Next Article in Journal
The Snake with the Scorpion’s Sting: Novel Three-Finger Toxin Sodium Channel Activators from the Venom of the Long-Glanded Blue Coral Snake (Calliophis bivirgatus)
Next Article in Special Issue
Contrasting Roles of Deoxynivalenol and Nivalenol in Host-Mediated Interactions between Fusarium graminearum and Sitobion avenae
Previous Article in Journal
Cross-Neutralisation of In Vitro Neurotoxicity of Asian and Australian Snake Neurotoxins and Venoms by Different Antivenoms
Previous Article in Special Issue
Different Toxicity Mechanisms for Citrinin and Ochratoxin A Revealed by Transcriptomic Analysis in Yeast
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Higher Fusarium Toxin Accumulation in Grain of Winter Triticale Lines Inoculated with Fusarium culmorum as Compared with Wheat †

1
Department of Plant Pathology, Plant Breeding and Acclimatization Institute-National Research Institute, Radzików, 05-870 Blonie, Poland
2
Institute of Plant Genetics, Polish Academy of Sciences, 34 Strzeszynska str., 60-479 Poznan, Poland
*
Author to whom correspondence should be addressed.
This paper is an extended version of paper published in the conference: 8th International Triticale Symposium, Ghent, Belgium, 10–14 June 2013.
Submission received: 1 September 2016 / Revised: 8 October 2016 / Accepted: 11 October 2016 / Published: 18 October 2016
(This article belongs to the Collection Understanding Mycotoxin Occurrence in Food and Feed Chains)

Abstract

:
Resistance to Fusarium head blight in 32 winter triticale and 34 winter wheat accessions was evaluated. Triticale and wheat were sown in field experiments in two locations. At the time of flowering, heads were inoculated with three Fusarium culmorum isolates. Fusarium head blight index was scored and after the harvest percentage of Fusarium damaged kernels was assessed. Grain was analysed for type B trichothecenes (deoxynivalenol and derivatives, nivalenol) and zearalenone (ZEN) content. The average Fusarium head blight indexes were 28.0% for wheat and 19.2% for triticale accessions. The percentage of Fusarium damaged kernels was also higher for wheat and came to 55.6%, while for triticale this figure was 40.2%. The average content of deoxynivalenol (DON) for wheat amounted to 11.65 mg/kg and was lower than the result for triticale which was 14.12 mg/kg. The average contents of nivalenol were similar in both cereals: 4.13 mg/kg and 5.19 mg/kg for wheat and triticale respectively. Considerable amounts of DON derivatives in the cereals were also detected. The ZEN content in the grain was 0.60 mg/kg for wheat and 0.66 mg/kg for triticale. Relationships between Fusarium head blight index, Fusarium damaged kernels and mycotoxin contents were statistically significant for wheat and mostly insignificant for triticale. Triticale proved to have less infected heads and kernels than wheat. However, the content of type B trichothecenes was higher in triticale grain than in wheat grain.

Graphical Abstract

1. Introduction

Hexaploid triticale (× Triticosecale Wittmack) is an artificially created cereal, resulting from the crossing of wheat (Triticum sp. Linnaeus) and rye (Secale cereale Linnaeus) [1]. The maternal parents were bread wheat (T. aestivum Linnaeus) or durum wheat (T. durum Desfontaines). Stable hexaploid types of triticale were obtained directly from crosses with durum wheat or crosses between hexaploid and octoploid forms which resulted in secondary triticale populations. Hexaploid triticale includes the A and B genomes of Triticum and R of S. cereale.
There is great interest in this cereal in Poland, due to the considerable share of poor and acid soils in the overall area of arable land. Advantages of triticale are the high yielding capacity and good quality grains intended for feed, characterised by a high content of proteins of the favorable composition of aminoacids and a high digestibility coefficient [2].
Triticale, as an entirely synthetic genus, has low genetic variation due to lack of transition through the process of evolution. In addition, the selection of donors of triticale subgenomes (wheat, rye), led by breeders contributes to the reduction of the genetic variability of varieties including limited diversity of traits responsible for the resistance to the biotic and abiotic stresses.
The development of breeding techniques, such as the production of doubled haploids, have strongly accelerated the process of breeding by introducing pure lines, but have also narrowed the genetic variation. The lack of an intentional selection pressures towards resistance to stresses and the conditions of the cultivation of plants used in breeding stations have caused modern varieties to be poorly adapted to biotic and abiotic stresses [3,4,5].
Fusarium head blight (FHB) is a disease of cereals caused by pathogenic fungi of the genus Fusarium [6,7]. Pathogenesis of FHB is complex. There are several types of resistance to FHB: resistance to initial infection (type I); resistance to Fusarium spread along the rachis (type II), resistance to kernel infection (type III); tolerance against FHB or trichothecenes (type IV); and resistance to accumulation of trichothecenes (type V) [8,9]. Resistance to FHB is complex and is a multigenic feature. Presence or a few or more quantitative trait loci (QTL) for resistance provides sufficient field resistance of plants to diseases [10,11]. Each of the genes (QTLs) determines a relatively small quantitative effect, however, combining their effects increases disease resistance levels [12,13]. Expression of quantitative resistance (e.g., to FHB) is substantially modified by the environmental conditions. High air humidity, wind and rain are the factors promoting the development of FHB [14].
Fusarium head blight may lead to a reduction in yield of grain. However, the concern related to FHB is contamination of grain with mycotoxins such as deoxynivalenol (DON), nivalenol (NIV), zearalenone (ZEN), which are extremely stable; they are not metabolized and are harmful to humans and animals [15,16]. Contamination of grain with mycotoxins is observed even when there is no reduction in the yield [17].
Fungi of the genus Fusarium produce several toxins that can be strongly or chronically toxic to both humans and animals, depending on the type of toxin and the amount of consumed food or feed. The consumption of food or feed contaminated with mycotoxins causes a variety of diseases in humans and animals known generally as mycotoxicoses. Trichotecenes (DON, NIV) have strong toxic effects, such as skin irritation, vomiting, diarrhea, weakness, decreased appetite, hemorrhages, neurological disorders, miscarriages and may even lead to death [18]. Zearalenone causes hyperestrogenic syndromes in pigs and can lead to disrupted conception. Some types of Fusarium mycotoxins (zearalenone, fumonisins) are associated with a growing number of cancers in humans [15]. Taking into consideration the facts above, the content of mycotoxins in grain cereals requires control and should be reduced. The limits of Fusarium toxins in food are regulated by Commission Regulation No. 1126/2007 of 28 September 2007 amending Regulation (EC) No. 1881/2006, which sets maximum levels for certain contaminants in foodstuffs with regard to Fusarium toxins in maize and maize products. Limits for animal feed are less restrictive and are regulated by Commission Recommendation No. 2006/576/EC on the presence of deoxynivalenol, zearalenone, ochratoxin A, T-2 and HT-2 and fumonisins in products intended for animal feed. However, for pig feed, standards are much tougher, the latter standards are particularly important for triticale grain, which is used mostly for feed, to a large extent in feeding pigs.
Fusarium head blight of wheat has been studied for many years in different countries, and there is much data on this cereal. However, the resistance of triticale to this disease is not as well known. Fusarium head blight is the most damaging to bread wheat and durum wheat. In comparison to other cereals, durum wheat is the most susceptible to this disease. Most of the published papers on triticale show that in terms of FHB resistance, it is more resistant than bread wheat and less resistant than rye [19,20,21,22,23]. However, there are results available showing that susceptibility of triticale to Fusarium head blight may be higher and even equal to that of wheat and considerable amounts of Fusarium toxins can be accumulated in triticale grain [24,25,26]. There are a small number of studies of the topic, due to the fact that triticale is a relatively new species and it is grown in much smaller areas of the world than wheat. However, in Poland, acreage of triticale is about 50% of the wheat acreage. Hence, it is important to obtain knowledge about the resistance of this cereal to Fusarium head blight, which can be used in breeding programs.
Many new varieties of triticale are susceptible to FHB, at a level similar to wheat. There are reports that in the triticale grain the amount of accumulated mycotoxin may be similar or even higher than that found in wheat, despite a lower severity of disease on spikes and kernels. So far there is no explanation for this phenomenon. Canadian researchers suggest that increased accumulation of Fusarium toxins results from higher susceptibility of triticale pericarp to Fusarium damage [26,27]. Using scanning electron microscope, we have observed that triticale kernels were more damaged by Fusarium in comparison to wheat [28,29]. The other reason for the vulnerability of part of the genetic pool of triticale (mainly spring), may be that the original forms were obtained from crosses of rye and durum wheat, which have a very high susceptibility to FHB, e.g., early Canadian cultivar “Rosner” [30] or “Armadillo” developed in CIMMYT (International Maize and Wheat Improvement Center, Mexico) [31]. In contrast, the European winter triticale genetic pool was developed in Hungary and Poland from secondary triticales obtained by hexaploid x octoploid crosses which included the genome of bread wheat, which is more resistant to FHB [1].
The main source of resistance is the Fhb1 gene located in the short arm of chromosome 3B. This is a major gene for resistance to FHB, present in Chinese spring wheat variety “Sumai 3”, which is the main source of resistance to this disease. Additionally, another gene, Fhb2, located on the short arm of chromosome 6B, is well characterised. It has, however, much less of an impact on the total resistance to FHB [32].
In addition, in triticale, as an artificial form, the erosion of the genetic base of varieties is at risk if no crosses of parental species are made. This can lead to a decrease in resistance of this species for pathogens, including Fusarium spp. There are attempts being made to broaden the variation of triticale by introducing genes from, for example, Triticum monococcum and Aegilops species and from the highly resistant bread wheat “Sumai 3” [33,34,35,36].
This study evaluated winter triticale and winter wheat breeding lines for their reactions to FHB after inoculations with Fusarium culmorum in field trials. Data were analysed to reveal if there was a statistical difference between triticale and wheat in head infection, kernel damage and accumulation of Fusarium toxins (type B trichothecenes, zearalenone) in grain.

