Mycorrhizal Effects on Growth and Expressions of Stress-Responsive Genes (aquaporins and SOSs) of Tomato under Salt Stress

Environmentally friendly arbuscular mycorrhizal fungi (AMF) in the soil can alleviate host damage from abiotic stresses, but the underlying mechanisms are unclear. The objective of this study was to analyze the effects of an arbuscular mycorrhizal fungus, Paraglomus occultum, on plant growth, nitrogen balance index, and expressions of salt overly sensitive genes (SOSs), plasma membrane intrinsic protein genes (PIPs), and tonoplast intrinsic protein genes (TIPs) in leaves of tomato (Solanum lycopersicum L. var. Huapiqiu) seedlings grown in 0 and 150 mM NaCl stress. NaCl stress severely inhibited plant growth, but P. occultum inoculation significantly improved plant growth. NaCl stress also suppressed the chlorophyll index, accompanied by an increase in the flavonoid index, whereas inoculation with AMF significantly promoted the chlorophyll index as well as reduced the flavonoid index under NaCl conditions, thus leading to an increase in the nitrogen balance index in inoculated plants. NaCl stress regulated the expression of SlPIP1 and SlPIP2 genes in leaves, and five SlPIPs genes were up-regulated after P. occultum colonization under NaCl stress, along with the down-regulation of only SlPIP1;2. Both NaCl stress and P. occultum inoculation induced diverse expression patterns in SlTIPs, coupled with a greater number of up-regulated TIPs in inoculated versus uninoculated plants under NaCl stress. NaCl stress up-regulated SlSOS2 expressions of mycorrhizal and non-mycorrhizal plants, while P. occultum significantly up-regulated SlSOS1 expressions by 1.13- and 0.45-fold under non-NaCl and NaCl conditions, respectively. It was concluded that P. occultum inoculation enhanced the salt tolerance of the tomato, associated with the nutrient status and stress-responsive gene (aquaporins and SOS1) expressions.


Introduction
The greenhouse cultivation of horticultural crops has become a major mode, but irrational irrigation, the excessive application of fertilizers, and poor air mobility tend to cause salt accumulation and soil secondary salinization, leading to a decrease in the yield and quality of horticultural crops [1]. Therefore, soil secondary salinization has become a major factor in the occurrence of successive cropping obstacles in greenhouse horticultural crops [2]. The tomato is a worldwide important vegetable crop with a global annual production of nearly 1.78 × 10 8 tons, and China ranks first in the world in terms of tomato cultivation areas and production [3]. Of the 1.1 million hectares of tomatoes grown in China, greenhouse tomatoes account for 58% [3]. In addition, cultivated tomatoes are moderately sensitive to soil salt levels and irrigation water [4]. As a result, it is key to find suitable methods to improve the salt tolerance of tomatoes under greenhouse conditions. A class of beneficial fungi, arbuscular mycorrhizal fungi (AMF), exists around tomato roots [5], where they colonize roots and establish a mutualistic symbiosis that provides nutrients and water to the host tomato, thus promoting plant growth, yield, and fruit quality [6][7][8].
The presence of arbuscular mycorrhizae in tomato roots has been known to enhance the resistance of the tomato to biotic and abiotic stresses, including salt stress [9][10][11]. In the tomato, AMF mainly induces ion balance, photo-chemistry, and an antioxidant defense system in response to salt stress [12,13], while the underlying mechanism is not yet understood. Under salt stress, mycorrhizal fungal colonization dramatically elevates biomass production, reduces shoot Na + concentrations, and does not alter shoot K + concentrations of the tomato [9]. The change in Na + and K + concentrations is associated with the Na + /H + antiporter salt overly sensitive 1 (SOS1) gene, coupled with the synergistic effect of SOS2 and SOS3 [14]. There is no information on whether and how SOS genes of tomatoes respond to AMF colonization under salt stress.
Salt-stressed tomatoes represent higher leaf water potential and root hydraulic conductance under mycorrhizated versus non-mycorrhizated conditions [15]. Changes in water potential under salt stress are associated with expressions of aquaporins (AQPs), especially plasma membrane intrinsic proteins genes (PIPs) and tonoplast intrinsic proteins genes (TIPs) [16,17]. He et al. [15] also reported the down-regulation of a TIP gene and two PIP genes in a tomato under salt stress, accompanied by the up-regulation of only SlAQP2. In fact, in the Genome-Wide of tomatoes, Reuscher et al. [18] identified 47 AQPs, including 14 homologs in the PIP family and 11 homologs in the TIP family. The study of a single or small amount of AQP gene expression could not reveal the regulation effect of mycorrhizal fungi on host AQPs.
The objective of this study was to evaluate the effects of AMF on the growth, physiological activities, and the expression of stress-responsive genes (SOSs, TIPs, and PIPs) in tomato seedlings under salt and non-salt stress, which was expected to reveal the molecular mechanism of the salt tolerance of mycorrhizal tomato plants.

