1. Introduction
Global warming has received significant interest because of the concerns regarding its impact on food security, quality, and safety. The challenge of increasing crop productivity to meet the demand of an ever-growing world population may be further exacerbated by climate change (CC) scenarios [
1]. Under CC conditions, plant growth and physiology will be modified together with the exposure to different fungal pathogens and pests [
2,
3]. This has been shown to also change the regions where suitable environmental conditions occur for fungal infection and mycotoxin contamination [
4,
5]. Indeed, it has been shown that the colonization of maize by
Aspergillus flavus under CC-related abiotic factors results in the stimulation of aflatoxin B
1 (AFB
1) contamination [
6,
7]. Recently, Baazeem et al. [
8] showed that strains of
A. flavus isolated from pistachio nuts grew optimally at around 35 °C on both pistachio nut-based media and on raw pistachio nuts. In contrast, AFB
1 production was optimum at around 30 °C. The impact of CC conditions of elevated temperature (35 vs. 37 °C) and CO
2 (400 vs. 1000 ppm) under conducive and stressed water availability conditions had little effect on the growth of strains of
A. flavus. However, there were indications of a stimulation of AFB
1 production, both
in vitro and on raw pistachio nuts [
9]. Indeed, there were also changes in the expression of some of the structural and regulatory genes (
aflD and
aflR) involved in toxin biosynthesis. Some strain variabilities were also observed.
There has been interest in the resilience of fungal pathogens, including mycotoxigenic species, when repeatedly exposed to CC interacting abiotic conditions. This is usually referred to as “acclimatization”. This is defined as a process in which an individual organism adjusts to a change in its environment, allowing it to maintain fitness. This may be important, especially if pathogenicity/virulence is modified or if mycotoxin production is increased. Vary et al. [
10] carried out one of the first studies that examined the acclimatization of fungal pathogens of wheat in relation to CC abiotic factors. They found that wheat plants exposed to 350 vs. 650 ppm CO
2 in controlled plant growth chambers had effects on crop physiology and severity of wheat diseases. Thus, ripening wheat ears exposed to CC conditions changed the stomatal number, position, and physiology of the plant.
Septoria tritici and
Fusarium graminearum sub-cultured for 10 and 20 generations in elevated CO
2 conditions, respectively, were found to change their infection and disease symptoms after such acclimatization. Thus, the acclimatized strains of the two fungal pathogens had increased pathogenicity under CC conditions, with both disease symptoms and fungal biomass using molecular approaches shown to increase. While there was an increase in
Fusarium Head Blight symptoms, no quantification was made of whether concomitant contamination with type B trichothecenes also occurred. Recently, Mshelia et al. [
11] acclimatized one strain each of
F. verticillioides and
F. graminearum for 10 generations on a milled maize-based media. However, this was only in relation to temperature, with exposure to step-wise increases in 0.5 °C steps for each generation, from 30 to 35 °C for the former, and from 30 to 33 °C for the latter species. No acclimatization by exposing to elevated CO
2 were included. Subsequent exposure of these pathogens to changes in temperature × elevated CO
2 (400 vs. 800, and 1200 ppm) × water activity (0.92, 0.95, and 0.98 a
w) showed little effect on growth or fumonisins, and deoxynivalenol or zearalenone production by
F. verticilioides and
F. graminearum, respectively.
Pistachio nuts are known to be more prone to contamination with AFB1 when there is increased insect infection and poor post-harvest practices, which could, under CC scenarios, predispose these tree nuts to A. flavus infection and perhaps increased AFB1 contamination. The evolution of acclimatization to facilitate better resilience to climate change scenario abiotic conditions and thus ecological fitness, by perhaps increasing toxin production, has not been examined previously in any food raw commodities. Indeed, to our knowledge, there have been no studies on the impact that the acclimatization of A. flavus strains to elevated CO2 may have on the colonization and AFB1 contamination of tree nuts.
The objectives of the present study were to examine whether acclimatization to 1000 ppm elevated CO2 + 37 °C of A. flavus strains (AB3 and AB10) for five generations would affect (a) mycelial colonization and (b) AFB1 contamination of raw pistachio nuts under interacting CC conditions (35 vs. 37 °C, 0.98 or 0.93 aw × 400 vs. 1000 ppm CO2), and to compare this with non-acclimatized strains under existing and future environmental conditions.
2. Materials and Methods
2.1. Apergillus flavus Strains
Two strains of
A. flavus were selected for this study due to their ecophysiological similarities to the type strain based on preliminary experiments. These strains were AB3 and AB10 [
7].
2.2. Acclimatization Experimental System
Both A. flavus strains were acclimatized by exposure to 1000 ppm elevated CO2 at 37 °C with repeated sub-culturing for five generations. Each generation was incubated for 7–10 days on a 2% milled pistachio nut-based medium in a climate change growth chamber. For each generation, the mycelial hyphal tips (2.5 mm agar blocks) from the edge of the growing colony were carefully cut with a surface-sterilized scalpel blade and centrally placed on a fresh pistachio nut-based medium to initiate the next generation. This process was repeated for five generations.