2. Results

Triticale flowered in both locations about 7–10 days earlier than wheat (Supplementary Materials Table S1). Initiation of flowering of both cereals was about 5 days earlier in Cerekwica than in Radzików. Weather conditions in Cerekwica during inoculations of triticale accession were unfavourable, because of high air temperatures and lack of precipitation (Supplementary Materials Figure S1). However, in Cerekwica mist irrigation was applied post-inoculation. In Radzików, weather during triticale inoculation was more favourable for Fusarium infections because of daily occurrence of rainfall. However, air temperature was low at the beginning of June (10.1 °C on 2 June). Weather conditions during inoculation of wheat in Cerekwica were more favourable than for triticale, because of occurrence of rainfall (Supplementary Materials Figure S1). The temperature was low only during the first three days of inoculations (10.2 °C on 5 June). In Radzików, weather conditions were even better because of the high temperature accompanied by frequent rainfalls.
Post-inoculation conditions in both locations were favorable for FHB development and mycotoxin production (Supplementary Materials Table S2). Weather, until the end of harvest, was rainy and with medium to high average daily air temperatures.
The average severity of FHB in 32 winter triticale lines was similar in both locations and amounted to 19.8% in Radzików and 18.7% in Cerekwica. The range of reactions was from 13.7% to 32.0% in Radzików and from 4.8% to 40.0% in Cerekwica. The proportion of Fusarium damaged kernels was higher in Cerekwica (53.7%) than in Radzików (26.8%). The range of reaction was from 9.4% to 45.0% in Radzików and from 27.5% to 68.9% in Cerekwica.
Average DON content in grain in Radzików amounted to 8.69 mg/kg and was lower than in the second location, which had DON content of 19.54 mg/kg. DON content ranged from 7.36 to 37.39 in Cerekwica, and from 4.41 to 17.43 mg/kg in Radzików. In grain samples from Cerekwica there were also high quantities of NIV. The average content was 10.05 mg/kg. In Radzików NIV content was low—0.32 mg/kg on average. There was also a significant amount of DON derivatives (3-acetyldeoxynivalenol [3AcDON], 15-acetyldeoxynivalenol [15AcDON]) in triticale grain in both locations (1.82 mg/kg of 3AcDON and 1.91 mg/kg of 15AcDON, on average). The content of ZEN in triticale grain from Cerekwica was very high and amounted to 1.12 mg/kg (0.51–2.75 mg/kg), while in the grain from Radzików this figure was 6 times lower at 0.20 mg/kg (0.03–1.08 mg/kg). Average values from the locations for 32 winter triticale accessions are presented in Supplementary Materials Table S3.
In both locations, parallel inoculation experiments with 34 winter wheat lines were carried out. The average severity of FHB in winter wheat lines was higher in Radzików than in Cerekwica and amounted to 34.2% and 21.8%, respectively. The range of reactions was from 22.5% to 55.0% in Radzików and from 8.3% to 49.5% in Cerekwica. The proportion of Fusarium damaged kernels was higher in Cerekwica (83.3%) than in Radzików (28.1%). The range of reaction was from 13.7% to 49.5% in Radzików and from 55.1% to 95.3% in Cerekwica.
Average content of DON in grain in Radzików amounted to 8.70 mg/kg and was lower than in the second location, which had a content of 14.87 mg/kg. DON content ranged from 7.36 to 37.39 mg/kg in Cerekwica, and from 4.41 to 17.43 mg/kg in Radzików. In grain samples from Cerekwica there were also high quantities of NIV. The average content was 7.88 mg/kg. In Radzików NIV content was low—0.39 mg/kg on average. There was also a significant amount of derivatives of DON in wheat grain in both locations (2.00 mg/kg of 3AcDON and 1.47 mg/kg of 15AcDON, on average). The content of ZEN in wheat grain from Cerekwica was very high and amounted to 1.03 mg/kg (0.41–3.15 mg/kg), while in the grain from Radzików this figure was six times lower—0.17 mg/kg (0.03–0.83 mg/kg). Average values from the locations for 32 winter wheat accessions are presented in Supplementary Materials Table S4.
Triticale lines were less Fusarium-infected than wheat with regard to heads and kernels (Figure 1). The differences were statistically significant (Table 1). However, the content of all trichothecene toxins was higher in triticale grain than in wheat grain (Figure 1). Statistically significantly higher was the content of DON, 15AcDON and NIV (Table 1). ZEN content was higher in triticale grain; however, the difference was not statistically significant. Variability in wheat and triticale was similar for FHB index, Fusarium damaged kernels (FDK), type B trichothecenes and ZEN (Figure 1). No significant differences were found between variances for FHB index, FDK, sum of type B trichothecenes and ZEN contents. However, for individual trichothecenes (DON, 15AcDON and NIV) variances were 2 times higher in triticale than in wheat.
In the principal component analysis of FHB index, Fusarium damaged kernels and concentration of type B trichothecenes and zearalenone for both cereals showed a clear division into two groups (Figure 2). In the first group most of triticale lines were grouped (except “Fredro” cv.), which showed lower head and kernel infection and higher toxin accumulation. Wheat lines of more infected heads and kernels and lower accumulation of Fusarium toxins formed the second group. The exceptions were two wheat lines (“DD 414/07-4”, “HRSM 789”) which were highly infected and accumulated high amount of toxins in the grain. Two susceptible lines “DC 44/08-4 (S)” and “KBP 09 20 (S)” showed medium toxin accumulation lower than some less infected triticale lines e.g., “DC 04294/04/2”, “MAH 33881-1/3”, “DC 04294/04/1”, “CM 9/10”, “Borwo”, “DD 466/07”.
In triticale average FHB index correlated significantly with FDK, and concentrations of DON, 3AcDON and sum of type B trichothecenes (Table 2). Coefficients, however, were low. On the other hand, FDK proportion correlated significantly with content of NIV, ZEN and sum of type B trichothecenes. Coefficients were higher than for FHB index. The accumulation of type B trichothecenes and ZEN also correlated highly significantly. We found significant, negative correlation of DON and NIV concentrations.
In wheat, average FHB index correlated significantly with FDK proportion and mycotoxin concentrations, except 15AcDON and NIV (Table 2). FDK also correlated significantly with mycotoxins, except NIV and ZEN content. The accumulation of type B trichothecenes and ZEN did not correlate significantly. Coefficients of correlations of FHB index versus FDK, DON, TCT B were higher in wheat (0.538–0.604) than in triticale (0.357–0.408).