Preparation of Mycorrhizal Inoculums
An arbuscular mycorrhizal fungus used in this study was Paraglomus occultum, which was isolated from peach trees grown in saline soils (pH 8.15, organic carbon 8.5 g/kg, Olsen-P 9.81 mg/kg, and total P 59 mg/kg) in Beijing, identified at the morphological level, and kept in our laboratory [19]. The chlamydospores of P. occultum were solitary in the soil and (65−)75−100(−140) µm in diameter, or a few existed on the tip of the mycelium; the spore shape was globose or subglobose, with no auxiliary cells; the spore wall had two layers, 2.5 µm, all colorless and transparent; in Melzer's reagent, the spores were orange [19]. In addition to morphological recognition, this fungus was also identified at the molecular level by Wang et al. [20] using the cad 5.1 primer (5 -GAAGTCTGTCGCAGTCTG-3 ). The fungus had been preserved in the Bank of Glomeromycota in China (BGC), and its number was BGC BJ04B. The fungus was propagated in potted white clover (Trifolium repens L. var. Olwen) for approximately 10 weeks, and the root segments and potting substrates were collected as mycorrhizal inoculums, in which spore density was 15 spores per g inoculum.

Plant Culture and Salt and AMF Treatments
Tomato (S. lycopersicum L. var. Huapiqiu) seeds from Hezhiyuan Seed Industry Co., Ltd. (Weifang, China) were surface-sterilized in 75% ethanol and sown into 32-hole trays containing an autoclaved mixture of perlite, vermiculite, and peat with an environment of 28 • C/20 • C (day/night temperature, 16 h/8 h) and 80% relative humidity. After 20 days, the tomato seedlings were transplanted into pots containing 1.9 kg of an autoclaved mixture of soil and sand (3:1, v/v). After autoclaving (121 • C, 0.11 MPa, 2 h), the mixture properties were as follows: pH 6.0, 27.5 cmol/kg of cation exchange capacity, 41.9 mg/kg of NH 4 + -N, 74.3 mg/kg of NO 3 − -N, 0.50 g/kg of available K, and 46.2 mg/kg of Olsen-P. The sand was less than 0.5 mm in diameter, with 68% of SiO 2 . Meanwhile, mycorrhizal fungus-inoculated plants received an additional 120 g of P. occultum inoculums containing approximately 1800 spores, while uninoculated plants received the same amount of autoclaved P. occultum inoculums plus 2 mL of filtrate (25 µm) of the same weight of inoculums that had not been autoclaved, in order to re-establish the background microflora. The filtrate was applied into the rhizosphere of potted seedlings. Therefore, there was a total of 2.02 kg of materials in each pot, evenly distributed. These inoculated plants were then placed in a greenhouse for growth with a photosynthetic photon density of 900 µmol/m 2 /s, a day/night temperature of 28 • C/20 • C (16 h/8 h), and a relative air humidity of 70%. Potted soil water was controlled daily at 75% of the maximum soil water holding capacity. After one month, inoculated and uninoculated plants were subjected to 0 and 150 mM NaCl treatments. The concentration of 150 mM NaCl was achieved with gradual increases in a gradient of 50 mM NaCl per day to avoid salt shock. For the salt treatment, 100 mL of the set salt concentration was watered per pot at an interval of 3 days, maintaining a total of 10 irrigations. Then, all treated plants were harvested. At the end of the experiment, the pH value of the substrate was 8.3. As a result, the experiment included the following four treatments: the tomato plants not inoculated with P. occultum were subjected to 0 mM NaCl (Po − Na − ); the plants inoculated with P. occultum were subjected to 0 mM NaCl (Po + Na − ); the plants not inoculated with P. occultum were subjected to 150 mM NaCl (Po − Na + ); the plants inoculated with P. occultum were subjected to 150 mM NaCl (Po + Na + ). Each treatment was replicated six times and arranged randomly.

