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Article

MaAzaR, a Zn2Cys6/Fungus-Specific Transcriptional Factor, Is Involved in Stress Tolerance and Conidiation Pattern Shift in Metarhizium acridum

by
Jinyuan Zhou
1,2,3,
Siqin Wang
1,2,3,
Yuxian Xia
1,2,3,* and
Guoxiong Peng
1,2,3,*
1
Genetic Engineering Research Center, School of Life Sciences, Chongqing University, Chongqing 401331, China
2
Chongqing Engineering Research Center for Fungal Insecticide, Chongqing 401331, China
3
Key Laboratory of Gene Function and Regulation Technologies Under Chongqing Municipal Education Commission, Chongqing 401331, China
*
Authors to whom correspondence should be addressed.
J. Fungi 2024, 10(7), 468; https://doi.org/10.3390/jof10070468
Submission received: 11 June 2024 / Revised: 28 June 2024 / Accepted: 29 June 2024 / Published: 4 July 2024
(This article belongs to the Collection Entomopathogenic and Nematophagous Fungi)
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Abstract

:
Entomopathogenic fungi are valuable sources of biological pesticides, with conidial yield and quality being pivotal factors determining their broad applications. AzaR, a fungus-specific zinc-cluster transcription factor, is known to regulate the biosynthesis of polyketone secondary metabolites in Aspergillus niger; however, its role in pathogenic fungi remains unclear. This study investigated the role of MaAzaR in the growth, development, and environmental tolerance of Metarhizium acridum. MaAzaR deletion slowed down conidial germination rate, caused reduction in conidial yield, lowered fungal tolerance to UV radiation, did not affect fungal heat-shock tolerance, and increased fungal sensitivity to the cell-wall-destructive agent calcofluor white. Furthermore, MaAzaR deletion transformed microcycle conidiation to normal conidiation on the microcycle conidiation medium. Transcription profile analysis demonstrated that MaAzaR could regulate transformation of the conidiation pattern by controlling the expression of genes related to cell division, mycelium growth and development, and cell wall integrity. Thus, this study identified a new gene related to fungal conidiation and environmental tolerance, enriching our understanding of the molecular mechanism of microcycle conidiation and providing theoretical support and genetic resources for the development of high-yielding strains.

1. Introduction

Entomopathogenic fungi serve as an optimal resource for pest management, characterized by their propensity to induce low levels of pest resistance and their environmental compatibility [1]. Metarhizium acridum, an entomopathogenic fungus, has been effectively utilized as a fungal insecticide to manage locust infestations in Africa, Asia, and Australia and serves as a prototypical organism for research on insecticidal strategies [2,3]. Conidia represent both the origin and terminal stages of differentiation within the fungal life cycle, having a critical function in the reproductive and survival mechanisms of fungi. Consequently, the capacity for conidiation and the quality of conidia are pivotal characteristics that govern the efficacy of large-scale production and deployment of mycopesticides [4]. In field applications, biopesticides still present issues such as their unstable protective effect due to environmental sensitivity and high costs, which constrain their widespread use. Therefore, investigation of the sporulation mechanism and stress resistance of Entomopathogenic fungi is crucial, representing a critical strategy for advancing the mycoinsecticides industry.
Fungal conidiation serves as a response to environmental modifications, and the vegetative growth of the fungi often stops and transits to conidiation under adverse conditions such as nutrient limitation [5], pH [6], or temperature stress [7]. In general, two modes of conidiation are observed in filamentous fungi, namely normal conidiation and microcycle conidiation [8]. Normal conidiation refers to the onset of conidiation following a protracted period of vegetative growth [9]. Microcycle conidiation functions as a survival strategy for certain fungi under detrimental conditions and is characterized by the absence or minimal growth of vegetative mycelium and immediate recurrence of conidiation following the germination of (sexual or asexual) conidia [9]. Anderson et al. observed that high-temperature exposure led to direct production of conidia in Aspergillus niger without associated hyphal growth, representing the initial documentation of microcycle conidiation [7]. Microcycle conidiation has been reported in over 100 fungal species, including Penicillium, Alternaria, etc. [5,7,9].
Extensive research has been conducted to elucidate the regulatory mechanisms of the normal conidiation pathway in Aspergillus spp., and the transcription factors (TFs) BrlA, AbaA, and WetA have been found to be involved in the fundamental regulatory pathway in Aspergillus nidulans [10,11]. In addition to the core regulatory pathway, various upstream activators and negative inhibitors, central regulatory factors, and light response and villus regulatory factors such as FluG, FlbA, FlbB, FlbC, FlbD, and FlbE [12,13,14,15] have been identified to function along with BrlA, AbaA, and WetA in controlling conidiation in A. nidulans. In contrast, studies on the molecular mechanism underlying microcycle conidiation are rather inadequate. When compared with normal conidiation, microcycle conidiation in M. acridum was noted to cause a faster conidial production rate, increased conidial yield, uniform conidial size, enhanced stress resistance, and superior conidial quality [16]. Several genes in M. acridum have been found to play a role in modulating conidiation patterns, including MaH1 [17], MaOpy2 [4], MaNCP1 [18], etc.; however, the regulatory mechanisms controlling them remain elusive. Therefore, further investigation and identification of novel genes involved in microcycle conidiation and the molecular mechanisms governing microcycle conidiation are imperative, which can provide theoretical support and valuable resources for enhancing the fermentation processes and selecting high-yielding strains.
Numerous studies have demonstrated that various abiotic stress conditions, including UV radiation and high temperature, significantly constrain entomopathogenic fungi, limiting their field performance and virulence [19,20,21]. Temperature is a pivotal factor that affects the efficacy of Entomopathogenic fungi in controlling microbial pests, with heat stress particularly influencing the entire infection process [22]. The tolerance of fungi towards environmental stress is closely linked to the metabolic activities of specific biochemical components within their cells, such as protein [23] and trehalose [24]. Consequently, to sustain high efficiency of Entomopathogenic fungi in practical applications, it is crucial to enhance their UV and hygrothermal resistance. TFs are vital in signal transduction pathways and are key regulators of cellular functions [25]. Zinc-cluster TFs play pivotal roles as regulators in various biological processes in fungi and are involved in asexual sporulation, sexual morphogenesis, secondary metabolism, stress response, drug resistance, and pathogenesis [26,27,28,29]. For instance, BbTpc1 governs hyphal development and pathogenicity [30], whereas Pcz1 in Penicillium roqueforti is crucial for conidial formation and germination [31]. In Aspergillus flavus, 135 zinc-cluster TFs genes were identified to participate in critical processes such as hyphal growth and sporulation [32]. It was reported that AzaR (Azaphilone cluster-specific TF), a Zn2Cys6/fungus-specific TF, regulates the biosynthesis of polyketone secondary metabolites in A. niger [33]; however, our understanding of the functional role of AzaR is limited. Moreover, the AzaR gene homolog in the entomopathogenic fungus M. acridum, named MaAzaR, has not yet been characterized for its function. Therefore, in the present study, we examined the role of MaAzaR in conferring conidiation ability and stress resistance in M. acridum. The results revealed that MaAzaR is a novel gene related to conidiation and environmental tolerance of M. acridum, affecting the transformation of conidial formation patterns by regulating genes related to conidial formation and development.