3. Discussion

The main finding of the present research is that in certain conditions triticale can accumulate in grain more type B trichothecene toxins than wheat. Accumulation of large amounts of DON in triticale grain was found previously in different studies [19,20,37,38]. Published results, however, were highly dependent on the triticale population was used in the experiments. Miedaner et al. [19] and Góral and Ochodzki [38] found that German and/or Polish triticale cultivars were more resistant to accumulation of DON in the grain than wheat. In contrast, Polish [37] and German breeding lines [20] accumulated high amounts of DON in grain exceeding that reported for wheat [39].
A possible explanation of the high DON content in triticale grain could be the different structure of triticale kernel as compared to wheat kernel. Triticale kernels are, on average, softer than wheat and tend to have higher water uptake rate than wheat kernels [40,41]. Canadian researchers observed that triticale kernels are (as compared to wheat), more susceptible to damage caused by Fusarium [25,26,27]. The pericarp of triticale is fragile to Fusarium infection/toxin contamination, which results in greater kernel destruction than in wheat [29]. However, it should be noted that proportion of Fusarium damaged kernels in triticale is mostly lower than in wheat (Figure 1) [21,42]. This is the effect of lower head infection observed in triticale as compared to wheat [20,21,43,44,45,46].
The other factor influencing observed FHB severity in triticale and wheat heads could be differences in flowering time between the two cereals. Triticale generally flowers earlier than wheat. In our research the difference was 7–10 days. Weather conditions have significant effect on infection of heads with Fusarium and later development of FHB symptoms [14]. Weather also strongly modifies Fusarium mycotoxins production under a field conditions [47,48]. Similar head infection symptoms or kernel damage under different environmental conditions does not result in the same DON levels. Application of mist irrigation post-inoculation can partially remove the effect of unfavourable weather conditions [49,50]. In present research mist irrigation was applied in one experimental location—Cerekwica. However, under field conditions, we cannot control the air temperature, which also affects the development of FHB symptoms and mycotoxin production.
Resistance to FHB in wheat and in triticale is described by different types controlled, partially, by different QTLs [32,51]. Type IV refers to the resistance to DON accumulation by inhibition of toxin synthesis or chemical modification of DON [9,52]. The latter is a glycosylation process which ends with production of DON-glucoside, showing no toxicity to plant cells [53]. DON-glucoside and other so called “masked mycotoxins” were detected in different cereal species, usually at up to 20% of unconjugated DON [54]. Rassmussen et al. [55] studied the proportion of this form of DON in different cereal grains and found the highest relative content of deoxynivalenol-3-β-d-glucoside (up to 37% of DON) in triticale. Average concentrations of DON in grain of studied wheat and triticale cultivars were similar and amounted to 6.54 mg/kg and 6.91 mg/kg, respectively. It should be noted that DON content in triticale was slightly higher. These results and results of our research are unfavorable for triticale. Masked mycotoxins can be digested back to their toxic form [54], hence toxic potential of infected triticale grain may be even higher.
We have analysed relationships of FHB resistance components (FHB index, FDK, mycotoxins) in triticale and wheat. In both cereals FHB index correlated significantly with kernel damage and DON and type B trichothecenes accumulation. However, coefficients for wheat were higher and highly significant.
As compared to wheat, in triticale lower coefficients of correlations between FHB symptoms on heads and kernel damage and mycotoxins have been reported. One of the reasons could be more difficult FHB scoring in triticale than in wheat [20,56,57]. As Miedaner et al. [20] stated, this is because of the widely varying colors of triticale heads and awns and the differing shape of its heads. The same conclusions were drawn by Oettler and Wahle [57]. They stated that triticale breeding materials showed significant differences in spike type, awn length and color, or glume color. This made make it difficult in individual genotypes to differentiate clearly visually between bleached spikelets because of infection or bleaching owing to the ripening process. Miedaner et al. [20] found that FDK rating had a higher correlation to DON content than FHB rating and was similar to that for wheat. In our research we found no correlation between FDK and DON in triticale; however, coefficient of correlation with sum of trichothecenes was significant and only slightly lower than that for wheat.
With regard to relationships between mycotoxins, we found high correlations of DON vs. DON acetyl derivatives. It is obvious as 3AcDON or 15AcDON are metabolized to DON by removing of acetyl units by wheat or fungal esterases (deacetylases) [58]. The deacetylation to DON by the fungus occurs slowly, so that during the Fusarium infection process the plant is most likely confronted primarily with either 15-ADON or 3-ADON [59]. The non-acetylated DON is next accumulated in wheat grain at amounts much larger than acetylated forms [60].
We found a lack of correlation between NIV and DON (3AcDON, 15AcDON) accumulation for wheat and significant negative correlation DON vs. NIV in triticale. Trichothecenes (DON, 3AcDON, 15AcDON) are Fusarium virulence factors inhibiting plant defense response in advance of the invading intercellular hyphae [61]. Lack of trichothecene synthesis capacity of Fusarium graminearum resulted in susceptible plants being able to slow down or even block Fusarium spread which remained restricted to the infected florets [62]. F. graminearum with disrupted Tri5 (encoding trichodiene synthase) gene produced much fewer symptoms than wild-type isolates [63]. It was found that also NIV is a FHB virulence factor and causes similar symptoms on wheat heads to those produced by DON [64]. However, differences in the detoxification mechanism of both toxins were observed. Lemmens et al. [64] postulated that the mechanism of resistance of wheat to NIV is different from the one described for DON. In Fusarium species able to produce both DON and NIV (F. culmorum, F. graminearum) these toxins are produced by different chemotypes. Yoshida et al. [65] inoculated wheat with mixture of DON and NIV isolates of F. graminearum. They found similar kinetics of production of both toxins. However, results showed different DON:NIV ratio depending on genotype. This was observed in our study and resulted in low or negative correlation coefficients. Different DON:NIV ratios could be the effect of competition between different isolates [66]. Co-inoculations can decrease toxin production. The proportion of toxins in individual genotype in specific experimental conditions can be the effect of an isolate-specific response.
Concentration of zearalenone in triticale grain correlated significantly with type B trichothecenes content. However, we found some lines with low or moderate trichothecene content and high amount of ZEN in grain. In wheat, no correlation ZEN vs. trichothecenes was observed, only a significant correlation with NIV content. We found eight lines with high amounts of ZEN in grain, but showing different trichothecene contents. In contrast to DON, zearalenone was not specified as Fusarium virulence factor. It is produced later than DON (or trichothecenes) during pathogenesis [67] or in higher amounts late in the growing season [68,69]. ZEN concentration is greatly affected by the weather conditions late in the season [50]. Late rainfall significantly increased ZEN amount accumulated in wheat grain.

