RESUMEN
Mycobacterium avium subspecies paratuberculosis (MAP) is the causative organism of Johne's Disease, a chronic intestinal infection of ruminants. Infected cows begin shedding MAP within the asymptomatic, subclinical stage of infection before clinical signs, such as weight loss, diarrhoea and reduced milk yields develop within the clinical stages of disease. Herein, we examine the milk metabolomic profiles of naturally MAP-infected Holstein-Friesian cows. The study used biobanked milk samples which were collected 73.4 ± 3.79 (early lactation) and 143 ± 3.79 (mean ± SE) (mid-lactation) days post-calving from 5 MAP-infected and 5 control multiparous cows. The milk metabolome was assessed using flow infusion electrospray high-resolution mass spectrometry (FIE-HRMS) for sensitive, non-targeted metabolite fingerprinting. Metabolite fingerprinting assessments using partial least squares discriminate analyses (PLS-DA) indicated that lactation stage was a larger source of variation than MAP status. Examining each lactation stage separately for changes associated to MAP-infection status identified 45 metabolites, 33 in early lactation and 12 in mid-lactation, but only 6 metabolites were targeted in both stages of lactation. Pathway enrichment analysis suggested that MAP affected the malate-aspartate shuffle during early lactation. Pearson's correlation analysis indicated relationships between milk lactose concentrations in mid-lactation and 6 metabolites that were tentatively linked to MAP-infection status. The targeted metabolites were suggestive of wider changes in the bioenergetic metabolism that appear to be an acceleration of the effects of progressing lactation in healthy cows. Additionally, milk lactose concentrations suggest that MAP reduces the availability of lactose derivatives.
Asunto(s)
Enfermedades de los Bovinos , Mycobacterium avium subsp. paratuberculosis , Paratuberculosis , Femenino , Bovinos , Animales , Lactancia , Lactosa/análisis , Lactosa/metabolismo , Enfermedades de los Bovinos/microbiología , Paratuberculosis/microbiología , Leche/metabolismoRESUMEN
Bovine tuberculosis (bTB) is increasing in incidence in the UK. Effective control strategies could involve vaccination; BCG, either alone or in prime-boost strategies, remains the most effective vaccine against bovine tuberculosis. However, BCG vaccination of cattle would require development of diagnostic tests able to accurately discriminate Mycobacterium bovis-infected from BCG-vaccinated animals. Herein, we demonstrate that the detection of secreted IFN-gamma following short term culture (4h) of whole blood with purified protein derived from M. bovis (PPD-B) allows such discrimination. This reflects, in part, the differential kinetics of IFN-gamma secretion in infected compared to vaccinated cattle. This is the first study to demonstrate that accurate, rapid distinction of BCG-vaccinated from M. bovis-infected cattle can be achieved in a short time period without the need for production of M. bovis-specific antigens, complex antigen mixtures or extensive laboratory procedures. We were also able to detect PPD-specific IFN-gamma release during short term culture of blood from a number of humans with active TB indicating that this test may have wider application and is potentially useful for the rapid diagnosis of disease in humans.
Asunto(s)
Vacuna BCG/inmunología , Mycobacterium bovis/inmunología , Tuberculosis Bovina/inmunología , Animales , Antígenos Bacterianos/biosíntesis , Antígenos Bacterianos/genética , Linfocitos T CD4-Positivos/inmunología , Linfocitos T CD4-Positivos/metabolismo , Bovinos , Citocinas/biosíntesis , Citocinas/genética , Citometría de Flujo , Humanos , Interferón gamma/análisis , Interferón gamma/biosíntesis , Cinética , Tuberculosis Pulmonar/inmunología , VacunaciónRESUMEN
The immune response against mycobacterial infections is dependant upon a complex interaction between T lymphocytes and macrophages in the context of the granuloma. For this study, we performed the analysis of 18 stage I or II, and 13 stage III or IV granulomas found in lymph nodes from 8 experimentally and 2 naturally infected cattle. T-cell subpopulations (CD3(+), CD4(+), CD8(+), WC1(+), CD25(+)) were investigated by immunohistochemistry. In the majority of stage I/II lesions, CD8(+) and CD25(+) cells were predominantly found in the lymphocytic outer region of the granuloma, suggesting a possible role for activated CD8(+) cells in the initial attempt to restrain the granuloma growth. CD4(+) T cells appeared equally distributed in the lymphocytic mantle and in the internal areas of the granulomas. WC1(+) cells appeared interspersed among the macrophages. We speculated that this could indicate a role for these 2 subsets in the maintenance and the maturation of the granuloma. In stage III/IV lesions, all of the T-cell subsets investigated appeared interspersed among the mononuclear component of the granulomas. In general terms, there was a higher density of CD8(+) cells compared with CD4(+) cells. However, there was no sense of rimming effect for any of the investigated cell populations.