2. Materials and Methods

2.1. Strains and Growth Conditions

Metarhizium acridum strain CQMa102, preserved in the China General Microbiological Culture Collection Center (Strain No. CGMCC 0877), was cultured on 1/4-strength Sabouraud’s dextrose agar (1/4 SDAY; 1% dextrose, 0.25% mycological peptone, 0.5% yeast extract, and 1.8% agar, w/v) at 28 °C.

2.2. Constructions of Mutants

The MaAzaR (Gene ID: MAC-06365) deletion mutant was constructed by homologous recombination. In brief, the upstream (about 1.2 kb) of the MaAzaR coding sequence was amplified by MaAzaR-LF and MaAzaR-LR, and the downstream flanking fragment (about 1.2 kb) was amplified by MaAzaR-RF and MaAzaR-RR and inserted into the pK2-PB vector harboring a bar cassette. The constructed pK2-PB-MaAzaR-LR vector was transformed into M. acridum using a Agrobacterium tumefaciens-mediated method. To rescue the deleted MaAzaR, the full-length MaAzaR sequence with flanking region (full length: 3.1 kb) was amplified and inserted into the pK2-sur vector containing the chlorimuron ethyl resistance gene sur [18] to construct the complementary vector pK2-sur-MaAzaR. The developed vector was transformed into ΔMaAzaR, and the complementary transformant (CP) was screened on Czapek medium (sucrose 30 g/L, NaNO3 2 g/L, K2HPO4 1 g/L, MgSO4·7H2O 0.5 g/L, KCl 0.5 g/L, FeSO4·7H2O 0.01 g/L, and agar 18 g/L) containing 60 μg/mL chlorsulfuron ethyl.

2.3. Growth Analysis

We prepared the conidia suspension of fungal strains according to the established method [18], using 0.05% Tween-80 aseptic solution and filtering through four layers of aseptic lens paper to remove potential mycelium. Then, the concentration of the conidia suspension was accurately determined by hematology analyzer. Next, the same amount of conidia suspension (1 × 107 conidia/mL) was inoculated into 1/4 SDAY plates at 28 ℃. To monitor the germination process of the wild-type (WT), ΔMaAzaR, and CP strains, culture medium of equal amounts was taken out every 2 h and placed on a slide, and the conidia germination rate of different strains was counted under an optical microscope. In total, 100 conidia were counted each time, and the counting was repeated three times to calculate the germination rate of the conidia of different strains. This experiment was repeated three times. The conidial yield was assayed as previously described [18]. Specifically, the conidia suspensions of WT, ΔMaAzaR, and CP (1 × 106 conidia/mL) were added to 24-well plates with 1 mL medium per well and cultured continuously at 28 °C for fifteen days. During this period, we washed the pore plate with 1 mL 0.1% Tween-80 solution every three days, collected conidia for counting, and accurately determined the spore production of each strain through the blood cell counter.

2.4. Stress Resistance Analysis

Fungal tolerance to UV irradiation and heat shock was assayed as previously described [4]. In brief, 50 µL of conidial suspension (1 × 107 conidia/mL) of the WT, ∆MaAzaR, and CP strains were, respectively, inoculated onto 1/4 SDAY plates and subjected to either UV-B irradiation (1350 mW/m2) for 0, 1.5, 3.0, 4.5, and 6.0 h or incubated at 46 °C for 0, 3, 6, 9, and 12 h. Subsequently, the plates were incubated at 28 °C for 20 h, and their conidial germination rates were calculated using a hemocytometer as described earlier. Fungal tolerances to hyperosmotic and oxidative stresses were determined by spot assays on 1/4 SDAY plates with 1 M/L NaCl, 1 M/L sorbitol, and 6 mM/L H2O2, respectively. The fungal sensitivities to cell wall stressors were ascertained by spot assays on 1/4 SDAY plates with 0.01% w/v sodium dodecyl sulfate, 50 µg/mL calcofluor white (CFW), and 500 µg/mL Congo red. The conidial suspension (2 µL of 1 × 106 conidia/mL) of the WT, ∆MaAzaR, and CP strains was, respectively, spotted on 1/4 SDAY without or with stressors and incubated for 6 days at 28 °C before photographing the fungal colonies.

2.5. Microscopic Observation of Conidiation

To observe the conidiation process of the fungal strains, the conidial suspension (100 µL of 1 × 107 conidia/mL) was inoculated onto 1/4 SDAY plate and microcycle conidiation induction medium (SYA; 0.5% yeast extract, 3% sucrose, 0.05% MgSO4, 0.001% MnSO4, 0.05% KCl, 0.3% NaNO3, 0.1% KH2PO4, 0.001% FeSO4, and 2% agar, w/v) and incubated at 28 °C. After 10, 12, 18, 24, and 36 h of incubation, approximately 1 cm2 of the culture medium was cut for observation under a microscope (Motic, Guangzhou, China). The hyphal samples were stained with 10 µL of CFW (50 µg/mL) for 30 min after 18, 24, and 36 h of cultivation to visualize the mycelial septa under a fluorescent microscope (Nikon Eclipse Ci-E, Tokyo, Japan).

2.6. Determination of Trehalose Content

The trehalose content was extracted as previously described [34]. In brief, 0.1 g of mature conidia was cultured in 1/4 SDAY medium for 15 days. Subsequently, 1 mL of extraction liquid was added to the culture, and the conidia were crushed by ultrasonic wave, transferred to a centrifuge tube, allowed to stand at room temperature for 45 min, oscillated for 3–5 times, and centrifuged at 8000× g at room temperature for 10 min, and the supernatant was collected. The trehalose content in the supernatant was determined using a trehalose determination kit (Solarbio Biotechnology, Beijing, China) according to the manufacturer’s instructions.

2.7. RNA Sequencing

Transcriptional profiles of the WT and ∆MaAzaR strains were obtained using RNA sequencing (RNA-seq). In brief, the total RNA was extracted from the WT and ∆MaAzaR strains cultured on SYA plates at 28 °C for 10 h. The total RNA was extracted from each sample using an RNA kit (Invitrogen, Carlsbad, CA, USA) with RNase-free DNaseI and reverse-transcribed into cDNA with an oligo-dT primer using the PrimeScript RT Master Mix (TaKaRa, Dalian, China). Sequencing libraries were prepared, and sequencing was conducted on BGISEQ-500 (BGI, Beijing, China). The sequencing data were filtered using SOAPnuke for quality control to obtain clean reads and mapped to the reference genome of M. acridum using HISAT2 [35]. The differential splicing gene (DSG) was fused with Ericscript and rMATS. Clean reads were compared with the gene set by Bowtie2, and the gene expression level was calculated by RSEM. Basically, DESeq2 [36] was used for differential expression analysis, and the Q value was 0.05. In order to annotate DEGs, based on hypergeometric test, phyper was used for GO enrichment analysis (http://www.geneontology.org/ accessed on 14 February 2022). Bonferroni was used to correct the significance level (Q value of ≤0.05), which had a strict threshold. The DEGs were defined with a Q value of ≤0.005, and a fold change ≥1.5. RT-qPCR was used to verify the reliability of RNA-seq data. The RNA-seq data in this study were deposited in the NCBI BioProject database under the accession number No. PRJNA884297. Differentially expressed genes (DEGs) were classified and annotated using gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis.

2.8. Data Analysis

All experiments were performed in triplicate. Statistical analysis was performed using Statistical Package for Social Sciences (SPSS Inc., Chicago, IL, USA, version 26.0 for Windows). All the data are expressed as mean ± standard error. Student’s t-test was used for comparisons of normally distributed data between the groups, and values with p < 0.05 were considered as statistically significant.

