1. Introduction
The culture degeneration or attenuation of the entomopathogenic fungus
Beauveria bassiana has long been reported to be parallel to its widespread application in integrated pest management (IPM). Several fungi degenerate after successive subculturing in vitro, such as on potato dextrose agar (PDA) and Sabouraud dextrose agar (SDA). The degenerated cultures show a reduction or loss in virulence [
1,
2], which is partially attributed to the reduced secretion of host-cuticle-degrading protease and a reduction in conidiation [
3,
4]. Entomopathogenic fungi with inconsistent conidial yield or virulence become unattractive to agricultural practitioners [
5].
The physiological changes in degenerated
Beauveria bassiana cultures were recently unraveled via proteomics analysis. Late in vitro subcultures had increased levels of proteins, which were associated with oxidative stress response, autophagy, amino acid homeostasis and apoptosis, whilst decreased levels of proteins were associated with DNA repair, ribosome biogenesis, energy metabolism and virulence [
6]. The finding that two effectors of target of rapamycin (TOR) signaling were elevated in late subcultures suggested the contribution of TOR signaling components in
B. bassiana degeneration.
TOR signaling is the master regulator of growth and is highly conserved in eukaryotes [
7]. It is mediated by two functionally distinct complexes, TOR complex 1 (TORC1) and TORC2. The better understood TORC1, which is rapamycin sensitive, responds to nutrient availability and promotes growth by stimulating nutrient uptake and the synthesis of proteins, lipids and nucleotides [
8]. TORC2, which is marginally rapamycin sensitive, coordinates with its major downstream effector Ypk1 and serves as the major regulator of plasma membrane lipid homeostasis [
9]. Intriguingly, numerous studies have suggested that TORC1 inhibition effectively extended the lifespan across different eukaryotes such as yeast,
Caenorhabditis elegans, Drosophila melanogaster and mice [
10,
11,
12,
13]. Nonetheless, few reports establish a link between TOR inhibition and culture degeneration, analogous to the in vitro lifespan, in filamentous fungi.
Beauveria bassiana BCC 2660 has a single copy of the TOR kinase gene,
tor2, which serves as a common core component of TORC1 and TORC2, similarly to most eukaryotes. In this study, a
B. bassiana PTet-On tor2 mutant was used to investigate exogenous
tor2 expression induction [
14], which helped to document a correlation between
tor2 expression levels and the affected phenotypes as a result of culture degeneration. We aim to determine the contribution of TOR kinase in growth and development in the fungus, and to determine if the relevant contributions are dose dependent. We demonstrate the significance of
tor2 in mycelial growth, conidiation, virulence and oxidative stress tolerance in this fungus.
2. Materials and Methods
2.1. Fungal/Bacterial Strains and Culture Conditions
Beauveria bassiana BCC 2660 was acquired from BIOTEC Culture Collection (BCC), Thailand and was maintained on potato dextrose agar (PDA; Difco, Franklin Lakes, NJ, USA) at 25–28 °C. To ensure the highest virulence, the fungus was first passaged through
Spodoptera exigua following Jirakkakul et al.’s (2018) [
6] protocol. In subculturing, conidia from 7-day-old cultures were harvested. Conidial suspension containing 1 × 10
7 conidia was spread on half-strength PDA and incubated for 7 days at 25–28 °C. Wild-type (WT) strain of
B. bassiana BCC 2660 was subcultured from the 2nd to 20th subcultures for the examination of culture degeneration. For isolation of genomic DNA or total RNA,
B. bassiana was shaken in potato dextrose broth (PDB) at 150 rpm at 25–28 °C for 4 days. The Tet-On inducer, doxycycline (Dox), at 0, 0.1, 0.5, 1 or 20 µg·mL
−1 was also supplemented in culture medium for total RNA extraction.
Escherichia coli DH5α was routinely used in molecular cloning. Culture media were supplemented with ampicillin for the recombinant DNA cloning of pCB1534 (Fungal Genetic Stock Center, Kansas, MO, USA; [
15]), pFC332 and pFC334 [
16].
