Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
1.
J Fish Dis ; 37(1): 51-62, 2014 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-24206018

RESUMEN

Cobia, Rachycentron canadum L., is a very important aquatic fish that faces the risk of infection with the bacterial pathogen Photobacterium damselae ssp. piscicida, and there are few protective approaches available that use multiple antigens. In the present study, potent bivalent antigens from P. damselae ssp. piscicida showed more efficient protection than did single antigens used in isolation. In preparations of three antigens that included recombinant heat shock protein 60 (rHSP60), recombinant α-enolase (rENOLASE) and recombinant glyceraldehyde-3-phosphate dehydrogenase (rGAPDH), we analysed the doses that elicited the best immune responses and found that this occurred at a total of 30 µg of antigen per fish. Subsequently, vaccination of fish with rHSP60, rENOLASE and rGAPDH achieved 46.9, 52 and 25% relative per cent survival (RPS), respectively. In addition, bivalent subunit vaccines--combination I (rHSP60 + rENOLASE), combination II (rENOLASE + rGAPDH) and combination III (rHSP60 + rGAPDH)--were administered and the RPS in these groups (65.6, 64.0 and 48.4%, respectively), was higher than that achieved with single-antigen administration. Finally, in combination IV, the trivalent vaccine rHSP60 + rENOLASE + rGAPDH, the RPS was 1.6%. Taken together, our results suggest that combinations of two antigens may achieve a better efficiency than monovalent or trivalent antigens, and this may provide new insights into pathogen prevention strategies.


Asunto(s)
Antígenos Bacterianos/inmunología , Vacunas Bacterianas/inmunología , Enfermedades de los Peces/prevención & control , Infecciones por Bacterias Gramnegativas/veterinaria , Perciformes/microbiología , Photobacterium/inmunología , Vacunación/veterinaria , Animales , Anticuerpos Antibacterianos/sangre , Ensayo de Inmunoadsorción Enzimática/veterinaria , Enfermedades de los Peces/mortalidad , Infecciones por Bacterias Gramnegativas/mortalidad , Infecciones por Bacterias Gramnegativas/prevención & control , Distribución Aleatoria , Análisis de Supervivencia , Factores de Tiempo , Vacunación/normas
2.
Dev Biol (Basel) ; 121: 175-80, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-15962480

RESUMEN

Oral vaccination is considered as the most desirable method for immunizing fish because it is non-stressful, user-friendly and is capable of easy administration to large numbers of fish. However, many publications have indicated that the current oral vaccines still lack the desired efficacy. Here we reported on an oral vaccine method to deliver recombinant subunit vaccine based on the food chain of fish, in that live Artemia nauplii are encapsulated with recombinant bacteria containing the antigen. The feasibility and efficacy of this method for delivering protein antigen was tested in a zebrafish model, where immunisation took place through feeding Artemia encapsulated with recombinant E. coli. By this oral vaccine method the antigen could be delivered to the hindgut as confirmed by immuno-histochemistry, and its efficacy was demonstrated by the ability to protect vaccinated fish significantly from a direct injection of a native Pseudomonas exotoxin and bacterial pathogen. Combined with the recombinant technology for producing desired protein antigens, this oral vaccine delivery method provides the capacity to deliver a variety of different antigens, including the option for delivery of multivalent vaccines by the oral route.


Asunto(s)
Acuicultura/métodos , Vacunas Bacterianas/administración & dosificación , Sistemas de Liberación de Medicamentos/métodos , Administración Oral , Animales , Antígenos Bacterianos/metabolismo , Artemia/metabolismo , Vacunas Bacterianas/metabolismo , Escherichia coli/genética , Escherichia coli/metabolismo , Inmunohistoquímica , Intestinos/anatomía & histología , Vacunas de Subunidad/administración & dosificación , Vacunas de Subunidad/metabolismo , Vacunas Sintéticas/administración & dosificación , Vacunas Sintéticas/metabolismo , Pez Cebra
3.
Zoonoses Public Health ; 57(7-8): e95-101, 2010 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-19968850

