Comparison of bovine and human O26 EHEC strains by the Whole Genome PCR ScanningBardiau, Marjorie ; ; et alConference (2008, March) Detailed reference viewed: 8 (0 ULg) Creating hybrid proteins by insertion of exogenous peptides into permissive sites of a class A beta-lactamaseRuth, Nadia ; ; Mainil, Jacques et alin FEBS Journal (2008), 275 Detailed reference viewed: 28 (10 ULg) Purification of the recombinant beta2 toxin (CPB2) from an enterotoxaemic bovine Clostridium perfringens strain and production of a specific immune serum; Filée, Patrice ; Galleni, Moreno et alin Protein Expression & Purification (2007), 55(1), 119-131 Overgrowth of Clostridium perfringens clones with production of one or more of its toxin(s) results in diverse digestive and systemic pathologies in human and animals, such as cattle enterotoxaemia. The ... [more ▼] Overgrowth of Clostridium perfringens clones with production of one or more of its toxin(s) results in diverse digestive and systemic pathologies in human and animals, such as cattle enterotoxaemia. The so-called beta2 toxin (CPB2) is the most recently described major toxin produced by C perfringens. In this study, the cpb2 ORF (cpb2FM) from a cattle C perfringens-associated enterotoxaemia was cloned and sequenced. The cpb2FM and its deduced nucleotide sequence clearly corresponded to the epb2 allele considered as "consensus" and not to "atypical" allele, despite its "non-porcine" origin. Expression assays of the recombinant toxin CPB2FM were performed in Escherichia coli and Bacillus subtilis with the expression vector pBLTS72, and by genomic integration by double recombination in B. subtilis. Highest level of production was obtained with the expression vector in B. subtilis 168 strain. The recombinant CPB2FM protein was purified and a specific rabbit polyclonal antiserum was produced. Polyclonal antibodies could detect CPB2 production in supernatants of C. perfringens from enterotoxaemic cattle. (C) 2007 Elsevier Inc. All rights reserved. [less ▲] Detailed reference viewed: 23 (6 ULg) Application of suppressive subtractive hybridization to identify specific host virulence factors of enterohemorrhagic Escherichia coli strains of serogroup O26Bardiau, Marjorie ; Labrozzo, Sabrina ; Mainil, Jacques ![]() Conference (2007, June) Detailed reference viewed: 10 (0 ULg) Identification, par hybridation suppressive soustractive (SSH) et par microarray, de facteurs de virulence impliqués dans l’attachement initial et dans la spécificité d’hôte de souches entérohémorragiques d’Escherichia coli (EHEC) appartenant au sérogroupe O26Bardiau, Marjorie ; Labrozzo, Sabrina ; Mainil, Jacques ![]() Conference (2007, May) Detailed reference viewed: 9 (1 ULg) The expression of Clostridium perfringens consensus beta2 toxin is associated with bovine enterotoxaemia syndrome; Filée, Patrice ; Mousset, Bénédicte et alin Veterinary Microbiology (2007), 120(1-2), 151-157 Clostridium perfringens has been implicated in a broad array of enteric infections including the fatal haemorrhagic enteritis/enterotoxaemia syndrome in cattle. The beta2 toxin (CPB2), encoded by cpb2, is ... [more ▼] Clostridium perfringens has been implicated in a broad array of enteric infections including the fatal haemorrhagic enteritis/enterotoxaemia syndrome in cattle. The beta2 toxin (CPB2), encoded by cpb2, is suspected to be implicated in this syndrome. However, among C. perfringens isolates from cattle suspected of clostridial disease, an atypical allele was recently found to predominate at the cpb2 locus and atypical corresponding CPB2 proteins were shown to be poorly expressed, thus arguing against a biologically significant role of the beta2 toxin in clostridial diseases in cattle. This study compared genotype and phenotype of the beta2 toxin between C. perfringens isolates from a group of healthy calves (n = 14, 87 isolates) and from a group of enterotoxaemic calves (n = 8,41 isolates). PCR results revealed the exclusive presence of the typical "consensus" cpb2 in the enterotoxaernic group. Western blot analysis demonstrated that the typical variant of CPB2 was often expressed in isolates from enterotoxaemic calves (43.9%) and infrequently in isolates from healthy cattle (6.9%). These data suggest that the typical variant of the CPB2 toxin may play a role in the pathogenesis of cattle enterotoxaemia. (c) 2006 Elsevier B.V. All rights reserved. [less ▲] Detailed reference viewed: 46 (16 ULg) Profils de résistance aux antibiotiques de souches d'Enterococcus sp et d'Escherichia coli isolées dans les matières fécales de sangliers et cervidés sauvages; ; Duprez, Jean-Noël et alin Annales de Médecine Vétérinaire (2007), 151 Detailed reference viewed: 59 (8 ULg) Helenalin reduces Staphylococcus aureus infection in vitro and in vivo; ; et al in Veterinary Microbiology (2007), 119(2-4), 330-338 Staphylococcus (S.) aureus is a