3. Results

3.1. Characteristics of MaAzaR and Verification of Mutant Strain

The MaAzaR coding sequence spans a total length of 1599 bp, including 348 bp introns encoding 416 amino acids with a molecular weight of 46.72 kDa. Prediction of structure domains using the online resource SMART (http://smart.embl.de/, accessed on 16 June 2021) revealed a Zn(II)2Cys6 bimodular cluster domain similar to GAL4 and a Fungal_trans domain (regulatory intermediate homology region of fungal TFs) (Figure 1A). Sequence comparison showed that the GAL4 sequence of Zn(II)2Cys6 zinc-cluster domain at MaAzaR was conserved, especially the Cys6 motif (Figure 1B). The sequence similarity was analyzed by DNAMAN version 8.0, and the phylogenetic tree was constructed by neighbor-joining method through MEGA-X version 10.1.8, which was tested by bootstrap (1000 repeats). The results indicated that MaAzaR exhibited high homology in filamentous fungi, with a closer relationship to Metarhizium anisopiae and significant sequence identity (Figure 1C).
Deletion and complementation vectors were developed through homologous recombination and random insertion strategy (Figure 2A). Successful knockout and recovery of the targeted genes were achieved through PCR amplification and quantitative verification (Figure 2B,C). In the subsequent experimental operation, we selected the knockout transformant 1# and the complementary transformant C1 for the experiment.

3.2. Disruption of MaAzaR Delayed Germination and Decreased Fungal Conidial Yield

To investigate the effect of MaAzaR on the growth and conidiation process of M. acridum, we first was evaluated the conidial germination rates of WT, ΔMaAzaR, and CP strains on nutrient-rich 1/4 SDAY solid medium (Figure 3A). When compared with the WT and CP strains, the germination rate of the ΔMaAzaR strain was extremely significantly lower at 4 h (p < 0.001). Further analysis of the median germination time (GT50) revealed that the GT50 of the ΔMaAzaR strain (8.02 ± 0.20 h) was extremely significantly higher than that of the WT (7.08 ± 0.36 h) and CP (7.11 ± 0.23 h) strains (p < 0.001; Figure 3B), indicating that the absence of MaAzaR delayed germination of M. acridum. Subsequently, the conidial yields were determined and found to be significantly reduced for the ΔMaAzaR strain when compared with those for the WT and CP strains (Figure 3C).
At 18 h, while the WT and CP strains were already showing obvious conidiation structures, the ΔMaAzaR strain was still in a mycelial growth state and did not produce conidiation structures until 24 h. At 36 h, while both the WT and CP strains presented significant conidial production, the ΔMaAzaR strain produced only very few conidia. These results consistently suggest that the absence of MaAzaR affected the growth and conidiation characteristics of CP, as evidenced by delayed germination, delayed formation of conidiation structures, and reduced conidial yields.

3.3. Disruption of MaAzaR Decreased Fungal Tolerance to UV-B Irradiation and Cell Wall Disrupting Agents

The conidial germination test was performed after UV-B radiation and heat-shock treatments. As shown in Figure 4A, the conidial germination rate of the ΔMaAzaR strain was significantly lower than those of the WT and CP strains after 3 h of UV-B radiation. Half-inhibition time analysis revealed that the ΔMaAzaR strain had a shorter half-inhibition time of about 0.5 h when compared with the WT and CP strains, indicating that the ΔMaAzaR strain was more sensitive to UV-B radiation than the WT and CP strains. In contrast, heat shock had no significant effect on the ΔMaAzaR strain (Figure 4C,D). Subsequently, we observed the growth of ΔMaAzaR strain in 1/4 SDAY medium supplemented with various types of chemical reagents in the presence of high salt content, oxygen, and osmosis as well as in the presence of fungal cell-wall- and cell-membrane-disrupting agents under adverse conditions. As shown in Figure 4A, colonies of the ΔMaAzaR strain grew slightly larger on the 1/4 SDAY medium without any added chemical reagents, with a slightly whitened periphery, loose folds in the center, and more developed mycelium, when compared with those of the WT and CP strains. In contrast, with the addition of the cell wall disruptor CFW, colonies of the ΔMaAzaR strain were considerably smaller and growth-restricted, presenting a significant slowdown in the growth rate (p < 0.001; Figure 5B) and significant increase in the relative growth inhibition rate (p < 0.001; Figure 5C) when compared with those of the WT and CP strains. This result suggests that the ΔMaAzaR strain is more sensitive to the cell wall disruptor CFW. Moreover, the intracellular trehalose content, which is important for fungal stress response, decreased to 32% in the ΔMaAzaR conidia when compared with that in the WT conidia (p < 0.01) (Figure 5D).

3.4. MaAzaR Regulates Conidiation Pattern Shift

To investigate whether MaAzaR affected the microcycle conidiation mode of M. acridum, the conidiation patterns of different fungal strains were observed on the SYA medium. As shown in Figure 6A, the ΔMaAzaR strain exhibited a shift in the conidiation mode. While microcycle conidiation commenced at 18 h in the WT and CP strains, the ΔMaAzaR strain grew as long hyphae without conidiation until 24 h. At 36 h, the conidia falling from the hyphal tips of the ΔMaAzaR strain were significantly fewer than those produced by the WT and CP strains through microcycle conidiation. Therefore, we speculated that deletion of MaAzaR might have reduced the conidial yield of M. acridum. From day 6 to day 15, the conidial yield of the ΔMaAzaR strain was significantly lower than those of the WT and CP strains (p < 0.001) (Figure 6B). Observation of the macroscopic colony status of each strain on the SYA medium revealed that ΔMaAzaR colonies were smaller and whitened, with a small amount of conidia on the surface, when compared with the WT colonies (Figure 6C). CFW staining revealed that MaAzaR contributed to chitin distribution in the hyphae. When compared with the WT and CP strains, chitin was not only distributed in the septa and tips of the hyphae but was also irregularly distributed in the extended hyphae of the ΔMaAzaR strain (Figure 6D). Moreover, disruption of MaAzaR also caused a significant increase in the apical cell length on the SYA medium (p < 0.001; Figure 6D,E).

3.5. Identification of DEGs Regulated by MaAzaR during Conidiation Pattern Shift Using RNA-seq

To elucidate the role of MaAzaR in conidiation pattern shift, the MaAzaR-regulated genes involved in conidiation pattern transition process were identified through RNA-seq (Accession No. PRJNA884297). Subsequently, WT and ΔMaAzaR samples cultured on SYA medium for 10 h were analyzed based on microscopic observations and expression patterns of MaAzaR during the conidiation pattern shift. A total of 64 DEGs were identified, among which 13 genes (20.3%) were upregulated, and 51 genes (79.7%) were downregulated (Figure 7A), which may include those involved in the conidiation pattern shift induced by MaAzaR. Furthermore, 15 DEGs (23.4%) were annotated as putative proteins (Table S1). To further validate the accuracy of DEGs, the upregulated and downregulated genes among the 64 DEGs were randomly selected for RT-qPCR verification. The results revealed that all the DEGs expressions were close to the RNA-seq data, and the expression trend was consistent, indicating that the RNA-seq data are valid (Figure S2). These findings further suggest the crucial role of MaAzaR in the conidiation pattern shift as well as the specific gene expression patterns associated with this process. KEGG pathway enrichment was performed on DEGs, and the enrichment bubble diagram shown in Figure 7B reveals that the DEGs were mainly enriched in various metabolic pathways, including carbon metabolism, purine metabolism, TCA cycle, and caffeine metabolism. The carbon metabolism pathway was the most enriched, and the caffeine metabolism pathway was the most significantly enriched.
Further GO functional enrichment analysis of the DEGs demonstrated that a total of 13 GO terms were enriched in DEGs, which could be classified into three major categories (Figure 7C). In the present study, the DEGs enriched for metabolic processes were predominantly concentrated in carbon metabolism, followed by cellular components involving the cell, cell membrane, etc., and molecular function including catalytic activity and binding. In summary, MaAzaR may influence the growth, development, and nutrient utilization of M. acridum by regulating the expression of genes related to cellular processes, components, metabolism, and catalytic functions, resulting in a switch in conidiation pattern.

