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. 2015 Jan-Feb;5(1):34–42.

Efficacy of Cuminum cyminum essential oil on FUM1 gene expression of fumonisin-producing Fusarium verticillioides strains

Ali Reza Khosravi 1,*, Hojjatollah Shokri 2, Ali Reza Mokhtari 1
PMCID: PMC4352531  PMID: 25767755

Abstract

Objectives: The purpose of this study was to evaluate the effect of Cuminum cyminum (C. cyminum) essential oil on the growth and FUM1 gene expression of fumonisin-producing Fusarium verticillioides (F. verticillioides) strains isolated from maize.

Materials and Methods: All fungal strains were cultured on potato dextrose agar (PDA) slopes at 30°C for 7 days. The antifungal activity was evaluated by broth microdilution assay. One set of primers was F. verticillioides species specific, which selectively amplified the intergenic space region of rDNA. The other set of primers was specific to FUM1 gene region of fumonisin-producing F. verticillioides. FUM1 transcript levels were quantified using a reverse transcription-polymerase chain reaction (RT-PCR) protocol.

Results: Minimum inhibitory concentration (MIC) values of C. cyminum oil against F. verticillioides strains varied from 0.195 to 0.781 µl.ml-1 (mean MIC value: 0.461 µl.ml-1) indicating 54.5% of the fungal strains inhibited at 0.390 µl.ml-1. PCR analysis of FUM1 gene expression revealed that DNA fragment of 183 bp was amplified in all the isolates of F. verticillioides before treatment with C. cyminum essential oil. Based on RT-PCR analyses, reduction in the expression of fumonisin biosynthetic genes was significant only for FUM1 gene (p<0.05), while no effect was observed on ITS gene.

Conclusions: This study showed that all F. verticillioides isolates were susceptible to C. cyminum essential oil, indicating a significant reduction in the growth of fungal isolates. In addition, this oil completely inhibited the expression of FUM1 gene in concentrations dose-dependently.

Key Words: Fusariumverticillioides, Fumonisin, Cuminumcyminum, RT-PCR, FUM1gene

Introduction

The genus Fusarium represents one of the major fungal genera, which are ubiquitous in distribution and are found frequently on freshly harvested and stored agricultural commodities such as cereals. Fusarium verticillioides (Gibberella moniliformis, Gibberella fujikuroi mating population A) is the main source of fumonisins, a group of toxins which contaminates commodities, causing chronic and acute diseases in humans (Gonzalez-Jaen et al., 2004 ▶). In addition, fumonisins cause several diseases in animals such as leukoencephalomalacia in horses, pulmonary edema in swine and hepatic cancer in rats. They are considered to be Group 2B carcinogens by the International Agency for Research on Cancer (Nelson et al., 1993 ▶).

The importance of F. verticillioides as a causal agent of several diseases in cereals, and the production of fumonisins during the course of host infection, even when no visible symptoms are observed, emphasize the need to control both pathogen growth and the production of fumonisin. In order to develop efficient strategies to achieve these goals, it is crucial to have more information regarding the population structure and variability of the species as well as the biosynthetic and regulatory pathways of mycotoxin production. This information could also be used to develop rapid, sensitive, and specific assays to detect the presence of mycotoxigenic species or lineages in the early stages of infection and to prevent mycotoxins entering the food chain.

Various PCR assays have been developed for the identification of toxigenic species of Fusarium. Some of them are based on single copy genes directly involved in mycotoxin biosynthesis while others are species-specific (Gonzalez-Jaen et al., 2004 ▶; Mule et al., 2004 ▶). Biochemical analyses indicated that fumonisins are products of a polyketide synthase (PKS) gene called FUM1 (Desjardins et al., 2002 ▶; Proctor et al., 2003 ▶) whose regulation occurs at the transcriptional level (Seo et al., 2001 ▶). Recent reports indicate significant correlation between FUM1 transcripts, quantified by reverse transcription-PCR (RT-PCR), and phenotypic fumonisin production (Jurado 2006 ▶; Lopez-Errasquın et al., 2007 ▶). The quantitation of FUM1 transcripts by RT-PCR permits a sensitive and specific approach to evaluate the effects of various treatments on fumonisin biosynthesis.

