Colonization ability of Herbaspirillum spp. B501gfp1 in sugarcane, a non-host plant in the presence of indigenous diazotrophic endophytes

Inoculating sugarcane with a mixture of diazotrophic endophytic bacteria has shown that they can provide substantial amount of biologically fixed nitrogen to the plant. The genera of diazotrophic endophytes previously isolated from sugarcane have been reported associating with other nonleguminousplants showing a broad host range. This study examined the colonization ability of a wild rice isolate, Herbaspirillum spp., in sugarcane plants in the presence of indigenous endophytes using two inoculum concentrations (102 and 108 bacterial cells ml-1). Internal tissue colonization was observed in plants inoculated with both the 102 and 108 B501gfp1 bacterial cells ml-1 inoculum concentrations. However, extensive colonization and higher bacterial numbers were determined only in the basal stem tissues of plants inoculated with the 108 bacterial cells ml-1

Establishment and characterization of a low-dose Mycoplasma haemofelis infection model

Hemotropic mycoplasma are small, cell-wall-free bacteria that can infect various mammalian species, including humans. They cannot be cultured in vitro; therefore, animal models play an important role, e.g. for pathogenesis studies. Mycoplasma haemofelis (Mhf) is the most pathogenic of the three feline hemotropic mycoplasma species; it is known to induce severe hemolytic anemia in infected cats. The aims of this study were to establish and characterize a low-dose Mhf transmission model. Five specified pathogen-free cats were subcutaneously exposed to 1000 copies of Mhf per cat corresponding to 0.05 μL of infectious blood with 2×10(7) copies/mL as determined by real-time PCR. All cats became PCR-positive within 34 days post-exposure and reached a maximum blood Mhf load of 10(9) copies/mL, similar to previously reported high-dose infections. In a selected sample of modified Wright-stained blood smears, small epicellular coccoid structures on the surface of the red blood cells were identified by light microscopy. Additionally, using an Mhf rDnaK ELISA, seroconversion was demonstrated in all cats within 4-5 weeks after Mhf exposure. Four out of five cats developed anemia. While three cats showed only mild clinical signs of hemoplasmosis, one cat developed severe anemia and required antibiotic treatment. Our study demonstrated that minimal contact with Mhf infectious blood was sufficient for transmission of the infection and the induction of hemoplasmosis. This low-dose Mhf infection might more accurately mirror the natural route of infection, i.e., by arthropod vectors or aggressive interaction among cats. We therefore recommend this protocol for use in future animal model studies