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Updated: Sep 7, 2026

Modeling Ascending Vaginal Infection, Preterm Birth, and Neonatal Morbidity in Mice
Published on: October 10, 2025
Factors determining pathogenicity of variants of ECHO 9 virus for newborn mice
Abstract:
While some strains of ECHO 9 virus were found to be completely incapable of multiplying in newborn mice or even of being adsorbed by their tissues (e.g., the prototype Hill strain), other naturally occurring strains readily multiplied even after inoculation of as little as 3 TCD(50) of virus. With the multiplying strains, the infection remained clinically inapparent except after inoculation of very large doses, usually in the range of 10(5) to 10(7.5) TCD(50). Investigation of the question why such large doses were required to produce paralysis indicated that for paralysis to occur virus multiplication had to reach a level of 10(8) TCD(50) or more within 4 days after inoculation of mice less than 1 day old. The reason for this was found in the fact that at 5 to 6 days of age the mice lost their susceptibility to paralysis even when multiplication was capable of progressing to the indicated high level. Thus, speed of multiplication and extent of muscle involvement before the 5th day of life were the determining factors. Passage in tissue culture had no effect except to yield a larger dose for inoculation, while serial propagation in mice resulted in a gradual enrichment of virus particles capable of more rapid multiplication in mice and in a concurrent greater paralytogenic activity of smaller doses.
Insights
ECHO 9 virus strains vary in newborn mouse infectivity. Rapid multiplication within 4 days is crucial for paralysis, as mice lose susceptibility after 5-6 days.
Area of Science:
- Virology
- Pathogenesis
- Animal Models
Background:
- ECHO 9 virus exhibits variable pathogenicity in newborn mice.
- Some strains are non-infectious, while others replicate efficiently.
Purpose of the Study:
- To investigate the factors determining ECHO 9 virus-induced paralysis in newborn mice.
- To understand the role of viral replication speed and host susceptibility.
Main Methods:
- Inoculation of newborn mice with different ECHO 9 virus strains and doses.
- Monitoring clinical signs, viral multiplication, and host age-related susceptibility.
- Serial propagation of virus in mice.
Main Results:
- High viral titers (≥10(8) TCD(50)) within 4 days are necessary for paralysis.
- Mice older than 5-6 days lose susceptibility to paralysis.
- Serial mouse passage enriches for faster-replicating, more paralytogenic strains.
Conclusions:
- Paralysis is dependent on rapid viral replication and host susceptibility window in early life.
- Viral strain adaptation through serial mouse passage enhances paralytogenic potential.

