MaNrtB, a Putative Nitrate Transporter, Contributes to Stress Tolerance and Virulence in the Entomopathogenic Fungus Metarhizium acridum

Abstract

Nitrogen is an essential nutrient that frequently determines the growth rate of fungi. Nitrate transporter proteins (Nrts) play a crucial role in the cellular absorption of nitrate from the environment. Entomopathogenic fungi (EPF) have shown their potential in the biological control of pests. Thus, comprehending the mechanisms that govern the pathogenicity and stress tolerance of EPF is helpful in improving the effectiveness and practical application of these fungal biocontrol agents. In this study, we utilized homologous recombination to create MaNrtB deletion mutants and complementation strains. We systematically investigated the biological functions of the nitrate transporter protein gene MaNrtB in M. acridum. Our findings revealed that the disruption of MaNrtB resulted in delayed conidial germination without affecting conidial production. Stress tolerance assays demonstrated that the MaNrtB disruption strain was more vulnerable to UV-B irradiation, hyperosmotic stress, and cell wall disturbing agents, yet it exhibited increased heat resistance compared to the wild-type strain. Bioassays on the locust Locusta migratoria manilensis showed that the disruption of MaNrtB impaired the fungal virulence owing to the reduced appressorium formation on the insect cuticle and the attenuated growth in the locust hemolymph. These findings provide new perspectives for understanding the pathogenesis of EPF.

1. Introduction

Numerous insect pests are prevalent in the natural environment, presenting significant challenges to agriculture, ecological balance, and human well-being [1]. Entomopathogenic fungi (EPF), a group of fungi that can cause infections and death in insects and other arthropods, have emerged as a promising and eco-friendly alternative to chemical insecticides and are extensively utilized as biocontrol agents against insect pests [2]. Well-known EPFs, such as Metarhizium acridum and Beauveria bassiana, have shown their potential and advantages in the biological control of pests within agricultural ecosystems [3]. Therefore, understanding the mechanisms that govern the pathogenicity and stress tolerance of EPF is helpful in improving the effectiveness and practical application of these fungal biocontrol agents.

In fungi, detecting and effectively utilizing nutrients are crucial for the successful establishment and rapid expansion of fungal colonies, and nitrogen, a critical nutrient, often dictates the growth rate of fungi [4]. The metabolism of nitrogen sources encompasses a range of biochemical pathways and mechanisms, such as the assimilation of ammonia, the reduction of nitrates, the fixation of nitrogen, the synthesis of amino acids, and so on [5]. Within this metabolic network, nitrate metabolism is an important part of nitrogen source metabolism in fungi.

Nitrate transporter proteins (Nrts) are pivotal in the cellular uptake of nitrate from the surroundings, playing a critical role in the assimilation, metabolism, and utilization of nitrate. The genetic exploration of these transporters in eukaryotes began in 1991 with the discovery of the CrnA gene, which encodes a transmembrane protein, in Aspergillus nidulans [6]. The CrnA-deficient strains exhibited nitrate uptake defects in both the conidial and the mycelial growth phases [7]. These high-affinity transport systems are part of the nitrate/nitrite porter family, a unique subset within the major facilitator superfamily (MFS), the largest group of secondary transporters [8]. Most eukaryotic organisms possess multiple Nrt protein variants, each encoded by distinct genes [9]. For instance, in the yeast Hansenula polymorpha (syn Ogataea angusta), the YNT1 mutants exhibits a deficiency in the uptake of nitrate [10]. In the pathogenic fungus Fusarium oxysporum f. sp. Lycopersici, the targeted deletion of the nitrate-transporting gene Ntr1 significantly impairs fungal growth when nitrate serves as the nitrogen source [11]. Similarly, in Ustilago maydis (syn Mycosarcoma maydis), the growth of nitrate transporter protein mutants is hindered in media where nitrate is the sole nitrogen source and their pathogenicity is diminished [12]. Trichoderma atroviride, a prevalent plant growth-promoting fungus, has been shown to rely on the nitrate transporter CHL1 for nitrogen uptake in MS medium supplemented with NH₄NO₃ [13]. Collectively, these findings underscore the influence of nitrate transporter proteins on fungal growth and pathogenicity. Despite their importance, the characterization of nitrate transporter genes in entomopathogenic fungi remains unexplored. Here, we investigated some biological processes that may be affected by the activity of a putative nitrate transporter, MaNrtB, in M. acridum.