Variable Determinations
The potted mixture's pH was determined using the pH meter (Sartorius Scientific Instruments Co., Ltd., Beijing, China). The cation exchange capacity of the substrate was determined by the NH 4 Cl-NH 4 OAc method [21]. The NH 4 + -N, NO 3 − -N, available K, and Olsen-P levels of the substrate were measured with a Soil Fertilizer Nutrient Tester (HM-TYD; Shandong Hengmei Electronic Technology Co., Ltd., Weifang, China) according to the user's guidelines.
On the day of the harvest, plant height and stem diameter were measured directly, and then the chlorophyll index (Chi), flavonoids index (Flav), and nitrogen balance index (Nbi) (the ratio of Chi to Flav) were measured by a portable plant polyphenol-chlorophyll apparatus (Dualex Scientific+, Force-A, Orsay, France).
At harvest, the biomass of the whole plant was weighed. The roots were scanned with the Flatbed Scanner (V700, EPSON), along with the analysis of root length, surface area, and volume by the WinRHIZO pro software (2007c) (Regent Instruments Inc., Quebec city, Canada).
The 1-2 cm long root segments were collected and stained with trypan blue in lactic acid phenol solution for mycorrhizal staining [22], and then a further microscopic observation was performed. The colonization rate of mycorrhizal fungi in roots was estimated as the percentage of the root segment length colonized by mycorrhizal fungi versus the observed root segment length.
Then, the total RNA of leaf samples was extracted with the EASY spin Plus Plant RNA Rapid Extraction Kit (Aidlab, RN38, Beijing, China) according to the manufacturer's protocol. After testing the integrity and purity of the obtained RNA, the RNA was reversely transcribed into cDNA using the PrimeScript TM RT Reagent Kit with gDNA Eraser (TaKaRa, RR047A, Beijing, China). SlPIP and SlTIP gene sequences were obtained from the Solanaceae Genomics Network (https://solgenomics.net/, accessed on 15 July 2022), and SlSOS1 and SlSOS2 gene sequences were obtained from NCBI (http://github.ncbi, accessed on 15 July 2022). The online tool PrimerQuest TM (http://sg.idtdna.com/primerquest/ Home/Index, accessed on 15 July 2022) was used to design corresponding specific primers (Supplementary Material Table S1). A quantitative real-time PCR analysis was performed using the ChamQ Universal SYBR qPCR Master Mix (Vazyme, Q711) with β-actin as the housekeeping gene. The 2 −∆∆Ct method [23] was used to analyze the relative expression of genes, and the Po − Na − treatment was used for the normalization.

Data Analysis
Sigmaplot 10.0 software was used for plotting. The experimental data were subjected to a one-way ANOVA using SAS 8.0 software, and then further tested for the significance of differences between treatments (p < 0.05) using the Duncan's multiple range test.

Effects of NaCl on Root Colonization of Tomato by P. occultum
No signs of mycorrhizal colonization were observed in tomato roots without P. occultum inoculation, while mycorrhizal fungal colonization was clearly visible in the roots of inoculated plants (Figure 1), with the root colonization rate ranging from 38.6% to 49.1% ( Table 1). The treatment with 150 mM NaCl significantly inhibited the mycorrhizal fungal colonization in roots by 0.21-fold, compared to the 0 mM NaCl treatment. Similar results were observed in trifoliate orange seedlings colonized by Funneliformis mosseae exposed to 100 mM NaCl for 32 days [16]. The decrease in the root mycorrhizal colonization rate in response to NaCl stress may be attributed to the inhibition of spore germination and mycelial growth and the decreased transfer of plant carbohydrates to root mycorrhizae [24]. merquest/Home/Index, accessed on 15 July 2022) was used to design corresponding specific primers (Supplementary Material Table S1). A quantitative real-time PCR analysis was performed using the ChamQ Universal SYBR qPCR Master Mix (Vazyme, Q711) with β-actin as the housekeeping gene. The 2 −ΔΔCt method [23] was used to analyze the relative expression of genes, and the Po − Na − treatment was used for the normalization.

