Pyloric Ceca Research Articles

Ascaridoid Nematodes Infection in Anadromous Fish Coilia nasus from Yangtze River

The longjaw tapertail anchovy Coilia nasus, which migrates from ocean to freshwater for spawning in spring, is an important anadromous fish with ecological and cultural significance. To determine parasite infection in anadromous C. nasus, a total of 103 fish from the Yangtze River were collected and examined in 2021 and 2022. The overall infection prevalence of nematodes in C. nasus was 100%, with a mean intensity of 13.81 ± 16.45. The mean intensity of nematode infections in 2022 was significantly higher than that observed in 2021 across all sampling sites (p < 0.05). Nematodes were widely detected in the mesentery, pyloric cecum, stomach, and liver, among which the mesentery accounted for the highest proportion, reaching up to 53.52%. A total of eight ascaridoid nematodes belonging to the family Anisakidae and Raphidascarididae were identified by using morphological characters and molecular biological techniques, including two species of Anisakis, five species of Hysterothylacium, and one species of Raphidascaris. A. pegreffii was found as the predominant species, accounting for 48.65% of all identified parasitic nematodes in liver, while Raphidascaris sp. was the most common nematode in the mesentery, pyloric cecum, and stomach, reaching up to 39.81%, 36.21%, and 74.36%, respectively. The present study systematically investigated the parasitic status and community structure of the nematode in C. nasus during its migration in the Yangtze River. This research provides a foundation for studying the impact of nematode parasitism on the reproductive migration and population recruitment of C. nasus, and offers valuable insights for biomarker screening and nematode identification in C. nasus.

Mechanisms of Digestive Enzyme Response to Acute Salinity Stress in Juvenile Yellowfin Tuna (Thunnus albacares).

This study investigates the effect of a sudden change in salinity for 48 h on the digestive enzyme activity of juvenile yellowfin tuna. The treatment included a control salinity of 32‱ in natural seawater and an experimental salinity of 29‱. Acute stress experiments were carried out on 72 juvenile yellowfin tuna (646.52 ± 66.32 g) for 48 h to determine changes in digestive enzyme activity in different intestinal sections over time (0 h, 12 h, 24 h, 48 h). The activities of pepsin, trypsin, α-amylase, lipase, and chymotrypsin in the digestive organs (stomach, foregut, and pyloric ceca) of juvenile yellowfin tuna were measured. Pepsin and pancreatic protease in the experimental group were significantly lower than in the control group (p < 0.05). α-amylase showed a fluctuating trend of decreasing and then increasing, and its activity trend was pyloric ceca > foregut > stomach. The lipase activity of gastric tissues decreased at the beginning and then increased, reaching a minimum at 24 h (2.74 ± 1.99 U·g protein-1). The change of lipase in the pyloric ceca and foregut was increasing and then decreasing. The lipase activity trend was pyloric ceca > foregut > stomach. The chymotrypsin showed a decreasing and increasing trend and then stabilized at 48 h with a pattern of pyloric ceca > foregut > stomach. Similarly, the gut villi morphology was not significantly altered in the acutely salinity-stressed compared to the non-salinity-stressed. This study suggests that salinity may change the digestive function of juvenile yellowfin tuna, thereby affecting fish feeding, growth, and development. On the contrary, yellowfin tuna is highly adapted to 29‱ salinity. However, excessive stress may negatively affect digestive enzyme activity and reduce fish digestibility. This study may provide a scientific basis for a coastal aquaculture water environment for yellowfin tuna farming, which may guide the development and cultivation of aquaculture.

Tissue-specific transcriptomes reveal potential mechanisms ofmicrobiome heterogeneity inan ancient fish.

