# Establishing the roles of lncRNAs in placental infection by Listeria monocytogenes

> **NIH NIH R03** · OHIO STATE UNIVERSITY · 2021 · $78,000

## Abstract

PROJECT SUMMARY
The placental barrier is an efficient cell barrier that protects the fetus from most infections. However, some
pathogens such as the Gram-positive bacterium Listeria monocytogenes (Lm) have evolved virulence
mechanisms to breach this barrier. Infection and inflammation of the fetoplacental unit have devastating
consequences including preterm birth, intrauterine growth restriction, fetal death, or severe infection of the
neonate with long-term neurological sequelae. Cytotrophoblasts (CYT) and the syncytiotrophoblast (SYN) are
fetal epithelial cells that form the placental barrier. The multinucleated SYN is a true syncytium that is
generated upon fusion of underlying CYT and is known to be resistant to microbes. However, we lack
knowledge regarding the defense mechanisms of the placental barrier and know little about the mechanisms
that allow some pathogens to overcome this barrier. To address these gaps in our knowledge, we study the
interaction of Lm with primary CYT/SYN isolated from healthy, term human placentas. RNA sequencing (RNA-
seq, n=3) of infected versus non-infected primary culture of CYT/SYN established that there is a transcriptional
inflammatory response 5 h post-infection. Pathway analysis revealed several inflammatory pathways
upregulated in the presence of Lm and a cytokine array confirmed that the transcriptional response was
paralleled with a significant increase in the production of cytokines. Importantly, several long non-coding RNAs
(lncRNAs) transcripts were significantly upregulated after infection with Lm. However, the roles of these
lncRNAs remain unknown. LncRNAs play a critical role in regulating the expression of immune and
inflammatory genes in infected macrophages, but they have been understudied in general and in particular in
the context of infection of placental cells. This work will test the hypothesis that 4 selected lncRNAs affect
placental cell susceptibility to Lm infection and/or their transcriptional and inflammatory responses to Lm. Aim 1
will establish the role of the lncRNAs in placental cell susceptibility to Lm infection. The expression of the
lncRNAs will be modulated and the resulting susceptibility to infection by Lm will be monitored for up to 24 h.
Aim 2 will establish the roles of the lncRNAS in the placental cell transcriptome and in the production of
cytokines during infection. The expression of selected lncRNAs will be silenced, cell culture supernatants will
be subjected to a cytokine array and RNA-seq will be performed on cell lysates. At the completion of this work,
we will have established the roles of the lncRNAs in the susceptibility of cells that form the human placental
barrier to Lm infection, the production of cytokines, and the cell transcriptional response to infection. These
data will allow us to develop a new project that will focus on establishing the roles and mechanisms of action of
the identified lncRNAs in the placental immune defense against infections. In ...

## Key facts

- **NIH application ID:** 10092106
- **Project number:** 5R03AI149371-02
- **Recipient organization:** OHIO STATE UNIVERSITY
- **Principal Investigator:** Stephanie M M Seveau
- **Activity code:** R03 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2021
- **Award amount:** $78,000
- **Award type:** 5
- **Project period:** 2020-02-01 → 2022-01-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10092106

## Citation

> US National Institutes of Health, RePORTER application 10092106, Establishing the roles of lncRNAs in placental infection by Listeria monocytogenes (5R03AI149371-02). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10092106. Licensed CC0.

---

*[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*