Data Analysis
Sigmaplot 10.0 software was used for plotting. The experimental data were subjected to a one-way ANOVA using SAS 8.0 software, and then further tested for the significance of differences between treatments (p < 0.05) using the Duncan's multiple range test.

Effects of NaCl on Root Colonization of Tomato by P. occultum
No signs of mycorrhizal colonization were observed in tomato roots without P. occultum inoculation, while mycorrhizal fungal colonization was clearly visible in the roots of inoculated plants (Figure 1), with the root colonization rate ranging from 38.6% to 49.1% ( Table 1). The treatment with 150 mM NaCl significantly inhibited the mycorrhizal fungal colonization in roots by 0.21-fold, compared to the 0 mM NaCl treatment. Similar results were observed in trifoliate orange seedlings colonized by Funneliformis mosseae exposed to 100 mM NaCl for 32 days [16]. The decrease in the root mycorrhizal colonization rate in response to NaCl stress may be attributed to the inhibition of spore germination and mycelial growth and the decreased transfer of plant carbohydrates to root mycorrhizae [24].

Effects of P. occultum on Plant Growth of Tomato Exposed to NaCl Stress
In the present study, NaCl stress somewhat inhibited plant growth performance as well as biomass production, especially in plant height and total plant biomass (Table 1). On the other hand, compared with the non-inoculation treatment, P. occultum inoculation also significantly increased the stem diameter and total plant biomass under non-NaCl stress conditions by 20.00% and 48.04%, respectively; P. occultum colonization also significantly increased plant height, stem diameter, and total plant biomass under NaCl stress by 40.51%, 36.84%, and 43.33%, respectively. Similarly, Ait-El-Mokhtar et al. [25] also reported positive effects of a mixture of AMF on the growth parameters of date palm seedlings under 240 mM NaCl stress conditions. The improvement of plant growth by mycorrhization under salt stress implied that mycorrhizal plants have greater adaptability of

Effects of P. occultum on Plant Growth of Tomato Exposed to NaCl Stress
In the present study, NaCl stress somewhat inhibited plant growth performance as well as biomass production, especially in plant height and total plant biomass (Table 1). On the other hand, compared with the non-inoculation treatment, P. occultum inoculation also significantly increased the stem diameter and total plant biomass under non-NaCl stress conditions by 20.00% and 48.04%, respectively; P. occultum colonization also significantly increased plant height, stem diameter, and total plant biomass under NaCl stress by 40.51%, 36.84%, and 43.33%, respectively. Similarly, Ait-El-Mokhtar et al. [25] also reported positive effects of a mixture of AMF on the growth parameters of date palm seedlings under 240 mM NaCl stress conditions. The improvement of plant growth by mycorrhization under salt stress implied that mycorrhizal plants have greater adaptability of salinity than non-mycorrhizal plants, which is partly associated with the mycorrhizal enhancement of plant mineral element acquisition, maintenance of improved ionic balance, and tolerance indicators such as proline [25,26].
3.3. Effects of P. occultum on Index of N Balance, Chlorophyll, and Flavonoids of Tomato Exposed to NaCl Stress It is well-known that when plants are in a healthy state, their chlorophyll content is high, and relatively few polyphenols (flavonoids) are produced at this time; once plants are subjected to nitrogen deficit, chlorophyll synthesis is inhibited, and a large number of polyphenols (flavonoids) are produced, causing an imbalance of nutrients in plants [27]. Therefore, plant Nbi can quickly and effectively evaluate the nutritional status of plants. In the present study, NaCl stress significantly inhibited leaf Nbi in inoculated and uninoculated tomato plants as well as Chi in uninoculated tomato plants, but distinctly increased Flav in inoculated tomato plants, compared with non-NaCl stress (Figure 2a-c). On the other hand, P. occultum inoculation under non-NaCl stress significantly inhibited Flav by 60.00% but dramatically increased Nbi by 170.41%, along with no change in Chi, as compared with non-inoculation. Under NaCl stress, P. occultum inoculation significantly increased leaf Chi and Nbi by 70.88% and 127.80%, respectively, but also inhibited it by 24.14%, as compared with non-inoculation. Dai et al. [28] also reported that in tea, Claroideoglomus etunicatum inoculation significantly increased leaf Nbi and Chi under soil drought stress, as compared with non-inoculation.

