Vignette d'image

Pfister, Kurt

Nom
Pfister, Kurt
Affiliation principale
Fonction
Ancien.ne collaborateur.trice
Identifiants
https://libra.unine.ch/handle/123456789/345
_
0000-0002-8443-1726

Résultat de la recherche

Filtres

1
1
1
1
Réinitialiser les filtres

Paramètres

Voici les éléments 1 - 1 sur 1
  • Publication
    Accès libre
    Analysis of "Anaplasma marginale" strains grown "in vitro"
    (2015)
    Lis, Katarzyna
    ;
    Pfister, Kurt 
    Anaplasma marginale is a tick-borne pathogen that affects ruminants worldwide, causing a disease called anaplasmosis. The disease is endemic in tropical and subtropical regions of the New World, Europe, Africa, Asia and Australia where it causes large economic losses in the cattle industry.
    A. marginale is an obligatory intracellular bacterium that multiplies only within tick cells or ruminants' erythrocytes. Many differences among A. marginale strains have emerged, which were probably driven by continuous exposure to different host immune systems during the transition of bacteria between ticks and vertebrates. The vast majority of studies aiming at elucidating differences between strains were conducted on the genomic level, and little is known about protein expression. Thus, this thesis investigates differences in protein regulation among A. marginale strains.
    A. marginale cultivated in vitro are in general an excellent source of organisms for experimentation. Furthermore, culture-derived organisms offer an alternative to the use of experimental animals.
    Many studies require intracellular organisms free from host cell debris. Therefore the use of Percoll gradients for the separation of A. marginale was evaluated. Bacteria isolated in this way contained only minimal amounts of IDE8 cell stroma but most importantly they retained their viability. A. marginale purified this way can be used directly for proteomic studies or for vaccination trials.
    In this thesis three geographical A. marginale strains grown in vitro have been partially characterized by gene and serological analyses. The differences on the proteomic level have been assessed by the 2D-DIGE technique, indicating that many antigenic membrane proteins are differentially regulated among the strains examined. Some of these proteins are also known to be virulence-associated.
    Increasing the number of strains in continuous in vitro cultivation, and improving purification methods for rickettsia, allow researchers to investigate differences in protein expression between A. marginale strains, and therefore identify proteins which could be incorporated into an improved vaccine against anaplasmosis.