A histological atlas for the Palinuridae (Crustacea: Decapoda: Achelata): A guide to parasite discovery and spotting the abnormal in spiny lobsters.

Crustaceans suffer from diseases that can alter their survival and ecology with additional economic consequences for fisheries and aquaculture. Many parasites have been described from crustaceans and with the advent of novel technologies such as next generation sequencing, the discovery of novel parasites has become increasingly efficient. Molecular techniques are beginning to surpass more conventional tools for parasite discovery, but they typically do not provide information on pathology. Histopathology remains one of the least expensive methods for parasite discovery and allows for both detection of parasites and descriptions of the pathology they cause. When used in concert with modern molecular and electron microscopy techniques, the approach is powerful; however, there are few informational tools for the interpretation of histological slides from crustaceans. Those available do not provide comprehensive images of all organs and early works were limited to lower resolution than currently available. More recent texts provide in-depth details of infection in histological section, but few provide images of healthy material or describe a baseline from which to compare. Here, we provide a series of image plates derived from histologically processed tissues from three palinurid lobsters: Panulirus argus, Palinurus elephas and Panulirus guttatus. Histology from these lobsters shows high visual similarity in all tissue types. We provide a histological atlas of healthy tissue that can be used as a baseline resource for pathobiologists working on these common species (and related crustaceans) and we discuss how disease may result in visual aberrations to these tissues.

Ionotropic crustacean olfactory receptors.

The nature of the olfactory receptor in crustaceans, a major group of arthropods, has remained elusive. We report that spiny lobsters, Panulirus argus, express ionotropic receptors (IRs), the insect chemosensory variants of ionotropic glutamate receptors. Unlike insects IRs, which are expressed in a specific subset of olfactory cells, two lobster IR subunits are expressed in most, if not all, lobster olfactory receptor neurons (ORNs), as confirmed by antibody labeling and in situ hybridization. Ligand-specific ORN responses visualized by calcium imaging are consistent with a restricted expression pattern found for other potential subunits, suggesting that cell-specific expression of uncommon IR subunits determines the ligand sensitivity of individual cells. IRs are the only type of olfactory receptor that we have detected in spiny lobster olfactory tissue, suggesting that they likely mediate olfactory signaling. Given long-standing evidence for G protein-mediated signaling in activation of lobster ORNs, this finding raises the interesting specter that IRs act in concert with second messenger-mediated signaling.

Sea urchin coelomocytes are resistant to a variety of DNA damaging agents.

Increasing anthropogenic activities are creating environmental pressures that threaten marine ecosystems. Effective environmental health assessment requires the development of rapid, sensitive, and cost-effective tools to predict negative impacts at the individual and ecosystem levels. To this end, a number of biological assays using a variety of cells and organisms measuring different end points have been developed for biomonitoring programs. The sea urchin fertilization/development test has been useful for evaluating environmental toxicology and it has been proposed that sea urchin coelomocytes represent a novel cellular biosensor of environmental stress. In this study we investigated the sensitivity of coelomocytes from the sea urchin Lytechinus variegatus to a variety of DNA-damaging agents including ultraviolet (UV) radiation, hydrogen peroxide (H(2)O(2)), methylmethane sulfonate (MMS) and benzo[a]pyrene (BaP). LD(50) values determined for coelomocytes after 24h of exposure to these DNA damaging agents indicated a high level of resistance to all treatments. Significant increases in the formation of apurinic/apyrimidinic (AP or abasic) sites in DNA were only detected using high doses of H(2)O(2), MMS and UV radiation. Comparison of sea urchin coelomocytes with hemocytes from the gastropod mollusk Aplysia dactylomela and the decapod crustacean Panulirus argus indicated that sensitivity to different DNA damaging agents varies between species. The high level of resistance to genotoxic agents suggests that DNA damage may not be an informative end point for environmental health assessment using sea urchin coelomocytes however, natural resistance to DNA damaging agents may have implications for the occurrence of neoplastic disease in these animals.

Robust microcircuit synchronization by inhibitory connections.

