{"title":"Why are nematodes so successful extremophiles?","authors":"Amir Sapir","doi":"10.1080/19420889.2021.1884343","DOIUrl":"https://doi.org/10.1080/19420889.2021.1884343","url":null,"abstract":"<p><p>Extreme environments constitute the largest habitat on earth, but our understanding of life in such environments is rudimentary. The hostility of extreme environments such as the deep sea, earth's crust, and toxic lakes limits the sampling, culturing, and studying of extremophiles, the organisms that live in these habitats. Thus, in terms of ecological research, extreme environments are the earth's final frontier. A growing body of data suggests that nematodes are the most common animal taxon in different types of extreme settings such as the deep-subsurface and sediments in the deep sea. Notably, the reasons for the abundance of nematodes in extreme habitats remain mostly unknown. I propose that a unique combination of several characteristics of nematodes may explain, additively or synergistically, their successful adaptation to extreme habitats. Novel functional genetic and genomic approaches are expected to reveal molecular mechanisms of adaptation of nematodes to the many fascinating extreme environments on earth.</p>","PeriodicalId":39647,"journal":{"name":"Communicative and Integrative Biology","volume":"14 1","pages":"24-26"},"PeriodicalIF":0.0,"publicationDate":"2021-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/19420889.2021.1884343","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25427470","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Endosomal Rab GTPases regulate secretory granule maturation in <i>Drosophila</i> larval salivary glands.","authors":"Cheng-I Jonathan Ma, Julie A Brill","doi":"10.1080/19420889.2021.1874663","DOIUrl":"https://doi.org/10.1080/19420889.2021.1874663","url":null,"abstract":"<p><p>Secretory granules (SGs) are organelles responsible for regulated exocytosis of biologically active molecules in professional secretory cells. Maturation of SGs is a crucial process in which cargoes of SGs are processed and activated, allowing them to exert their function upon secretion. Nonetheless, the intracellular trafficking pathways required for SG maturation are not well defined. We recently performed an RNA interference (RNAi) screen in <i>Drosophila</i> larval salivary glands to identify trafficking components needed for SG maturation. From the screen, we identified several Rab GTPases (Rabs) that affect SG maturation. Expression of constitutively active (CA) and dominant-negative (DN) forms narrowed down the Rabs important for this process to Rab5, Rab9 and Rab11. However, none of these Rabs localizes to the limiting membrane of SGs. In contrast, examination of endogenously YFP-tagged Rabs (YRabs) in larval salivary glands revealed that YRab1 and YRab6 localize to the limiting membrane of immature SGs (iSGs) and SGs. These findings provide new insights into how Rab GTPases contribute to the process of SG maturation.</p>","PeriodicalId":39647,"journal":{"name":"Communicative and Integrative Biology","volume":"14 1","pages":"15-20"},"PeriodicalIF":0.0,"publicationDate":"2021-02-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/19420889.2021.1874663","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25402446","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Koji Okayasu, Koh Aoki, Ken-Ichi Kurotani, Michitaka Notaguchi
{"title":"Tissue adhesion between distant plant species in parasitism and grafting.","authors":"Koji Okayasu, Koh Aoki, Ken-Ichi Kurotani, Michitaka Notaguchi","doi":"10.1080/19420889.2021.1877016","DOIUrl":"https://doi.org/10.1080/19420889.2021.1877016","url":null,"abstract":"<p><p>Plant grafting is generally performed between closely related species. Recently, we have discovered that <i>Nicotiana</i> species of Solanaceae show the ability to graft with distantly related plant species beyond the family. Graft adhesion with diverse angiosperms by <i>Nicotiana</i> species was probably facilitated by the secretion of a subclade of ß-1,4-glucanases. The capability of interfamily grafting was also found in the model Orobanchaceae hemiparasitic plant, <i>Phtheirospermum japonicum</i>, which naturally invades to the tissues of host plants of different families. Transcriptome analysis indicated that the same clade of ß-1,4-glucanase plays an important role in plant parasitism. Thus, the tissue adhesion between distant plant species occurs both naturally and artificially. Here, we further observed the capability of interfamily grafting in the stem holoparasitic genus, <i>Cuscuta</i>. These findings indicate that the natural process of tissue adhesion is a potential clue to improve plant-grafting techniques.