Lorella Navazio
Elide Formentin
Laura Cendron
Ildikò Szabò- 1Department of Biology, University of Padova, Padova, Italy
- 2Botanical Garden, University of Padova, Padova, Italy
Calcium has long been known to regulate the metabolism of chloroplasts, concerning both light and carbon reactions of photosynthesis, as well as additional non photosynthesis-related processes. In addition to undergo Ca2+ regulation, chloroplasts can also influence the overall Ca2+ signaling pathways of the plant cell. Compelling evidence indicate that chloroplasts can generate specific stromal Ca2+ signals and contribute to the fine tuning of cytoplasmic Ca2+ signaling in response to different environmental stimuli. The recent set up of a toolkit of genetically encoded Ca2+ indicators, targeted to different chloroplast subcompartments (envelope, stroma, thylakoids) has helped to unravel the participation of chloroplasts in intracellular Ca2+ handling in resting conditions and during signal transduction. Intra-chloroplast Ca2+ signals have been demonstrated to occur in response to specific environmental stimuli, suggesting a role for these plant-unique organelles in transducing Ca2+-mediated stress signals. In this mini-review we present current knowledge of stimulus-specific intra-chloroplast Ca2+ transients, as well as recent advances in the identification and characterization of Ca2+-permeable channels/transporters localized at chloroplast membranes. In particular, the potential role played by cMCU, a chloroplast-localized member of the mitochondrial calcium uniporter (MCU) family, as component of plant environmental sensing is discussed in detail, taking into account some specific structural features of cMCU. In summary, the recent molecular identification of some players of chloroplast Ca2+ signaling has opened new avenues in this rapidly developing field and will hopefully allow a deeper understanding of the role of chloroplasts in shaping physiological responses in plants.
Introduction
Calcium is a fundamental intracellular messenger involved in a wide range of different signaling pathways in all eukaryotes. In plants, Ca2+ has been shown to participate in the transduction of a large variety of environmental stimuli of both abiotic and biotic nature (Dodd et al., 2010). A complex Ca2+ homeostatic and signaling machinery allows for a tight regulation of the intracellular concentration of the ion ([Ca2+]) and its variations during signal transduction (Kudla et al., 2018). Plant organellar Ca2+ signaling is a rapidly expanding field of investigation, also thanks to the increasing availability of novel genetically encoded Ca2+ indicators, specifically targeted to different intracellular compartments (Costa et al., 2018). In addition to the vacuole, considered as the main stimulus-releasable Ca2+ store in the plant cell, other organelles, i.e. chloroplasts, have recently come to the fore. The detection of stimulus-specific intra-chloroplast Ca2+ signals in response to different environmental cues has highlighted the contribution of chloroplasts to shaping cytosolic Ca2+ signatures. In this mini-review we present the most recent research works dealing with the monitoring of chloroplast Ca2+ concentration and its changes during signal transduction events. Moreover, we focus on the recently reported identification and biochemical characterization of some molecular players involved in chloroplast Ca2+ handling. Current evidence for a crucial role of chloroplasts as stress sensors and future avenues of investigation in this promising field are also discussed.
The Emerging Role of Chloroplast Calcium Signaling in the Transduction of Biotic and Abiotic Stress Signals
Chloroplasts have long been known to be involved in intracellular Ca2+ homeostasis and signaling. The regulatory role played by these organelles on intracellular Ca2+ handling is two-fold: i) a tight control of intra-organellar [Ca2+] is essential for the proper functioning of the chloroplast physiology, e.g. the regulation of photosynthesis, as well as other chloroplast-localized processes (Stael et al., 2012b; Rocha and Vothknecht, 2012; Nomura and Shiina, 2014; Hochmal et al., 2015); ii) transient changes in stromal [Ca2+] ([Ca2+]str), evoked in response to different stress stimuli, in turn can shape intracellular Ca2+ signals, thereby affecting Ca2+-mediated signaling circuits.