Numerous studies have been performed on the plant compounds with the intent to reduce the growth of mycotoxin-producing fungi, inhibit toxin production, and suppress the major toxin encoded genes in these organisms. Cuminum cyminum (Apiaceae) is an annual herbaceous plant (height: 15-50 cm) with green seeds which have aromatic characteristics. It is believed to the natives of the Mediterranean and Near Eastern regions. It is applied in Iranian folk medicine since more than 200 years ago. It has been shown that its fruits have medicinal application in treatment of diarrhea, toothache, and epilepsy (Zargari, 1994 ▶). It also has diuretic, carminative, emmanogogic, and antispasmodic properties (Janahmadi et al., 2006 ▶). Besides its use in traditional medicine in the treatment of some ailments, C. cyminum is widely used in food. It is one of the popular spices regularly used as a flavoring agent and possesses numerous antimicrobial activities (Iacobellis et al., 2005 ▶; Nostro et al., 2005 ▶). Major constituents in C. cyminum essential oil are gamma-terpinene, 2-methyl-3-phenyl-propanal, myrtenal, and glucopyranosides (Jalali-Heravi et al., 2007 ▶). There is no report regarding the effect of C. cyminum essential oil on fumonisin-producing F. verticillioides strains. The objective of this study was to evaluate the effect of C. cyminum essential oil on the growth and FUM1 gene expression in fumonisin-producing strains of F. verticillioides. These relationships are important as they clarify the ecophysiological basis for the establishment and survival in crop residue and for subsequent spread and infection of maize.

Materials and Methods

Fungal isolates

Fourteen F. verticillioides strains, F1-14, were prepared from Mycology Research Center, University of Tehran, Tehran, Iran. All fungal strains, originally isolated from the maize farm in Iran, were cultured on potato dextrose agar (PDA, Merck Co., Darmstdt, Germany) slopes at 30°C for 7 days.

Slopes were flooded with phosphate-buffered saline (PBS) containing 0.05% Tween 80. Fungal growth was gently probed and the resulting suspension was removed and mixed thoroughly by a vortex mixer. After the settling of the large rparticles, suspension was adjusted by hemocytometer to final inoculums concentration of 0.5×106 cell.ml-1.

Extraction of C. cyminum oil

The seeds of C. cyminum were dried at room temperature (20-23ºC) and ground into a powder using a blender. The essential oil was obtained from 50 g of powdered seeds by water-distillation using a Clevenger-type system for 3 h. The aqueous phase was extracted three times with 50 ml dichloromethane. The organic phase was dried with sodium sulphate and filtered. The solvent was allowed to evaporate until dryness. Oil sample was stored at −25ºC in a sealed glass vial (FarmacopeiaBrasileira, 2000 ▶).

Antifungal activity assay

Broth microdilution testing was performed based on M38-A protocol for filamentous fungi (NCCLS, 2002). Briefly, a series of doubling dilutions of cumin oil ranging from 0.0975 to 3.12 µl.ml-1 was prepared in a 96-well microdilution plate, with a final concentration of 0.001% (v/v) Tween 80 to enhance cumin oil solubility. After the addition of inocula (prepared as described above), plates were incubated at 35°C for 48 h. Minimum inhibitory concentrations (MICs) were determined visually with the aid of a reading mirror, according to NCCLS guidelines. Minimum fungicidal concentrations (MFCs) were also determined by using 0.01 ml from each well without visible growth onto PDA plates. MFCs were determined as the lowest concentration resulting in no growth on subculture. Each experiment was repeated in duplicate.

