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1.
J Neurosci ; 37(4): 768-780, 2017 01 25.
Artículo en Inglés | MEDLINE | ID: mdl-28123014

RESUMEN

Cephalopods in nature undergo highly dynamic skin coloration changes that allow rapid camouflage and intraspecies communication. The optic lobe is thought to play a key role in controlling the expansion of the chromatophores that generate these diverse body patterns. However, the functional organization of the optic lobe and neural control of the various body patterns by the optic lobe are largely unknown. We applied electrical stimulation within the optic lobe to investigate the neural basis of body patterning in the oval squid, Sepioteuthis lessoniana Most areas in the optic lobe mediated predominately ipsilateral expansion of chromatophores present on the mantle, but not on the head and arms; furthermore, the expanded areas after electrical stimulation were positively correlated with an increase in stimulating voltage and stimulation depth. These results suggest a unilaterally dominant and vertically converged organization of the optic lobe. Furthermore, analyzing 14 of the elicited body pattern components and their corresponding stimulation sites revealed that the same components can be elicited by stimulating different parts of the optic lobe and that various subsets of these components can be coactivated by stimulating the same area. These findings suggest that many body pattern components may have multiple motor units in the optic lobe and that these are organized in a mosaic manner. The multiplicity associated with the nature of the neural controls of these components in the cephalopod brain thus reflects the versatility of the individual components during the generation of diverse body patterns. SIGNIFICANCE STATEMENT: Neural control of the dynamic body patterning of cephalopods for camouflage and intraspecies communication is a fascinating research topic. Previous studies have shown that the optic lobe is the motor command center for dynamic body patterning. However, little is known about its neural organization and the mechanisms underlying its control of body pattern generation. By electrically stimulating the optic lobe of the oval squids and observing their body pattern changes, surprisingly, we found that there is no somatotopic organization of motor units. Instead, many of these components have multiple motor units within the optic lobe and are organized in a mosaic manner. The present work reveals a novel neural control of dynamic body patterning for communication in cephalopods.


Asunto(s)
Tipificación del Cuerpo/fisiología , Cromatóforos/fisiología , Decapodiformes/fisiología , Lóbulo Óptico de Animales no Mamíferos/fisiología , Animales , Decapodiformes/anatomía & histología , Estimulación Eléctrica/métodos , Femenino , Masculino , Lóbulo Óptico de Animales no Mamíferos/anatomía & histología
2.
J Comput Neurosci ; 44(2): 219-231, 2018 04.
Artículo en Inglés | MEDLINE | ID: mdl-29327161

RESUMEN

Action potentials are the information carriers of neural systems. The generation of action potentials involves the cooperative opening and closing of sodium and potassium channels. This process is metabolically expensive because the ions flowing through open channels need to be restored to maintain concentration gradients of these ions. Toxins like tetraethylammonium can block working ion channels, thus affecting the function and energy cost of neurons. In this paper, by computer simulation of the Hodgkin-Huxley neuron model, we studied the effects of channel blocking with toxins on the information transmission and energy efficiency in squid giant axons. We found that gradually blocking sodium channels will sequentially maximize the information transmission and energy efficiency of the axons, whereas moderate blocking of potassium channels will have little impact on the information transmission and will decrease the energy efficiency. Heavy blocking of potassium channels will cause self-sustained oscillation of membrane potentials. Simultaneously blocking sodium and potassium channels with the same ratio increases both information transmission and energy efficiency. Our results are in line with previous studies suggesting that information processing capacity and energy efficiency can be maximized by regulating the number of active ion channels, and this indicates a viable avenue for future experimentation.


Asunto(s)
Potenciales de Acción/fisiología , Axones/fisiología , Simulación por Computador , Canales Iónicos/metabolismo , Modelos Neurológicos , Neuronas/citología , Potenciales de Acción/efectos de los fármacos , Animales , Decapodiformes/anatomía & histología , Entropía , Canales Iónicos/antagonistas & inhibidores , Neuronas/efectos de los fármacos , Neuronas/fisiología , Ruido , Procesos Estocásticos
3.
Dev Genes Evol ; 227(6): 375-387, 2017 11.
Artículo en Inglés | MEDLINE | ID: mdl-28105525