2. Materials and Methods

2.1. Strains and Culture Conditions

The wild-type strain of M. acridum (WT) has been archived at the China General Microbiological Culture Collection Center (CGMCC) with the accession number 0877. In conducting the genetic engineering and fungal transformation for this study, we employed Escherichia coli DH5α (Solarbio, Beijing, China) and Agrobacterium tumefaciens AGL1 (Solarbio, Beijing, China), respectively. The fungal strains employed in this investigation were cultivated on a modified Sabouraud dextrose agar medium, specifically a one-quarter-strength formulation (1/4 SDAY). This medium is composed of 1% dextrose, 0.25% mycological peptone, 0.5% yeast extract, and 2% agar, measured by the weight to volume ratio. The cultures were maintained at a temperature of 28 °C for a period of 15 days to ensure the conidia reached maturity [14].

2.2. Bioinformatic Analyses

All the protein sequences were sourced from the NCBI genome database, accessible at https://www.ncbi.nlm.nih.gov/ (accessed on 25 December 2024). The specific nucleic acid sequence (MAC_03189) and protein sequence (XP_007809529.2) were obtained in FASTA format. Utilizing these protein sequences, a selection of diverse filamentous and non-filamentous fungi were made for BLASTp sequence alignment to identify similarities. Protein 3D structure maps were retrieved from the AlphaFold Protein Structure Database at https://alphafold.ebi.ac.uk/ (accessed on 25 December 2024). For constructing the phylogenetic tree, MEGA v7.0 was employed with the neighbor-joining approach. The sequences were aligned using the ClustalW algorithm integrated within MEGA and employing a bootstrap test with 1000 replicates. Another alignment parameter was set to default settings. The aligned sequences were then exported to GeneDoc 2.7 for homology analysis. Domain prediction was conducted using the SMART tool, available at http://smart.embl.de/ (accessed on 25 December 2024), and TMH prediction was performed using TMHMM at https://services.healthtech.dtu.dk/ (accessed on 25 December 2024). Additionally, BioXM v2.7.1 software was used to calculate the molecular weights and isoelectric points of the proteins.

2.3. Fungal Mutant Generation

The MaNrtB nucleic acid sequence (2535 bp) and an additional 2000 bp flanking the MaNrtB gene on both sides were obtained from the NCBI database. Among them, a 1.3 kb (left border) and a 1.4 kb (right border) flanking sequence of the MaNrtB gene locus were amplified using the primer pairs of MaNrtB-LF/MaNrtB-LR and MaNrtB-RF/MaNrtB-RR, respectively (Supplementary Table S1). The fragments were then successively ligated into the HindIII/XbaI and EcoRV/EcoRI-restricted pK2-PB vectors and verified by PCR using the primers LF/Pt-R and Bar-F/RR [15], respectively. Fungal transformation and validation of the transformants followed the methods described previously [16]. Potential ΔMaNrtB mutants were identified on Czapek–Dox (CZA) medium supplemented with 500 μg/mL glufosinate ammonium (Sigma, St. Louis, MO, USA), and the presence of the desired recombinant sequences was confirmed by PCR using the primer pairs of NrtB-VF/Pt-R and NrtB-VR/Bar-F. The pK2-sur vector was employed to generate the MaNrtB complemented strains (CPs). Initially, the full-length eGFP and TtrpC genes were cloned and ligated into the pK2-sur vector to create the pK2-eGFP-sur vector. Then, the promoter and ORF fragments were amplified from the WT genome using the primers NrtB-CP-F and NrtB-CP-R, and ligated to the HindIII/BamHI-restricted pK2-eGFP-sur vector by one-step cloning to create the pK2-sur-MaNrtB construct [17], which was introduced into the ΔMaNrtB strain. Candidate CP strains were selected on CZA medium with 20 μg/mL chlorimuron ethyl (Sigma, Bellefonte, PA, USA), and recombinant events were verified by PCR using the primer pair of NrtB-CP-VF/GFP-VR. Reverse transcription quantitative PCR (RT-qPCR) analysis was performed to confirm the ΔMaNrtB and CP strains. The schematic diagrams of the pK2-PB and pK2-sur vectors are shown in Figure S1. A complete list of the primers utilized in this study is provided in Table S1.

2.4. Conidial Germination and Conidial Yield Assays

Conidial suspensions at a concentration of 1 × 10⁷ conidia/mL were prepared with mature and freshly harvested conidia and a 0.05% Tween-80 solution. An aliquot of 50 μL was uniformly spread onto 1/4 SDAY plates. Over a period of 10 h, at 2-h intervals, three 1 cm² sections were excised from each strain’s plate. The number of germinated conidia was counted for every 100 conidia observed. Germination was defined as the emergence of a bud whose length was more than one-third of the width of the conidium. The germination rate was determined by the following formula: (number of germinated conidia/total number of conidia) × 100%. For assessing the conidial yield, 2 μL of the conidial suspension (1 × 10⁶ conidia/mL) was deposited into 24-well plates with 1 mL of 1/4 SDAY medium in each plate well. Every three days, the yield of conidia was measured. Briefly, the fungal cultures were transferred to a 2 mL centrifuge tube. After adding 1 mL of 0.05% Tween-80 solution for grinding, the mixture was vortexed. The suspension was then diluted, and the conidial concentration was determined using a hemocytometer. Each experiment was independently performed a minimum of three times to ensure reliability.

2.5. Stress Tolerance Assays

The 1/4 SDAY medium was amended with 0.5 M NaCl, 1 M sorbitol (SOR), 500 μg/mL Congo red (CR), 0.01% w/v sodium dodecyl sulfate (SDS), 50 μg/mL Calcofluor white (CFW), and 60 mmol/L H₂O₂ to simulate adverse conditions. A 2 µL aliquot of conidial suspension (1 × 10⁶ conidia/mL) from each strain was spread onto the modified culture plates and incubated at 28 °C for 6 days. The colony growth was then photographed and measured. To evaluate the heat-shock sensitivity of the fungal strains, the conidial suspensions (1 × 10⁷ conidia/mL) were subjected to a water bath at 45 °C for durations of 2, 4, 6, and 8 h. Post-treatment, the suspensions were spread onto 1/4 SDAY medium and incubated at 28 °C for 20 h to determine the germination rates. For the UV-B tolerance of the fungal strains, the conidial suspensions (1 × 10⁷ conidia/mL) were spread on 1/4 SDAY medium and exposed to UV-B radiation at a dose of 1350 mW/m² for periods of 0.5, 1.0, 1.5, and 2.0 h. Following exposure, the cultures were incubated at 28 °C for 20 h to assess the conidial germination. Each experiment was conducted in triplicate.

2.6. Bioassays

Two distinct bioassay methods were employed as previously described [15]. Briefly, in the topical inoculation approach, suspensions of the WT, ΔMaNrtB, and CP strains, prepared in paraffin oil at a concentration of 1 × 10⁷ conidia/mL, were applied to the fifth-instar nymphs of locusts, Locusta migratoria manilensis (5 μL per nymph). For the intrahemocoel injection method, the conidia from the fungal strains were suspended in double-distilled water (ddH₂O) at a concentration of 1 × 10⁶ conidia/mL and injected directly into the locust hemocoel (5 μL per nymph). For both inoculation techniques, each experimental group contained 20 fifth-instar nymphs, and the negative control groups were treated with pure paraffin oil and ddH₂O, respectively. The survival rates of the locusts were monitored and documented at intervals of 12 h throughout the experiment.

To investigate the nutrient utilization efficiency of the various fungal strains, we employed liquid CZA medium along with two modified versions of CZA, SPM and TPM, to assess the fungal development under distinct nutritional conditions. The CZA medium was supplemented with 3% sucrose and 0.3% NaNO₃, while the SPM contained 3% sucrose and 0.5% peptone, and the TPM was formulated with 3% trehalose and 0.5% peptone. Among the three media, CZA has nitrate as the main nitrogen source donor and thus can be used to assess the nitrate transport activity of NrtBp in M. acridum. TPM is used to mimic insect hemolymph, as described previously [18]. These media were designed to replicate and evaluate the growth of fungi in a variety of nutrient-rich environments. Briefly, a 30 μL sample of a conidial suspension at a concentration of 10⁷ conidia/mL was introduced into each 30 mL medium, which was then incubated for 60 h at 28 °C with a shaker speed of 200 rpm to determine the biomass. This procedure was conducted in triplicate for each condition. To evaluate the host immune response, the total RNA was extracted from the fat bodies in the nymphs of locusts after injection to assess the expression levels of two key antimicrobial peptide (AMP) genes, Attacin and Defensin, using the protocol outlined in a previous study [19]. Each bioassay experiment was repeated three times.

