Effect of atmospheric CO2 on plant defense against leaf and root pathogens of Arabidopsis


Climate change and the associated increase in atmospheric CO2 levels may affect the severity of plant diseases and threaten future crop yields. Here, we compared responses of the model plant Arabidopsis thaliana to leaf and root pathogens with hemi-biotrophic or necrotrophic infection strategies under pre-industrial, current, and future atmospheric CO2 conditions. Defenses against biotrophs are generally regulated by salicylic acid (SA) signaling, whereas jasmonic acid (JA) signaling controls defenses against necrotrophs. Under the CO2 conditions tested, basal expression of the JA-responsive marker gene PDF1.2 increased at increasing CO2 concentrations. The SA-responsive marker genes ICS1 and FRK1 showed an opposite behavior, being lower expressed under high CO2 and higher expressed under low CO2, respectively. Accordingly, plants showed enhanced resistance to the necrotrophic leaf pathogen Botrytis cinerea under high CO2, while resistance to the hemi-biotrophic leaf pathogen Pseudomonas syringae pv. tomato was reduced. The opposite was true for plants grown under low CO2. Disease severity caused by the soil-borne pathogens Fusarium oxysporum f.sp. raphani and Rhizoctonia solani was similar under all CO2 conditions tested. Collectively, our results stress the notion that atmospheric CO2 impacts the balance between SA- and JA-dependent defenses and concomitant resistance against foliar (hemi)biotrophic and necrotrophic pathogens. The direction of the CO2-mediated effects on SA- and JA-mediated defenses varies between reported studies, suggesting that the defense output is influenced by environmental context. These findings highlight that a wider dynamic range of climate change parameters should be studied simultaneously to harness plant traits for the development of future climate-resilient crops.


Climate change due to increasing CO2 levels in the Earth’s atmosphere may affect interactions between plants and their attackers resulting in significant effects on crop yields in agriculture. In order to secure food production for the increasing human population it is essential to anticipate on this development. Plants are exposed to a wide array of pathogenic microbes. It is only since one and a half centuries that microbes have been recognized as causal agents of plant diseases. Early pioneers in plant pathology, such as Johanna Westerdijk – who gave her inaugural address in 1917 at Utrecht University entitled “New directions in phytopathological research” (Westerdijk 1917) – laid the foundation of present-day plant pathology (Kerling et al. 1986). Nowadays, plant pathogens are typically distinguished by their infection strategy. Pathogens with a biotrophic lifestyle, like the oomycete pathogen Hyaloperonospora arabidopsidis, commonly feed on living host cells, whereas pathogens with a necrotrophic lifestyle, like the fungal pathogen Botrytis cinerea, derive nutrients from killed plant tissues (Glazebrook 2005). Many pathogens, for example the bacterial pathogen Pseudomonas syringae pv. tomato (Pst), have both a biotrophic and a subsequent necrotrophic infection stage and are thus referred to as hemi-biotrophs (Glazebrook 2005). To defend themselves against pathogenic invaders, plants have developed a sophisticated defense system that recognizes pathogen-associated molecules and subsequently activate downstream defense cascades. The mutually antagonistic phytohormones salicylic acid (SA) and jasmonic acid (JA) are crucial for the regulation of the plant immune signaling network (Pieterse et al. 2009), in which the SA pathway typically regulates defenses against biotrophic pathogens, whereas JA is effective against necrotrophic pathogens and insect herbivores.

Atmospheric CO2 concentration can induce changes in hormone levels in many plant species (Noctor and Mhamdi 2017). In general, SA, auxin, and gibberellin levels and signaling increase under elevated CO2 conditions, whereas ABA and JA levels and signaling decrease, but effects vary between studies and plant species (Arteca et al. 1980; Li et al. 2011a, b; Teng et al. 2006; Zavala et al. 2008; Mhamdi and Noctor 2016; Noctor and Mhamdi 2017; Zhou et al. 2017; Williams et al. 2018a). For example, suppression of JA-related signaling by high CO2 levels was associated with increased susceptibility of maize to Fusarium verticillioides (Vaughan et al. 2014) and of soybean to herbivores (Zavala et al. 2008, 2013). In tomato plants, elevated CO2 levels induced an increase in SA levels and concomitantly a decrease in JA signaling. This was associated with enhanced resistance against yellow leaf curl virus, tobacco mosaic virus and Pst, which are typically sensitive to SA-dependent defenses, and increased susceptibility to B. cinerea, which is sensitive to JA-dependent defenses (Huang et al. 2012; Zhang et al. 2015). In Arabidopsis thaliana (hereafter Arabidopsis), elevated CO2 similarly conferred enhanced resistance to the biotrophic pathogens H. arabidopsidis and Pst, but also to the necrotrophic fungi Plectosphaerella cucumerina and B. cinerea (Mhamdi and Noctor 2016; Williams et al. 2018a). In another study, the resistance to Pst in Arabidopsis was found to be reduced at high CO2 levels, while low CO2 levels increased the level of resistance against this pathogen (Zhou et al. 2017). This was correlated with enhanced pre-invasion, stomatal defenses and so far uncharacterized post-invasion defenses.

Most studies on the effects of different CO2 levels on plant diseases and pests have focused on foliar pathogens and herbivores (Braga et al. 2006; Guo et al. 2014; Jwa and Walling 2001; Li et al. 2015; Mhamdi and Noctor 2016; Williams et al. 2018a). Compared to the detailed knowledge generated for interactions between plants and leaf pathogens, relatively little is known about the interactions with soil-borne pathogens, both for necrotrophs (Okubara and Paulitz 2005) and hemi-biotrophs (Chen et al. 2014; Yadeta and Thomma 2013). The few studies on the effects of enhanced atmospheric CO2 levels on soil-borne diseases show ambiguous results. For example, the incidence of sheath blight in rice caused by the necrotrophic fungus Rhizoctonia solani was increased under elevated CO2 (Kobayashi et al. 2006). Similarly, disease incidence of Fusarium pseudograminearum was increased in wheat plants grown under elevated CO2 (Melloy et al. 2014). By contrast, the tolerance of tomato plants to infection by the hemi-biotroph Phytophthora parasitica increased at elevated CO2 (Jwa and Walling 2001). In other studies, elevated CO2 levels did not significantly influence disease incidence. In lettuce, disease caused by Fusarium oxysporum f.sp. lactucae was not affected by elevated atmospheric CO2 (Ferrocino et al. 2013), and in soybean elevated CO2 did not affect the severity of the sudden death syndrome caused by Fusarium virguliforme (Eastburn et al. 2010).