RESUMEN

The protein Crumbs is a determinant of apical-basal cell polarity and plays a role in apoptosis of epithelial cells and their protection against photodamage. Using the squid-vibrio system, a model for development of symbiotic partnerships, we examined the modulation of the crumbs gene in host epithelial tissues during initiation and maintenance of the association. The extracellular luminous symbiont Vibrio fischeri colonizes the apical surfaces of polarized epithelia in deep crypts of the Euprymna scolopes light organ. During initial colonization each generation, symbiont harvesting is potentiated by the biochemical and biophysical activity of superficial ciliated epithelia, which are several cell layers from the crypt epithelia where the symbionts reside. Within hours of crypt colonization, the symbionts induce the cell death mediated regression of the remote superficial ciliated fields. However, the crypt cells directly interacting with the symbiont are protected from death. In the squid host, we characterized the gene and encoded protein during light organ morphogenesis and in response to symbiosis. Features of the protein sequence and structure, phylogenetic relationships, and localization patterns in the eye supported assignment of the squid protein to the Crumbs family. In situ hybridization revealed that the crumbs transcript shows opposite expression at the onset of symbiosis in the two different regions of the light organ: elevated levels in the superficial epithelia were attenuated whereas low levels in the crypt epithelia were turned up. Although a rhythmic association in which the host controls the symbiont population over the day-night cycle begins in the juvenile upon colonization, cycling of crumbs was evident only in the adult organ with peak expression coincident with maximum symbiont population and luminescence. Our results provide evidence that crumbs responds to symbiont cues that induce developmental apoptosis and to symbiont population dynamics correlating with luminescence-based stress throughout the duration of the host-microbe association.


Asunto(s)
Aliivibrio fischeri/fisiología , Decapodiformes/microbiología , Decapodiformes/fisiología , Proteínas de la Membrana/metabolismo , Simbiosis , Secuencia de Aminoácidos , Animales , Apoptosis , Polaridad Celular , Decapodiformes/anatomía & histología , Decapodiformes/citología , Células Epiteliales/citología , Células Epiteliales/microbiología , Ojo/microbiología , Expresión Génica , Proteínas de la Membrana/química , Proteínas de la Membrana/genética
4.
Soft Matter ; 13(42): 7740-7752, 2017 Nov 01.
Artículo en Inglés | MEDLINE | ID: mdl-29043368

RESUMEN

The beak of the Humboldt squid is a biocomposite material made solely of organic components - chitin and proteins - which exhibits 200-fold stiffness and hardness gradients from the soft base to the exceptionally hard tip (rostrum). The outstanding mechanical properties of the squid beak are achieved via controlled hydration and impregnation of the chitin-based scaffold by protein coacervates. Molecular-based understanding of these proteins is essential to mimic the natural beak material. Here, we present detailed studies of two histidine-rich beak proteins (HBP-1 and -2) that play central roles during beak bio-fabrication. We show that both proteins have the ability to self-coacervate, which is governed intrinsically by the sequence modularity of their C-terminus and extrinsically by pH and ionic strength. We demonstrate that HBPs possess dynamic structures in solution and achieve maximum folding in the coacervate state, and propose that their self-coacervation is driven by hydrophobic interactions following charge neutralization through salt-screening. Finally, we show that subtle differences in the modular repeats of HBPs result in significant changes in the rheological response of the coacervates. This knowledge may be exploited to design self-coacervating polypeptides for a wide range of engineering and biomedical applications, for example bio-inspired composite materials, smart hydrogels and adhesives, and biomedical implants.


Asunto(s)
Pico/química , Decapodiformes/anatomía & histología , Proteínas/química , Animales , Quitina/química , Histidina/química , Conformación Proteica , Reología
5.
J Exp Biol ; 219(Pt 9): 1317-26, 2016 05 01.
Artículo en Inglés | MEDLINE | ID: mdl-26944502