Microcircuits in different brain areas share similar architectural and biophysical properties with compact motor networks known as central pattern generators (CPGs). Consequently, CPGs have been suggested as valuable biological models for understanding of microcircuit dynamics and particularly, their synchronization. We use a well known compact motor network, the lobster pyloric CPG to study principles of intercircuit synchronization. We couple separate pyloric circuits obtained from two animals via artificial synapses and observe how their synchronization depends on the topology and kinetic parameters of the computer-generated synapses. Stable in-phase synchronization appears when electrically coupling the pacemaker groups of the two networks, but reciprocal inhibitory connections produce more robust and regular cooperative activity. Contralateral inhibitory connections offer effective synchronization and flexible setting of the burst phases of the interacting networks. We also show that a conductance-based mathematical model of the coupled circuits correctly reproduces the observed dynamics illustrating the generality of the phenomena.

Identification of putative neuroblasts at the base of adult neurogenesis in the olfactory midbrain of the spiny lobster, Panulirus argus.

Continuous neurogenesis persists during adulthood in the olfactory midbrain of decapod crustaceans, including spiny lobsters, Panulirus argus. This encompasses generation of projection and local interneurons, whose somata are in the lateral soma cluster (LC) and medial soma cluster (MC), respectively. Both neuronal types originate from immediate precursors labeled by a single injection of BrdU and located in a small proliferation zone within each cluster. The aim of this study was to identify neuroblasts as a source of the dividing cells by multiple injections of BrdU over 2 days. All animals receiving multiple injections had one or a few 'extra' BrdU-positive nuclei near the proliferation zones, and these nuclei were significantly larger than nuclei of neurons or BrdU-positive cells in the proliferation zones. Since the defining morphological feature of neuroblasts in preadult neurogenesis in arthropods is being larger than their progeny, these large extra BrdU-positive nuclei represent "putative adult neuroblasts." Multiple BrdU-injections revealed a clump of small cells enclosing the putative adult neuroblasts in LC and MC, and these cells shared morphological characteristics with newly identified putative glial cells in the soma clusters and perivascular cells in the walls of arterioles. These results on P. argus suggest that adult neurogenesis is based on one adult neuroblast per soma cluster, adult neurogenesis appears to be a continuation of embryonic and larval neurogenesis, and the newly identified clumps of cells surrounding the putative adult neuroblasts might provide them with specific microenvironments necessary for their unusual lifelong proliferative and self-renewal capacity.

Panulirus interruptus Ih-channel gene PIIH: modification of channel properties by alternative splicing and role in rhythmic activity.

We cloned 10 full-length variants of PIIH, the gene for I(h) from the spiny lobster, Panulirus interruptus, using reverse transcription-PCR (RT-PCR) and rapid amplification of cDNA ends (RACE). This gene shows a significant amount of alternative splicing in the S3-S4 and S4-S5 linkers, in the P-loop and the entire S6 transmembrane domain, in the cyclic nucleotide binding domain (CNBD), and near the 3' end of the gene. Functional expression of seven splice variants in Xenopus oocytes generated slowly activating hyperpolarization-activated inward currents, which were blocked by the I(h) channel blockers CsCl and ZD7288. The different splice variants had markedly varying activation kinetics and voltage dependence of activation. Bath application of 8-Br-cAMP shifted the V(1/2) to more positive potentials and accelerated the activation kinetics in an isoform-specific manner. Two variants containing a segment with an ER-retention motif in the S4-S5 loop did not produce currents in oocytes. Overexpression of one splice variant, PIIH AB(S)-I, in pyloric dilator (PD) neurons in the lobster stomatogastric ganglion produced an average threefold increase in I(h) without evoking a compensatory increase in I(A). The voltage for half-maximal activation of I(h) in PIIH AB(S)-I-expressing PDs was shifted in the depolarizing direction by 9 mV, whereas the slope factor decreased by 3.8 mV. Moreover, its activation kinetics were significantly faster than in control PDs. PIIH AB(S)-I overexpression enhanced PD neuron rhythmic firing in an amplitude-dependent manner above a minimal threshold two- to threefold increase in amplitude.

Distinct synaptic dynamics of heterogeneous pacemaker neurons in an oscillatory network.