CO2 concentrations in soils with active microbial communities are 10–50 times higher than the atmospheric CO2 levels (Drigo et al. 2008). Thus, it is unlikely that the increase in atmospheric CO2 levels foreseen for the future have an effect on the CO2 concentration in the soil. Nonetheless, increases in atmospheric CO2 concentration can alter plant photosynthetic rate, stimulate plant growth, and lead to increased carbon allocation to the belowground plant tissue, resulting in changes in the release of organic compounds in the rhizosphere (Drigo et al. 2008, 2010). It has been postulated that the composition of these rhizodeposits plays an essential role in shaping the rhizosphere microbiome (Berendsen et al. 2012). Indeed, Williams et al. (2018b) showed a profound effect of the interaction between atmospheric CO2 and soil nutritional status on the impact of beneficial rhizobacteria on plant growth and induced systemic resistance. Changes in atmospheric CO2 levels may affect the richness, composition and structure of soil microbial communities through changes in carbon allocation and root exudation (Drigo et al. 2009), which in turn can affect the impact of the root microbiome on plant performance (Bakker et al. 2018). Such effects may also influence growth and virulence of soil-borne plant pathogens.

In this study, we examined the effect of pre-industrial, current, and future levels of CO2 in the atmosphere on resistance of Arabidopsis to the foliar pathogens Pst and B. cinerea, and to the soil-borne pathogens F. oxysporum f.sp. raphani and R. solani. Pst and F. oxysporum are considered as hemi-biotrophic pathogens (Glazebrook 2005; Kidd et al. 2011; Ma et al. 2013), while B. cinerea and R. solani are nectrotrophic pathogens that cause severe damage on a wide range of host plants (Foley et al. 2013; Van Kan 2006). We observed contrasting effects of high and low CO2 levels on SA- and JA-dependent defense responses in Arabidopsis leaves and associated resistances against the hemi-biotrophic and necrotrophic leaf pathogens. This is partly in line with previous findings (Mhamdi and Noctor 2016; Williams et al. 2018a), showing shifts in the expression of SA- and JA-dependent defenses. This points to the notion that other environmental factors may influence the defense output of a plant and that effects of climate change on plant immunity should be studied by taking into account a more dynamic range of environmental parameters. This is in line with what the first Dutch female professor Johanna Westerdijk already stressed during her inaugural address at Utrecht University (Westerdijk 1917): it is important to study the physiology of both host and parasite in their environmental context (Kerling et al. 1986).

Material and methods

Plant material and cultivation

Seeds of Arabidopsis thaliana accession Col-0 and mutant line ein2–1 (Alonso et al. 1999) were sown on sand under ambient CO2 conditions (450 ppm). Two weeks later, seedlings were transferred to 60-ml pots containing a sand/potting soil mixture (v/v, 5:12) that was autoclaved twice for 20 min, after which they were transferred to a growth chamber with continuous high (800 ppm), ambient (450 ppm) or low (150 ppm) atmospheric CO2 conditions as described (Zhou et al. 2017). Plants were cultivated with a 10-h day at 20 °C and 14-h night at 18 °C cycle (350 μmol/m2/s) with 70% relative humidity for 4 weeks. The technical specifications of the growth chambers used in this study have been described in detail by Temme et al. (2015).

RT-qPCR analysis

For gene expression analysis, total RNA was isolated as described (Oñate-Sánchez and Vicente-Carbajosa 2008). RNA was pretreated with DNAse I (Fermentas, St. Leon-Rot, Germany) and RevertAid H minus Reverse Transcriptase (Fermentas) was used to convert DNA-free RNA into cDNA using an oligo-dT primer. PCR reactions were performed in optical 384-well plates (Applied Biosystem) with a ViiA 7 realtime PCR system (Applied Biosystems, Carlsbad, CA, USA), using SYBR® Green to monitor the synthesis of double-stranded DNA. Transcript levels were calculated relative to the constitutively expressed reference gene PP2A-A3 (At1g13320), encoding the protein phosphatase 2A subunit A3, as described previously (Schmittgen and Livak 2008). Primers used for RT-qPCR were as follows. At1g13320 _F, 5′-TAA CGT GGC CAA AAT GAT GC-3′; At1g13320_R, 5′-GTT CTC CAC AAC CGC TTG GT-3′. PDF1.2_F, 5’-CAC CCT TAT CTT CGC TGC TCT T-3′; PDF1.2_R, 5’-GCC GGT GCG TCG AAA G-3′. PR1_F, 5’-CTC GGA GCT ACG CAG AAC AAC T-3′; PR1_R, 5’-TTC TCG CTA ACC CAC ATG TTC A-3′. FRK1_F, 5′- TTT CAA CAG TTG TCG CTG GA-3′; FRK1_R, 5’-AGC TTG CAA TAG CAG GTT GG-3′. ICS1_F, 5′- GGC AGG GAG ACT TAC G-3′; ICS1_R, 5′-AGG TCC CGC ATA CAT T-3′.

B. cinerea bioassay

Botrytis cinerea cultivation and disease resistance bioassays were performed essentially as described previously (Van Wees et al. 2013). B. cinerea strain B05.10 (Van Kan et al. 1997) was cultivated on half-strength potato dextrose agar (PDA) plates for 10 days at 22 °C. B. cinerea spores were collected and resuspended in half-strength potato dextrose broth to a final density of 5 × 105 spores/ml. Four-week-old plants were inoculated by applying 10-μl droplets to six leaves per plant. Symptoms were scored 4 days later. Disease severity was expressed as the percentage of leaves showing symptoms in the following three classes of disease severity: restricted lesion (<2 mm; class I), spreading lesion (>2 mm; class II), and spreading lesion with accompanying sporulation (class III).

P. syringae bioassay

Pseudomonas syringae pv. tomato DC3000 (Pst; Whalen et al. 1991) was cultured at 28 °C on King’s medium B (King et al. 1954) agar plates supplemented with 50 μg/ml rifampicin. Bacteria were transferred and cultivated overnight in liquid KB medium at 28 °C in an orbital shaker at 220 rpm. Subsequently, bacteria were collected by centrifugation for 10 min at 14,500 g and resuspended in 10 mM MgSO4. The suspension was adjusted to OD600 = 1.0 (= 109 cfu/ml). For dip inoculation, the bacterial inoculum was diluted to a final density of 5 × 107 cfu/ml of 10 mM MgSO4 containing 0.015% (v/v) Silwet L-77 (Van Meeuwen Chemicals, Weesp, Netherlands). For disease assessment, leaf discs from treated plants were harvested, surface sterilized in 70% ethanol for 8 s, and subsequently washed with water. Eight biological replicates were included for each data point. Each leaf disc was ground thoroughly in 200 μl of 10 mM MgSO4 and 10 μl aliquots of different dilutions were plated onto KB plates containing 25 μg/ml rifampicin. After 48 h incubation at room temperature, bacterial colonies were counted and the growth of Pst was calculated.

