2018
DOI: 10.1016/j.fsi.2018.01.023
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Expression and functional characterization of transferrin in Nile tilapia (Oreochromis niloticus) in response to bacterial infection

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Cited by 54 publications
(26 citation statements)
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“…Transferrin is an iron-binding glycoprotein involved in the transport and storage of iron, it participates in the regulation of breathing, cell proliferation and differentiation, and also plays an important role in host defence against pathogenic infection, not only because it inhibits the growth and proliferation of pathogens, but it also activates anti-microbial responses in macrophages [72]. Similarly, the expression of transferrin was significantly up-regulated in other fish species exposed to bacterial [73] and parasitic [74] pathogens, in the latter case also in gills. The higher expression of transferrin in P gills could correlate with a higher need of iron to transport the low oxygen available or alternatively it could be an effort to increase iron storage to deprive its availability for the parasite.…”
Section: Discussionmentioning
confidence: 99%
“…Transferrin is an iron-binding glycoprotein involved in the transport and storage of iron, it participates in the regulation of breathing, cell proliferation and differentiation, and also plays an important role in host defence against pathogenic infection, not only because it inhibits the growth and proliferation of pathogens, but it also activates anti-microbial responses in macrophages [72]. Similarly, the expression of transferrin was significantly up-regulated in other fish species exposed to bacterial [73] and parasitic [74] pathogens, in the latter case also in gills. The higher expression of transferrin in P gills could correlate with a higher need of iron to transport the low oxygen available or alternatively it could be an effort to increase iron storage to deprive its availability for the parasite.…”
Section: Discussionmentioning
confidence: 99%
“…Nile tilapia, about 80 ± 10 g (for challenge experiment) and 300 ± 20 g (for cell separation) were procured from the Guangdong Tilapia Breeding Farm (Guangzhou, China), which were cultured as previously described ( 28 , 31 ). The Balb/c female mice for the preparation of polyclonal antibody (pAb) were purchased from Guangdong Medical Laboratory Animal Center (Guangzhou, China).…”
Section: Methodsmentioning
confidence: 99%
“…To characterize the tissue distribution of OnMAp34 , the samples from healthy O. niloticus were collected, including liver, head kidney, hind kidney, spleen, skin, gills, peripheral blood, thymus, muscle, and intestine. To explore the variation of OnMAp34 after bacterial challenges, the experimental fish were intraperitoneally injected with 0.1 mL live S. agalactiae (ZQ0910, 1 × 10 7 CFU/mL) or A. hydrophila (BYK00810, 1 × 10 7 CFU/mL) ( 28 , 31 ). The control group was stimulated with 0.1 mL sterilized phosphate-buffered saline (PBS, 10 mM phosphate, 150 mM NaCl, pH 7.4) per fish.…”
Section: Methodsmentioning
confidence: 99%
“…The cells were cultured in 96‐well plate (Corning, USA; 100 μl/well) with the final concentration of 1 × 10 6 cells/ml per well and then stimulated with poly (I:C) (50 μg/ml), S. agalactiae (1 × 10 7 CFU/ml) (Mu et al, ; Wang, Seymour, Sundberg, & Hogenesch, ) and A. hydrophila (1 × 10 7 CFU/ml) at 25℃. Bacteria of S. agalactiae and A. hydrophila (Tang et al, ; Yin et al, ) were cultured and inactivated and control group with the equal volume of 1 × PBS as same as our previous study. Preparation and application of bacteria were the same as laboratory methods (Mu et al, ).…”
Section: Methodsmentioning
confidence: 99%
“…agalactiae (1 × 10 7 CFU/ml) (Mu et al, 2017; and A. hydrophila (1 × 10 7 CFU/ml) at 25℃. Bacteria of S. agalactiae and A. hydrophila (Tang et al, 2014;Yin et al, 2018) were cultured and inactivated and control group with the equal volume of 1 × PBS as same as our previous study. Preparation and application of bacteria were the same as laboratory methods .…”
Section: Primersmentioning
confidence: 99%