2.2. Construction of CRISPR/Cas9 tor2-Targeted Vector and Tet-On-Carrying Donor Vector
CRISPR/Cas9-directed double-stranded break (DSB) and homology-directed repair were adopted to introduce the Tet-On promoter just upstream of the
tor2 coding sequence. The endogenous
tor2 promoter remained since it was shared between
tor2 and an adjacent gene, encoding a hypothetical protein. The
tor2-targeted CRISPR/Cas9 vector was cloned by following Nødvig et al.’s (2015) protocol and using the plasmids pFC332 and pFC334 [
16]. Two fragments were amplified for the construction of
tor2-targeted sgRNA cassette. The first fragment was amplified with primers CSN389 (5′-GGGTTTAAUGCGTAAGCTCCCTAATTGGC-3′) and tor2sgRNA-r (5′-AGCTT ACUCGTTTCGTCCTCACGGACTCATCAGGTCACTCGGTGATGTCTGCTCAGCG-3′). The second fragment was amplified with primers tor2sgRNA-f (5′-AGTAAGCUCGTCGTCACTGAATTGGGAAACCGGTTTTAGAGCTAGAAATAGCAAGTTAAA-3′) and CSN390 (5′-GGTCTTAAUGAGCCAAGAGCGGATTCCTC-3′). The two fragments integrated the
tor2-specific protospacer sequence (5′-GTCACTGAATTGGGAAACCGGGG-3′; PAM site is CCG;
Figure 1A), and were then cloned into the backbone vector pFC332 at the restriction site PacI/Nt.BbvCI via USER cloning (New England Biolabs, Ipswich, MA, USA), resulting in the recombinant plasmid pFC-TOR2.
The donor DNA vector contains the 2581 bp Tet-On sequence, flanked by a 991 bp 5′-homology arm (5′-HA) and a 900 bp 3′-homology arm (3′-HA) that have sequences complementary to the
tor2 promoter sequences and the 5′ end of the
tor2 coding sequence, respectively. For the construction of the donor DNA vector, the three DNA fragments were cloned into the vector pCB1534 via restriction cloning. The primers 5F-Bsi (5′-GATCGTACGCTGATGCTTCTCGAATCTGC-3′) and 5R-Nco (5′-GTACCATGG AAGCAAGCTTGCCCGCGCAA-3′) were used to amplify the 5′-HA from the genomic DNA of
Beauveria bassiana BCC 2660. The primers TetF-Nco (5′-GAACCATGGAA GCTTCCCTCGGCTGGTCTGT-3′) and TetR-Age (5′-GACACCGGTGTTTAAAC GGTGATGTCTGCT-3′) were used to amplify the Tet-On sequence from pFW22.1, a plasmid vector that carries the Tet-On inducible gene expression system. Lastly, the primers 3F-Age (5′-GATACCGGTAACTGGCGAGGACAGTGTGCA-3′) and 3R-Avr (5′-GCGCCTAGGTTCTTGTTTCCAGGTGTAATGC-3′) were used to amplify 3′-HA from the
B. bassiana genomic DNA. After PCR amplification, the 5′-HA fragment was introduced to pCB1534 via double digestion of both pCB1534 and 5′-HA by
BsiWI and
NcoI, followed by DNA ligation. This step generated the recombinant vector pCB-5HA. Next, the Tet-On sequence was introduced via double digestion of both pCB-5HA and the Tet-On fragment by
NcoI and
AgeI, followed by DNA ligation. The cloning generated pCB-5HA-Tet. Lastly, 3′-HA was introduced via double digestion of both pCB-5HA-Tet and 3′-HA by
AgeI and
AvrII and DNA ligation, hence generating pCB-5T3 (
Figure 1A). Both the CRISPR/Cas9 vector pFC-TOR2 and the donor vector pCB-5T3 were verified via DNA sequencing.