The lake sturgeon (Acipenser fulvescens) is an ancient, octoploid fish faced with conservation challenges across its range in North America, but a lack of genomic resources has hindered molecular research in the species. To support such research, we created a transcriptomic database from 13 tissues: brain, esophagus, gill, head kidney, heart, white muscle, liver, glandular stomach, muscular stomach, anterior intestine, pyloric cecum, spiral valve and rectum. The transcriptomes for each tissue were sequenced and assembled individually from a mean of 98.3 million (±38.9 million SD) reads each. In addition, an overall transcriptome was assembled and annotated with all data used for each tissue-specific transcriptome. All assembled transcriptomes and their annotations were made publicly available as a scientific resource. The non-gut transcriptomes provide important resources for many research avenues. However, we focused our analysis on messenger ribonucleic acid (mRNA) observations in the gut because the gut represents a compartmentalized organ system with compartmentalized functions, and seven of the sequenced tissues were from each of these portions. These gut-specific analyses were used to probe evidence of microbiome regulation by studying heterogeneity in microbial genes and genera identified from mRNA annotations. Gene set enrichment analyses were used to reveal the presence of photoperiod and circadian-related transcripts in the pyloric cecum, which may support periodicity in lake sturgeon digestion. Similar analyses were used to identify different types of innate immune regulation across the gut, while analyses of unique transcripts annotated to microbes revealed heterogeneous genera and genes among different gut tissues. The present results provide a scientific resource and information about the mechanisms of compartmentalized function across gut tissues in a phylogenetically ancient vertebrate. Database URL: https://figshare.com/projects/Lake_Sturgeon_Transcriptomes/133143.

A NEW SPECIES OF HENNEGUYA THÉLOHAN, 1892 (CNIDARIA: BIVALVULIDA: MYXOBOLIDAE) INFECTING THE SUBMUCOSA OF THE INTESTINE AND PYLORIC CECA OF RED DRUM, SCIAENOPS OCELLATUS (LINNAEUS) (PERCIFORMES: SCIAENIDAE) FROM COASTAL ALABAMA.

A new species of Henneguya Thélohan, 1892 (Bivalvulida: Myxobolidae) is described from the submucosa of the intestine and pyloric ceca of red drum (Sciaenops ocellatus [Linnaeus, 1766] [Perciformes: Sciaenidae]) from the Gulf of Mexico off Gulf Shores, Alabama. Henneguya albomaculata n. sp. differs from all congeners by the combination of myxospore dimensions, polar tubule coil count, the presence of an iodinophilic vacuole in the sporoplasm, and small-subunit ribosomal deoxyribonucleic acid (SSU rDNA) sequence. A phylogenetic analysis of the SSU rDNA recovered H. albomaculata sister to Henneguya cynosioniDykova, de Buron, Roumillat, and Fiala, 2011 in a clade composed of 11 species of Henneguya and 1 species of Myxobolus Bütschli, 1882 (Bivalvulida: Myxobolidae) that collectively infect fishes in marine or estuarine systems. Histologic sections of infected intestine and pyloric ceca revealed plasmodia of H. albomaculata n. sp. developing in the loose connective tissue of the submucosa. The new species comprises the second species of Henneguya reported from red drum.

Oxygenation of European seabass (Dicentrarchus labrax L.) in cages through aeration and effect on lipid metabolism.

Two groups of the same batch of European seabass were used in an industrial-scale trial in sea cages in Vorios Evoikos, Greece. For about one month, one of the two cages was oxygenated by use of compressed air injected in seawater through an AirX frame (Oxyvision A/S, Norway) at 3.5 m depth, while oxygen concentration and temperature were monitored every 30 min. The liver, gut, and pyloric ceca samples were taken from fish of both groups for measurement of gene expression of phospholipase A2 (PLA2) and hormone-sensitive lipase (HSL), and for histological analysis at the middle and end of the experiment. Real-time qPCR was performed with housekeeping genes ACTb, L17, and EF1a. The expression of PLA2 increased in pyloric caeca samples from the oxygenated cage, suggesting that aeration improved the absorption rate of dietary phospholipids (p < 0.05). Expression of HSL increased significantly in liver samples from the control cage, in comparison with the aerated cage (p < 0.05). Histological examination of sea bass samples revealed an increased fat accumulation in the hepatocytes of fish in the oxygenated cage. The results of the present study showed increased lipolysis induced by low DO levels in farmed sea bass in cages.

