González Roxana, Henríquez-Castillo Carlos, Lohrmann Karin B, Romero María Soledad, Ramajo Laura, Schmitt Paulina, Brokordt Katherina
Laboratorio de Fisiología y Genética Marina (FIGEMA), Departamento de Acuicultura, Facultad de Ciencias del Mar, Universidad Católica del Norte, Larrondo 1281, Coquimbo 1781421, Chile.
Centro de Estudios Avanzados en Zonas Áridas (CEAZA), Larrondo 1281, Coquimbo 1781421, Chile.
Microorganisms. 2022 Nov 25;10(12):2330. doi: 10.3390/microorganisms10122330.
Despite the great importance of gills for bivalve mollusks (respiration, feeding, immunity), the microbiota associated with this tissue has barely been characterized in scallops. The scallop is an important economic resource that is cultivated in areas where coastal upwelling is intensifying by climate change, potentially affecting host-microbiota interactions. Thus, we first characterized the bacterial community present in gills from cultivated scallops (by 16S rRNA gene amplicon sequencing) and assessed their stability and functional potential in animals under farm and laboratory conditions. Results showed that under both conditions the gill bacterial community is dominated by the phylum Campylobacterota (57%), which displays a chemoautotrophic potential that could contribute to scallop nutrition. Within this phylum, two phylotypes, namely symbionts A and B, were the most abundant; being, respectively, taxonomically affiliated to symbionts with nutritional functions in mussel gills, and to uncultured bacteria present in coral mucus. Additionally, in situ hybridization and scanning electron microscopy analyses allowed us to detect these symbionts in the gills of . Given that shifts in upwelling phenology can cause disturbances to ecosystems, affecting bacteria that provide beneficial functions to the host, we further assessed the changes in the abundance of the two symbionts (via qPCR) in response to a simulated upwelling intensification. The exposure to combined decreasing values in the temperature, pH, and oxygen levels (upwelling conditions) favored the dominance of symbiont B over symbiont A; suggesting that symbiont abundances are modulated by these environmental changes. Overall, results showed that changes in the main Campylobacterota phylotypes in response to upwelling intensification could affect its symbiotic function in under future climate change scenarios. These results provide the first insight into understanding how scallop gill-microbial systems adapt and respond to climate change stressors, which could be critical for managing health, nutrition, and scallop aquaculture productivity.
尽管鳃对于双壳贝类至关重要(用于呼吸、摄食、免疫),但与该组织相关的微生物群在扇贝中几乎未得到表征。扇贝是一种重要的经济资源,在因气候变化导致沿海上升流加剧的地区进行养殖,这可能会影响宿主与微生物群的相互作用。因此,我们首先对养殖扇贝鳃中存在的细菌群落进行了表征(通过16S rRNA基因扩增子测序),并评估了它们在养殖和实验室条件下动物体内的稳定性和功能潜力。结果表明,在这两种条件下,鳃细菌群落均以弯曲杆菌门为主(57%),该门具有化学自养潜力,可能有助于扇贝的营养。在这个门内,两种系统发育型,即共生体A和B最为丰富;它们在分类学上分别隶属于在贻贝鳃中具有营养功能的共生体,以及存在于珊瑚黏液中的未培养细菌。此外,原位杂交和扫描电子显微镜分析使我们能够在扇贝的鳃中检测到这些共生体。鉴于上升流物候的变化会导致生态系统受到干扰,影响为宿主提供有益功能的细菌,我们进一步评估了两种共生体丰度的变化(通过定量PCR)对模拟上升流增强的响应。暴露于温度、pH值和氧气水平的综合下降值(上升流条件)有利于共生体B相对于共生体A占优势;这表明共生体丰度受这些环境变化的调节。总体而言,结果表明,在未来气候变化情景下,弯曲杆菌门主要系统发育型对上升流增强的响应变化可能会影响其在扇贝中的共生功能。这些结果为理解扇贝鳃 - 微生物系统如何适应和应对气候变化压力源提供了首个见解,这对于管理扇贝的健康、营养和水产养殖生产力可能至关重要。