The aim of this study was to examine if synbiotics can function as alternatives to antibiotics in broiler production under heat stress (HS). Day-old broiler chicks (528 birds) were randomly placed in floor pens within 2 identical temperature-controlled rooms (11 birds/pen and 24 pens/room). The pens of each room were evenly divided among 3 treatments (n = 8): basal diet (CON), the basal diet mixed with 50 ppm of bacitracin methylene disalicylate (BMD) or a synbiotic (50 ppm of PoultryStar me^US, SYN). From d 15, room 2 was under thermoneutral (TN) conditions (TN-CON, TN-BMD, and TN-SYN), while HS was applied to room 1 at 32^oC for 9 hrs/d (0800 to 1700) (HS-CON, HS-BMD, and HS-SYN). Treatment effects on footpad dermatitis and gait score were measured on 5 birds/pen, and latency to lie (LTL) test was measured on 2 birds/pen at d 27 and d 41; and 1 broiler/pen was sampled on d 28 and d 42, respectively. Body, liver, and spleen weight were determined. Plasma levels of interleukins (IL), heat shock protein 70, immunoglobulin (Ig)Y, liver superoxide dismutase (SOD) and glutathione peroxidase (GPx) enzyme activities were examined. Heat stress suppressed BW and IgY concentrations on both d 28 and d 42, while suppressed plasma IL-6 concentrations, SOD activities, and LTL duration on d 28 only (P < 0.05). Among all treatments, SYN birds had the best foot and skeletal health scores on both d 27 and d 41 (P < 0.05). On d 42, SYN increased BW, and TN-SYN birds had higher relative spleen weight than both TN-BMD and TN-CON birds (P < 0.05). Antibiotic BMD increased BW (P < 0.05) but decreased SOD activities (P < 0.05) on d 42. These results indicate that the SYN supplementation decreases HS negative effect on broilers by improving BW, foot, and skeletal health, while BMD improves BW but also increases oxidative stress in broilers. The data suggest that synbiotic supplement may function as an alternative to antibiotics in broiler production during summer seasons, especially in the tropical and subtropical regions.

The LC-MS-based method has emerged as the preferred approach for quantifying food allergens. However, the preparation of a traditional calibration curve (MSCC) is labor-intensive and error-prone. Here, a sensitive and robust LC-MS/MS method for quantifying 10 major food allergens was developed and validated, where the one-sample multipoint external calibration curve (OSCC) was employed instead of MSCC. By employing the multiple isotopologue reaction monitoring (MIRM) technique with only one spiked level in the blank, OSCC can be effectively established. Results demonstrate that the proposed method exhibits excellent performance in selectivity, sensitivity, accuracy, and precision, comparable to that of the traditional MSCC. Additionally, this strategy allows for isotope sample dilution by monitoring the less abundant MIRM channel. Moreover, the developed method was successfully applied to investigate the contamination of 10 food allergens in commercial food products. With its high throughput and robustness, the MIRM-OSCC-LC-MS/MS methodology has many potential applications, especially in the MS-based protein quantification analysis.

Microcystin-LR (MC-LR) is a hepatotoxic metabolite that naturally occurs during some cyanobacterial blooms in eutrophic waterbodies, and irrigation of edible plants with MC-LR-contaminated water causes bioaccumulation of the toxin. However, sufficient information about accumulation and depuration mechanics in hydroculture-grown herb plants is still lacking. This work aimed at 1) investigating bioaccumulation and depuration of MC-LR in basil, 2) verifying the possible MC-LR detoxification mechanisms in the plant, and 3) detecting the natural occurrence of MC-LR in basil (n = 50) collected from the Belgian market. Basil plants grown in a hydroculture were exposed to MC-LR (5, 20, and 50 μg L⁻¹) spiked in a Hoagland solution for seven days. MC-LR depuration was also studied by transferring the plants to a non-contaminated Hoagland solution after exposure to MC-LR for another seven days. MC-LR concentrations in Hoagland solution, basil leaves, and roots were quantified using a validated UHPLC–MS/MS method. In addition, ELISA and LC–HRMS (only basil leaves) were used for confirmation. The results showed an increase in the accumulated levels of MC-LR at higher exposure doses, with higher MC-LR levels in roots than in leaves for all the treatment conditions. For MC-LR depuration, significant reductions were observed in all the treatment conditions for roots only. No MC-LR conjugates, potentially related to metabolism, were detected by LC–HRMS. Finally, MC-LR was detected in one store-bought basil sample, representing the first occurrence of cyanotoxins in an edible crop from Belgium.

