According to a recently published study in Science
translation medicine, the placental microbiome might be associated with
pre-term birth less than 37 weeks, and a remote history of antenatal infection in the
first trimester. In this study, which was based on placental collection from
320 subjects, the investigators analyzed the human placental microbiome and
provided details on microorganisms present, their probable functions and
overall structure of placental microbial community.
Due to recent advances in sequencing technologies, a large
number of studies have looked at the structure, function and diversity of human
microbiome across multiple body sites in both healthy and disease states.
Studies conducted on newborn babies have shown that the gut microbiome of
neonates show complex microbial communities in the first few weeks of life.
However, the source of these microbes and the time at which the infants acquire
those is not yet known. It has also been shown that gut microbiome of full-term
infants is different from that of low birth weight infants during the first few
weeks of life, indicating that the infants might acquire these microbes in
utero through a common source and that the composition of the microbiome might
change with length of gestation. The authors of this study hypothesized that
the human placenta could be that source.
The investigators of this study used whole-genome shotgun
(WGS), a technique involving sequencing long strands of DNA, to determine the
taxonomic classification of placental microbiome. They noted that several
species of oral microbiome were detected in the placenta. These included Prevotella tannerae and non-pathogenic Neisseria species. They also found high
abundance of E. coli in most
individuals. The authors further compared the microbial community observed in
placenta with those reported from other body sites (oral, stool, skin, nasal
and vaginal) from non-pregnant healthy subjects using publicly available HMP
(Human Microbiome Project) data. They observed that placental microbiota showed
similarity to oral phyla only. Furthermore, the relative abundance of metabolic
pathways was different in placenta when compared to other body sites. For
example, the metabolism of co-factors and vitamins showed a greater relative
abundance in placental functional gene profile.
The authors found a statistically significantly association
between placental microbiome and pre-term birth less than 37 weeks. The researchers
also identified various placental taxa whose abundance was enriched or
diminished among women who experienced pre-term births. They also observed a
statistically significant association between placental microbial community and
a remote history of antepartum infection. Streptococcus
and Acinetobacter were found to be enriched in women with a remote history
of antepartum infection.
In conclusion, Aagaard and colleagues show that in contrast
to the widespread believe that intra-uterine environment is sterile, human
placenta harbors a variety of non-pathogenic commensal species, and the overall
microbiome profile of placenta is most similar to that of non-pregnant human
oral cavity. They also observed correlation between placental microbiome and
pre-term birth and a history of antenatal infection.
The authors also noted several limitations of the study. The
authors compared the placental microbiome with microbiome of other body sites
from non-pregnant subjects. Moreover, the authors were not able to characterize
the placental microbiome in early preterm gestation in women who had a full
term delivery. Still, the study presents some interesting findings and
indicates towards an essential role of placental microbiota in human pregnancy.
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