RESUMEN

Although steady swimming has received considerable attention in prior studies, unsteady swimming movements represent a larger portion of many aquatic animals' locomotive repertoire and have not been examined extensively. Squids and cuttlefishes are cephalopods with unique muscular hydrostat-driven, dual-mode propulsive systems involving paired fins and a pulsed jet. These animals exhibit a wide range of swimming behavior, but turning performance has not been examined quantitatively. Brief squid, Lolliguncula brevis, and dwarf cuttlefish, Sepia bandensis, were filmed during turns using high-speed cameras. Kinematic features were tracked, including the length-specific radius of the turn (R/L), a measure of maneuverability, and angular velocity (ω), a measure of agility. Both L. brevis and S. bandensis demonstrated high maneuverability, with (R/L)min values of 3.4×10(-3)±5.9×10(-4) and 1.2×10(-3)±4.7×10(-4) (mean±s.e.m.), respectively, which are the lowest measures of R/L reported for any aquatic taxa. Lolliguncula brevis exhibited higher agility than S. bandensis (ωa,max=725.8 versus 485.0 deg s(-1)), and both cephalopods have intermediate agility when compared with flexible-bodied and rigid-bodied nekton of similar size, reflecting their hybrid body architecture. In L. brevis, jet flows were the principal driver of angular velocity. Asymmetric fin motions played a reduced role, and arm wrapping increased turning performance to varying degrees depending on the species. This study indicates that coordination between the jet and fins is important for turning performance, with L. brevis achieving faster turns than S. bandensis and S. bandensis achieving tighter, more controlled turns than L. brevis.


Asunto(s)
Decapodiformes/fisiología , Sepia/fisiología , Aletas de Animales/anatomía & histología , Aletas de Animales/fisiología , Animales , Fenómenos Biomecánicos , Tamaño Corporal , Decapodiformes/anatomía & histología , Sepia/anatomía & histología , Natación
7.
J Acoust Soc Am ; 137(5): 2522-32, 2015 May.
Artículo en Inglés | MEDLINE | ID: mdl-25994685

RESUMEN

Material properties of the flesh from three fish species (Merluccius productus, Symbolophorus californiensis, and Diaphus theta), and several body parts of the Humboldt squid (Dosidicus gigas) collected from the California Current ecosystem were measured. The density contrast relative to seawater varied within and among taxa for fish flesh (0.9919-1.036), squid soft body parts (mantle, arms, tentacle, braincase, eyes; 1.009-1.057), and squid hard body parts (beak and pen; 1.085-1.459). Effects of animal length and environmental conditions on nekton density contrast were investigated. The sound speed contrast relative to seawater varied within and among taxa for fish flesh (0.986-1.027) and Humboldt squid mantle and braincase (0.937-1.028). Material properties in this study are similar to values from previous studies on species with similar life histories. In general, the sound speed and density of soft body parts of fish and squid were 1%-3% and 1%-6%, respectively, greater than the surrounding seawater. Hard parts of the squid were significantly more dense (6%-46%) than seawater. The material properties reported here can be used to improve target strength estimates from acoustic scattering models, which could increase the accuracy of biomass estimates from acoustic surveys for these nekton.


Asunto(s)
Acústica , Decapodiformes/clasificación , Monitoreo del Ambiente/métodos , Gadiformes/clasificación , Movimientos del Agua , Animales , Biomasa , Decapodiformes/anatomía & histología , Decapodiformes/fisiología , Ecosistema , Gadiformes/anatomía & histología , Gadiformes/fisiología , Movimiento (Física) , Océano Pacífico , Densidad de Población , Agua de Mar , Procesamiento de Señales Asistido por Computador , Sonido , Especificidad de la Especie , Factores de Tiempo
9.
J Exp Biol ; 217(Pt 9): 1588-600, 2014 May 01.
Artículo en Inglés | MEDLINE | ID: mdl-24501132

RESUMEN

Squid are the largest jet propellers in nature as adults, but as paralarvae they are some of the smallest, faced with the inherent inefficiency of jet propulsion at a low Reynolds number. In this study we describe the behavior and kinematics of locomotion in 1 mm paralarvae of Dosidicus gigas, the smallest squid yet studied. They swim with hop-and-sink behavior and can engage in fast jets by reducing the size of the mantle aperture during the contraction phase of a jetting cycle. We go on to explore the general effects of a variable mantle and funnel aperture in a theoretical model of jet propulsion scaled from the smallest (1 mm mantle length) to the largest (3 m) squid. Aperture reduction during mantle contraction increases propulsive efficiency at all squid sizes, although 1 mm squid still suffer from low efficiency (20%) because of a limited speed of contraction. Efficiency increases to a peak of 40% for 1 cm squid, then slowly declines. Squid larger than 6 cm must either reduce contraction speed or increase aperture size to maintain stress within maximal muscle tolerance. Ecological pressure to maintain maximum velocity may lead them to increase aperture size, which reduces efficiency. This effect might be ameliorated by nonaxial flow during the refill phase of the cycle. Our model's predictions highlight areas for future empirical work, and emphasize the existence of complex behavioral options for maximizing efficiency at both very small and large sizes.