Asunto(s)
Granuloma/patología , Ganglios Linfáticos/patología , Activación de Linfocitos/fisiología , Subgrupos de Linfocitos T/fisiología , Tuberculosis Bovina/patología , Animales , Bovinos , Granuloma/microbiología , MasculinoRESUMEN
The source of bovine tuberculosis was investigated in 31 herds in north-east England that experienced confirmed breakdowns between January 2002 and June 2004; nine of the herds had been restocked after the UK outbreak of foot-and-mouth disease in 2001. In all but one of the breakdowns the most likely source of infection was identified as one or more purchased animals. In 17 of the breakdowns, reactor animals were traced to herds from which the same combination of spoligotype and variable number tandem repeats was isolated, and in five breakdowns a different spoligotype was isolated. The most likely sources were located in Wales and the west and north of England, and included a Cheshire herd that was the most likely source of nine of the breakdowns. Three breakdowns were traced to Irish imports. Reactors in five of the breakdowns included homebred as well as purchased animals, providing evidence for the likely spread of the disease within the herds. The lack of geographical clustering of molecular types pointed to the overwhelming source of infection being cattle that had been bought-in.
Asunto(s)
Comercio , Transmisión de Enfermedad Infecciosa/veterinaria , Mycobacterium bovis/genética , Tuberculosis Bovina/epidemiología , Tuberculosis Bovina/transmisión , Animales , Bovinos , Análisis por Conglomerados , ADN Bacteriano/análisis , Brotes de Enfermedades/veterinaria , Inglaterra/epidemiología , Monitoreo del Ambiente , Monitoreo Epidemiológico , Irlanda/epidemiología , Mycobacterium bovis/clasificación , Mycobacterium bovis/aislamiento & purificación , Factores de Riesgo , Secuencias Repetidas en Tándem , Gales/epidemiologíaRESUMEN
The pathognomonic characteristic of tuberculosis (TB) is the formation of a tuberculous granuloma. The objective of this study was to classify lymph node granulomas from experimentally infected calves into different histopathological stages and characterize them further by studying cell types and markers of fibrosis associated with each of the stages. Four stages of granuloma were identified and mRNA and protein expression for cell markers, cytokines and pro-fibrotic markers were studied by immunohistochemistry (IHC) and in-situ hybridization (ISH). In advanced stage granulomas, there was an increase in the expression of TGF-beta, and of type I procollagen as demonstrated by IHC and ISH. As the granulomas advanced, there were fewer CD3+T cells and they tended to be more prominent towards the periphery of the lesions, with a steady increase in the number of CD68+ cells and gammadelta (WC1+) T cells. Granuloma classification and application of cell cytokine markers will assist in improving understanding of the pathogenesis of bovine TB and may help to identify the immunopathology of active disease versus contained or inactive disease. Such disease correlates may help to inform the development of improved diagnostic methods and support vaccine development programmes.
Asunto(s)
Antígenos CD/análisis , Antígenos de Diferenciación Mielomonocítica/análisis , Colágeno Tipo I/biosíntesis , Granuloma/veterinaria , Macrófagos , Receptores de Antígenos de Linfocitos T gamma-delta/análisis , Subgrupos de Linfocitos T , Tuberculosis Bovina/patología , Animales , Antígenos CD/genética , Antígenos de Diferenciación Mielomonocítica/genética , Complejo CD3/biosíntesis , Complejo CD3/genética , Antígenos CD79/biosíntesis , Antígenos CD79/genética , Bovinos , Enfermedades de los Bovinos/genética , Enfermedades de los Bovinos/inmunología , Enfermedades de los Bovinos/metabolismo , Enfermedades de los Bovinos/patología , Colágeno Tipo I/genética , Expresión Génica , Granuloma/genética , Granuloma/inmunología , Granuloma/patología , Recuento de Linfocitos , Macrófagos/inmunología , Masculino , ARN Mensajero/biosíntesis , ARN Mensajero/genética , Receptores de Antígenos de Linfocitos T gamma-delta/genética , Subgrupos de Linfocitos T/inmunología , Factor de Crecimiento Transformador beta/biosíntesis , Factor de Crecimiento Transformador beta/genética , Tuberculosis Bovina/genética , Tuberculosis Bovina/inmunología , Tuberculosis Bovina/metabolismoRESUMEN
We report the first isolation of Mycobacterium microti from a dog with lesions of acute peritonitis. The isolate was demonstrated to be M. microti of Llama-Type by spoligotyping. Epidemiological implications of the isolation of this possibly zoonotic agent from a dog are discussed.