Treatment of F. verticillioides strains with C. cyminum oil

A 10 μl spore suspension was prepared from 7-day-old PDA cultures, of each F. verticillioides strain was inoculated into 250 μl of fumonisin-inducing liquid medium exposed to different concentrations of C. cyminum essential oil (0.195 and 0.390 µl.ml-1) and incubated at 20°C for 7 days. Mycelia were harvested by filtration through Whatman No.1 paper (Whatman International, Ltd, England), frozen in liquid nitrogen and kept at -70°C for RNA isolation. The fungal filtrates were used to analyze fumonisin contents by high-performance liquid chromatography (HPLC) according to the manufacturer’s protocol (Lopez-Errasquin et al., 2007 ▶).

DNA extraction and polymerase chain reaction (PCR) amplification

Genomic DNA of the fungal strains was obtained using the “GeneJET™ Plant Genomic DNA Purification Mini Kit” (Fermentas) following the manufacturer's instructions. DNA samples from F. verticillioides isolates as well as from the control sample (Aspergillus flavus) were subjected to PCR analyses using Fusarium species specific ITS and FUM1 primers: ITS Forward: 5'-AACTCCCAAACCCCTGTGAACATA-3', ITS Reverse: 5'-TTTAACGGCGTGGCCGC-3'), and FUM1 Forward: 5´-GCGGGAATTCAAAAG-3', FUM1 Reverse: 5´-GAGGGCGCGAAACGGATCGG-3') (Sreenivasa et al., 2006). The PCR reaction was carried out in 25 μl volume containing 10 ng of DNA sample, 10X Taq polymerase buffer (AB-gene Housse, UK), 25 mM MgCl2, 2 mMdNTPs, 20 pmol of each forward and reverse primer, and 0.5 μl (3U.μl-1) of Red Hot Taq. The PCR reactions were performed using Thermocycler (Techne, TC-512, UK). Samples were heated at 94ºC for 3 min and then subjected to 32 cycles of 1 min at 95ºC (denaturation), 1 min at 60ºC (annealing) and 3 min at 72ºC (extension). The final extension was set at 72°C for 5 min. Ten μl of the PCR product was electrophoresed on 1.5% agarose gel, stained with ethidium bromide, illuminated, and documented using Biorad UV Transilluminator.

RNA isolation and reverse transcription (RT)-PCR

Fungal total RNA was isolated using the “GeneJET Plant RNA PurificationMini Kit” (Fermentas) according to the manufacturer's instructions and stored at −80°C. DNAse I treatment to remove genomic DNA contamination from the samples was performed using RibolockRNase Inhibitor following the manufacturer's instructions. First strand cDNA was synthesized using the “RevertAid First Strand cDNA Synthesis Kit” (Fermentas). Each 20 μl reaction contained 500 ng of total RNA, 1 μl of oligo d(T)16 (50 μM), 4 μl of 5×RT-PCR buffer, 1 μl of MgCl2 (25 mM), 2 μl of dNTPs (10 mM), 2 μl of DTT (100 mM), 1 μl of RNAse inhibitor (20 U.μl-1), 1 μl of RevertAid M-MulV Reverse Transcriptase (200 U.μl-1), and sterile DEPC water up to the final volume. Synthesis of cDNA was performed in a Thermocycler (Techne, TC-512, UK) according to the following procedure: 94ºC for 4 min and then subjected to 35 cycles of 1 min at 94ºC (denaturation), 1 min at 58ºC (annealing) and 1 min at 72ºC (extension). The final extension was set at 72°C for 10 min. The cDNA samples were kept at −20°C. Samples incubated in the absence of reverse transcriptase were used as controls (Jurado et al., 2010 ▶; Marín et al., 2010 ▶).

Statistical analysis

The data of fungal growth and gene expression were subjected to the analysis of variance (One-way ANOVA) in Tukey range. The differences with p<0.05 were considered significant.

