Se is an important trace element and micronutrient, essentially needed for the biosynthesis of selenocysteine-containing selenoproteins. In humans, the selenoproteome comprises enzymes implicated in redox control, antioxidative defence, thyroid hormone metabolism, endoplasmic reticulum function and other important biochemical pathways including the systemic Se transport by selenoprotein P (SePP)( Reference Labunskyy, Hatfield and Gladyshev 1 ). A few cases of inherited defects in selenoprotein biosynthesis have been characterised. Symptoms may include severe muscular dystrophy, cognitive impairment, endocrine alterations and sensitivity towards oxidative noxae( Reference Schweizer, Dehina and Schomburg 2 ). On a population-wide scale, low Se intake and suboptimal selenoprotein expression have been associated with a number of health risks including cancer at various sites, infections, mortality in severe illness, autoimmune thyroiditis and other diseases( Reference Rayman 3 ).
Se status is mainly controlled by hepatic Se metabolism, which becomes impaired in response to cirrhosis( Reference Burk, Early and Hill 4 ), inflammation( Reference Renko, Hofmann and Stoedter 5 ) or hypoxia( Reference Becker, Martitz and Renko 6 ), causing diminished SePP biosynthesis and secretion. In turn, the Se concentration in blood may decline strongly. Serum Se has thus been characterised as a negative acute-phase reactant( Reference Nichol, Herdman and Sattar 7 ). Under such conditions, the central nervous system, endocrine glands and bone may become Se-deficient and highly sensitive to oxidative injury, as SePP is the major transport protein of Se supplying these organs with the essential trace element. Collectively, the negative acute-phase response of Se together with an increased susceptibility of Se-deficient subjects for infections may form a vicious cycle of disease-dependent Se decline and impaired defence mechanisms. For these reasons, Se supplementation is considered as a potentially meaningful adjuvant treatment option in severe diseases( Reference Heyland 8 , Reference Schomburg 9 ).
Clinically, Se status correlates with survival odds and regeneration in adult patients( Reference Forceville, Vitoux and Gauzit 10 – Reference Meyer, Endermann and Stephan 12 ). Similarly, in children, high plasma Se was associated with improved outcome in systemic inflammation( Reference Leite, Nogueira and de Oliveira Iglesias 13 , Reference Iglesias, Leite and Paes 14 ), and a respective Cochrane meta-analysis highlighted a reduction in sepsis incidence upon Se supplementation in preterm neonates( Reference Darlow and Austin 15 ). These findings are of high importance, as the immature immune system of neonates places them at increased risk for infections. High mortality rates from sepsis and pneumonia are observed in this vulnerable period, especially in poorly developed countries( 16 – Reference Seale, Blencowe and Manu 18 ). Markers of oxidative stress are elevated in newborns with sepsis( Reference Cancelier, Petronilho and Reinke 19 ), especially in preterm neonates( Reference Buonocore, Perrone and Longini 20 ). These findings may be related to the Se status, as it controls the biosynthesis of selenoproteins implicated in antioxidative defence reactions and immune cell functioning. In order to test the hypothesis that infection is associated with a Se deficit already during the first few days of life, we compared two well-established plasma biomarkers of Se in infected neonates and controls. We detected some neonates with severe Se deficiency, especially in the group of preterm neonates with infection, raising the issue of Se substitution or supplementation in these very vulnerable patients.
Methods
Study design
The present study was designed as an observational case–control study. This study was conducted according to the guidelines laid down in the Declaration of Helsinki, and all procedures involving human subjects/patients were approved by the ethics committee of the Charité Universitätsmedizin Berlin, Germany (application no; EA2/092/12). Enrolment started in February 2013 and ended in April 2014 in three neonatal care units of the Charité Universitätsmedizin Berlin. Neonates fulfilling inclusion criteria (Table 1) were identified, next of kin were contacted and informed written consent for participation was obtained from one or both parents. For this study, only the remaining plasma samples from the routine diagnostic analyses were available, were pseudonymised and frozen at −20°C until analysis. Leftover samples from the mothers were not available for analysis.
Table 1 Inclusion and exclusion criteria
INR, international normalised ratio; CRP, C-reactive protein.