Asunto(s)
Enfermedades de los Perros/microbiología , Mycobacterium/aislamiento & purificación , Peritonitis/veterinaria , Enfermedad Aguda , Animales , Biopsia con Aguja Fina/veterinaria , Enfermedades de los Perros/transmisión , Perros , Resultado Fatal , Humanos , Masculino , Mycobacterium/clasificación , Peritonitis/microbiología , ZoonosisRESUMEN
Injection of plasmid DNA encoding antigens into rodents followed by electroporation improved the immune response when compared with injection without electroporation (Widera et al. J Immunol 2000;164:4635-40; Zucchelli et al. J Virol 2000;74:11598-607; Kadowaki et al. Vaccine 2000;18:2779-88). The present study describes the extension of this technology to farm animals, by injecting plasmid DNA encoding mycobacterial antigens (MPB70, Ag85B and Hsp65) into the muscles of goats and cattle using two different types of electrodes, both allowing DNA delivery at the site of electroporation. The animals were vaccinated under local anaesthesia without any observed immediate or long-term distress or discomfort, or any behavioural signs of muscle damage or pathological changes after the electroporation. DNA-injected and electroporated goats showed increased humoral response after the primary vaccination when compared with nonelectroporated animals. Improved T-cell responses following electroporation were observed in hsp65 DNA-vaccinated cattle. DNA injection with or without electroporation did not compromise the specificity of the tuberculin skin test. In conclusion, a protocol applying in vivo electroporation free of side effects to farmed ruminants was established. In addition, we show that DNA vaccination in combination with electroporation can improve the primary immune responses to the encoded antigens.
Asunto(s)
Proteínas Bacterianas , Vacunas Bacterianas/administración & dosificación , Enfermedades de las Cabras/microbiología , Mycobacterium bovis/inmunología , Tuberculosis Bovina/inmunología , Vacunación/veterinaria , Vacunas de ADN/administración & dosificación , Animales , Antígenos Bacterianos/inmunología , Vacunas Bacterianas/inmunología , Bovinos , Chaperonina 60 , Chaperoninas/inmunología , Electroporación/veterinaria , Ensayo de Inmunoadsorción Enzimática/veterinaria , Femenino , Citometría de Flujo/veterinaria , Enfermedades de las Cabras/inmunología , Enfermedades de las Cabras/prevención & control , Cabras , Memoria Inmunológica , Interferón gamma/inmunología , Activación de Linfocitos/inmunología , Masculino , Prueba de Tuberculina/veterinaria , Tuberculosis Bovina/prevención & control , Vacunación/métodos , Vacunas de ADN/inmunologíaRESUMEN
The distribution of 20 variable regions resulting from insertion-deletion events in the genomes of the tubercle bacilli has been evaluated in a total of 100 strains of Mycobacterium tuberculosis, Mycobacterium africanum, Mycobacterium canettii, Mycobacterium microti, and Mycobacterium bovis. This approach showed that the majority of these polymorphisms did not occur independently in the different strains of the M. tuberculosis complex but, rather, resulted from ancient, irreversible genetic events in common progenitor strains. Based on the presence or absence of an M. tuberculosis specific deletion (TbD1), M. tuberculosis strains can be divided into ancestral and "modern" strains, the latter comprising representatives of major epidemics like the Beijing, Haarlem, and African M. tuberculosis clusters. Furthermore, successive loss of DNA, reflected by region of difference 9 and other subsequent deletions, was identified for an evolutionary lineage represented by M. africanum, M. microti, and M. bovis that diverged from the progenitor of the present M. tuberculosis strains before TbD1 occurred. These findings contradict the often-presented hypothesis that M. tuberculosis, the etiological agent of human tuberculosis evolved from M. bovis, the agent of bovine disease. M. canettii and ancestral M. tuberculosis strains lack none of these deleted regions, and, therefore, seem to be direct descendants of tubercle bacilli that existed before the M. africanum-->M. bovis lineage separated from the M. tuberculosis lineage. This observation suggests that the common ancestor of the tubercle bacilli resembled M. tuberculosis or M. canettii and could well have been a human pathogen already.
