References of "Baise, Etienne"
     in
Bookmark and Share    
Full Text
Peer Reviewed
See detailMolecular cloning and characterisation of the CD18 partner in ovine (Ovis aries) beta(2)-integrins
Zecchinon, Laurent ULg; Fett, Thomas ULg; Baise, Etienne ULg et al

in Gene (2004), 334

The leukocyte integrins play a critical role in a number of cellular adhesive interactions during the immune response. We describe here the isolation and characterization of the ovine beta(2) (CD18 ... [more ▼]

The leukocyte integrins play a critical role in a number of cellular adhesive interactions during the immune response. We describe here the isolation and characterization of the ovine beta(2) (CD18) subunit, common to the leukocyte beta(2)-integrin family. The deduced 770-amino-acid sequence reveals a transmembrane protein with 81%, 83% and 95% identity with its murine, human and bovine homologues, respectively. Comparisons of CD18 sequences emphasize the functional importance of the beta(2) subunit I-like domain and included metal ion-dependent adhesion site (MIDAS)-like motif and confirm that of the cytoplasmic tail. The data provided here will offer the possibility to explore new avenues in studies based on the ovine model. (C) 2004 Elsevier B.V. All rights reserved. [less ▲]

Detailed reference viewed: 11 (3 ULg)
Full Text
Peer Reviewed
See detailThe bovine (Bos taurus) CD11a-encoding cDNA: molecular cloning, characterisation and comparison with the human and murine glycoproteins
Fett, Thomas ULg; Zecchinon, Laurent ULg; Baise, Etienne ULg et al

in Gene (2004), 325

The bovine cDNA encoding CD11 a cell-surface glycoprotein involved in multiple leukocyte functions, was sequenced and compared with the human and murine sequences. Despite some focal differences, it ... [more ▼]

The bovine cDNA encoding CD11 a cell-surface glycoprotein involved in multiple leukocyte functions, was sequenced and compared with the human and murine sequences. Despite some focal differences, it shares all the main characteristics of its known mammalian homologs. Along with the bovine CD18-encoding cDNA, which is available for a long time, the sequence data provided here will allow the successful expression of bovine CD11a, thus giving the first opportunity to express the Bos taurus beta(2)-integrin CD11a/CD18 (LFA-1, alpha(L)beta(2)) in vitro as a tool to examine the specificities of inflammation in the bovine species. (C) 2003 Elsevier B.V. All rights reserved. [less ▲]

Detailed reference viewed: 29 (3 ULg)
Full Text
Peer Reviewed
See detailCharacterization of the caprine (Capra hircus) beta-2 integrin CD18-encoding cDNA and identification of mutations potentially responsible for the ruminant-specific virulence of Mannheimia haemolytica
Zecchinon, Laurent ULg; Fett, Thomas ULg; Baise, Etienne ULg et al

in Molecular Membrane Biology (2004), 21(5, Sep-Oct), 289-295

The leukocyte integrins play a critical role in a great number of cellular adhesive interactions during the immune response. We describe here the isolation and characterization of the caprine beta(2 ... [more ▼]

The leukocyte integrins play a critical role in a great number of cellular adhesive interactions during the immune response. We describe here the isolation and characterization of the caprine beta(2) (CD18) sub-unit, common to the leukocyte beta(2)-integrin family. The deduced 770-amino-acid sequence reveals a transmembrane protein with 80, 81, 83, 96 and 99% identity with its canine, murine, human, bovine and ovine homologues respectively. Analysis of CD18 sequences emphasizes the functional importance of the beta(2) sub-unit I-like domain, and included metal ion-dependent adhesion site-like motif and confirms that of the cytoplasmic tail. Moreover, comparisons of ruminant versus non-ruminant CD18 sequences allowed the identification of 16 potential mutation sites that could be held responsible for the unique virulence of Mannheimia haemolytica for ruminants. Mannheimiosis is known to be the major respiratory disease among ruminants, whereas it is not pathogenic for other mammals, an observation that has been attributed to a specific interaction between M. haemolytica leukotoxin and ruminants' CD18. Therefore, the data provided here offer the possibility to explore new avenues in studies based on the caprine model and provide key information for future studies aimed at elucidating the molecular mechanisms underlying the ruminant-specific virulence of M. haemolytica. [less ▲]