Asunto(s)
Decapodiformes/fisiología , Natación/fisiología , Animales , Fenómenos Biomecánicos , Decapodiformes/anatomía & histología , Modelos Teóricos
10.
J Exp Biol ; 217(Pt 6): 850-8, 2014 Mar 15.
Artículo en Inglés | MEDLINE | ID: mdl-24622892

RESUMEN

Squid display impressive changes in body coloration that are afforded by two types of dynamic skin elements: structural iridophores (which produce iridescence) and pigmented chromatophores. Both color elements are neurally controlled, but nothing is known about the iridescence circuit, or the environmental cues, that elicit iridescence expression. To tackle this knowledge gap, we performed denervation, electrical stimulation and behavioral experiments using the long-fin squid, Doryteuthis pealeii. We show that while the pigmentary and iridescence circuits originate in the brain, they are wired differently in the periphery: (1) the iridescence signals are routed through a peripheral center called the stellate ganglion and (2) the iridescence motor neurons likely originate within this ganglion (as revealed by nerve fluorescence dye fills). Cutting the inputs to the stellate ganglion that descend from the brain shifts highly reflective iridophores into a transparent state. Taken together, these findings suggest that although brain commands are necessary for expression of iridescence, integration with peripheral information in the stellate ganglion could modulate the final output. We also demonstrate that squid change their iridescence brightness in response to environmental luminance; such changes are robust but slow (minutes to hours). The squid's ability to alter its iridescence levels may improve camouflage under different lighting intensities.


Asunto(s)
Cromatóforos/fisiología , Decapodiformes/fisiología , Ambiente , Pigmentación , Animales , Conducta Animal , Encéfalo , Cromatóforos/citología , Decapodiformes/anatomía & histología , Desnervación , Estimulación Eléctrica , Luz , Neuronas Motoras/fisiología
11.
J Exp Biol ; 217(Pt 15): 2710-6, 2014 Aug 01.
Artículo en Inglés | MEDLINE | ID: mdl-25079893

RESUMEN

Many pelagic fishes engage prey at high speeds supported by high metabolic rates and anaerobic metabolic capacity. Epipelagic squids are reported to have among the highest metabolic rates in the oceans as a result of demanding foraging strategies and the use of jet propulsion, which is inherently inefficient. This study examined enzymatic proxies of anaerobic metabolism in two species of pelagic squid, Dosidicus gigas and Doryteuthis pealeii (Lesueur 1821), over a size range of six orders of magnitude. We hypothesized that activity of the anaerobically poised enzymes would be high and increase with size as in ecologically similar fishes. In contrast, we demonstrate that anaerobic metabolic capacity in these organisms scales negatively with body mass. We explored several cephalopod-specific traits, such as the use of tentacles to capture prey, body morphology and reduced relative prey size of adult squids, that may create a diminished reliance on anaerobically fueled burst activity during prey capture in large animals.


Asunto(s)
Decapodiformes/anatomía & histología , Decapodiformes/metabolismo , Metabolismo Energético , Conducta Alimentaria/fisiología , Natación/fisiología , Aminoácido Oxidorreductasas/metabolismo , Anaerobiosis , Animales , Tamaño Corporal/fisiología
12.
BMC Evol Biol ; 13: 187, 2013 Sep 08.
Artículo en Inglés | MEDLINE | ID: mdl-24010674