RESUMEN

The first case of Q fever in Taiwan was reported in 1993. The disease is considered to be emerging in Taiwan, but the route of transmission has remained unclear. The annual number of confirmed Q fever cases has been increasing up to more than 100 cases since 2005, comparing with less than 30 before 2003. The purpose of this study was to determine the seroprevalence and risk factors of Coxiella burnetii infection in veterinary-associated populations in southern Taiwan. A total of 228 serum samples of high risk individuals engaging in veterinary-related work or animal-farm work, were collected between March and June in 2007. The study individuals were interviewed by a structured questionnaire designed for Q fever investigation. Serum samples from different animal species were also obtained for Q fever analysis in the same study areas. Serological test was conducted by indirect immunofluorescence antibody assay (IFA). The result demonstrated the overall seroprevalence of Q fever was 26.3% in individuals engaging in veterinary and animal-related work in southern Taiwan. After multiple logistic regression analysis, goat exposure was significantly associated with seropositivity of Q fever in the study population in southern Taiwan (adjusted odds ratio: 2.62; 95% CI: 1.06-6.46). In addition, the highest seroprevalence (43.8%) of Q fever was identified in goats (P < 0.05). Finally, this study documented that people with prior knowledge of Q fever were less likely to be seropositive for C. burnetii. It was concluded that goat exposure was the most important risk factor associated with C. burnetii infection and appropriate health education could be useful to prevent high risk individuals from the infection in southern Taiwan.


Asunto(s)
Animales Domésticos/microbiología , Anticuerpos Antibacterianos/sangre , Coxiella burnetii/inmunología , Enfermedades Profesionales/epidemiología , Fiebre Q/epidemiología , Enfermedades de los Animales/epidemiología , Enfermedades de los Animales/microbiología , Animales , Coxiella burnetii/aislamiento & purificación , Técnica del Anticuerpo Fluorescente Indirecta , Modelos Logísticos , Enfermedades Profesionales/microbiología , Fiebre Q/diagnóstico , Fiebre Q/microbiología , Fiebre Q/transmisión , Factores de Riesgo , Estudios Seroepidemiológicos , Encuestas y Cuestionarios , Taiwán/epidemiología , Veterinarios
4.
J Appl Microbiol ; 95(6): 1375-80, 2003.
Artículo en Inglés | MEDLINE | ID: mdl-14633013

RESUMEN

AIMS: To detect Photobacterium damselae ssp. piscicida using the PCR technique and plating method. METHODS AND RESULTS: Two strains of P. damselae ssp. piscicida were isolated from cultured cobia (Rachycentron canadum) at two different fish farms in Taiwan. A pair of primers was designed to detect the capsular polysaccharide gene of P. damselae ssp. piscicida by PCR. Reference strains of different genus and different clinical strains were used for this study. The expected product (410 bp) was obtained from both P. damselae ssp. piscicida and P. damselae ssp. damselae, and they were differentiated by culturing on thiosulphate citrate bile salts-sucrose agar (TCBS-1). Photobacterium damselae ssp. damselae grew on TCBS-1 producing green colonies whereas P. damselae ssp. piscicida did not grow. CONCLUSIONS: The methods used are cost and labour effective when compared with the other methods and commercially available kits. SIGNIFICANCE AND IMPACT OF THE STUDY: This work provides an integrated set of methods to identify the species P. damselae and to differentiate P. damselae ssp. piscicida from P. damselae ssp. damselae.


Asunto(s)
Enfermedades de los Peces/diagnóstico , Infecciones por Bacterias Gramnegativas/veterinaria , Photobacterium/aislamiento & purificación , Animales , Acuicultura , Técnicas de Tipificación Bacteriana/métodos , Secuencia de Bases , ADN Bacteriano/genética , Peces/microbiología , Infecciones por Bacterias Gramnegativas/diagnóstico , Datos de Secuencia Molecular , Photobacterium/clasificación , Photobacterium/genética , Reacción en Cadena de la Polimerasa/métodos
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA