93 research outputs found
First feeding of Atlantic bluefin tuna (Thunnus thynnus) with copepods (Acartia tonsa) or rotifers /artemia - larval prey size preferences, growth, and development
The increase of dry weight, standard length and low incidence of skeletal anomalies clearly show that A. tonsa represents an optimal live food organism for tuna larvae
BONE DEVELOPMENT IN ATLANTIC BLUEFIN TUNA Thunnus thynnus AND SKELETAL EFFECTS OF FIRST FEEDING WITH COPEPODS Acartia tonsa OR ROTIFERS Brachionus ibericus
Juvenile production of Atlantic bluefin tuna (Thunnus thynnus) is characterized by high mortalities and low growth rates during the larval stage. Startfeeding of Bluefin tuna larvae in hatcheries depends on the traditional food organisms rotifers and Artemia nauplii (Biswas et al., 2006), and skeletal malformations have been observed in 70% of larvae and juveniles (Libert et al., 2013). When copepods are used as live food, the results are generally improved compared to the use of traditional live feed organisms (Evjemo et al., 2003), with higher survival, increased growth, normal development, earlier onset of ossification and less skeletal anomalies compared to larvae fed rotifers and Artemia (Imsland et al., 2006). The aims of this study were to describe the bone development in the Atlantic Bluefin tuna fed copepods, and to evaluate the effects of start-feeding with enriched rotifers or with cultivated copepods on skeletal deformities
Identification of the cathelicidin peptide LL-37 as agonist for the type I insulin-like growth factor receptor
The human cathelicidin antimicrobial protein-18 and its C terminal peptide, LL-37, displays broad antimicrobial activity that is mediated through direct contact with the microbial cell membrane. In addition, recent studies reveal that LL-37 is involved in diverse biological processes such as immunomodulation, apoptosis, angiogenesis and wound healing. An intriguing role for LL-37 in carcinogenesis is also beginning to emerge and the aim of this paper was to explore if and how LL-37 contributes to the signaling involved in tumor development. To this end, we investigated the putative interaction between LL-37 and growth factor receptors known to be involved in tumor growth and progression. Among several receptors tested, LL-37 bound with the highest affinity to insulin-like growth factor 1 receptor (IGF-1R), a receptor that is strongly linked to malignant cellular transformation. Furthermore, this interaction resulted in a dose-dependent phosphorylation and ubiquitination of IGF-1R, with downstream signaling confined to the mitogen-activated protein kinase/extracellular signal-regulated kinase (ERK)-pathway but not affecting phosphatidylinositol 3 kinase/Akt signaling. We found that signaling induced by LL-37 was dependent on the recruitment of β-arrestin to the fully functional IGF-1R and by using mutant receptors we demonstrated that LL-37 signaling is dependent on β-arrestin-1 binding to the C-terminus of IGF-1R. When analyzing the biological consequences of increased ERK activation induced by LL-37, we found that it resulted in enhanced migration and invasion of malignant cells in an IGF-1R/β-arrestin manner, but did not affect cell proliferation. These results indicate that LL-37 may act as a partial agonist for IGF-1R, with subsequent intra-cellular signaling activation driven by the binding of β-arrestin-1 to the IGF-1R. Functional experiments show that LL-37-dependent activation of the IGF-1R signaling resulted in increased migratory and invasive potential of malignant cells
Lack of Chemokine Signaling through CXCR5 Causes Increased Mortality, Ventricular Dilatation and Deranged Matrix during Cardiac Pressure Overload
RATIONALE: Inflammatory mechanisms have been suggested to play a role in the development of heart failure (HF), but a role for chemokines is largely unknown. Based on their role in inflammation and matrix remodeling in other tissues, we hypothesized that CXCL13 and CXCR5 could be involved in cardiac remodeling during HF. OBJECTIVE: We sought to analyze the role of the chemokine CXCL13 and its receptor CXCR5 in cardiac pathophysiology leading to HF. METHODS AND RESULTS: Mice harboring a systemic knockout of the CXCR5 (CXCR5(-/-)) displayed increased mortality during a follow-up of 80 days after aortic banding (AB). Following three weeks of AB, CXCR5(-/-) developed significant left ventricular (LV) dilatation compared to wild type (WT) mice. Microarray analysis revealed altered expression of several small leucine-rich proteoglycans (SLRPs) that bind to collagen and modulate fibril assembly. Protein levels of fibromodulin, decorin and lumican (all SLRPs) were significantly reduced in AB CXCR5(-/-) compared to AB WT mice. Electron microscopy revealed loosely packed extracellular matrix with individual collagen fibers and small networks of proteoglycans in AB CXCR5(-/-) mice. Addition of CXCL13 to cultured cardiac fibroblasts enhanced the expression of SLRPs. In patients with HF, we observed increased myocardial levels of CXCR5 and SLRPs, which was reversed following LV assist device treatment. CONCLUSIONS: Lack of CXCR5 leads to LV dilatation and increased mortality during pressure overload, possibly via lack of an increase in SLRPs. This study demonstrates a critical role of the chemokine CXCL13 and CXCR5 in survival and maintaining of cardiac structure upon pressure overload, by regulating proteoglycans essential for correct collagen assembly
The impact of DO and salinity on microbial community in poly(butylene succinate) denitrification reactors for recirculating aquaculture system wastewater treatment
Chapitre 14: Phytopathogènes et stratégies de contrôle en aquaponie
peer reviewedAmong the diversity of plant diseases occurring in aquaponics, soil-borne
pathogens, such as Fusarium spp., Phytophthora spp. and Pythium spp., are the most
problematic due to their preference for humid/aquatic environment conditions.
Phytophthora spp. and Pythium spp. which belong to the Oomycetes pseudo-fungi
require special attention because of their mobile form of dispersion, the so-called
zoospores that can move freely and actively in liquid water. In coupled aquaponics,
curative methods are still limited because of the possible toxicity of pesticides and
chemical agents for fish and beneficial bacteria (e.g. nitrifying bacteria of the
biofilter). Furthermore, the development of biocontrol agents for aquaponic use is
still at its beginning. Consequently, ways to control the initial infection and the
progression of a disease are mainly based on preventive actions and water physical
treatments. However, suppressive action (suppression) could happen in aquaponic
environment considering recent papers and the suppressive activity already
highlighted in hydroponics. In addition, aquaponic water contains organic matter
that could promote establishment and growth of heterotrophic bacteria in the system
or even improve plant growth and viability directly. With regards to organic
hydroponics (i.e. use of organic fertilisation and organic plant media), these bacteria
could act as antagonist agents or as plant defence elicitors to protect plants from
diseases. In the future, research on the disease suppressive ability of the aquaponic
biotope must be increased, as well as isolation, characterisation and formulation of
microbial plant pathogen antagonists. Finally, a good knowledge in the rapid
identification of pathogens, combined with control methods and diseases monitoring,
as recommended in integrated plant pest management, is the key to an efficient
control of plant diseases in aquaponics.Cos
Fixation of catecholamine-containing tissues for histochemical demonstration of catecholamines and for radioautography of steroid hormones in the same sections
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