R. solani bioassay

Rhizoctonia solani isolate AG2-2IIIB (Chapelle et al. 2016; Mendes et al. 2011) was grown on half-strength PDA at room temperature for 1 week. The PDA plates were chopped up and blended into a sand/potting soil mixture (0.5 Petri dish/kg soil). Two-week-old Arabidopsis seedlings were transferred to the R. solani-inoculated soil/sand mixture and from then on, the plants were cultivated in the growth rooms under the three different CO2 conditions. For the R. solani disease assessment, at least thirty plants were tested under each CO2 condition at 3 weeks after inoculation. Chlorotic symptoms, stunted growth and death of the plant was recorded as “diseased”. Additionally, fresh weight of the aboveground plant parts was determined.

F. oxysporum bioassay

Fusarium oxysporum f. sp. raphani strain WCS600 causes fusarium wilt disease in Arabidopsis (Pieterse et al. 1996). Before use, the fungus was cultivated on half-strength PDA at 28 °C for 3 days. The inoculum was prepared by transferring two PDA plugs to sucrose sodium nitrate liquid medium (Sinha and Wood 1968) and culturing while shaking for 3 days at 28 °C. Subsequently the culture was filtered over sterile glasswool to remove mycelium fragments and the suspension was adjusted to 107 conidia/ml sterile distilled water. Roots of two-week-old seedlings that were grown in sand were dipped in the conidial suspension. The seedlings were then transferred to soil mixed with sand (12:5) and grown under the three different CO2 conditions.

For the F. oxysporum f. sp. raphani disease assessment, twenty plants per CO2 treatment were analyzed and 3 weeks after inoculation disease symptoms were scored by determining the percentage of plants with Fusarium wilt symptoms in the leaves. The disease index (DI) was calculated from the percentage of leaves in four different disease severity classes as described (Van Wees et al. 1997). Class I. no symptoms; Class II. 1–2 wilted leaves; Class III. 3–5 wilted leaves; Class IV. >6 wilted leaves/dead plants. The aboveground plant parts were harvested and fresh weight was recorded. Relative growth (RG) was calculated as the weight of infected plants/the weight of control plants.

Three weeks after F. oxysporum inoculation, the aboveground plant parts were harvested. Per plant, 100–200 mg of leaf material was ground in 1 ml of 10 mM MgSO4. A dilution series of this suspension was made and 100 μl of each dilution (0, 10 and 100 times diluted) was plated in duplicate on Fusarium selective Komada medium (Komada 1975). Komada plates were incubated at 28 °C for 3–4 days. The numbers of colonies were counted to assess the population density of F. oxysporum in each plant. This experiment was repeated twice, with at least 12 biological replicates for each CO2 treatment.


Atmospheric CO2 affects JA- and SA-dependent gene expression in Arabidopsis

To investigate whether the activity of the JA or SA pathways is altered under different atmospheric CO2 conditions in Arabidopsis plants, we analyzed the expression of genes that are responsive to these two hormones in plants that had grown at three atmospheric CO2 concentrations. Two-week-old seedlings that had been cultivated at ambient CO2 were subsequently transferred to low (150 ppm), ambient (450 ppm), and high (800 ppm) CO2 conditions and gene expression was analyzed when plants were 4 weeks old. Previous studies identified PDF1.2 as a marker gene for JA-dependent defenses (Penninckx et al. 1996) and PR1, FLG22-INDUCED RECEPTOR-LIKE KINASE1 (FRK1), and ISOCHORISMATE SYNTHASE1 (ICS1) as marker genes for SA-dependent defenses (Asai et al. 2002; Wildermuth et al. 2001; Zhang et al. 1999). Analysis of the expression of these JA- and SA-responsive marker genes revealed that the various atmospheric CO2 concentrations differentially affected their basal expression levels (Fig. 1a–d). More specifically, expression of PDF1.2 was significantly higher in plants grown under the high atmospheric CO2 condition and reduced under the low CO2 conditions (Fig. 1a). Oppositely, the FRK1 gene was higher expressed at low atmospheric CO2 levels (Fig. 1c) and ICS1 expression was reduced under the high CO2 condition (Fig. 1d).

Fig. 1

RT-qPCR analysis of PDF1.2 (a), PR1 (b), FRK1 (c), and ICS1 (d) gene expression in 4-week-old Arabidopsis Col-0 plants grown under high (800 ppm), ambient (450 ppm) and low (150 ppm) levels of atmospheric CO2. Indicated are the expression levels relative to the reference gene PP2A-A3 (At1g13320). Different letters indicate significant differences between CO2 treatments (one-way ANOVA, Duncan’s multiple range test, P < 0.05). Error bars represent SD, n = 3 plants. Experiments were repeated with similar results

Atmospheric CO2 alters Arabidopsis resistance to the foliar pathogens B. cinerea and Pst

In order to investigate whether differences in atmospheric CO2 levels affect resistance to a foliar necrotrophic pathogen, we tested the resistance of Arabidopsis plants to B. cinerea at three atmospheric CO2 levels. Four days after inoculation, leaves of plants grown at high CO2 developed fewer spreading lesions, whereas at low CO2 significantly more spreading lesions developed (Fig. 2a and b). Thus, with increasing atmospheric CO2 levels the resistance of Arabidopsis plants to B. cinerea also increased.

Fig. 2

a Quantification of B. cinerea disease symptoms on leaves of Arabidopsis Col-0 plants grown under three atmospheric CO2 conditions. Disease severity of the inoculated leaves was scored in three classes at 4 days after inoculation. Percentage of leaves in each class was calculated per plant. Indicated above the brackets are the P values of comparisons between different atmospheric CO2 conditions (Χ2-test; n = 9 plants). b Representative leaves showing disease symptoms of plants grown under the three CO2 conditions 4 days after inoculation with B. cinerea. c The bacterial titers of Pst in leaves of Arabidopsis plants grown under the three atmospheric CO2 conditions. Bacterial population densities were determined at 5 days after inoculation. Indicated is the average of the log10-transformed bacterial titer per leaf area. Different letters indicate significant differences between CO2 treatments (one-way ANOVA, Fisher’s LSD test, P < 0.05). Error bars represent SD, n = 8 plants. Experiments were repeated with similar results

We also tested the resistance of Arabidopsis plants to the hemi-biotrophic leaf pathogen Pst at the different atmospheric CO2 levels. At 5 days after inoculation, the bacterial titer of Pst was significantly higher in high CO2-grown plants and significantly lower in low CO2-grown plants compared with bacterial densities in the ambient CO2-grown plants (Fig. 2c), confirming previously reported results (Zhou et al. 2017), showing that opposite to the increasing resistance level to B. cinerea, Pst resistance decreases at increasing CO2 levels under the conditions used in our experimental setup.