The pseudobranch is a gill-like structure that exhibits great variations in structure and function among fish species, and therefore, it has remained a topic of investigation for a long time. This study was conducted on adult Molly fish (Poecilia sphenops) to investigate the potential functions of their pseudobranch using histological, histochemical, immunohistochemical analysis, and scanning electron microscopy. The pseudobranch of Molly fish was of embedded type. It comprised many rows of parallel lamellae that were fused completely throughout their length by a thin connective tissue. These lamellae consisted of a central blood capillary, surrounded by large secretory pseudobranch cells (PSCs). Immunohistochemical analysis revealed the expression of PSCs for CD3, CD45, iNOS-2, and NF-κB, confirming their role in immunity. Furthermore, T-lymphocytes-positive CD3, leucocytes-positive CD45, and dendritic …

The adrenal gland is a vital endocrine gland that secretes many important hormones
in everyday bird life. The adrenal gland of the Japanese quail is grossly located ventromedially
the corresponding kidney and has a creamy to yellow color. The quail
gland is surrounded by a capsule and contains some ganglionic cells, and the capsule
is characterized by the presence of chromaffin cells. The adrenal gland is subdivided
into three concentric zones: subcapsular, peripheral, and central. The parenchyma
consists of interrenal tissue, chromaffin islets, and blood sinusoids. The interrenal
cells contain lipid droplets, are arranged in cords, and rest on the basement membrane.
Chromaffin cells are categorized as two types: epinephrine (E) and norepinephrine
(NE) cells. These cells contain the granules, and are characterized by the
presence of lipid droplets. In this study, the interrenal tissue was found to have a
higher proportion of chromaffin cells in quail as compared with other birds, which is
attributed to the fact that the Japanese quail is a migratory bird. Therefore, the present
investigation aims to provide a detailed study on the adrenal gland in the Japanese
quail to help physiologists understand the gland's function and the pathologist
to determine the implications for the differential diagnosis of adrenal gland tumors.

The retina consists of various cell types arranged in eight cell layers and two membranes
that originate from the neuroectodermal cells. In this study, the timing of differentiation
and distribution of the cellular components and the layers of the rabbit
retina are investigated using light and electron microscopy and immunohistochemical
techniques. There were 32 rabbit embryos and 12 rabbits used. The rabbit retina
begins its prenatal development on the 10th day of gestation in the form of optic
cup. The process of neuro- and gliogenesis occurs in several stages: In the first stage,
the ganglionic cells are differentiated at the 15th day. The second stage includes the
differentiation of Muller, amacrine, and cone cells on the 23rd day. The differentiation
of bipolar, horizontal, and rod cells and formation of the inner segments of the
photoreceptors consider the late stage that occurs by the 27th and 30th day of gestation.
On the first week of age postnatally, the outer segments of the photoreceptors
are developed. S100 protein is expressed by the Muller cells and its processes
that traverse the retina from the outer to the inner limiting membranes. Calretinin is
intensely labeled within the amacrine and displaced amacrine cells. Ganglionic cells
exhibited moderate immunoreactivity for calretinin confined to their cytoplasm and
dendrites. In conclusion, all stages of neuro- and gliogenesis of the rabbit retina occur
during the embryonic period. Then, the retina continues its development postnatally
by formation of the photoreceptor outer segments and all layers of the retina
become established.

The development of the cornea is a fascinating process. Its dual origin involves the
differentiation of surface ectoderm cells and the migration of mesenchymal cells of
neural crest origin. This research aimed to demonstrate the morphogenesis of the
rabbit cornea from fetal to postnatal life using light- and electron microscopy, and
immunohistochemical analysis. There were 27 rabbit embryos and nine rabbits used.
The rabbit cornea begins its prenatal development on the twelfth day of gestation.
The surface ectoderm differentiates into the corneal epithelium on day 13. Intriguingly,
telocytes were visible within the epithelium. The secondary stroma develops
on the sixteenth day of gestation by differentiation of keratocytes. At the age of
2 weeks, the lamellae of collagenous fibers become highly organized, and the stroma
becomes avascular, indicating that the cornea has become transparent. Bowman's
membrane appears on day 23 of pregnancy and disappears on day 30. The Descemet's
membrane appears at this time and continues to thicken postnatally. The corneal
endothelium appears on the twentieth gestational day as double layer of
flattened cells and becomes a single layer of cuboidal cells on day 30. The spaces
between the endothelial cells resemble craters. VEGF immunohistochemical expression
increases over the course of development, reaching its peak in the first week
after birth before decreasing in all corneal layers and becoming negative in the
stroma. In conclusion, numerous morphogenetic events contribute to corneal maturation
and transparency, allowing the cornea to perform its vital functions.