4. Conclusions

Winter triticale accessions showed weaker Fusarium head blight symptoms (head infection, proportion of damaged kernels) as compared to winter wheat accessions. However, accumulation of Fusarium toxins in triticale grain was significantly higher than in wheat grain for type B trichothecenes and there was no significant difference for zearalenone between two cereal species.
The results showed that there is a threat of contamination of triticale grain with mycotoxins despite lower severity of Fusarium head blight symptoms. It indicates that in Fusarium head blight resistance selection some other resistance components should be scored to avoid genotypes combining low disease symptoms with high toxin accumulation.

5. Materials and Methods

The resistance to Fusarium head blight was studied with respect to 29 winter triticale lines, and three cultivars: “Borwo”, “Fredro”, and “Mikado”, as well as 32 winter wheat lines and cultivars ”KWS Ozon” and “Tonacja”. All lines originated from Polish breeding companies and were selected from the large set of breeding lines based on low head infection in two environments (data not shown).
The accessions were sown in the field in Cerekwica near Poznań (GPS coordinates 52.522579, 16.688624) and in Radzików near Warsaw (GPS coordinates 52.212612, 20.633111). Both experiments were established as a randomized block design. Wheat cultivars were sown in 1 m2 plots in three replicates/blocks.
The infective material was a mixture of three isolates of Fusarium culmorum, producing deoxynivalenol (KF846, DON chemotype), nivalenol (KF350, NIV chemotype) and zearalenone (ZFR 112, DON chemotype) [42]. Isolates were incubated on autoclaved wheat kernels in glass flasks for about 1 week at 20 °C in darkness and then exposed to near UV light under a 16 h photoperiod for 3 weeks at 15 °C. The mycelium-colonised grain was air dried and stored in a refrigerator at 4 °C until usage.
On the date of inoculation, the grain with Fusarium mycelium was suspended in tap water for 2 h and then filtered through cheesecloth to obtain a conidial suspension. The suspensions from each of the three isolates were adjusted to 100,000 spores/mL with the aid of a haemocytometer. Equal volumes of suspension were mixed.
Wheat spikes were sprayed with a spore suspension at anthesis at a rate of 100 mL/m2. Inoculations were performed individually on each plot at the beginning of anthesis, and repeated about 3 days later at full anthesis. Inoculations were carried out in the evening, when relative air humidity was increasing.
In the experimental field in Cerekwica, in order to maintain a high humidity necessary to infection of heads, plots were mist irrigated for 3 days after inoculation. In the second location in the Radzików field experiment was conducted without mist irrigation, however, the experimental field was located near the river and this area had high relative air humidity.
Severity of Fusarium head blight was evaluated twice, 14 and 21 days post inoculation. The presence of FHB (percentage of heads infected per plot) and percentages of head infection were determined. Fusarium head blight index was calculated as the combination of disease severity and disease incidence.
After ripening, 30 randomly selected spikes per plot were harvested. Grain was threshed using laboratory thresher. Percentage of kernels damaged by Fusarium (FDK) was determined by dividing samples into two categories: healthy looking kernels (plump, normal color, no visual infection; slightly shrivelled of normal color) and kernels with visible symptoms of Fusarium damage (discolored kernels of normal size or slightly shrivelled, pinkish-white, shrivelled kernels = “tombstone”) [70].
The content of the type B trichothecenes (deoxynivalenol [DON], 3-acetyldeoxynivalenol [3AcDON], 15-acetyldeoxynivalenol [15AcDON], nivalenol [NIV]) in triticale and wheat grain was analysed, using the technique of gas chromatography.
Mycotoxins were extracted from 5 g of ground grains using 25 mL of an aqueous solution of acetonitrile (acetonitrile:water 84:16 v/v) was shaken on the laboratory shaker overnight. Samples were centrifuged (3000 rpm·min−1, 5 min), and the extract was purified with MycoSep® 227 Trich+ columns (Romer Labs Inc., Union, MO, USA). One microlitre of the internal standard solution (chloralose) was added to 4 mL of purified extract. The solvent was evaporated to dryness in the air stream. Mycotoxins were derivatised to the trimethylsilyl derivatives using the derivatising agent Sylon BTZ [BSA (N,O-Bis(trimethylsilyl)acetamide):TMCS (Chlorotrimethylsilane):TMSI (N-trimethylsilyimidazole), 3:2:3] (Supelco, Bellefonte, PA, USA). After dissolution of sample in isooctane, excess of derivatising agent was decomposed and removed with water. The organic layer was transferred to autosampler vial and analysed chromatographically with gas chromatograph SRI 8610C (SRI Instruments, Torrance, CA, USA), with BGB-5MS column of 30 m in length, and an internal diameter of 0.25 mm.
Hydrogen was a carrier. Elution was carried out in the temperature gradient. Mycotoxin detection was carried out using electron capture detector (ECD). Identification of individual compounds was made by comparing the retention times of the pure standards of mycotoxins. The concentration of mycotoxins was established on the basis of the calibration curve, using chloralose as the internal standard. The content of type B trichothecenes was expressed as toxin weight (mg) per grain weight (kg).
The content of zearalenone (ZEN) was determined using a quantitative direct competitive enzyme-linked immunosorbent assay (ELISA) AgraQuant® ZON 40/1000 (LOD 10 ppb) (Romer Labs Inc., Union, MO, USA). A 5 g of the ground sample was placed in a conical 50 mL Falcon centrifuge tube and then 25 mL of the solvent (methanol-water 70:30 v/v) was added. The sample was extracted for 1 h on a shaker and then centrifuged (1620 g, 5 min). The obtained extract was analysed with ELISA method according to the procedure described by Romer Labs. The content of zearalenone was expressed as toxin weight (mg) per grain weight (kg).
The statistical analysis was performed using Microsoft® Excel 2010/XLSTAT©-Pro (Version 2015.2.02.18135, Addinsoft, Inc., Brooklyn, NY, USA). Differences between the two cereal species were compared using the Kruskal–Wallis one-way analysis of variance (XLSTAT procedure: Comparison of k samples—Kruskal-Wallis, Friedman, …). The Kruskal-Wallis test was selected because most of the variables did not follow normal distribution. Comparison of the variances of triticale and wheat samples (FHBi, FDK and mycotoxin concentrations) were performed using parametric Fisher’s F test (XLSTAT procedure: Two-sample comparison of variances). The relationships between FHBi, FDK and mycotoxin concentrations for wheat and triticale were investigated by Pearson correlation tests (XLSTAT procedure: Correlation tests). Prior to analysis, data which did not follow normal distribution was log10 transformed to normalise residual distributions. Multivariate data analysis method was applied to the data on FHB resistance. Principal component analysis (XLSTAT procedure: Principal Component Analysis PCA) was used to show how the two cereal species are distributed with respect to the main variation described in the first two components and how variables influence the construction of the two components. PCA results also revealed associations among variables measured by the angle between variable vectors.