RESUMEN

BACKGROUND: We recently reported (Curr Biol 22:683-688, 2012) that the eyes of giant and colossal squid can grow to three times the diameter of the eyes of any other animal, including large fishes and whales. As an explanation to this extreme absolute eye size, we developed a theory for visual performance in aquatic habitats, leading to the conclusion that the huge eyes of giant and colossal squid are uniquely suited for detection of sperm whales, which are important squid-predators in the depths where these squid live. A paper in this journal by Schmitz et al. (BMC Evol Biol 13:45, 2013) refutes our conclusions on the basis of two claims: (1) using allometric data they argue that the eyes of giant and colossal squid are not unexpectedly large for the size of the squid, and (2) a revision of the values used for modelling indicates that large eyes are not better for detection of approaching sperm whales than they are for any other task. RESULTS AND CONCLUSIONS: We agree with Schmitz et al. that their revised values for intensity and abundance of planktonic bioluminescence may be more realistic, or at least more appropriately conservative, but argue that their conclusions are incorrect because they have not considered some of the main arguments put forward in our paper. We also present new modelling to demonstrate that our conclusions remain robust, even with the revised input values suggested by Schmitz et al.


Asunto(s)
Decapodiformes/anatomía & histología , Decapodiformes/genética , Cachalote , Animales , Ecosistema , Ojo/anatomía & histología , Cadena Alimentaria , Masculino , Tamaño de los Órganos
13.
BMC Evol Biol ; 13: 226, 2013 Oct 15.
Artículo en Inglés | MEDLINE | ID: mdl-24127991

RESUMEN

It has been hypothesized that sperm whale predation is the driver of eye size evolution in giant squid. Given that the eyes of giant squid have the size expected for a squid this big, it is likely that any enhanced ability of giant squid to detect whales is an exaptation tied to their body size. Future studies should target the mechanism behind the evolution of large body size, not eye size. Reconstructions of the evolutionary history of selective regime, eye size, optical performance, and body size will improve the understanding of the evolution of large eyes in large ocean animals.


Asunto(s)
Evolución Biológica , Decapodiformes/anatomía & histología , Decapodiformes/genética , Animales , Tamaño Corporal , Decapodiformes/fisiología , Ojo , Tamaño de los Órganos , Conducta Predatoria , Cachalote , Visión Ocular , Ballenas
14.
Proc Biol Sci ; 280(1769): 20131463, 2013 Oct 22.
Artículo en Inglés | MEDLINE | ID: mdl-23986106

RESUMEN

The deep-sea squid Grimalditeuthis bonplandi has tentacles unique among known squids. The elastic stalk is extremely thin and fragile, whereas the clubs bear no suckers, hooks or photophores. It is unknown whether and how these tentacles are used in prey capture and handling. We present, to our knowledge, the first in situ observations of this species obtained by remotely operated vehicles (ROVs) in the Atlantic and North Pacific. Unexpectedly, G. bonplandi is unable to rapidly extend and retract the tentacle stalk as do other squids, but instead manoeuvres the tentacles by undulation and flapping of the clubs' trabecular protective membranes. These tentacle club movements superficially resemble the movements of small marine organisms and suggest the possibility that G. bonplandi uses aggressive mimicry by the tentacle clubs to lure prey, which we find to consist of crustaceans and cephalopods. In the darkness of the meso- and bathypelagic zones the flapping and undulatory movements of the tentacle may: (i) stimulate bioluminescence in the surrounding water, (ii) create low-frequency vibrations and/or (iii) produce a hydrodynamic wake. Potential prey of G. bonplandi may be attracted to one or more of these as signals. This singular use of the tentacle adds to the diverse foraging and feeding strategies known in deep-sea cephalopods.


Asunto(s)
Decapodiformes/anatomía & histología , Decapodiformes/fisiología , Animales , Conducta Alimentaria , Femenino , Golfo de México , Movimiento , Océano Pacífico
15.
Proc Natl Acad Sci U S A ; 107(5): 2259-64, 2010 Feb 02.
Artículo en Inglés | MEDLINE | ID: mdl-20133870