</p>","PeriodicalId":39647,"journal":{"name":"Communicative and Integrative Biology","volume":"14 1","pages":"21-23"},"PeriodicalIF":0.0,"publicationDate":"2021-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/19420889.2021.1877016","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25343672","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Effects of spatial confinement on migratory properties of Dictyostelium discoideum cells.","authors":"Yuri Belotti, David McGloin, Cornelis J Weijer","doi":"10.1080/19420889.2021.1872917","DOIUrl":"https://doi.org/10.1080/19420889.2021.1872917","url":null,"abstract":"<p><p>Migratory environments of various eukaryotic cells, such as amoeba, leukocytes and cancer cells, typically involve spatial confinement. Numerous studies have recently emerged, aimed to develop experimental platforms that better recapitulate the characteristics of the cellular microenvironment. Using microfluidic technologies, we show that increasing confinement of Dictyostelium discoideum cells into narrower micro-channels resulted in a significant change in the mode of migration and associated arrangement of the actomyosin cytoskeleton. We observed that cells tended to migrate at constant speed, the magnitude of which was dependent on the size of the channels, as was the locomotory strategy adopted by each cell. Two different migration modes were observed, pseudopod-based and bleb-based migration, with bleb based migration being more frequent with increasing confinement and leading to slower migration. Beside the migration mode, we found that the major determinants of cell speed are its protrusion rate, the amount of F-actin at its leading edge and the number of actin foci. Our results highlighted the impact of the microenvironments on cell behavior. Furthermore, we developed a novel quantitative movement analysis platform for mono-dimensional cell migration that allows for standardization and simplification of the experimental conditions and aids investigation of the complex and dynamic processes occurring at the single-cell level.</p>","PeriodicalId":39647,"journal":{"name":"Communicative and Integrative Biology","volume":"14 1","pages":"5-14"},"PeriodicalIF":0.0,"publicationDate":"2021-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/19420889.2021.1872917","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25343671","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Adhesion stimulates Scar/WAVE phosphorylation in mammalian cells.","authors":"Shashi Prakash Singh, Robert H Insall","doi":"10.1080/19420889.2020.1855854","DOIUrl":"https://doi.org/10.1080/19420889.2020.1855854","url":null,"abstract":"<p><p>The Scar/WAVE complex catalyzes the protrusion of pseudopods and lamellipods, and is therefore a principal regulator of cell migration. However, it is unclear how its activity is regulated, beyond a dependence on Rac. Phosphorylation of the proline-rich region, by kinases such as Erk2, has been suggested as an upstream activator. We have recently reported that phosphorylation is not required for complex activation. Rather, it occurs after Scar/WAVE has been activated, and acts as a modulator. Neither chemoattractant signaling nor Erk2 affects the amount of phosphorylation, though in Dictyostelium it is promoted by cell-substrate adhesion. We now report that cell-substrate adhesion also promotes Scar/WAVE2 phosphorylation in mammalian cells, suggesting that the process is evolutionarily conserved.</p>","PeriodicalId":39647,"journal":{"name":"Communicative and Integrative Biology","volume":"14 1","pages":"1-4"},"PeriodicalIF":0.0,"publicationDate":"2020-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/19420889.2020.1855854","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38821041","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Interoception the foundation for: mind's sensing of 'self,' physiological responses, cognitive discrimination and dysregulation.","authors":"Pollard-Wright Holly","doi":"10.1080/19420889.2020.1846922","DOIUrl":"10.1080/19420889.2020.1846922","url":null,"abstract":"<p><p>This article presents a theory of mind whereby interoception (i.e., a sense of signals originating from the body) provides a transdisciplinary framework in which theories from diverse fields may be conformed to ideas from other areas of science. Through a science of interoception, the mind itself investigates the mind and thus can explore how the universe and consciousness came about and understand how interoceptive processing is shaped by experience. Interoception provides a metastable network that enables individuals to compute