Supplementary Materials

The following are available online at www.mdpi.com/2072-6651/8/10/301/s1. Figure S1: Daily air temperature and sum of precipitation in Cerekwica (C) and Radzików (R) during Fusarium inoculation of triticale and wheat heads. Table S1: Flowering periods of winter triticale and winter wheat in 2012 in two experimental locations. Table S2: Average daily air temperature and sum of precipitation in Cerekwica and Radzików from triticale and wheat flowering until the end of harvest in 2012. Table S3: Resistance to Fusarium head blight and mycotoxin accumulation in grain of 29 lines and three cultivars of winter triticale inoculated with Fusarium culmorum isolates in the field experiments in Radzików and Cerekwica. FHB: Fusarium head blight; FDK: Fusarium damaged kernels; DON: deoxynivalenol; 3AcDON: 3-acetyldeoxynivalenol; 15AcDON: 15-acetyldeoxynivalenol; NIV: nivalenol; TCT B: type B trichothecenes; ZEN: zearalenone. Table S4: Resistance to Fusarium head blight and mycotoxin accumulation in grain of 32 lines and two cultivars of winter wheat inoculated with Fusarium culmorum isolates in the field experiments in Radzików and Cerekwica. FHB: Fusarium head blight; FDK: Fusarium damaged kernels; DON: deoxynivalenol; 3AcDON: 3-acetyldeoxynivalenol; 15AcDON: 15-acetyldeoxynivalenol; NIV: nivalenol; TCT B: type B trichothecenes; ZEN: zearalenone.

Acknowledgments

Research was supported by the project from the Ministry of Agriculture and Rural Development: “Evaluation of resistance of triticale lines to Fusarium head blight and accumulation of Fusarium mycotoxins in grain” (HOR hn 801-8/12, HOR hn 801-11/12). Authors wish to thank triticale breeders from Strzelce Plant Breeding and Danko Plant Breeding and wheat breeders from Strzelce Plant Breeding, Danko Plant Breeding, Poznańska Plant Breeding, Smolice Plant Breeding and Małopolska Plant Breeding for providing triticale and wheat lines for the experiment.