RESUMEN

Mechanisms for controlling symbiont populations are critical for maintaining the associations that exist between a host and its microbial partners. We describe here the transcriptional, metabolic, and ultrastructural characteristics of a diel rhythm that occurs in the symbiosis between the squid Euprymna scolopes and the luminous bacterium Vibrio fischeri. The rhythm is driven by the host's expulsion from its light-emitting organ of most of the symbiont population each day at dawn. The transcriptomes of both the host epithelium that supports the symbionts and the symbiont population itself were characterized and compared at four times over this daily cycle. The greatest fluctuation in gene expression of both partners occurred as the day began. Most notable was an up-regulation in the host of >50 cytoskeleton-related genes just before dawn and their subsequent down-regulation within 6 h. Examination of the epithelium by TEM revealed a corresponding restructuring, characterized by effacement and blebbing of its apical surface. After the dawn expulsion, the epithelium reestablished its polarity, and the residual symbionts began growing, repopulating the light organ. Analysis of the symbiont transcriptome suggested that the bacteria respond to the effacement by up-regulating genes associated with anaerobic respiration of glycerol; supporting this finding, lipid analysis of the symbionts' membranes indicated a direct incorporation of host-derived fatty acids. After 12 h, the metabolic signature of the symbiont population shifted to one characteristic of chitin fermentation, which continued until the following dawn. Thus, the persistent maintenance of the squid-vibrio symbiosis is tied to a dynamic diel rhythm that involves both partners.


Asunto(s)
Aliivibrio fischeri/genética , Aliivibrio fischeri/metabolismo , Decapodiformes/genética , Decapodiformes/microbiología , Simbiosis/genética , Simbiosis/fisiología , Aliivibrio fischeri/ultraestructura , Anaerobiosis , Animales , Quitina/metabolismo , Ritmo Circadiano/genética , Ritmo Circadiano/fisiología , Decapodiformes/anatomía & histología , Decapodiformes/metabolismo , Dieta , Perfilación de la Expresión Génica , Genes Bacterianos , Metabolismo de los Lípidos , Microscopía Electrónica de Transmisión , Modelos Biológicos , Datos de Secuencia Molecular , Análisis de Secuencia por Matrices de Oligonucleótidos
16.
Proc Biol Sci ; 279(1745): 4243-52, 2012 Oct 22.
Artículo en Inglés | MEDLINE | ID: mdl-22896651

RESUMEN

Fast dynamic control of skin coloration is rare in the animal kingdom, whether it be pigmentary or structural. Iridescent structural coloration results when nanoscale structures disrupt incident light and selectively reflect specific colours. Unlike animals with fixed iridescent coloration (e.g. butterflies), squid iridophores (i.e. aggregations of iridescent cells in the skin) produce dynamically tuneable structural coloration, as exogenous application of acetylcholine (ACh) changes the colour and brightness output. Previous efforts to stimulate iridophores neurally or to identify the source of endogenous ACh were unsuccessful, leaving researchers to question the activation mechanism. We developed a novel neurophysiological preparation in the squid Doryteuthis pealeii and demonstrated that electrical stimulation of neurons in the skin shifts the spectral peak of the reflected light to shorter wavelengths (greater than 145 nm) and increases the peak reflectance (greater than 245%) of innervated iridophores. We show ACh is released within the iridophore layer and that extensive nerve branching is seen within the iridophore. The dynamic colour shift is significantly faster (17 s) than the peak reflectance increase (32 s), revealing two distinct mechanisms. Responses from a structurally altered preparation indicate that the reflectin protein condensation mechanism explains peak reflectance change, while an undiscovered mechanism causes the fast colour shift.


Asunto(s)
Decapodiformes/fisiología , Acetilcolina/metabolismo , Acetilcolina/fisiología , Animales , Conducta Animal , Color , Decapodiformes/anatomía & histología , Estimulación Eléctrica , Femenino , Masculino , Piel/inervación , Fenómenos Fisiológicos de la Piel
17.
Cell Microbiol ; 13(4): 518-26, 2011 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-21338463

RESUMEN

Because of its unique chemical properties, nitric oxide (NO) is a pluripotent signalling and effector molecule that is implicated in a variety of biological roles. Although NO is known to function in host innate immunity against pathogen invasion, its possible roles in microbial symbioses with animal and plant hosts remain relatively less well defined. In this review, we discuss the mechanisms by which bacteria sense and/or detoxify NO. We then focus specifically on its roles in microbial symbioses of diverse eukaryotic hosts. Using the squid-vibrio light-organ symbiosis as a well-characterized example, we discuss the ways in which NO serves as a signal, antioxidant and specificity determinant in this model symbiosis. Because beneficial microbial associations are older and much more prevalent than pathogenic ones, it seems likely that the former may be evolutionary precursors of the latter. Thus, knowledge of the roles played by NO in mutualisms will provide insights into its function in disease interactions as well.


