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1.
Pol J Vet Sci ; 17(4): 713-5, 2014.
Article in English | MEDLINE | ID: mdl-25638986

ABSTRACT

The aim of the present study was to investigate the occurrence of Borrelia burgdorferi sensu lato DNA in a group of 120 wild bison (Bison bonasus) from the Bialowieza Primeval Forest in eastern Poland. The PCR technique revealed the presence of 16S RNA of Borrelia burgdorferi sensu lato in the blood of 16 out of 120 examined animals. DNA amplification by means of primers SC1 and SC2 gave a product with a size of 300-bp. The sequences of the PCR products obtained showed 100% homology with each other and 100% homology with B. burgdorferi s.1. 16S RNA gene DQ111061. Results of this study suggest that wild bison are important in maintaining agents of Lyme borreliosis, and that studies of reservoir competence of this species are indicated.


Subject(s)
Bison/blood , Borrelia burgdorferi Group/isolation & purification , Lyme Disease/veterinary , Animals , Animals, Wild , Borrelia burgdorferi Group/genetics , DNA, Bacterial/genetics , Lyme Disease/blood , Lyme Disease/epidemiology , Lyme Disease/microbiology , Poland/epidemiology
2.
Pol J Vet Sci ; 16(3): 587-92, 2013.
Article in English | MEDLINE | ID: mdl-24195300

ABSTRACT

Proteomics including the studies of the structure, function and dependences between proteins is more and more extensively applied in human medicine and veterinary medicine. The analysis of protein profiles of tissues and body fluid from healthy and ill individuals allows to identify diagnostic, prognostic and predictive markers in various pathological states in people and animals. This paper presents preparation of urine samples for analysis in the mass spectrometer MALDI-TOF (Ultraflextreme, Bruker, Bremen, Germany) by means of two methods: liquid chromatography based on the system Nano-LC (PROTEINER FC II, Bruker Daltonics, Bremen Germany). and two-direction electrophoresis 2DE (GE Healthcare, United Kingdom). Both methods enable separation of the mixture under consideration into individual fractions of high purity indispensable for obtaining readable mass spectra. The purpose of this paper is to determine applicability of these methods in analysis of protein composition of urine samples.


Subject(s)
Chromatography, Liquid/veterinary , Electrophoresis, Gel, Two-Dimensional/veterinary , Proteomics/methods , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/veterinary , Urine/chemistry , Animals , Humans
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