Author Contributions

The experiments were conceived and designed by T.G. and H.W. The experiments were performed by T.G., H.W. and D.W.-G. Toxins were analysed by P.O. Data was analysed by T.G. The paper was written by T.G. and H.W.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Randhawa, H.; Bona, L.; Graf, R.J. Triticale breeding—Progress and prospect. In Triticale; Eudes, F., Ed.; Springer: Cham, Switzerland, 2015; pp. 15–32. [Google Scholar]
  2. Arseniuk, E.; Oleksiak, T. Production and breeding of cereals in Poland. In Proceedings of the 5th International Triticale Symposium, Radzików, Poland, 30 June–5 July 2002; pp. 11–20.
  3. Arseniuk, E.; Góral, T. Triticale biotic stresses—Known and novel foes. In Triticale; Eudes, F., Ed.; Springer: Cham, Switzerland, 2015; pp. 83–108. [Google Scholar]
  4. Audenaert, K.; Troch, V.; Landschoot, S.; Haesaert, G. Biotic stresses in the anthropogenic hybrid triticale (× Triticosecale Wittmack): Current knowledge and breeding challenges. Eur. J. Plant Pathol. 2014, 140, 615–630. [Google Scholar] [CrossRef]
  5. Arseniuk, E. Triticale abiotic stresses—An overview. In Triticale; Eudes, F., Ed.; Springer: Cham, Switzerland, 2015; pp. 69–81. [Google Scholar]
  6. Parry, D.W.; Jenkinson, P.; McLeod, L. Fusarium ear blight (scab) in small grain cereals—A review. Plant Pathol. 1995, 44, 207–238. [Google Scholar] [CrossRef]
  7. Siou, D.; Gélisse, S.; Laval, V.; Repinçay, C.; Canalès, R.; Suffert, F.; Lannou, C. Effect of wheat spike infection timing on Fusarium head blight development and mycotoxin accumulation. Plant Pathol. 2014, 63, 390–399. [Google Scholar] [CrossRef]
  8. Mesterházy, Á. Types and components of resistance to Fusarium head blight of wheat. Plant Breed. 1995, 114, 377–386. [Google Scholar] [CrossRef]
  9. Foroud, N.A.; Eudes, F. Trichothecenes in cereal grains. Int. J. Mol. Sci. 2009, 10, 147–173. [Google Scholar] [CrossRef] [PubMed]
  10. Kalih, R.; Maurer, H.P.; Miedaner, T. Genetic architecture of Fusarium head blight resistance in four winter triticale populations. Phytopathology 2015, 105, 334–341. [Google Scholar] [CrossRef] [PubMed]
  11. Faris, J.D.; Li, W.L.; Liu, D.J.; Chen, P.D.; Gill, B.S. Candidate gene analysis of quantitative disease resistance in wheat. Theor. Appl. Genet. 1999, 98, 219–225. [Google Scholar]
  12. Chen, J.; Griffey, C.A.; Saghai Maroof, M.A.; Stromberg, E.L.; Biyashev, R.M.; Zhao, W.; Chappell, M.R.; Pridgen, T.H.; Dong, Y.; Zeng, Z. Validation of two major quantitative trait loci for Fusarium head blight resistance in Chinese wheat line W14. Plant Breed. 2006, 125, 99–101. [Google Scholar] [CrossRef]
  13. Miedaner, T.; Wilde, F.; Steiner, B.; Buerstmayr, H.; Korzun, V.; Ebmeyer, E. Stacking quantitative trait loci (QTL) for Fusarium head blight resistance from non-adapted sources in an European elite spring wheat background and assessing their effects on deoxynivalenol (DON) content and disease severity. Theor. Appl. Genet. 2006, 112, 562–569. [Google Scholar] [CrossRef] [PubMed]
  14. Xu, X.M.; Monger, W.; Ritieni, A.; Nicholson, P. Effect of temperature and duration of wetness during initial infection periods on disease development, fungal biomass and mycotoxin concentrations on wheat inoculated with single, or combinations of, Fusarium species. Plant Pathol. 2007, 56, 943–956. [Google Scholar] [CrossRef]
  15. Bennett, J.W.; Klich, M. Mycotoxins. Clin. Microbiol. Rev. 2003, 16, 497–516. [Google Scholar] [CrossRef] [PubMed]
  16. Hazel, C.M.; Patel, S. Influence of processing on trichothecene levels. Toxicol. Lett. 2004, 153, 51–59. [Google Scholar] [CrossRef] [PubMed]
  17. Cowger, C.; Arrellano, C. Plump kernels with high deoxynivalenol linked to late Gibberella zeae infection and marginal disease conditions in winter wheat. Phytopathology 2010, 100, 719–728. [Google Scholar] [CrossRef] [PubMed]
  18. Sobrova, P.; Adam, V.; Vasatkova, A.; Beklova, M.; Zeman, L.; Kizek, R. Deoxynivalenol and its toxicity. Interdiscip. Toxicol. 2010, 3, 94–99. [Google Scholar] [CrossRef] [PubMed]
  19. Miedaner, T.; Reinbrecht, C.; Lauber, U.; Schollenberger, M.; Geiger, H.H. Effects of genotype and genotype-environment interaction on deoxynivalenol accumulation and resistance to Fusarium head blight in rye, triticale, and wheat. Plant Breed. 2001, 120, 97–105. [Google Scholar] [CrossRef]
  20. Miedaner, T.; Heinrich, N.; Schneider, B.; Oettler, G.; Rohde, S.; Rabenstein, F. Estimation of deoxynivalenol (DON) content by symptom rating and exoantigen content for resistance selection in wheat and triticale. Euphytica 2004, 139, 123–132. [Google Scholar] [CrossRef]
  21. Langevin, F.; Eudes, F.; Comeau, A. Effect of trichothecenes produced by Fusarium graminearum during Fusarium head blight development in six cereal species. Eur. J. Plant Pathol. 2004, 110, 735–746. [Google Scholar] [CrossRef]
  22. Veitch, R.S.; Caldwell, C.D.; Martin, R.A.; Lada, R.; Salmon, D.; Anderson, D.M.; MacDonald, D. Susceptibility of winter and spring triticales to Fusarium head blight and deoxynivalenol accumulation. Can. J. Plant Sci. 2008, 88, 783–788. [Google Scholar] [CrossRef]
  23. Arseniuk, E.; Góral, T.; Czembor, H.J. Reaction of triticale, wheat and rye accessions to graminaceous Fusarium spp. infection at the seedling and adult plant growth stages. Euphytica 1993, 70, 175–183. [Google Scholar] [CrossRef]
  24. Góral, T.; Cichy, H.; Buśko, M.; Perkowski, J. Resistance to head blight and mycotoxins concentrations in kernels of Polish winter triticale lines and cultivars inoculated with Fusarium culmorum. In Proceedings of the 5th International Triticale Symposium, Radzików, Poland, 30 June–5 July 2002; pp. 501–507.
  25. Randhawa, H.; Eudes, F.; Beres, B.; Graf, R.; Fedak, G.; Comeau, A.; Langevin, F.; Dion, Y.; Pozniak, C. Integrated approaches for triticale breeding. In Proceedings of the 8th International Triticale Symposium, Ghent, Belgium, 10–14 June 2013; p. 29.
  26. Comeau, A.; Langevin, F.; Savard, M.E.; Gilber, J.; Dion, Y.; Rioux, S.; Martin, R.A.; Haber, S.; Voldeng, H.; Fedak, G.; et al. Improving Fusarium head blight resistance in bread wheat and triticale for Canadian needs. Cereal Res. Commun. 2008, 36, 91–92. [Google Scholar]
  27. Langevin, F.; Eudes, F.; Comeau, A.; Dion, Y.; Rioux, S.; Randhawa, H.; Fedak, G.; Cao, W.; Gilbert, J.; Lachance, C.; et al. Sources of type II Fusarium resistance for triticale breeding. In Proceedings of the 6th Canadian Workshop on Fusarium Head Blight, Ottawa, ON, Canada, 1–4 November 2009; p. 66.
  28. Jackowiak, H.; Packa, D.; Wiwart, M.; Perkowski, J. Scanning electron microscopy of Fusarium damaged kernels of spring wheat. Int. J. Food Microbiol. 2005, 98, 113–123. [Google Scholar] [CrossRef] [PubMed]
  29. Packa, D.; Jackowiak, H.; Góral, T.; Wiwart, M.; Perkowski, J. Scanning electron microscopy of Fusarium-infected kernels of winter triticale (× Triticosecale Wittmack). Seed Sci. Biotechnol. 2008, 2, 27–31. [Google Scholar]
  30. Larter, E.N.; Shebeski, L.H.; McGinnis, R.C.; Evans, L.E.; Kaltsikes, P.J. Rosner, a hexaploid triticale cultivar. Can. J. Plant Sci. 1970, 50, 122–124. [Google Scholar] [CrossRef]
  31. Merker, A. Chromosome composition of hexaploid triticale. Hereditas 1975, 80, 41–52. [Google Scholar] [CrossRef]
  32. Buerstmayr, H.; Ban, T.; Anderson, J.A. QTL mapping and marker-assisted selection for Fusarium head blight resistance in wheat: A review. Plant Breed. 2009, 128, 1–26. [Google Scholar] [CrossRef]