2.3. Colonisation of Pistachio Nuts by Aspergillus flavus Isolates and Incubation Conditions
For experiments with non-acclimatized and acclimatized strains, the a
w of the raw pistachio nuts was modified to 0.98 and 0.93 a
w by adding known amounts of water based on the previously developed moisture sorption curves, and they were left overnight at 4 °C for equilibration [
7]. A conidial spore suspension from non-acclimatized and acclimatized strains (0.2 mL; 10
6 conidia/mL) was spread-plated using a bent surface sterilized glass rod on to 2% milled pistachio nut medium in 9 cm Petri pates. These were left overnight at 30 °C to allow initial germination to occur. Using a surface-sterilised 4 mm cork-borer and needle a single agar disc containing the conidial germlings was carefully placed in the centre of the layers of raw pistachio nuts in each replicate Petri plate for the different treatment a
w levels [
8]. They were incubated under existing conditions: 35 °C + 400 ppm CO
2 + 0.98 or 0.93 a
w, and CC conditions of 37 °C + 1000 ppm CO
2 + 0.98 or 0.93 a
w.
All of the experiments were carried out in environmental growth chambers, as described previously [
8]. Briefly, inoculated replicates and treatments were placed in plastic environmental chambers. Inoculated treatments of the same a
w were enclosed together in the environmental chambers containing switchable valves at each end: one for CO
2 intake and the other for exit. Two 500-mL beakers of glycerol/water solution with the same a
w as the treatment were included in the chamber in order to maintain the same equilibrium relative humidity (ERH) as the media a
w.
Colonization of the raw pistachio nut layers in 9 cm Petri plates was measured every two days. Immediately after measurement, the environmental chambers were flushed with the treatment CO2 for 10–15 min and then sealed and incubated at the treatment temperature. The chambers were flushed every 24 h with either 5 L of air (400 ppm CO2) or 1000 ppm CO2 from a specialty gas cylinder (British Oxygen Company Ltd., Guilford, Surrey, UK; 1000 ppm CO2 cylinder). They were incubated for 10 days at 35 and 37 °C.
At the end of the 10 days, the pistachio nuts were dried at 50 °C and milled for AFB1 extraction and quantification.
2.4. Quantification of Aflatoxin B1 Production
The dried pistachio nut samples were ground (Waring blender, Merck Ltd., Feltham, UK) and weighed (25 g). The background aflatoxin B1 levels in the nuts used in the experiments was 0.015 ng/g. This was taken into account as a correction factor in the final quantification of the results. Acetonitrile/water 60/40 (100 mL) was used as an extraction solvent. The mixture was blended for 3 min and the extract filtered into a smaller sample container. A PBS buffer (pH 7.4, Thermo Fisher Scientific, Waltham, MA, USA) was used for sample dilution, then the diluted extract was passed through an Immunoaffinity Column (IAC; AflaStar™; Romer Labs, Tulln, Austria) with a flow rate between 1–3 mL/min. The column was rinsed with 2 × 10 mL sterile distilled water. HPLC-grade methanol (1.5–3 mL) was then applied to the column and the eluent was collected in a new amber glass vial and left to dry overnight at room temperature before derivatisation.
Derivatisation of Aflatoxin B
1 extract: Derivatisation of the AFB
1 extract was performed according to the AOC method [
12]. First, 200 μL hexane was added to the tube, followed by 50 μL of triflouroacetic acid. The mixture was vortexed for 30 s and left for 5 min. A mixture of water/acetonitrile (9:1) was then added to the tube, and vortexed for 30 s and left for 10 min to allow for separation of the layers. Then, the aqueous layer was filtered using a nylon syringe filter (13 mm × 0.22 μm; Jaytee Biosciences Ltd., Herne Bay, UK) into amber salinized 2 mL HPLC vials (Agilent, Santa Clara, CA, USA) before the HPLC analysis. All of the analytical reagents used were HPLC-grade.
Quantification of aflatoxin B1 with High Performance Liquid Chromatography HPLC: A reverse-phase HPLC with fluorescence detection was used to confirm the identity and quantify AFB1. An Agilent 1200 series HPLC system was used for the analysis. It consisted of an in-line degasser, auto sampler, binary pump, and a fluorescence detector (excitation and emission wavelengths of 360 and 440 nm, respectively). Separation was achieved using a C18 column (Phenomenex Gemini; 150 × 4.6, 3 μm particle size; Phenomenex, Torrance, CA, USA) with a Phenomenex Gemini C18 3 mm, 3 μm guard cartridge. Isocratic elution with methanol/water/acetonitrile (30:60:10, v/v/v) as the mobile phase was performed at a flow rate of 1.0 mL/min. The injection volume was 20 µL. A set of standards was injected (1 to 5 ng AFB1, AFB2, AFG1, and AFG2 per injection) and standard curves were generated by plotting the area underneath the peaks against the amounts of AFB1 standard injected.