4. Discussion

The results of the present study reveal a shift from microcycle conidiation to normal conidiation in the ΔMaAzaR strain in SYA medium, along with a significant reduction in conidial yield. To further explore the molecular mechanism of MaAzaR regulation of conidiation, we analyzed conidiation transcriptome data. The caffeine metabolism pathway was the most significantly enriched in KEGG pathway. Caffeine metabolism pathway-related proteins have been reported to be associated with DNA damage in yeast cells [37], cell wall integrity [38], and MAPK pathway [39]. GO functional enrichment analysis showed that the DEGs enriched for metabolic processes were predominantly concentrated in carbon metabolism, followed by cellular components involving the cell, cell membrane, etc., and molecular function including catalytic activity and binding. This result suggests that MaAzaR affects a variety of biological processes in the growth and conidiation of M. acridum. A previous study found that cellular processes can influence fungal cell differentiation and development as well as play an important role in cell growth and proliferation [40]. It was shown that genes related to membrane composition and structure can influence fungal spore morphology and mycelial development by affecting membrane formation and structure [41], while genes with catalytic activity were noted to influence nutrient uptake and utilization during fungal conidial growth [42]. Moreover, genes with cell-binding functions were found to regulate the binding and division of fungal conidia to influence conidiation [43].
Analysis of differential genes revealed that 64 genes were significantly differentially expressed (13 upregulated and 51 downregulated), 33 of which have been reported to be involved in key biological processes such as fungal growth and development, conidiation, stress response, cell division, and cell wall integrity. These DEGs included genes encoding enzymes such as catalase (MAC_03712), whose knockout in C. albicans was found to block hyphal development and reduce virulence [44], and phospholipid transport ATPase (MAC_07309), which was noted to be a core regulator of the growth, conidiation, and response to various stress stimuli of B. bassiana [45]. Furthermore, deletion of the adhesion protein gene MAD1 (MAC_00987) in M. anisopliae was observed to suppress conidia formation [46]. Additionally, the DEGs also included genes encoding TFs such as MADS-boxMEF2t-type TF (MAC_07653), which was reported to play an important role in nutrient utilization, sexual development, secondary metabolism, and virulence in Fusarium verticillioides [47], and the unique TF cutinase G box binding protein (MAC_01008) of Ascomycetes, whose deletion in Ustilaginoidea virens was found to affect fungal development and virulence [48]. Moreover, genes encoding the TF MaSom1 (MAC_02477) downstream of the cAMP/PKA signaling pathway, which plays an important role in conidia formation and pathogenicity of M. acridum [49], were also found to be differentially expressed. These results suggest that MaAzaR regulates the expression of a variety of genes involved in fungal development during conidiation.
Among the 33 DEGs, 20 were downregulated, implying that MaAzaR mainly plays a negative regulatory role in the growth and conidiation processes in the ΔMaAzaR strain. A previous study indicated that deletion of MaCreA, a core regulator of carbon source metabolic blockade, in M. acridum significantly decreased conidiation by switching the conidiation mode from microcycle conidiation to normal conidiation [48]. Given that MaAzaR was downregulated and screened from a differential gene library for the switch in conidiation mode regulated by MaCreA in M. acridum, it can be presumed that MaCreA might regulate the expression of MaAzaR. Therefore, we searched for differential expression of genes associated with carbon source utilization in MaAzaR spore-producing transcriptome DEGs and identified that mannitol-1-phosphate 5-dehydrogenase (encoded by MAC_00279), which catalyzes the NAD(H)-dependent interconversion of D-fructose 6-phosphate and D-mannitol 1-phosphate in the mannitol metabolic pathway, and the key sugar isomerase-phosphoenolpyruvate carboxykinase (encoded by MAC_04725) were downregulated. Moreover, MaAzaR, in addition to regulating the expression of the abovementioned 33 DEGs, might also partly negatively regulate the expression of genes related to carbon source metabolism, inhibiting the nutrient utilization process of the strain and allowing the ΔMaAzaR strain to switch its conidiation pattern.
Stabilizing the effectiveness of the control is a major challenge for researchers studying entomopathogenic fungi. The survival of fungal conidia in the field is affected by exposure to abiotic factors such as high temperature, humidity, and UV-B radiation [50]. UV-B radiation was found to disrupt the cell wall and inactivate conidia in B. bassiana [51]. In the present study, a highly significant decrease in the conidial germination rate of the ΔMaAzaR strain was noted after 3 and 4.5 h of UV-B radiation, along with a significant reduction in the half-inhibition time, reduced tolerance to UV-B radiation, and unaffected hygrometric tolerance. The cell wall of filamentous fungi is a complex structure mainly composed of polysaccharides, primarily α-glucans, β-glucans, galactomannans, and chitins [46]. It is highly dynamic and plastic, possessing a heterogeneous composition that is pivotal for cell viability, morphogenesis, and pathogenesis. Furthermore, as the outermost layer, the cell wall serves as a protective barrier against environmental physical and chemical factors, regulating permeability and safeguarding cells from mechanical or osmotic stress [46]. In the present study, the ΔMaAzaR strain exhibited increased sensitivity to CFW. In particular, the growth of the ΔMaAzaR strain was constrained following supplementation of CFW to 1/4 SDAY medium, resulting in significantly smaller colonies when compared with those of the WT and CP strains. These observations are consistent with the findings reported by Bermejo et al., who demonstrated that CFW and other compounds interacting with cell wall components can lead to alterations in the cell wall, ultimately causing significant changes in cell morphology and appearance [52]. In Saccharomyces cerevisiae, application of CFW was found to cause the formation of abnormal septum, preventing the detachment and normal separation of daughter cells [53]. Studies in B. bassiana show that BbpksP impaired the cell wall structure of conidia and therefore UV tolerance [54]. Genes related to fungal cell wall composition, such as MAC_03926 (guanosine-diphosphatase) and MAC_03926 (guanosine-diphosphatase), were found in the RNA-seq database, which further explains the effect of the MaAzaR gene on the stress tolerance of M. acridum conidia. As a cell wall disruptor, CFW is known to exert its antifungal effect by binding to chitin components within the cell wall. In the present study, CFW staining of the hyphae evidently showed that the chitin distribution in the ΔMaAzaR strains was irregular. These abnormalities were not only confined to the mycelial tips and septum but were also observed as random distributions throughout the hyphae. This finding suggests that MaAzaR plays a pivotal role in regulating the growth and development of hyphae by influencing the distribution of chitin within the fungal cell wall.

5. Conclusions

In summary, the zinc-cluster TF MaAzaR, which is examined in the present study, plays a pivotal role in the biocontrol traits of M. acridum, including stress tolerance, conidiation ability, and conidiation mode. The results not only reveal the fundamental function of MaAzaR in M. acridum but also clarify the molecular mechanism underlying the conidiation mode shift. Thus, the present study provides a substantial theoretical foundation for the selection of Entomopathogenic fungi as well as the promotion and utilization of mycoinsecticides.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/jof10070468/s1, Figure S1. Transcription levels of MaAzaR on SYA medium. Figure S2. RT-qPCR validation of DEGs identified in RNA-seq analysis. Table S1. The DEGs in conidiation of ΔMaAzaR compared to WT. Table S2. Primers used in the study.

Author Contributions

Conceptualization, Y.X., and G.P.; investigation, J.Z. and S.W.; methodology, Y.X. and G.P.; project administration, G.P.; funding acquisition, G.P.; writing—original draft, J.Z.; software, S.W.; writing—review and editing, G.P. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by International Cooperation and Exchange Program of the National Natural Science Foundation of China (Nos. 82261128004 and 2022YMFL1002), the technology innovation and application development project of Chongqing (No. CSTB2023TIAD-KPX0045), and the fundamental research funds for the central universities (No. 2023CDJXY009 and 2023CDJKYJH043).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

RNA-seq data were deposited in the NCBI BioProject database (accession No. PRJNA884297).

