Biology subjects

Bahrami, R.

Publications and source records attributed to Bahrami, R..

4 recordsLinked to original sources

bioRxiv2026

Microbiota-driven, strain-specific Asaia colonisation modulates mosquito vector competence

Microbiota-based mosquito control strategies are founded on the ability of bacterial symbionts to modify host biology and/or pathogen transmission. However, symbionts do not operate in isolation. Their colonisation, persistence and biological effects arise within a complex ecological network comprising the host and its resident microbiota. We hypothesized that colonisation success is not only an intrinsic property of a bacterial symbiont but emerges from interactions between bacterial strain, host background, and the native microbial community. To test this, we compared recolonisation by endogenous and exogenous Asaia strains in the invasive mosquito Aedes koreicus using wild-type and axenic mosquitoes to experimentally manipulate the microbial composition. We found that endogenous and exogenous strains followed distinct colonisation trajectories. Depletion of the resident microbiota selectively rescued colonisation by the endogenous strain, whereas both strains successfully disseminated to transmission-relevant tissues despite contrasting early gut dynamics. Furthermore, these strain-specific colonisation dynamics were associated with increased Semliki Forest virus (SFV) transmission and enhanced adult longevity, particularly following colonisation by the exogenous strain. Our findings indicate that resident microbial communities act as selective ecological filters that shape symbiont colonisation in a strain-dependent manner. More broadly, this study demonstrates that the biological effects of mosquito symbionts emerge from interactions between bacterial strains and the microbial community context, providing an ecological framework for the rational and effective development of microbiota-based vector control strategies.

microbiology↗

bioRxiv2026

Evidence of thermal selection from experimental evolution in the arboviral vector Aedes albopictus

The extent to which phenotypic plasticity and adaptation are coupled during ectotherm thermal evolution is poorly understood. We carried out thermal experimental evolution for 20 generations in the arboviral vector Aedes albopictus, an efficient invasive species that has newly conquered climatically diverse regions in the past few decades. During acclimation (one generation of evolution) we saw accelerated development and increased reproduction that traded off against survival. After only another 10 generations, we saw adaptation in the form of major changes in mosquito fitness, metabolism and gene expression, revealing the consolidation of a temperature-dependent trade-off between reproduction and longevity. These shifts demonstrate that Ae. albopictuscan adapt at the pace of warming. When selection was relaxed, most of the thermally shifted phenotypes reverted to control levels, revealing the importance of plasticity after prolonged evolution. Furthermore, 250 warm evolution-altered genes did not return to control levels. These genes exhibited significant negative correlation between mean and variance in warm-evolved mosquitoes, but a two-fold variance reduction without mean change in relaxed-selection mosquitoes. Both signals are consistent with the action of selection operating on a polygenic trait architecture. Ecological modelling identified egg-to-adult viability as the primary driver of thermal reproductive success, highlighting juvenile stages as a crucial control target under continued warming.

evolutionary biology↗

bioRxiv2026

Thermal responses of an emerging temperate mosquito reshape arboviral transmission risk

Global warming is known to increase arboviral disease risk by enabling the expansion of tropical vectors such as Aedes aegypti and Aedes albopictus. However, whether climate-driven shifts in seasonal dynamics within temperate regions, such as warmer springs and shorter winters, create thermal settings favourable for additional vectors, which can reshape disease risk maps, is poorly understood. To answer this question, we used the invasive temperate mosquito species Aedes koreicus and tested its thermal developmental resilience, along with its vector competence for dengue and chikungunya viruses. We observed significant phenotypic variation in thermal tolerance across life stages, which translates into distinct thermal performance curves for life-history traits, ultimately shaping overall mosquito fitness. We further found that temperature effects are virus-specific, with differential impacts on infection and transmission between dengue and chikungunya viruses. These stage- and pathogen-specific responses generate carry-over effects across life stages, indicating that thermal responses may be constrained by life-history trade-offs rather than be defined by a single thermal optimum. Our results highlight the need to move beyond static, species-based risk assessments toward mechanistic frameworks that integrate thermal biology across life stages and vector-pathogen systems. As climate change increasingly reshapes seasonal structure rather than simply elevating mean temperatures, cold-adapted and temperate vectors such as Ae. koreicus, provide critical model systems to understand how transmission risk emerges outside mosquito classical thermal optima, calling for a broader paradigm shift in how global change and vector-borne disease risk are conceptualised.

ecology↗

bioRxiv2023

Population-specific responses to developmental temperature in the arboviral vector : implications for climate change

The increase of environmental temperature due to current global warming is not only favoring the expansion of the distribution range of many insect species, but it is also changing their phenology. Insect phenology is tightly linked to developmental timing, which is regulated by environmental temperatures. However, the degree to which effects of developmental temperatures extend across developmental stages and their inter-stage relationships have not been thoroughly quantified in mosquitoes. Here, we used the mosquito Aedes albopictus, which is an aggressive invasive species and an arboviral vector to study how developmental temperature influences fitness across developmental stages, thermal traits, energy reserves, transcriptome, and Wolbachia prevalence in populations from either temperate or tropical regions. We show that hatchability, larval and pupal viability, and developmental speed are strongly influenced by temperature and these effects extend to wing length, body mass, longevity, content of water, protein and lipids in adults, in a population-specific manner. On the contrary, neither adult thermal preference nor heat resistance significantly change with temperature. Development at 18{degrees}C revealed to be a limiting factor for the proliferation of Wolbachia in adults and transcriptome analysis showed enrichment for functions linked to stress responses (i.e. cuticle proteins and chitin, cytochrome p450, and heat shock proteins) in mosquitoes reared at both 18{degrees}C and 32{degrees}C. Our data showed an overall reduced vector fitness performance when mosquitoes were reared at 32{degrees}C, and the absence of isomorphy in the relationship between developmental stages and temperature in the temperate population. Altogether these results have important implications for reliable model projections of the invasion potentials of Ae. albopictus and its epidemiological impact.

ecology↗