Atmospheric CO2 does not affect disease resistance against the soil-borne pathogens R. solani and F. oxysporum

To study effects of different atmospheric CO2 levels on the interaction between Arabidopsis and the necrotrophic soil-borne pathogen R. solani, two-week-old seedlings, grown at ambient CO2, were transplanted into R. solani-inoculated soil and subsequently grown for 3 weeks at the three different atmospheric CO2 conditions. Under ambient CO2 conditions the percentage of diseased plants was nearly 50% and neither high nor low CO2 conditions affected the disease incidence (Fig. 3a). R. solani infection significantly reduced shoot fresh weight of Arabidopsis plants, but also for this parameter no significant differences between high, ambient and low CO2 levels were observed (Fig. 3b). These results show that varying atmospheric CO2 conditions from 150 ppm to 800 ppm has no significant impact on the disease severity caused by R. solani infection of Arabidopsis.

Fig. 3

Effect of atmospheric CO2 conditions on disease caused by the soil-borne pathogens R. solani and F. oxysporum in Arabidopsis grown under high (800 ppm), ambient (450 ppm), or low (150 ppm) CO2 conditions.a Disease incidence at 24 days after transplantation of Arabidopsis accession Col-0 seedlings to soil mixed with R. solani inoculum. Chlorotic, stunted or dead plants were considered as diseased. b Inhibition of plant growth by R. solani. At 24 days after inoculation, the aboveground plant parts were harvested and fresh weight was recorded. The weight of R. solani-infected plants relative to non-inoculated control plants is depicted. c The density of F. oxysporum in leaves of Arabidopsis. Arabidopsis accession Col-0 seedlings were inoculated with F. oxysporum by root dipping and grown in soil. Arabidopsis leaves were harvested 3 weeks later. The density of F. oxysporum was determined by dilution plating on Komada agar medium. Statistical analysis was performed using one-way ANOVA (Duncan’s multiple range test), treatments did not differ significantly. Error bars represent SD, n = 6 replicated blocks, existing of 9 plants per block for R. solani bioassays, and n = 12 plants for F. oxysporum bioassays. Experiments were repeated with similar results

We also investigated effects of atmospheric CO2 on the performance of Arabidopsis plants inoculated with the hemi-biotrophic soil-borne pathogen F. oxysporum. Two-week-old seedlings were inoculated by root dipping in a conidial suspension of F. oxysporum f.sp. raphani, and transferred to high, ambient, or low CO2 conditions. Disease symptoms were scored 3 weeks after inoculation. Throughout the course of the study, the disease severity caused by F. oxysporum infection in Arabidopsis Col-0 plants varied among experiments, and the different atmospheric CO2 levels had inconsistent effects on disease caused by F. oxysporum among the five independent experiments that were performed (Table 1). For example, in experiment 2, plants grown at either high or low CO2 levels both showed a significantly lower disease index than the plant grown at ambient CO2 levels, whereas in experiment 3, the disease index was significantly lower under the high CO2 and higher under the low CO2 condition than under ambient CO2 conditions, while in experiment 4 no significant effects were observed at all (Table 1). Since the disease development in these experiments was relatively low, we investigated if atmospheric CO2 might affect disease in a more susceptible Arabidopsis line. Mutations that disrupt the ethylene signaling pathway increase plant susceptibility to F. oxysporum (Berrocal-Lobo and Molina 2004; Pantelides et al. 2013) and therefore, we included a mutant impaired in ethylene responsiveness (ein2–1) in the experiments. Indeed, in four out of the five experiments, the ein2–1 mutant exhibited a higher disease index (Table 1, experiment 1, 2, 3, and 5). However, also in ein2–1 the different atmospheric CO2 levels did not influence the disease severity consistently (Table 1). In addition to disease symptoms, the effect of F. oxysporum infection on the growth of Arabidopsis was determined. The shoot fresh weight of infected plants relative to non-infected control plants was calculated. The effects of CO2 levels were again not consistent when comparing the five independent experiments that were performed (Table 2).

Table 1 Disease index (DI) of Arabidopsis wild-type Col-0 plants and a mutant defective in ethylene signaling (ein2–1) 3 weeks after root inoculation with F. oxysporum and grown under high (800 ppm), ambient (450 ppm), or low (150 ppm) CO2 conditions in five independent experiments
Table 2 Growth of F. oxysporum-inoculated Arabidopsis wild-type Col-0 plants and a mutant defective in ethylene signaling (ein2–1) relative to non-inoculated plants under high (800 ppm), ambient (450 ppm), or low (150 ppm) CO2 conditions in five independent experiments

Finally, the colonization of Arabidopsis shoots by F. oxysporum was determined under the different CO2 conditions at 3 weeks after inoculation of the roots. As shown in Fig. 3c, fungal titer in the leaves was not affected by the atmospheric CO2 conditions under which the plants were grown. Overall, the results on the three parameters suggest that there is no significant impact of atmospheric CO2 levels on the interaction between Arabidopsis and the soil-borne pathogen F. oxysporum.


Various climate change models predict elevation of atmospheric CO2 levels in the future and this has boosted research on plant-pathogen interactions under high atmospheric CO2 conditions (Chakraborty and Datta 2003; Huang et al. 2012; Lake and Wade 2009; Pangga et al. 2011; Zhang et al. 2015; Noctor and Mhamdi 2017; Velásquez et al. 2018; Williams et al. 2018a). It has been shown that altered atmospheric CO2 levels have only a limited direct influence on the overall growth of plant-associated microbes, including pathogenic ones (Drigo et al. 2008; Wells 1974). Nevertheless, altered levels of atmospheric CO2 are likely to affect infection by plant pathogens through interference with host plant defense responses. Metabolic and transcriptional analyses of plants grown under ambient and high CO2 conditions revealed distinct alterations in different hormone signaling pathways in different plant species (Casteel et al. 2008; Matros et al. 2006; Teng et al. 2006; Mhamdi and Noctor 2016; Williams et al. 2018a). Plants grown under high CO2 are slow in photorespiration, but are induced in defense, which may be related to enhancement of reactive oxygen species (ROS) signaling (Noctor and Mhamdi 2017). High CO2 can affect disease resistance to foliar pathogens. In both tomato and Arabidopsis plants this was shown to be associated with altered activation of SA- and JA-dependent defense pathways, resulting in reduced resistance against the (hemi)biotrophs Pst and H. arabidopsidis, and enhanced resistance against the necrotrophs B. cinerea and P. cucumerina (Zhang et al. 2015; Mhamdi and Noctor 2016; Williams et al. 2018a).

Under our experimental conditions, we also see contrasting effects of the level of CO2 on SA- and JA-dependent defenses and biotroph and necrotroph resistance, respectively, but these effects are partly opposite from the effects observed in some other studies (Mhamdi and Noctor 2016; Williams et al. 2018a). Hence, the effect of different CO2 levels on disease resistance may be dependent on the environmental context. Under our experimental conditions, we found a generally enhanced expression of SA-responsive genes in Arabidopsis plants grown under low atmospheric CO2 conditions, in comparison to plants grown under high CO2 conditions (Fig. 1). These results match with the observed enhanced resistance against the hemi-biotroph Pst under low CO2 and the reduced resistance under high CO2 conditions (Fig. 2c). Previously, we showed that the effects of atmospheric CO2 likely impact both pre- and post-invasive immune responses to Pst infection (Zhou et al. 2017). The recorded changes in the level of SA-responsive gene expression as shown in Fig. 1 are in line with these observations and suggest that altered intensities of SA-dependent defenses under low and high CO2 may contribute to the observed differences in Pst resistance. However, our observations contrast those reported by Mhamdi and Noctor (2016), who found that high CO2 (1000 and 3000 ppm) stimulated SA responses and Pst resistance in Arabidopsis, rather than reducing it. These contrasting outcomes are not unrealistic, because antagonism between the SA and the JA defense pathways is known to be dependent on the environmental context (Pieterse et al. 2012). Whether differences in environmental parameters, such as day length (10-h short day versus 16-h long day), and light intensity (350 versus 200 μM/m2/s) have influenced the defense outputs in both studies is not known. Notwithstanding, both studies show that different levels of CO2 antagonistically impact the outcome of plant defenses against pathogens with contrasting infection strategies.

The expression of the JA-responsive marker gene PDF1.2 was significantly enhanced under the high atmospheric CO2 condition and reduced under the low CO2 condition used in our study (Fig. 1a), suggesting that increasing atmospheric CO2 levels stimulated the JA response pathway in Arabidopsis plants. This is in line with the enhanced resistance to the necrotrophic leaf pathogen B. cinerea in high CO2-grown plants and the reduced resistance to this pathogen in low CO2-grown plants (Fig. 2a and b). Similar results have been reported by Williams et al. (2018a) who found elevated levels of the JA marker gene VSP2 and increased resistance to the necrotrophic fungus P. cucumerina. In contrast, other studies with Arabidopsis, tomato and soybean showed that elevated CO2 levels induced the SA signaling pathway and concomitantly repressed the JA signaling pathway, leading to enhanced resistance to (hemi)biotrophs and increased susceptibility to diverse necrotrophic pathogens and herbivores (Huang et al. 2012; Zavala et al. 2008; Zhang et al. 2015; Mhamdi and Noctor 2016). As mentioned above, these differential effects of altered atmospheric CO2 levels on hormonal signaling between the studies might be attributed to the plant species examined, concentration and duration of CO2 treatments, or differences in other environmental conditions that may have shifted the balance between SA- and JA-dependent defenses in contrasting directions. Nevertheless, these studies highlight that changes in the level of atmospheric CO2 can differentially affect the level of resistance against plant pathogens with contrasting infection strategies.

Additionally, we studied to what extent atmospheric CO2 levels affect the disease severity caused by soil-borne pathogens with different infection strategies. Previous studies on the influence of CO2 levels on disease caused by the necrotroph R. solani showed that elevated CO2 concentrations reduced the disease in radish and sugar beet seedlings (Papavizas and Davey 1962), but in rice the disease incidence of R. solani was increased (Kobayashi et al. 2006). In our study with Arabidopsis, we observed no effect of different levels of atmospheric CO2 on the level of disease caused by R. solani (Fig. 3a and b). Atmospheric CO2 levels also did not consistently affect development of disease caused by the hemi-biotrophic pathogen F. oxysporum f.sp. raphani (Fig. 3c; Tables 1 and 2). This was not only observed for the moderately susceptible wild-type accession line Col-0, but also for the more susceptible ein2–1 mutant. In lettuce, elevated CO2 also did not influence the disease severity caused by F. oxysporum (Ferrocino et al. 2013). But in rice, wheat, and maize elevated CO2 caused an increased in the susceptibility to Fusarium (Kobayashi et al. 2006; Melloy et al. 2014; Vaughan et al. 2014). Hence, it appears that atmospheric CO2 can affect soil-borne diseases, but the effects depend on the host-pathogen system and environmental context.

In summary, our study confirms that alterations in atmospheric CO2 levels differentially affect SA and JA defense-related pathways, resulting in contrasting effects on pathogens with a (hemi)biotrophic and necrotrophic lifestyle. The study-dependent outcome of the defense outputs suggests that the environmental context is likely to be decisive in the CO2-mediated shift in the balance between SA- and JA-dependent defenses and concomitant effects on resistance to biotrophic and necrotrophic pathogens. We found no significant effects of high and low CO2 on the level of disease caused by the soil-borne pathogens R. solani and F. oxysporum. Like in most other studies, we only varied the level of CO2 to monitor the effect of this climate change parameter on disease resistance. However, during the anticipated global environmental changes, disease resistance will also be influenced by other parameters, such as elevated O3, humidity, drought, and increased temperature (Eastburn et al. 2011; Velásquez et al. 2018). Hence, to fully understand the consequences of climate change for the outcome of above- and below-ground plant-pathogen interactions, future research should capture a wider dynamic range of environmental conditions in order to identify plant traits that allow for the development of future climate-resilient crops.


  1. Alonso, J. M., Hirayama, T., Roman, G., Nourizadeh, S., & Ecker, J. R. (1999). EIN2, a bifunctional transducer of ethylene and stress responses in Arabidopsis. Science, 284, 2148–2152.

    Article  CAS  PubMed  Google Scholar 

  2. Arteca, R. N., Poovaiah, B., & Smith, O. E. (1980). Use of high performance liquid chromatography for the determination of endogenous hormone levels in Solanum tuberosum L. subjected to carbon dioxide enrichment of the root zone. Plant Physiology, 65, 1216–1219.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Asai, T., Tena, G., Plotnikova, J., Willman, M. R., Chiu, W. L., Gomez-Gomez, L., Boller, T., Ausubel, F. M., & Sheen, J. (2002). MAP kinase signalling cascade in Arabidopsis innate immunity. Nature, 415, 977–983.

    Article  CAS  PubMed  Google Scholar 

  4. Bakker, P. A. H. M., Pieterse, C. M. J., De Jonge, R., & Berendsen, R. L. (2018). The soil-borne legacy. Cell, 172, 1178–1180.