2.3. Transformation of Beauveria bassiana Protoplasts with the CRISPR/Cas9 Vector and Donor Vectors
The CRISPR/Cas9 vector and the donor vector were co-introduced to
Beauveria bassiana via PEG-mediated protoplast transformation with modifications from Srisuksam et al.’s (2015) protocol [
17]. Conidial suspension containing 1 × 10
8 conidia from 5-day culture was inoculated to 50 mL of PDB. The culture was shaken at 150 rpm at 25 °C for 16 h, and the young mycelia were harvested via centrifugation at 1500×
g. For protoplast preparation, cell-well-degrading enzyme mix VinoTaste Pro (Novozymes, Frederiksberg, Denmark) was added at a final concentration of 35 mg·mL
−1 in 0.6 M MgSO
4. The mix was incubated at 28 °C at 90 rpm until most of the mycelia were digested to protoplasts. Equal volumes of 0.6 M sorbitol and 100 mM Tris buffer (pH 7.0) were added, followed by centrifugation at 1500×
g to collect the protoplast pellet. Protoplasts were then resuspended in 500 µL of 1 M sorbitol, 10 mM Tris buffer (pH 7.5) and 10 mM CaCl
2. Then, the protoplasts were added to a transformation mixture comprising 50 µL of transformation solution (40% PEG (50%,
v/
v), 0.6 M KCl (15%,
v/
v), 50 mM Tris buffer (pH 8.0) (5%,
v/
v), 50 mM CaCl
2 (5%,
v/
v), water (25%,
v/
v)), CRISPR/Cas9 vector and donor vector (20 µg each). After incubation on ice for 30 min, an additional 1 mL of transformation solution was added to the mix and it was left to incubate in RT for 45 min. Transformation mix was subsequently transferred to 15 mL of molten PDA supplemented with 0.8 M sucrose and 250 µg·mL
−1 hygromycin B (hyg) before pouring into a Petri dish. The culture was incubated at 28 °C until emergence of fungal colonies.
2.4. Beauveria bassiana PTet-On tor2 Mutant Selection and Verification
Fungal colonies from transformation culture were isolated and transferred to new selection media (PDA with 250 µg mL−1 of hyg). Hyg selection was repeated for five generations. Afterwards, colonies were propagated on half PDA and then in PDB for genomic DNA isolation.
Tet-On introduction in transformants was verified by two rounds of PCR. The first PCR verified the presence of Tet-On promoter in transformants, using Tet primer pair HindIII_Tet_F (5′-AAGCTTCCCTCGGCTGGTCTGTCTTAC-3′) and Tet_plus_R (5′-ATCCAGATTGCACACTGTCCGTTTAAACGGTGATGTCTGCTC-3′). The second PCR verified Tet-On insertion downstream of tor2 promoter. The primer pair TorTet-seqF (5′-GCAATACCAGCCACACCTGCA-3′) and TorTet-seqR (5′-GCGAGTAACT AGCCAGGTCAG-3′) amplified partial Tet sequence and tor2 coding sequence. Transformants showing correct DNA band sizes in both PCR were subjected to Sanger DNA sequencing.
2.5. Gene Expression Analyses of tor2 in PTet-On tor2 Mutant under Different Dox Inductions
PTet-On tor2 mutants induced with 0, 0.1, 0.5, 1 and 20 µg·mL
−1 of Dox were determined for their
tor2 expression levels using qPCR. Total RNA was extracted with Ambion TRIzol Reagent (Thermo Fisher Scientific, Waltham, MA, USA). Traces of DNA were removed using Ambion DNase I (Thermo Fisher Scientific). First-strand cDNA was then synthesized using RevertAid First Strand cDNA Synthesis Kit (Thermo Fisher Scientific). All procedures were conducted according to the manufacturer’s protocol. First-strand cDNA from samples were verified via PCR using
tor2-specific primer pair tor2-f (5′-GCAATGTCAGCGTCCAGAAT-3′) and tor2-r (5′-AAAAGTACCCGGAGCGT GTA-3′), as well as the housekeeping gene, M1PD (mannitol 1-phosphate dehydrogenase). The primer pairs amplified intron-inclusive coding sequence in genome so as to distinguish PCR product bands between
tor2 cDNA and control (genomic DNA). qPCR was performed using SYBR Green Master Mix (Bio-Rad, Hercules, CA, USA). Thermal cycle was as follows: 95 °C for 10 min; 39 cycles of 95 °C for 15 s; 55 °C for 30 s; and 72 °C for 30 s. M1PD was used as internal control. Expression fold change of
PTet-On tor2 mutant treatments relative to WT was normalized and calculated using the 2
–ΔΔCt method [
18]. Experiments were repeated twice.