FIRST RECORD OF LARVAE OF Hysterothylacium (NEMATODA: RAPHIDASCARIDIDAE) INFECTING Hoplias malabaricus (CHARACIFORMES: ERYTHRINIDAE) IN PIAUÍ STATE, BRAZIL

Nematode larvae can cause damage to fish and diseases to consumers. In this paper we record the first occurrence of Hysterothylacium sp. in Hoplias malabaricus captured by artisanal fishers in the Poti River, State of Piauí, northeast Brazil. In the laboratory the fish were investigated for the collection of helminths. Sixteen hosts (63.3%) were parasitized by 94 nematodes larvae that were morphologically identified as Hysterothylacium sp. parasitizing the liver, intestine, stomach, pyloric cecum, abdominal cavity and swim bladder. The parasitic diversity in H. malabaricus is composed of thirty-two taxa, with the larvae of Contracaecum being dominant. This work records the parasitological inventory of nematodes in H. malabaricus and we add morphological and morphometric data for Hysterothylacium sp. in the state of Piauí, parasitizing fish of commercial importance.

Aspectos macro e micromorfológicos e histológicos do intestino do pirarucu Arapaima gigas (SCHINZ, 1822) (Osteoglossiformes: Arapaimidae)

Currently, the fish farming with Arapaima gigas has suffered from technological obstacles in the fields of reproduction, health and nutrition, making it necessary to know the morphology of its structures, so that it can advance in more technified research in scope of production in Rondônia state, as well as in aquaculture nutrition and health. Therefore, the aimed is to characterize the macro and microscopic morphology of posterior digestive system of A. gigas. The intestine of six specimens A. gigas in ideal slaughter size was analyzed. The analyzes were performed using light-sheet microscopy (LM) and scanning electron (SEM) techniques. The intestine basically showes similar histological characteristics in three analyzed portions (proximal, middle and distal). Same type of simple columnar epithelium with goblet cells was evidenced, with subtle variations in pattern of villi in each segment, and in number of goblet cells. In the rectum, the amount of goblet cells and evident longitudinal villi was expressive. Macroscopic anatomy and histology of the intestine A. gigas analyzed showes characteristics of adaptation to cultivation, according to their diet and habitat. The intestinal mucosa can divided into three distinct portions: proximal, middle and final intestine, in addition to the rectum and anus. In the pyloric cecum, the folds are slightly higher and poorly branched. The rectum, compared to the midgut, showed a higher occurrence of goblet cells in the mucosa. This increase in goblet cells observed in the posterior portion may related to the assimilation of ions and fluids that occur at this location.

Examination of Paraffin Sections of Different Rainbow Trout (Oncorhynchus mykiss) Tissues by Light and Scanning Electron Microscope

The current study aimed to highlight histopathological findings in paraffin block sections of the liver, gill kidney, and pyloric cecum of rainbow trout (Oncorhynchus mykiss) by different imagining devices such as Scanning Electron (SEM) and Light Microscope (LM). To determine the performance of different imagining methods two different thickness paraffin sections such as 5 and 15 µm about various rainbow trout tissue were prepared for imagining different devices. That sections were imagined by SEM and LM, both sections including 5 and 15 µm were imagined by SEM while just 5 µm was an image by LM. In LM imagining, it was detected that hydropic degeneration and vacuole formations in the liver hepatocytes of fish, as well as hyperplasia in bile ducts. Lamellar epithelial cell hyperplasia/hypertrophy was mild and histopathological findings such as secondary lamellar elevation and edema were more severe in rainbow trout gills. Glomerular atrophy/hypertrophy was moderately detected in the kidneys and hydropic degeneration of tubular epithelium was more severe. No degeneration or necrosis was observed in the lamina epithelium of the pyloric cecum. In SEM imagining of different thickness paraffin sections, cartilage and secondary lamellar structure in the gills, glomerulus, and Bowman’s capsule structure in the kidneys, and the structure of the pyloric cecum was observed. In the SEM imaging of the paraffin block sections of hepatocytes of the liver, the cell nuclei were determined, and also the grooves in the cytoplasm were thought to be vacuoles. As a consequence, the structural elements of the organ had higher clarity in SEM imaging from paraffin block sections, but the histopathological alterations remained unclear. As a result, SEM imaging of fish tissue is more suited for seeing tissue architecture, although LM imaging is better suited for determining and scoring histopathological variations.

