Biology subjects

Ouattara, A.

Publications and source records attributed to Ouattara, A..

3 recordsLinked to original sources

bioRxiv2026

Ecological dynamics and stability in the Taï and Comoe national parks in Cote dIvoire

The accelerated loss of biodiversity in sub-Saharan Africa threatens the functioning of tropical ecosystems. In Cote dIvoire, the Comoe National Park (PNCOMOE), a Sudano-Guinean savannah, and the Tai National Park (PNTAI), a dense rainforest, both UNESCO World Heritage Sites, are home to fauna assemblages of global importance, whose long-term resilience remains insufficiently quantified. This study assesses and compares, over a decade (2014-2025), the functional stability of vertebrate communities in these two contrasting ecosystems, using nine metrics covering resistance, invariance, persistence, interspecific synchrony, Tilmans stability, Jacobian resilience and a Composite Stability Index (CSI). Abundance data for 107 vertebrate species were collected via foot transects at PNTAI and aerial surveys at PNCOMOE. The stability metrics were calculated using the R package estar, integrated with an alpha diversity analysis (Shannon H', species richness S, Pielous evenness J') and a Jacobian spectral analysis within a multidimensional ecological assessment. PNTAI (0.708) exhibits significantly higher alpha diversity (H' = 2.82; S = 55.7 taxa) and community resilience 4.6 times higher than in the PNCOMOE (0.153). Its interspecific asynchrony index (0.504) reveals a strong portfolio effect, absent in the PNCOMOE (0.232). In contrast, PNCOMOE exhibits higher temporal invariance (0.382 versus 0.116) and Tilman stability (0.276 versus 0.152), reflecting more predictable dynamics. The overall ICS favours the PNTAI (0.484) and (0.370). The Jacobian analysis detects local instability in both parks (Re({lambda}max) = 5.58 at the PNTAI; 3.73 at the PNCOMOE). The two parks exhibit distinct yet complementary stability architectures: PNTAI relies on dynamic stability based on resilience and interspecific compensation, whilst PNCOMOE demonstrates conservative stability through temporal regularity. The absence of calculable resilience at PNCOMOE suggests a potential crossing of a functional degradation threshold, arguing for urgent restoration interventions and differentiated conservation strategies, tailored to the resilience mechanisms specific to each ecosystem.

ecology↗

bioRxiv2026

Molecular and spatial profiling identifies immune endotypes for the stratification of OA patients

Osteoarthritis (OA) is a prevalent and heterogeneous joint disease in which synovial inflammation drives structural progression and pain. Despite the recognized heterogeneity of OA, the cellular and molecular organization of synovial tissue remains poorly characterized and defining distinct histological and immune endotypes could guide precision medicine and therapeutic targeting. We show that histologically defined synovial pathotypes are conserved across independent cohorts and correspond to distinct molecular immune endotypes. Integration of bulk and spatial transcriptomics with proteomics revealed niche-specific gene and protein signatures, reflecting the anatomical and functional diversity of OA synovium. The lympho-myeloid pathotype was characterized by mature ectopic lymphoid structures containing CD21+CD23+ follicular dendritic cells, spatially organized T and B cell zones, and clonally expanded T and B cells with shared immune cell receptor motifs, consistent with local adaptive immune activity correlating with radiological joint damage. These findings highlight how immune organization and cellular composition shape OA pathogenesis and provide a framework for endotype-guided stratification and therapeutic targeting.

immunology↗

bioRxiv2019

Strains used in whole organism Plasmodium falciparum vaccine trials differ in genome structure, sequence, and immunogenic potential

BackgroundPlasmodium falciparum (Pf) whole-organism sporozoite vaccines have provided excellent protection against controlled human malaria infection (CHMI) and naturally transmitted heterogeneous Pf in the field. Initial CHMI studies showed significantly higher durable protection against homologous than heterologous strains, suggesting the presence of strain-specific vaccine-induced protection. However, interpretation of these results and understanding of their relevance to vaccine efficacy (VE) have been hampered by the lack of knowledge on genetic differences between vaccine and CHMI strains, and how these strains are related to parasites in malaria endemic regions.\n\nMethodsWhole genome sequencing using long-read (Pacific Biosciences) and short-read (Illumina) sequencing platforms was conducted to generate de novo genome assemblies for the vaccine strain, NF54, and for strains used in heterologous CHMI (7G8 from Brazil, NF166.C8 from Guinea, and NF135.C10 from Cambodia). The assemblies were used to characterize sequence polymorphisms and structural variants in each strain relative to the reference Pf 3D7 (a clone of NF54) genome. Strains were compared to each other and to clinical isolates from South America, Sub-Saharan Africa, and Southeast Asia.\n\nResultsWhile few variants were detected between 3D7 and NF54, we identified tens of thousands of variants between NF54 and the three heterologous strains both genome-wide and within regulatory and immunologically important regions, including in pre-erythrocytic antigens that may be key for sporozoite vaccine-induced protection. Additionally, these variants directly contribute to diversity in immunologically important regions of the genomes as detected through in silico CD8+ T cell epitope predictions. Of all heterologous strains, NF135.C10 consistently had the highest number of unique predicted epitope sequences when compared to NF54, while NF166.C8 had the lowest. Comparison to global clinical isolates revealed that these four strains are representative of their geographic region of origin despite long-term culture adaptation; of note, NF135.C10 is from an admixed population, and not part of recently-formed drug resistant subpopulations present in the Greater Mekong Sub-region.\n\nConclusionsThese results are assisting the interpretation of VE of whole-organism vaccines against homologous and heterologous CHMI, and may be useful in informing the choice of strains for inclusion in region-specific or multi-strain vaccines.

genomics↗