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A Murine Model of Group B Streptococcus Vaginal Colonization
Published on: November 16, 2016
Bacterial and host factors affecting acquisition of Streptococcus pneumoniae in a murine model
Daniel P Fecko1, Cindy Wu1, Jeffrey N Weiser1
1Department of Microbiology, New York University Grossman School of Medicine, New York, New York, USA.
Abstract:
Initial acquisition is a critical step in the establishment of colonization that in turn enables transmission to new hosts and potentially leads to invasive disease. Here, we studied host and bacterial factors affecting acquisition, as distinct from those affecting colonization density, using Streptococcus pneumoniae (Spn) in a mouse model. Acquisition was quantified using nasal inocula of limiting size to determine the proportion of hosts infected, as well as the median infectious dose. Infant mice (<7 days of age) were highly susceptible to acquisition (ID50<30 CFU) compared with adults (>6 weeks of age), with rates declining with increasing host age. Prior influenza A infection greatly increased acquisition in adults. Expression of Spn capsule was also an important factor influencing acquisition in adults, with less of a role for the highly susceptible infants. Prior Spn colonization with a heterologous or homologous strain effectively blocked acquisition in infants by completely occupying the upper respiratory tract niche. Immunity due to prior colonization and nasal microbiota were not found to be factors limiting acquisition. Together, our findings show how high carriage rates of encapsulated Spn during early life and in the setting of recent viral infection could be explained by effects on acquisition. Our study describes an approach for studying factors that specifically affect the step of acquisition.
Insights
Host age, prior influenza A infection, and Streptococcus pneumoniae (Spn) capsule expression significantly impact bacterial acquisition. Early-life colonization effectively blocks Spn acquisition in infant mice.
Area of Science:
- Microbiology
- Immunology
- Infectious Disease Epidemiology
Background:
- Initial acquisition is crucial for bacterial colonization, host transmission, and potential disease.
- Understanding factors influencing acquisition is key to controlling pathogen spread.
Purpose of the Study:
- To investigate host and bacterial factors specifically affecting Streptococcus pneumoniae (Spn) acquisition, distinct from colonization density.
- To elucidate mechanisms underlying high Spn carriage rates in early life and during viral infections.
Main Methods:
- Utilized a mouse model to quantify Spn acquisition using limiting nasal inocula and determining median infectious dose (ID50).
- Assessed the impact of host age, prior influenza A infection, Spn capsule expression, and prior Spn colonization on acquisition rates.
Main Results:
- Infant mice (<7 days) showed high susceptibility to Spn acquisition (ID50 <30 CFU), declining with age.
- Prior influenza A infection significantly increased acquisition in adult mice.
- Spn capsule expression was important for adult acquisition, less so for infants. Prior Spn colonization completely blocked acquisition in infants.
Conclusions:
- Host age and viral infections influence Spn acquisition, explaining high carriage rates in early life and post-viral infection.
- Spn capsule and prior colonization are key factors modulating acquisition, with prior colonization acting as a potent blocking mechanism in infants.
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