major udder pathogen causing bovine mastitis. Some pro-inflammatory cytokines, including tumor necrosis factor-alpha (TNF-alpha), enhance extracellular and intracellular ... [more ▼] Staphylococcus (S.) aureus is a major udder pathogen causing bovine mastitis. Some pro-inflammatory cytokines, including tumor necrosis factor-alpha (TNF-alpha), enhance extracellular and intracellular growth of S. aureus, indicating that the inflammatory process favors S. aureus infection. Helenalin is a sesquiterpene lactone with potent anti-inflammatory properties. This study was designed to evaluate the effects of helenalin on S. aureus infection. First, in vitro experiments were conducted. These studies revealed that proliferation of S. aureus in bovine mammary epithelial MAC-T cells treated in the presence or absence of TNF-alpha was markedly reduced in the presence of helenalin. Secondly, in vivo effects of helenalin were investigated. Lactating mice treated in the presence or absence of helenalin were challenged by the intramammary route with S. aureus and the bacteria in the mammary glands were counted 12 h after infection. Significantly less numbers of bacteria were recovered from the infected glands of helenalin-treated mice compared with untreated mice. Moreover, histological examination of mammary tissue from helenalin-treated mice that were challenged with S. aureus indicated that helenalin is able to significantly reduce leukocyte infiltration in the mammary gland following S. aureus inoculation. Our results show that helenalin reduces S. aureus intracellular growth and experimental S. aureus infection. We conclude that helenalin may be of potential interest in the treatment of S. aureus-induced mastitis in the bovine species. [less ▲] Detailed reference viewed: 78 (18 ULg) Infectious agents associated with epizootic rabbit enteropathy: Isolation and attempts to reproduce the syndromeMarlier, Didier ; ; Lassence, Cédric et alin Veterinary Journal (2006), 172(3), 493-500 Epizootic rabbit enteropathy (ERE), a highly lethal (30-80% mortality) disease of broiler rabbits aged 6-14 weeks, first appeared in 1997 in French intensive enclosed rabbitries and is of unknown ... [more ▼] Epizootic rabbit enteropathy (ERE), a highly lethal (30-80% mortality) disease of broiler rabbits aged 6-14 weeks, first appeared in 1997 in French intensive enclosed rabbitries and is of unknown aetiology. Bacteriological, virological and parasitical examination of the intestinal contents of rabbits that had died either in spontaneous field cases or after experimental reproduction of ERE, were undertaken in an attempt to identify infectious agents that may play a role in the disease. Two bacterial strains, Clostridium perfringens and non-enteropathogenic Escherichia coli, were repeatedly isolated at high faecal counts from naturally infected animals. In field cases, a correlation between typical gross lesions of epizootic enteropathy and the presence of the alpha toxin of Cl. perfringens was observed (P < 0.0001; Chi-squared test). Although attempts to reproduce the disease by inoculation with different pools of cultivable bacterial strains failed, the disease was successfully reproduced by inoculation with one French and two Belgian samples of caecal contents. (c) 2005 Elsevier Ltd. All rights reserved. [less ▲] Detailed reference viewed: 63 (5 ULg) Common virulence factors and genetic relationships between O18 : K1 : H7 Escherichia coli isolates of human and avian origin; ; et al in Journal of Clinical Microbiology (2006), 44(10), 3484-3492 Extraintestinal pathogenic (ExPEC) Escherichia coli strains of serotype 018:K1:H7 are mainly responsible for neonatal meningitis and sepsis in humans and belong to a limited number of closely related ... [more ▼] Extraintestinal pathogenic (ExPEC) Escherichia coli strains of serotype 018:K1:H7 are mainly responsible for neonatal meningitis and sepsis in humans and belong to a limited number of closely related clones. The same serotype is also frequently isolated from the extraintestinal lesions of colibacillosis in poultry, but it is not well known to what extent human and avian strains of this particular serotype are related. Twenty-two ExPEC isolates of human origin and 33 isolates of avian origin were compared on the basis of their virulence determinants, lethality for chicks, pulsed-field gel electrophoresis (PFGE) patterns, and classification in the main phylogenetic groups. Both avian and human isolates were lethal for chicks and harbored similar virulence genotypes. A major virulence pattern, identified in 75% of the isolates, was characterized by the presence of F1 variant fimbriae; S fimbriae; IbeA; the aerobactin system; and genomic fragments A9, A12, D1, D7, D10, and D11 and by the absence of P fimbriae, F1C fimbriae, Afa adhesin, and CNF1. All but one of the avian and human isolates also