Inclusion and exclusion criteria
Clinical signs of infections are subtle and often non-specific in neonates( Reference Arnon and Litmanovitz 21 , Reference Shah and Padbury 22 ). No validated diagnosis score system for infections in early life has been established. In addition, the specificity of blood cultures in neonates is low( Reference Vergnano, Menson and Kennea 23 ). On the basis of previous data( 24 – Reference Dollner, Vatten and Austgulen 26 ) and internal standard procedures, we defined an infection as the presence of at least one characteristic clinical sign and simultaneously a laboratory evidence for inflammation, as described in Table 1. To this end, we chose IL-6 or C-reactive protein (CRP), as they are used as diagnostic markers for infections in infants and correlate with severity of infection( Reference Arnon and Litmanovitz 21 , Reference Chiesa, Pacifico and Natale 27 , Reference Ng and Lam 28 ).
Procedures
Neonates with clinically suspected infections were screened for an increase in the concentration of IL-6 and/or CRP. The first blood analysis took place immediately after detection of alarming clinical signs, in case of early-onset infection on the day of birth (day 1). Antibiotic (ampicillin and gentamicin) therapy was initiated if the IL-6 or CRP concentrations exceeded a predefined threshold (IL-6>100 ng/l; CRP>10 mg/l). To evaluate the effect of the therapy and control gentamicin blood levels, a second sample was collected after 48 h (day 3). These two time points were available for analysis from our infected newborns, as the study protocol allowed Se status analysis from leftover samples only. Control plasma samples were available from neonates admitted to the neonatal care units at the time of birth for diagnostic purposes unrelated to acute infections. Severe infection was defined as IL-6 concentrations exceeding a threshold of 500 ng/l( Reference Bloos and Reinhart 29 ).
Subjects
In total, 108 newborns were considered on the basis of clinical presentation, of which seventy-two fulfilled all inclusion criteria including the availability of remaining plasma samples exceeding 20 µl. Informed consent was obtained from forty-four parents; twenty-three from the control group and twenty-one from the infected neonates group.
Measurements
IL-6 and CRP concentrations were determined by the local commercial diagnostics provider conducting the routine clinical measurements (Labor Berlin – Charité Vivantes GmbH). CRP was measured by a turbidometric assay and IL-6 by an electro-chemical luminescence immunoassay (COBAS 6000 or COBAS 8000; Roche Diagnostics), respectively. Se contents were determined by total reflection X-ray fluorescence analysis (S2 Picofox; Bruker Nano GmbH) as described earlier( Reference Hughes, Fedirko and Jenab 30 ). In brief, 10 µl plasma samples were spiked with an internal gallium standard (Sigma-Aldrich). Samples were applied to polished quartz glass carriers, dried at 37°C for 3 h and analysed in duplicates. Quantification of SePP was carried out by analysing duplicate plasma samples using a colorimetric enzyme immunoassay (Selenotest®; ICI immunochemical intelligence GmbH) as described earlier( Reference Hughes, Fedirko and Jenab 30 ). Inter-assay and intra-assay CV were below 15 % as determined using a commercial human reference serum sample (Seronorm; SERO AS).
Western blot analysis
Plasma samples (0·2 µl) were diluted in ultrapure water (Biochrom AG) and 4× sample buffer (200 mm-Tris-HCl, pH 7·5; 50 % glycerin; 4 % SDS; 0·04 % bromophenol blue and 125 mm-dithiothreitol). Samples were size fractionated by SDS-PAGE and blotted by semi-dry transfer onto nitrocellulose membranes (Optitran; Schleicher & Schuell). A SePP-specific antibody (1:2000 dilution; ICI) was used, and signals were developed using the Western-Bright Quantum chemiluminescence substrate Sirius (Biozym Scientific) with the Fluor Chem FC2 detection system (Biozym).
Statistics
Statistical Package for the Social Sciences (SPSS, version 21; IBM) and GraphPad Prism (version 5; GraphPad Software, Inc.) were used for biostatistical analyses. For independent and normally distributed data, t test to compare means and Pearson’s test for correlation analyses were conducted. For independent and not-normally distributed variables, the Mann–Whitney U and Spearman’s rank correlation tests were used. For dependent and normally distributed variables, a paired t test was used. Probability values (P) of <0·05 were defined as significant. Univariate analyses were conducted to examine the effect of several factors on one variable. Before we conducted a univariate analysis of SePP, we performed a square root transformation to gain normally distributed groups (SePPsqrt). The Se concentration of one neonate from the infected group was three times the interquartile range (IQR) above the 75 % percentile (69·26 µg/l), and was consequently excluded from the Se analysis.
