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1.
Pol J Vet Sci ; 19(3): 627-632, 2016 Sep 01.
Artículo en Inglés | MEDLINE | ID: mdl-27760034

RESUMEN

The aim of this study was to use matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) for the identification of coagulase-negative staphylococci (CNS) isolated from the milk of cows with subclinical mastitis. The study material consisted of 33 isolates of CNS, identified by the results of API Staph tests, obtained from the milk of cows with subclinical mastitis. Based on the spectra analyses, MALDI-TOF MS tests of 33 bacterial samples allowed identification of the microorganisms in 27 cases (81.8%). The most frequent cause of subclinical mastitis was found to be Staphylococcus sciuri (39%), while S. vitulinus was detected in 15% of the milk samples. The results obtained indicate that MALDI-TOF MS can be used for the identification of CNS isolated from bovine mastitis as a method supplementary to biochemical tests.


Asunto(s)
Mastitis Bovina/microbiología , Espectrometría de Masa por Láser de Matriz Asistida de Ionización Desorción/métodos , Infecciones Estafilocócicas/veterinaria , Staphylococcus/clasificación , Staphylococcus/aislamiento & purificación , Animales , Bovinos , Femenino , Mastitis Bovina/diagnóstico , Leche/microbiología , Filogenia , Espectrometría de Masa por Láser de Matriz Asistida de Ionización Desorción/veterinaria , Infecciones Estafilocócicas/microbiología , Staphylococcus/enzimología , Staphylococcus/genética
2.
Pol J Vet Sci ; 18(3): 573-7, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26618590

RESUMEN

In this study, we used PCR to detect and characterize B. canis from naturally infected dogs in Poland with subclinical babesiosis by amplifying and sequencing a portion of the 18S ribosomal RNA (rRNA) gene. Venous blood samples were collected from ten dogs with subclinical babesiosis. A 559-bp fragment of the B. canis 18S rRNA gene was amplified by PCR. Sequencing of the PCR products led to the identification of a new variant of Babesia canis, differing from the previously detected protozoa genotypes (18S rRNA-A and 18S rRNA-B) with nucleotide substitutions in positions 150 and 151 of the tested gene fragment. The results indicate the emergence within the Polish territory of a new, previously unencountered Babesia canis genotype responsible for the development of subclinical babesiosis.


Asunto(s)
Babesia/genética , Babesiosis/parasitología , Enfermedades de los Perros/parasitología , ARN Protozoario/genética , ARN Ribosómico 18S/genética , Animales , Babesia/clasificación , Perros , Femenino , Masculino , Filogenia
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