Detailed reference viewed: 17 (1 ULg)
Full Text
Peer Reviewed
See detailConditional expression of type I interferon-induced bovine Mx1 GTPase in a stable transgenic vero cell line interferes with replication of vesicular stomatitis virus
Baise, Etienne ULg; Pire, Grégory; Leroy, Michael et al

in Journal of Interferon & Cytokine Research (2004), 24(9), 513-521

In some vertebrate species, type I interferon(IFN)-induced Mx gene expression has been shown to confer resistance to some single-stranded RNA (ssRNA) viruses in vitro. Because the bovine species is ... [more ▼]

In some vertebrate species, type I interferon(IFN)-induced Mx gene expression has been shown to confer resistance to some single-stranded RNA (ssRNA) viruses in vitro. Because the bovine species is subject to an exceptionally wide array of infections caused by such viruses, it is anticipated that an antiviral allele should have been retained by evolution at the bovine Mx locus. The identification of such allele may help in evaluating the real significance of the Mx genotype for disease resistance in vivo, in deciphering host-virus molecular interactions involved, or in improving innate disease resistance of livestock through marker-assisted selection. We validated a double transgenic Vero cell clone in which the bovine Mx1 reference allele is placed under control of the human cytomegalovirus (CMV) enhancer-promoter sequence containing elements from the bacterial tetracycline resistance operon to regulate transcription. In the selected clone, transgene repression was very tight, and derepression by doxycycline led to homogeneous 48-h duration expression of physiologic levels of bovine Mx1. Expression of the transgene caused a dramatic decrease in cytopathic efficiency and a 500-5000-fold yield reduction of the Indiana and New Jersey serotypes of vesicular stomatitis virus (VSV). To our knowledge, the transgenic clone developed here is the first ever reported that allows conditional expression of an Mx protein, thus providing a valuable tool for studying functions of Mx proteins in general and that of bovine Mx1 in particular. This latter may henceforward be included in the group of Mx proteins with authenticated anti-VSV activity, which offers new research avenues into the field of host-virus interactions. [less ▲]

Detailed reference viewed: 43 (14 ULg)
Full Text
Peer Reviewed
See detailGenomic structure, organisation, and promoter analysis of the bovine (Bos taurus) Mx1 gene
Gérardin; Baise, Etienne ULg; Pire, Grégory et al

in Gene (2004), 326

Some MX proteins are known to confer a specific resistance against a panel of single-stranded RNA viruses. Many diseases due to such viruses are known to affect cattle worldwide, raising the possibility ... [more ▼]

Some MX proteins are known to confer a specific resistance against a panel of single-stranded RNA viruses. Many diseases due to such viruses are known to affect cattle worldwide, raising the possibility that the identification of an antiviral isoform of a bovine MX protein would allow the implementation of genetic selection programs aimed at improving innate resistance of cattle. With this potential application in mind, the present study was designed to isolate the bovine Mx1 gene including its promoter region and to investigate its genomic organisation and promoter reactivity. The bovine Mx1 gene is made up of 15 exons. All exon-intron boundaries conformed to the consensus sequences. A PCR product that contained a approximately 1-kb, 5'-flanking region upstream from the putative transcription start site was sequenced. Unexpectedly, this DNA region did not contain TATA or CCAAT motifs. A computer scan of the region disclosed a series of putative binding sites for known cytokines and transcription factors. There was a GAAAN(1-2)GAAA(C/G) motif, typical of an interferon-sensitive responsive element, between -118 and -107 from the putative transcription start site. There were also a NF-kappaB, two interleukin-6 binding sites, two Sp1 sites and five GC-rich boxes. The region also contained 12 stretches of the GAAA type, as described in all IFN-inducible genes. Bovine Mx1 expression was assessed by Northern blotting and immunofluorescence in the Madin Darby bovine kidney cells (MDBK) cell line treated with several stimuli. In conclusion, the bovine Mx1 gene and promoter region share the major structural and functional characteristics displayed by their homologs described in the rainbow trout, chicken, mouse and man. [less ▲]

Detailed reference viewed: 28 (1 ULg)
Full Text
See detailLa myopathie atypique des équidés: particularités cliniques, examens complémentaires et hypothèses étiologiques.
Votion, Dominique ULg; Delguste, Catherine ULg; Amory, Hélène ULg et al

in Journée AVEF (Association des Vétérinaires Equins Français) (2003, October)

