Price Donald K, West Kristian, Cevallos-Zea Michelle, Cahan Sara Helms, Nunez Joaquin C B, Longman Emily K, Yew Joanne Y, Mederios Matthew J
School of Life Sciences, University of Nevada, 4505 S. Maryland Pkwy, Las Vegas, NV 89154. USA.
Dept. of Biology, University of Vermont, Burlington, VT 05405. USA.
bioRxiv. 2025 Jun 7:2025.06.03.657679. doi: 10.1101/2025.06.03.657679.
Hawaiian picture-winged are undergoing rapid biodiversity loss, with twelve species listed as endangered and others in decline. Gut microbiota are increasingly recognized as contributors to host adaptation that are capable of influencing stress tolerance, reproduction, and other fitness-related traits. We investigated the role of microbial communities in local adaptation using two populations of from Hawaiian rainforests at 900 m and 1200 m elevation. Microbiome profiling of wild flies by high throughput amplicon sequencing revealed distinct bacterial and fungal communities between sites. Whole-genome resequencing of the two populations identified weak but significant population genetic structure, with evidence of admixture and gene flow. Despite this connectivity, 16 outlier SNPs across 18 genes showed patterns consistent with divergent selection, suggesting localized adaptation. To test microbiome effects on host physiology experimentally, we conducted a fully factorial research design with microbiome inoculations in laboratory-reared flies acclimated to 18 °C (control) or 24 °C (stressful). Flies treated with low-elevation microbiota had higher survival across temperatures, whereas those treated with high-elevation microbiota produced more eggs, indicating microbiome-mediated differences in reproductive investment. Activity levels at 18 °C were higher when flies received microbiota from their native population. Measures of critical thermal maximum (CTmax) and male accessory gland size showed complex interactions among microbiome source, temperature, and fly population. These results indicate that microbes may modulate host thermal tolerance and reproduction in environmentally-dependent and population-specific ways. Our findings suggest that microbiome-host-environment interactions may contribute to both phenotypic plasticity and evolutionary adaptation to enhance resilience to environmental stress, with important implications for conservation in rapidly changing Hawaiian ecosystems.
夏威夷 picture-winged 正经历着生物多样性的迅速丧失,有12个物种被列为濒危物种,其他物种数量也在减少。肠道微生物群越来越被认为是宿主适应性的贡献者,能够影响应激耐受性、繁殖和其他与适应性相关的特征。我们使用来自夏威夷雨林海拔900米和1200米处的两个种群,研究了微生物群落在局部适应性中的作用。通过高通量扩增子测序对野生果蝇进行微生物组分析,结果显示不同地点之间存在明显的细菌和真菌群落。对这两个种群进行全基因组重测序,发现了微弱但显著的种群遗传结构,并有混合和基因流动的证据。尽管存在这种连通性,但18个基因中的16个异常单核苷酸多态性(SNP)显示出与分歧选择一致的模式,表明存在局部适应性。为了通过实验测试微生物组对宿主生理的影响,我们进行了一项全因子研究设计,在适应18°C(对照)或24°C(应激)的实验室饲养果蝇中接种微生物组。用低海拔微生物群处理的果蝇在不同温度下具有更高的存活率,而用高海拔微生物群处理的果蝇产卵更多,这表明微生物组介导了繁殖投入的差异。当果蝇接受来自其本地种群的微生物群时,在18°C时的活动水平更高。临界热最大值(CTmax)和雄性附腺大小的测量结果显示,微生物组来源、温度和果蝇种群之间存在复杂的相互作用。这些结果表明,微生物可能以环境依赖和种群特异性的方式调节宿主的热耐受性和繁殖。我们的研究结果表明,微生物组-宿主-环境相互作用可能有助于表型可塑性和进化适应,以增强对环境压力的恢复力,这对快速变化的夏威夷生态系统中的保护具有重要意义。