Effects of P. occultum on Index of N Balance, Chlorophyll, and Flavonoids of Tomato Exposed to NaCl Stress
It is well-known that when plants are in a healthy state, their chlorophyll content is high, and relatively few polyphenols (flavonoids) are produced at this time; once plants are subjected to nitrogen deficit, chlorophyll synthesis is inhibited, and a large number of polyphenols (flavonoids) are produced, causing an imbalance of nutrients in plants [27]. Therefore, plant Nbi can quickly and effectively evaluate the nutritional status of plants.
In the present study, NaCl stress significantly inhibited leaf Nbi in inoculated and uninoculated tomato plants as well as Chi in uninoculated tomato plants, but distinctly increased Flav in inoculated tomato plants, compared with non-NaCl stress (Figure 2a-c). On the other hand, P. occultum inoculation under non-NaCl stress significantly inhibited Flav by 60.00% but dramatically increased Nbi by 170.41%, along with no change in Chi, as compared with non-inoculation. Under NaCl stress, P. occultum inoculation significantly increased leaf Chi and Nbi by 70.88% and 127.80%, respectively, but also inhibited it by 24.14%, as compared with non-inoculation. Dai et al. [28] also reported that in tea, Claroideoglomus etunicatum inoculation significantly increased leaf Nbi and Chi under soil drought stress, as compared with non-inoculation.  Table 1 for abbreviations. Data (means ± SD, n = 6) followed by different letters on the bar indicate significant differences among treatments at the 0.05 level. See Table 1 for abbreviations.
Based on our study, it can be understood that mycorrhizal plants promoted Nbi by increasing leaf Chi and decreasing Flav under NaCl stress, thus indicating that the nutritional status of mycorrhizal plants was significantly better than that of non-mycorrhizal plants under salinity. Earlier studies also observed greater nutrient levels in mycorrhizal versus non-mycorrhizal plants under salt stress, such as pistachio [29], wheat [30], and trifoliate orange [31].

