BUSCADOR RECOLECTA

BC cluster rotation in control (tslGFP; mirrGal4) and EHBP1mCh overexpressing (tslGFP; mirr>EHBP1mCh) egg chambers, related to Fig 3. Scale bar, 10 μm., Peer reviewed

Peer reviewed

Current clinical guidelines support the concomitant administration of seasonal influenza vaccines and COVID-19 mRNA boosters vaccine. Whether dual vaccination may impact vaccine immunogenicity due to an interference between influenza or SARS-CoV-2 antigens is unknown. We aimed to understand the impact of mRNA COVID-19 vaccines administered concomitantly on the immune response to influenza vaccines. For this, 128 volunteers were vaccinated during the 22-23 influenza season. Three groups of vaccination were assembled: FLU vaccine only (46, 35%) versus volunteers that received the mRNA bivalent COVID-19 vaccines concomitantly to seasonal influenza vaccines, FluCOVID vaccine in the same arm (42, 33%) or different arm (40, 31%), respectively. Sera and whole blood were obtained the day of vaccination, +7, and +28 days after for antibody and T cells response quantification. As expected, side effects were increased in individuals who received the FluCOVID vaccine as compared to FLU vaccine only based on the known reactogenicity of mRNA vaccines. In general, antibody levels were high at 4 weeks post-vaccination and differences were found only for the H3N2 virus when administered in different arms compared to the other groups at day 28 post-vaccination. Additionally, our data showed that subjects that received the FluCOVID vaccine in different arm tended to have better antibody induction than those receiving FLU vaccines for H3N2 virus in the absence of pre-existing immunity. Furthermore, no notable differences in the influenza-specific cellular immune response were found for any of the vaccination groups. Our data supports the concomitant administration of seasonal influenza and mRNA COVID-19 vaccines., This work was supported by American Lung Association: [COVID-1034091]. Centro de Investigación Biomedica en Red de Enfermedades Infecciosas, CIBERINFEC, Instituto de Salud Carlos III, Ministerio de Ciencia e Innovacion and Union Europea – NextGeneration EU (Grant Number CB21/13/00006); Consejeria de Economia, Conocimiento, Empresas y Universidad, Secretaria General de Universidades, Investigacion y Tecnologia, Junta de Andalucia, Spain (P18-RT-3320). SEM-CIVIC National Institute of Allergy and Infectious Diseases: [Grant Number 75N93019C00051]. CEIRR-CRIPT: [75N93021C00014]., Peer reviewed

BC migration in tslGFP; mirrGal4 and tslGFP; mirr>EHBP1mCh egg chambers. tslGFP is in green and EHBP1mCh in red, related to Fig 2. Scale bar, 20 μm., Peer reviewed

Appendix S1-S5 and References., Peer reviewed

BC migration in tslGFP; tjGal4 and tslGFP; tj>EHBP1mCh egg chambers, related to S3 Fig. tslGFP is in green and EHBP1mCh in red, related to S4 Fig. Scale bar, 20 μm., Peer reviewed

Supplementary Tables (S1-S6) and Figures (S1-S3)., Peer reviewed

Migration of control (C306; slbo; tslGFPGal4) and LanB1RNAi expressing BCs (C306;slbo;tsl;GFP>LanB1 RNAi), related to S3 Fig. Scale bar, 20 μm., Peer reviewed