After the pioneering work conducted by Johnson et al. (Johnson et al., 1995) and Sai and Johnson (Sai and Johnson, 2002), who monitored [Ca2+] in the chloroplast stroma by means of a chloroplast-targeted aequorin chimera, precise measurements of Ca2+ levels inside the different chloroplast subcompartments have been lacking for a long time. However, in the last few years the increasing availability of specifically targeted Ca2+ reporters has rapidly expanded the possibility of accurately monitoring organellar Ca2+ dynamics. The set up of a toolkit of aequorin-based probes targeted to the different subcompartments of chloroplasts (outer and inner envelope membranes, stroma, thylakoids) has allowed for the elucidation of stimulus-specific intra-organellar Ca2+ signals and their contribution to fine-tuning cytosolic Ca2+ signatures (Mehlmer et al., 2012; Sello et al., 2016; Sello et al., 2018). A complementary approach based on the design of a cameleon probe directed to the chloroplast stroma further permitted Ca2+ imaging in single chloroplasts, highlighting organelle-autonomous Ca2+ transients (Loro et al., 2016). The establishment of aequorin reporters targeted to the thylakoid lumen and thylakoid membrane highlighted the ability of thylakoids to store 3- to 5-fold higher [Ca2+] with respect to the stroma (about 500 nM in the thylakoid lumen versus 100÷150 nM in the stroma, in resting conditions in the dark), as well as their contribution to the modulation of intra-chloroplast Ca2+ signals (Sello et al., 2018).
Chloroplast Ca2+ signals have been shown to be triggered by a large number of different stimuli of both biotic and abiotic nature. Elicitors of plant defence responses, such as the fungal-derived protein cryptogein and the plant cell wall-derived pectin fragments oligogalacturonides, were found to evoke transient Ca2+ elevations in the chloroplast stroma of Nicotiana tabacum and Arabidopsis thaliana plant cell suspension cultures (Manzoor et al., 2012; Sello et al., 2018). Moreover, the bacterial flagellin peptide flg22 was demonstrated to trigger a chloroplast Ca2+ response in the chloroplast stroma of Arabidopsis rosette leaves, peaking later than the cytosolic Ca2+ elevation (Nomura et al., 2012; Nomura and Shiina, 2014). In this latter work, a striking chloroplast-mediated transcriptional reprogramming during plant immune responses was demonstrated, uncovering an unanticipated link between chloroplast and nuclear plant innate immunity via ROS and Ca2+ signaling (Stael et al., 2015). The calcium-sensing receptor CAS, a thylakoid-localized protein of not yet well-defined function, was found to be involved in the generation of the flg22-induced stromal Ca2+ transient and chloroplast-mediated activation of defence gene expression (Nomura et al., 2012).
Different abiotic cues, such as cold, oxidative, salt and osmotic stresses were found to evoke stimulus-specific Ca2+ signals in the chloroplast stroma (Nomura et al., 2012; Sello et al., 2016; Sello et al., 2018; Teardo et al, 2019). Whereas these stimuli were shown to activate Ca2+ responses in both chloroplasts and non-green plastids (Sello et al., 2016), the light-to-dark transition was found to elicit a chloroplast-specific response (Sello et al., 2016; Loro et al., 2016). Although the precise mechanisms underlying dark-induced chloroplast Ca2+ fluxes remain to be unravelled, the circadian gating of dark-induced chloroplast and cytosolic Ca2+ elevations has recently been demonstrated (Martí Ruiz et al., 2020), uncovering an intriguing link between eukaryotic circadian clocks and chloroplasts.
In contrast to the above-mentioned stimuli, that have been demonstrated to trigger Ca2+ transients in both chloroplasts and the cytosol, increases in absolute temperature were found to evoke Ca2+ responses specific to chloroplasts, as no corresponding elevations were detected in the cytosol (Lenzoni and Knight, 2019). Interestingly, also in this case the chloroplast Ca2+ response was found to be partially dependent on CAS (Lenzoni and Knight, 2019).
Taken together, the above findings strongly highlight the ability of chloroplasts to perceive and transduce environmental signals in a Ca2+-dependent manner. However, compared to the large amount of information progressively cumulating on the generation of chloroplast Ca2+ signals, information about Ca2+-permeable channels/transporters localized at chloroplast membranes has long lagged behind.
Current Knowledge of the Molecular Players Involved in Ca2+ Handling in Chloroplasts
The extent, duration and frequency (i.e. signature) of free Ca2+ elevation in the cytosol ([Ca2+]cyt) acts as a signal to be implemented in the transducing machinery of the cell. Different stimuli are followed by different Ca2+ signatures, leading in turn to different specific responses, in terms of gene expression, protein activity and localization. The Ca2+ signature is shaped by the activity of Ca2+-permeable channels and transporters regulating the ion entry into and exit from the cytosol, respectively. Ca2+-permeable channels are grouped in five families: cyclic nucleotide-gated channels (CNGCs), glutamate receptors-like channels (GLRs), two-pore channels (TPCs), mechanosensitive channels (MCAs), hyperosmolality gated channels (OSCAs) (Demidchik et al., 2018). Ca2+ transport off the cytosol to restore the resting [Ca2+]cyt is mediated by energy-driven pumps/transporters belonging to the P-type ATPases, such as P1B-type calcium/heavy metal cation-transporting ATPase (AtHMA1), P2A-type calcium cation-transporting ATPase (ECAs) and P2B-type calcium cation-transporting ATPase (ACAs) (García Bossi et al., 2020). Other Ca2+ transporters are grouped in the CaCA family (CAX-type proton:calcium cation exchanger, CCX-type cation:calcium cation exchanger, MHX-type proton:magnesium cation exchanger, NCL/EF-CAX-type cation exchanger, EF-CAX-type cation exchanger) (Pittman and Hirschi, 2016) and CaCA2 family (PAM71-type manganese/calcium cation transporter).
The transduction of the Ca2+ signal is mediated by Ca2+ -dependent/binding proteins. The Arabidopsis genome encodes for 250 proteins harbouring at least one Ca2+ binding domain (EF-hand), hence acting as putative Ca2+ sensors [e.g. (Ranty et al., 2016)]. Calmodulins (CaMs), calmodulin-like (CaMLs), calcineurin B-like proteins (CBLs) and Ca2+-dependent protein kinases (CPKs) all harbour EF hand motifs. Ca2+ sensors directly (CPKs) or indirectly (CaMs, CaMLs, CBLs) [e.g. (Sanyal et al., 2015; Kudla et al., 2018)] modulate protein activity (e.g. ion channels, metabolic enzymes) and/or protein subcellular localization (e.g. transcription factors). The redundancy of sensor isoforms allows the discrimination between different signals and carry the specificity of the message brought by the Ca2+ signature.
To our knowledge, Ca2+-binding proteins acting as buffers in the chloroplast have not yet been identified. Nevertheless, organellar Ca2+ buffering mechanisms are likely to play an essential role, generating heterogeneity in local Ca2+ concentrations inside chloroplasts. How Ca2+ is stored in the chloroplast remains an open question for future investigations, aimed to unravel whether Ca2+ interacts with specific Ca2+ binding proteins or with the thylakoid surface, which harbours a significant amount of phosphorylated proteins that have been suggested to bind calcium ions (Rocha and Vothknecht, 2012; Stael et al., 2012a; Stael et al., 2012b).
The major part of research carried out so far has focused on the analysis of the cytosolic Ca2+ signature, but the possibility to study Ca2+ dynamics in organelles by targeting Ca2+ probes to plastids has recently allowed the understanding of the existence of organellar Ca2+ transients in response to external stimuli. These findings pose the question of the identity of players involved in shaping and transducing the Ca2+ signal coming from organelles. The existence of peculiar and dedicated pathways for Ca2+ handling in organelles can be a possibility, and/or the machinery may comprise some already known players that may localize to chloroplasts as well (Finazzi et al., 2015; Pottosin and Shabala, 2015; Carraretto et al., 2016).
Recently, two proteins belonging to the family of the mitochondrial calcium uniporter (MCU) have been found to mediate Ca2+ transport across the mitochondria and chloroplast membranes, respectively AtMCU1 (Teardo et al, 2017) and AtMCU6 (later renamed AtcMCU (Teardo et al., 2019). In animal cells the only isoform, MCU (De Stefani et al., 2011; Baughman, 2011) is responsible for Ca2+ loading into mitochondria, thus helping recovery of resting [Ca2+]cyt. New evidence supports the involvement of MCU isoforms in shaping the organellar Ca2+ signatures in plants as well (Wagner et al., 2015; Teardo et al., 2017; Selles et al., 2018; Teardo et al., 2019). In particular, cMCU is involved in the generation of the stromal Ca2+ transient specific for the osmotic stress and mutants lacking cMCU showed an improved drought tolerance (Stael, 2019; Teardo et al., 2019).
It is now commonly acknowledged that a protein can localize to different cell compartments (Karniely and Pines, 2005), as it has been proven also for proteins involved in Ca2+ handling (Table 1). AtGLR3.4 and AtGLR3.5, two Ca2+ -permeable channels belonging to the GLR family, have a dual localization, at the plasma membrane and chloroplasts the former (Teardo et al., 2010; Teardo et al., 2011), in mitochondria and chloroplasts the latter (Teardo et al., 2015). Both seem to play a role in ABA signaling under abiotic stress (Cheng et al., 2018; Ju et al., 2020), although their direct involvement in organellar Ca2+ signaling under abiotic stress has to be investigated more in depth.
Table 1 List of proteins involved in Ca2+ handling predicted to be located in plastids.
Querying the protein databases Uniprot (The UniProt Consortium, 2019), SUBA4 (Hooper et al., 2017) and Aramemnon (Schwacke et al., 2003) for A. thaliana records with plastidial localization and using “calcium” as keyword, 682 hits can be found in SUBA4, only 43 in Aramemnon and 42 in Uniprot. Table 1 shows all those proteins belonging to the above-mentioned classes of channels/transporters, sensors and kinases involved in Ca2+ signature formation and signaling, whose plastidial localization has been predicted or demonstrated by MS/MS or by fusion to fluorescent proteins (FP).
23 out of 47 proteins belong to Ca2+ channels/transporters: 6 are confirmed to be located in plastid membranes either by biochemical and cell biology methods or by mass spectrometry. Among them, for AtcMCU, AtGLR3.4 and AtGLR3.5 a role in stress response was suggested. Altogether, these channels/transporters can be involved in the formation of the plastidial Ca2+ transients, along with the putative calcium-transporting protein PAM71/BICAT (Frank et al., 2019). However, this latter protein seems to play a prevalent role in manganese homeostasis rather than in calcium homeostasis (Schneider et al., 2016; Zhang et al., 2018). In addition to Ca2+ channels and transporters, Ca2+ sensors, namely 21 proteins, are predicted to be located in plastids. However, only three have been confirmed so far: AtCPK20, AtCPK31, and AtCAS. It is worth to mention that CPK20, besides the plastidial localization that was confirmed by MS/MS approaches (Behrens et al., 2013), showed a plasma membrane localization when fused to reporter genes or co-expressed with other CPK members (Gutermuth et al., 2013). CPK31 has also been shown to localize at the plasma membrane when interacting with the arsenite transporter NIP1;1 (Ji et al., 2017). In addition, localization of many CPKs with chloroplast-targeting sequence can be affected by N-acylation. For example, AtCPK20 and 31 are located in the chloroplast, only if its N-acylation is prevented (Stael et al., 2011). Interestingly, AtGRF9, a Ca2+-regulated 14-3-3 protein, although not predicted to be located in chloroplasts, has been demonstrated to be present in many compartments, including plastids. This regulatory protein is involved in root and leaf development under water stress (He et al., 2015) and leaf development in general (Omidbakhshfard et al., 2018), but its role in chloroplasts has not yet been explored.
The presence of members of protein families involved in Ca2+ transport/sensing supports the idea of a core-machinery determining the observed Ca2+ transients in the chloroplast stroma, and putatively in the thylakoid lumen as well. Ca2+ sensors are indeed present in plastids, although their activity in deciphering organellar Ca2+ signatures has not been fully demonstrated so far. Nevertheless, a recent work points to CAS as mediator of light response and photoacclimation (Cutolo et al., 2019).
The multiple localizations shown by some proteins in Table 1 awaits further investigation. Recent evidence is pointing to the hypothesis of an inter-connection between organelles and nucleus for material exchanging or signal propagation (Kmiecik et al., 2016). The presence of the Ca2+ handling machinery in multiple positions can be part of the retrograde signaling in response to adverse environmental conditions (Pornsiriwong et al., 2017).
Structural and Functional Comparison Between MCU Isoforms From Different Organisms and the Chloroplast-Localized Homologue in Plants
As mentioned above, AtcMCU is one of the very few molecular entities among the plastidial Ca2+ channels/transporters shown to work as a Ca2+-permeable ion channel, to mediate indeed Ca2+ flux across chloroplast envelope and to participate in the drought stress response in Arabidopsis. While many organisms have only one MCU isoform (Bick et al., 2012), Arabidopsis harbours 6 different isoforms: 5 with clear predicted subcellular localization to mitochondria, whereas AtMCU6/At5g66650 has a predicted localization to either chloroplasts and/or to mitochondria. Localization prediction was confirmed for AtMCU1/At1g09575 (Teardo et al., 2017), AtMCU2/At1g57610 (Wagner et al., 2015; Selles et al., 2018), AtMCU3/At2g23790 (Carraretto et al., 2016). For AtMCU6 an interesting situation was observed: in tissues harbouring mature chloroplasts, AtMCU6 was efficiently targeted to these photosynthetic organelles, whereas in roots the protein was found in mitochondria (Teardo et al., 2019). Thus, either plastid-specific partners promote targeting of AtMCU6/AtcMCU or targeting depends on the metabolic state of a given cell. However, among the possible partners (https://string-db.org/network/3702.AT5G66650.1) no proteins with unique localization to chloroplasts are present. Thus, the mechanism by which dual localization occurs awaits clarification.
The N-terminal domain (NTD) of AtcMCU harbours motifs rich in acidic residues, one of which (107-118) playing a role in Ca2+ uptake by cMCU, as demonstrated by mutagenesis studies (D107A/E118K mutant) and Ca2+ uptake assays in an aequorin-based E. coli system (Teardo et al., 2019). Two groups independently set up the same system to study MCU activity, namely that exploiting E. coli stably expressing aequorin (Teardo et al., 2019) or the fluorescent Ca2+ reporter GCaMP2 (Fan et al., 2018). This valuable tool allows a quick screening of the effect of MCU residues' mutations and of chemical modulators on the Ca2+ flux-mediating activity and may become a method of choice for further structure-function studies.
One common feature of MCU homologs from fungi and Arabidopsis is that they can function as Ca2+-permeable channels on their own in contrast to vertebrates, where the uniporter is a complex (MCUC) consisting of multiple subunits, including: 1) the channel forming unit (MCU) with two transmembrane segments and a conserved DXXE sequence forming the Ca2+ selectivity filter (see Figure 1); 2) regulatory EF-hand proteins MICU1-3; 3) a small, single-pass transmembrane protein, EMRE (Essential MCU REgulator) [for review see e.g.(Wagner et al., 2016)]. The structure of MCU homologs from various organisms has been recently solved: 1) from Fusarium graminearum and Metarhizium acridum revealing a dimer assembly of MCU (Fan et al., 2018); 2) from Neurospora crassa (Yoo et al., 2018); 3) from Neosartorya fischeri (Nguyen et al., 2018b); and from 4) zebrafish and Cyphellophora europaea (Baradaran et al., 2018). All these homologues share high sequence similarity in their transmembrane domains, show a similar pore architecture and a high structural similarity of the NTDs (despite relatively low sequence homology). The amino acid sequence is more similar between Arabidopsis and Dictyostelium discoideum than between AtMCUs and human MCU (Teardo et al., 2017). This similarity apparently translates also to the tertiary structure of the two proteins, at least regarding the N-terminal domain, whose structure has been recently resolved for Dictyostelium MCU, proving its divergent evolution (doi: https://doi.org/10.1101/848002) (see Figure 1).
Figure 1 Structural features of chloroplast MCU from Arabidopsis thaliana, modelled by Phyre V 2.0. From the left to the right: (panel A) cartoon view of the superposition of MCU structure from Neurospora crassa (cryoEM, 3.7 Å resolution, PDB:6DT0, grey), used as a reference, and predicted A. thaliana cMCU transmembrane tetrameric assembly (coloured chains); (panel B, C) details of the transmembrane (TM) and coiled-coil domain (CCD) tetrameric assembly and selectivity filter (panel C), where the four chains are shown in yellow, orange, pale violet and green. The key acidic residues within the highly conserved motif (WDXXEP, where X is any hydrophobic residue) of cMCU are highlighted in sticks, as well as the coordinated calcium ion, shown as dark grey sphere; (panel D) superposition of the model of one monomer of A. thaliana cMCU channel (orange and red) and N. crassa MCU tetramers (light grey); cMCU model shown here includes the transmembrane domain (TM), part of the coil-coiled region and the N-terminal domain (NTD), the last predicted according to our previous homology searches and its similarity toward Dictyostelium discoideum NTD (PDB:5Z2H, doi: https:/doi.org/10.1101/848002). The superposition underlines the divergence from metazoan NTDs and other structure-known fungal homologues such as NcMCU, CeMCU, MaMCU, and NfMCU.
In plants and fungi, the pore-forming unit MCU alone is able to allow Ca2+ flux, without the need of EMRE, as confirmed by different groups (Tsai et al., 2016; Teardo et al., 2017; Fan et al., 2018; Teardo et al., 2019). In fact, homologs of EMRE are not present in these organisms. The cryo-EM structure of the human MCU-EMRE complex (Wang et al., 2019) suggests that NTD mediates the dimerization of two human MCU tetramers, thereby modulating the function of the channel [although deletion of NTD does not affect Ca2+ flux (Lee et al., 2015)]. In contrast to other MCUs, an (R/K)/Q/(R/K/D)/K/L motif is found in the L2 (Oxenoid et al., 2016) (now called CC2a for coiled-coiled domain 2a) (Wang et al., 2019) region of Arabidopsis, Dictyostelium and NfMCU (Teardo et al., 2017; Wang et al., 2019), all being able to form functional MCU without EMRE. It has been proposed that the extended side chain of HsMCU R297 (missing in the above MCUs) on CC2a connects the gate-forming juxtamembrane loop (JML) of MCU to EMRE by forming hydrogen bonds with the hydroxyl group of highly conserved T285 (on the JML of MCU) and a valine residue of EMRE. Interaction between CC2a and EMRE has been proposed as a crucial factor determining the conductivity of the channel formed by MCU tetramers. On the other hand, in the EMRE-independent Dictyostelium MCU, deletion of either CC1 or CC2 caused the loss of function of MCU (Yamamoto et al., 2019), suggesting that these two domains are crucial for MCU function independently of their ability to bind EMRE. Altogether, determination of structural differences among various MCUs accounting for the requirement of EMRE for channel function requires further work.
Conclusions and Perspectives
In these last few years there has been a surge of papers on Ca2+ signaling in chloroplasts, witnessing the crucial role increasingly attributed to these plant-unique organelles in the orchestration of the complex Ca2+ signaling network of the plant cell. We foresee that the newly available experimental tools to investigate the role of thylakoids in Ca2+-mediated signal transduction, the molecular identification of Ca2+ channels/transporters in chloroplast membranes and the determination of the structure of transmembrane proteins by cryo-EM will lead to a rapid development of this exciting field of plant research. Future plant organellar Ca2+ signaling studies should also focus on non-photosynthetic plastids, which have recently been proposed to trigger tissue-specific signaling involved in mounting plant systemic stress response (Beltran et al., 2018). Furthermore, the potential interplay of chloroplasts with other intracellular Ca2+-mobilizable stores should also be taken into consideration, in view of the well-known structural and functional interactions established by plastids with other organelles (Mathur et al., 2012).
Author Contributions
LN, EF, and IS jointly contributed to the writing of this manuscript. LC designed the structural model of cMCU presented in Figure 1. All authors reviewed and approved the final version of the submitted manuscript.
Funding
This work was supported by HFSP RG0052 to IS and the University of Padova (PRID 2018, BIRD180317) to LN.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Keywords: chloroplasts, organellar calcium signaling, calcium-permeable channels, calcium transporters, calcium binding proteins, genetically encoded calcium indicators, chloroplast calcium uniporter
Citation: Navazio L, Formentin E, Cendron L and Szabò I (2020) Chloroplast Calcium Signaling in the Spotlight. Front. Plant Sci. 11:186. doi: 10.3389/fpls.2020.00186
Received: 09 December 2019; Accepted: 07 February 2020;
Published: 11 March 2020.
Edited by:
Jürgen Soll, Ludwig Maximilian University of Munich, GermanyReviewed by:
Markus Teige, University of Vienna, AustriaCornelia Spetea, University of Gothenburg, Sweden
Copyright © 2020 Navazio, Formentin, Cendron and Szabò. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Ildikò Szabò, ildiko.szabo@unipd.it
†These authors have contributed equally to this work