Results

Our findings showed that all isolates were susceptible to the essential oil, indicating a significant reduction in the growth of fungal isolates. The MIC values of C. cyminum oil against F. verticillioides strains varied from 0.195 to 0.781 µl.ml-1 (mean MIC value: 0.461 µl.ml-1) representing 54.5% of the strains inhibited at 0.390 µl.ml-1 (Table 1). C. cyminum oil exhibited a remarkable fungicidal activity against the fungal isolates with MFC values ranging from 0.390 to 1.56 µl.ml-1.

Table 1.

Antifungal susceptibility of Cuminum cyminum essential oil against Fusarium verticillioides isolates (µl.ml-1).

Strains F1 F2 F3 F4 F5 F6 F7 F8 F9 F10 F11 F12 F13 F14
Value
MIC 0.195 0.781 0.781 0.390 0.390 0.390 0.781 0.390 0.195 0.390 0.390 0.195 0.781 0.390
MFC 0.390 1.56 1.56 0.781 0.781 0.781 1.56 0.781 0.390 0.781 0.781 0.390 1.56 0.781
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In PCR analysis, all F. verticillioides strains were positive for the ITS region and exhibited the expected 431 bp DNA fragment except A. flavus, which was used as control (Figure 1). In addition, all the tested strains of F. verticillioides revealed the FUM1 gene expression and amplified fragment with the molecular size of 183 bp, corresponding to the expected molecular size of the FUM1 gene sequence, while this band could not be detected in the control sample (A. flavus) (Figure 2).

Figure 1.

Figure 1

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Agarose gel showing amplified products using primers for ITS region (431 bp). Lane marker (left): 100bp DNA ladder. Lanes 1-11 (from left to right): Fusarium verticillioides (F1-11). Lane 12: Aspergillus flavus

Figure 2.

Figure 2

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Agarose gel showing amplified products using primers for FUM1 region (183 bp) before treatment with C. cyminum essential oil. Lane marker (left): 100bp DNA ladder. Lanes 1-11 (from left to right): Fusarium verticillioides (F1-11). Lane 12: Aspergillus flavus

In order to evaluate the effect of C. cyminum oil on expression of ITS and FUM1 genes, F. verticillioides isolates were cultured on fumonisin-inducing liquid medium in presence of C. cyminum oil (0.195 and 0.390 µl.ml-1) at 20°C for 7 days. The results revealed that C. cyminum oil completely inhibited the expression of FUM1 gene in both concentrations dose-dependently (Figure 3). Based on the statistical analyses, reduction in the expression of fumonisin biosynthetic genes was significant only for FUM1 gene (p<0.05), while no effect was observed on ITS gene.

Figure 3.

Figure 3

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Agarose gel showing amplified products using primers for ITS and FUM1 regions after treatment with C. cyminum essential oil. Lane marker (left): 100bp DNA ladder. Lanes 1-11 (from left to right): Fusarium verticillioides (F1-11). Lane 12: Aspergillus flavus

Discussion

The antimicrobial properties of volatile aromatic oils from plants have been recognized since antiquity. Here, we evaluated the antifungal activity of essential oil obtained from C. cyminum against fumonisin-producing strains of F. verticillioides. Our results confirmed that all of the tested isolates were susceptible to the essential oil, indicating a significant reduction in the growth of fungal isolates. The rate of growth reduction was directly proportional to the concentrations of tested oil in the medium. In fact, higher concentrations of the oil led to lower fungal developments. As illustrated in Table 1, MIC values of C. cyminum oil against F. verticillioides strains varied from 0.195 to 0.781 µl.ml-1 (mean MIC value: 0.461 µl.ml-1) representing 54.5% of the strains inhibited at 0.390 µl.ml-1.