2.7. Appressorium Formation Assays

Conidial suspensions for each strain were prepared in sterilized ddH₂O to a density of 1 × 10⁷ conidia/mL. The sterilized locust hindwings were first coated with the conidial suspensions and then carefully spread onto pristine microscope slides for incubation at a controlled temperature of 28 °C. The conidia germination rate was monitored and recorded every two hours. Additionally, after a 12 h incubation period, the appressorium formation rate was also counted. This experimental procedure was conducted in triplicate to ensure reliability.

To assess the fungal penetration capability, we placed sterilized locust hindwings on 1/4 SDAY plates. A 2 µL aliquot of conidial suspension from each fungal strain, diluted to a concentration of 1 × 10⁶ conidia/mL, was dropped on the wings carefully. These were then incubated at 28 °C for 44 h. Following photography and documentation, the wings were removed to allow continued incubation for an additional four days, with photographs taken to document the colony morphology. As a control, conidial suspensions were also directly inoculated onto 1/4 SDAY medium and incubated at 28 °C for a duration of 6 days. Each treatment contained 10 wings and these assays were repeated three times.

2.8. Data Analyses

A one-way ANOVA test was conducted to evaluate the phenotypic estimates, followed by Tukey’s honestly significant difference (HSD) test to ascertain the significance of any observed differences among the groups.

3. Results

3.1. Features of MaNrtB and Mutant Generation

Bioinformatics analysis revealed that there is only one putative Nrt gene, designated as MaNrtB, in M. acridum. The MaNrtB gene spans 1612 base pairs and encodes a protein of 502 amino acids, distributed across two exons. The calculated molecular weight for the MaNrtB protein is 53.75 kDa, with an isoelectric point of 7.8. Domain analysis, conducted via the SMART online tool, indicated the presence of an MFS domain. As with other reported Nrt homologues [6,11,12,20,21,22], the tertiary structure of NrtB in M. acridum putatively contains 12 transmembrane-spanning alpha helices (TMHs)that are colored in blue with a less conserved intracellular central loop (Figure 1A and Figure S2). The sequence alignment of the orthologous NrtB proteins revealed that these TMH domains are highly conserved, whereas the central loop region exhibits a lack of order (Figure S3). Additionally, phylogenetic analysis grouped MaNrtB together with several of its homologs that have been evidenced to possess nitrate transport capacity, such as A. nidulans [6] and F. oxysporum [11] (Figure 1B), and these domains are notably conserved in filamentous fungi and exhibit lower conservation in yeast (Figure 1B). Overall, the significant similarity in the tertiary structures of these proteins suggests that they likely have similar functions. MaNrtB-knockout transformants were generated through homologous recombination. The CP strain was derived using the ectopic strategy (Figure 2B). The ΔMaNrtB and CP strains were validated by PCR (Figure S4). Furthermore, the expression levels of the MaNrtB gene in the WT, ΔMaNrtB, and CP strains were quantified using RT-qPCR. The expression levels of MaNrtB in the WT and CP strains were markedly higher than in the ΔMaNrtB strain, confirming the successful generation of both the ΔMaNrtB and CP strains (Figure 2C).

3.2. Disruption of MaNrtB Impaired Conidial Germination but Not Conidial Yield

Our initial assessment focused on the germination rates and conidial yields of the different fungal strains. It was observed that the ΔMaNrtB strain exhibited a considerably reduced germination rate compared to both the WT and CP strains after 4 h of incubation (Figure 3A). Furthermore, the ΔMaNrtB strain required a significantly longer time to reach 50% germination (GT₅₀) (Figure 3B). In contrast, the conidial yield among the three strains was found to be statistically indistinguishable (Figure 3C). Collectively, these findings suggest that the disruption of the MaNrtB gene in M. acridum led to the retardation of conidial germination without impacting the conidial production.