    Article  CAS  PubMed  Google Scholar 

  5. Berendsen, R. L., Pieterse, C. M. J., & Bakker, P. A. H. M. (2012). The rhizosphere microbiome and plant health. Trends in Plant Science, 17, 478–486.

    Article  CAS  PubMed  Google Scholar 

  6. Berrocal-Lobo, M., & Molina, A. (2004). Ethylene response factor 1 mediates Arabidopsis resistance to the soilborne fungus Fusarium oxysporum. Molecular Plant-Microbe Interactions, 17, 763–770.

    Article  CAS  PubMed  Google Scholar 

  7. Braga, M. R., Aidar, M. P., Marabesi, M. A., & De Godoy, J. R. (2006). Effects of elevated CO2 on the phytoalexin production of two soybean cultivars differing in the resistance to stem canker disease. Environmental and Experimental Botany, 58, 85–92.

    Article  CAS  Google Scholar 

  8. Casteel, C. L., O'Neill, B. F., Zavala, J. A., Bilgin, D. D., Berenbaum, M. R., & Delucia, E. (2008). Transcriptional profiling reveals elevated CO2 and elevated O3 alter resistance of soybean (Glycine max) to Japanese beetles (Popillia japonica). Plant, Cell & Environment, 31, 419–434.

    Article  CAS  Google Scholar 

  9. Chakraborty, S., & Datta, S. (2003). How will plant pathogens adapt to host plant resistance at elevated CO2 under a changing climate? New Phytologist, 159, 733–742.

    Article  CAS  Google Scholar 

  10. Chapelle, E., Mendes, R., Bakker, P. A. H. M., & Raaijmakers, J. M. (2016). Fungal invasion of the rhizosphere microbiome. ISME Journal, 10, 265–268.

    Article  CAS  PubMed  Google Scholar 

  11. Chen, Y. C., Kidd, B. N., Carvalhais, L. C., & Schenk, P. M. (2014). Molecular defense responses in roots and the rhizosphere against Fusarium oxysporum. Plant Signaling & Behavior, 9(12), e977710.

    Article  CAS  Google Scholar 

  12. Drigo, B., Kowalchuk, G. A., & Van Veen, J. A. (2008). Climate change goes underground: effects of elevated atmospheric CO2 on microbial community structure and activities in the rhizosphere. Biology and Fertility of Soils, 44, 667–679.

    Article  Google Scholar 

  13. Drigo, B., Van Veen, J. A., & Kowalchuk, G. A. (2009). Specific rhizosphere bacterial and fungal groups respond differently to elevated atmospheric CO2. ISME Journal, 3, 1204–1217.

    Article  CAS  PubMed  Google Scholar 

  14. Drigo, B., Pijl, A. S., Duyts, H., Kielak, A. M., Gamper, H. A., Houtekamer, M. J., Boschker, H. T., Bodelier, P. L., Whiteley, A. S., & Van Veen, J. A. (2010). Shifting carbon flow from roots into associated microbial communities in response to elevated atmospheric CO2. Proceedings of the National Academy of Sciences of the United States of America, 107, 10938–10942.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Eastburn, D. M., Degennaro, M. M., Delucia, E. H., Dermody, O., & McElrone, A. J. (2010). Elevated atmospheric carbon dioxide and ozone alter soybean diseases at SoyFACE. Global Change Biology, 16, 320–330.

    Article  Google Scholar 

  16. Eastburn, D. M., McElrone, A. J., & Bilgin, D. D. (2011). Influence of atmospheric and climatic change on plant–pathogen interactions. Plant Pathology, 60, 54–69.

    Article  Google Scholar 

  17. Ferrocino, I., Chitarra, W., Pugliese, M., Gilardi, G., Gullino, M. L., & Garibaldi, A. (2013). Effect of elevated atmospheric CO2 and temperature on disease severity of Fusarium oxysporum f. sp. lactucae on lettuce plants. Applied Soil Ecology, 72, 1–6.

    Article  Google Scholar 

  18. Foley, R. C., Gleason, C. A., Anderson, J. P., Hamann, T., & Singh, K. B. (2013). Genetic and genomic analysis of Rhizoctonia solani interactions with Arabidopsis; evidence of resistance mediated through NADPH oxidases. PLoS One, 8, e56814.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Glazebrook, J. (2005). Contrasting mechanisms of defense against biotrophic and necrotrophic pathogens. Annual Review of Phytopathology, 43, 205–227.

    Article  CAS  PubMed  Google Scholar 

  20. Guo, H., Sun, Y., Li, Y., Liu, X., Zhang, W., & Ge, F. (2014). Elevated CO2 decreases the response of the ethylene signaling pathway in Medicago truncatula and increases the abundance of the pea aphid. New Phytologist, 201, 279–291.

    Article  CAS  PubMed  Google Scholar 

  21. Huang, L., Ren, Q., Sun, Y., Ye, L., Cao, H., & Ge, F. (2012). Lower incidence and severity of tomato virus in elevated CO2 is accompanied by modulated plant induced defence in tomato. Plant Biology, 14, 905–913.

    Article  CAS  PubMed  Google Scholar 

  22. Jwa, N.-S., & Walling, L. L. (2001). Influence of elevated CO2 concentration on disease development in tomato. New Phytologist, 149, 509–518.

    Article  CAS  Google Scholar 

  23. Kerling, L. C. P., Ten Houten, J. G., & De Bruin-Brink, G. (1986). Johanna Westerdijk: pioneer leader in plant pathology. Annual Review of Phytopathology, 24, 33–41.

    Article  CAS  PubMed  Google Scholar 

  24. Kidd, B. N., Kadoo, N. Y., Dombrecht, B., Tekeoglu, M., Gardiner, D. M., Thatcher, L. F., Aitken, E. A., Schenk, P. M., Manners, J. M., & Kazan, K. (2011). Auxin signaling and transport promote susceptibility to the root-infecting fungal pathogen Fusarium oxysporum in Arabidopsis. Molecular Plant-Microbe Interactions, 24, 733–748.

    Article  CAS  PubMed  Google Scholar 

  25. King, E. O., Ward, M. K., & Raney, D. E. (1954). Two simple media for the demonstration of pyocyanin and fluorescin. Journal of Laboratory and Clinical Medicine, 44, 301–307.

    CAS  PubMed  Google Scholar 

  26. Kobayashi, T., Ishiguro, K., Nakajima, T., Kim, H., Okada, M., & Kobayashi, K. (2006). Effects of elevated atmospheric CO2 concentration on the infection of rice blast and sheath blight. Phytopathology, 96, 425–431.

    Article  CAS  PubMed  Google Scholar 

  27. Komada, H. (1975). Development of a selective medium for quantitative isolation of Fusarium oxysporum from natural soil. Review of Plant Protection Research, 8, 114–124.

