Westaway Jacob A F, Huerlimann Roger, Miller Catherine M, Kandasamy Yoga, Norton Robert, Rudd Donna
James Cook University, 1 McGregor Road, Smithfield, QLD, 4878, Australia.
James Cook University, 1 James Cook Dr, Douglas, QLD, 4811, Australia.
Matern Health Neonatol Perinatol. 2021 Mar 8;7(1):11. doi: 10.1186/s40748-021-00131-9.
The premature infant gut microbiome plays an important part in infant health and development, and recognition of the implications of microbial dysbiosis in premature infants has prompted significant research into these issues. The approaches to designing investigations into microbial populations are many and varied, each with its own benefits and limitations. The technique used can influence results, contributing to heterogeneity across studies. This review aimed to describe the most common techniques used in researching the preterm infant microbiome, detailing their various limitations. The objective was to provide those entering the field with a broad understanding of available methodologies, so that the likely effects of their use can be factored into literature interpretation and future study design. We found that although many techniques are used for characterising the premature infant microbiome, 16S rRNA short amplicon sequencing is the most common. 16S rRNA short amplicon sequencing has several benefits, including high accuracy, discoverability and high throughput capacity. However, this technique has limitations. Each stage of the protocol offers opportunities for the injection of bias. Bias can contribute to variability between studies using 16S rRNA high throughout sequencing. Thus, we recommend that the interpretation of previous results and future study design be given careful consideration.
早产婴儿的肠道微生物群在婴儿健康和发育中起着重要作用,对早产婴儿微生物群失调影响的认识促使人们对这些问题进行了大量研究。设计微生物种群研究的方法多种多样,每种方法都有其自身的优点和局限性。所使用的技术会影响结果,导致不同研究之间存在异质性。本综述旨在描述研究早产婴儿微生物群时最常用的技术,并详细说明其各种局限性。目的是让该领域的新手广泛了解可用的方法,以便在文献解读和未来研究设计中考虑使用这些方法可能产生的影响。我们发现,尽管有许多技术用于表征早产婴儿的微生物群,但16S rRNA短扩增子测序是最常用的。16S rRNA短扩增子测序有几个优点,包括高准确性、可发现性和高通量能力。然而,这项技术也有局限性。该方案的每个阶段都可能引入偏差。偏差会导致使用16S rRNA高通量测序的不同研究之间存在差异。因此,我们建议在解读以往结果和设计未来研究时应仔细考虑。