3.3. Disruption of MaNrtB Affected Fungal Stress Tolerances

The ability to withstand environmental stress is crucial for EPF. Thus, we examined the UV-B and heat-shock stress tolerances of the WT, ΔMaNrtB, and CP strains. Post-UV-B irradiation, the ΔMaNrtB strain exhibited a markedly reduced conidial germination rate after one hour and a significantly lower GT₅₀ compared to the WT and CP strains (Figure 4A,B). Conversely, under heat-shock conditions, the ΔMaNrtB strain displayed a higher germination rate after four hours of treatment, with a notably elevated GT₅₀ (Figure 4C,D). These findings suggest that the disruption of MaNrtB in M. acridum compromised its UV-B resistance but enhanced its heat tolerance. Furthermore, spot assays revealed that the ΔMaNrtB strain formed smaller colonies relative to the WT and CP strains on 1/4 SDAY medium supplemented with SOR, NaCl, H₂O₂, CR, and CFW (Figure 5), indicating that the ΔMaNrtB strain was more susceptible to hyperosmotic, oxidative, and cell wall stresses.

3.4. Disruption of MaNrtB Attenuated Fungal Virulence

To assess the role of MaNrtB in virulence, we conducted bioassays using two infection methods, topical application and direct intrahemocoel injection. With topical application of the WT or CP strains, all the locusts succumbed by 8.5 days post-inoculation (dpi), whereas those inoculated with the ΔMaNrtB strain died after 10.0 dpi (Figure 6A). The median lethal time (LT₅₀) for the ΔMaNrtB strain was 6.26 ± 0.80 days, which was significantly longer than the 4.90 ± 0.69 days for the WT and 5.32 ± 0.73 days for the CP strain (p < 0.05; Figure 6B). Similarly, when using the intrahemocoel injection method, the survival rates of the locusts infected with the ΔMaNrtB strain were also significantly higher than those infected with the WT or CP strains (Figure 6C). Likewise, the LT₅₀ for the ΔMaNrtB strain, at 4.64 ± 0.67 days, was significantly longer than the 3.55 ± 0.56 days for the WT and 3.97 ± 0.60 days for the CP strains (p < 0.05; Figure 6D). Collectively, these findings indicate that MaNrtB plays a significant role in the virulence of M. acridum.

To explore whether the MaNrtB deletion impacts fungal penetration, we inoculated M. acridum on the hind wings of locusts and analyzed the penetration ability of each strain. The results showed that compared to the WT and CP, the ΔMaNrtB strain formed the smallest colony with the lowest penetration ability (Figure 7A). To elucidate the functions of MaNrtB in the infectious process, we analyzed the germination of conidia and the formation of appressoria on the locust hind wings for the WT, ΔMaNrtB, and CP strains. The absence of MaNrtB led to slower conidial germination on the locust hind wings (Figure 7B,C). Microscopic observation showed that all three strains formed normal appressorium, but the MaNrtB mutation also resulted in significantly decreased appressorium formation (p < 0.01; Figure S5 and Figure 7D). After a 24 h induction on locust wings, the ΔMaNrtB strain formed about 30% normal appressoria, in contrast to the over 50% observed in both the WT and CP strains (Figure 7D).

To verify whether the MaNrtB deletion impacts fungal colonization in hemolymph, we first simulated fungal growth in different media, then quantified the biomass, and analyzed the uptake of carbon and nitrogen sources. It was found that the fungi accumulated the most biomass in SPM medium containing sucrose and peptone, which were the preferable choice for both nitrogen and carbon sources, and the ΔMaNrtB mutant accumulated about 22% biomass less than the WT (Figure 8A). Replacing sucrose with trehalose widened the gap to about 43% in TPM (Figure 8A). In the nutrient-poor CZA standard medium, the gap in accumulated biomass reached 56% (Figure 8A). Furthermore, to probe whether the MaNrtB gene contributed to the ability of the fungus to evade host immune defenses, the expression levels of Defensin and Attacin, Toll- and/or Imd-activating antimicrobial peptide genes involved in fungal recognition and immune response in the insect fat bodies were analyzed after injection with conidial suspension from different fungal strains. The results displayed that lower levels of expression of Attacin (32%) and Defensin (43%) were found in the locusts infected by the MaNrtB strain compared to those infected by the WT after 24 dpi (Figure 8B).

