the coral holobiont
- 7.5 Summary and Outlook
- References
- Chapter 8: Extra-intestinal regulation of the gut microbiome: The case of C. elegans TGFß/SMA signaling
- 8.1 Introduction: Caenorhabditis elegans as a model for studying the holobiont
- 8.2 The C. elegans gut microbiome and the factors that shape it
- 8.3 The intestinal niche
- 8.4 Host immunity and its role in shaping the intestinal niche
- 8.5 Multitissue contributions of TGFß signaling control anterior gut commensal abundance and function
- 8.6 TGFß signaling and cell nonautonomous regulation of intestinal function
- 8.7 Conclusions and future prospects: Convergence with other systems of host-symbiont interactions
- Acknowledgments
- References
- Chapter 9: Multiple roles of bacterially produced natural products in the bryozoan Bugula neritina.
- 9.1 Introduction
- 9.2 Bryozoans, Bugula spp., and Bugula neritina
- 9.3 Bryostatins
- 9.4 Bryostatin production by the bacterial symbiont of B. neritina
- 9.5 Defensive role of bryostatins
- 9.6 Impacts of symbiont and symbiont-produced metabolites on host physiology
- 9.7 Bryostatins and symbionts in closely related genera
- 9.8 Future directions
- Acknowledgments
- References
- Chapter 10: The molecular dialogue through ontogeny between a squid host and its luminous symbiont
- 10.1 Introduction
- 10.2 Features of the Euprymna scolopes-Vibrio fischeri association as a model symbiosis
- 10.3 Host activities before symbiont colonization: Embryogenesis and early posthatching
- 10.4 Early posthatching activity that mediates species and strain specificity of the association
- 10.5 Colonization and early development
- 10.6 The basis of a stable symbiosis: Daily rhythms and maturation of the symbiotic organ
- 10.7 Conclusions
- Acknowledgments
- References
- Chapter 11: Evolving integrated multipartite symbioses between plant-sap feeding insects (Hemiptera) and their endosymbionts
- 11.1 Introduction
- 11.2 Roles of Hemipteran symbionts: Nutrition and beyond
- 11.3 Genome evolution in Hemipteran symbionts
- 11.4 Symbiont bearing organs: Transmission and development
- 11.4.1 Intracellular symbioses: Transovarial transmission and bacteriome development
- 11.4.2 Extracellular symbioses: External transmission and the midgut
- 11.5 Maintaining and regulating microbial symbionts
- 11.5.1 Evolution of mechanisms to maintain and regulate symbionts
- 11.5.2 Symbiont self-help and self-regulation
- 11.5.3 Symbiont-symbiont support
- 11.5.4 Host support and regulation of nutritional synthesis in symbionts
- 11.5.5 Host support and regulation of other symbiont cell functions
- 11.6 Conclusion
- References.
- Chapter 12: Symbiosis for insect cuticle formation
- 12.1 Introduction
- 12.2 Weevil-Nardonella endosymbiosis
- 12.3 Nardonella genome is extremely reduced and specialized for tyrosine synthesis
- 12.4 Nardonella endosymbiotic system in Pachyrhynchus infernalis
- 12.5 Nardonella-harboring bacteriome as a tyrosine-producing organ
- 12.6 Suppression of Nardonella by antibiotic and its effects on tyrosine and DOPA provisioning
- 12.7 Contribution of Nardonella to adult cuticle formation in Pachyrhynchus infernalis
- 12.8 Incomplete tyrosine synthesis pathway of Nardonella and complementation by host genes
- 12.9 Insights from weevil-Nardonella symbiosis: Host's final step control over symbiont's metabolic pathway
- 12.10 Insights from weevil-Nardonella symbiosis: How do symbiont replacements proceed?
- 12.11 Symbiosis for insect cuticle formation: General phenomena across diverse insect taxa
- 12.12 Conclusion and perspective
- Acknowledgments
- References
- Chapter 13: Microbial determinants of folivory in insects
- 13.1 Introduction
- 13.2 Deconstructing the plant cell wall
- 13.3 Symbiont-mediated evasion of plant defenses
- 13.4 Niche preservation
- 13.5 Conclusions
- References
- Chapter 14: Right on cue: Microbiota promote plasticity of zebrafish digestive tract
- 14.1 Introduction
- 14.2 Development under immune surveillance
- 14.3 Developmental plasticity at the luminal interface
- 14.4 Beyond the lumen: A secreted bacterial protein impacts pancreas development
- 14.5 Conclusions
- References
- Chapter 15: Uncovering the history of intestinal host-microbiome interactions through vertebrate comparative genomics
- 15.1 Introduction
- 15.2 A history of symbiotic interactions captured within microbial and host genomes
- 15.3 Capturing symbiotic signals within coding regions of the host genome.
- 15.4 Uncovering specific symbiotic signals in host transcriptional programs.