Effects of AMF on PIPs' Expressions in Leaves of Tomato under NaCl Stress
Plant PIPs are divided into two classes, PIP1 and PIP2, localized on the plasma membrane, where PIP1 acts as water transport as well as root conductivity maintenance and stomatal conductance, but PIP2 has a higher water transport activity than PIP1 [32]. In this study, we found that NaCl stress up-regulated the expression of SlPIP1 and SlPIP2 genes in leaves of both inoculated and uninoculated plants in almost all cases, except for no change in the expression of SlPIP1;3, SlPIP2;4, SlPIP2;8, SlPIP2;11, and SlPIP2;12 in uninoculated plants (Figure 3). This reveals that PIPs of AMF-inoculated tomato were able to rapidly up-regulate their expression and thus promoted water uptake and root hydraulic conductance; therefore, inoculated plants have a higher salt tolerance than uninoculated plants. On the other hand, P. occultum colonization under non-NaCl stress conditions barely altered the expression of SlPIP1 and SlPIP2, except for the down-regulation in SlPIP1;1, SlPIP2;4, and SlPIP2;10, and the up-regulation in SlPIP2;12. This is because under non-salt stress, there is sufficient water in the soil surrounding roots, and plants can obtain enough water by relying on roots, thus reducing the regulatory role of mycorrhiza in AQPs [24,33]. In contrast, under NaCl stress conditions, P. occultum colonization distinctly up-regulated SlPIP1;5, SlPIP2;4, SlPIP2;6, SlPIP2;10, and SlPIP2;11 expressions by 0.47-, 0.63-, 0.48-, and 0.87-fold, respectively, along with no change in SlPIP1;2, SlPIP1;3, SlPIP2;1, SlPIP2;8, SlPIP2;9, and SlPIP2;12, and down-regulation of SlPIP1;2, compared with non-fungus colonization. Such results suggested that AMF diversifies to regulate the expression of host PIPs in response to NaCl stress, which is consistent with the results of Chen et al. [34] in salt-stressed black locust PIPs in response to AMF inoculation. The maintenance of the higher expression of PIPs in mycorrhizal plants versus non-mycorrhizal plants under NaCl stress would mean that more water could be taken up from saline soil conditions in mycorrhizal plants [35], thus enhancing the salt tolerance of host plants.
this study, we found that NaCl stress up-regulated the expression of SlPIP1 and genes in leaves of both inoculated and uninoculated plants in almost all cases, ex no change in the expression of SlPIP1;3, SlPIP2;4, SlPIP2;8, SlPIP2;11, and SlPIP uninoculated plants (Figure 3). This reveals that PIPs of AMF-inoculated tomato w to rapidly up-regulate their expression and thus promoted water uptake and root h lic conductance; therefore, inoculated plants have a higher salt tolerance than u lated plants. On the other hand, P. occultum colonization under non-NaCl stress con barely altered the expression of SlPIP1 and SlPIP2, except for the down-regula SlPIP1;1, SlPIP2;4, and SlPIP2;10, and the up-regulation in SlPIP2;12. This is beca der non-salt stress, there is sufficient water in the soil surrounding roots, and pla obtain enough water by relying on roots, thus reducing the regulatory role of myc in AQPs [24,33]. In contrast, under NaCl stress conditions, P. occultum colonizat tinctly up-regulated SlPIP1;5, SlPIP2;4, SlPIP2;6, SlPIP2;10, and SlPIP2;11 express 0.47-, 0.63-, 0.48-, and 0.87-fold, respectively, along with no change in SlPIP1;2, S SlPIP2;1, SlPIP2;8, SlPIP2;9, and SlPIP2;12, and down-regulation of SlPIP1;2, com with non-fungus colonization. Such results suggested that AMF diversifies to regu expression of host PIPs in response to NaCl stress, which is consistent with the re Chen et al. [34] in salt-stressed black locust PIPs in response to AMF inoculati maintenance of the higher expression of PIPs in mycorrhizal plants versus non-my zal plants under NaCl stress would mean that more water could be taken up from soil conditions in mycorrhizal plants [35], thus enhancing the salt tolerance of host  Table 1 for a tions.  Table 1 for abbreviations.

Effects of AMF on TIPs' Expressions in Leaves of Tomato under NaCl Stress
Tonoplast intrinsic proteins (TIPs) in plants are localized in the tonoplast of cells and can transport a variety of small solutes, including water, hydrogen peroxide, ammonia, etc.; thus, they are associated with salt stress tolerance [17,33,36]. In this study, NaCl stress triggered SlTIP1;1, SlTIP2;1, and SlTIP2;2 expressions in non-mycorrhizal plants, coupled with the down-regulation of SlTIP4;1 and no change in SlTIP1;2, SlTIP1;3, SlTIP2;3, and SlTIP3;2 expressions ( Figure 4). Similarly, in mycorrhizal plants, NaCl stress distinctly induced the up-regulated expressions of SlTIP1;3, SlTIP2;1, SlTIP2;2, SlTIP2;3, and SlTIP4;1, followed by no change in SlTIP1;1, and the down-regulated expressions of SlTIP1;2 and SlTIP3;2. A greater number of up-regulated TIPs in inoculated versus uninoculated plants under NaCl stress means that AMF-inoculated plants can tolerate NaCl stress by the up-regulated expression of more TIPs. Under non-NaCl stress conditions, P. occultum colonization significantly increased SlTIP1;2 and SlTIP3;2 expressions by 13.10-and 9.48-fold, suggesting that mycorrhizae under non-saline conditions mainly regulate the expression patterns of SlTIP1;2 and SlTIP3;2. Moreover, TIP1;2 was confirmed to transport hydrogen peroxide [37], suggesting that mycorrhizal effects on tomato plants under non-NaCl stress conditions may be associated with the balance of reactive oxygen species. In trifoliate orange, P. occultum colonization dramatically up-regulated PtTIP4;1 and PtTIP5;1 expressions under non-NaCl stress conditions and PtTIP4;1 expressions under NaCl stress conditions [38]. This suggests that mycorrhiza-modulated TIPs expressions depend on the host plant species. patterns of SlTIP1;2 and SlTIP3;2. Moreover, TIP1;2 was confirmed to transport hyd peroxide [37], suggesting that mycorrhizal effects on tomato plants under non-NaCl conditions may be associated with the balance of reactive oxygen species. In trifolia ange, P. occultum colonization dramatically up-regulated PtTIP4;1 and PtTIP5;1 ex sions under non-NaCl stress conditions and PtTIP4;1 expressions under NaCl stres ditions [38]. This suggests that mycorrhiza-modulated TIPs expressions depend o host plant species.  Table 1 for abb tions.