Asunto(s)
Evolución Molecular , Genoma Bacteriano , Mycobacterium tuberculosis/clasificación , Mycobacterium tuberculosis/genética , Tuberculosis/microbiología , Secuencia de Bases , Genes Bacterianos/genética , Humanos , Datos de Secuencia Molecular , Filogenia , Eliminación de Secuencia/genética , Factores de TiempoRESUMEN
Mycobacterium bovis has the broadest host range of species in the Mycobacterium tuberculosis complex and is responsible for disease in humans and diverse animal species. We report on genotypic differences at multiple loci among 13 isolates derived from a range of human and animal infections. All isolates were classified as M. bovis by phenotypic analysis but could be subdivided into five distinct genotypes based on polymorphisms at the pncA and oxyR loci, the status of the RD5 deletion region, and the spoligotype pattern. These findings suggest the existence of a spectrum of strains with genotypic characteristics between those of M. tuberculosis and M. bovis.
Asunto(s)
Variación Genética , Mycobacterium bovis/clasificación , Mycobacterium bovis/aislamiento & purificación , Tuberculosis/microbiología , Anciano , Anciano de 80 o más Años , Amidohidrolasas/genética , Animales , Técnicas de Tipificación Bacteriana , Gatos , Bovinos , Femenino , Genotipo , Humanos , Masculino , Persona de Mediana Edad , Mycobacterium bovis/genética , Oligonucleótidos/análisis , Fenotipo , Tuberculosis/veterinariaAsunto(s)
Proteínas Bacterianas/química , Mycobacterium bovis/química , Mycobacterium tuberculosis/química , Antígenos Bacterianos/química , Proteínas Bacterianas/inmunología , Humanos , Mycobacterium bovis/inmunología , Mycobacterium tuberculosis/inmunología , Mycobacterium tuberculosis/patogenicidad , Resonancia Magnética Nuclear Biomolecular , Estructura Secundaria de ProteínaRESUMEN
In order to gain a better understanding of the molecular epidemiology of Mycobacterium bovis isolates in Cameroon, 75 isolates of M. bovis collected in three provinces of northern Cameroon were studied by spoligotyping. For 65 of these isolates, typing was also carried out by pulsed-field gel electrophoresis (PFGE) with DraI, and 18 of the isolates were also typed by restriction fragment length polymorphism (RFLP) analysis with probe IS6110-RHS. Molecular typing of the isolates by these techniques revealed a high degree of homogeneity, with 10 spoligotypes for 75 isolates, four PFGE profiles for 65 isolates, and three RFLP types for 18 isolates. Some types were present in the three different provinces, while some were confined to one or two areas. These results suggest that geographical mapping of M. bovis strains could be helpful for the control of bovine tuberculosis at the regional level. An interesting feature of all the spoligotypes was the absence of spacer 30, suggesting a common origin for all of the Cameroon isolates tested; an evolutionary scenario for the isolates is discussed. In addition, a comparison of the three techniques showed that for M. bovis strain differentiation in Cameroon and in surrounding countries, spoligotyping would be a more discriminating and practical tool for molecular typing than the other two techniques used in this study.
Asunto(s)
Técnicas de Tipificación Bacteriana , Mycobacterium bovis/clasificación , Mycobacterium bovis/genética , Tuberculosis Bovina/microbiología , Animales , Camerún/epidemiología , Bovinos , Elementos Transponibles de ADN/genética , ADN Bacteriano/análisis , ADN Bacteriano/genética , Electroforesis en Gel de Campo Pulsado/métodos , Oligonucleótidos/análisis , Oligonucleótidos/genética , Polimorfismo de Longitud del Fragmento de Restricción , Tuberculosis Bovina/epidemiologíaAsunto(s)
Infecciones por Mycobacterium/diagnóstico , Infecciones por Mycobacterium/veterinaria , Mycobacterium/clasificación , Animales , Animales Domésticos , Arvicolinae/microbiología , Camélidos del Nuevo Mundo/microbiología , Carnívoros/microbiología , Gatos/microbiología , Bovinos/microbiología , Humanos , Mycobacterium/aislamiento & purificación , Infecciones por Mycobacterium/microbiología , Reino UnidoRESUMEN
The effects of mutagenesis of residues of a major T cell epitope were investigated in order to expand knowledge from synthetic peptides to the naturally processed antigen. The impact of substitutions within the core of the immunodominant p61-80/PT19 mycobacterial epitope was ascertained in respect of this epitope per se, or of a C-terminal (140-159) overlapping T/B epitope and of a conformational B epitope. The core substitution A71L impaired T immunogenicity of the target epitope within the protein, but not in the peptide, whereas the N73A substitution impaired the responses in both instances. Notably, each of these single amino acid mutations abrogated the T but not the B immunogenicity of the C-terminal epitope. Furthermore, mutation of five core residues (71-76) also ablated expression of a monoclonal antibody defined conformational B epitope. In conclusion, immunological analysis of mutated proteins revealed functional associations between topographically distinct antigenic determinants which may account for the previously observed differences in the specificity of immune responses between immunised and infected hosts.