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Members of the genus Lysinibacillus attract attention for their mosquitocidal, bioremediation, and plant growth-promoting abilities. Despite this interest, comprehensive studies focusing on genomic traits governing plant growth and stress resilience in this genus using whole-genome sequencing are still scarce. Therefore, we sequenced and compared the genomes of three endophytic Lysinibacillus irui strains isolated from Canary Island date palms with the ex-type strain IRB4-01. Overall, the genomes of these strains consist of a circular chromosome with an average size of 4.6 Mb and a GC content of 37.2%. Comparative analysis identified conserved gene clusters within the core genome involved in iron acquisition, phosphate solubilization, indole-3-acetic acid biosynthesis, and volatile compounds. In addition, genome analysis revealed the presence of genes encoding carbohydrate-active enzymes, and proteins that confer resistance to oxidative, osmotic, and salinity stresses. Furthermore, pathways of putative novel bacteriocins were identified in all genomes. This illustrates possible common plant growth-promoting traits shared among all strains of L. irui. Our findings highlight a rich repertoire of genes associated with plant lifestyles, suggesting significant potential for developing inoculants to enhance plant growth and resilience. This study is the first to provide insights into the overall genomic signatures and mechanisms of plant growth promotion and biocontrol in the genus Lysinibacillus. Key points: • Pioneer study in elucidating plant growth promoting in L. irui through comparative genomics. • Genome mining identified biosynthetic pathways of putative novel bacteriocins. • Future research directions to develop L. irui-based biofertilizers for sustainable agriculture. [ABSTRACT FROM AUTHOR]

Objective: Women with psoriatic arthritis (PsA) may have reduced tumor necrosis factor inhibitor (TNFi) effectiveness compared to men. We examined sex differences in treatment response and retention rates during 24 months of follow‐up among patients with PsA initiating their first TNFi. Methods: Data from patients with PsA across 13 European Spondyloarthritis Research Collaboration Network registries starting their first TNFi were pooled. Logistic regression was used to analyze the association between sex and treatment response using low disease activity (LDA) according to the Disease Activity Score in 28 joints using the C‐reactive protein level (DAS28‐CRP) (<3.2) at six months as the primary outcome. Analyses were adjusted for age, country, conventional synthetic disease‐modifying antirheumatic drug treatment, and TNFi start year. Retention rates were explored using the Kaplan–Meier estimator. Results: We analyzed the treatment response of 7,679 patients with PsA (50% women) with available data on LDA at six months. At baseline, women and men had similar characteristics, including mean DAS28‐CRP (women vs men, 4.4 [SD 1.2] vs 4.2 [SD 1.2]), though patient‐reported outcome measures were worse in women. At six months, 64% of women and 78% of men had LDA (relative risk [RR] 0.82; 95% confidence interval [CI] 0.80–0.84). This difference was similar after adjustment (RR 0.83; 95% CI 0.81–0.85). TNFi retention rates were evaluated in 17,842 patients with PsA. Women had significantly lower retention rates than men at all time points (women 79%, 64%, and 50% vs men 88%, 77%, and 64% at 6, 12, and 24 months, respectively). Conclusion: Despite comparable disease characteristics at baseline, women with PsA have reduced treatment response and retention rates to their first TNFi, highlighting the need to consider sex differences in PsA research and management. [ABSTRACT FROM AUTHOR]

Protected Areas (PAs) are important wildlife refuges and act as climate change buffers, but they may impact human livelihoods, particularly engendering a high risk of negative human-wildlife interactions (HWI). Understanding synergies and tradeoffs among the drivers of overall human vulnerability within PAs is needed to ensure good outcomes for conservation and human wellbeing. We examined how climate variability, HWI, and socio-demographics affect livelihood vulnerability across three PAs in Mozambique, Southeast Africa. We used structured questionnaires to obtain information on livelihood vulnerability and socialecological context-specific variables. We applied principal component analysis to understand synergies and trade-offs between the dimensions of vulnerability and linear models to test the effect of social-ecological drivers on vulnerability. We show that households are mostly vulnerable within PAs due to exposure to climate variability and to HWI, and their low capacity to employ livelihood strategies or to have a strong social network. Furthermore, we show that vulnerability to HWI and climate variability increases with distance to strict protection areas within the PAs and distance to rivers, which implies that proximity to strict protection areas and rivers within PAs still promotes better livelihood conditions than elsewhere. On the other hand, we also found that lower access to infrastructure and other livelihood assets enhances vulnerability, which reflects a trade-off within PAs that potentially limits the benefits of socially inclusive conservation. Our results show that the impacts of PAs, HWI, and climate on community vulnerability should not be viewed in isolation, but instead, conservation and livelihood improvement strategies should reflect their interconnectedness. Although livelihood vulnerability appears to be shaped by these general effects of PAs, it is important also to consider the local PA context when addressing or mitigating livelihood vulnerability in and around them [ABSTRACT FROM AUTHOR]

• Many patients are still treated with glucocorticoids when they are starting a TNF-inhibitor, abatacept or tocilizumab for rheumatoid arthritis. • All these bDMARDs were associated with a decrease in the use of glucocorticoid over time. • No bDMARD was superior to another when looking at glucocorticoid discontinuation. • Tapering of glucocorticoids occurs at a much slower rate compared to what is recommended by current international guidelines. To evaluate and compare the use of oral glucocorticoids with three classes of bDMARDs in patients with rheumatoid arthritis (RA). We included patients from 13 observational registries treated with a TNF-inhibitor, abatacept or tocilizumab and with available information on the use of oral glucocorticoids. The main outcome was oral glucocorticoid withdrawal. A McNemar test was used to analyse the change in the use of glucocorticoids after 1 year. Kaplan-Meier estimates and Cox regressions, adjusted for patient, treatment, and disease characteristics, were used to evaluate glucocorticoid discontinuation in patients with glucocorticoids at baseline. Because of heterogeneity, analyses were done by registers and pooled using random-effects meta-analysis. A total of 12,334 participants treated with TNF-inhibitors, 2100 with tocilizumab and 3229 with abatacept were included. At one-year, oral glucocorticoid use decreased in all treatment groups (odds ratio for stopping vs. starting of 2.19 [95% CI 1.58; 3.04] for TNF-inhibitors, 2.46 [1.39; 4.35] for tocilizumab; 1.73 [1.25; 2.21] for abatacept). Median time to glucocorticoid withdrawal was ≈2 years or more in most countries, with a gradual decrease over time. Compared to TNF-inhibitors, crude hazard ratios of glucocorticoid discontinuation were 0.65[0.48–0.87] for abatacept, and 1.04 [0.76–1.43] for tocilizumab, and adjusted hazard ratios were 1.1 [0.83–1.47] for abatacept, and 1.30 [0.96–1.78] for tocilizumab. After initiation of a bDMARD, glucocorticoid use decreased similarly in all treatment groups. However, glucocorticoid withdrawal was much slower than advocated by current international guidelines. More effort should be devoted to glucocorticoid tapering when low disease activity is achieved. [ABSTRACT FROM AUTHOR]