  33. Sodkiewicz, W.; Strzembicka, A. Application of Triticum monococcum for the improvement of triticale resistance to leaf rust (Puccinia triticina). Plant Breed. 2004, 123, 39–42. [Google Scholar] [CrossRef]
  34. Kwiatek, M.; Wiśniewska, H.; Apolinarska, B. Cytogenetic analysis of Aegilops chromosomes, potentially usable in triticale (× Triticosecale Witt.) breeding. J. Appl. Genet. 2013, 54, 147–155. [Google Scholar] [CrossRef] [PubMed]
  35. Salmanowicz, B.P.; Langner, M.; Wiśniewska, H.; Apolinarska, B.; Kwiatek, M.; Błaszczyk, L. Molecular, physicochemical and rheological characteristics of introgressive Triticale/Triticum monococcum ssp. monococcum lines with wheat 1D/1A chromosome substitution. Int. J. Mol. Sci. 2013, 14, 15595–15614. [Google Scholar] [PubMed]
  36. Dürr, S.R. Evaluation of Three Winter Triticale (× Triticosecale Wittmack) Populations and a Collection of Triticale Cultivars and Breeding Lines for Resistance against Fusarium Head Blight. Master’s Thesis, University of Natural Resources and Life Sciences, Vienna, Austria, October 2014. [Google Scholar]
  37. Góral, T.; Buśko, M.; Cichy, H.; Jackowiak, H.; Perkowski, J. Resistance of winter triticale lines and cultivars to Fusarium head blight and deoxynivalenol accumulation in kernels. J. Appl. Genet. 2002, 43, 237–248. [Google Scholar]
  38. Góral, T.; Ochodzki, P. Resistance of Polish winter triticale cultivars to Fusarium head blight and accumulation of Fusarium-myctoxins in grain. In Proceedings of the 6th International Triticale Symposium, Stellenbosch, South Africa, 3–7 September 2006; Botes, W.C., Boros, D., Darvey, N., Gustafson, P., Jessop, R., Marais, G.F., Oettler, G., Salmon, D., Eds.; Stellenbosch University: Stellenbosch, South Africa, 2007; pp. 140–143. [Google Scholar]
  39. Góral, T.; Ochodzki, P. Effect of severity of Fusarium head blight and kernel infection with Fusarium culmorum on mycotoxin content in grain of winter wheat cultivars. In Proceedings of the 28th Mykotoxin-Workshop, Bydgoszcz, Poland, 29–31 May 2006; Grajewski, J., Twaruzek, M., Szymanska, A., Eds.; Kazimierz Wielki University: Bydgoszcz, Poland, 2006; p. 84. [Google Scholar]
  40. Clarke, J.M.; Depauw, R.M. Water imbibition rate of wheat kernels as affected by kernel color, weather damage, and method of threshing. Can. J. Plant Sci. 1989, 69, 1–7. [Google Scholar] [CrossRef]
  41. Wiwart, M.; Moś, M.; Wójtowicz, T. Studies on the imbibition of triticale kernels with a different degree of sprouting, using digital shape analysis. Plant Soil Environ. 2006, 52, 328–334. [Google Scholar]
  42. Góral, T.; Wiśniewska, H.; Ochodzki, P.; Walentyn-Góral, D.; Kwiatek, M. Reaction of winter triticale breeding lines to Fusarium head blight and accumulation of Fusarium metabolites in grain in two environments under drought conditions. Cereal Res. Commun. 2013, 41, 106–115. [Google Scholar] [CrossRef]
  43. Góral, T. Evaluation of resistance of breeding lines of wheat and triticale to Fusarium head blight, snow mold, and leaf rust in Radzików in 2006. Short communication. Biul. IHAR 2007, 246, 31–44. [Google Scholar]
  44. Góral, T. Resistance of winter triticale cultivars to Fusarium head blight caused by Fusarium culmorum. Biul. IHAR 2009, 254, 41–50. [Google Scholar]
  45. Wiśniewska, H.; Góral, T.; Ochodzki, P.; Walentyn-Góral, D.; Kwiatek, M.; Majka, M.; Grzeszczak, I.; Belter, J.; Banaszak, Z.; Pojmaj, M.; et al. Resistance of winter triticale breeding lines to Fusarium head blight. Biul. IHAR 2014, 271, 29–43. [Google Scholar]
  46. Wiśniewska, H.; Góral, T.; Ochodzki, P.; Walentyn-Góral, D.; Kwiatek, M.; Majka, M.; Belter, J.; Banaszak, Z.; Pojmaj, M.; Kurleto, D.; et al. Resistance of winter triticale breeding lines to infection of spike with Fusarium culmorum. Biul. IHAR 2015, 276, 39–56. [Google Scholar]
  47. Cowger, C.; Arellano, C. Fusarium graminearum infection and deoxynivalenol concentrations during development of wheat spikes. Phytopathology 2013, 103, 460–471. [Google Scholar] [CrossRef] [PubMed]
  48. Lemmens, M.; Buerstmayr, H.; Krska, R.; Schuhmacher, R.; Grausgruber, H.; Ruckenbauer, P. The effect of inoculation treatment and long-term application of moisture on Fusarium head blight symptoms and deoxynivalenol contamination in wheat grains. Eur. J. Plant Pathol. 2004, 110, 299–308. [Google Scholar] [CrossRef]
  49. Imathiu, S.; Edwards, S.; Ray, R.; Back, M. Review article: Artificial inoculum and inoculation techniques commonly used in the investigation of Fusarium head blight in cereals. Acta Phytopathol. Entomol. Hung. 2014, 49, 129–139. [Google Scholar] [CrossRef]
  50. Kharbikar, L.L.; Dickin, E.T.; Edwards, S.G. Impact of post-anthesis rainfall, fungicide and harvesting time on the concentration of deoxynivalenol and zearalenone in wheat. Food Addit. Contam. A 2015, 32, 2075–2085. [Google Scholar] [CrossRef] [PubMed]
  51. Somers, D.J.; Fedak, G.; Savard, M. Molecular mapping of novel genes controlling Fusarium head blight resistance and deoxynivalenol accumulation in spring wheat. Genome 2003, 46, 555–564. [Google Scholar] [CrossRef] [PubMed]
  52. Boutigny, A.-L.; Richard-Forget, F.; Barreau, C. Natural mechanisms for cereal resistance to the accumulation of Fusarium trichothecenes. Eur. J. Plant Pathol. 2008, 121, 411–423. [Google Scholar] [CrossRef]
  53. Berthiller, F.; Dall’Asta, C.; Schuhmacher, R.; Lemmens, M.; Adam, G.; Krska, R. Masked mycotoxins: determination of a deoxynivalenol glucoside in artificially and naturally contaminated wheat by liquid chromatography-tandem mass spectrometry. J. Agric. Food Chem. 2005, 53, 3421–3425. [Google Scholar] [CrossRef] [PubMed]
  54. Berthiller, F.; Crews, C.; Dall’Asta, C.; De Saeger, S.; Haesaert, G.; Karlovsky, P.; Oswald, I.P.; Seefelder, W.; Speijers, G.; Stroka, J. Masked mycotoxins: A review. Mol. Nutr. Food Res. 2013, 57, 165–186. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Rasmussen, P.H.; Nielsen, K.F.; Ghorbani, F.; Spliid, N.H.; Nielsen, G.C.; Jørgensen, L.N. Occurrence of different trichothecenes and deoxynivalenol-3-β-d-glucoside in naturally and artificially contaminated Danish cereal grains and whole maize plants. Mycotoxin Res. 2012, 28, 181–190. [Google Scholar] [CrossRef] [PubMed]
  56. Oettler, G.; Heinrich, N.; Miedaner, T. Estimates of additive and dominance effects for Fusarium head blight resistance of winter triticale. Plant Breed. 2004, 123, 525–530. [Google Scholar] [CrossRef]
  57. Oettler, G.; Wahle, G. Genotypic and environmental variation of resistance to head blight in triticale inoculated with Fusarium culmorum. Plant Breed. 2001, 120, 297–300. [Google Scholar] [CrossRef]
  58. Alexander, N.J.; McCormick, S.P.; Waalwijk, C.; van der Lee, T.; Proctor, R.H. The genetic basis for 3-ADON and 15-ADON trichothecene chemotypes in Fusarium. Fungal Genet. Biol. 2011, 48, 485–495. [Google Scholar] [CrossRef] [PubMed]
  59. Schmeitzl, C.; Warth, B.; Fruhmann, P.; Michlmayr, H.; Malachová, A.; Berthiller, F.; Schuhmacher, R.; Krska, R.; Adam, G. The metabolic fate of deoxynivalenol and its acetylated derivatives in a wheat suspension culture: Identification and detection of DON-15-O-glucoside, 15-acetyl-DON-3-O-glucoside and 15-acetyl-DON-3-sulfate. Toxins 2015, 7, 3112–3126. [Google Scholar] [CrossRef] [PubMed]