La myopathie atypique (MA) des équidés, encore appelée myoglobinurie atypique des chevaux au pré, est un syndrome caractérisé par l’apparition soudaine de faiblesse musculaire, de raideur, de tremblements ... [more ▼]

La myopathie atypique (MA) des équidés, encore appelée myoglobinurie atypique des chevaux au pré, est un syndrome caractérisé par l’apparition soudaine de faiblesse musculaire, de raideur, de tremblements et de sudation profuse généralisée ou localisée. L’animal adopte rapidement une position en décubitus sternal ou latéral. Lorsque de l’urine est émise, celle-ci a une couleur brune « chocolatée ». L’examen clinique révèle fréquemment de la tachycardie, de l’hypothermie et de la dyspnée. Le dosage de l’activité sérique de la créatinine kinase contribue à la présomption de MA en démontrant une destruction musculaire massive mais le diagnostic définitif repose nécessairement sur l’examen histologique des muscles intervenant dans la posture et la respiration, muscles généralement atteints lors de cette maladie ainsi que sur l’examen du muscle cardiaque où des lésions de dégénérescence sont occasionnellement observées. Diverses hypothèses étiologiques sont en cours d’investigation et les plus probables incriminent l’action d’une mycotoxine ou d’une toxine d’origine bactérienne, ingérée ou produite dans le tractus digestif. Néanmoins, une carence nutritionnelle n’est pas exclue. Quelle que soit la cause, il semble que des conditions climatiques défavorables favorisent le déclenchement des symptômes. La récolte de données épidémiologiques permettra de mieux définir les moyens de prévention de cette maladie souvent fatale. [less ▲]

Detailed reference viewed: 74 (7 ULg)
Full Text
Peer Reviewed
See detailDiagnostic différentiel en cas de présomption de myopathie atypique des équidés : illustration au travers de cas référés à la Faculté de Médecine Vétérinaire de l’Université de Liège au cours du printemps 2003
Votion, Dominique ULg; Delguste, Catherine ULg; Baise, Etienne ULg et al

in Annales de Médecine Vétérinaire (2003), 147

Atypical myopathy is a frequently fatal disease inducing extensive and severe muscular damage, occurring during autumn and spring in grazing horses. The main features of the syndrome are the sudden onset ... [more ▼]

Atypical myopathy is a frequently fatal disease inducing extensive and severe muscular damage, occurring during autumn and spring in grazing horses. The main features of the syndrome are the sudden onset of non pathognomonic symptoms such as weakness, stiffness, sudation, recumbency and when observed, emission of dark urine. Confirmation of the diagnosis is of paramount importance since the disease can be recurrent on limited geographic area. This paper discusses the methodology applied on 7 clinical cases referred with a symptomatology suggestive of atypical myopathy to the Faculty of Veterinary Medicine at Liege University during the spring 2003. Two of those cases were confirmed for atypical myopathy. A presumption of atypical myopathy may be drawn on history and clinical signs. On living animals, the serum concentration of the creatinine phosphokinase enzyme is the most useful biochemical tests as an aid to diagnosis because it confirms the presence of muscle damage. Nevertheless, the definitive diagnosis requires the histological examination of specific muscular samples obtained post-mortem. [less ▲]

Detailed reference viewed: 183 (19 ULg)
Full Text
Peer Reviewed
See detailMyopathies atypiques chez les chevaux au pré: une série de cas en Belgique
Delguste, Catherine ULg; Cassart, Dominique ULg; Baise, Etienne ULg et al

in Annales de Médecine Vétérinaire (2002), 146(4, AUG-SEP), 235-247

Atypical myoglobinuria in grazing horses was described in United Kingdom and Germany between 1984 and 1996. Fourteen horses were presented at the University of Liege between November 2000 and April 2001 ... [more ▼]

Atypical myoglobinuria in grazing horses was described in United Kingdom and Germany between 1984 and 1996. Fourteen horses were presented at the University of Liege between November 2000 and April 2001, with a clinical history suggesting atypical myoglobinuria. Lesions were similar to those previously described. All horses were at rest and grazing when they developed clinical signs. Three times, the syndrome killed several horses grazing together. Horses were generally found recumbent, nearly or totally unable to stand up. They were presenting tachycardia, polypnoea, myoglobinuria and died rapidly. When performed, blood analysis revealed severe muscular enzymatic activity rises. Histopathology revealed pulmonary congestion and oedema, and squeletal muscular fibers degeneration, mostly in respiratory and postural muscles. These observations are in accordance with cases of atypical myoglobinuria previously described in UK and Germany. The aetiology of this pathology is still unknown, despite of research attempts. [less ▲]

Detailed reference viewed: 221 (9 ULg)
Full Text
Peer Reviewed
See detailCold-Adapted Beta-Galactosidase from the Antarctic Psychrophile Pseudoalteromonas Haloplanktis
Hoyoux, A.; Jennes, I.; Dubois, P. et al

in Applied and Environmental Microbiology (2001), 67(4), 1529-35

The beta-galactosidase from the Antarctic gram-negative bacterium Pseudoalteromonas haloplanktis TAE 79 was purified to homogeneity. The nucleotide sequence and the NH(2)-terminal amino acid sequence of ... [more ▼]

The beta-galactosidase from the Antarctic gram-negative bacterium Pseudoalteromonas haloplanktis TAE 79 was purified to homogeneity. The nucleotide sequence and the NH(2)-terminal amino acid sequence of the purified enzyme indicate that the beta-galactosidase subunit is composed of 1,038 amino acids with a calculated M(r) of 118,068. This beta-galactosidase shares structural properties with Escherichia coli beta-galactosidase (comparable subunit mass, 51% amino sequence identity, conservation of amino acid residues involved in catalysis, similar optimal pH value, and requirement for divalent metal ions) but is characterized by a higher catalytic efficiency on synthetic and natural substrates and by a shift of apparent optimum activity toward low temperatures and lower thermal stability. The enzyme also differs by a higher pI (7.8) and by specific thermodynamic activation parameters. P. haloplanktis beta-galactosidase was expressed in E. coli, and the recombinant enzyme displays properties identical to those of the wild-type enzyme. Heat-induced unfolding monitored by intrinsic fluorescence spectroscopy showed lower melting point values for both P. haloplanktis wild-type and recombinant beta-galactosidase compared to the mesophilic enzyme. Assays of lactose hydrolysis in milk demonstrate that P. haloplanktis beta-galactosidase can outperform the current commercial beta-galactosidase from Kluyveromyces marxianus var. lactis, suggesting that the cold-adapted beta-galactosidase could be used to hydrolyze lactose in dairy products processed in refrigerated plants. [less ▲]

Detailed reference viewed: 37 (5 ULg)
Full Text
Peer Reviewed
See detailEnzyme Activity Determination on Macromolecular Substrates by Isothermal Titration Calorimetry: Application to Mesophilic and Psychrophilic Chitinases
Lonhienne, T.; Baise, Etienne ULg; Feller, Georges ULg et al

in Biochimica et Biophysica Acta (2001), 1545(1-2), 349-56

Isothermal titration calorimetry has been applied to the determination of the kinetic parameters of chitinases (EC 3.2.1.14) by monitoring the heat released during the hydrolysis of chitin glycosidic ... [more ▼]

Isothermal titration calorimetry has been applied to the determination of the kinetic parameters of chitinases (EC 3.2.1.14) by monitoring the heat released during the hydrolysis of chitin glycosidic bonds. Experiments were carried out using two different macromolecular substrates: a soluble polymer of N-acetylglucosamine and the insoluble chitin from crab shells. Different experimental temperatures were used in order to compare the thermodependence of the activity of two chitinases from the psychrophile Arthrobacter sp. TAD20 and of chitinase A from the mesophile Serratia marcescens. The method allowed to determine unequivocally the catalytic rate constant k(cat), the activation energy (E(a)) and the thermodynamic activation parameters (DeltaG(#), DeltaH(#), DeltaS(#)) of the chitinolytic reaction on the soluble substrate. The catalytic activity has also been determined on insoluble chitin, which displays an effect of substrate saturation by chitinases. On both substrates, the thermodependence of the activity of the psychrophilic chitinases was lower than that observed with the mesophilic counterpart. [less ▲]