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Wang, J.B.; St. Leger, R.J.; Wang, C. Chapter Three—Advances in Genomics of Entomopathogenic Fungi. In Advances in Genetics; Lovett, B., St. Leger, R.J., Eds.; Genetics and Molecular Biology of Entomopathogenic Fungi; Academic Press: Cambridge, MA, USA, 2016; Volume 94, pp. 67–105. [Google Scholar]
  2. Peng, G.; Wang, Z.; Yin, Y.; Zeng, D.; Xia, Y. Field Trials of Metarhizium anisopliae Var. acridum (Ascomycota: Hypocreales) against Oriental Migratory Locusts, Locusta migratoria manilensis (Meyen) in Northern China. Crop Prot. 2008, 27, 1244–1250. [Google Scholar] [CrossRef]
  3. Lomer, C.J.; Bateman, R.P.; Johnson, D.L.; Langewald, J.; Thomas, M. Biological Control of Locusts and Grasshoppers. Annu. Rev. Entomol. 2001, 46, 667–702. [Google Scholar] [CrossRef] [PubMed]
  4. Wen, Z.; Fan, Y.; Xia, Y.; Jin, K. MaOpy2, a Transmembrane Protein, Is Involved in Stress Tolerances and Pathogenicity and Negatively Regulates Conidial Yield by Shifting the Conidiation Pattern in Metarhizium acridum. J. Fungi 2022, 8, 587. [Google Scholar] [CrossRef] [PubMed]
  5. Sekiguchi, J.; Gaucher, G.; Costerton, J. Microcycle Conidiation in Penicillium Urticae—Ultrastructural Investigation of Conidiogenesis. Can. J. Microbiol. 1975, 21, 2069–2083. [Google Scholar] [CrossRef] [PubMed]
  6. Pazout, J.; Schroder, P. Microcycle Conidiation in Submerged Cultures of Penicillium-Cyclopium Attained Without Temperature-Changes. J. Gen. Microbiol. 1988, 134, 2685–2692. [Google Scholar] [CrossRef] [PubMed]
  7. Anderson, J.G.; Smith, J.E. The Production of Conidiophores and Conidia by Newly Germinated Conidia of Aspergillus niger (Microcycle Conidiation). J. Gen. Microbiol. 1971, 69, 185–197. [Google Scholar] [CrossRef] [PubMed]
  8. Hanlin, R.T. Microcycle Conidiation–A Review. Mycoscience 1994, 35, 113–123. [Google Scholar] [CrossRef]
  9. Jung, B.; Kim, S.; Lee, J. Microcyle Conidiation in Filamentous Fungi. Mycobiology 2014, 42, 1–5. [Google Scholar] [CrossRef]
  10. Adams, T.H.; Boylan, M.T.; Timberlake, W.E. BrlA Is Necessary and Sufficient to Direct Conidiophore Development in Aspergillus nidulans. Cell 1988, 54, 353–362. [Google Scholar] [CrossRef]
  11. Boylan, M.T.; Mirabito, P.M.; Willett, C.E.; Zimmerman, C.R.; Timberlake, W.E. Isolation and Physical Characterization of Three Essential Conidiation Genes from Aspergillus Nidulans. Mol. Cell. Biol. 1987, 7, 3113–3118. [Google Scholar] [CrossRef]
  12. Seo, J.-A.; Guan, Y.; Yu, J.-H. FluG-Dependent Asexual Development in Aspergillus nidulans Occurs via Derepression. Genetics 2006, 172, 1535–1544. [Google Scholar] [CrossRef]
  13. Guo, C.-T.; Luo, X.-C.; Ying, S.-H.; Feng, M.-G. Differential Roles of Five Fluffy Genes (flbA–flbE) in the Lifecycle In Vitro and In Vivo of the Insect–Pathogenic Fungus Beauveria Bassiana. J. Fungi 2022, 8, 334. [Google Scholar] [CrossRef]
  14. Yu, J.H.; Wieser, J.; Adams, T.H. The Aspergillus FlbA RGS Domain Protein Antagonizes G Protein Signaling to Block Proliferation and Allow Development. EMBO J. 1996, 15, 5184–5190. [Google Scholar] [CrossRef]
  15. Garzia, A.; Etxebeste, O.; Herrero-Garcia, E.; Fischer, R.; Espeso, E.A.; Ugalde, U. Aspergillus nidulans FlbE Is an Upstream Developmental Activator of Conidiation Functionally Associated with the Putative Transcription Factor Flbb. Mol. Microbiol. 2009, 71, 172–184. [Google Scholar] [CrossRef]
  16. Zhang, S.; Peng, G.; Xia, Y. Microcycle Conidiation and the Conidial Properties in the Entomopathogenic Fungus Metarhizium Acridum on Agar Medium. Biocontrol Sci. Technol. 2010, 20, 809–819. [Google Scholar] [CrossRef]
  17. Gao, P.; Li, M.; Jin, K.; Xia, Y. The Homeobox Gene MaH1 Governs Microcycle Conidiation for Increased Conidial Yield by Mediating Transcription of Conidiation Pattern Shift-Related Genes in Metarhizium Acridum. Appl. Microbiol. Biotechnol. 2019, 103, 2251–2262. [Google Scholar] [CrossRef]
  18. Li, C.; Xu, D.; Hu, M.; Zhang, Q.; Xia, Y.; Jin, K. MaNCP1, a C2H2 Zinc Finger Protein, Governs the Conidiation Pattern Shift through Regulating the Reductive Pathway for Nitric Oxide Synthesis in the Filamentous Fungus Metarhizium acridum. Microbiol. Spectr. 2022, 10, e00538-22. [Google Scholar] [CrossRef]
  19. Fang, W.; St. Leger, R.J. Enhanced UV Resistance and Improved Killing of Malaria Mosquitoes by Photolyase Transgenic Entomopathogenic Fungi. PLoS ONE 2012, 7, e43069. [Google Scholar] [CrossRef]
  20. Braga, G.U.L.; Flint, S.D.; Miller, C.D.; Anderson, A.J.; Roberts, D.W. Both Solar UVA and UVB Radiation Impair Conidial Culturability and Delay Germination in the Entomopathogenic Fungus Metarhizium anisopliae. Photochem. Photobiol. 2001, 74, 734–739. [Google Scholar] [CrossRef]
  21. Thaochan, N.; Benarlee, R.; Prabhakar, C.S.; Hu, Q. Impact of Temperature and Relative Humidity on Effectiveness of Metarhizium guizhouense PSUM02 against Longkong Bark Eating Caterpillar Cossus chloratus Swinhoe under Laboratory and Field Conditions. J. Asia-Pac. Entomol. 2020, 23, 285–290. [Google Scholar] [CrossRef]
  22. Khan, M.A.; Ahmad, W. (Eds.) Microbes for Sustainable Insect Pest Management. Volume 1: An Eco-Friendly Approach; Sustainability in Plant and Crop Protection; Springer: Cham, Switzerland, 2019; ISBN 978-3-030-23044-9. [Google Scholar]
  23. Yu, L.; Xu, S.-Y.; Luo, X.-C.; Ying, S.-H.; Feng, M.-G. Comparative Roles of Rad4A and Rad4B in Photoprotection of Beauveria Bassiana from Solar Ultraviolet Damage. J. Fungi 2023, 9, 154. [Google Scholar] [CrossRef]
  24. McMillan, S.D.; Oberlie, N.R.; Hardtke, H.A.; Montes, M.M.; Brown, D.W.; McQuade, K.L. A Secondary Function of Trehalose-6-Phosphate Synthase Is Required for Resistance to Oxidative and Desiccation Stress in Fusarium verticillioides. Fungal Biol. 2023, 127, 918–926. [Google Scholar] [CrossRef]
  25. Shelest, E. Transcription Factors in Fungi. FEMS Microbiol. Lett. 2008, 286, 145–151. [Google Scholar] [CrossRef]
  26. Chang, P.-K.; Ehrlich, K.C. Genome-Wide Analysis of the Zn(II)2Cys6 Zinc Cluster-Encoding Gene Family in Aspergillus Flavus. Appl. Microbiol. Biotechnol. 2013, 97, 4289–4300. [Google Scholar] [CrossRef]
  27. He, R.; Zhang, L.; Lan, J.; Mei, S.; Li, Y. Cmcrf1, a Putative Zn2Cys6 Fungal Transcription Factor, Is Involved in Conidiation, Carotenoid Production, and Fruiting Body Development in Cordyceps Militaris. Biology 2022, 11, 1535. [Google Scholar] [CrossRef]
  28. Liao, L.-S.; Li, C.-X.; Zhang, F.-F.; Yan, Y.-S.; Luo, X.-M.; Zhao, S.; Feng, J.-X. How an Essential Zn2Cys6 Transcription Factor PoxCxrA Regulates Cellulase Gene Expression in Ascomycete Fungi? Biotechnol. Biofuels 2019, 12, 105. [Google Scholar] [CrossRef]
  29. Zhang, Z.; Jia, H.; Liu, N.; Li, H.; Meng, Q.; Wu, N.; Cao, Z.; Dong, J. The Zinc Finger Protein StMR1 Affects the Pathogenicity and Melanin Synthesis of Setosphaeria turcica and Directly Regulates the Expression of DHN Melanin Synthesis Pathway Genes. Mol. Microbiol. 2022, 117, 261–273. [Google Scholar] [CrossRef]
  30. Qiu, L.; Zhang, J.; Song, J.-Z.; Hu, S.-J.; Zhang, T.-S.; Li, Z.; Wang, J.-J.; Cheng, W. Involvement of BbTpc1, an Important Zn(II)2Cys6 Transcriptional Regulator, in Chitin Biosynthesis, Fungal Development and Virulence of an Insect Mycopathogen. Int. J. Biol. Macromol. 2021, 166, 1162–1172. [Google Scholar] [CrossRef]
  31. Gil-Durán, C.; Rojas-Aedo, J.F.; Medina, E.; Vaca, I.; García-Rico, R.O.; Villagrán, S.; Levicán, G.; Chávez, R. The Pcz1 Gene, Which Encodes a Zn(II)2Cys6 Protein, Is Involved in the Control of Growth, Conidiation, and Conidial Germination in the Filamentous Fungus Penicillium Roqueforti. PLoS ONE 2015, 10, e0120740. [Google Scholar] [CrossRef]