Mucin O-glycosylation and pathogen binding ability differ between rainbow trout epithelial sites

Mucins are highly glycosylated proteins that make up the mucus covering internal and external surfaces of fish. Mucin O-glycans regulate pathogen quorum sensing, growth, virulence and attachment to the host. Knowledge on this mucosal defense system can enable alternative treatments to diseases posing a threat to productivity and welfare in aquaculture. Here, we characterize the rainbow trout (Oncorhynchus mykiss) gill, skin, pyloric ceca and distal intestinal mucin O-glycosylation and compare it to known teleost O-glycomes. We identified 54 O-glycans, consisting of up to nine monosaccharide residues. Skin glycans were most acidic, shortest on average and consisted mainly of NeuAcα2-6GalNAc. Glycans from the gills were less acidic with predominantly core 1 and 2 glycans, whereas glycans from pyloric ceca and distal intestine expressed an increased number of core 5 glycans, distinctly decorated with NeuAcα2-8NeuAc- like epitopes. When compared to Atlantic salmon and Arctic charr, trends on the core distribution, average size and overall acidity remained similar, although the epitopes varied. Rainbow trout mucins from gill and intestine bound A. salmonicida and A. hydrophila more efficiently than skin mucins. This is in line with a model where skin mucins with small glycans limit bacterial adhesion to the fish surface whereas the complex intestinal mucin glycans aid in trapping and removing pathogens from the epithelial surface.

Developmental stages of the ballan wrasse from first feeding through metamorphosis: Cranial ossification and the digestive system.

We have described six developmental stages for the ballan wrasse, from the first feeding until the juvenile stage, supported by specific descriptions of cranial ossification, maturation of the digestive tract, and growth‐correlated stages. The initial formation and development of bones are closely linked to the functional anatomical structures required for the mechanics of its feeding behavior and ingestion, particularly the jaws and branchial regions involved in opening the mouth and capturing food particles. The overall ontogeny of the cranial structure compares to that of other teleosts. The cranial ossification of the ballan wrasse skull and the development of its dentary apparatus—first pharyngal teeth and later oral teeth—is linked to the development of the digestive system and to their feeding habits, from preying on zooplankton to feeding on crustaceans and invertebrates on rocks and other substrates. As ballan wrasse is a nibbler, eating small meals, the digestive tract is short compared to the length of the fish; there is no stomach or peptic digestion and also no distinctive bulbus and pyloric ceca. The liver and exocrine pancreas and their outlets terminating in the lumen of the most anterior part of the intestine are important in the digestive process and develop with a larger volume than that in gastric teleosts, relative to the digestive system.

Deploying an In Vitro Gut Model to Assay the Impact of the Mannan-Oligosaccharide Prebiotic Bio-Mos on the Atlantic Salmon (Salmo salar) Gut Microbiome.

