Argania spinosa is among the most important species of the Moroccan forest in terms of ecological, environmental, and socio-economic aspects. However, it faces a delicate balance between regeneration and degradation in its natural habitat. Hence, the efforts to preserve and regenerate argan forests are crucial for biodiversity, soil quality, and local livelihoods, yet they face challenges like overgrazing and climate change. Sustainable management practices, including reforestation and community engagement, are vital for mitigating degradation. Similarly, exploiting the argan tree’s rhizosphere can enhance soil quality by leveraging its rich microbial diversity. This approach not only improves crop growth but also maintains ecosystem balance, ultimately benefiting both agriculture and the environment. This enrichment can be achieved by different factors: mycorrhizae, plant extracts, algae extracts, and plant growth-promoting rhizobacteria (PGPR). The benefits provided by PGPR may include increased nutrient availability, phytohormone production, shoot, root development, protection against several plant pathogens, and disease reduction. In this study, the effect of rhizobacteria isolated from the Agran rhizosphere was evaluated on germination percentage and radicle length for Argania spinosa in vitro tests, growth, collar diameter, and branching number under greenhouse conditions. One hundred and twenty (120) bacteria were isolated from the argan rhizosphere and evaluated for their capacity for phosphate solubilization and indole acetic acid production. The results showed that 52 isolates could solubilize phosphorus, with the diameters of the solubilization halos varying from 0.56 ± 0.14 to 2.9 ± 0.08 cm. Among 52 isolates, 25 were found to be positive for indole acetic acid production. These 25 isolates were first tested on maize growth to select the most performant ones. The results showed that 14 isolates from 25 tested stimulated maize growth significantly, and 3 of them by 28% (CN005, CN006, and CN009) compared to the control. Eight isolates (CN005, CN006, CN004, CN007, CN008, CN009, CN010, and CN011) that showed plant growth of more than 19% were selected to evaluate their effect on argan germination rate and radicle length and were subjected to DNA extraction and conventional Sanger sequencing. The 8 selected isolates were identified as: Brevundimonas naejangsanensis sp2, Alcaligenes faecalis, Brevundimonas naejangsanensis sp3, Brevundimonas naejangsanensis sp4, Leucobacter aridicollis sp1, Leucobacter aridicollis sp2, Brevundimonas naejangsanensis sp1, and Staphylococcus saprophyticus. The results showed that Leucobacter aridicollis sp2 significantly increased the germination rate by 95.83%, and the radicle length with a value of 2.71 cm compared to the control (1.60 cm), followed by Brevundimonas naejangsanensis sp3 and Leucobacter aridicollis sp1 (2.42 cm and 2.11 cm, respectively). Under greenhouse conditions, the results showed that the height growth increased significantly for Leucobacter aridicollis sp1 (42.07%) and Leucobacter aridicollis sp2 (39.99%). The isolates Brevundimonas naejangsanensis sp3 and Leucobacter aridicollis sp1 increased the gain of collar diameter by 41.56 and 41.21%, respectively, followed by Leucobacter aridicollis sp2 and Staphyloccocus saprophyticus (38.68 and 22.79%). Leucobacter aridicollis sp1 increased the ramification number per plant to 12 compared to the control, which had 6 ramifications per plant. The use of these isolates represents a viable alternative in sustainable agriculture by improving the germination rate and root development of the argan tree, as well as its development, while increasing the availability of nutrients in the soil and consequently improving fertilization.

Green mold, caused by Penicillium digitatum, is a serious disease of citrus fruit during postharvest. The focus of this study was to evaluate possible biological alternatives to chemical fungicides for P. digitatum control. Four Pseudomonas isolates (Q110B, Q125B, Q112B, and Q004B) were isolated from rhizospheric soil and evaluated for their antagonistic activity against P. digitatum. The in vitro evaluations of these isolates by dual culture revealed an important zone of inhibition after 3 days of incubation at 25 ± 2°C. The Q004B isolate provided a high zone of inhibition in vitro at 45 mm diameter. Four Pseudomonas isolates tested showed antagonistic activity against P. digitatum on orange fruit after 7 days of inoculation under postharvest conditions. Inhibition percentage of P. digitatum on orange fruit ranged from 22 to 85% for Q004B and Q112B, respectively. Regarding the mechanism of action, the four tested isolates produced volatile compounds in vitro with inhibition percentage ranging from 35% to 79%, respectively for Q004B andQ125B. The Q004B isolate caused a high spore inhibition rate of 46%, while Q110B had no effect on spore germination. The four isolates of Pseudomonas produced siderophores in CAS medium. Additionally, Q125B, Q112B, and Q004B showed a positive chitinolytic activity, whereas Q110B provided negative results to the chitinase assay. These isolates represent potential candidates for biological control of citrus green mold and may be effectively used as a sustainable alternative measure to chemical fungicide control.

The argane tree (Argania spinosa L.) is a mostly self-incompatible species that must be cross-pollination. However, the cross-pollination is often insufficient to obtain a desirable fruit yield in the absence of compatibility between the orchard’s argane trees. Proper pollination design is therefore essential to ensure a supply of compatible pollen. In this study, pollen germination and pollen development following cross- and self-pollination were investigated in A. spinosa. The choice of compatible parents or a pollinizer is currently a new research topic for the production of argane fruits in the framework of argane farming programs. Different pollination experiments were designed with two main objectives: (i) to study cross/self-(in)compatibility in the argane tree, and (ii) to determine the degree of compatibility between selected superior genotypes for pollination strategies to improve fruit set in argane orchards. Thus, to determine if a pollination deficit exists, experiments were carried out on 14 genotypes, and 5421 flowers served as sampling. The germination rate of pollen was lower than 50% for three genotypes, and only four genotypes bloom twice a year. From cross-pollination trials, traits related to the mother trees, such as the shape of the fruit and fruit ripening duration, are not influenced by the gene flow transmitted by pollens. Self-pollination was very low (0.2%) for both hand- and free self-pollination but the highest fruit set rate observed was 5.3%. Based on the pollen effect study results, it can be concluded that different pollen sources affected the fruit set. Thus, the choice of an efficient pollinizer genotype must be inter-compatible with the main variety, bloom at the same time, and be regular (no alternation). This is the first time that a pollinizer tree was reported and studied for argane. To meet future argane farming requirements, the number and location of compatible pollinizers is very important in the argane orchard design. This design of pollination remains to be checked by alternately planting a row of pollinizer trees or inter-rows with main varieties.