4. Discussion

NrtB, a conserved nitrate transporter in filamentous fungi, has been the subject of limited research regarding its molecular mechanisms and their relation to fungal growth. In our study, we employed homologous recombination to generate MaNrtB deletion and complementation transformants, conducting a thorough analysis of the MaNrtB functions. Our results indicated that MaNrtB, the nitrate transporter gene, plays important roles in the conidial germination, stress tolerances, and virulence of the entomopathogenic fungus M. acridum. These findings provide new perspectives for understanding the biological properties and pathogenesis of EPF.

Nitrogen sources play a pivotal role in the morphological development, production of secondary metabolites, and virulence of EPF [23]. Typically, fungi prioritize certain nitrogen sources, such as ammonium, and repress the assimilation of others, such as nitrate, a phenomenon termed nitrogen catabolite repression (NCR) [24]. In Ascomycetes, including A. nidulans, the key regulators AreA and AreB govern nitrogen metabolism, with nitrate metabolism gene activation primarily under the control of the transcription factors AreA and NirA [25,26,27]. AreA acts as a positive regulator that can alleviate NCR, while NirA is a transcription factor specific to the nitrate assimilation pathway, induced by nitrate or nitrite [28]. NmrA is another central regulator within the NCR pathway, modulating fungal nitrogen metabolism by interacting with and suppressing the activity of AreA and AreB [29,30,31,32]. In our previous research, we established a library of differentially expressed genes responsive to nitrate [33]. Among the genes, MaNCP1, a C2H2-type transcription factor gene, was identified to modulate nitrate metabolism by interacting with the MaNmrA in M. acridum [34,35]. MaNCP1 influences nitrate metabolism and impacts nitric oxide (NO) synthesis [34], which can engage in various signal transduction pathways, leading to phenotypic alterations in the fungus [36]. Nitrate can trigger the upregulation of MaNCP1 and MaNmrA, and the expression of the nitrate transporter gene MaNrtB is downregulated following the deletion of MaNCP1 or MaNmrA [34]. This suggests reduced transport of nitrate from the extracellular environment into the cell, yet the nitrate content in the ΔMaNCP1 and ΔMaNmrA strains was significantly higher than in the wild-type strain, indicating a severe disruption in nitrate catabolism [34]. As a key component of the conserved nitrate assimilation pathway, Nrts regulate cellular nitrogen utilization and further influence fungal growth and development [37]. In our research, the ΔMaNrtB strain displayed slower growth, reduced stress resistance, and decreased virulence against locusts, just like the mutant of ΔMaNCP1 [38] and ΔMaNmrA strains [39], underscoring the important role of nitrate metabolism in sustaining fungal growth.

The capacity of conidia to withstand environmental stress is critical for the efficacy of EPF in the field, underscoring the importance of identifying robust strains for practical applications [40]. Our research revealed that the ΔMaNrtB strain showed reduced tolerances to UV-B and cell wall stress but enhanced resistance to heat shock. The fungal cell wall is the primary defense against external stressors [41]. Compounds such as CFW and CR are commonly utilized to challenge fungal cell walls in vitro [42]. CFW interferes with chitin assembly, and CR inhibits β-glucan synthesis, both leading to cell wall damage and triggering cell wall stress responses [43]. In Arabidopsis thaliana, a co-expression analysis of cell wall remodeling genes with nitrate and ammonium transporters revealed that there is a notably strong correlation between the regulation of cell wall remodeling and nitrate assimilation processes, while ammonium transporters appeared to have a more limited role in these co-expression networks [44]. Thus, the inhibited growth of ΔMaNrtB on 1/4 SDAY medium containing CR and CFW suggests that MaNrtB also plays a role in maintaining cell wall integrity.

The conidial germination rate of the ΔMaNrtB strain was diminished, echoing observations in U. maydis [12] and F. oxysporum [11]. However, the production of conidia remained unaffected in the ΔMaNrtB strain, suggesting that the MaNrtB gene is pivotal for conidial germination but exerts minimal influence on the process of conidiation. In F. fujikuroi, a reduction in biomass was noted in mutants of the nitrate transporter protein compared to the wild type [45]. Consistent with prior fungal studies, the growth rate of F. graminearum is dependent on the availability and type of nitrogen sources [46]. In B. bassiana, deprivation of nitrogen nutrients leads to reduced conidium production [47]. Disrupting the gene encoding the nitrate-responsive transcription factor NirA in B. bassiana causes reduced growth rates and diminished efficiency in utilizing nitrate and urea [48]. This supports the notion that the highly conserved nitrate assimilation pathway is crucial for promoting growth across various filamentous fungi.