Asunto(s)
Bacterias/metabolismo , Óxido Nítrico/metabolismo , Simbiosis , Animales , Antioxidantes/metabolismo , Decapodiformes/anatomía & histología , Decapodiformes/microbiología , Interacciones Huésped-Patógeno , Plantas/metabolismo , Plantas/microbiología , Transducción de Señal/fisiología , Vibrio/metabolismo
18.
Cell Microbiol ; 13(4): 527-37, 2011 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-21091598

RESUMEN

Bacterial pathogens typically upregulate the host's production of nitric oxide synthase (NOS) and nitric oxide (NO) as antimicrobial agents, a response that is often mediated by microbe-associated molecular patterns (MAMPs) of the pathogen. In contrast, previous studies of the beneficial Euprymna scolopes/Vibrio fischeri symbiosis demonstrated that symbiont colonization results in attenuation of host NOS/NO, which occurs in high levels in hatchling light organs. Here, we sought to determine whether V. fischeri MAMPs, specifically lipopolysaccharide (LPS) and the peptidoglycan derivative tracheal cytotoxin (TCT), attenuate NOS/NO, and whether this activity mediates the MAMPs-induced light organ morphogenesis. Using confocal microscopy, we characterized levels of NOS with immunocytochemistry and NO with a NO-specific fluorochrome. When added exogenously to seawater containing hatchling animals, V. fischeri LPS and TCT together, but not individually, induced normal NOS/NO attenuation. Further, V. fischeri mutants defective in TCT release did not. Experiments with NOS inhibitors and NO donors provided evidence that NO mediates apoptosis and morphogenesis associated with symbiont colonization. Attenuation of NOS/NO by LPS and TCT in the squid-vibrio symbiosis provides another example of how the host's response to MAMPs depends on the context. These data also provide a mechanism by which symbiont MAMPs regulate host development.


Asunto(s)
Aliivibrio fischeri/fisiología , Decapodiformes/microbiología , Interacciones Huésped-Patógeno , Óxido Nítrico/metabolismo , Simbiosis/fisiología , Animales , Decapodiformes/anatomía & histología , Decapodiformes/metabolismo , Luz , Morfogénesis , Donantes de Óxido Nítrico/metabolismo , Óxido Nítrico Sintasa/metabolismo
19.
An Acad Bras Cienc ; 84(4): 1015-28, 2012 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-23207705

RESUMEN

Morphological and morphometric variability of the small-sized coastal squid Lolliguncula brevis was assessed along the largest part of its latitudinal range in the southern hemisphere, off the Brazilian coast (8º S - 27º S). A general homogeneity in form was found throughout the entire latitudinal range. In terms of body proportions, no latitudinal gradients were evident, but a few local "morphotypes" could be distinguished. The distinctive egg mass morphology, and size and form features, including a hectocotylus 20-40% longer than the opposing ventral arm and the presence of suckers on the buccal membrane, indicated that Lolliguncula from northern and southern hemispheres might comprise two different taxa.


Asunto(s)
Decapodiformes/anatomía & histología , Animales , Océano Atlántico , Brasil , Decapodiformes/clasificación , Decapodiformes/crecimiento & desarrollo , Femenino , Masculino
20.
Nat Rev Microbiol ; 19(10): 654-665, 2021 10.
Artículo en Inglés | MEDLINE | ID: mdl-34089008

RESUMEN

As our understanding of the human microbiome progresses, so does the need for natural experimental animal models that promote a mechanistic understanding of beneficial microorganism-host interactions. Years of research into the exclusive symbiosis between the Hawaiian bobtail squid, Euprymna scolopes, and the bioluminescent bacterium Vibrio fischeri have permitted a detailed understanding of those bacterial genes underlying signal exchange and rhythmic activities that result in a persistent, beneficial association, as well as glimpses into the evolution of symbiotic competence. Migrating from the ambient seawater to regions deep inside the light-emitting organ of the squid, V. fischeri experiences, recognizes and adjusts to the changing environmental conditions. Here, we review key advances over the past 15 years that are deepening our understanding of these events.


Asunto(s)
Aliivibrio fischeri/fisiología , Decapodiformes/microbiología , Interacciones Microbiota-Huesped , Simbiosis , Animales , Decapodiformes/anatomía & histología , Evolución Molecular , Hawaii , Agua de Mar/microbiología
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