The purpose of this study was to investigate the growth-promoting effects of four rhizobacterial isolates (RS60, RS65, RS46, and RP6) isolated from the tomato rhizosphere. These isolates were screened for key plant growth-promoting rhizobacteria (PGPR) mechanisms, including ammonia production, nitrogen fixation, phosphate solubilization, indole-3-acetic acid (IAA) production, and siderophore synthesis. Their potential to enhance seed germination and tomato plant growth was investigated in controlled and greenhouse conditions. Four isolates exhibited multiple PGPR attributes, notably IAA and ammonia production as well as phosphate solubilization. The results revealed that these strains significantly enhanced tomato seed germination and shoot growth in vitro, with RS65 showing the highest germination rate (70%). However, no significant differences in early seedling responses were observed under greenhouse conditions when compared to the control. Thirty days after inoculation, greenhouse results revealed that the four studied strains significantly increased growth metrics including shoot length, number of leaves, collar diameter, and dry weight. The isolate RP6 showed a significant effect on the growth of the plant, with an average shoot length of 34.40 cm and nine leaves per plant. In vitro antagonism assays demonstrated that isolates RS60, RS65, and RP6 effectively inhibited the growth of Botrytis cinerea, Alternaria alternata, and Oidium lycopersici, with inhibition rates exceeding 65%. These antagonistic activities were linked to the production of hydrolytic enzymes (chitinase, cellulase, pectinase, protease), siderophores, and hydrogen cyanide (HCN). Molecular identification through 16S rRNA gene sequencing confirmed the isolates as Bacillus cereus (RS60), Bacillus pumilus (RS46), Bacillus amyloliquefaciens (RP6), and Bacillus velezensis (RS65), each showing over 97% sequence similarity with reference strains. These findings underscore the potential of the selected Bacillus spp. as promising biofertilizers and biocontrol agents for sustainable tomato cultivation and support their inclusion in integrated disease and nutrient management strategies.

In agroecosystems, soil biodiversity is increasingly becoming more recognized as providing benefits to both plants and human health. It performs a wide variety of ecological services beyond the recycling of nutrients to plant growth and manage pests and diseases below the economic injury level. This study investigated the effects of three Pseudomonas isolates (Q172B, Q110B and Q036B), isolated from untreated tomato rhizospheric soil, as a biological control agent of Bemisia tabaci which is a key pest of tomato crops. The study was conducted under laboratory and glasshouse conditions and the water treatment was used as a control. Adult mortality rates were assessed during three days at 24h interval and larva mortality rates were evaluated during six days after treatment at 48h interval. Results indicate that Q036B isolate has a faster effect on B. tabaci adult and larvae. Under laboratory conditions, all three Pseudomonas isolates (Q110B, Q036B and Q172B) have a significant effect on B. tabaci adult mortality compared to control. The earliest and the most important mortality rate of 76% was recorded by Q036B. Two isolates Q036B and Q110B caused a significant mortality on B. tabaci larvae; with highest mortality effect (79%) was observed for Q036B compared to control. However, Q172B has no mortality effects on B. tabaci larvae under laboratory conditions. In glasshouse conditions, only Q036B provided high mortality rates of 91% at 168h after treatment. The results of this study indicate that the Pseudomonas isolate Q036B significantly suppresses B. tabaci in tomato plant and could substitute the excessive use of chemicals. Current research indicates that soil biodiversity could be promising to preserve agro-ecological sustainability.

This study aimed to investigate the biocontrol activity of rhizosphere isolates against late blight disease of tomatoes caused by the fungus Phytophthora infestans. A total of 30 rhizospheric bacterial isolates were evaluated for their antagonistic activity against P. infestans in vitro and in vivo. The results demonstrated that among the 30 isolates tested, six (RS65, RP6, RS47, RS46, RP2, and RS61) exhibited a highly significant inhibitory effect (p < 0.001) on the mycelial growth of P. infestans in vitro, with the inhibition rate exceeding 67%. Among the isolates, RS65 exhibited the highest inhibition rate at 78.48%. For antagonistic mechanisms, the results demonstrated that the six isolates exhibited significant enzymatic activity, including proteolytic, lipolytic, and chitinolytic activity, as well as the production of HCN, cellulase, and pectinase. Isolate RS65, which showed the highest inhibition rate, was further evaluated under greenhouse conditions. This investigation revealed significant differences in the severity of late blight between the control and the RS65 treatment. The control showed a severity level of 31.26%, whereas the RS65 treatment achieved the lowest severity of 16.54%. Molecular identification results indicated that the RS65 isolate (accession numbers PV208381) is a Bacillus genus with 99% proximity to Bacillus velezensis. This finding suggests that the Bacillus RS65 treatment could provide effective protection against P. infestans infection in tomato plants. These findings highlight the potential of Bacillus RS65 as a biocontrol agent in integrated disease management for tomato late blight.