Résumé
Functional soil microbial communities, including phosphate solubilizing bacteria (PSB), are known for their ability to enhance P availability along with additional properties such as the immobilization of trace elements like cadmium (Cd). Bacterial P solubilization and tolerance to Cd are important biological processes that might occur simultaneously with positive influence on plant growth, thus physiological mechanisms controlling both processes need to be deciphered. This interplay was investigated in three PSB isolates (Bacillus siamensis "B. Siam", Rahnella aceris “R. Acer” and Bacillus cereus “B. Cer”) and their consortium (PSBCs) with contrasting P solubilizing capacities (high-medium-low), through bacterial culture-based and plant inoculation experiments under increasing Cd concentrations and low P availability conditions (Tri-calcium P “TCP” and Rock P “RP”). Results show that PSB, particularly R. Acer and PSBCs, significantly increased P bioavailability (from TCP) under increasing Cd2+ concentrations (33 ppm “Cd33”, 67 ppm “Cd67”, 134 ppm “Cd134” and 201 ppm “Cd201”). The enhanced bioavailable P strongly correlated (B. Siam and PSBCs) with Cd bioaccumulation capacity, phosphatase enzyme activity, and organic acids (OA) production. Co-application of RP and PSB inoculation under Cd2+ stress (Cd8 and Cd16) improved wheat seedling root growth, P acquisition, and root hairs density in the piliferous zone and root cap. Moreover, inoculation with B. Cer significantly improved root inorganic P (Pi) (384 and 752%) and root acid phosphatases (176 and 131%) under Cd8 and Cd16 compared to uninoculated Cd-stressed seedlings. Such a beneficial root adaptation mechanism could be explained by the significant correlations (mainly under Cd16) between Pi content and morphological traits of wheat roots. Findings from this study demonstrate that P solubilization and Cd tolerance are likely interconnected rhizosphere processes triggered by inoculation that presumably induced the elongation of root hairs and likely the rigidity of the root cell wall to reduce Cd entrance while increasing P acquisition