Many rhythmically active networks involve heterogeneous populations of pacemaker neurons with potentially distinct synaptic outputs that can be differentially targeted by extrinsic inputs or neuromodulators, thereby increasing possible network output patterns. To understand the roles of heterogeneous pacemaker neurons, we characterized differences in synaptic output from the anterior burster (AB) and pyloric dilator (PD) neurons in the lobster pyloric network. These intrinsically distinct neurons are strongly electrically coupled, coactive, and constitute the pyloric pacemaker ensemble. During pyloric oscillations, the pacemaker neurons produce compound inhibitory synaptic connections to the follower lateral pyloric (LP) and pyloric constrictor (PY) neurons, which fire out of phase with AB/PD and with different delay times. Using pharmacological blockers, we separated the synapses originating from the AB and PD neurons and investigated their temporal dynamics. These synapses exhibited distinct short-term dynamics, depending on the presynaptic neuron type, and had different relative contributions to the total synaptic output depending on waveform shape and cycle frequency. However, paired comparisons revealed that the amplitude or dynamics of synapses from either the AB or PD neuron did not depend on the postsynaptic neuron type, LP or PY. To address the functional implications of these findings, we examined the correlation between synaptic inputs from the pacemakers and the burst onset phase of the LP and PY neurons in the ongoing pyloric rhythm. These comparisons showed that the activity of the LP and PY neurons is influenced by the peak phase and amplitude of the synaptic inputs from the pacemaker neurons.

Primary culture of hemocytes from the Caribbean spiny lobster, Panulirus argus, and their susceptibility to Panulirus argus Virus 1 (PaV1).

Primary cultures of hemocytes from the Caribbean spiny lobster Panulirus argus were developed for studies on the in vitro propagation of Panulirus argus Virus 1 (PaV1). A modified Leibovitz L-15 medium supported the best survival of hemocytes in in vitro primary cultures. However, degradation of the cultures occurred rapidly in the presence of granulocytes. A Percoll step gradient was used to separate hemocytes into three subpopulations enriched in hyalinocytes, semigranulocytes, and granulocytes, respectively. When cultured separately, hyalinocytes and semigranulocytes maintained higher viability ( approximately 80%) after 18 days incubation compared with granulocytes, which degraded over 2-3 days. Susceptibility of the cell types was investigated in challenge studies with PaV1. Hyalinocytes and semigranulocytes were susceptible to PaV1. Cytopathic effects (CPE) were observed as early as 12h post-inoculation, and as the infection progressed, CPE became more apparent, with cell debris and cellular exudates present in inoculated cultures. Cell lysis was noticeable within 24h of infection. The presence of virus within cells was further confirmed by in situ hybridization using a specific DNA probe. The probe gave a unique staining pattern to cells infected with PaV1 24-h post-inoculation. Cells in the control treatment were intact and negative to hybridization. This assay was further applied to the quantification of infectious virus in hemolymph using a 50% tissue culture infectious dose assay (TCID(50)) based on CPE. These tools will now allow the quantification of PaV1 using established culture-based methods.

Experimental transmission and tissue tropism of white spot syndrome virus (WSSV) in two species of lobsters, Panulirus homarus and Panulirus ornatus.

The susceptibility of two species of lobsters, Panulirus homarus and Panulirus ornatus to white spot syndrome virus (WSSV) was tested by oral route and intramuscular injection. The results revealed that these lobsters were as highly susceptible as marine shrimp when the WSSV was administered intramuscularly. The WSSV caused 100% mortality in both Panulirus homarus and Panulirus ornatus, at 168 and 120 h, respectively, after intramuscular injection and failed to cause mortality when given orally. The presence of WSSV in moribund lobsters was confirmed by single-step and nested PCR, Western blot, histology, and bioassay test. It was found in eyestalk, gill, head muscle, tail muscle, hemolymph, appendages, and stomach. In lobsters with oral route infection, all tested organs except stomach and head muscle was negative for WSSV by nested PCR at 120 h post-inoculation. The stomach and head muscle was positive by nested PCR at 120 h p.i., but negative at 168 h p.i. Western blot analysis was negative in all the tested organs of both species of lobster at 120 h post-inoculation by oral route.

Mechanical functions of setae from the mouth apparatus of seven species of decapod crustaceans.

The mouthpart setae of seven species of decapods were examined with macro-video recordings and scanning electron microscopy. The general mechanical (nonsensory) functions of the different mouthparts are described and an account of their setation is given. This offers the possibility to determine the mechanical functions of the different types of setae. Pappose setae do not participate in food handling but in general make setal barriers. Plumose setae likewise do not contact food objects but assist in current generation. Papposerrate setae are rare but they were seen to assist in pushing food particles into the mouth. Serrulate setae are very common and mainly participate in gentle food handling and grooming. Serrate setae are used for more rough food manipulation and grooming. The roughest shredding, tearing, and manipulation of prey items are handled by the cuspidate setae. Simple setae seem to be divided into two populations with very different functions. On the maxillipeds of Panulirus argus they are used for shredding, tearing, and holding the food objects, but on the basis of maxilla 2 of three other species they appear to have very little mechanical influence and only when handling small prey items. The functional scheme seems to be consistent within the Decapoda.