ABSTRACTAlpha mannose-oligosaccharide (MOS) prebiotics are widely deployed in animal agriculture as immunomodulators as well as to enhance growth and gut health. Their mode of action is thought to be mediated through their impact on host microbial communities and their associated metabolism. Bio-Mos is a commercially available prebiotic currently used in the agri-feed industry, but studies show contrasting results of its effect on fish performance and feed efficiency. Thus, detailed studies are needed to investigate the effect of MOS supplements on the fish microbiome to enhance our understanding of the link between MOS and gut health. To assess Bio-Mos for potential use as a prebiotic growth promoter in salmonid aquaculture, we have modified an established Atlantic salmon in vitro gut model, SalmoSim, to evaluate its impact on the host microbial communities. The microbial communities obtained from ceca compartments from four adult farmed salmon were inoculated in biological triplicate reactors in SalmoSim. Prebiotic treatment was supplemented for 20 days, followed by a 6-day washout period. Inclusion of Bio-Mos in the media resulted in a significant increase in formate (P = 0.001), propionate (P = 0.037) and 3-methyl butanoic acid (P = 0.024) levels, correlated with increased abundances of several, principally, anaerobic microbial genera (Fusobacterium, Agarivorans, Pseudoalteromonas). DNA metabarcoding with the 16S rDNA marker confirmed a significant shift in microbial community composition in response to Bio-Mos supplementation with observed increase in lactic acid producing Carnobacterium. In conjunction with previous in vivo studies linking enhanced volatile fatty acid production alongside MOS supplementation to host growth and performance, our data suggest that Bio-Mos may be of value in salmonid production. Furthermore, our data highlights the potential role of in vitro gut models to complementin vivo trials of microbiome modulators.IMPORTANCE In this paper we report the results of the impact of a prebiotic (alpha-MOS supplementation) on microbial communities, using an in vitro simulator of the gut microbial environment of the Atlantic salmon. Our data suggest that Bio-Mos may be of value in salmonid production as it enhances volatile fatty acid production by the microbiota from salmon pyloric ceca and correlates with a significant shift in microbial community composition with observed increase in lactic acid producing Carnobacterium. In conjunction with previous in vivo studies linking enhanced volatile fatty acid production alongside MOS supplementation to host growth and performance, our data suggest that Bio-Mos may be of value in salmonid production. Furthermore, our data highlights the potential role of in vitro gut models to augment in vivo trials of microbiome modulators.

Atlantic Salmon Mucins Inhibit LuxS-Dependent A. Salmonicida AI-2 Quorum Sensing in an N-Acetylneuraminic Acid-Dependent Manner.

One of the most important bacterial diseases in salmonid aquaculture is furunculosis, caused by Aeromonas salmonicida. Bacterial communication through secreted autoinducer signals, quorum sensing, takes part in the regulation of gene expression in bacteria, influencing growth and virulence. The skin and mucosal surfaces, covered by a mucus layer, are the first point of contact between fish and bacteria. Mucins are highly glycosylated and are the main components of mucus. Here, we validate the Vibrio harveyi BB170 bioreporter assay for quantifying A. salmonicida quorum sensing and study the effects of Atlantic salmon mucins as well as mono- and disaccharides on the AI-2 levels of A. salmonicida. Atlantic salmon mucins from skin, pyloric ceca, proximal and distal intestine reduced A. salmonicida AI-2 levels. Among the saccharides abundant on mucins, fucose, N-acetylneuraminic acid and GlcNAcβ1-3Gal inhibited AI-2 A. salmonicida secretion. Removal of N-acetylneuraminic acid, which is the most abundant terminal residue on mucin glycans on Atlantic salmon mucins, attenuated the inhibitory effects on AI-2 levels of A. salmonicida. Deletion of A. salmonicida luxS abolished AI-2 production. In conclusion, Atlantic salmon mucins regulate A. salmonicida quorum sensing in a luxS and N-acetylneuraminic acid-dependent manner.

Macronutrients and essential amino acids on digestive process of the freshwater teleost Matrinxã

The objective of this work was to evaluate the effect of macronutrients and essential amino acids on digestive process of the freshwater teleost Matrinxã (Brycon amazonicus). Juveniles were fed with diets containing starch plus free amino acids or oil plus free amino acids for 15 days. These fish were compared with others fed with diets containing starch or oil without addition of free amino acids. After the experimental span, 12 fish from each treatment were randomly sampled to collect stomach, pyloric cecum, anterior and posterior intestine for assaying digestive enzymes activity. Increase of gastric proteolysis due to dietary amino acids were observed. Amylolytic, proteolytic and lipolytic activities in intestine sections were also positive related to dietary amino acids. However, proteolytic and lipolytic activities in pyloric cecum were not responsive to dietary changes. Moreover, the absence of starch in the diets resulted in decrease of amylolysis, and very low levels of oil did not change the lipolytic activity. In conclusion, activities of amylase, protease and lipase of Matrinxãare selectively responsive to addition of free essential amino acids concerning the gut section.