In addition, C. cyminum oil exhibited a remarkable fungicidal activity against the fungal isolates with MFC values ranging from 0.390 to 1.56 µl.ml-1. Previous studies showed that C. cyminum is effective on the growth of some microorganisms including fungi (Megalla et al., 1980 ▶; Naeini et al., 2009 ▶; Mohammadpour et al., 2012 ▶). In a study by Naeini et al. (2010), ▶ high anti-Fusarium activity was found at a very low concentration of C. cyminum oil against non-toxigenic (F. solani, and F. oxysporum) and toxigenic (F. verticillioides, F. poae, and F. equiseti) species. In agreement with our findings, Salehi Surmaghi (2006) ▶ reported strong antifungal activity of C. cyminum against Fusarium species.

Early and specific detection of toxigenic fungi lead to the better understanding of the pathogens, which pave the way of effective disease control. The PCR assay provides a useful tool for rapid and sensitive detection and differentiation of potential mycotoxin-producing fungi. In this study F. verticillioides isolates were subjected to PCR analysis using ITS genus specific and FUM1 gene specific primers. All F. verticillioides strains were positive for the ITS region and exhibited the expected 431 bp DNA fragment except A. flavus, which was used as control (Figure 1). In addition, all the tested strains of F. verticillioides revealed the FUM1 gene expression and amplified fragment with the molecular size of 183 bp, corresponding to the expected molecular size of the FUM1 gene sequence, while this band could not be detected in the control sample (A. flavus) (Figure 2). Some investigators have used PCR primers from genes directly involved in fumonisin-biosynthesis, like FUM1, to identify the fumonisin-producing Fusarium species (Abd-Elsalam et al., 2003 ▶; Bluhm et al., 2004 ▶; Patino etal., 2004 ▶). Sreenivasa et al. (2008) ▶ found that, when the isolates of Fusarium species were subjected to PCR analysis, the expected 183-bp DNA was amplified in all F. verticillioides (45/45), all F. proliferatum (04/04), and all F. anthophilum (04/04). Amplification was not detected in other isolates of Fusarium species (F. pallidoroseum, F. sporotrichioides, and F. oxysporum).

In order to evaluate the effect of C. cyminum oil on expression of ITS and FUM1 genes encoding proteins involved in fumonisin biosynthesis, F. verticillioides isolates were cultured on fumonisin-inducing liquid medium in presence of C. cyminum oil (0.195 and 0.390 µl.ml-1) at 20°C for 7 days. The fungal mycelia were separated by filtration, then total RNA was extracted and the expression of ITS and FUM1 genes was evaluated by RT-PCR. The results showed that C. cyminum oil completely inhibited the expression of FUM1 gene in both concentrations dose-dependently (Figure 3).

Based on the statistical analyses, reduction in the expression of fumonisin biosynthetic genes was significant only for FUM1 gene (p<0.05), while no effect was observed on ITS gene. Lopez-Errasquin et al. (2007) ▶ demonstrated a very good linear regression between FUM1 transcript levels and fumonisin production using RT-PCR. Despite the known antifungal activity of C. cyminum, no information has been reported about its effect on fumonisin biosynthesis in gene expression level. To date, different studies have been conducted to find out bioactive compounds from plants and microorganisms with inhibitory effect on toxigenic fungal growth and mycotoxin production. In a study by Khosravi et al. (2011) ▶, C. cyminum essential oil showed significant reductions in values of 94.2% for aflatoxin (AF) B1, 100% for AFB2, 98.9% for AFG1, 100% for AFG2, and 97.5% for total aflatoxin. Another study by Bluma et al. (2008) ▶ showed that thyme and clove essential oils were effective to control aflatoxigenic fungi in stored maize. In conclusion, we reported for the first time that C. cyminum oil inhibited expression of FUM1 gene in F. verticillioides strains. All together, these results indicated that C. cyminum may be employed successfully as a good candidate in controlling toxigenic F. verticillioides on food and feed and subsequent contamination with fumonisin in practice.

Acknowledgments

This work was supported by the Research Council of University of Tehran.

Conflict of interest

The authors declare that they have no conflicts of interest concerning this article.

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