belonged to major phylogenetic group B2. However, various subclonal populations could be distinguished by PFGE in relation to animal species and geographical origin. These results demonstrate that very closely related clones can be recovered from extraintestinal infections in humans and chickens and suggest that avian pathogenic E. coli isolates of serotype 018:K1:H7 are potential human pathogens. [less ▲] Detailed reference viewed: 22 (6 ULg) Identification of specific host virulence factors of enterohemorrhagic Escherichia coli strains of serogroup O26 by substractive suppressive hybridyzationBardiau, Marjorie ; Mainil, Jacques ![]() Conference (2006, September) Detailed reference viewed: 7 (0 ULg)![]() Prévalence d’Escherichia coli enterohémorragiques du sérotype O157 et d’autres Escherichia coli attachantes et effaçantes sur des carcasses bovines en Algérie.; ; Mainil, Jacques et alPoster (2006, July) Detailed reference viewed: 23 (0 ULg)![]() Fluctuations dans la sensibilité à l’enrofloxacine des populations nasales chez le porcelet au cours d’un traitement parentéralMainil, Jacques ; ; et alin Proceedings: 3ème Colloque International Francophone de Bactériologie Vétérinaire (2006) Detailed reference viewed: 31 (9 ULg) Infectious agents associated with epizootic rabbit enteropathy : isolation and attempts to reproduce the syndromeMarlier, Didier ; ; et alin Veterinary Journal (2006), 172 Detailed reference viewed: 8 (2 ULg) Prevalence of enterohaemorrhagic Escherichia coli from serotype O157 and other attachning and effacing Escherichia coli on bovine carcasses in Algeria; ; Mainil, Jacques et alin Journal of Applied Microbiology (2006), 101 Detailed reference viewed: 8 (4 ULg) Serotypes and intimin types of intestinal and faecal strains of eae+ Escherichia coli from weaned pigs; ; et al in Veterinary Microbiology (2006), 114 Detailed reference viewed: 12 (1 ULg) Le lipopolysaccharide d’Escherichia coli : structure, biosynthèse et rôlesSzalo, Ioan Mihai ; Taminiau, Bernard ; Mainil, Jacques ![]() in Annales de Médecine Vétérinaire (2006), 150 The lipopolysaccharide (LPS) is a major component of the surface of the Gram negative bacteria. The LPS is composed of three separately synthesized entities: the lipid A, the core oligosaccharide and the ... [more ▼] The lipopolysaccharide (LPS) is a major component of the surface of the Gram negative bacteria. The LPS is composed of three separately synthesized entities: the lipid A, the core oligosaccharide and the O antigen, that will be linked together after their respective synthesis. The lipid A, embedded inside the outer membrane, is the proximal part of the LPS and the core is the medial part, whereas the O antigen represents the distal part free in the external environment. Amongst the Enterobacteriaceae family, the lipid A is structurally highly conserved and the variation in the structure of the core oligosaccharide is limited whereas the O antigen is the hypervariable region. Diverse biological activities have been associated with LPS, amongst which the endotoxinic activity carried by the lipid A, and the strain immunogenic specificity carried by the O antigen. In this review manuscript we summarize the state of knowledge on the structures and biosynthesis of the different components of the LPS of Escherichia coli and on their respective roles in the virulence of pathogenic bacteria. [less ▲] Detailed reference viewed: 57 (9 ULg) Prevalence of enterohaemorrhagic Escherichia coli from serotype O157 and other attaching and effacing Escherichia coli on bovine carcasses in Algeria; ; Mainil, Jacques et alin Journal of Applied Microbiology (2006), 101(2), 361-368 AIMS: Bovine meat is the principal source of human contamination of attaching and effacing Escherichia coli, including enterohaemorrhagic E. coli O157. The aim was to study the prevalence of these strains ... [more ▼] AIMS: Bovine meat is the principal source of human contamination of attaching and effacing Escherichia coli, including enterohaemorrhagic E. coli O157. The aim was to study the prevalence of these strains on bovine carcasses in Algeria. METHODS AND RESULTS: Two-hundred and thirty carcasses were swabbed and analysed by classical microbiological methods for total E. coli counts and for the presence of pathogenic E. coli. The E. coli counts were high, with a 75th percentile of 444.75 CFUs cm(-2). For pathogenic E. coli, more than 7% of the tested carcasses were positive for E. coli O157. Eighteen E. coli O157 strains were isolated and typed by multiplex PCR. The main isolated pathotype (78%) was eae+ stx2+ ehxA+. In addition to E. coli O157, other attaching and effacing E. coli (AEEC) were also detected from carcasses by colony hybridization after pre-enrichment and plating on sorbitol MacConkey agar using eae, stx1 and stx2 probes. Thirty carcasses (13%) on the 230 analysed harboured