Molecular characterization of the aryl hydrocarbon receptor 2 gene in black rockfish, Sebastes schlegelii, and its expression patterns upon exposure to benzo[a]pyrene, 2,3,7,8-tetrachlorodibenzo-p-dioxin, and β-naphthoflavone.

The aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor that mediates the toxicity of halogenated and polycyclic aromatic hydrocarbons in vertebrates. Thus, increased knowledge of AhR-mediated responses to xenobiotics is imperative. Sebastes schlegelii is increasingly being used as a model for studying environmental toxicology; hence, in this study, the presence of AhR2 was evaluated in S. schlegelii. The results showed that the predicted AhR2 amino acid sequence contained regions characteristic of other vertebrate AhRs, including the basic helix-loop-helix and PER-ARNT-SIM domains in the N-terminal half, but it had minor similarity with other vertebrate AhRs across the C-terminal half; it did not contain the distinct glutamine-rich domains found in mammalian AhR2. Phylogenetic analysis demonstrated that S. schlegelii AhR2 was clustered within the teleost AhR2 branch. Additionally, AhR2 mRNA was detectable in all 11 tissues tested, with the highest mRNA levels in the heart, pyloric ceca, and liver. Furthermore, exposure to the AhR agonists showed that 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD, 1 μg/g body weight) induced a significantly higher increases in AhR2 expression in the gills, liver, kidneys, and spleen in 48 h than benzo[a]pyrene (2 μg/g body weight), and β-naphthoflavone (50-μg/g body weight); AhR2 mRNA levels upon TCDD exposure were up-regulated by 16- and 10-fold in the gills and liver, respectively. These findings indicated that AhR was a highly sensitive receptor against TCDD. Thus, investigating AhR2 expression in the presence of other xenobiotics might offer further information for the elucidation of its crucial role in mediating toxicant metabolism in S. schlegelii.

Practical Euthanasia Method for Common Sea Stars (Asterias rubens) That Allows for High-Quality RNA Sampling.

Simple SummarySea stars are iconic marine invertebrates and are important for maintaining the biodiversity in their ecosystems. As humans, we interact with sea stars when they are used as research animals or displayed at public or private aquaria. Molecular research requires fresh tissues that have thus far been considered to be of the best quality if collected without euthanasia. This is the first paper describing a method to euthanize sea stars that still allows for sampling of high-quality tissue that can be used for advanced research. Since it can be difficult to tell if an invertebrate has died, it is important to use a two-step method where the first step makes it non-responsive and the next step ensures it has died. Sea stars were placed in a solution of magnesium chloride until they no longer reacted to having their underside or oral surface tapped. Sea stars did not seemingly find the magnesium chloride solution unpleasant. After they were no longer reactive, the sea stars were immediately sampled. Tissue from their digestive glands was extracted and interpreted to be of adequate quality for molecular research techniques. This study promotes animal welfare while maintaining high-quality tissue sampling for molecular research.Sea stars in research are often lethally sampled without available methodology to render them insensible prior to sampling due to concerns over sufficient sample quality for applied molecular techniques. The objectives of this study were to describe an inexpensive and effective two-step euthanasia method for adult common sea stars (Asterias rubens) and to demonstrate that high-quality RNA samples for further use in downstream molecular analyses can be obtained from pyloric ceca of MgCl2-immersed sea stars. Adult common sea stars (n = 15) were immersed in a 75 g/L magnesium chloride solution until they were no longer reactive to having their oral surface tapped with forceps (mean: 4 min, range 2–7 min), left immersed for an additional minute, and then sampled with sharp scissors. RNA from pyloric ceca (n = 10) was isolated using a liquid–liquid method, then samples were treated with DNase and analyzed for evaluation of RNA integrity number (RIN) for assessment of the quantity and purity of intact RNA. Aversive reactions to magnesium chloride solution were not observed and no sea stars regained spontaneous movement or reacted to sampling. The calculated RIN ranged from 7.3–9.8, demonstrating that the combination of animal welfare via the use of anesthesia and sampling for advanced molecular techniques is possible using this low-cost technique.