Elucidating the impact of nitrogen sources on fungal virulence is helpful in developing novel pest control strategies. A successful infection hinges on the ability of a pathogen to overcome host defenses and secure vital nutrients necessary to complete its life cycle [49]. The nitrate assimilation pathway plays a significant role in fungal virulence. In Colletotrichum acutatum, a strain with a deletion of the NirA1 gene could not grow on media using nitrate or nitrite as the sole nitrogen source and displayed reduced virulence on strawberry leaves [50]. In N. crassa, growth tests with nitrate as the sole nitrogen source showed that the homologous protein nit-10 mutant was unable to grow with a low nitrate concentration [51]. In the plant pathogen Magnaporthe oryzae, the trehalose-6-phosphate synthase enzyme (Tps1) links glucose-6-phosphate metabolism to nitrogen source utilization, modulating nitrate reductase activity [52]. Moreover, a study showed that there is a genetic switch that consists of Tps1 and the nitrogen metabolite repressor gene NMR1 [53]. This genetic switch controls the expression of certain nitrogen-utilization GATA-factor transcriptional factors downstream, including ASD4 (the homologous protein to AreB in M. oryzae), and it is necessary for regulation of a set of genes that are expressed during appressorium-mediated infection in M. oryzae [53]. Further research has reported that targeted deletion of Asd4 led to an increase in glutamine levels in M. oryzae, which can further activate the TOR pathway and promote autophagy, thereby promoting hyphal growth while impeding appressorium formation [54,55]. The phenotypic observations of the ΔMaAreB strain [55] were consistent with the M. oryzae ASD4 mutant [56]. In our study, the disruption of the MaNrtB gene led to delayed conidial germination, reduced appressorium formation, and attenuated growth within the insect host; thus, we speculate that the disorder of the nitrate assimilation pathways may have led to changes in the glutamine levels in vivo and influenced the TOR pathway, ultimately resulting in impaired growth and virulence in M. acridum.

For entomopathogenic fungi, the capacity to penetrate the insect cuticle and proliferate in the hemolymph is crucial for fungal virulence [57]. Fungi not only need to overcome the host immune response but also compete for nutrients with other microorganisms within the host; for instance, M. rileyi generates compounds that inhibit the proliferation of competing microorganisms, thereby facilitating its own swift expansion and contributing to the demise of the host [58]. In our study, media containing different carbon and nitrogen sources were used to simulate the growth pattern of fungi facing different nutrient environments. Correspondingly, the ΔMaNrtB strain showed significantly decreased total biomass in each media compared to the WT and CP strains, suggesting that the deletion of MaNrtB contributes to trehalose utilization, which would further affect fungal growth and dimorphic transformation within the host haemocoele, and hence fungal virulence [56]. In the nutrient-poor CZA standard medium, the gap in accumulated biomass reached 56%, while the absence of Nrts greatly limited fungal growth in nitrate-containing environments, which is consistent with previous studies [7,10,11,12]. Furthermore, fungal cells must overcome the host immune activity to propagate by yeast-like budding in the host haemocoele [59]. We assessed the immune response of locusts by quantifying the expression levels of two AMP genes, Attacin and Defensin. In this study, the locusts infected by ΔMaNrtB displayed decreased AMP gene expression, implicating an impaired ability of the ΔMaNrtB mutant in the fungal evasion from locust immunity defense. Given that the mutant strain exhibits a reduced growth rate in media with varying nutrient compositions, this could potentially impair its development under diverse conditions. Such developmental constraints might, in turn, account for the insect’s diminished defensive response.

In summary, our study sheds light on the multifaceted functions of the NrtB gene in the entomopathogenic fungus M. acridum. We have demonstrated that NrtB plays a pivotal role in multi-stress tolerance, nutrient assimilation, and fungal pathogenicity. These insights contribute to a deeper understanding of the molecular mechanisms underlying fungal virulence.