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  • Genetic modification, characterization, and co-infection of Franken Sphingomonas and Anaplasma phagocytophilum in tick cells.

Genetic modification, characterization, and co-infection of Franken Sphingomonas and Anaplasma phagocytophilum in tick cells.

STAR protocols (2023-09-11)
Lorena Mazuecos, Almudena González-García, José de la Fuente
ZUSAMMENFASSUNG

Paratransgenesis through genetic manipulation of symbiotic or commensal microorganisms has been proposed as an effective and environmentally sound approach for the control of vector-borne diseases, including tick bite-related pathologies, and reducing pathogen transmission. Here, we present a protocol for Sphingomonas transformation with Anaplasma phagocytophilum major surface protein 4 and heat shock protein 70. We describe a step-by-step protocol for in vitro study of interactions between transformed Franken Sphingomonas and Ixodes scapularis ISE6 tick cells during A. phagocytophilum infection. For complete details on the use and execution of this protocol, please refer to Mazuecos et al. (2023).1.

MATERIALIEN
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Produktbeschreibung

Sigma-Aldrich
Natriumselenit, BioReagent, suitable for cell culture, ≥98%
Sigma-Aldrich
Anti-Kaninchen-IgG (Gesamtmolekül)-FITC in Ziege hergestellte Antikörper, affinity isolated antibody, buffered aqueous solution
Sigma-Aldrich
Monoclonal Anti-Heat Shock Protein 70 antibody produced in mouse, clone BRM-22, ascites fluid
Sigma-Aldrich
Anti-Maus-IgG (Gesamtmolekül) – FITC in Ziege hergestellte Antikörper, affinity isolated antibody, buffered aqueous solution
Sigma-Aldrich
HRP-conjugated Anti-Rabbit IgG Concentrate (Item I1)
Sigma-Aldrich
Rabbit Anti-Goat IgG Antibody, FITC conjugate, Chemicon®, from rabbit