Localized ablation of olfactory receptor neurons induces both localized regeneration and widespread replacement of neurons in spiny lobsters.

The peripheral olfactory system of the spiny lobster Panulirus argus--located on paired antennules--undergoes continual postembryonic development. This process includes continuous addition of olfactory receptor neurons (ORNs) related to indeterminate growth, continuous replacement, and regeneration when necessitated by damage. We have shown previously that new olfactory tissue is continually added to the proximal margin of these populations, called the proximal proliferation zone (PPZ). Here, we show that focal damage to mature portions of the olfactory system causes localized degeneration of ORNs over 1-10 days after damage. Studies using the cell proliferation marker 5-bromo-2'-deoxyuridine show that localized degeneration was followed by rapid and localized regeneration of olfactory tissue. Rapidly dividing cells were recorded up to 40 days after damage, with regeneration of ORN clusters complete within 80 days. Focal damage appeared to stimulate widespread cell replacement (cell death and proliferation) within mature, undamaged ORN clusters. This response was observed in ORN clusters outside the damaged zone, including mature clusters in the contralateral antennule. The degree of widespread cell replacement was less than local repair after local damage, but it increased with more extensive damage. However, changes in on-going proliferation in the PPZ were not detected, at least not 20 days or longer after damage, suggesting damage-induced widespread proliferation may be specific to mature populations of ORNs. We speculate that localized regeneration involves activity of resident precursor cells not destroyed by the ablation and that unidentified regulatory signals released in response to localized damage induce widespread ORN replacement.

Inducible transcript expressed by reactive epithelial cells at sites of olfactory sensory neuron proliferation.

The continuous replacement of cells in the spiny lobster olfactory organ depends on proliferation of new cells at a specific site, the proximal proliferation zone (PPZ). Using representational difference analysis of cDNA, we identified transcripts enriched in the PPZ compared to the mature zone (MZ) of the organ. The 12 clones identified included four novel sequences, three exoskeletal proteins, a serine protease, two protease inhibitors, a putative growth factor, and a sequence named PET-15 that has similarity to antimicrobial proteins of the crustin type. PET-15 mRNA was only detected in epithelial cells. It was abundant in all epithelial cells of the PPZ, but was only detected in the MZ at sites of damage to the olfactory organ. PET-15 mRNA was increased by types of damage that are known to induce proliferation of new olfactory sensory neurons in the olfactory organ. It increased in the PPZ after partial ablation of the olfactory organ and in the MZ after shaving of aesthetasc sensilla. These ipsilateral effects were mirrored by smaller increases in the undamaged contralateral olfactory organ. These contralateral effects are most parsimoniously explained by the action of a diffusible signal. Because epithelial cells are the source of proliferating progenitors in the olfactory organ, the same diffusible signal may stimulate increases in both cellular proliferation and PET-15 mRNA. The uniformity of expression of PET-15 in the PPZ epithelium suggests that the epithelial cells that give rise to new olfactory sensory neurons are a subset of cells that express PET-15.

Calcium signaling components of oscillating invertebrate neurons in vitro.

We have studied the Ca(2+) dynamics of bursting-spiking neurons in the lobster stomatogastric ganglion. Neurons in this ganglion undergo spontaneous oscillations in membrane voltage with a period of 1-10 s in situ. We found that neurons isolated from the ganglion and filled with the fluorescent calcium indicator Fluo-4 show simultaneous changes of membrane potential and cytoplasmic Ca(2+) concentration ([Ca(2+)](I)). These Ca(2+) signals are highly heterogeneous both in terms of amplitude and time constants. They showed variable spatial distributions with the soma exhibiting low and slow signals, and a region in the process with large and fast signals. Ca(2+) transients in the processes are dependent on external Ca(2+) and can be blocked by Co(2+), but not other, more specific Ca(2+) current blockers. Rather, nifedipine a known Ca(2+) current blocker, affects the distribution of the Ca(2+) signal, which suggests a specific localization of Ca(2+) channels. Although the signal is not absolutely dependent on action potentials, it is greatly reduced when action potentials are blocked by tetrodotoxin. Termination of the signal depends only slightly on Ca(2+) buffering mechanisms such as mitochondria, Ca(2+)/Na(+) and Ca(2+)/H(+) exchangers. We also demonstrate the presence of caffeine-sensitive internal stores in stomatogastric ganglion cells. The store distribution is different but overlaps with the voltage-dependent distribution. The maximal caffeine-activated Ca(2+) signal is in the soma and it is smaller in the processes. Unlike the voltage-activated Ca(2+) signal this signal is not blocked by Co(2+). Nevertheless, the two types of signal interact during caffeine application. This unique spatial separation of two Ca(2+) sources may have important functional implication.

