Nanopore-based metagenomics analysis reveals microbial presence in amniotic fluid: A prospective study.

BACKGROUND

Current research on amniotic fluid (AF) microbiota yields contradictory data, necessitating an accurate, comprehensive, and scientifically rigorous evaluation.

OBJECTIVE

This study aimed to characterise the microbial features of AF and explore the correlation between microbial information and clinical parameters.

METHODS

76 AF samples were collected in this prospective cohort study. Fourteen samples were utilised to establish the nanopore metagenomic sequencing methodology, whereas the remaining 62 samples underwent a final statistical analysis along with clinical information. Negative controls included the operating room environment (OE), surgical instruments (SI), and laboratory experimental processes (EP) to elucidate the background contamination at each step. Simultaneously, levels of five cytokines (IL-1β, IL-6, IL-8, TNF-α, MMP-8) in AF were assessed.

RESULTS

Among the 62 AF samples, microbial analysis identified seven without microbes and 55 with low microbial diversity and abundance. No significant clinical differences were observed between AF samples with and without microbes. The correlation between microbes and clinical parameters in AF with normal chromosomal structure revealed noteworthy findings. In particular, the third trimester exhibited richer microbial diversity. demonstrated higher detection rates and relative abundance in the second trimester and Preterm Birth (PTB) groups. in the PTB group exhibited elevated detection frequencies and relative abundance. Notably, negatively correlated with activated partial thromboplastin time (APTT) (r = -0.329,  = 0.016), while showed positive correlations with APTT (r = 0.395,  = 0.003). Furthermore, negatively correlated with birth weight (r = -0.297,  = 0.034).

CONCLUSION

Most AF samples exhibited low microbial diversity and abundance. Certain microbes in AF may correlate with clinical parameters such as gestational age and PTB. However, these associations require further investigation. It is essential to expand the sample size and undertake more comprehensive research to elucidate the clinical implications of microbial presence in AF.