Effects of Short-Term Fasting on mRNA Expression of Ghrelin and the Peptide Transporters PepT1 and 2 in Atlantic Salmon (Salmo salar).

Food intake is a vital process that supplies necessary energy and essential nutrients to the body. Information regarding luminal composition in the gastrointestinal tract (GIT) collected through mechanical and nutrient sensing mechanisms are generally conveyed, in both mammals and fish, to the hypothalamic neurocircuits. In this context, ghrelin, the only known hormone with an orexigenic action, and the intestinal peptide transporters 1 and 2, involved in absorption of dietary di- and tripeptides, exert important and also integrated roles for the nutrient uptake. Together, both are potentially involved in signaling pathways that control food intake originating from different segments of the GIT. However, little is known about the role of different paralogs and their response to fasting. Therefore, after 3 weeks of acclimatization, 12 Atlantic salmon (Salmo salar) post-smolt were fasted for 4 days to explore the gastrointestinal response in comparison with fed control (n = 12). The analysis covered morphometric (weight, length, condition factor, and wet content/weight fish %), molecular (gene expression variations), and correlation analyses. Such short-term fasting is a common and recommended practice used prior to any handling in commercial culture of the species. There were no statistical differences in length and weight but a significant lower condition factor in the fasted group. Transcriptional analysis along the gastrointestinal segments revealed a tendency of downregulation for both paralogous genes slc15a1a and slc15a1b and with significant lowered levels in the pyloric ceca for slc15a1a and in the pyloric ceca and midgut for slc15a1b. No differences were found for slc15a2a and slc15a2b (except a higher expression of the fasted group in the anterior midgut), supporting different roles for slc15 paralogs. This represents the first report on the effects of fasting on slc15a2 expressed in GIT in teleosts. Transcriptional analysis of ghrelin splicing variants (ghrl-1 and ghrl-2) showed no difference between treatments. However, correlation analysis showed that the mRNA expression for all genes (restricted to segment with the highest levels) were affected by the residual luminal content. Overall, the results show minimal effects of 4 days of induced fasting in Atlantic salmon, suggesting that more time is needed to initiate a large GIT response.

Maturation of the digestive system of Downs herring larvae (Clupea harengus, Linnaeus, 1758): identification of critical periods through ontogeny

Digestive system functionality is a key process linked to larval recruitment and survival. However, little is known about organ development and enzyme maturation of the digestive system of North Sea Atlantic herring (Clupea harengus). In this study, herring larvae were reared at 13 °C from hatching to 69 day post hatch, covering four developmental stages: (1) yolk sac (8–9 mm), (2) pre-flexion (9–14 mm), (3) flexion (12–18 mm) and (4) post-flexion stages (15–30 mm). Combined histological (semi-quantitative scoring) and enzyme analyses (pancreatic and intestinal) showed that developmental stages are strongly linked to physiological changes. The larvae lack a functional stomach and use the intestine as the primary site of digestion which is mainly supported by pancreatic enzyme activity. The intestine acquired adult enzymatic digestive features with a functional brush border at the end of the flexion stage and pyloric ceca started to develop during the post-flexion stage. The transition from pre-flexion to flexion stage and the end of the post-flexion stage are energetically taxing periods as indicated by a reduced number and size of liver vacuoles. Based on these findings, we consider these moments as critical periods, where herring larvae could be dramatically affected by suboptimal feeding conditions in the field. This implies that pre-flexion stage larvae with low or no liver reserves may not be able to proceed to the next developmental stage. Hence, the level of energy storage in first-feeding larvae needs to be examined for its use as a field indicator of survival and development.