the significance of stimuli as physiological changes in its complex global context. Both sensory and much cognitive discrimination and integration are affected by the flow of interoceptive information that acts as <i>cues</i> whereby unconscious events may be correlated with conscious events and the reportable content of mental life. Heightened interoceptive sensitivity and individuals who show augmented interoceptive sensitivity are susceptible to a wide range of neuropsychiatric as well as general medical conditions. Physiological responses can be measured and interoceptive awareness cultivated to generate well-being and stress resilience in the treatment of emotional dysregulation and interoceptive abnormalities.</p>","PeriodicalId":39647,"journal":{"name":"Communicative and Integrative Biology","volume":" ","pages":"198-213"},"PeriodicalIF":0.0,"publicationDate":"2020-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/19420889.2020.1846922","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38734669","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Why isn't sex optional? Stem-cell competition, loss of regenerative capacity, and cancer in metazoan evolution.","authors":"Chris Fields, Michael Levin","doi":"10.1080/19420889.2020.1838809","DOIUrl":"10.1080/19420889.2020.1838809","url":null,"abstract":"<p><p>Animals that can reproduce vegetatively by fission or budding and also sexually via specialized gametes are found in all five primary animal lineages (Bilateria, Cnidaria, Ctenophora, Placozoa, Porifera). Many bilaterian lineages, including roundworms, insects, and most chordates, have lost the capability of vegetative reproduction and are obligately gametic. We suggest a developmental explanation for this evolutionary phenomenon: obligate gametic reproduction is the result of germline stem cells winning a winner-take-all competition with non-germline stem cells for control of reproduction and hence lineage survival. We develop this suggestion by extending Hamilton's rule, which factors the relatedness between parties into the cost/benefit analysis that underpins cooperative behaviors, to include similarity of cellular state. We show how coercive or deceptive cell-cell signaling can be used to make costly cooperative behaviors appear less costly to the cooperating party. We then show how competition between stem-cell lineages can render an ancestral combination of vegetative reproduction with facultative sex unstable, with one or the other process driven to extinction. The increased susceptibility to cancer observed in obligately-sexual lineages is, we suggest, a side-effect of deceptive signaling that is exacerbated by the loss of whole-body regenerative abilities. We suggest a variety of experimental approaches for testing our predictions.</p>","PeriodicalId":39647,"journal":{"name":"Communicative and Integrative Biology","volume":" ","pages":"170-183"},"PeriodicalIF":0.0,"publicationDate":"2020-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7746248/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38786424","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Giant, highly diverse protists in the abyssal Pacific: vulnerability to impacts from seabed mining and potential for recovery.","authors":"Andrew J Gooday, Jennifer M Durden, Craig R Smith","doi":"10.1080/19420889.2020.1843818","DOIUrl":"https://doi.org/10.1080/19420889.2020.1843818","url":null,"abstract":"<p><p>Xenophyophores, giant deep-sea agglutinated foraminifera, dominate the benthic megafauna in the eastern equatorial Pacific Clarion-Clipperton Zone. This abyssal (>4000 m depth) region hosts major deposits of polymetallic nodules targeted for future seabed mining, an activity that would destroy these highly diverse and delicate protists, particularly those living on the nodules themselves. Since the cell occupies only a small proportion of their test volume, xenophyophores may make a fairly modest contribution to benthic biomass and carbon cycling. Nevertheless, xenophyophore tests can passively enhance particle deposition, concentrate food, and provide habitat structure utilized by diverse organisms. Their destruction could therefore influence the recovery of benthic communities. Species requiring nodule substrates will likely not recover, since nodules take millions of years to form. However, xenophyophores can grow quickly and colonize extensive volcanic ash deposits within years, suggesting that sediment-dwelling species could be among the first large immobile organisms to reappear in mining-impacted areas.</p>","PeriodicalId":39647,"journal":{"name":"Communicative and Integrative Biology","volume":" ","pages":"189-197"},"PeriodicalIF":0.0,"publicationDate":"2020-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/19420889.2020.1843818","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38716836","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Justin Maire, Bessem Chouaia, Anna Zaidman-Rémy, Abdelaziz Heddi