  32. Carrillo, A.J.; Schacht, P.; Cabrera, I.E.; Blahut, J.; Prudhomme, L.; Dietrich, S.; Bekman, T.; Mei, J.; Carrera, C.; Chen, V.; et al. Functional Profiling of Transcription Factor Genes in Neurospora crassa. G3 Genes|Genomes|Genet. 2017, 7, 2945–2956. [Google Scholar] [CrossRef]
  33. Zabala, A.O.; Xu, W.; Chooi, Y.-H.; Tang, Y. Characterization of a Silent Azaphilone Gene Cluster from Aspergillus Niger ATCC 1015 Reveals a Hydroxylation-Mediated Pyran-Ring Formation. Chem. Biol. 2012, 19, 1049–1059. [Google Scholar] [CrossRef]
  34. Chen, J.-F.; Tan, J.-J.; Wang, J.-Y.; Mao, A.-J.; Xu, X.-P.; Zhang, Y.; Zheng, X.; Liu, Y.; Jin, D.; Li, X.-B.; et al. The Zinc Finger Transcription Factor BbCmr1 Regulates Conidium Maturation in Beauveria Bassiana. Microbiol. Spectr. 2022, 10, e02066-21. [Google Scholar] [CrossRef]
  35. Cock, P.J.A.; Fields, C.J.; Goto, N.; Heuer, M.L.; Rice, P.M. The Sanger Fastq File Format for Sequences with Quality Scores, and the Solexa/Illumina Fastq Variants. Nucleic Acids Res. 2010, 38, 1767–1771. [Google Scholar] [CrossRef]
  36. Love, M.I.; Huber, W.; Anders, S. Moderated Estimation of Fold Change and Dispersion for RNA-Seq Data with DESeq2. Genome Biol. 2014, 15, 550. [Google Scholar] [CrossRef]
  37. Ciccia, A.; Elledge, S.J. The DNA Damage Response: Making It Safe to Play with Knives. Mol. Cell 2010, 40, 179–204. [Google Scholar] [CrossRef]
  38. Levin, D.E. Cell Wall Integrity Signaling in Saccharomyces cerevisiae. Microbiol. Mol. Biol. Rev. 2005, 69, 262–291. [Google Scholar] [CrossRef]
  39. Truman, A.W.; Kim, K.-Y.; Levin, D.E. Mechanism of Mpk1 Mitogen-Activated Protein Kinase Binding to the Swi4 Transcription Factor and Its Regulation by a Novel Caffeine-Induced Phosphorylation. Mol. Cell. Biol. 2009, 29, 6449–6461. [Google Scholar] [CrossRef]
  40. Ribeiro, L.F.C.; Chelius, C.L.; Harris, S.D.; Marten, M.R. Insights Regarding Fungal Phosphoproteomic Analysis. Fungal Genet. Biol. 2017, 104, 38–44. [Google Scholar] [CrossRef]
  41. Roberts, S.K.; Milnes, J.; Caddick, M. Characterisation of AnBEST1, a Functional Anion Channel in the Plasma Membrane of the Filamentous Fungus, Aspergillus Nidulans. Fungal Genet. Biol. 2011, 48, 928–938. [Google Scholar] [CrossRef]
  42. Wang, S.; Lin, R.; Tumukunde, E.; Zeng, W.; Bao, Q.; Wang, S.; Wang, Y. Glutamine Synthetase Contributes to the Regulation of Growth, Conidiation, Sclerotia Development, and Resistance to Oxidative Stress in the Fungus Aspergillus Flavus. Toxins 2022, 14, 822. [Google Scholar] [CrossRef]
  43. Peñalva, M.A.; Tilburn, J.; Bignell, E.; Arst, H.N. Ambient pH Gene Regulation in Fungi: Making Connections. Trends Microbiol. 2008, 16, 291–300. [Google Scholar] [CrossRef] [PubMed]
  44. Nakagawa, Y. Catalase Gene Disruptant of the Human Pathogenic Yeast Candida albicans Is Defective in Hyphal Growth, and a Catalase-specific Inhibitor Can Suppress Hyphal Growth of Wild-type Cells. Microbiol. Immunol. 2008, 52, 16–24. [Google Scholar] [CrossRef] [PubMed]
  45. Wang, J.; Zhou, G.; Ying, S.; Feng, M. P-type Calcium ATPASE Functions as a Core Regulator of Beauveria bassiana Growth, Conidiation and Responses to Multiple Stressful Stimuli through Cross-talk with Signalling Networks. Environ. Microbiol. 2013, 15, 967–979. [Google Scholar] [CrossRef] [PubMed]
  46. Wang, C.; St Leger, R.J. The MAD1 Adhesin of Metarhizium anisopliae Links Adhesion with Blastospore Production and Virulence to Insects, and the MAD2 Adhesin Enables Attachment to Plants. Eukaryot. Cell 2007, 6, 808–816. [Google Scholar] [CrossRef] [PubMed]
  47. Ortiz, C.S.; Shim, W.-B. The Role of MADS-Box Transcription Factors in Secondary Metabolism and Sexual Development in the Maize Pathogen Fusarium verticillioides. Microbiology 2013, 159, 2259–2268. [Google Scholar] [CrossRef]
  48. Chen, X.; Li, P.; Liu, H.; Chen, X.; Huang, J.; Luo, C.; Li, G.; Hsiang, T.; Collinge, D.B.; Zheng, L. A Novel Transcription Factor UvCGBP1 Regulates Development and Virulence of Rice False Smut Fungus Ustilaginoidea virens. Virulence 2021, 12, 1563–1579. [Google Scholar] [CrossRef] [PubMed]
  49. Du, Y.; Jin, K.; Xia, Y. Involvement of MaSom1, a Downstream Transcriptional Factor of cAMP/PKA Pathway, in Conidial Yield, Stress Tolerances, and Virulence in Metarhizium acridum. Appl. Microbiol. Biotechnol. 2018, 102, 5611–5623. [Google Scholar] [CrossRef]
  50. Mascarin, G.M.; Jaronski, S.T. The Production and Uses of Beauveria Bassiana as a Microbial Insecticide. World J. Microbiol. Biotechnol. 2016, 32, 177. [Google Scholar] [CrossRef] [PubMed]
  51. Li, F.; Shi, H.-Q.; Ying, S.-H.; Feng, M.-G. WetA and VosA Are Distinct Regulators of Conidiation Capacity, Conidial Quality, and Biological Control Potential of a Fungal Insect Pathogen. Appl. Microbiol. Biotechnol. 2015, 99, 10069–10081. [Google Scholar] [CrossRef]
  52. Bermejo, C.; García, R.; Straede, A.; Rodríguez-Peña, J.M.; Nombela, C.; Heinisch, J.J.; Arroyo, J. Characterization of Sensor-Specific Stress Response by Transcriptional Profiling of Wsc1 and Mid2 Deletion Strains and Chimeric Sensors in Saccharomyces Cerevisiae. OMICS J. Integr. Biol. 2010, 14, 679–688. [Google Scholar] [CrossRef]
  53. Roncero, C.; Durán, A. Effect of Calcofluor White and Congo Red on Fungal Cell Wall Morphogenesis: In Vivo Activation of Chitin Polymerization. J. Bacteriol. 1985, 163, 1180–1185. [Google Scholar] [CrossRef] [PubMed]
  54. Wang, J.; Ma, Y.; Liu, Y.; Tong, S.; Zhu, S.; Jin, D.; Pei, Y.; Fan, Y. A Polyketide Synthase, BbpksP, Contributes to Conidial Cell Wall Structure and UV Tolerance in Beauveria Bassiana. J. Invertebr. Pathol. 2020, 169, 107280. [Google Scholar] [CrossRef] [PubMed]
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Figure 1. Structural and phylogenetic features of MaAzaR. (A) Domain structure analysis of MaAzaR. GAL4: GAL4-like Zn(II)2Cys6 binuclear cluster DNA binding domain; Fungal_trans: fungal TF regulatory middle homology region. (B) Domain sequence alignments of MaAzaR with other species. (C) Phylogenetic analysis of AzaR protein sequence from different fungi, including Metarhizium anisopliae (KAF5129833.1), Metarhizium acridum (CQMa102, XP_007812705.1), Aspergillus fumigatus (KAH1485999.1), Beauveria bassiana (XP_008596496.1), Aspergillus niger (GKZ68934.1), Neurospora crassa (XP_964064.3), Ustilago maydis (XP_011389956.1), Saccharomyces cerevisiae (NP_010031.1), Canidia albicans (KAF6072832.1), and Pyricularia oryzae (XP_003720741.1).
Figure 1. Structural and phylogenetic features of MaAzaR. (A) Domain structure analysis of MaAzaR. GAL4: GAL4-like Zn(II)2Cys6 binuclear cluster DNA binding domain; Fungal_trans: fungal TF regulatory middle homology region. (B) Domain sequence alignments of MaAzaR with other species. (C) Phylogenetic analysis of AzaR protein sequence from different fungi, including Metarhizium anisopliae (KAF5129833.1), Metarhizium acridum (CQMa102, XP_007812705.1), Aspergillus fumigatus (KAH1485999.1), Beauveria bassiana (XP_008596496.1), Aspergillus niger (GKZ68934.1), Neurospora crassa (XP_964064.3), Ustilago maydis (XP_011389956.1), Saccharomyces cerevisiae (NP_010031.1), Canidia albicans (KAF6072832.1), and Pyricularia oryzae (XP_003720741.1).
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Figure 2. Construction of MaAzaR knockout and complementary vectors and verification of the corresponding strains. (A) Schematic diagram of the construction of the MaAzaR knockout and complementary vector; (B) PCR validation of knockout and complementary transformant. ΔMaAzaR-VF/Pt-R indicates left-arm validation of knockout transformant #1 and #2 (1323 bp); Bar-F/MaAzaR-VR denotes right-arm validation of knockout transformant #1 and #2 (1488 bp); MaAzaR-SF/GFP-VR indicates validation of complementary transformant C1 and C2 (3019 bp). The mutants used in subsequent experiments are marked in red font. (C) Analysis of MaAzaR gene expression in each strain. The expression level of MaAzaR in WT strain was used as a control. WT: wild type; ΔMaAzaR: MaAzaR knockout strain; CP: complementary strain. ***: p < 0.001; ns: no significant difference, p > 0.05. Error bars denote standard deviation for different strains.