2.6. Radial Growth Assays and Oxidative Stress Tolerance Analysis of PTet-On tor2 Mutant
Radial growth assay for PTet-On tor2 mutant was conducted to determine optimal Dox concentration and to assess tor2-associated radial growth change. Conidial drop prepared as above was inoculated to PDA supplemented with 0, 0.1, 0.5, 1, 5, 50, 100, 200 and 500 µg·mL−1 of Dox. WT was used as comparative control. Colony diameter was measured daily. Each treatment consisted of 4 replicates, and the experiment was repeated twice.
Tolerance of PTet-On tor2 mutant against oxidative stress under different tor2 inductions was assessed. Mutant was cultured with 0 or 20 µg·mL−1 of Dox and was compared to WT. Ferrous ion (Fe2+) was introduced as FeSO4 at 0 or 10 µM to induce oxidative stress. Ten-microliter drops of conidial suspension at 1 × 107 conidia·mL−1 were cultured on minimal media agar (0.02% (w/v) dextrose, 0.51% (w/v) (NH4)2SO4, 0.17% (w/v) yeast nitrogen base (YNB) without amino acids) and incubated at 25–28 °C for 12 days with daily examination and measurement of colony diameter. Each datum was averaged from two perpendicular measurements. Each treatment consisted of 3 replicate plates with 2 colonies per replicate, and the experiment was repeated twice.
2.7. Conidiation Analyses of PTet-On tor2 Mutant and Beauveria bassiana WT Culture Degeneration
Subcultures of Beauveria bassiana WT or PTet-On tor2 mutant were cultured on PDA for 7 days. Mutant tor2 was induced by 0, 0.1, 0.5, 1 or 20 µg·mL−1 of Dox. For successive subcultures of WT, subcultures S2, S4, S8, S12, S16 and S20 were analyzed. Two hundred microliters of conidial suspension at 5 × 107 conidia·mL−1 was spread on PDA plate and incubated at 28 °C for 7 days. Conidia were then harvested by rinsing with 10 mL of 0.1% Tween 20 and counted. Each treatment consisted of 3 replicates, and the experiment was repeated twice.
2.8. Insect Bioassay of Beauveria bassiana PTet-On tor2 Mutant and WT
Fungal culture and
tor2 induction were prepared similarly as above. For
B. bassiana WT, S2, S8, S12 and S20 were analyzed. Conidial suspension was prepared with saline (0.85% NaCl) and was adjusted to 1 × 10
5 conidia·mL
−1. Conidia were introduced to the larvae of
Spodoptera exigua via intrahemocoelic injection, adapted from Toopaang et al.’s (2017) protocol [
19]. Fourth-instar beet armyworm (
S.
exigua) larvae were obtained from the Viral Technology for Biocontrol Research Team (BIOTEC, Pathum Thani, Thailand). Three microliters of the conidial suspension was injected to the insect larvae with a specialized 33-gauge microliter syringe set (Hamilton, NV, USA). Injected larvae were then transferred to individual wells of a 24-well plate coated with mung-bean-based semi-synthetic diet (in 1 L: (
w/
v) 13% mung bean, 1% brewer’s yeast, 0.3% ascorbic acid, 0.125% sorbic acid, 0.25% methyl paraben, 0.3% casein, 0.15% vitamin E, 0.05% choline chloride and 1.2% agar; (
v/
v) 0.3% vitamin stock and 0.08% formalin). Control larvae were injected with saline. Each treatment consisted of ten larvae. Cumulative insect mortality was recorded for 7 days on a daily basis. The experiment was repeated twice. Median lethal time (LT
50) was determined using SPSS’s probit analysis.
2.9. Statistical Analyses
Experiments in this study were conducted either two or three times with three or four replicates for each treatment. Statistical significance was determined using one-way ANOVA. Univariate linear model was used, and Duncan’s test was used as the post hoc test. The significance letters represent the different homogenous subsets in Duncan’s post hoc test. LT50 in insect bioassay was calculated using Probit regression analysis. LT50 was determined by recording the days required for killing half of the beet armyworm population. All significance tests were completed using SPSS package version 23 (IBM, Chicago, IL USA).
4. Discussion
The morphological changes in degenerated fungal cultures include the attenuation of sporulation and impairment in sexuality, fruiting body formation and secondary metabolism [
20]. It is important to understand the mechanisms contributing to culture degeneration, since the phenotypic stability of fungal strains in in vitro cultivation is industrially important in the manufacture of mycoinsecticides [
21,
22]. TOR signaling regulates fungal growth, energy metabolism, survival and the secondary metabolism in response to nutrient availability, growth factors and stresses; thus, TOR reasonably plays a potential role in maintaining the phenotypic stability in filamentous fungi. The deletion of the sole TOR kinase gene in filamentous fungi is lethal such as in
Fusarium fujikuroi,
Aspergillus fumigatus,
Trichoderma atroviridae,
Verticilium dahliae [
23,
24,
25,
26] and
Beauveria bassiana BCC2660 (unpublished data). In this study, we selected the TOR kinase 2 gene ‘
tor2’ to target both the TOR complexes that generally exist in most organisms, TORC1 and TORC2. The Tet-On introduction was precisely placed just upstream of the
tor2 coding sequence. The native
tor2 promoter remained at the locus since it is likely shared with an adjacent gene. The CRISPR/Cas9-mediated Tet-On promoter introduction enabled exogenous
tor2 expression induction via Dox. Here, our data from various characterizations of the
PTet-On tor2 mutant demonstrate the significance of the TOR kinase in
B. bassiana’s mycelial growth, conidiation, virulence and oxidative stress tolerance. It is also interesting how this essential developmental program may contribute to the culture degeneration of
B. bassiana.
Fungal conidiation, vegetative growth and oxidative stress tolerance predominately determine virulence against insect hosts. In nature, firstly, the fungal dispersal is principally carried out by means of ‘conidiation’ and subsequent release into the surrounding area. The dispersed
Beauveria bassiana conidia attach to the host cuticle. Secondly, these cells germinate, grow ‘vegetatively’ and form the cuticle-penetrating appressorium for hemolymph access. The fungus then gradually infects and colonizes the host by exploiting the host’s nutrients for proliferation, releasing insecticidal compounds whilst evading the host’s immune response. The fungus later emerges from the host cadaver and releases conidia, where the infection cycle repeats [
27]. Conidiation and hyphal growth therefore determine the success of conidial attachment to the host and pathogenesis.
Thirdly, ‘oxidative stress tolerance’ plays an important role as the stress response when exposed to the host’s ‘oxidative burst’ upon microbial detection [
28] or to adverse stresses from habitat niches [
29]. TOR signaling coordinates these machineries in
Beauveria bassiana through an intricate regulation network, as supported by knockdown studies. TORC1 inhibition via rapamycin often leads to a serious or complete loss of fungal sporulation. The antisense RNA knockdown of the TOR kinase gene in
B. bassiana increased the fungus’s sensitivity to osmotic stress, heat stress, cell-wall-perturbing agents and oxidative stress [
30]. The TOR-regulated transcription factor Msn2/4 negatively regulates the production of protease, lipase and oosporein in
B. bassiana [
31], which are important in facilitating host cuticle penetration and minimizing microbial competition in the host cadaver [
31,
32], while in the fungal plant pathogen
V. dahliae, TORC1 inhibition via rapamycin significantly inhibits fungal mycelial growth and pathogenicity [
26]. Similarly, in
Fusarium graminearum, the TOR downstream component Tap42 interacts with different types of 2A phosphatases Pp2A, Sit4 and Ppg1, which regulate the cell wall integrity, mycelial growth, mycotoxin production and virulence [
33]. TOR also regulates the secondary metabolism, including polyketide biosynthesis, in mycoparasitic fungus
T. atroviridae [
25], which is essential for its mycoparasitism. Therefore, TOR plays a crucial role in mediating fungal pathogenesis.