    Google Scholar 

  28. Lake, J. A., & Wade, R. N. (2009). Plant–pathogen interactions and elevated CO2: morphological changes in favour of pathogens. Journal of Experimental Botany, 60, 3123–3131.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. Li, X., Zhang, L., Li, Y., Ma, L., Chen, Q., Wang, L., & He, X. (2011a). Effects of elevated carbon dioxide and/or ozone on endogenous plant hormones in the leaves of Ginkgo biloba. Acta Physiologiae Plantarum, 33, 129–136.

    Article  CAS  Google Scholar 

  30. Li, X., Zhang, L., Ma, L., & Li, Y. (2011b). Elevated carbon dioxide and/or ozone concentrations induce hormonal changes in Pinus tabulaeformis. Journal of Chemical Ecology, 37, 779–784.

    Article  CAS  PubMed  Google Scholar 

  31. Li, X., Sun, Z., Shao, S., Zhang, S., Ahammed, G. J., Zhang, G., Jiang, Y., Zhou, J., Xia, X., Zhou, Y., Yu, J., & Shi, K. (2015). Tomato–Pseudomonas syringae interactions under elevated CO2 concentration: the role of stomata. Journal of Experimental Botany, 66, 307–316.

    Article  CAS  PubMed  Google Scholar 

  32. Ma, L. J., Geiser, D. M., Proctor, R. H., Rooney, A. P., O'Donnell, K., Trail, F., Gardiner, D. M., Manners, J. M., & Kazan, K. (2013). Fusarium pathogenomics. Annual Review of Microbiology, 67, 399–416.

    Article  CAS  PubMed  Google Scholar 

  33. Matros, A., Amme, S., Kettig, B., Buck-Sorlin, G. H., Sonnewald, U., & Mock, H.-P. (2006). Growth at elevated CO2 concentrations leads to modified profiles of secondary metabolites in tobacco cv. SamsunNN and to increased resistance against infection with potato virus Y. Plant, Cell & Environment, 29, 126–137.

    Article  CAS  Google Scholar 

  34. Melloy, P., Aitken, E., Luck, J., Chakraborty, S., & Obanor, F. (2014). The influence of increasing temperature and CO2 on Fusarium crown rot susceptibility of wheat genotypes at key growth stages. European Journal of Plant Pathology, 140, 19–37.

    Article  CAS  Google Scholar 

  35. Mendes, R., Kruijt, M., De Bruijn, I., Dekkers, E., Van der Voort, M., Schneider, J. H. M., Piceno, Y. M., DeSantis, T. Z., Andersen, G. L., Bakker, P. A. H. M., & Raaijmakers, J. M. (2011). Deciphering the rhizosphere microbiome for disease-suppressive bacteria. Science, 332, 1097–1100.

    Article  CAS  Google Scholar 

  36. Mhamdi, A., & Noctor, G. (2016). High CO2 primes plant biotic stress defences through redox-lined pathways. Plant Physiology, 172, 929–942.

    CAS  PubMed  PubMed Central  Google Scholar 

  37. Noctor, G., & Mhamdi, A. (2017). Climate change, CO2, and defense: the metabolic, redox, and signaling perspectives. Trends in Plant Science, 22, 857–870.

    Article  CAS  PubMed  Google Scholar 

  38. Okubara, P. A., & Paulitz, T. C. (2005). Root defense responses to fungal pathogens: a molecular perspective. Plant and Soil, 274, 215–226.

    Article  CAS  Google Scholar 

  39. Oñate-Sánchez, L., & Vicente-Carbajosa, J. (2008). DNA-free RNA isolation protocols for Arabidopsis thaliana, including seeds and siliques. BMC Research Notes, 1, 93.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. Pangga, I. B., Hanan, J., & Chakraborty, S. (2011). Pathogen dynamics in a crop canopy and their evolution under changing climate. Plant Pathology, 60, 70–81.

    Article  Google Scholar 

  41. Pantelides, I., Tjamos, S., Pappa, S., Kargakis, M., & Paplomatas, E. (2013). The ethylene receptor ETR1 is required for Fusarium oxysporum pathogenicity. Plant Pathology, 62, 1302–1309.

    Article  CAS  Google Scholar 

  42. Papavizas, G., & Davey, C. (1962). Activity of rhizoctonia in soil as affected by carbon dioxide. Phytopathology, 52, 759–766.

    CAS  Google Scholar 

  43. Penninckx, I. A. M. A., Eggermont, K., Terras, F. R. G., Thomma, B. P. H. J., De Samblanx, G. W., Buchala, A., Metraux, J. P., Manners, J. M., & Broekaert, W. F. (1996). Pathogen-induced systemic activation of a plant defensin gene in Arabidopsis folows a salicylic acid-independent pathway. The Plant Cell, 8, 2309–2323.

    CAS  PubMed  PubMed Central  Google Scholar 

  44. Pieterse, C. M. J., Van Wees, S. C. M., Hoffland, E., Van Pelt, J. A., & Van Loon, L. C. (1996). Systemic resistance in Arabidopsis induced by biocontrol bacteria is independent of salicylic acid accumulation and pathogenesis-related gene expression. The Plant Cell, 8, 1225–1237.

    CAS  PubMed  PubMed Central  Google Scholar 

  45. Pieterse, C. M. J., Leon-Reyes, A., Van der Ent, S., & Van Wees, S. C. M. (2009). Networking by small-molecule hormones in plant immunity. Nature Chemical Biology, 5, 308–316.

    Article  CAS  PubMed  Google Scholar 

  46. Pieterse, C. M. J., Van der Does, D., Zamioudis, C., Leon-Reyes, A., & Van Wees, S. C. M. (2012). Hormonal modulation of plant immunity. Annual Review of Cell and Developmental Biology, 28, 489–521.

    Article  CAS  PubMed  Google Scholar 

  47. Schmittgen, T. D., & Livak, K. J. (2008). Analyzing real-time PCR data by the comparative CT method. Nature Protocols, 3, 1101–1108.

    Article  CAS  PubMed  Google Scholar 

  48. Sinha, A., & Wood, R. (1968). Studies on the nature of resistance in tomato plants to Verticillium albo-atrum. Annals of Applied Biology, 62, 319–327.

    Article  Google Scholar 

  49. Temme, A. A., Liu, J. C., Cornwell, W. K., Cornelissen, J. H. C., & Aerts, R. (2015). Winners always win: growth of a wide range of plant species from low to future high CO2. Ecology and Evolution, 5, 4949–4961.

    Article  PubMed  PubMed Central  Google Scholar 

  50. Teng, N., Wang, J., Chen, T., Wu, X., Wang, Y., & Lin, J. (2006). Elevated CO2 induces physiological, biochemical and structural changes in leaves of Arabidopsis thaliana. New Phytologist, 172, 92–103.