Detailed reference viewed: 14 (0 ULg)
Full Text
Peer Reviewed
See detailReceptors as screening tools in the detections of hormones. Applications in the control of meat production
Maghuin-Rogister, Guy ULg; Baise, Etienne ULg; Carpeaux, Rudy et al

in Biotechnologie, Agronomie, Société et Environnement = Biotechnology, Agronomy, Society and Environment [=BASE] (1999), 4(1), 21-22

Detailed reference viewed: 42 (13 ULg)
See detailCold enzymes : a hot topic
Gerday, Charles ULg; Aittaleb, M.; Arpigny, J. L. et al

in Margesin, R.; Schinner, F. (Eds.) Cold-adapted Organisms : Ecology, Physiology, Enzymology and Molecular Biology (1999)

Detailed reference viewed: 30 (5 ULg)
Full Text
Peer Reviewed
See detailPsychrophilic Enzymes: A Thermodynamic Challenge
Gerday, Charles ULg; Aittaleb, Mohamed; Arpigny, Jean Louis et al

in Biochimica et Biophysica Acta (1997), 1342(2), 119-31

Psychrophilic microorganisms, hosts of permanently cold habitats, produce enzymes which are adapted to work at low temperatures. When compared to their mesophilic counterparts, these enzymes display a ... [more ▼]

Psychrophilic microorganisms, hosts of permanently cold habitats, produce enzymes which are adapted to work at low temperatures. When compared to their mesophilic counterparts, these enzymes display a higher catalytic efficiency over a temperature range of roughly 0-30 degrees C and a high thermosensitivity. The molecular characteristics of cold enzymes originating from Antarctic bacteria have been approached through protein modelling and X-ray crystallography. The deduced three-dimensional structures of cold alpha-amylase, beta-lactamase, lipase and subtilisin have been compared to their mesophilic homologs. It appears that the molecular adaptation resides in a weakening of the intramolecular interactions, and in some cases in an increase of the interaction with the solvent, leading to more flexible molecular edifices capable of performing catalysis at a lower energy cost. [less ▲]

Detailed reference viewed: 11 (0 ULg)
Peer Reviewed
See detailPsychrophiles et thermophiles : un problème d’enzyme
Gerday, Charles ULg; Aittaleb, M.; Arpigny, J. L. et al

in Chimie Nouvelle (1997), 15

Detailed reference viewed: 34 (3 ULg)
Peer Reviewed
See detailEnzymes from psychrophiles
Feller, Georges ULg; Narinx, Emmanuel; Arpigny, Jean Louis et al

Conference (1996)

Detailed reference viewed: 6 (0 ULg)
Full Text
Peer Reviewed
See detailEnzymes from psychrophilic organisms
Feller, Georges ULg; Narinx, E.; Arpigny, J. L. et al

in FEMS Microbiology Reviews (1996), 18(2-3), 189-202

Psychrophilic organisms such as micro-organisms and other ectothermic species living in polar, deep- sea or any constantly low temperature environments, produce enzymes adapted to function at low ... [more ▼]

Psychrophilic organisms such as micro-organisms and other ectothermic species living in polar, deep- sea or any constantly low temperature environments, produce enzymes adapted to function at low temperature. These enzymes are characterized by a high catalytic efficiency at low and moderate temperatures but are rather thermolabile. Due to their high specific activity and their rapid inactivation at temperatures as low as 30 degrees C, they offer, along with the producing micro-organisms, a great potential in biotechnology. The molecular basis of the adaptation of cold cu-amylase, subtilisin, triose phosphate isomerase from Antarctic bacteria and of trypsin from fish living in North Atlantic and in Antarctic sea waters have been studied. The comparison of the 3D structures obtained either by protein modelling or by X-ray crystallography (North Atlantic trypsin) with those of their mesophilic counterparts indicates that the molecular changes tend to increase the flexibility of the structure by a weakening of the intramolecular interactions and by an increase of the interactions with the solvent. For each enzyme, the most appropriate strategy enabling it to accommodate the substrate at a low energy cost is selected. There is a price to pay in terms of thermosensibility because the selective pressure is essentially oriented towards the harmonization of the specific activity with ambient thermal conditions. However, as demonstrated by site-directed mutagenesis experiments carried out on the Antarctic subtilisin, the possibility remains to stabilize the structure of these enzymes without affecting their high catalytic efficiency. [less ▲]

Detailed reference viewed: 51 (6 ULg)