Activity-independent homeostasis in rhythmically active neurons.

The shal gene encodes the transient potassium current (I(A)) in neurons of the lobster stomatogastric ganglion. Overexpression of Shal by RNA injection into neurons produces a large increase in I(A), but surprisingly little change in the neuron's firing properties. Accompanying the increase in I(A) is a dramatic and linearly correlated increase in the hyperpolarization-activated inward current (I(h)). The enhanced I(h) electrophysiologically compensates for the enhanced I(A), since pharmacological blockade of I(h) uncovers the physiological effects of the increased I(A). Expression of a nonfunctional mutant Shal also induces a large increase in I(h), demonstrating a novel activity-independent coupling between the Shal protein and I(h) enhancement. Since I(A) and I(h) influence neuronal activity in opposite directions, our results suggest a selective coregulation of these channels as a mechanism for constraining cell activity within appropriate physiological parameters.

In the spiny lobster (Panulirus interruptus) the prophenoloxidase is located in plasma not in haemocytes.

In the spiny lobster (Panulirus interruptus), unlike other crustaceans most of the prophenoloxidase (proPO) was detected in cell-free plasma (86.3%). In spite of its location, lobster proPO activating system has a similar activation mechanism to other crustacean proPO systems. Haemocyte lysate was able to activate the plasma proPO indicating location of the prophenoloxidase activating enzyme (PPAE) in haemocytes. Lobster haemocyte PPAE was isolated by affinity chromatography and its participation as activating enzyme was demonstrated. This enzyme is a serine-proteinase that transforms the inactive form (proPO) to an active one (phenoloxidase). The PPAE was also present in the cell-free supernatant of haemocytes previously incubated with Vibrio alginolyticus.

Adaptation in chemoreceptor cells. II. The effects of cross-adapting backgrounds depend on spectral tuning.

1. The cross-adapting effects of chemical backgrounds on the response of primary chemoreceptor cells to superimposed stimuli were studied using NH(4) receptor cells, of known spectral tuning from the lobster (Homarus americanus). 2. Spectrum experiments: The spectral tuning of NH(4) receptor cells was investigated using NH(4)C1 and 7 other compounds selected as the most stimulatory non-best compounds for NH(4) cells from a longer list of compounds tested in previous studies. Based on their responses to the compounds tested, 3 spectral subpopulations of NH(4) Bet cells which responded second-best to Betaine (Bet; and 'pure' NH(4) cells, which responded to NH(4)C1 only (Fig.1). 3. Cross-adaptation experiments: Overall, cross-adaptation with Glu and Bet backgrounds caused suppression of response of NH(4) receptor cells to various concentrations of NH(4)C1. However, the different subpopulations of NH(4) cells were affected differently: (a) The stimulus-response functions of NH(4)-Glu cells were significantly suppressed by both a 3 micrometre (G3) and 300 micrometre (G300) Glu backgrounds. (b) The stimulus-response functions of NH(4)-Bet cells was not affected by a 3 micrometre (B3), but significantly suppressed by a 300 micrometre (B300) Bet background. (c) The stimulus-response functions of pure NH(4) cells were not affected by any of the Glu or Bet back grounds (Figs. 3, 4). 4. The stimulus-response functions of 5 cells from all different subpopulations were enhanced by cross-adaptation with the G300 and B300 back-grounds (Fig 4, Table 1). 5. Whereas self-adaptation caused parallel shifts in stimulus-response functions (Borroni and Atema 1988), cross-adaptation caused a decrease in slope of stimulus-response functions. Implications of the results from cross- and self-adaptation experiments on NH(4) receptor cells, for a receptor cell model are discussed.