{"title":"Endosymbiosis morphological reorganization during metamorphosis diverges in weevils.","authors":"Justin Maire, Bessem Chouaia, Anna Zaidman-Rémy, Abdelaziz Heddi","doi":"10.1080/19420889.2020.1840707","DOIUrl":"https://doi.org/10.1080/19420889.2020.1840707","url":null,"abstract":"<p><p>Virtually all animals associate with beneficial symbiotic bacteria. Whether and how these associations are modulated across a host's lifecycle is an important question in disentangling animal-bacteria interactions. We recently reported a case of complete morphological reorganization of symbiosis during metamorphosis of the cereal weevil, <i>Sitophilus oryzae</i>. In this model, the bacteriome, a specialized organ that houses the intracellular bacterium <i>Sodalis pierantonius</i>, undergoes a two-phase remodeling program synchronously driven by host and endosymbiont, resulting in a localization shift and the formation of multiple new bacteriomes. Here, we provide comparative data in a closely-related coleopteran, the red palm weevil <i>Rhynchophorus ferrugineus</i>, which is associated with the ancestral endosymbiont <i>Nardonella</i>. Using cell imaging experiments, we show that the red pal weevil bacteriome remains unchanged during metamorphosis, hence contrasting with what we reported in the cereal weevil <i>S. oryzae</i>. These findings highlight the complexity and divergence of host-symbiont interactions and their intertwining with host development, even in closely-related species. <b>Abbreviations</b>: DAPI: 4',6-diamidino-2-phenylindole; FISH: Fluorescence <i>in situ</i> hybridization; T3SS: Type III secretion system.</p>","PeriodicalId":39647,"journal":{"name":"Communicative and Integrative Biology","volume":" ","pages":"184-188"},"PeriodicalIF":0.0,"publicationDate":"2020-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/19420889.2020.1840707","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38605739","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
María Fernanda Gonzalez, Freddy Magdama, Luis Galarza, Daynet Sosa, Christian Romero
{"title":"Evaluation of the sensitivity and synergistic effect of <i>Trichoderma reesei</i> and mancozeb to inhibit under <i>in vitro</i> conditions the growth of <i>Fusarium oxysporum</i>.","authors":"María Fernanda Gonzalez, Freddy Magdama, Luis Galarza, Daynet Sosa, Christian Romero","doi":"10.1080/19420889.2020.1829267","DOIUrl":"https://doi.org/10.1080/19420889.2020.1829267","url":null,"abstract":"<p><p>Trichoderma is a saprophytic, soil-borne fungus with a worldwide distribution that has been extensively studied due to their capacity to synthesize secondary metabolites with antimicrobial activity, parasitize other fungi and directly interact with plant roots, inducing resistance to disease and tolerance to abiotic stresses. <i>Fusarium</i> wilt caused by the soil-inhabiting fungus <i>Fusarium oxysporum</i> is considered one of the most important diseases that affect banana cultivars. Currently, more environmentally friendly alternatives to control this disease are being proposed, these strategies include the application of low doses of synthetic fungicides and the use of biocontrol agents such as <i>Trichoderma</i> or <i>Xylaria</i>. Thus, this study aimed to evaluate under <i>in vitro</i> conditions the synergistic effect of the biological control agent <i>T. reesei</i> C2A combined with low doses of mancozeb to inhibit the mycelial growth of <i>F. oxysporum</i> F1. To perform the synergistic essays, 0.1 mg/mL of mancozeb was suspended in PDA plates, then plugs of <i>T. ressei</i> C2A were placed at the center of the Petri dishes, the plates were incubated for 7 days at 28°C. Results showed that the mycoparasitic capacity of the biocontrol strain to inhibit the mycelial growth of <i>F. oxysporum</i> F1 was enhanced approximately 36% compared to the control plates. Although these results are promising, future studies under greenhouse and field conditions are necessary to corroborate the effectiveness of this approach.</p>","PeriodicalId":39647,"journal":{"name":"Communicative and Integrative Biology","volume":" ","pages":"160-169"},"PeriodicalIF":0.0,"publicationDate":"2020-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/19420889.2020.1829267","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38569379","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}