datasheet.xlsx Data used in the analyses, consists on two sheets: - boxplotindices: data with stability, synchrony and richness values for each plot or community, the approach used to calculate each index (long-term or year-to-year), and the treatment applied in each plot (control or fertilized). - matrixalldatacom: data used to carry out the analyses at the community level. For each community it is given: the number of the plot or community, stability, synchrony, richness, functional composition and diversity of the five traits studied, and treatment (control or fertilized). For each of these variables there are two columns, one with the variable calculated using the long-term approach (named "longterm_" or "cum_") and the other one for the variable calculated using the year-to-year approach (named "yeartoyear_" or "mean_"). - matrixalldataspp: data used to carry out the analyses at the species level. For each species it is given: species name, long-term and year-to-year stability, species values for the five traits studied, and treatment (control or fertilized). Missing values are indicated by NAs., Understanding the mechanisms underlying community stability has become an urgent need in order to protect ecosystems from global change and resulting biodiversity loss. While community stability can be influenced by richness, synchrony in annual fluctuations of species, species stability and functional traits, the relative contributions of these drivers to stability are still unclear. In semi-natural grasslands, land-use changes such as fertilization might affect stability by decreasing richness and influencing year-to-year fluctuations. In addition, they can promote long-term directional trends, shifting community composition and influencing grassland maintenance. Thus, it is important to consider how species and community stability vary year-to-year but also in the long term. Using a 14-year vegetation time series of a species-rich semi-natural Mediterranean grassland, we studied the relative importance of richness, synchrony, species stability and functional traits on community stability. To assess land-use change effects on stability, we applied a fertilization treatment. To distinguish stability patterns produced by year-to-year fluctuations from those caused by long-term trends, we compared the results obtained using a detrending approach from those without detrending. Stability is influenced by richness, synchrony and functional traits. Fertilization decreases species and community stability by promoting long-term trends in species composition, favouring competitive species and decreasing richness. Studying stability at the community and species level, and accounting for the effect of trends is essential to understand stability and its drivers more comprehensively., [Methods] Study site and experimental design: In 2003, 12 plots of 15x5 m (hereafter called macro-plots) were established inside an area of 5500 m2. Half of the macro-plots (six) were used as control plots and half were fertilized with sewage sludge in a single event in 2003, applying manually to the soil surface 5 kg m-2 . The sludge came from a municipal urban wastewater treatment plant located in Tudela (Navarra, Spain), and it was sludge previously dried to 28% dry matter by centrifugation. To accurately assess vegetation changes, a 1x1 m permanent plot was placed in the centre of each macro-plot. Every year for 14 consecutive years (from 2004 to 2017), at the end of June, vegetation was sampled by R. Ibáñez, who identified and recorded every vascular plant species present in each of the permanent plots. The 1x1 m permanent plots were divided into 100 10x10 cm subplots to measure species abundance (frequency) by counting the number of 10x10 cm subplots in which the species was present (presence was recorded if shoots overlapped with the sampling unit/subplot, not according to rooted plants). Richness, synchrony and stability measures: Species richness in each permanent plot was measured both as cumulative species richness, counting the number of species found at least once in a permanent plot during the 14 years of the study, and as mean species richness, averaging the number of species found in a permanent plot over the 14 years (Lepš et al., 2018). Community-level synchrony for each permanent plot was calculated using the log variance ratio index (“Logvar”), which is the log-transformation of the ratio of observed to expected variance (i.e. the ratio of variance of the total community abundance to the sum of variances of the abundance of each species; Lepš et al., 2018; Roscher et al., 2011). Stability at both the community and the species level was calculated as the inverse of the coefficient of variation (CV-1) across years of cumulative or individual species abundances in each permanent plot. In order to distinguish the patterns produced by long-term trends from those caused by year-to-year fluctuations, we also used the three-term local quadrat variance detrending method (T3; Hill, 1973), which consists in calculating the variance in three year time periods, to remove the effect of long-term trends both on synchrony and stability indices (Lepš, Götzenberger, et al., 2019). Thus, we calculated synchrony (log variance ratio) and stability (CV-1) indices using both the non-detrending (hereafter “long-term” synchrony and stability) and the T3-detrending approach (hereafter “year-to-year” synchrony and stability; for which the original variance used in the log variance ratio index or in the inverse of the coefficient of variation was replaced by the three-term local-quadrat variance) (Valencia, de Bello, Lepš, et al., 2020). All synchrony and stability indices were calculated using the calc_sync function of the package “tempo” in R (Lepš, Götzenberger, et al., 2019). Plant functional traits and indices: We obtained data for five functional traits (plant height, Leaf Dry Matter Content or LDMC, Specific Leaf Area or SLA, Leaf Area or LA and Seed Mass or SM) for most of the species present in the 1x1 m permanent plots (data available for 98%, 78%, 84%, 98% and 85% of the species, respectively). Trait data were collected in-situ. Although the number of individuals measured for each trait varied, traits were measured following the protocols provided by Cornelissen et al. (2003). Missing data were obtained from BROT, a trait database for Mediterranean Basin species (Tavşanoğlu & Pausas, 2018), or from TRY database (Kattge et al., 2020). Mean trait values and abundance data for each species were used to calculate community functional composition and functional diversity for the five traits studied. Functional composition was measured as the Community Weighted Mean (CWM; Garnier et al., 2004) and functional diversity as the Rao Quadratic Index (Rao, 1982), which is the sum of pairwise functional distances between species weighted by relative abundance (Mouchet et al., 2010). To calculate these indices, we used the function dbFD of the “FD” package in R (Laliberté & Legendre, 2010; Laliberté et al., 2014). Data analysis: To study how fertilization influenced stability, synchrony and species richness at the community level, and to test if the values displayed by these indices and their response to fertilization changed depending on the approach used to calculate them (e.g. long-term or year-to-year), we carried out three multiple linear regression models using as response variables the stability, synchrony or species richness index in each plot, respectively. As explanatory variables we used the treatment applied in each plot (i.e. control or fertilized), the approach used to calculate the index (i.e. long-term or year-to-year stability and synchrony, and cumulative or mean species richness), and the interaction between both. In order to discover the main drivers of community stability, we used different linear regression models to test for relationships between community stability (long-term and year-to-year) and synchrony, richness, functional composition and diversity of the five traits studied and treatment. The explanatory variables were calculated in different ways depending on if we studied long-term or year-to-year stability, so that the variables would as well reflect “accumulated” or “yearly” values. For long-term stability we used long-term synchrony and cumulative species richness, and the functional composition and diversity indices were calculated using the cumulative abundance of each species across all years. By contrast, for year-to-year stability we used year-to-year synchrony and mean species richness across years, and the functional composition and diversity were calculated separately for each plot and year and then averaged across all years. This way, the first type of models was more focused on detecting processes acting across years and promoting trends, while the second type was focused on year-to-year processes. We build linear regression models by first running simple regression models for each explanatory variable and then applied multiple regression models with synchrony, richness, treatment and the functional indices selected as significant or marginally significant in the simple models. We then studied stability at the species level. Species stability was averaged over control and over fertilized plots. As we found some extreme values corresponding to highly stable species (Brachypodium retusum (Pers.) P.Beauv. and Aphyllanthes monspeliensis L.), we log transformed average species stability. We tested for relationships between log-transformed species stability (long-term and year-to-year) and the five functional traits studied. We first used simple models for each trait and when a certain trait was significant we did multiple models using trait, treatment and the interaction between both as explanatory variables. On the other hand, we also studied how fertilization influenced species stability, checking if results changed when using the long-term or year-to-year approach. We calculated the Pearson’s correlation coefficient and applied a paired t-test to test for differences in species stability between control and fertilized plots and between the long-term and year-to-year approach. All analyses were carried out with the lm, cor.test and t.test functions in R software (v. 4.0.3; R Core Team, 2020)., Fundación Caja Navarra, Award: Ref. 10833 (Programa “Tú Eliges, Tú Decides”), University of Navarra, Award: Project “Biodiversity Data Analytics and Environmental Quality”, University of Navarra, Award: Project “Red de Observatorios de la Biodiversidad de Navarra (ROBIN)”, Departamento de Educación, Award: Ayudas predoctorales para la realización de programas de doctorado de interés para Navarra; Plan de Formación y de I+D 2018, Ministerio de Ciencia e Innovación, Award: Ref. RTI2018-096884-B-C31 (Project FORMAL), Czech Academy of Sciences, Award: No. RVO 67985939, Peer reviewed

BC migration in control (tslGFP; tjGal4) and laminin (tslGFP; tj>LanB1RNAi, tslGFP; Lanb1hyp) or Col IV (tslGFP;tj>Col IV RNAi)-depleted egg chambers, related to Fig 1. Scale bar, 20 μm., Peer reviewed