  60. Burlakoti, R.R.; Ali, S.; Secor, G.A.; Neate, S.M.; McMullen, M.P.; Adhikari, T.B. Comparative mycotoxin profiles of Gibberella zeae populations from barley, wheat, potatoes, and sugar beets. Appl. Environ. Microbiol. 2008, 74, 6513–6520. [Google Scholar] [CrossRef] [PubMed]
  61. Brown, N.A.; Bass, C.; Baldwin, T.K.; Chen, H.; Massot, F.; Carion, P.W.C.; Urban, M.; van de Meene, A.M.L.; Hammond-Kosack, K.E. Characterisation of the Fusarium graminearum-wheat floral interaction. J. Pathog. 2011, 2011, 626345. [Google Scholar] [PubMed]
  62. Wagacha, J.M.; Muthomi, J.W. Fusarium culmorum: Infection process, mechanisms of mycotoxin production and their role in pathogenesis in wheat. Crop Prot. 2007, 26, 877–885. [Google Scholar] [CrossRef]
  63. Proctor, R.H.; Hohn, T.M.; McCormick, S.P. Reduced virulence of Gibberella zeae caused by disruption of a trichothecene toxin biosynthetic gene. Mol. Plant-Microbe Interact. 1995, 8, 593–601. [Google Scholar] [CrossRef] [PubMed]
  64. Lemmens, M.; Koutnik, A.; Steiner, B.; Buerstmayr, H.; Berthiller, F.; Schuhmacher, R.; Maier, F.; Schäfer, W. Investigations on the ability of Fhb1 to protect wheat against nivalenol and deoxynivalenol. Cereal Res. Commun. 2008, 36, 429–435. [Google Scholar] [CrossRef]
  65. Yoshida, M.; Nakajima, T. Deoxynivalenol and nivalenol accumulation in wheat infected with Fusarium graminearum during grain development. Phytopathology 2010, 100, 763–773. [Google Scholar] [CrossRef] [PubMed]
  66. Siou, D.; Gélisse, S.; Laval, V.; Elbelt, S.; Repinçay, C.; Bourdat-Deschamps, M.; Suffert, F.; Lannou, C. Interactions between head blight pathogens: Consequences for disease development and toxin production in wheat spikes. Appl. Environ. Microbiol. 2015, 81, 957–965. [Google Scholar] [CrossRef] [PubMed]
  67. Waśkiewicz, A.; Morkunas, I.; Bednarski, W.; Mai, V.C.; Formela, M.; Beszterda, M.; Wiśniewska, H.; Goliński, P. Deoxynivalenol and oxidative stress indicators in winter wheat inoculated with Fusarium graminearum. Toxins 2014, 6, 575–591. [Google Scholar] [CrossRef] [PubMed]
  68. Brinkmeyer, U.; Dänicke, S.; Valenta, H.; Flachowsky, G. Progression of deoxynivalenol and zearalenone concentrations in straw of wheat infected artificially with Fusarium culmorum. Mycotoxin Res. 2005, 21, 97–99. [Google Scholar] [CrossRef] [PubMed]
  69. Matthäus, K.; Dänicke, S.; Vahjen, W.; Simon, O.; Wang, J.; Valenta, H.; Meyer, K.; Strumpf, A.; Ziesenib, H.; Flachowsky, G. Progression of mycotoxin and nutrient concentrations in wheat after inoculation with Fusarium culmorum. Arch. Anim. Nutr. 2004, 58, 19–35. [Google Scholar] [CrossRef] [PubMed]
  70. Argyris, J.; Van Sanford, D.; TeKrony, D. Fusarium graminearum infection during wheat seed development and its effect on seed quality. Crop Sci. 2003, 43, 1782–1788. [Google Scholar] [CrossRef]
Figure 1. Fusarium head blight index (FHBi), Fusarium damaged kernels (FDK) proportion and accumulation type B trichothecenes (TCT B) and zearalenone (ZEN) in grain of triticale and wheat inoculated with F. culmorum. Boxes represent first quartile, median, and third quartile. Whiskers show lower and upper limits.
Figure 1. Fusarium head blight index (FHBi), Fusarium damaged kernels (FDK) proportion and accumulation type B trichothecenes (TCT B) and zearalenone (ZEN) in grain of triticale and wheat inoculated with F. culmorum. Boxes represent first quartile, median, and third quartile. Whiskers show lower and upper limits.
Toxins 08 00301 g001
Figure 2. Biplot of the principal component analysis of Fusarium head blight index (FHBi), Fusarium damaged kernels (FDK), type B trichothecenes (TCT B) and zearalenone (ZEN) accumulation in grain for 32 lines of winter triticale (squares) and 34 lines of winter wheat (circles) inoculated with F. culmorum in Radzików and Cerekwica. (S): susceptible checks of winter wheat.
Figure 2. Biplot of the principal component analysis of Fusarium head blight index (FHBi), Fusarium damaged kernels (FDK), type B trichothecenes (TCT B) and zearalenone (ZEN) accumulation in grain for 32 lines of winter triticale (squares) and 34 lines of winter wheat (circles) inoculated with F. culmorum in Radzików and Cerekwica. (S): susceptible checks of winter wheat.
Toxins 08 00301 g002
Table 1. Comparison of wheat and triticale in resistance to Fusarium head blight and Fusarium toxin accumulation in grain.
Table 1. Comparison of wheat and triticale in resistance to Fusarium head blight and Fusarium toxin accumulation in grain.
CerealFHB Index (%)FDK (%)DON (mg/kg)3AcDON (mg/kg)15AcDON (mg/kg)NIV (mg/kg)TCT B (mg/kg)ZEN (mg/kg)
Wheat (n = 34)28.0 b55.6 b11.65 a **2.00 a1.47 a **4.13 a *19.25 a **0.60 a
Triticale (n = 32)19.2 a40.2 a14.12 b **1.82 a1.91 b **5.19 b *23.03 b **0.66 a
Values within the same column followed by the different letters are significantly different at the level of probability < 0.001, ** < 0.01 or * < 0.05. FHB: Fusarium head blight; FDK: Fusarium damaged kernels; DON: deoxynivalenol; 3AcDON: 3-acetyldeoxynivalenol; 15AcDON: 15-acetyldeoxynivalenol; NIV: nivalenol; TCT B: type B trichothecenes; ZEN: zearalenone.
Table 2. Coefficients of correlations between FHB (Fusarium head blight) index, Fusarium damaged kernels (FDK), and type B trichothecenes (DON, 3AcDON, 15AcDON, NIV, TCT B) and zearalenone (ZEN) accumulation in grain of 32 triticale lines (below, diagonal), and 34 wheat lines (above, diagonal) from experiments in Cerekwica and Radzików.
Table 2. Coefficients of correlations between FHB (Fusarium head blight) index, Fusarium damaged kernels (FDK), and type B trichothecenes (DON, 3AcDON, 15AcDON, NIV, TCT B) and zearalenone (ZEN) accumulation in grain of 32 triticale lines (below, diagonal), and 34 wheat lines (above, diagonal) from experiments in Cerekwica and Radzików.
VariablesFHB IndexFDKDON3AcDON15AcDONNIVTCT B aZEN
FHB index-0.604 ***0.538 ***0.630 ***0.333 ns0.326 ns0.576 ***0.412 *
FDK0.408 b,*-0.451 **0.529 ***0.336 *0.314 ns0.504 **0.233 ns
DON0.398 *0.214 ns-0.845 ***0.889 ***0.251 ns- c-0.014 ns
3AcDON0.536 **0.347 ns0.885 ***-0.736 ***0.262 ns-0.170 ns
15AcDON0.267 ns0.232 ns0.890 ***0.804 ***-0.057 ns--0.165 ns
NIV0.180 ns0.465 **-0.406 *-0.262 ns-0.339 ns--0.406 *
TCT B a0.357 *0.451 **-----0.115 ns
ZEN0.166 ns0.490 **0.350 *0.472 **0.285 ns0.295 ns0.501 **-
a Sum of DON, 3AcDON, 15AcDON, and NIV; b ns not significant. *, **, and *** correlation coefficient is significant at p < 0.05, 0.01, and 0.001, respectively; c Coefficients of correlation between TCT B and individual trichothecenes were not included in the table.

Share and Cite

MDPI and ACS Style

Góral, T.; Wiśniewska, H.; Ochodzki, P.; Walentyn-Góral, D. Higher Fusarium Toxin Accumulation in Grain of Winter Triticale Lines Inoculated with Fusarium culmorum as Compared with Wheat. Toxins 2016, 8, 301. https://0-doi-org.brum.beds.ac.uk/10.3390/toxins8100301

AMA Style

Góral T, Wiśniewska H, Ochodzki P, Walentyn-Góral D. Higher Fusarium Toxin Accumulation in Grain of Winter Triticale Lines Inoculated with Fusarium culmorum as Compared with Wheat. Toxins. 2016; 8(10):301. https://0-doi-org.brum.beds.ac.uk/10.3390/toxins8100301

Chicago/Turabian Style

Góral, Tomasz, Halina Wiśniewska, Piotr Ochodzki, and Dorota Walentyn-Góral. 2016. "Higher Fusarium Toxin Accumulation in Grain of Winter Triticale Lines Inoculated with Fusarium culmorum as Compared with Wheat" Toxins 8, no. 10: 301. https://0-doi-org.brum.beds.ac.uk/10.3390/toxins8100301

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop