Reproductive biology of the skate, Rioraja agassizii (Müller and Henle, 1841), off Puerto Quequén, Argentina

A total of 230 specimens of the skate, Rioraja agassizii, was collected from the commercial bottom trawl fishery of Puerto Quequén, Argentina. During the warmer seasons greater proportions of females were sampled. The largest male and female sampled were 629 and 698 mm total length (TL), respectively. Sexual dimorphism was detected in the relationship between weight ( W )−TL and disc width (DW)−TL, in that females were heavier and wider than males. The smallest mature male and female were 485 and 530 mm TL, respectively. TL at 50% maturity (TL_50%) was estimated at 504 and 570 mm for males and females, respectively. Females exhibited heavier livers than males throughout their lifetimes. Seasonal variations in the gonadosomatic (GSI) and hepatosomatic (HSI) indices, and in the width of the left oviducal gland (OG), along with the greater number of pregnant females sampled during spring, suggested that the peak of the egg laying season could be during this season. The egg cases presented a mean length of 69.01 ± 5.53 mm, mean width of 43.40 ± 1.86 mm and mean weight of 17.00 ± 4.59 g. According to these results specimens from Puerto Quequén and southern Brazil appeared to differ in size, the peak of the egg-laying season and in egg dimensions.     

Calling Patterns in Male Responses to Conspecific Playbacks in the Johnstone's Whistling Frog Eleutherodactylus johnstonei

Vocal interactions are common in chorusing frogs. Changes in the calling patterns of Eleutherodactylus johnstonei males were analyzed by recording their responses to playbacks of conspecific calls repeated at fixed periods (long: 1.7 s, short: 0.98 s). The call period and timing, estimated through the onset response time, were determined for each male. Males reduced and regularized the period of their calls in response to both stimuli, regardless of their absolute and relative period (i.e., the difference between the male's period and the stimulus period). Males avoided initiating their calls during ongoing stimuli, but did not time their calls in the silent gap between successive stimuli in ways that reduced the probability of overlap: the proportion of calls without overlap did not depart from random expectations when the silent gap was long, and was smaller than expected when the gap was short. This result indicated that males react to the presence of the virtual competitor but not to its particular characteristics. Fixed responses have been described in other anurans, and often relate to trade-offs between female attraction, male competition, predator attraction, and depletion of energy reserves. Lack of coordination with the stimuli, beyond inhibition of calling during an ongoing stimulus, also indicates somewhat rigid vocal strategies, at least under the experimental conditions. Results from the short period trials suggested a compromise between maintaining a call period and avoiding call overlap. Whether female behavior is influenced by call interference and whether males pay selective attention to distant males instead of to close neighbors must be investigated to better understand the vocal behavior of E. johnstonei .     

Mitochondrial DNA Variant Discovery and Evaluation in Human Cardiomyopathies through Next-Generation Sequencing

Mutations in mitochondrial DNA (mtDNA) may cause maternally-inherited cardiomyopathy and heart failure. In homoplasmy all mtDNA copies contain the mutation. In heteroplasmy there is a mixture of normal and mutant copies of mtDNA. The clinical phenotype of an affected individual depends on the type of genetic defect and the ratios of mutant and normal mtDNA in affected tissues. We aimed at determining the sensitivity of next-generation sequencing compared to Sanger sequencing for mutation detection in patients with mitochondrial cardiomyopathy. We studied 18 patients with mitochondrial cardiomyopathy and two with suspected mitochondrial disease. We “shotgun” sequenced PCR-amplified mtDNA and multiplexed using a single run on Roche''s 454 Genome Sequencer. By mapping to the reference sequence, we obtained 1,300× average coverage per case and identified high-confidence variants. By comparing these to >400 mtDNA substitution variants detected by Sanger, we found 98% concordance in variant detection. Simulation studies showed that >95% of the homoplasmic variants were detected at a minimum sequence coverage of 20× while heteroplasmic variants required >200× coverage. Several Sanger “misses” were detected by 454 sequencing. These included the novel heteroplasmic 7501T>C in tRNA serine 1 in a patient with sudden cardiac death. These results support a potential role of next-generation sequencing in the discovery of novel mtDNA variants with heteroplasmy below the level reliably detected with Sanger sequencing. We hope that this will assist in the identification of mtDNA mutations and key genetic determinants for cardiomyopathy and mitochondrial disease.     

Mutations in the GlyT2 Gene (SLC6A5) Are a Second Major Cause of Startle Disease

Hereditary hyperekplexia or startle disease is characterized by an exaggerated startle response, evoked by tactile or auditory stimuli, leading to hypertonia and apnea episodes. Missense, nonsense, frameshift, splice site mutations, and large deletions in the human glycine receptor α1 subunit gene (GLRA1) are the major known cause of this disorder. However, mutations are also found in the genes encoding the glycine receptor β subunit (GLRB) and the presynaptic Na(+)/Cl(-)-dependent glycine transporter GlyT2 (SLC6A5). In this study, systematic DNA sequencing of SLC6A5 in 93 new unrelated human hyperekplexia patients revealed 20 sequence variants in 17 index cases presenting with homozygous or compound heterozygous recessive inheritance. Five apparently unrelated cases had the truncating mutation R439X. Genotype-phenotype analysis revealed a high rate of neonatal apneas and learning difficulties associated with SLC6A5 mutations. From the 20 SLC6A5 sequence variants, we investigated glycine uptake for 16 novel mutations, confirming that all were defective in glycine transport. Although the most common mechanism of disrupting GlyT2 function is protein truncation, new pathogenic mechanisms included splice site mutations and missense mutations affecting residues implicated in Cl(-) binding, conformational changes mediated by extracellular loop 4, and cation-π interactions. Detailed electrophysiology of mutation A275T revealed that this substitution results in a voltage-sensitive decrease in glycine transport caused by lower Na(+) affinity. This study firmly establishes the combination of missense, nonsense, frameshift, and splice site mutations in the GlyT2 gene as the second major cause of startle disease.     

Heterocyclic acetamide and benzamide derivatives as potent and selective β3-adrenergic receptor agonists with improved rodent pharmacokinetic profiles

A series of amide derived β₃-adrenergic receptor (AR) agonists is described. The discovery and optimization of several series of compounds derived from 1, is used to lay the SAR foundation for second generation β₃-AR agonists for the treatment of overactive bladder.     

Decreased expression of the endothelial cell-derived factor EGFL7 in systemic sclerosis: potential contribution to impaired angiogenesis and vasculogenesis

Introduction

Microvascular damage and defective angiogenesis and vasculogenesis have a major role in the pathogenesis of systemic sclerosis (SSc). Epidermal growth factor-like domain 7 (EGFL7) is a proangiogenic molecule which is predominantly expressed and secreted by endothelial cells and their progenitors and controls vascular development and integrity. In this study, we investigated the possible involvement of EGFL7 in SSc.

Methods

Serum EGFL7 levels from 60 patients with SSc and 35 age- and sex-matched healthy controls were examined by colorimetric sandwich enzyme-linked immunosorbent assay. The expression of EGFL7 in forearm skin biopsies (n = 16 SSc, n = 10 controls), cultured dermal microvascular endothelial cells (MVECs) (n = 3 SSc, n = 3 controls) and late-outgrowth peripheral blood endothelial progenitor cell (EPC)-derived endothelial cells (n = 15 SSc, n = 8 controls) was investigated by immunofluorescence and Western blotting.

Results

Serum EGFL7 levels were detectable in 68.6% of healthy controls and 45% of SSc cases (P < 0.05). Circulating levels of EGFL7 were significantly decreased in SSc patients compared with healthy controls (P = 0.01). Serum levels of EGFL7 were significantly lower in both limited cutaneous SSc and diffuse cutaneous SSc patients than in controls (P = 0.02 and P = 0.04, respectively). In SSc, decreased serum EGFL7 levels were significantly correlated with the severity of nailfold capillary abnormalities. Patients with the most severe capillary changes and digital ulcers had serum EGFL7 levels significantly lower than healthy controls, while the EGFL7 levels did not differ significantly between controls and SSc patients with less capillary damage and lack of digital ulcers. Endothelial EGFL7 expression was strongly downregulated or even almost completely undetectable in SSc-affected dermis compared with controls (P < 0.001). In cultured SSc dermal MVECs and late-outgrowth peripheral blood EPC-derived endothelial cells, EGFL7 was significantly downregulated compared with cells obtained from healthy subjects (P < 0.01 and P < 0.001, respectively).

Conclusions

Our findings suggest that the loss of EGFL7 expression in endothelial cells and their progenitors might play a role in the development and progression of peripheral microvascular damage and the defective vascular repair process characteristic of SSc.     

Evaluation of Alpha 1-Antitrypsin and the Levels of mRNA Expression of Matrix Metalloproteinase 7, Urokinase Type Plasminogen Activator Receptor and COX-2 for the Diagnosis of Colorectal Cancer

Background

Colorectal cancer (CRC) is the second most common cause of death from cancer in both men and women in the majority of developed countries. Molecular tests of blood could potentially provide this ideal screening tool.

Aim

Our objective was to assess the usefulness of serum markers and mRNA expression levels in the diagnosis of CRC.

Methods

In a prospective study, we measured mRNA expression levels of 13 markers (carbonic anhydrase, guanylyl cyclase C, plasminogen activator inhibitor, matrix metalloproteinase 7 (MMP7), urokinase-type plasminogen activator receptor (uPAR), urokinase-type plasminogen activator, survivin, tetranectin, vascular endothelial growth factor (VEGF), cytokeratin 20, thymidylate synthase, cyclooxygenase 2 (COX-2), and CD44) and three proteins in serum (alpha 1 antitrypsin, carcinoembryonic antigen (CEA) and activated C3 in 42 patients with CRC and 33 with normal colonoscopy results.

Results

Alpha 1-antitrypsin was the serum marker that was most useful for CRC diagnosis (1.79±0.25 in the CRC group vs 1.27±0.25 in the control group, P<0.0005). The area under the ROC curve for alpha 1-antitrypsin was 0.88 (0.79–0.96). The mRNA expression levels of five markers were statistically different between CRC cases and controls: those for which the ROC area was over 75% were MMP7 (0.81) and tetranectin (0.80), COX-2 (0.78), uPAR (0.78) and carbonic anhydrase (0.77). The markers which identified early stage CRC (Stages I and II) were alpha 1-antitrypsin, uPAR, COX-2 and MMP7.

Conclusions

Serum alpha 1-antitrypsin and the levels of mRNA expression of MMP7, COX-2 and uPAR have good diagnostic accuracy for CRC, even in the early stages.     

Population parameters of the Pacific flagfin mojarra Eucinostomus currani (Perciformes: Gerreidae) captured by shrimp trawling fishery in the Gulf of California

Shrimp trawling fishery in the Gulf of California captures a wide variety of non-target species of fish, crustaceans, and mollusks that are relatively unknown. The Pacific flagfin mojarra Eucinostomus currani is a frequently found species in these catches, nevertheless, nothing is currently known about its population dynamics. To contribute to the knowledge on this fish species, we studied the size structure, growth, mortality, and the recruitment pattern during the 2004-2005 seasons. A total of 6,078 mojarra were captured from 350 samples, with minimum and maximum lengths of 4.5 cm and a maximum of 21.0 cm. The average total length of the four major cohorts was 11.4, 13.7, 15.6 and 18.0 cm, corresponding to ages 0.9, 1.2, 1.6 and 2.2 years, respectively, being the most abundant the 1.2 year-old group. The instant growth coefficient indicated moderate growth rates (K(s) = 0.81/year, K(E) = 0.85/year), corresponding to individuals living between 3.5 to 3.7 years. The estimated asymptotic lengths was L (infinity) = 21.8 cm. In general, the population could be considered healthy: natural mortality (M = 1.53/year); total mortality (Z = 2.73/year); condition factor (K = 0.01072); fishery mortality (F = 1.2/year) and exploitation rate (E = 0.43/year). The maximum reproduction period almost coincided with the closed season for shrimp fishing (March to August), thus we concluded that survival of the species is ensured because reproduction is indirectly protected.     

Facial Structure Alterations and Abnormalities of the Paranasal Sinuses on Multidetector Computed Tomography Scans of Patients with Treated Mucosal Leishmaniasis

Background/Objectives

Mucosal leishmaniasis (ML) is a progressive disease that affects cartilage and bone structures of the nose and other upper respiratory tract structures. Complications associated with ML have been described, but there is a lack of studies that evaluate the structural changes of the nose and paranasal sinuses in ML using radiological methods. In this study, we aimed to assess the opacification of the paranasal sinuses in patients with treated ML and any anatomical changes in the face associated with ML using multidetector computed tomography scans (MDCT) of the sinuses. We compared the findings with a control group.

Methodology/Principal Findings

We evaluated 54 patients with treated ML who underwent CT scans of the sinuses and compared them with a control group of 40 patients who underwent orbital CT scans. The degree of sinus disease was assessed according to the Lund-Mackay criteria. Forty of the 54 patients with a history of ML (74.1%) had a tomographic score compatible with chronic sinusitis (Lund-Mackay ≥4). CT scans in the leishmaniasis and control groups demonstrated significant differences in terms of facial structure alterations. Patients from the ML group showed more severe levels of partial opacification and pansinus mucosal thickening (42.6%) and a greater severity of total opacification. Patients from the ML group with a Lund-Mackay score ≥4 presented longer durations of disease before treatment and more severe presentations of the disease at diagnosis.

Conclusion/Significance

CT scans of the sinuses of patients with ML presented several structural alterations, revealing a prominent destructive feature of the disease. The higher prevalence in this study of chronic rhinosinusitis observed in CT scans of patients with treated ML than in those of the control group suggests that ML can be considered a risk factor for chronic rhinosinusitis in this population (p<0.05).