2.5. Statistical Analysis
Three replicates per treatment were used in all of the experimental studies. The means were obtained by taking the average of each three measurements with the standard error of the means (±SE). Analysis of variance (ANOVA) was applied to analyze the variation of means with a 95% confidence interval. Normal distribution of data were checked with the normality test of Kolmogorov−Smirnov using Minitab statistical software. Fisher’s least significant difference (LSD) was used to identify the differences between the means, with p < 0.05 as a significant difference using the same statistical software.
4. Discussion
This study suggests that the effect of acclimatization on the colonization of pistachio nuts and perhaps other nuts may need further investigation. The effect of the acclimatization treatment on the two strains differed, although both were isolated from pistachio nuts [
8]. The resilience of one strain was increased by acclimatization with faster colonization of the raw pistachio nuts and a clear stimulation of AFB
1 production. In contrast, for the other strain, there was no difference from the control treatments. It may be that comparisons need to be made of such strains after 5, 10, or perhaps 20 generations in climate-related abiotic conditions in order to determine the real impact of the adaptation and stability of resilience to these factors and what influence this may have on toxin biosynthesis.
The only comparable study was by Vary et al. [
10], who used 10 and 20 generations of acclimatization of wheat fungal pathogens. However, they did not examine inter-strain differences. This certainly requires more in-depth research to examine how exposure to climate-related abiotic conditions for different generations affects the expression of the key genes involved in the biosynthesis of AFs. Certainly, changes in the relative expression of some of the biosynthetic genes (
aflD and
aflR) in
A. flavus under climate change-related abiotic factors in pistachio nuts and in maize have been shown to occur [
5,
6,
9]. Indeed, Vary et al. [
10] found that
F. graminearum exposed for 10 generations to elevated CO
2 had a higher pathogenicity, with more fungal biomass of this species present in the ripening ears of wheat, as well as an increase in visible symptoms. Unfortunately, the effects on deoxynovalenol contamination of the wheat grain were not quantified. The only other study was with
F. verticillioides and
F. graminearum, where step changes were made by increasing the temperature slowly for 10 generations. However, this acclimatization was done under existing CO
2 conditions only. They found little impact on growth or on fumonisins or type B trichothecenes and zearalenone production, respectively [
11]. Medina et al. [
13] and Perrone et al. [
3] pointed out that the three-way interaction between increased temperature, exposure to elevated CO
2, and drought stress together may be more important for influencing the evolving resilience of such fungal pathogens than single or two-way climate-related abiotic factors.
If we consider climate-related abiotic factor effects without acclimatization, then certainly they suggest significant influences on mycotoxin production in different food-related matrices. Thus, colonization and ochratoxin A (OTA) production by strains of
A. westerdijkiae were stimulated, while there was practically no effect on strains of
A. carbonarius [
14,
15] in coffee-based media and stored coffee beans. Studies of the colonization of maize by
A. flavus strains under existing and three-way climate-related abiotic factors showed little effect on growth but a significant stimulation of AFB
1 contamination of maize [
7].
In contrast to studies with coffee, strains of
A. carbonarius from grapes were found to be significantly affected by fluxes in day/night temperature, elevated CO
2 (400 vs. 1000 ppm), and drought/wet conditions [
16]. This study showed an up-regulation of both structural (
AcOTApks,
AcOTAnrps,
AcOTAhal, AcOTAp450, and
AcOTAbZIP) and regulatory genes of the velvet complex (
laeA/
veA/
velB, “velvet complex”) involved in OTA biosynthesis and phenotypic OTA production.
Other studies with non-xerophilic species such as
Fusarium langsethiae, which grows under cooler conditions on oats, were also found to respond to three-way climate-related abiotic factors [
17]. These showed that the
Tri5 gene expression was reduced in all conditions except at the elevated temperature, 30 °C, when compared to 25 °C, and exposure to 1000 ppm CO
2 with a 5.3-fold significant increase in expression. Other biosynthetic genes (
Tri6 and
Tri16) were upregulated in elevated CO
2 conditions. In stored oats, at 0.98 a
w, elevated CO
2 led to a significant increase (73-fold) in the T2/HT-2 toxin, especially at 30 °C [
17]. With
F. verticillioides, Vaughan et al. [
18] showed an increase in pathogen biomass during the infection of ripening maize cobs, but no effect on fumonisins production when exposed to 650 ppm CO
2. However, when drought stress was included, there was a stimulation of fumonisins in ripening maize cobs [
19].
In terms of further investigations of acclimatization, perhaps a broader approach needs to be utilized including RNAseq, that may help to better understand the possible role of acclimatization, in relation to changes in the transcriptome and key biosynthetic pathways, for the production of other toxic secondary metabolites by A. flavus, including cyclopiazonic acid and related compounds. This would provide a better understanding of the physiological/functional basis for the evolution of resilience in such acclimatized strains. Perhaps acclimatization for at least 10–20 generations in elevated CO2 + increased temperature stress is required in order to better understand the evolution of the potential development of tolerance and effects on secondary metabolite production in climate change scenarios.