Results
A total of forty-four subjects fulfilled all inclusion criteria (Table 1) and were included in our study, of which twenty-three were classified as control and twenty-one as neonates with infection. The other samples initially collected were not analysed, as the sample volume was insufficient or consent from the parent(s) was not available (denied or incomplete, n 28). Table 2 presents the anthropometric and clinical characteristics of the neonates finally enrolled in the study. Overall, neonates in the control group had on average a lower gestational age and a lower birth weight. Sex distribution differed between the groups with more female newborns in the control group than in the group with connatal infection (Table 2).
Table 2 Group characteristics (Medians and interquartile ranges (IQR) and standard deviations)
CRP, C-reactive protein.
* Significant difference (P<0·05).
The average Se concentration on day 0 of the newborns in our study was 34·5 (sd 11·6) µg/l, considerably below the levels usually observed in adults. Se and SePP concentrations were strongly correlated (b=0·025, r p =0·78, P<0·001), verifying the notion that Se status was suboptimal in the newborns. The positive correlation was present both in the control group (Fig. 1(a)) and in the group of infected newborns (Fig. 1(b)). When comparing the infected neonates before (day 1) and after (day 3) initiation of antibiotic therapy, the correlation was stronger at day 1 compared with day 3 (Fig. 1(c) and (d)).
Fig. 1 Comparison of the two selenium biomarkers analysed in this study. Total selenium and selenoprotein P (SePP) show a strong and positive correlation in (a) the control and (b) in the group of infected newborns. The strong correlation of selenium and SePP is observed in the infected newborns both at (c) birth and (d) 48 h after initiation of treatment. These data indicate that both total selenium and SePP concentrations are suitable for Se status assessment in healthy and infected newborns. *** P<0·001.
On average and without considering covariates, mean plasma Se concentrations of the infected infants were lower compared with the control group at day 1, but not significantly different (Fig. 2(a)). Very low Se concentrations (Se<20 µg/l) were observed in four infected subjects (11·7, 14·3, 15·1 and 15·7 µg/l) and one control subject (15·8 µg/l). Similarly, mean SePP concentrations in our study were not significantly different between control and infected newborns (Fig. 2(b)). Notably, the two biomarkers of Se status showed a relatively wide range of concentrations both in the controls (median Se, 36·2 (IQR 10·8) µg/l; median SePP, 0·99 (IQR 0·50) mg/l) and in the infected newborns (Se, 31·8 (IQR 10·5) µg/l; SePP, 0·98 (IQR 0·53) mg/l)).
Fig. 2 Plasma concentrations of selenium and selenoprotein P (SePP) in control and infected newborns. (a) The selenium concentrations in both groups cover a relatively wide range and are on average not different between controls and infected neonates. (b) The ranges of SePP concentrations are similarly wide in both groups and do not differ on average between control and infected. Notably, the lowest selenium and SePP concentrations are detected in the group of infected newborns.
Gestational age was not correlated with Se or SePP concentrations in the group of controls (Fig. 3(a) and (c)). However, both biomarkers of Se status were positively correlated with gestational age in the group of infected newborns (Fig. 3(b) and (d)). In particular, preterm infants (gestational age <37 weeks) had lower SePP concentrations (median SePP, 0·91 (IQR 0·51) mg/l) than term infants (SePP, 1·04 (IQR 0·57) mg/l). This difference was statistically significant (U=145, z=−2·192, P=0·028). In comparison, Se concentrations were not significantly different between preterm and term infants (median (preterm)=32·6 µg/l; v. median (term)=39·0 µg/l; U=175, z=−1·481, P=0·139).
Fig. 3 Association of selenium status with gestational age. (a, c) Concentrations of selenium and selenoprotein P (SePP) were unrelated to gestational age in the neonates of the control group. (b, d) In the infected neonates, selenium and SePP concentrations were positively associated with gestational age; (b) P=0·006, and (d) P=0·004. Notably, the lowest levels of selenium and SePP observed in this study were detected in premature neonates with infection. (e, f) Separating all newborns into term (>37 weeks) and preterm, there was no significant difference in (e) selenium concentrations, whereas (f) SePP concentrations differed significantly. 
, Preterms. * P<0·05, ** P<0·01.
Next, we conducted a univariate analysis with gestational age as a covariate and infection status as a fixed factor to examine their influence on Se and SePP concentrations. No previous studies have created evidence for a positive correlation between infection risk and gestational age, and therefore the difference in age between the groups seems to be a random error (Table 2)(31). In this analysis, gestational age was significantly related to Se concentration (P=0·045, b=1·48, 95 % CI 0·038, 2·923). After controlling for gestational age, infection had a significant effect on concentrations of Se (P=0·027, b=−8·584, 95 % CI −16·143, −1·026) and SePPsqrt (P=0·045, b=−0·125, 95 % CI −0·247, −0·003). The univariate analysis with birth weight as a covariate and infection status as a fixed factor yielded a similarly strong significant relation to Se concentrations (P=0·031, b=−8·381, 95 % CI −0·796, −15·966), but failed to reach statistical significance for SePPsqrt concentrations (P=0·087, b=−0·109, 95 % CI −0·235, 0·017).
With respect to effects of therapy, Se concentrations were not significantly different between day of birth (day 1) and 48 h after initiation of treatment (day 3) (Fig. 4(a)). However, SePP concentrations increased significantly from day 1 to day 3 (Fig. 4(b)). There was a significant negative correlation between gentamicin and Se concentrations on day 3 (Fig. 4(c)). Western blot analysis was performed in order to verify the data obtained from ELISA and to test for differently migrating SePP isoforms (Fig. 4(e)). Measured SePP concentrations were congruent with the optical density of the SePP-specific Western blot bands, and no indications for additional SePP isoforms were noted.
Fig. 4 Analysis of selenium and selenoprotein P (SePP) concentrations in infected neonates on day 1 and day 3 of treatment. (a) Average selenium concentrations do not differ between the two time points. The relatively wide range of selenium concentrations observed on day 1 is diminished on day 3. (b) SePP is significantly (P<0·001) elevated in the samples from the treated newborns (day 3) as compared with treatment initiation (day 1). (c) The blood concentration of gentamicin correlates negatively with selenium concentrations on day 3 (d) In parallel, no such correlation is observed between SePP and gentamicin. (e) Immunoreactive SePP band density (SePP) was in agreement with the concentrations determined by ELISA (SePP-ELISA), and no indication for a shift in SePP isoform pattern was observed. The Western blot analysis of four infected neonates along with standards (low, medium and high SePP) and controls (control and an adult sample) is shown. * P<0·05, *** P<0·001.
The influence of infection on Se status was evident in the early stage (Fig. 5(a) and (b)). IL-6 levels were inversely correlated to both Se and SePP on day 1 in neonates with severe infection (IL-6>500 ng/l), whereas on day 3 there was no correlation between Se or SePP with CRP concentrations.
Fig. 5 Association of severe infection with biomarkers of selenium status. IL-6 is negatively associated with (a) selenium and (b) selenoprotein P (SePP) at birth (day 1) in neonates with severe infection (IL-6>500 ng/l). On day 3 (48 h after initiation of therapy), C-reactive protein (CRP) concentrations were neither associated with (c) selenium nor with (d) SePP. * P<0·05.
Discussion
Se deficiency is associated with increased mortality in adults in intensive care( Reference Forceville, Vitoux and Gauzit 10 , Reference Angstwurm, Engelmann and Zimmermann 11 , Reference Sakr, Reinhart and Bloos 32 ). Whether the same association holds in neonates is unknown. We decided to assess the Se status of newborns with and without infection as a first step towards a better understanding of this potential interaction in the first few days of life. We hypothesised that infection negatively affects hepatic selenoprotein biosynthesis as shown before in model systems( Reference Renko, Hofmann and Stoedter 5 , Reference Wang, Forceville and Van Antwerpen 33 ). Therefore, we aimed to determine the two important biomarkers of Se status – that is, total plasma Se and SePP concentrations.
