Rice straw was divided into moist straw, soaked straw for 24 h without pasteurization and soaked for 24 h and pasteurized at 100 °C/1 h, and all of them were inoculated with different microbial inoculants.
Figure 2A-C depicts the time difference of E. coli PR02 cultures that were inoculated with different replication tools.
704) seeds were planted in each pot and were inoculated with different AM treatments including control (M1), Iranian Glomus mosseae (M2), Iranian G. etunicatum (M3), and Canadian G. mosseae, received from GINCO (Glomales In Vitro Collection), Canada (M4).
The bark and sapwood of Pinus radiata log segments were inoculated with different propagules to see if logs could be colonised and so potentially act as carriers of Phytophthora species.
To analyze this hypothesis wt and C57BL/6Je/e mice were inoculated with different concentrations of B16-melanoma cells.
Ten-day-old sterile in vitro grown cauliflower plantlets were inoculated with different Rhizoctonia AGs.
At ∼3 weeks post agro-infiltration, plants were inoculated with different pathogens and disease was investigated as described above.
To ascertain whether the expression of other COPTs was also response to pathogen infection, rice plants were inoculated with different Xoo strains.
Blood agar, chocolate agar, and Mueller-Hinton agar plates (Beijing Laboratory Biology Technology of China, Beijing, China) were inoculated with different bacterial species and incubated at 37°C for 12 16 h.
Twelve-day-old embryonated special pathogen free (SPF) chicken eggs procured from Venkatershwara Hatcheries, Pune were inoculated with different dilutions (200 μl/egg) of CHPV (n = 4 per dilution) through the allantoic route and incubated at 37°C with 90% humidity and observed for 48 hr.