Effects of AMF on SOS Expressions in Leaves of Tomato under NaCl Stress
NaCl stress up-regulated SlSOS2 expressions of mycorrhizal and non-mycor plants, while it inhibited SlSOS1 expressions of mycorrhizal plants ( Figure 5). Belve [39] observed that SlSOS2 over-expression could raise the exchange of Na + /H + plasma membrane load Na + into the xylem and the compartmentalization of Na + an This suggests that the tomato variety tolerates salt stress mainly by activating SlSOS not SlSOS1. On the other hand, P. occultum significantly up-regulated SlSOS1 expres by 1.13-and 0.45-fold under non-NaCl and NaCl conditions, respectively. Howeve SlSOS2, P. occultum down-regulated its expressions by 0.39-fold under non-NaCl c tions but did not alter its expressions under NaCl conditions. Porcel et al. [40] al ported the up-regulation of OsSOS1 expressions in rice subjected to salt stress. Und  Table 1 for abbreviations.

Effects of AMF on SOS Expressions in Leaves of Tomato under NaCl Stress
NaCl stress up-regulated SlSOS2 expressions of mycorrhizal and non-mycorrhizal plants, while it inhibited SlSOS1 expressions of mycorrhizal plants ( Figure 5). Belver et al. [39] observed that SlSOS2 over-expression could raise the exchange of Na + /H + at the plasma membrane load Na + into the xylem and the compartmentalization of Na + and K + . This suggests that the tomato variety tolerates salt stress mainly by activating SlSOS2, but not SlSOS1. On the other hand, P. occultum significantly up-regulated SlSOS1 expressions by 1.13-and 0.45-fold under non-NaCl and NaCl conditions, respectively. However, for SlSOS2, P. occultum down-regulated its expressions by 0.39-fold under non-NaCl conditions but did not alter its expressions under NaCl conditions. Porcel et al. [40] also reported the up-regulation of OsSOS1 expressions in rice subjected to salt stress. Under 100 mM NaCl conditions, Funneliformis mosseae inoculation up-regulated SlSOS1 expressions in shoots of Suaeda salsa [41]. It is known that SOS1 is the Na + /H + exchanger in the plasma membrane that controls the extrusion and distribution of Na + in tomatoes exposed to salt stress [42]. It was concluded that AMF activated expressions of SlSOS1 to tolerate salt stress in tomato plants. mM NaCl conditions, Funneliformis mosseae inoculation up-regulated SlSOS1 expressions in shoots of Suaeda salsa [41]. It is known that SOS1 is the Na + /H + exchanger in the plasma membrane that controls the extrusion and distribution of Na + in tomatoes exposed to salt stress [42]. It was concluded that AMF activated expressions of SlSOS1 to tolerate salt stress in tomato plants.  Table 1 for abbreviations.

Conclusions
In this study, P. occultum inoculation was able to improve plant growth as well as  Table 1 for abbreviations.

Conclusions
In this study, P. occultum inoculation was able to improve plant growth as well as nutritional status (e.g., Nbi), and also showed the higher expression of SlSOS1, as well as the diverse regulation of SlPIPs' expression and higher number of up-regulated SlTIPs on inoculated versus uninoculated tomato plants under NaCl stress. This implies that P. occultum-inoculated tomato plants had higher salt tolerance than uninoculated plants; therefore, P. occultum has good potential for application in tomatoes under greenhouse and salt stress. However, how SlSOS1 is activated by P. occultum and how its signal is transmitted under mycorrhization conditions have yet to be further investigated.