A vast microbial community inhabits in the rhizosphere, among which, specialized bacteria known as Plant Growth-Promoting Rhizobacteria (PGPR) confer benefits to host plants including growth promotion and disease suppression. PGPR taxa vary in the ways whereby they curtail the negative effects of invading plant pathogens. However, a cumulative or synergistic effect does not always ensue when a bacterial consortium is used. In this review, we reassess the disease-suppressive mechanisms of PGPR and present explanations and illustrations for functional diversity and/or stability among PGPR taxa regarding these mechanisms. We also provide evidence of benefits when PGPR mixtures, rather than individuals, are used for protecting crops from various diseases, and underscore the critical determinant factors for successful use of PGPR mixtures. Then, we evaluate the challenges of and limitations to achieving the desired outcomes from strain/species-rich bacterial assemblages, particularly in relation to their role for plant disease management. In addition, towards locating additive or synergistic outcomes, we highlight why and how the benefits conferred need to be categorized and quantified when different strains/species of PGPR are used in combinations. Finally, we highlight the critical approaches needed for developing PGPR mixtures with improved efficacy and stability as biocontrols for utilization in agricultural fields.

Salt stress inhibits photosynthetic process and triggers excessive formation of reactive oxygen species (ROS). This study examined the role of arbuscular mycorrhizal (AM) association in regulating photosynthetic capacity and antioxidant activity in leaves of two maize genotypes (salt-tolerant JD52 and salt-sensitive FSY1) exposed to salt stress (100 mM NaCl) in soils for 21 days. The leaf water content, chlorophyll content, and photosynthetic capacity in non-mycorrhizal (NM) plants were decreased by salt stress, especially in FSY1, with less reduction in AM plants than NM plants. Salinity increased the activities of antioxidant enzymes (superoxide dismutase (SOD), catalase (CAT), ascorbate peroxidase (APX), and glutathione reductase (GR)) in both genotypes regardless of AM inoculation, but decreased the contents of non-enzymatic antioxidants (reduced glutathione (GSH) and ascorbate (AsA)), especially in FSY1, with less decrease in AM plants than NM plants. The AM plants, especially JD52, maintained higher photosynthetic capacity, CO₂ fixation efficiency, and ability to preserve membrane integrity than NM plants under salt stress, as also indicated by the higher antioxidant contents and lower malondialdehyde (MDA)/electrolyte leakage in leaves. To conclude, the higher salt tolerance in AM plants correlates with the alleviation of salinity-induced oxidative stress and membrane damage, and the better performance of photosynthesis could have also contributed to this effect through reduced ROS formation. The greater improvements in photosynthetic processes and antioxidant defense systems by AM fungi in FSY1 than JD52 under salinity demonstrate genotypic variation in antioxidant defenses for mycorrhizal amelioration of salt stress.