Department of Infection Biology and Microbiomes, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.
NIHR Health Protection Research Unit in Gastrointestinal Infections, Liverpool, UK.
BMC Microbiol. 2023 Nov 18;23(1):354. doi: 10.1186/s12866-023-03098-z.
The immunogenicity and effectiveness of oral rotavirus vaccines (ORVs) against severe rotavirus-associated gastroenteritis are impaired in low- and middle-income countries (LMICs) where the burden of disease is highest. Determining risk factors for impaired ORV response may help identify strategies to enhance vaccine effectiveness. In this study, we use metagenomic sequencing to provide a high-resolution taxonomic analysis of stool samples collected at 6 weeks of age (coinciding with the first ORV dose) during a prospective study of ORV immunogenicity in India and Malawi. We then analyse the functional capacity of the developing microbiome in these cohorts. Microbiome composition differed significantly between countries, although functional capacity was more similar than taxonomic composition. Our results confirm previously reported findings that the developing microbiome is more diverse in taxonomic composition in ORV non-seroconverters compared with seroconverters, and we additionally demonstrate a similar pattern in functional capacity. Although taxonomic or functional feature abundances are poor predictors of ORV response, we show that skews in the direction of associations within these microbiome data can be used to identify consistent markers of ORV response across LMIC infant cohorts. We also highlight the systemic under-representation of reference genes from LMICs that limit functional annotation in our study (7% and 13% annotation at pathway and enzyme commission level, respectively). Overall, higher microbiome diversity in early life may act as marker for impaired ORV response in India and Malawi, whilst a holistic perspective of functional capacity may be hidden in the "dark matter" of the microbiome.
口服轮状病毒疫苗(ORV)在疾病负担最高的中低收入国家(LMICs)中对严重轮状病毒相关胃肠炎的免疫原性和有效性受损。确定 ORV 反应受损的风险因素可能有助于确定增强疫苗有效性的策略。在这项研究中,我们使用宏基因组测序对印度和马拉维进行的 ORV 免疫原性前瞻性研究中,在 6 周龄(恰逢第一剂 ORV 时)收集的粪便样本进行高分辨率分类分析。然后,我们分析这些队列中发育中微生物组的功能能力。尽管功能能力比分类组成更相似,但国家之间的微生物组组成差异显着。我们的研究结果证实了先前报道的发现,即与血清转化者相比,ORV 非血清转化者的发育中微生物组在分类组成上具有更多的多样性,我们还证明了功能能力存在类似的模式。尽管分类或功能特征丰度是 ORV 反应的不良预测指标,但我们表明,这些微生物组数据中关联方向的倾斜可以用于识别跨越 LMIC 婴儿队列的 ORV 反应的一致标志物。我们还强调了限制我们研究中功能注释的来自 LMIC 的参考基因的系统代表性不足(分别在途径和酶委员会级别为 7%和 13%的注释)。总体而言,生命早期更高的微生物组多样性可能是印度和马拉维 ORV 反应受损的标志物,而功能能力的整体观点可能隐藏在微生物组的“暗物质”中。