The strong correlation observed between these two biomarkers indicates that both parameters are suitable for assessing Se status in neonates. It is well established that selenoprotein expression becomes saturated at sufficiently high Se intake, causing a disruption of the strong positive correlation between Se and SePP( Reference Hurst, Armah and Dainty 34 ). Consequently, our data indicate that the majority of neonates in our study were not sufficiently well supplied with Se for maximal selenoprotein expression. This is further substantiated by comparing the absolute concentrations in relation to adults; average Se and SePP concentrations of the neonates in our study at day 1 were 35·2 (sd 12·6) µg Se/l and 1·1 (sd 0·4) mg SePP/l, respectively, which corresponds to only 40 and 25 % of the concentrations found in adults, respectively, as, for example, determined in a recent large study of colorectal cancer risk in Europe( Reference Hughes, Fedirko and Jenab 30 ). Even German vegetarians, who are at high risk of Se deficiency, had about 2-fold higher Se concentrations as compared with the neonates in this study( Reference Hoeflich, Hollenbach and Behrends 35 ). Similarly, the reference value determined in Swiss and German infants <1 month of age lies at 0·64 µm-Se (corresponding to 50·6 µg/l), again 1·4 times above the average of the neonates in our study( Reference Loui, Raab and Braetter 37 ).
Thus, the relatively low average plasma Se concentrations determined in both groups of neonates may reflect that many of the enrolled infants were very premature and in a postnatal phase in which Se status may still increase continuously with each day of life. Moreover, we observed that preterm infants have significantly lower SePP levels than term infants. This notion is in agreement with similar findings of Se concentrations in other studies( Reference Iranpour, Zandian and Mohammadizadeh 36 – Reference Sievers, Arpe and Schleyerbach 38 ). The underlying reason for higher plasma SePP in term as compared with preterm neonates is unknown, but may be related to the maturation of the hepatic selenoprotein biosynthesis machinery during development, to an increasing generation of a hepatic Se store until delivery or to changes in intestinal absorption and chorionic villi function as hypothesised in a recent meta-analysis on Se deficiency in preterm infants( Reference Freitas, Nogueira and Antonio 39 ).
The univariate analysis with gestational age as a covariate revealed a significant effect of an infection on both Se and SePP concentrations, supporting the hypothesis that the Se status of neonates declines during infection. Whether a reduced Se status has a negative impact on the severity, duration of stay in the intensive care unit or treatment success of neonatal infection needs to be examined in future studies.
As we were not able to analyse blood from healthy neonates, for ethical reasons, we determined whether there is an association of clinical markers of infection with Se status. An inverse relationship was observed when comparing Se and SePP levels with IL-6 concentrations (Fig. 5(a) and (b)). In particular, two infants with very high levels of IL-6 at birth (13 690, 5247 pg/ml) displayed very low concentrations of Se (11·7, 15·7 µg/l) and SePP (0·27, 0·91 mg/l). This finding is in agreement with our recent analysis on the impact and importance of IL-6 for hepatic SePP biosynthesis and secretion( Reference Martitz, Becker and Renko 40 ).
Previous studies have shown that both biomarkers – that is, total Se and SePP – are suitable to determine a Se-deficient state, whereas only total Se assessment appears suitable to detect Se intoxication( Reference Combs 41 ). The positive and almost linear correlation of both biomarkers observed in countries with marginal intake suggests that it may make no difference if measuring one or the other in order to assess Se status. In this respect, neonates were already showing the same strong association as known from healthy or diseased adults in Se-deficient populations( Reference Burk and Hill 42 ). Yet, our two recent large-scale studies on the influence of Se status on bone turnover in healthy postmenopausal women( Reference Hoeg, Gogakos and Murphy 43 ) and on colorectal cancer risk in European adults( Reference Hughes, Fedirko and Jenab 30 ) both indicated that the interactions of Se status and clinical parameters are in general stronger for SePP than for total Se. This may be because of the role of SePP as the major determinant of plasma Se concentrations and its transport function in blood, being specifically recognised and taken up by receptors on target cells as the peripherally bioavailable fraction of Se in blood( Reference Olson, Winfrey and Hill 44 , Reference Olson, Winfrey and Nagdas 45 ).
In addition to the differences between the control and infection groups, we found a significant difference between day 1 and day 3 in SePP concentrations. The antibiotic treatment successfully corrected the severe Se and SePP deficiency of the newborns with highest IL-6 concentrations and lowest Se status. During this time period, SePP concentrations increased significantly, whereas total Se concentrations remained unchanged. This difference may indicate an improved rate of SePP biosynthesis in hepatocytes and a more efficient anabolic usage of circulating Se forms during therapy, again highlighting SePP as the probably more suitable and sensitive biomarker under these conditions. The biosynthesis of Se-poor SePP isoforms terminating before the Se-rich protein domain may provide an alternative explanation( Reference Kurokawa, Bellinger and Hill 46 ). Similarly, a more efficient selenoprotein biosynthesis read-through due to the effects of the aminoglycoside treatment on ribosomal amino acid insertion may have caused increasing SePP concentrations during therapy, as described before in in vitro studies for selenoproteins glutathione peroxidase 1( Reference Handy, Hang and Scolaro 47 ) and SePP( Reference Becker, Martitz and Renko 6 ). Notably, under aminoglycoside exposure, the error rate of UGA (stop-codon) decoding increases strongly, giving rise to inactive and Se-deprived selenoprotein variants, as convincingly shown in breast cancer cells by Tobe et al. ( Reference Tobe, Naranjo-Suarez and Everley 48 ) using a combination of radioactive labelling, protein and activity analyses as well as MS.
