# Lymphocytic Choriomeningitis Virus Seroprevalence among Urban Pregnant Women and Newborns, Philadelphia, Pennsylvania, USA, 2021

**Authors:** Dustin D. Flannery, Caitlin M. Cossaboom, Timothy D. Flietstra, Alvaro Zevallos Barboza, Heather H. Burris, Karen M. Puopolo, Aridth Gibbons, Deborah L. Cannon, Inna Krapiunaya, Leanna Sayyad, Katrin S. Sadigh, Kami Smith, Joel M. Montgomery, Trevor Shoemaker, John D. Klena, Scott M. Gordon

PMC · DOI: 10.3201/eid3203.250910 · 2026-03-01

## TL;DR

This study found a low but notable LCMV seroprevalence among urban pregnant women in Philadelphia, highlighting the risk of rodent-borne infections during pregnancy.

## Contribution

The study provides new seroprevalence data for LCMV in urban pregnant populations and identifies risk factors like neighborhood deprivation.

## Key findings

- LCMV IgG seroprevalence was 2.4% in high-risk and 2.7% in randomly selected pregnant women.
- Seroprevalence varied by hospital site, maternal race or ethnicity, and neighborhood deprivation level.
- All maternal LCMV IgM tests were negative, and 37 fetuses with neurologic malformations were LCMV seronegative.

## Abstract

Lymphocytic choriomeningitis virus (LCMV) is a globally distributed rodentborne pathogen that can cause severe congenital infections. We conducted a retrospective cross-sectional seroepidemiologic study using remnant serum samples from pregnant women and newborns at 2 hospitals in Philadelphia, Pennsylvania, USA. We tested samples for LCMV IgG and IgM in 3 phases: a high-risk group determined by neighborhood deprivation index scores, a random sample of all birthing women, and a group with prenatally diagnosed neurologic malformations. We found LCMV IgG seroprevalence was 2.4% among 700 high-risk and 2.7% among 300 randomly selected pregnant women. Seroprevalence varied by hospital site, maternal race or ethnicity, and neighborhood deprivation level. All seropositive maternal samples were IgM-negative. Thirty-seven pregnant women carrying fetuses with neurologic malformations were seronegative. Our findings highlight the risk for LCMV exposure in urban settings and emphasize the need for pregnant women to avoid contact with rodents to prevent this rare but serious congenital infection.

## Full-text entities

- **Genes:** DDIT3 (DNA damage inducible transcript 3) [NCBI Gene 1649] {aka AltDDIT3, C/EBPzeta, CEBPZ, CHOP, CHOP-10, CHOP10}
- **Diseases:** fetal neurologic disease (MESH:D005315), open neural tube defect (MESH:D009436), Zika (MESH:D000071243), Listeria (MESH:D008088), ventriculomegaly (MESH:D006849), retinal hemorrhage (MESH:D012166), abnormal cerebral ventricle (MESH:D002551), encephalocele (MESH:D004677), syphilis (MESH:D013587), fetal death (MESH:D005313), hydrops (MESH:D004487), Dandy-Walker malformation (MESH:D003616), varicella (MESH:D002644), congenital disease (MESH:D030342), fetal brain anomalies (MESH:D000013), sexually transmitted infections (MESH:D012749), cerebral calcification (MESH:D002114), neurodevelopmental problems (MESH:D019973), posterior fossa cyst (MESH:D015192), corpus callosum abnormalities (MESH:D061085), Treponema (MESH:C531782), congenital neurologic malformations (MESH:D009421), rubella (MESH:D012409), Infections (MESH:D007239), congenital malformations (OMIM:163000), lipomyelomeningocele (MESH:C537030), intracranial calcifications (MESH:C537905), intracranial cystic lesion (MESH:D052177), congenital pathogen (MESH:D008209), septum pellucidum (MESH:C535562), LCMV (MESH:D008216), Birth Defects (MESH:D000014), Toxoplasma (MESH:D014125), cytomegalovirus (MESH:D003586), intellectual disability (MESH:D008607), myelomeningocele (MESH:D008591), HPO (MESH:D001734), chorioretinitis (MESH:D002825), microcephaly (MESH:D008831)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], LCMV [taxon 11623], Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC13016026/full.md

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Source: https://tomesphere.com/paper/PMC13016026