    Article  CAS  PubMed  Google Scholar 

  51. Van Kan, J. A. L. (2006). Licensed to kill: the lifestyle of a necrotrophic plant pathogen. Trends in Plant Science, 11, 247–253.

    Article  CAS  PubMed  Google Scholar 

  52. Van Kan, J. A. L., Van't Klooster, J. W., Wagemakers, C. A. M., Dees, D. C. T., & Van der Vlugt-Bergmans, C. J. B. (1997). Cutinase A of Botrytis cinerea is expressed, but not essential, during penetration of gerbera and tomato. Molecular Plant-Microbe Interactions, 10, 30–38.

    Article  PubMed  Google Scholar 

  53. Van Wees, S. C. M., Pieterse, C. M. J., Trijssenaar, A., Van't Westende, Y. A., Hartog, F., & Van Loon, L. C. (1997). Differential induction of systemic resistance in Arabidopsis by biocontrol bacteria. Molecular Plant-Microbe Interactions, 10, 716–724.

    Article  PubMed  Google Scholar 

  54. Van Wees, S.C.M., Van Pelt, J.A., Bakker, P.A.H.M., & Pieterse, C.M.J. (2013). Bioassays for assessing jasmonate-dependent defenses triggered by pathogens, herbivorous insects, or beneficial rhizobacteria. In: A. Goossens & L. Pauwels (Eds.), Jasmonate signaling- methods and protocols, Methods in Molecular Biology (Vol. 1011, pp. 35–49). Berlin: Springer.

  55. Vaughan, M. M., Huffaker, A., Schmelz, E. A., Dafoe, N. J., Christensen, S., Sims, J., Martins, V. F., Swerbilow, J., Romero, M., & Alborn, H. T. (2014). Effects of elevated CO2 on maize defence against mycotoxigenic Fusarium verticillioides. Plant, Cell & Environment, 37, 2691–2706.

    Article  CAS  Google Scholar 

  56. Velásquez, A. C., Castroverde, C. D. M., & He, S. Y. (2018). Plant-pathogen warfare under changing climate conditions. Current Biology, 28, 619–634.

    Article  CAS  Google Scholar 

  57. Wells, J. M. (1974). Growth of Erwinia carotovora, E. atroseptica and Pseudomonas fluorescens in low oxygen and high carbon dioxide atmospheres. Phytopathology, 64, 1012–1015.

    Article  Google Scholar 

  58. Westerdijk, J. (1917). De nieuwe wegen van het phytopathologisch onderzoek. Inaugural Address Utrecht University. Amsterdam: J.H. de Bussy. 38 pp.

  59. Whalen, M. C., Innes, R. W., Bent, A. F., & Staskawicz, B. J. (1991). Identification of Pseudomonas syringae pathogens of Arabidopsis and a bacterial locus determining avirulence on both Arabidopsis and soybean. The Plant Cell, 3, 49–59.

    CAS  PubMed  PubMed Central  Google Scholar 

  60. Wildermuth, M. C., Dewdney, J., Wu, G., & Ausubel, F. M. (2001). Isochorismate synthase is required to synthesize salicylic acid for plant defence. Nature, 414, 562–571.

    Article  CAS  PubMed  Google Scholar 

  61. Williams, A., Pétriacq, P., Schwarzenbacher, R. E., Beerling, D. J., & Ton, J. (2018a). Mechanisms of glacial-to-future atmospheric CO2 effects on plant immunity. New Phytologist, 218, 752–761.

  62. Williams, A., Pétriacq, P., Beerling, D. J., Cotton, T. E. A., & Ton, J. (2018b). Impacts of atmospheric CO2 and soil nutritional value on plant responses to rhizosphere colonization by soil bacteria. Frontiers in Plant Science, 9, 1493.

    Article  PubMed  PubMed Central  Google Scholar 

  63. Yadeta, K. A., & Thomma, B. P. H. J. (2013). The xylem as battleground for plant hosts and vascular wilt pathogens. Frontiers in Plant Science, 4, 97.

    PubMed  PubMed Central  Google Scholar 

  64. Zavala, J. A., Casteel, C. L., DeLucia, E. H., & Berenbaum, M. R. (2008). Anthropogenic increase in carbon dioxide compromises plant defense against invasive insects. Proceedings of the National Academy of Sciences of the United States of America, 105, 5129–5133.

    Article  PubMed  PubMed Central  Google Scholar 

  65. Zavala, J. A., Nabity, P. D., & DeLucia, E. H. (2013). An emerging understanding of mechanisms governing insect herbivory under elevated CO2. Annual Review of Entomology, 58, 79–97.

    Article  CAS  PubMed  Google Scholar 

  66. Zhang, Y., Fan, W., Kinkema, M., Li, X., & Dong, X. (1999). Interaction of NPR1 with basic leucine zipper protein transcription factors that bind sequences required for salicylic acid induction of the PR-1 gene. Proceedings of the National Academy of Sciences of the United States of America, 96, 6523–6528.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  67. Zhang, S., Li, X., Sun, Z., Shao, S., Hu, L., Ye, M., Zhou, Y., Xia, X., Yu, J., & Shi, K. (2015). Antagonism between phytohormone signalling underlies the variation in disease susceptibility of tomato plants under elevated CO2. Journal of Experimental Botany, 66, 1951–1963.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  68. Zhou, Y., Vroegop-Vos, I., Schuurink, R. C., Pieterse, C. M. J., & Van Wees, S. C. M. (2017). Atmospheric CO2 alters resistance of Arabidopsis to Pseudomonas syringae by affecting abscisic acid accumulation and stomatal responsiveness to coronatine. Frontiers in Plant Science, 8, 700.

Download references


This work was supported by a Chinese Scholarship Council (CSC) PhD scholarship (Y.Z.), Advanced Investigator Grant 269072 of the European Research Council (C.M.J.P), and VIDI grant no. 11281 of the Dutch Technology Foundation STW (S.C.M.V.W.).

Author information



Corresponding author

Correspondence to Saskia C. M. Van Wees.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Human and animal rights

No human and/or animal participants were involved in this research.

Informed consent

All authors consent to this submission.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Zhou, Y., Van Leeuwen, S.K., Pieterse, C.M.J. et al. Effect of atmospheric CO2 on plant defense against leaf and root pathogens of Arabidopsis. Eur J Plant Pathol 154, 31–42 (2019). https://doi.org/10.1007/s10658-019-01706-1

Download citation


  • Atmospheric CO2
  • Arabidopsis
  • Disease resistance
  • Foliar pathogens
  • Soil-borne pathogens
  • Defense signaling