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iparous and multiparous postpartum cows, highlighting the importance of oxidative stress profiles in the assessment of metabolic health status during transition.
Veterinary health care is an emergent area in animal sciences and innovative therapeutic approaches happen to be imperative in the present days. In view of the importance of cattle health and production, it is necessary to take up contemporary approach of stem cell therapy in this sector also. This study aimed to standardize an explant culture method of bovine umbilical tissue offcut to isolate mesenchymal stem cells (MSCs) because considerable efforts are required for ensuring easy accessibility and availability of MSCs in bulk quantity, as well as in establishing and characterizing the cell lines.
The umbilical cord (UC) tissue matrix offcut was collected after calving. A simplified
cell isolation technique was followed to collect the emerged out cells from the explants of UC. Further, we expanded these isolated cells
, observed its growth kinetics, and characterized to confirm as per the criterion of bovine MSCs.
A considerable exponential growth rate of the UC-derived cells was noticed. In addition to their confirmation as MSCs, the cells also exhibited plastic adherent property and maintained the spindle-shaped morphology throughout the
culture. The cultured cells were found positive MSC-specific surface markers CD105, CD90, and CD73 and were negative for hematopoietic cell marker CD45. Cytochemical studies revealed the ability of the cells to differentiate into osteogenic, chondrogenic, and adipogenic lineages.
This simplified method of isolation and culture of bovine multipotent MSCs from the UC offcut collected after calving could be extrapolated for the greater availability of the cells for prospective therapeutic applications.
This simplified method of isolation and culture of bovine multipotent MSCs from the UC offcut collected after calving could be extrapolated for the greater availability of the cells for prospective therapeutic applications.
The amino acid content of feed can affect growth performance of poultry during the first 6 weeks of life or the starter phase. Unlike for broiler and layer chickens, there is no information concerning standard requirements for tryptophan and threonine during the starter phase. This study aimed to determine the amount of threonine and tryptophan that should be supplemented in chicken feed to maximize growth performance and small intestinal morphology of native chickens during the starter phase.
A total of 128 day-old native chickens were divided into four treatment groups with four replications based on a completely randomized design. The treatment diets were as follows T
(control feed); T
(T
+0.10% L-tryptophan+0.35% L-threonine); T
(T
+0.17% L-tryptophan+0.68% L-threonine); and T
(T
+0.25% L-tryptophan+1.00% L-threonine).
The feed intake was highest for the T
and T
groups (123.06 and 124.18 g/bird/week, respectively). The T
group had the highest body weight gain (49.35 g/bird/week) and carcass weight (201.44 g/bird) relative to the other groups, while the T
and T
groups showed similar, significant (p<0.05) increases in feed conversion ratio (2.57 and 2.51, respectively) and carcass percentage (60.88 and 60.99%/bird, respectively) compared to the other groups. This study showed villi height, crypt depth, and villi width of duodenum, the highest jejunum and ileum of T3 (1109.00±27.26, 1325.50±75.00, 1229.50±101.68, 225.50±17.52, 236.00±24.81, 219.75±17.25, 192.25±14.41, 191.75±4.79, and 184.75±6.40, respectively) compare to other treatment.
These results indicate that supplementation of feed with 0.17% L-tryptophan and 0.68% L-threonine positively affected the growth performance and small intestinal morphology of native chickens during the starter phase.
These results indicate that supplementation of feed with 0.17% L-tryptophan and 0.68% L-threonine positively affected the growth performance and small intestinal morphology of native chickens during the starter phase.
Saprolegniasis is a fungal disease that infects freshwater fish. The condition is characterized by a cotton-like appearance in the gills and body. This study aimed to isolate
from common carp,
, raised in a floating cage in Wana district, Mosul, Iraq.
Samples were collected from 15 infected fish and examined microbiologically, molecularly, and histopathologically.
DNA was extracted which was amplified using universal primers give a 540 bp DNA fragment, and gill and muscle tissue were also examined for histopathological changes.
Isolated colonies of
were characterized by a circular, white cottony appearance with long hair. Lactophenol staining demonstrated hyphae as branched non-septate, transparent masses. The genomic DNA of isolates was consistent with
spp. The infected tissue samples showed variable pathology in gills. Severe hemorrhage and edema were observed in primary gill filaments with hyperplasia in epithelial cells and infusion in secondary gill filaments. Hyphae of
were seen between necrotic and edematous myofiber with inflammatory cells infiltration.
can cause economic impacts through lethal infection of fish. Clinical signs of
infection were confirmed molecularly and microscopically, and these findings were supported by histopathological lesions in gill and muscle tissues.
Saprolegnia can cause economic impacts through lethal infection of fish. Clinical signs of Saprolegnia infection were confirmed molecularly and microscopically, and these findings were supported by histopathological lesions in gill and muscle tissues.
The present study was conducted to record the prevalence of multidrug-resistant (MDR), extended-spectrum β-lactamases (ESBLs) producing
from pig population of organized and unorganized farms of Mizoram and to record the presence of ESBLs, non-ESBLs, and integrons.
Fecal samples were collected from pigs under organized (n=40) and unorganized (n=58) farms of Mizoram. Samples were processed for isolation and identification of
by conventional techniques, BD Phoenix™ automated bacterial system, and polymerase chain reaction (PCR) based confirmatory test. All the isolates were subjected to antimicrobial sensitivity test by disk diffusion assay and ESBLs production by double-disk synergy test (DDST). The ESBLs producing isolates were subjected to PCR for determination of ESBLs genes and all the isolates were screened for non-ESBLs genes and integrons by PCR.
A total of 258
was isolated and identified from organized (n=120) and unorganized farms (n=138). https://www.selleckchem.com/products/Triciribine.html Majority of the
isolates exhibited high level of resistance against amoxicillin (Ax) (81.
My Website: https://www.selleckchem.com/products/Triciribine.html
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