The digestive system of mandarin fish (Siniperca chuatsi) can adapt to domestication by feeding with artificial diet

Mandarin fish (Siniperca chuatsi) is an economically important aquaculture species in China. Mandarin fish prefers to feed on live prey fish and can be domesticated by artificial diet. Artificial diet culture could realize large-scale aquaculture and minimize the ecological damage caused by catching bait fish. In this study, we analyzed morphological changes and gene expression profiles of the liver, stomach, and intestines after artificial diet feeding. The skin of the domesticated mandarin fish became darker. Remarkable morphological changes in the stomach, intestines, and pyloric cecum of mandarin fish were observed. The stomach and intestinal walls of the domesticated fish became thinner, the lumen became larger, and the muscle layer became thinner. The villi of the intestines became longer and had more branches. Compared with the mandarin fish fed with live prey fish (control group), the fish domesticated by artificial diet feeding had 4194, 2505, and 4579 differentially expressed genes (DEGs) in the liver, stomach, and intestines, respectively. These DEGs were most enriched in the signal pathways of protein processing in the endoplasmic reticulum and the PI3K-Akt signaling pathway. The most significantly upregulated genes were glucokinase, microfibril-associated glycoprotein 4, and amnion-associated transmembrane protein in the liver, stomach, and intestines. The most significantly downregulated genes were insulin-like growth factor-binding protein 1, MHC class II antigen alpha chain, and neuralized E3 ubiquitin protein ligase 3 in the liver, stomach, and intestines. Twelve categories of digestive enzymes were obtained from the DEGs, including lipase, trypsin, pepsin, cathepsin, nuclease, lysozyme, aminopeptidase, chitinase, elastase, chymotrypsin, maltase, and lactase. Most of these categories were sequenced for the first time. Results suggested that mandarin fish have a certain degree of adaptability to artificial diet feeding. Multigeneration screening must be performed to obtain strains that are easy to domesticate to achieve extensive artificial diet culture.

Comparative morphomolecular identification and pathological changes associated with Anisakis simplex larvae (Nematoda: Anisakidae) infecting native and imported chub mackerel (Scomber japonicus) in Egypt

Native and imported Scomber Japonicus were collected from Egypt and found to be infected with the third stage larvae (L3) of Anisakidae. The Anisakidae larvae were found encapsulated tightly coiled in the mesenteries associated with pyloric ceca and the serosal surface of visceral organs and/or uncoiled larvae free in the abdominal cavity of infected S. japonicus. The prevalence, mean intensity, and mean abundance of L3 were 80%, 24.4, and 19.5 in imported fish, and they were 36%, 7.36, and 2.65 in native fish, respectively. These larvae were identified as Anisakis simplex type 1 based on their morphological and molecular characteristics. The larvae were cylindrical in shape, and the oral openings had a prominent boring tooth. The esophago-intestinal junction (ventriculus) was oblique. The bodies of the larvae were covered with a transversely striated cuticle. The posterior end of the larvae had a short mucron or spine. Subsequently, phylogenetic analysis of the internal transcribed spacer region and COI gene of investigated larvae confirmed the identification of A. simplex when compared with relevant species sequences in GenBank. Histopathological examination revealed multiple A. simplex larvae in the abdominal cavity near the pyloric appendages, stomach, and under the visceral peritoneum, which appeared as a very thin and glistening capsule covering the larvae with a prominent adhesive fibrinous peritonitis together with mononuclear and eosinophilic granular cell infiltration. The importance of A. simplex infection in both native and imported S japonicus in Egypt is emphasized.

Morphohistology and histopathology of the digestive organs of the deep-water fish greater forkbeard, Phycis blennoides

Abstract The aim of this paper was to report on an examination of the digestive organs in the deep-water fish Phycis blennoides (Brünnich) from Algerian coastal waters. A total of 1,019 specimens (5.7–62.7 cm in total length) obtained from commercial fisheries were examined between December 2013 and May 2017. The anatomical study was conducted using morphometric measurements of different sections of the digestive tract of P. blennoides. The histological features of the digestive tract were examined in the esophagus, stomach, intestine, and pyloric cecum. They were compatible with carnivorous feeding behavior and confirmed by a low intestinal quotient (IQ = 0.72 ± 0.13). The histopathological assessment highlighted the hepatic steatosis and parasitic infestation in its intestine from Anisakis simplex, which also occurs in Algerian coastal waters. According to our knowledge, this paper reports for the first time the morphohistological analysis of the digestive tract of a Phycidae species in Africa and provides the first histopathological assessment of the digestive organs of the greater forkbeard in the southwestern Mediterranean Sea.