This hypothesis is supported by our data on the relation of Se and SePP after gentamicin treatment. If gentamicin causes increased read-through at UGA stop codons, yielding Se-poor SePP variants as a consequence of amino acid mis-incorporation, then plasma Se concentrations should negatively correlate with the gentamicin level (Fig. 4(c)), without leading to a similar effect on plasma SePP concentrations, which may under such conditions reflect both full-length Se-rich and Se-poor SePP variants (Fig. 4(d)). This hypothesis should be tested in future studies with respect to the Se content of circulating SePP, which will likely be only possible with adult patients under aminoglycoside therapy, because of the high demand for serum or plasma volume. Under these conditions, we found no indications in our Western blot analyses that different or shorter SePP isoforms were generated. The amount of full-size SePP increased in most of the neonates from day 1 to day 3 in agreement with ELISA results. This increase may be due to an improved control of the inflammatory cytokines during therapy, and may have resulted from the above-mentioned stimulation of selenoprotein biosynthesis by the aminoglycosides. Alternatively, or in addition to the effects described, the antibiotic may have affected the composition of the intestinal microflora, which has been shown in a mouse model to affect Se availability to the host and hepatic selenoprotein biosynthesis( Reference Kasaikina, Kravtsova and Lee 49 ). From a therapeutic point of view, the bioavailabilities of SePP being synthesised in the presence or absence of aminoglycosides need to be compared, in order to determine whether Se transport becomes impaired under gentamicin therapy.
The low sample requirement in combination with the ease and speed of immunological detection may favour SePP assessment over total Se determination as the preferred method of analysis in infected subjects in future studies. Especially in neonates, only minute amounts of plasma are usually available and highly sensitive techniques are needed. If a fast and reliable bedside test for SePP quantification could be established, it would allow the identification of severely Se-deficient neonates already during intensive care unit admission and a fast initiation of measures for correcting a potential Se deficit. Luckily, all neonates included in our study survived the connatal infection. Nevertheless, a severe Se deficiency needs to be considered as a relevant mortality risk factor, and Se supplementation may have beneficial effects in severely diseased neonates as documented in some but not all respective studies with adult patients( Reference Leite, Nogueira and de Oliveira Iglesias 13 , Reference Alhazzani, Jacobi and Sindi 50 – Reference Kong, Wang and Ji 53 ). Alternatively, the Se status of the mothers may be adjusted for avoiding Se deficiency during pregnancy. Such measures would not only be of likely advantage to the unborn child but may also reduce the risks of adverse pregnancy outcomes( Reference Mariath, Bergamaschi and Rondo 54 ). Therefore, this direction of research needs to be continued, as reducing child mortality is among the millennium goals( Reference Lozano, Wang and Foreman 55 ). We hope that our study contributes to this challenge and supports the initiation of more focused studies on the health importance of Se in connatal infections for the sake of the most vulnerable patients.
Acknowledgements
The authors express the gratitude to all parents and children who took part in this study, and to the clinical colleagues taking care of the patients in the Department of Neonatology, Charité – Universitätsmedizin Berlin, Campus Virchow-Klinikum, Germany.
This work was supported by Deutsche Forschungsgemeinschaft (DFG) grants RE3038/1–1 (to K. R.) and Scho849/4–1 (to L. S.), and an Elsa-Neumann stipend from the City of Berlin (to J. M.).
L. W., M. C., M. W., N.-P. B., C. B. and L. S. formulated the research question and designed the study. L. W., M. W., N.-P. B., E. R., J. M., S. H. and K. R. conducted the experimental analyses; all authors contributed to the statistical analysis and interpretation of the data. All authors contributed to writing and editing the manuscript.
None of the authors has any conflicts of interest to disclose.