at least one colony positive for one of the tested probes. These positive carcasses were different from those positive for E. coli O157. Sixty-six colonies (2.9%) positive by colony hybridization were isolated. The majority (60.6%) of the positive strains harboured an enteropathogenic E. coli-like pathotype (eae+ stx-). Only three enterohaemorrhagic E. coli (EHEC)-like (eae+ stx1+) colonies were isolated from the same carcass. These strains did not belong to classical EHEC serotypes. CONCLUSIONS: In this study, the global hygiene of the slaughterhouse was low, as indicated by the high level of E. coli count. The prevalence of both E. coli O157 and other AEEC was also high, representing a real hazard for consumers. SIGNIFICANCE AND IMPACT OF THE STUDY: This is the first study of this type in Algeria, which indicates that the general hygiene of the slaughterhouse must be improved. [less ▲] Detailed reference viewed: 80 (5 ULg) Lipopolysaccharide of Escherichia coli: structure, biosynthesis and roles; Taminiau, Bernard ; Mainil, Jacques ![]() in Annales de Médecine Vétérinaire (2006), 150(2), 108-124 The lipopolysaccharide (LPS) is a major component of the surface of the Gram negative bacteria. The LPS is composed of three separately synthesized entities: the lipid A, the core oligosaccharide and the ... [more ▼] The lipopolysaccharide (LPS) is a major component of the surface of the Gram negative bacteria. The LPS is composed of three separately synthesized entities: the lipid A, the core oligosaccharide and the O antigen, that will be linked together after their respective synthesis. The lipid A, embedded inside the outer membrane, is the proximal part of the LPS and the core is the medial part, whereas the O antigen represents the distal part free in the external environment. Amongst the Enterobacteriaceae family, the lipid A is structurally highly conserved and the variation in the structure of the core oligosaccharide is limited whereas the O antigen is the hypervariable region. Diverse biological activities have been associated with LPS, amongst which the endotoxinic activity carried by the lipid A, and the strain immunogenic specificity carried by the O antigen. In this review manuscript we summarize the state of knowledge on the structures and biosynthesis of the different components of the LPS of Escherichia coli and on their respective roles in the virulence of pathogenic bacteria. [less ▲] Detailed reference viewed: 28 (1 ULg) Immunochemical, biomolecular and biochemical characterization of bovine epithelial intestinal primocultures; ; Peulen, Olivier et alin BMC Cell Biology (2005), 6 Background: Cultures of enterocytes and colonocytes represent valuable tools to study growth and differentiation of epithelial cells. In vitro models may be used to evaluate passage or toxicity of drugs ... [more ▼] Background: Cultures of enterocytes and colonocytes represent valuable tools to study growth and differentiation of epithelial cells. In vitro models may be used to evaluate passage or toxicity of drugs, interactions of enteropathogenes bacteria strains with intestinal epithelium and other physiologic or pathologic phenomenon involving the digestive tract. Results: Cultures of bovine colonocytes and jejunocytes were obtained from organoid-enriched preparations, using a combination of enzymatic and mechanical disruption of the intestine epithelium, followed by an isopicnic centrifugation discarding most single cells. Confluent cell monolayers arising from plated organoids exhibited epithelium typical features, such as the pavement-like structure, the presence of apical microvilli and tight junctions. Accordingly, cells expressed several markers of enterocyte brush border (i.e. maltase, alkaline phosphatase and fatty acid binding protein) as well as an epithelial cytoskeleton component (cytokeratin 18). However, enterocyte primocultures were also positive for the vimentin immunostaining (mesenchyme marker). Vimentin expression studies showed that this gene is constitutively expressed in bovine enterocytes. Comparison of the vimentin expression profile with the pattern of brush border enzymes activities, suggested that the decrease of cell differentiation level observed during the enterocyte isolation procedure and early passages of the primoculture could result from a post-transcriptional de-repression of vimentin synthesis. The low differentiation level of bovine enterocytes in vitro could partly be counteracted adding butyrate (1-2 mM) or using a glucose-deprived culture medium. Conclusion: The present study describes several complementary approaches to characterize bovine primary cultures of intestinal cells. Cultured cells kept their morphologic and functional characteristics during several generations. [less ▲] Detailed reference viewed: 16 (1 ULg) |
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