In this study, the mutant
PTet-On tor2 ‘T41’ serves as a tool for evaluating the fungal phenotypes according to the TOR expression levels. Our results from these phenotypic characterizations support TOR’s significance in the growth, survival and pathogenesis of the fungus.
tor2’s downregulation from the absence of Dox resulted in the hampering of
PTet-On tor2’s radial growth, a lower oxidative stress tolerance and a decrease in conidiation and virulence against
S. exigua compared to those under the presence of Dox. The upregulation of
tor2 induced by Dox resulted in different extents of improvement in these phenotypes depending on the Dox concentration. A low range of concentrations of Dox at 0.1–1 µg·mL
−1 induced
tor2 upregulation by up to 30%, resulting in an increasing gradient of conidiation and radial growth. However, at a relatively higher Dox concentration at 20 µg·mL
−1, the oxidative stress tolerance increased, but the conidiation significantly dropped. The conidiation decrease in T41 is akin to the deteriorating conidiation in the
Beauveria bassiana WT after successive subcultures in vitro [
6], supporting a notion of correlation of elevated TOR signaling in repetitive subcultures and degeneration in conidiation after a certain TOR expression threshold. However, the finding that virulence against
S. exigua of T41 with 20 µg·mL
−1 of Dox did not exhibit a similar drop to that found in conidiation suggests that the regulatory spectrum by the TOR signaling pathway may be different depending on the phenotypes. Alternatively, the TOR pathway may not be the sole factor for the declined insect virulence; instead, this may be caused by multiple factors that were not determined in our
PTet-On tor2 model.
Apart from its role in virulence, the TOR signaling pathway was reported to be associated with
Beauveria bassiana’s culture degeneration [
6]. TOR negatively regulates catabolic activities such as mRNA degradation, ubiquitin-dependent proteolysis and autophagy, which are potential stress-responsive cellular processes that may contribute to lifespan extension [
34]. Temporally, TOR’s role in aging control may begin in adulthood. In
C. elegans, TOR inhibition during development is growth inhibitory; yet, inhibition starting from the first day of adulthood lengthens its lifespan [
11]. Our experimental data confirm TOR’s inhibitory effect on conidiation, radial growth and virulence when the TOR kinase gene is downregulated in early development. Further experiments on the effect of TOR inhibition on the degeneration of in vitro subcultures of
B. bassiana could attest to TOR’s potential role in culture degeneration at ‘adulthood’, which we speculate to be a representation of the restriction of
B. bassiana to a saprophytic mode of nutrition during cultivation on axenic media.
TOR’s contribution to culture degeneration could stem from the failure to select longevity-promoting traits in natural selection [
35]. Under in vitro cultures, individuals with robust TOR activity are selected, which could drive cellular hyperfunction and pathogenicity [
36]. This could explain some observations of the phenotypic and physiological changes in culture degeneration, including the change in the color of the conidia in
M. anisopliae, the development of a sterile sector in
A. nidulans as well as the altered energy metabolism in
Beauveria bassiana [
6,
20,
37]. Nonetheless, further studies need to be conducted to clarify the mechanisms of how degenerated cultures often restore to maximum virulence after the reintroduction to an insect host.
The culture degeneration of entomopathogenic fungi probably results from a combination of inter-connected factors [
5], where strains, culture media and environmental cues could contribute to the degeneration in addition to TOR signaling. The reliance of stimuli from an insect host partially explains their ability to rejuvenate and restore to full pathogenicity potential after one or two passages through an insect host; yet, axenic culture media fail to select virulent offspring. The possible involvement of TOR in these processes raises a possible strategy of alleviating the fungal culture degeneration via TOR inhibition, as shown in other organisms. Indeed, our data demonstrate that a tight regulation of the TOR signaling pathway would be the key to rejuvenate these fungal cultures. Our study aims to shed light on the culture degeneration in entomopathogenic fungi and the linkage between TOR, aging and culture degeneration.