Subramanian Poorani, Romero-Soto Hector N, Stern David B, Maxwell George L, Levy Shira, Hourigan Suchitra K
National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, United States.
Women's Service Line, Inova Health System, Falls Church, Virginia, United States.
medRxiv. 2023 Nov 13:2023.11.13.23298307. doi: 10.1101/2023.11.13.23298307.
Cesarean section delivery is associated with altered early-life bacterial colonization and later adverse inflammatory and immune health outcomes. Although gut bacteriophages can alter gut microbiome composition and impact host immune responses, little is known about how delivery mode impacts bacteriophage colonization over time. To begin to address this we examined how delivery mode affected bacteriophage colonization over the first two years of life.
Shotgun metagenomic sequencing was conducted on 272 serial stool samples from 55 infants, collected at 1-2 days of life and 2, 6, 12 and 24 months. 33/55 (60%) infants were born by vaginal delivery. DNA viruses were identified, and by host inference, 94% of the viral sequences were found to be bacteriophages. Alpha diversity of the virome was increased in vaginally delivered infants compared to cesarean section delivered infants at 2 months (Shannon index, p=0.022). Beta diversity significantly differed by delivery mode at 2, 6, and 12 months when stratified by peripartum antibiotic use (Bray-Curtis dissimilarity, all p<0.05). Significant differentially abundant predicted bacteriophage hosts by delivery mode were seen at all time points. Moreover, there were differences in predicted bacteriophage functional gene abundances up to 24 months by delivery mode. Many of the functions considered to play a role in host response were increased in vaginal delivery.
Clear differences in bacteriophage composition and function were seen by delivery mode over the first two years of life. Given that phages are known to affect host immune response, our results suggest that future investigation into how delivery mode may lead to adverse inflammatory outcomes should not only include bacterial microbial colonization but also the potential role of bacteriophages and transkingdom interactions.
剖宫产与早期细菌定植改变以及后期不良的炎症和免疫健康结局相关。尽管肠道噬菌体可改变肠道微生物群组成并影响宿主免疫反应,但关于分娩方式如何随时间影响噬菌体定植却知之甚少。为了开始解决这个问题,我们研究了分娩方式如何在生命的头两年影响噬菌体定植。
对55名婴儿的272份系列粪便样本进行了鸟枪法宏基因组测序,这些样本在出生后1 - 2天以及2、6、12和24个月时采集。33/55(60%)的婴儿通过阴道分娩出生。鉴定出了DNA病毒,通过宿主推断,发现94%的病毒序列为噬菌体。与剖宫产出生的婴儿相比,阴道分娩的婴儿在2个月时病毒群落的α多样性增加(香农指数,p = 0.022)。在按围产期抗生素使用分层时,2、6和12个月时的β多样性因分娩方式而有显著差异(布雷 - 柯蒂斯差异度,所有p < 0.05)。在所有时间点都观察到了按分娩方式显著不同的预测噬菌体宿主丰度。此外,按分娩方式在24个月时预测的噬菌体功能基因丰度也存在差异。许多被认为在宿主反应中起作用的功能在阴道分娩中增加。
在生命的头两年,按分娩方式观察到噬菌体组成和功能存在明显差异。鉴于已知噬菌体可影响宿主免疫反应,我们的结果表明,未来关于分娩方式如何导致不良炎症结局的研究不仅应包括细菌微生物定植,还应包括噬菌体的潜在作用和跨界相互作用。