Figure 2. Construction of MaAzaR knockout and complementary vectors and verification of the corresponding strains. (A) Schematic diagram of the construction of the MaAzaR knockout and complementary vector; (B) PCR validation of knockout and complementary transformant. ΔMaAzaR-VF/Pt-R indicates left-arm validation of knockout transformant #1 and #2 (1323 bp); Bar-F/MaAzaR-VR denotes right-arm validation of knockout transformant #1 and #2 (1488 bp); MaAzaR-SF/GFP-VR indicates validation of complementary transformant C1 and C2 (3019 bp). The mutants used in subsequent experiments are marked in red font. (C) Analysis of MaAzaR gene expression in each strain. The expression level of MaAzaR in WT strain was used as a control. WT: wild type; ΔMaAzaR: MaAzaR knockout strain; CP: complementary strain. ***: p < 0.001; ns: no significant difference, p > 0.05. Error bars denote standard deviation for different strains.
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Figure 3. Characterization of growth and conidiation of the fungal strains on 1/4 SDAY medium. (A) Conidial germination rates (%) of the WT, ΔMaAzaR, and CP strains on 1/4 SDAY medium. (B) Analysis of GT50. (C) Conidial yields of the WT, ΔMaAzaR, and CP strains assessed on 1/4 SDAY medium. (D) Conidiation of the WT, ΔMaAzaR, and CP strains on 1/4 SDAY medium. Arrows indicate conidia on the conidiophores. Error bars denote the standard error of the mean. *: p < 0.05; **: p < 0.01; ***: p < 0.001; ns: no significant difference, p > 0.05.
Figure 3. Characterization of growth and conidiation of the fungal strains on 1/4 SDAY medium. (A) Conidial germination rates (%) of the WT, ΔMaAzaR, and CP strains on 1/4 SDAY medium. (B) Analysis of GT50. (C) Conidial yields of the WT, ΔMaAzaR, and CP strains assessed on 1/4 SDAY medium. (D) Conidiation of the WT, ΔMaAzaR, and CP strains on 1/4 SDAY medium. Arrows indicate conidia on the conidiophores. Error bars denote the standard error of the mean. *: p < 0.05; **: p < 0.01; ***: p < 0.001; ns: no significant difference, p > 0.05.
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Figure 4. Assessment of UV-B irradiation and heat-shock tolerance. (A) Germination rates of the WT, ΔMaAzaR, and CP strains after 1.5, 3, 4.5, and 6 h of UV-B irradiation (1350 mW/m2). (B) Median inhibition time (IT50) of the WT, ΔMaAzaR, and CP strains after UV-B irradiation. (C) Germination rates of the WT, ΔMaAzaR, and CP strains after 46 °C heat-shock treatment for 3, 6, 9, and 12 h. (D) Median inhibition time (IT50) of the WT, ΔMaAzaR, and CP strains after damp heat treatment. Error bars indicate standard error of mean. *: p < 0.05; **: p < 0.01; ***: p < 0.001; ns: no significant difference, p > 0.05.
Figure 4. Assessment of UV-B irradiation and heat-shock tolerance. (A) Germination rates of the WT, ΔMaAzaR, and CP strains after 1.5, 3, 4.5, and 6 h of UV-B irradiation (1350 mW/m2). (B) Median inhibition time (IT50) of the WT, ΔMaAzaR, and CP strains after UV-B irradiation. (C) Germination rates of the WT, ΔMaAzaR, and CP strains after 46 °C heat-shock treatment for 3, 6, 9, and 12 h. (D) Median inhibition time (IT50) of the WT, ΔMaAzaR, and CP strains after damp heat treatment. Error bars indicate standard error of mean. *: p < 0.05; **: p < 0.01; ***: p < 0.001; ns: no significant difference, p > 0.05.
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Figure 5. Chemical resistance analysis. (A) Colony growth status of each strain on various stress media supplemented with different chemical reagents. (B) Growth rate of each strain on different stress media. (C) Relative growth inhibition (RGI) of the fungal strains. (D) Intracellular trehalose accumulation in 15-day-old aerial conidia incubated on 1/4 SDAY. *: p < 0.05; ***: p < 0.001; ns: no significant difference, p > 0.05.
Figure 5. Chemical resistance analysis. (A) Colony growth status of each strain on various stress media supplemented with different chemical reagents. (B) Growth rate of each strain on different stress media. (C) Relative growth inhibition (RGI) of the fungal strains. (D) Intracellular trehalose accumulation in 15-day-old aerial conidia incubated on 1/4 SDAY. *: p < 0.05; ***: p < 0.001; ns: no significant difference, p > 0.05.
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Figure 6. Characterization of growth and conidiation of different fungal strains on SYA medium. (A) Colony growth status of the WT, ΔMaAzaR, and CP strains after 5 days of growth on SYA medium (B) Conidial yields of ΔMaAzaR, WT, and CP strains on SYA medium. (C) Initial stage of conidiation of the WT, ΔMaAzaR, and CP strains on SYA medium (white arrow: microcycle conidiation; black arrow: normal conidiation). Error bars indicate standard error of mean. (D) Microscopic observation of chitin in hyphae stained with CFW. White arrows indicate irregular distributions of chitin. (E) Length of apical hyphal cells in the WT, ΔMaAzaR, and CP strains. *: p < 0.05; ***: p < 0.001; ns: no significant difference, p > 0.05.
Figure 6. Characterization of growth and conidiation of different fungal strains on SYA medium. (A) Colony growth status of the WT, ΔMaAzaR, and CP strains after 5 days of growth on SYA medium (B) Conidial yields of ΔMaAzaR, WT, and CP strains on SYA medium. (C) Initial stage of conidiation of the WT, ΔMaAzaR, and CP strains on SYA medium (white arrow: microcycle conidiation; black arrow: normal conidiation). Error bars indicate standard error of mean. (D) Microscopic observation of chitin in hyphae stained with CFW. White arrows indicate irregular distributions of chitin. (E) Length of apical hyphal cells in the WT, ΔMaAzaR, and CP strains. *: p < 0.05; ***: p < 0.001; ns: no significant difference, p > 0.05.
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Figure 7. Number of DEGs in the conidiation stage transcriptome and analysis of the KEGG pathway and GO functional enrichment. (A) The number of upregulated and downregulated DEGs. (B) Enrichment analysis of DEGs in the KEGG pathway. (C) GO functional enrichment analysis of DEGs.
Figure 7. Number of DEGs in the conidiation stage transcriptome and analysis of the KEGG pathway and GO functional enrichment. (A) The number of upregulated and downregulated DEGs. (B) Enrichment analysis of DEGs in the KEGG pathway. (C) GO functional enrichment analysis of DEGs.
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Zhou, J.; Wang, S.; Xia, Y.; Peng, G. MaAzaR, a Zn2Cys6/Fungus-Specific Transcriptional Factor, Is Involved in Stress Tolerance and Conidiation Pattern Shift in Metarhizium acridum. J. Fungi 2024, 10, 468. https://doi.org/10.3390/jof10070468

AMA Style

Zhou J, Wang S, Xia Y, Peng G. MaAzaR, a Zn2Cys6/Fungus-Specific Transcriptional Factor, Is Involved in Stress Tolerance and Conidiation Pattern Shift in Metarhizium acridum. Journal of Fungi. 2024; 10(7):468. https://doi.org/10.3390/jof10070468

Chicago/Turabian Style

Zhou, Jinyuan, Siqin Wang, Yuxian Xia, and Guoxiong Peng. 2024. "MaAzaR, a Zn2Cys6/Fungus-Specific Transcriptional Factor, Is Involved in Stress Tolerance and Conidiation Pattern Shift in Metarhizium acridum" Journal of Fungi 10, no. 7: 468. https://doi.org/10.3390/jof10070468

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